Brazilian Society for Angiology and Vascular Surgery guidelines on abdominal aortic aneurysm

Abstract

The Brazilian Society of Angiology and Vascular Surgery, through the Guidelines Project, presents new Abdominal Aortic Aneurysm Guidelines, on the subject of care for abdominal aortic aneurysm patients. Its development prioritized descriptive guidelines, using the EMBASE, LILACS, and PubMed databases. References include randomized controlled trials, systematic reviews, meta-analyses, and cohort studies. Quality of evidence was evaluated by a pair of coordinators, aided by the RoB 2 Cochrane tool and the Newcastle Ottawa Scale forms. The subjects include juxtarenal aneurysms, infected aneurysms, and new therapeutic techniques, especially endovascular procedures. The current version of the guidelines include important recommendations for the primary topics involving diagnosis, treatment, and follow-up for abdominal aortic aneurysm patients, providing an objective guide for medical practice, based on scientific evidence and widely available throughout Brazil.

Keywords:  aortic aneurysm; aorta; aortic disease; endovascular procedures

Resumo

A Sociedade Brasileira de Angiologia e Cirurgia Vascular, por meio do projeto Diretrizes, apresenta as novas Diretrizes de Aorta Abdominal, referentes aos cuidados de pacientes com aneurisma de aorta abdominal. Para sua elaboração, foram priorizadas diretrizes descritivas, utilizando as bases EMBASE, LILACS e PubMed. As referências incluem ensaios clínicos randomizados, revisões sistemáticas, metanálises e estudos de coorte. A qualidade das evidências foi examinada por uma dupla de coordenadores, com auxílio da ferramenta RoB 2 da Colaboração Cochrane e dos formulários da Newcastle Ottawa Scale. Aneurismas justarrenais, infectados e novas técnicas terapêuticas, principalmente no âmbito endovascular, estão entre os temas estudados. A versão atual das Diretrizes apresenta importantes recomendações para os principais itens que envolvem o diagnóstico, tratamento e acompanhamento de pacientes com aneurisma de aorta abdominal, oferecendo um guia objetivo para prática médica, construído a partir de evidências científicas e amplamente acessível em todo o território nacional.

Palavras-chave:  aneurisma da aorta; aorta, doenças da aorta; procedimentos endovasculares

INTRODUCTION

The Guidelines Project was established in 2002, by the combined efforts of the Federal Medical Council (CFM) and the Brazilian Medical Association (AMB).¹ The Guidelines are a set of medical information about a given subject, organized by and based on high-quality scientific evidence. The intent at the time, and the project's guiding star to this day, was to provide information that could help medical professionals make diagnostic, therapeutic, and follow-up decisions for their patients.

In 2016, the Brazilian Ministry of Health published a document discussing the importance of medical guidelines and suggesting a methodology to enable the production of documents characterized by high scientific quality.² The accumulated experience and the development of standard procedure protocols seem to have a direct influence on improved results, lowering morbidity and mortality for patients.

AMB maintains a website (http://www.projetodiretrizes.org.br/) where physicians throughout Brazil can read Guidelines divided by topic and medical specialty societies. One of the guiding principles of this project is to increase the accessibility and dissemination of the documents produced, and the AMB website makes guidelines available free of charge. The Brazilian Society of Angiology and Vascular Surgery (SBACV) is a very representative group, as expressed by the number of members of the organization—in 2022, there were 4,232 associates. Considering the Guidelines require constant updates to continuously provide specialists with information and security, this year, SBACV has updated and added new guidelines to its library. The goal is to provide a work instrument capable of assisting clinical reasoning, but also preserves physician autonomy, as described in the CFM Code of Medical Ethics.

Abdominal aortic aneurysms (AAA) are the most frequent form of aortic aneurysm. The disease increases with age, and is most prevalent among patients over 60. Smoking is one of the primary risk factors for its growth and rupture, its most feared complication.³ When they occur, ruptures are lethal in most cases. In Brazil, it is estimated that between 2000 and 2016, ruptures were the direct cause of 38,000 deaths, representing 55 percent of all aortic aneurysm-related mortality.⁴

Objective

To develop new Abdominal Aortic Aneurysm Guidelines, with well-defined methods and widely disseminated in society.

METHODS

To develop the Abdominal Aortic Aneurysm Guidelines, the SBACV Scientific Department chose a group of authors working in clinical practice with quality scientific publications on the subject. The previous Guidelines, published in 2015, were rewritten to answer new questions and discuss previously uncovered topics.⁵ The subjects include juxtarenal aneurysms, infected aneurysms, and new therapeutic techniques, especially endovascular procedures.

Prior to writing the guidelines themselves, the group gathered and took classes on how to sort and assess evidence quality with Prof. Dr. Wanderley Marques Bernardo, one of the authors of the Guidelines Project, who has vast experience and is dedicated to working with groups such as this. Descriptive guidelines presenting a synthetic recommendation were prioritized. The following reference databases were consulted in writing these guidelines: EMBASE, LILACS, and PubMed.

The EMBASE (Elsevier) database lists indexed periodicals, conference abstracts, and technical notes, among others. In Brazil, it is available free of charge through the CAPES journal portal. The PICO process (P: Population; I: Intervention; C: Comparators; O: Outcome) was developed based on that website. The list of questions or subjects was developed in advance by the group coordinator, while the authors provided input into how the writing process would be divided. Each author wrote one section, or two at the most.

The topics addressed in this document are:

1. Methods

2. Definition

3. Epidemiology and screening

4. Etiology, pathophysiology and risk factors

5. Clinical status

6. Diagnosis

7. Treatment

a. Clinical indications, regulatory aspects, choice of devices

b. Conventional open treatment

c. Endovascular treatment of infrarenal aneurysms

d. Endovascular treatment of juxtarenal aneurysms

8. Clinical follow-up

9. Postoperative complications

a. Graft infection

b. Endoleak

10. Ruptured abdominal aortic aneurysm

11. Inflammatory aneurysm

12. Aneurysms in women

Three primary articles were used as our starting point: the last version of the Brazilian Guidelines on Aortic Aneurysm (2015),⁵ the European Society for Vascular Surgery (ESVS) Clinical Practice Guidelines (2019),⁶ and the Society for Vascular Surgery practice guidelines (2018).⁷ Articles were also selected based on the following publication categories: randomized controlled trials, systematic reviews, meta-analyses, and cohort studies. Neither case series, case reports, nor experimental trials were accepted as sources of evidence.

Evidence quality was examined by a pair of coordinators chosen in advance. Randomized controlled trials were evaluated using the RoB 2 Cochrane tool.⁸ Cohort studies, systematic reviews, and meta-analyses were used to supplement the responses, while evidence quality was assessed using the New Castle Ottawa Scale.⁹

Guideline quality is variable and can be audited using specific instruments. Despite the existence of several assessment protocols, Appraisal of Guidelines for Research and Evaluation (AGREE) is the most frequently used instrument to assess guidelines.¹⁰ Assessment comprises six domains: scope and purpose, stakeholder involvement, rigor of development, clarity of presentation, applicability, and editorial independence. Scores above 80 percent are acceptable for guidelines. Only four abdominal aortic aneurysm guidelines achieve that score (European Society of Cardiology, Society for Vascular Surgery, European Society of Vascular Surgery, and National Institute of Health).⁶,⁷,¹¹,¹²

Evidently, each guideline covering a given subject or pathology must take into consideration the economic situation of their region or country. Cost-benefit analyses and local surveys for each intervention are necessary, as well as assessing the characteristics of the local health system. The recommendations from one guideline may apply at some centers and not others, but can guide treatment even in suboptimal situations.

Development of this guideline was approved by Plataforma Brasil and the Research Ethics Committee under CAAE number 62177722.2.0000.0068. SBACV was registered as a sponsor of scientific research for the first time in its history.

DEFINITION

Aortic aneurysms comprise a dilation of two standard deviations or 50 percent greater than the expected diameter for an artery in the region. This guideline discusses infrarenal aneurysms and, therefore, dilations greater than 3 cm of diameter. Diameter measurement techniques are widely discussed, but in order to consider the greatest dilation, antero-posterior and/or transversal measurements are accepted, from the external aortic wall, via abdominal ultrasonography or computed tomography.⁶,⁷

Definitions of terms such as hostile neck, short neck and juxtarenal are also widely discussed, possibly due to advancements in endovascular repair techniques, as well as in instructions for use (IFUs) for endografts.¹³ For standardization purposes, this guidelines classifies as juxtarenal or pararenal aneurysms those extending to a renal artery but not involving it, or with neck below 1 cm, also known as short neck or hostile neck.⁶,⁷

A hostile neck, in turn, has at least one of the following characteristics: infrarenal neck longer than 28 mm, infrarenal angle smaller than 60º, neck length < 1.5 cm, thrombus thickness greater than 50 percent of circumference, conical neck (tapering greater than 0,2 cm in a 1 cm infrarenal segment), bosselation (growth greater than 0.3 cm in the initial 1.5 cm infrarenal segment).¹³,¹⁴

Taking into account the anatomical treatment frontiers explored over the last decade, this guideline considered including open and endovascular repair of juxtarenal, infrarenal, and hostile neck aneurysms, following the example of recent international guidelines.⁶,⁷

EPIDEMIOLOGY AND SCREENING

The current prevalence of AAA in men over the age of 65 is 1.7 percent in the Swedish population screening study (in addition, 0.5 percent had already been diagnosed),¹⁵ 1.3 percent in the British screening study,¹⁶ 3 percent in Denmark (men aged 65-74),¹⁷ and 5 percent in the U.S., where screening was only made available for smokers.¹⁸ In Brazil, there are no population-level screening data. Prevalence was four to six times higher among men than women in Brazilian and international studies,⁴,¹⁹,²⁰ and a 2016 meta-analysis estimated a 0.7 percent prevalence rate among women over the age of 60.¹⁹

In developed countries, the prevalence and incidence of AAA has decreased significantly in recent decades, which can partly be attributed to lower rates of smoking.⁶,¹⁵,²¹,²² According to an analysis of Datasus data published in 2020, AAA mortality in Brazil increased between 2000 and 2008, followed by a decrease between 2008 and 2016.⁴ Brazil had one of the highest rates of smoking cessation between 1990 and 2015, which may partly explain the decrease.⁴

SCREENING

There are four major population-level AAA screening studies, in the United Kingdom, Australia, and Denmark, and a smaller screening study for women in the United Kingdom,²³-²⁷ all for patients 65 and older. A Cochrane review²⁸ of these studies assessing AAA-related mortality found an odds ratio of 0.60 (95% CI 0.47-0.78) in favor of screening. In the longest follow-up available, all-cause mortality was significantly lower in the screening group, with an odds ratio of 0,987 (95% CI 0.975-0.999, p = 0.03).²⁹ The primary harm associated with screening is the number of elective procedures, which increases twofold. However, this problem is partly compensated by the reduction in emergency procedure.¹⁶ Due to the high mortality associated with ruptured aneurysms and low morbidity and mortality of elective treatment, the number of men in the screening needed to prevent one aneurysm-related death would be 667, and the number of aneurysms treated 1.5.³⁰ With the data available at the moment, one cannot determine the optimum age for screen in cost-benefit terms. However, a standalone abdominal ultrasound is currently recommended for men over the age of 65.⁶ There is low evidence for screening women, considering the only randomized trial focusing on the issue was underpowered for a proper statistical analysis. Therefore, at the moment, population-level screening for women is not recommended.³¹

Relatively small studies found an association between peripheral arterial disease and AAA. However, the higher prevalence rates among members of this subgroup are counterbalanced by their shorter life expectancy and high surgical risk. At the moment, there is no unequivocal evidence for screen peripheral arterial disease patients.³² Solid evidence correlate positive family history with risk of AAA, rapid aortic growth, and higher risk of rupture. Though the subgroup has not been adequately assessed in current studies, routine screening for patients of both genders is suggested.³³,³⁴ Likewise, given the frequent concomitances of peripheral aneurysms (iliac, femoral, popliteal) and AAA, screening every 5 to 10 years is also recommended for this group.³⁵

The ideal periodicity of subsequent examinations was not properly assessed in randomized trials, but a model developed using a 15,000-patient database³⁶ suggests intervals should be stratified according to aneurysm diameter. For aneurysms between 3 and 3.9 cm, a 3 year interval between examinations is suggests, while for AAAs between 4 and 4.9 cm, annual examinations are recommended. When the aneurysm reaches 5 cm, intervals between examinations drop to 3-6 months. Though the information on the ideal management of patients with ectatic aortas (diameter < 3 cm) is limited, a new ultrasound every 5-10 years for patients with good life expectancy is reasonable.³⁷ Recommendations for abdominal aortic aneurysms can be found in Table 1.

Table 1
Level of recommendation for abdominal aortic aneurysm screening.

Recommendation	Level of evidence
Men over the age of 65 should be screened for abdominal aortic aneurysms with an abdominal ultrasound.	IIa
Men and women with a positive family history of abdominal aortic aneurysm should be screened starting at age 50.	IIb
The use of ultrasonography to track aortic diameters greater than 3 cm is recommended, with periodicity depending on initial diameter.	I

ETIOLOGY, PATHOPHYSIOLOGY AND RISK FACTORS

Few countries have population-wide early screening and diagnosis programs for AAA. This means knowledge about the true incidence of new cases and the prevalence of existing ones is subject to real constraints. Consequently, we have limited data available for a more precise understanding of its major risk factors. The dearth of global data causes distortions and biases interpretation when it comes to the causes and formation mechanisms of AAA. The pursuit of that data has practical effects, since countries with national diagnosis and prevention programs (such as the United Kingdom, Sweden, and Australia) have in recent years observed remarkable decreases in rates of mortality and other complications from AAA compared to the same rates for countries with similar socioeconomic status, such as Hungary, Austria, and Romania.³²,³⁸-⁴²

Male gender, advanced age, low levels of low-density lipoprotein, and smoking are the risk factors historically related to AAA, and are considered criteria for screening tests.⁴³,⁴⁴ Likewise, studies have found a relationship between some diseases and concomitant AAA:³,¹¹,⁴³,⁴⁵ hypertension, peripheral arterial disease, ischemic heart failure, prior myocardial infarction, and chronic obstructive pulmonary disease (COPD).⁴⁶,⁴⁷

“How” and especially “why” of aneurysms form are frequent questions from patients and their family members after the AAA diagnosis, directed to angiologists and vascular surgeons. These questions embody the natural drive to understand what could be done to prevent further dilations and their frightening complications. Therefore, this section of the Guidelines discusses important aspects of what is currently known about the causes (etiology), formation (pathophysiology), and risk factors of AAA.

Etiology

“Hereditary or behavioral”?

Is having an AAA predetermined at birth or are environmental factors and issues outside the body more important? Is it true that “a human being is as old as their arteries” and that dilations are the inevitable consequences of genetically determined senescence, or is aortic senility with dilation a predictable and preventable disease?

Discussing the etiology of AAAs (as well as any other pathological process) necessarily means discussing genetics as well as its younger sister, epigenetics. Both try to explain why the walls of a vessel as sturdy as the aorta can weaken to the point of becoming aneurysmal. In fact, AAA cases cluster in certain families, and there is evidence for a strong genetic component to AAA risk.⁴⁸,⁴⁹ Twin studies report genetic heritability may be as high as 70 percent. The Swedish twin register reports a monozygotic twin has a 24 percent chance of having an aneurysm if the other twin has it, compared to 4.8 percent for dizygotic twins.¹⁵,⁵⁰-⁵² Positive family history approximately doubles the risk of developing AAA in these studies.

The literature also contains reports that individuals with a family history of AAA are more likely to suffer ruptures and are less likely to have heart disease compared to aneurysm cases with no family history of the disease.⁵³,⁵⁴ This has led some specialists to consider interventions for smaller diameters than usual for cases without positive family history.

AAA inheritance may be Mendelian (single gene) or non-Mendelian, with a more complex cause stemming from various genes. Rare genetic diseases, such as Ehlers-Danlos syndrome, Marfan syndrome, Loeys-Dietz syndrome, and fibromuscular dysplasia, which may cause AAA, are examples of Mendelian inheritance. However, these diseases are rare, and epidemiological analyses find that only 10 to 20 percent of AAA patients have at least one relative who suffer from a genetic disease. This may suggest that a more complex mechanism, rather than changes to a single gene, are behind the genetic causes of AAA. Further evidence suggests epigenetic mechanisms (environmental and behavioral risk factors) play an important role in vascular disease and the smooth muscle cell plasticity in the vascular system associated with the process.⁵⁵

Epigenetics refers to hereditary and acquired changes to the genome affecting gene expression without changing DNA sequences. In some cases, epigenetic changes are stable and passed down across generations, but many are relatively dynamic and respond to environmental cues.⁵⁶ Epigenetic changes include DNA methylation, histone modifications, and non-coding RNA, which may interact directly with the primary nucleotide sequence and regulate gene expression. Methyltransferases are enzymes that methylate DNA and their support elements, including histones, to change genetic activity and chromatin structure. DNA methylation is a powerful epigenetic mechanism, important in the preservation of DNA structure, chromosomal stability, chromosome inactivation and even activation. It is a natural consequence of aging and cell differentiation, but is also acknowledged as an important modifier of disease risk. In DNA methylation, a methyl group is added to a region where a cytosine base 5' is linked to a guanine by enzymes called DNA methyltransferases. Recent studies have looked into the role of that process in the pathogenesis of AAA. A major study evaluated the DNA of control peripheral blood mononuclear cells from AAA patients and reported that global DNA methylation was significantly higher for men with large major AAA compared to small AAA and controls. Smooth muscle cells from isolated vessels from aneurysm patients show altered DNA methylation levels. Advanced age, smoking, and inflammation are the primary risk factors for AAA, and may have a substantial impact on DNA methylation patterns. Studies of aging find hypomethylation throughout the genome and hypermethylation of the senescence/senility-specific promoter. Smokers have lower methylation levels than non-smokers. Smoking cessation results in partial restoration of DNA methylation patterns, but never to the same levels found in non-smokers. However, it is still unclear whether DNA methylation changes are a cause or a consequence of inflammatory and degenerative processes.⁵⁷

Pathophysiology

Smooth muscle cell (SMC) loss, extracellular matrix (ECM) destruction, inflammation, and oxidative stress are key phenomena in the pathophysiology of AAA.⁵⁸ Recent in vivo and in vitro studies in genetics and epigenetics have shown that certain patterns of SMC differentiation and proliferation, combined with structural changes in the ECM, lead to senile degeneration and subsequent dilation of the arterial wall. The studies also detected cellular and fluid infiltrates typical of inflammatory reactions.⁵⁹,⁶⁰

The five main physiopathological processes observed in AAA formation are:

1. Changes to connective tissue proteins;

2. Imbalance between metalloproteinases and tissue inhibitors of metalloproteinases (both produced by SMC);

3. Chronic inflammation with cytokine release, as well as metalloproteinases by neutrophils and macrophages;

4. SMC transdifferentiation (turning them into macrophage-like cells);

5. Early cell death (apoptosis).

One factor suggesting a key role for SMC in the pathogenesis of AAA is that these aortic abdominal cells come from a different embryonic lineage than other aortic segments, making the infrarenal segment more prone to enlargement. The peculiar embryonic origin of abdominal aortic SMC leads to a specific condition for gene transcription in those cells, with different cell content, genetic activity, and histological structure.

Elastin degradation in the infrarenal aorta is greater than in ascending aortic segments or the aortic arch, and is one of the most powerful mechanisms promotion dilation in this particular aortic segment. All these factors make it more susceptible to specific clinical conditions.⁶¹

In general, inflammation is a trademark of aneurysm formation, and its role in AAA is well-documented compared to thoracic aortic aneurysms. Initially, neutrophils infiltrate the aortic wall very early, though only transiently. They are sources of metalloproteinases and oxygen free radicals that can trigger ECM degradation and weakening of the aortic wall.⁶² SMC are more consistently influenced by another type of inflammatory cells: macrophages. Macrophages are hematopoietic cells. A relatively recent development is that even differentiated tissue cells, such as vessel SMC, can “trans” differentiate into macrophage-like metalloproteinase producers. This is a well-documented phenomenon in tissue samples from human AAA vessel walls.⁶³-⁶⁵

We now know that the DNA demethylation process may be responsible for changes in protein coding and synthesis that ultimately result in the phenotypic expression of certain genetic codes. Histone H3/Lisin K4 demethylation of the MyH11 gene has been shown to be specific to SMC in guine pig as well as human tissue. This epigenetic change may be a clue to where the inflammatory process begins, to the imbalance between metalloproteinases and their tissue inhibitor factor, leading to the degeneration and degradation of the extracellular matrix of the aortic wall and subsequent AAA formation.

One of the earliest tissue changes identified in the pathophysiology of AAA is the increased concentration of highly reactive oxygen species, such as superoxide. These chemical compounds, known to cause oxidative stress, can induce and potentiate pro-inflammatory gene activity, increase local metalloproteinase concentration, and cause SMC apoptosis. Administering vitamin E as an antioxidant has led to reductions in AAA size and rupture in animal models.⁶⁶-⁶⁹

Risk factors

For practical purposes, in developing these guidelines, risk factors were related to the most expressive and best documented odds ratios found in the literature.⁷⁰

Age

Age is one of the most important risk factors for AAA development. Compared to a man aged 40-44, the risk increases almost 200-fold for a man aged 75-79 (0.83 versus 164 per 100,000). Most studies use 65 as the age cutoff, the inflection point in the AAA prevalence curve.

Gender

There is a wide consensus in the literature that AAA is more prevalent in males. The overwhelming majority of studies considering this variable points to a higher likelihood of diagnosis for men and a higher risk of rupture for women (see section on AAA in women). The Male:Female odds ratio ranges from 4.26 to 8.25 (mean 5.93), according a recent meta-analysis which included thirteen studies that looked into gender differences in AAA.

Smoking

Increased risk of AAA in current and former smokers ranges from 1.20 to 7.30 (mean 2.97), according to six recent studies. Current smokers have aneurysms at younger ages. In addition, current smokers are at higher risk of AAA than former smokers, and the risk increases proportionally with time of smoking.

Systemic hypertension

Diagnosis of hypertension increases the risk of being diagnosed with AAA. The risk increases 1.55 times, ranging from 1.02 to 2.34.

Diabetes mellitus

Diabetes mellitus diagnosis is unrelated with significant risk of AAA, having actually been considered a protective factor rather than a risk factor. Though the subject is controversial, diabetes is associated with a 1.18 risk of AAA. Since the confidence interval of this odds ratio ranges from 0.99 to 1.41, crossing the 1.0 neutral threshold, current evidence leads us to state that diabetes is not a significant risk factor for AAA, but neither is it a protective factor.

Coronary artery disease

Closely related to peripheral arterial disease (PAD), coronary artery disease (CAD), when present, also increases the likelihood of AAA. According to recent studies, a CAD diagnosis increases the risk of AAA 2.29 times (from 1.75 to 3.01).

Family history

Though relatively rare, some studies do include data on the family history of AAA patients. However, this is a more relevant risk factor in practice, since the risk of first-degree relatives being diagnosed with an aneurysm and their complications is almost 10 times higher. Studies point to an odds ratio of 9.64 (ranging from 1.72 to 53.98).

Sedentary lifestyle

The impact of lifestyle on noncommunicable chronic disease risk is a growing cause of concern, and represents one of the most important risk factors for PAD and for CAD in general. In the case of AAA, there is little evidence of a direct relation with physical exercise at the moment. Adequate blood pressure (BP) control is known to improve general cardiovascular health. Performing moderate-intensity aerobic exercise at least 3-4 times a week, 30-60 minutes per session, achieves that goal. However, resistance training can increase central aortic BP, so benefits for patients with aneurysms are less well understood. In theory, increases in BP can contribute to subsequent aortic growth and aneurysm complications. High-intensity isotonic and isometric training can increase systolic BP to approximately 300 mmHg with associated Valsalva maneuver. Further longitudinal studies are required.

Recommendantions regarding etiology and physiopathology are on Table 2.

Table 2
Recommendations for environmental and genetic risk factors for the genesis of abdominal aortic aneurysms.

Recommendation	Level of evidence
Considering the role of epigenetic changes on the phenotypic expression of genes related to the genesis of the dilation may be useful to understand the cause of abdominal aortic aneurysms. Cases with genetic-familial history have a higher likelihood of rupture and lower association with heart disease, facts which may be decisive for an indication of earlier intervention.	IIa
Presence of chronic inflammation, oxidative stress, and transdifferentiation of smooth muscle cells of the aortic wall into macrophages producing extracellular matrix-degrading proteolytic enzymes seems reasonable. However, an analysis of inflammatory markers still requires validation for use as prognostic factor.	IIb
Age over 65, male gender, smoking, systemic hypertension, family history, and coronary artery disease are factors that significantly increase the risk of being diagnosed with an abdominal aortic aneurysm.	IIa

CLINICAL STATUS

Most AAA patients are asymptomatic. At times, some mention feeling a pulse in their stomach. Asymptomatic aneurysms are occasionally found during routine abdominal palpation or by imaging examinations performed for other purposes. Since aneurysm progression means growth, it can compress neighboring structures, causing various symptoms:

• For duodenal compression, symptoms may include vomiting;

• Vena cava compression can cause lower limb edema, progressing to vein thrombosis;

• Ureter compression can result in hydronephrosis and even renal failure;

• Spinal cord compression may cause back pain and sometimes progresses to vertebral body erosion;

• Radicular compression causes neuropathic symptoms in lower limbs.

An additional symptom is lower limb ischemia caused by aortic aneurysm thrombosis or distal artery embolism. In case of acute expansion of the aneurysm, an important symptom is intense abdominal pain in the aneurysm area, usually subsiding only after the aneurysm is repaired. When the aneurysm ruptures, its most frequent complication, the patient usually indicates high-intensity abdominal pain, and may also swoon or pass out due to hypotension.

DIAGNOSIS

AAA can be diagnosed by clinical examination, but is primarily associated with the use of imaging methods, whether directly or as an incidental finding of examinations performed for other purposes. This section assess different diagnostic methods for AAA, including clinical diagnosis and imaging methods. In imaging methods, we assess their capacity to diagnose and detail aneurysm anatomy, in addition to their advantages and disadvantages.⁷¹,⁷²

Clinical examination

Physical examination may reveal the presence of an pulsatile abdominal mass, but its sensitivity is low, especially in obese patients or those with large abdominal circumference⁷³,⁷⁴

Imaging examinations

Ultrasonography: Doppler and non-Doppler abdominal ultrasonography is the examination of choice for AAA diagnosis. As a low-cost, non-invasive, and widely available test, it is the most frequently used in initial diagnosis.⁷⁵ Some authors have shown the high sensitivity and specificity of ultrasounds to diagnose abdominal aneurysms, which can exceed 95 percent. However, it is an examiner-dependent method, and has limitations: different methods among examiners, obesity, presence of gas in intestinal loops, diameter variations between systole and diastole, limited view of suprarenal aorta, inability to create imaging sequences for later reconstruction and planning.⁷⁶

Ultrasonography has also become an important diagnostic method that does not require the use of iodinated contrast material or radiation. However, it has some limitations, cannot provide enough detail for surgical planning, and does not enable the surgeon to manipulate and reconstruct images for treatment planning purposes, whether open or endovascular repair.

Computed tomography: computed tomography (CT) is a more reproducible method than ultrasonography and does not depend on the examiner for the interpretation and manipulation of images. Interobserver variability is also lower than for ultrasonography.⁷⁷ In addition, tomography allows for a single examination to assess the thoracic and thoracoabdominal aorta, as well as the iliac and femoral arteries, essential for preoperative planning. It can also better detail aneurysms for surgical planning, providing measurements and characteristics of the aneurysm wall, proximal neck, and presence and location of main and accessory renal arteries, as well as accesses for treatment and possible presence of synchronous aneurysms. Radiation is inherent to tomography, but the use of contrast materials can be avoided, or at least reduced, in various situations with less complex anatomy, as well as in the case of allergies and renal dysfunction.

Standardizing measurements is still required, however, such as establishing the diameter from the outer edge of the aortic wall. Greater access to medical imaging software, with the use of centerlines and multiplanar and three-dimensional reconstructions, has enabled greater accuracy and reproducibility in measurements. Software advances have even enabled us to fuse CT images with intraoperative digital angiography images for greater surgical precision. The diameter of the aneurysm and the sealing zones (proximal neck and iliac arteries) should be measured on the true axial direction of the aorta, thus avoiding errors attributed to vessel tortuosity and inclination.

Though there are limits associated with tomography equipment, software availability, and patient characteristics, such as artifacts and renal dysfunction, it should be stressed that the ideal examination uses iodinated contrast material, axial sections with thickness equal to or greater than 0.2 cm, and appropriate software to analyze the images using multiplanar and three-dimensional reconstruction.⁷⁷,⁷⁸

Other imaging methods:

Simple spin or abdominal x-rays may incidentally discover AAAs, especially in heavily calcified aortas. These methods are not indicated for that purpose, however. Magnetic nuclear resonance (MNR) has limitations compared to tomography, such as availability, claustrophobia, and presence of metallic devices. However, an MNR does not require the use of radiation and iodinated contrast material. It is neither easily interpreted nor widely adopted by vascular surgeons. For aneurysms, there are few studies comparing resonances with the gold standard method, CT angiography.⁷⁷,⁷⁸

Positron emission tomography (PET/CT) is of limited use for aneurysms, adopted for select cases of inflammatory aneurysms, mycotic aneurysms, and graft infection, where one can identify increased metabolic activity.⁷⁹

Digital subtraction angiography is not an adequate method for diagnosis of aortic aneurysms. Though widely used in the past, it does not enable an accurate measurement of aortic diameter, showing only the true lumen. Aneurysm dimensions may also be understated due to the presence of a parietal thrombus or arterial wall thickening. Angiography is an invasive method, requiring arterial access, and should not be used as a standalone diagnostic method, but rather intraoperatively during endovascular repair.

Recommendations for diagnosis of AAAs can be found in Table 3.

Table 3
Recommendations for diagnostic methods for abdominal aortic aneurysm patients.

Recommendation	Level of evidence
In cases of suspected abdominal aortic aneurysm, standalone clinical examination for diagnosis is not recommended.	IIb
Ultrasonography is the recommended examination for initial diagnosis in investigations of abdominal aortic aneurysms.	I
Ultrasonography is the examination of choice to track small aneurysms, for which there is no surgical planning at the moment.	I
Computed tomography angiography is the examination of choice in therapeutic decision-making and surgical planning for abdominal aortic aneurysms.	I
The aortic diameter should be measured from the outer edge of the vessel wall.	IIb
Imaging processing for CT angiography and multiplanar reconstruction using three perpendicular planes should be used to correctly measure diameters.	IIb

TREATMENT

Clinical treatment, indications for surgical treatment, regulatory aspects, choice of devices

Clinical treatment

The primary goal of medical treatment for this group of patients is to retard growth, lower the risk of rupture, and consequently obviate the need for surgical or endovascular repair. Periodical imaging examinations (such as Doppler ultrasound and CT angiography) are important for monitoring growth. In addition, strict blood pressure control, treatment for dyslipidemia and diabetes, smoking cessation, and assessment of other risk factors for atherosclerosis are also recommended.

Hypertension control

There is a well established association between uncontrolled hypertension and increased frequency of cardiovascular, acute myocardial infarction (AMI), and strokes, as well as rapid aneurysm growth or aortic dissection. The use of beta-blockers and antihypertensives (angiotensin II receptor blockers) to maintain systolic pressure below 130 mmHg and diastolic pressure below 80 mmHg, associated with statins, retards growth as well as minimizes the frequency of these events.

According to the American College of Cardiology/American Heart Association (ACC/AHA)⁸⁰ and European Society of Cardiology (ESC) guidelines,¹¹ treatment of AAAs with angiotensin-converting enzyme inhibitor (ACEI) and beta-blockers is a Class IIa recommendation, meaning the benefits of the treatment outweigh the risks and that using the treatment is reasonable. However, the weight of the evidence supporting the use of ACEIs and beta-blockers for AAA has Level of Evidence B, meaning the evidence comes primarily from nonrandomized or observational studies.⁸¹-⁸⁵

Use of statins

Several studies looked into the impact of statin therapy on aortic aneurysm growth, with mixed results. While some found statin therapy can retard the growth of aortic aneurysms and reduce the risk of rupture, others found no significant impact.

Reducing LDL levels by 50 percent in patients 75 and younger led to a decrease in the number of strokes and cardiovascular events. Another meta-analysis showed that statin use retarded aneurysm growth due to its action on the matrix metalloproteinase-9 or interleukin-6 concentrations. That reduction had a favorable effect on the process of medial degeneration of the aortic wall while acting on the progression of inflammation and atherosclerosis.

A meta-analysis of several studies published in the Journal of Vascular Surgery in 2018 found that statin therapy is associated with a significant reduction in the risk of aneurysm expansion and aneurysm-related deaths, as well as a significant reduction in abdominal aortic aneurysm growth rates in patients who underwent repair.⁸⁵

Statin use before and/or after endovascular treatment of AAA is associated with a 5-year increase in survival compared to the group that did not use statin; however, it should be stressed that these studies have limitations, and further research is required to fully understand the impact of statin therapy on aortic aneurysm growth. It should also be stressed that statin therapy is not specific to aortic aneurysms, and its use should be considered as part of a more comprehesive approach to the management of risk factors associated with aortic aneurysms.⁸²,⁸⁶-⁸⁹

Smoking cessation

Smoking cessation is considered a critical recommendation for treatment of AAA, since it is strongly correlated with aneurysm growth and rupture. Smoking is a key risk factor for the development of AAAs and is associated with higher incidences of aneurysm growth and rupture.

The ACC/AHA⁸⁰ and ESC guidelines¹¹ for AAA management list smoking cessation as a Class I recommendation. The level of evidence for smoking cessation in AAA management is listed as Level B, meaning the evidence comes primarily from observational studies or nonrandomized trials. The studies show that smokers are at a much higher risk of developing AAA and of aneurysm rupture than nonsmokers.

Smoking cessation has been shown to reduce the risk of aneurysm growth and rupture by lowering the pressure on the aneurysm, reducing inflammation and oxidative stress in the aorta, and improving aortic wall health. In addition, smoking cessation reduces the risk of other cardiovascular diseases, AMI, stroke, and peripheral arterial disease. Therefore, health professionals should strongly encourage AAA patients to quit smoking and, if necessary, refer them to smoking cessation programs. Smoking is an independent risk factor for AAA development, growth and complications, in addition to increasing the morbidity and mortality of surgical and endovascular repair.⁹⁰-⁹²

Use of antiplatelet drugs

Antiplatelet therapy, such as aspirin and clopidogrel, is considered an important aspect of AAA management, used to reduce the risk of cardiovascular events. The ACC/AHA⁸⁰ and ESC guidelines¹¹ for AAA management recommend the use of antiplatelet therapy for all AAA patients unless contraindicated. The use of antiplatelet therapy, such as acetylsalicylic acid at 75-162 mg/day, reduces the risk of cardiovascular events in this group of patients and is listed as a Class I recommendation, indicating the benefits of treatment outweigh the risks and that treatment should be administered.

However, when we assess growth speed, the data is controversial. Some studies show that among patients with AAA larger than 4 cm in diameter, aneurysm growth slowed down. On the other hand, a Danish study found higher mortality after rupture in the antiplatelet group compared with nonusers.⁹³,⁹⁴

Screening and surveillance

The Aneurysm Detection and Management Study (ADAM) is a multicenter randomized controlled clinical trial with the goal of determining the best strategy to detect and treat AAAs. The study compared two strategies: one, ultrasound screening followed by surveillance for aneurysms with diameter equal to or larger than 3 cm; the other, no screening and treatment of AAAs only when found incidentally or when causing symptoms.⁹⁵

The results showed that ultrasound screening followed by surveillance for aneurysms with diameter equal to or larger than 3 cm was associated with a significant reduction in the number of AAA-related deaths compared to the non-screening strategy. Ultrasound screening followed by surveillance for aneurysms with diameter equal to or larger than 3 cm is listed as Class of Recommendation I and Level of Evidence A. Table 4 summarizes recommendations for clinical treatment and follow-up.

Table 4
Recommendations for clinical treatment and follow-up for abdominal aortic aneurysm patients.

Recommendation	Level of evidence
Consider prescribing beta-blockers and/or angiotensin II receptor blockers to keep blood pressure below 130 and 80 mmHg. Consider prescribing statins to retard the growth or reduce the incidence of cardiovascular events.	IIa
Smoking cessation is recommended for all patients diagnosed with abdominal aortic aneurysm.	IIa
Antiplatelet therapy is recommended for all patients diagnosed with abdominal aortic aneurysm, unless expressly contraindicated.	IIa
Regular abdominal ultrasound for follow-up of patients with aortic diameter greater than 3 cm is recommended.	I

Indication for surgical and endovascular treatment

Currently, most international guidelines recommend using endovascular aneurysm repair (EVAR) as the treatment of choice for most AAA patients, but open surgery (OS) is still recommended for some patients, especially those poorly suited for EVAR due to the extent, site and anatomy of the aneurysm. Indications for AAA repair, both surgical and endovascular, may be described in simpler terms as:

13. Fusiform aneurysm with diameter larger than 5 cm for women and 5.5 cm for men;

14. Rapid growth fusiform aneurysm, faster than 0.5 cm in 6 months or 1 cm in 1 year;

15. AAA associated with complications and/or symptoms;

16. Dilation shape: saccular aneurysm.

However, key considerations are required in terms of indications for treatment, discussed in the following paragraphs.

DIAMETER

Even though basing indications for treatment only on large aneurysm diameters is controversial, that criteria is still the most frequently utilized. Therefore, the current thresholds of 5 cm for women and 5.5 cm for men are the most frequently cited for indication for surgical or endovascular treatment. However, the issue is not without controversy in the literature and recommendations may vary, depending on aneurysm site, clinical condition, and the patient's individual risk factors.

The use of EVAR in small and asymptomatic AAAs is still the topic of discussion and research, and recommendation may change as new evidence emerges. Considering the significant decrease in surgical morbidity and mortality from the use of endovascular procedures, early repair of small aneurysms (4-5 cm) is once again the subject of ongoing debate. However, currently available data shows no evidence of the benefits of early treatment for small aneurysms compared to conservative treatment. The UK Small Aneurysm Trial, ADAM, and Comparison of surveillance versus aortic endografting for small aneurysm repair (CAESAR): results from a randomised trial⁹⁶-⁹⁸ corroborate these premises—even though there is significant crossover in the groups compared in all three studies, as well as the finding that one in every six aneurysms in clinical follow-ups lose optimal anatomy for endovascular repair.⁹⁵-⁹⁹ Randomized trials have yet to find evidence of the effectiveness of repair for aneurysms smaller than 5.5 cm, but that does not mean that they cannot be more efficient.¹⁰⁰ Variables such as delays in referrals, the conditions of health system access, and mortality rates at the center where the intervention is to be performed all impact these numbers. Therefore, it is plausible that with aneurysms between 5 and 5.5 cm, a given intervention may be justified.⁶,⁹⁹,¹⁰⁰

For aneurysms smaller than 4 cm in diameter, with no growth or significant symptoms, rigorous monitoring with imaging examinations is usually recommended. For aneurysms between 4 and 5 cm in diameter, with no growth or significant symptoms, rigorous monitoring with imaging examinations is recommended. EVAR may be considered for aneurysms with significant growth or in case of other risk factors for rupture.

RAPID GROWTH

Two factors associated with aneurysm rupture are its diameter and rapid growth rate. The mean annual growth rate for AAAs is approximately 0.26 cm per year for aneurysms smaller than 5 cm, increasing to 0.5 cm per year for aneurysms larger than 5 cm. Therefore, faster growth, i.e., greater than 0.5 cm in 6 months⁸⁰ or 1 cm in 1 year,⁶,⁸⁰ is considered a primary criteria for elective AAA repais.

PRESENCE OF SYMPTOMS

AAAs are typically asymptomatic, and often found incidentally during imaging examinations prescribed for other conditions. It should be noted that AAA symptoms may be subtle, and often barely perceptible. However, as the aneurysm increases, it may cause symptoms such as:

17. Abdominal or back pain;

18. Back pain radiating to the inguinal region;

19. Feeling of fullness or abdominal discomfort;

20. Pulsating feeling in the abdomen.

Multivariate analysis of a number of studies has determined that the strongest predictors of risk of rupture are rapid documented expansion and presence of significant abdominal or back pain, regardless of AAA size.¹⁰¹-¹⁰⁴

SACCULAR SHAPE

Aneurysms are considered saccular when the alteration or deformity is found only on one side of the aorta, creating a focal dilation in saccular shape. Saccular aneurysms are less frequent, and data on their natural progression is scarce. According to studies, they are more frequent in women and, compared to fusiform aneurysms, symptoms manifest at smaller diameters. Overall, endovascular or surgical repair is indicated for saccular aneurysms, despite the lack of data and the lack of consensus regarding their size.

In general, the level of evidence for treatment of saccular aneurysms is moderate to low. This is due to the lack of high-quality randomized controlled trials for this type of aneurysm. Most of the evidence available comes from observational studies and case series, which can provide useful information, but are considered less reliable than randomized controlled trials. For example, the Society for Vascular Surgery recommends endovascular repair for saccular aneurysms smaller than 5 cm in diameter, but lists it as a weak recommendation.⁷ The reason is the low quality of the evidence supporting that recommendation, and the decision to treat should be based on the patient's individual characteristics and preferences. Do keep in mind that treatment recommendations for saccular aneurysms may vary, depending on the guidelines or specific sources used, and are based on the current state of knowledge and understanding about the condition.¹⁰⁵,¹⁰⁶

Recommendations for elective surgical repair of AAA can be found in Table 5.

Table 5
Recommendations for elective surgical repair for asymptomatic abdominal aortic aneurysm patients.

Recommendation	Level of evidence
Conventional or endovascular surgical repair is recommended for fusiform aortic aneurysms greater than 5 cm in diameter for women and 5.5 cm for men.	I
Elective abdominal aortic aneurysm repair may justified for diameters between 5 and 5.5 cm based on the patient's clinical and anatomical conditions, health system access, hospital mortality rate.	IIb
Conventional or endovascular surgical repair is recommended for fusiform aortic aneurysms with growth rates greater than 5 cm per year.	Ib
Conventional or endovascular surgical repair is recommended for symptomatic fusiform aortic aneurysms.	IIb
Conventional or endovascular surgical repair is recommended for saccular aortic aneurysms regardless of diameter.	IIb

Conventional and endovascular surgery

AAAs can be treated with two types of procedure: EVAR and OS. For over 50 years, surgical procedures with the interposition of a straight or bifurcated graft was the first choice of treatment for AAA repair. However, with the development of new endovascular procedures, the strategy came to be replaced by minimally invasive procedures. Despite the high technological level involved, the issue of whether one technique is superior to the other on the short, medium, and long term has always been controversial. Currently, there is consensus in the literature that given the same risk conditions, i.e., patients with the same clinical characteristics and adequate anatomy for endovascular repair, both approaches can be used, with similar outcomes—therefore, the decision about which technique to employ should be made jointly by the medical team and the patient. There is Class of Recommendation I and Quality Level A data in the literature in that direction.¹⁰⁷,¹⁰⁸

Choice of procedure depends on several factors, including patient age, risk factors, and aneurysm size and site. The physician can discuss the best option after assessing the patient's medical history and clinical condition. Several studies and international guidelines are used to guide the treatment of AAA patients.⁶,⁷,¹²,⁸⁰

Physicians should also consider the Brazilian Abdominal Aortic Aneurysm Treatment Guidelines published in August 2016 by the Brazilian Unified Health System (SUS) National Committee for Technology Incorporation (CONITEC).¹⁰⁹ Based on a thorough literature review and analysis of outcomes from endovascular treatment of AAA compared to conventional surgery in SUS reference hospitals, the guideline strongly recommends the use of endovascular repair to treat AAAs, reserving OS exclusively for situations where EVAR is not possible.

Long term outcomes may be influenced by many different factors related to patient characteristics, quality of repair, and extent of follow-up. In addition, long-term studies also show that the durability of the endografts used in EVAR may be limited, especially first-generation grafts, and reintervention may be necessary in the future in order to replace, complement, or repair endograft migration. Again, it should be stressed that rates of reintervention and adverse events are usually more frequent for EVAR compared to OS, but the mortality rates are still lower.

Currently, most international guidelines and randomized trials recommend EVAR as the treatment of choice for most AAA patients. These are all considered high-quality studies, providing strong evidence for the use of EVAR, but OS is still recommended for some patients, specially those poorly suited for endovascular repair due to the extent, site and anatomy of the aneurysm.

Decision-making

The decision-making process for AAA treatment should be individualized, based on patient characteristics. The decision should be discussed by a multidisciplinary team involving a vascular surgeon as well as other specialists, such as interventional practitioners and cardiologists. A multidisciplinary approach enables the team to consider a wide range of factors that might influence treatment choice. The approach is key to determine whether the patient meets the conditions for various treatment options as well as to consider the long term outcomes and possible complications of each option. A multidisciplinary team can integrate various perspectives and sources of knowledge, leading to a more accurate and comprehensive decision-making process and better outcomes for patients. The collective approach also enables the team to manage possible complications and to coordinate patient follow-up, which may improve continuity of care. Shared decision-making in medicine, now a major topic of discussion in the area, where the patient is at the center of the decision-making process, still has room to grow in AAA management.

Adherence to instructions

IFUs are mandatory for endovascular repair of aneurysms to ensure the safety and efficacy of the product and the procedure. They provide information such as indications, contraindications, warnings, precautions, and instructions for use of endovascular devices, such as the endografts used in EVAR. Noncompliance with IFUs can lead to complications, such as device failure, endoleaks, and device migration, among others. In some cases, complications may require reintervention or conversion to OS. However, according to the literature, approximately 42 percent of cases met the most conservative recommendations of device IFUs; and 69 percent met the most liberal recommendations, while all others fail to meet recommendations of use.¹³

Adherence to IFUs includes following proper implantation procedures, ensuring correct sizing and placement of device, and monitoring patient condition during and after the procedure to detect potential complications. It is also important to note that IFUs may change over time as new or updated information becomes available, so practitioners should keep abreast of the most recent version of the IFU and contact the manufacturer for additional information.

Conventional open treatment

Indication for open repair

Indications for OS for AAA include asymptomatic and rapidly expanding aneurysms, distal embolization or rupture, and do not differ from indications for EVAR. On the other hand, OS is indicated for most infected aneurysms or when requiring conversion after unsuccessful endovascular repair.

Major contraindications for OS include hostile abdomen, comorbidities (especially heart and renal), and short life expectancy.⁷,³⁸,¹¹⁰

Open repair technique

The steps of OS procedures have changed little over the last 7 decades. Typically, a xiphoid-to-pubis midline incision is made and the retroperitoneum approached after right visceral rotation. Dissection of the retroperitoneum is carried out from the proximal neck of the aneurysm to the common iliac arteries or iliac bifurcation, depending on patient anatomy. After systemic heparinization, aortic and iliac clamping is performed, the aneurysm sac is opened, and the lumbar arteries are ligated. A straight or bifurcated graft is then interposed; end-to-end anastomoses are then created using continuous sutures. A teflon ring can be used to reinforce the proximal anastomosis in select cases. After releasing the vascular clamps, the anastomoses and the ligation sites of the lumbar arteries are inspected for bleeding. The aneurysm sac is then brought over the graft, and laparosynthesis is performed.

Maintenance of pelvic and visceral flow

Pelvic and visceral perfusion depends on the communication between the superior mesenteric, inferior mesenteric, and hypogastric arteries. Occlusion of hypogastric arteries may lead to erectile dysfunction, buttock claudication and, more rarely, to colon and medular ischemia. During OS, all efforts should be directed at maintaining flow to at least one of the hypogastric arteries.

The risk of colon ischemia increases significantly when revascularization excludes both hypogastric arteries (aortobifemoral bypass with hypogastric exclusion).⁶,⁷ In a Canadian prospective study, risk of colon ischemia increased eightfold when both iliac arteries were excluded (from 0.3 to 2.6 percent).¹¹¹

Inferior mesenteric artery reimplantation to prevent colon ischemia has conflicting results. Considering reimplantation is reasonable in very specific situations, such as previous colectomy, occluded collateral pathways between the superior mesenteric artery (SMA) and the inferior mesenteric artery (IMA), SMA occlusion and/or stenosis, or absence of the arc of Riolan.¹¹²,¹¹³ A 2006 randomized prospective trial concluded that IMA reimplantation could be beneficial for elderly patients and those with considerable intraoperative blood loss.¹¹⁴ The Canadian prospective study¹¹¹ found that postoperative bleeding was more frequent in patients who underwent reimplantation (5 percent of the series).

Type of incision

Transverse versus midline incision

A randomized prospective study from 2005 assessed select patients randomized to transverse versus longitudinal incision.¹¹⁵ Logistic regression analysis after over 4 years found, for a small study group comprised of 69 patients, a higher rate of incisional hernia for the midline incision group (p = 0.010). Transverse incision is a reasonable recommendation for COPD patients because of its lower respiratory restriction.⁷

Midline versus retroperitoneal incision

Even randomized trials comparing midline to retroperitoneal incisions had conflicting results.¹¹⁶-¹¹⁸ Only two measurable variables—shorter period of adynamic ileus and earlier feeding—favored retroperitoneal incision. Limited exposure of the right renal artery and right iliac artery are drawbacks of retroperitoneal incisions. In the prospective randomized trial conducted by Sieunarine et al.,¹¹⁶ no significant differences were found between the two incisions, except for bulging and longer and more intense pain in the retroperitoneal group. On the other hand, longitudinal incisions were associated with more frequent hernias. It seems clear that the retroperitoneal incision should be reserved for cases of hostile abdomen and select cases of inflammatory aneurysm¹¹⁹ and horseshoe kidney.

Mesh reinforcement in midline incision

A randomized trial¹²⁰ and a 2018 meta-analysis¹²¹ have shown that the prophylactic use of mesh reinforcement reduces the risk of incisional hernia in xiphoid-to-pubis midline incisions. However, there was no long-term follow-up for these groups and the number of reinterventions was not reported for a more appropriate analysis. Table 6 lists recommendations for open surgery for AAAs.

Table 6
Recommendations for open surgical repair for abdominal aneurysms.

Recommendation	Level of evidence
Preserving flow into at least one internal iliac artery is recommended, both in open surgery and endovascular procedures.	I
Using a transverse incision in chronic obstructive pulmonary disease patients is recommended.	IIb
A retroperitoneal incision is recommended in cases of horseshoe kidney, inflammatory aneurysm, and hostile abdomen.	IIa

Juxtarenal aneurysm

By definition, a juxtarenal aneurysm is characterized by a proximal neck short enough to demand suprarenal clamping in open repair, but no anatomical involvement of the aorta at the origin of the renal arteries.¹²² Approximately 15 percent of AAAs are classified as juxtarenal.¹²² Several clinical series do not to properly define this anatomical status, include pararenal aneurysms, and fail to provide long-term outcomes.

There are no randomized controlled trials comparing OS to EVAR at the moment, which represents the main obstacle to comparing the two techniques. It is important to note that branched (BrEVAR) and fenestrated endovascular repair (FEVAR), with low rates of complications, are performed at highly experienced centers with low mortality rates. The decision on whether to use open or endovascular repair for a juxtarenal aneurysm is absolutely multifactorial. Therefore, this document has no intention of comparing the two techniques.

The low mortality rate of OS for juxtarenal aneurysms is evident in various clinical series and meta-analyses. A 2010 meta-analysis assessed the results of OS, including 1,256 patients from 21 nonrandomized trials from the MEDLINE, EMBASE, and Cochrane databases. Perioperative mortality was 2.9 percent (95% CI, 1.8 to 4.6) and incidence of new onset of dialysis was 3.3 percent (95% CI, 2.4 to 4.5).¹²³ A recent retrospective study in five french academic centers,¹²⁴ including 315 consecutive patients, also found low mortality for OS (0.9 percent).

With the advent of endovascular repair with branched, parallel stent, or fenestrated endografts,¹²⁵,¹²⁶ several clinical series and a few meta-analyses have compared OS to endovascular repair. A 2022 meta-analysis confirmed the excellent outcomes of fenestrated endografts in treating juxtarenal aneurysms,¹²⁷ but with no significant reduction in mortality, compared to endovascular treatment; the latter was associated with a higher number of reinterventions, despite lower morbidity. That same year saw the publication of a meta-analysis by Doonan et al.,¹²⁸ which included pararenal aneurysms and several endovascular procedures. That systematic review found lower mortality rates for EVAR. A more recent meta-analysis (UK-COMPASS) of 7,000 patients compared OS to various forms of endovascular repair,¹²⁹ including the use of conventional endografts outside IFUs, parallel stent grafts, and fenestrated endografts. There was a lower mortality rate for EVAR, but difference was not seen at 30 months.

A comparative study in elderly patients found no difference in operative mortality for OS and fenestrated endografts,¹³⁰ but one should bear in mind that comparisons are not possible, and that even with paired patients, anatomical differences, patient selection criteria, and differences in team experience, both for OS and for FEVAR and BrEVAR, present difficulties for this kind of analysis.

The obvious obstacles for a wider indication of fenestrated endografts are related to their high cost, low availability, and requirement of proper training in endovascular techniques. On the other hand, OS of juxtarenal aneurysms has its own technical difficulties and requires additional surgical team expertise and highly specific postoperative intensive care.

OS should preferably be performed by teams treating AAA with in-hospital mortality rates less than 5 percent and depends on the number of repairs completed per year at the center.¹³¹ This means endovascular repair should be reserved for patients with considerable comorbidities and/or centers completing high volumes of endovascular procedures.

Table 7 summarizes OS and endovascular indications for juxtarenal aneurysms.

Table 7
Recommendations for repair of juxtarenal aneurysms.

Recommendation	Level of evidence
Open surgery is recommended for juxtarenal aneurysms in centers reporting mortality rates below 5 percent.	IIb

Endovascular treatment of infrarenal aneurysms

EVAR has staked its place as an important technical advance and has become the therapy of choice is several countries. The primary goal of EVAR is to achieve a proximal and distal seal, preventing contact between blood and the aneurysm wall and ultimately preventing rupture. Since the first implantation, and since the first in Brazil in 1994, many endografts have been modified in terms of diameter, material, proximal fixation mechanism, and navigability, among others. Many anatomical constraints have been overcome, and hundreds of vascular surgeons have been trained in the technique; today, it is widely available throughout the country, both in the private health insurance system and in the Brazilian Unified Health System (SUS). IFUs may vary among manufacturers, and we strongly recommend checking the anatomical requirements in the product's manual.

There are many randomized controlled trials on EVAR. One of the most important is the Randomized Controlled Trial of Endovascular Repair versus Open Repair for Abdominal Aortic Aneurysm (EVAR 1).¹³² The trial showed EVAR was associated with a lower short-term risk of death compared to OS. Another important study is Endovascular Aneurysm Repair (EVAR 2), where patients considered unfit for OS underwent EVAR with no improvement in mortality rates and increased need for reintervention.¹³³

DREAM is an additional randomized trial to find lower perioperative mortality in the EVAR group.¹³⁴ As well as previous studies, it also showed EVAR was associated with lower risk of death and lower risk of complications compared to OS, despite the higher number of reinterventions.¹³⁵ That advantage evidently favors EVAR during the first 6 months, but does not hold over the long term. Even long-term trials, such as Open versus Endovascular Repair of Abdominal Aortic Aneurysm (OVER), show that survival at long-term follow-up periods (4-8 years) was similar between both groups.¹³⁶

In 2008, a meta-analysis of randomized and observational studies which included 42 studies and totaled 21,178 patients compared OS to EVAR. In elective procedures, the findings were shorter surgery times, less blood loss, lower 30-day mortality, shorter hospital stays, shorter ICU stays, and fewer cardiac and respiratory complications in patients who underwent EVAR. The authors recommend EVAR be the treatment of choice for patients with adequate anatomy, both for elective and emergency surgeries.¹³⁷

The meta-analysis by Sajid et al.¹³⁸ included three randomized trials comparing EVAR to OS (totaling 1,468 patients), confirming EVAR is associated with lower operative mortality, less postoperative pain, shorter ICU stays, and shorter hospital stays. The authors conclude EVAR can be recommended as the treatment of choice for elderly and high-risk patients. A Cochrane Review published in 2014 compared EVAR to OS in AAA repair. Five studies were included, finding a statistical difference favoring EVAR for short-term mortality, but no medium and long-term difference. The reintervention rate in the EVAR group was statistically higher compared to open surgery, but the result should be interpreted with caution, given the heterogeneity between studies. Most reinterventions used endovascular procedures and were associated with low mortality.¹³⁹

The evidence indicates that the decision-making should involve the patient, especially frail and very high surgical risk patients, some of who possibly should be advised not to undergo an operation. For all others, with adequate anatomy and good to moderate surgical risk, EVAR and OS may be suggested as therapies.

Recommendations for EVAR for AAA can be found in Table 8.

Table 8
Recommendations for endovascular repair for abdominal aneurysms.

Recommendation	Level of evidence
Endovascular repair is recommended as the preferred mode of treatment in the presence of a trained team and favorable anatomical conditions.	IIa
Open repair is recommended for young patients and those with low clinical and surgical risk.	IIa
Ultrasound-guided percutaneous access and closing at the conventional surgical access site is recommended to reduce operation time, blood loss, length of hospital stay, wound healing time, and pain.	IIb

ACCESS CHOICE FOR EVAR

The greater availability of percutaneous closure devices and low-profile endografts have made ultrasound-guided percutaneous access and closure more feasible. Two randomized trials¹⁴⁰,¹⁴¹ and a major retrospective review found favorable results for percutaneous access and closure of the common femoral artery, with shorter operative time, less blood loss, and better patient-centered results, such as less pain.

The PEVAR trial showed total percutaneous access and closure of the common femoral artery for EVAR patients with adequate anatomy was not inferior.¹⁴⁰ The Percutaneous access in Endovascular Repair vs Open (PiERO) trial found less pain and improved wound healing among patients who underwent percutaneous access compared to those who underwent groin access approaches.¹⁴¹ There was no difference in the incidence of infection at the access site between groups. In addition, a multicenter observational study of common femoral artery access showed a significant reduction in groin hematomas with routine ultrasound-guided accesses.¹⁴²

In patients undergoing endovascular repair of AAAs with adequate common femoral artery anatomy, ultrasound-guided percutaneous access and closing at the conventional surgical access site is recommended to reduce operation time, blood loss, length of hospital stay, wound healing time, and pain.⁸⁰

Table 8 lists a recommendation regarding access for EVAR.

Endovascular treatment of juxtarenal aneurysms

EVAR has lower mortality rates, short operative time and shorter hospital stays compared to OS in the short and medium term, making it the most widely used treatment method at present.¹³²,¹³⁴,¹⁴³ However, all commercially available endografts have inclusion criteria defined in their IFUs. These instructions establish the minimum anatomical requirements to use these devices. For most endografts, minimum proximal neck length is 1-1.5 cm, maximum angulation of 45-60º, and absence of calcification and circumferential thrombus.¹⁴⁴

Despite these explicit recommendations in instructions for use, a retrospective study using a database of patients who underwent endovascular repair showed only 42 percent of patients had anatomy that met the most conservative criteria, and 69 percent met the most liberal definition.¹³ In follow-up, these patients had aneurysm sac enlargement > 0.5 cm in 41 percent of cases. The risk factors associated with enlargement were: presence of endoleak, age above 80, proximal neck diameter > 2.8 cm, angulation > 60º, and common iliac artery diameter > 2 cm.

The presence of a hostile neck, especially short, reverse conical or irregular necks, increases the risk of endoleak fourfold, and the risk of aneurysm-related death ninefold in 1 year.¹⁴⁵ The combination of hostile neck criteria and implantation of the endograft in off-label anatomies, i.e., those that did not meet the IFUs, increases the need for adjunctive procedures, presence of intraoperative endoleaks, and all-cause mortality.¹⁴⁶

Therefore, endovascular repair of short neck, juxtarenal or pararenal aneurysms requires more advanced techniques than conventional EVAR to ensure an adequate sealing zone, with a high rate of technical success, as well as a long-lasting repair.

Parallel stenting

One of those techniques is the use of parallel stents, whether chimney, periscope or sandwich stenting.¹⁴⁷-¹⁴⁹ The advantage of this technique is that it does not use customized devices, which take time to manufacture, but it has the drawback of forming “gutters” that can lead to endoleaks.

Several studies about the procedure are registered rather than prospective studies, suffer from patient selection bias, and problems associated with definition, procedure standardization, patency assessment, and long-term follow-up.¹⁴⁷ Most data comes from the PERICLES registry, and 95 percent of the 517 patients had juxtarenal aneurysms.¹⁵⁰ For elective cases, 30-day mortality was 3.7 percent. The incidence of transient renal dysfunction was 28 percent, and 3 percent required permanent dialysis. Technical success was achieved in 97.1 percent of cases, while 2.9 percent of patients had persistent endoleaks. Global survival at 17 months was 79 percent. Chimney patency in patients for whom imaging examinations were available was 94 percent. Mean aneurysm sac regression was 0.44 cm, though there was no mention of how many patients presented no regression.

In a systematic review of the literature, the incidence of endoleaks was 7.6 percent, compared to 3.7 percent for FEVAR.¹⁵¹ The better outcomes from parallel stenting come from patients where the physician can create a sealing zone ≥ 1.5 cm, oversize the endograft by 30 percent, and use two chimneys maximum.¹⁵¹,¹⁵² With the development of fenestrated and branched grafts, the use of parallel stenting is increasingly the province of emergency situations, with anatomy unsuited for FEVAR, or as a salvage procedure in cases of inadvertent occlusion of branch vessels.

Endoanchors

Endosuture devices were developed to increase endograft fixation to the aortic wall, improving alignment and preventing migration of type Ia endoleaks in cases where conventional EVAR would not be enough due to short or angulated necks. Experimental studies show the use of these devices increases the strength required to dislodge the graft from the aortic wall, approaching or even exceeding that of conventionally hand-sutured grafts.¹⁵³

The use of this device is relatively simple, adding on average only 17 minutes to total operative time,¹⁵⁴ and it has a short learning curve.

In the ANCHOR multicenter registry, endoanchors were deployed prophylactically in 208 cases where surgeons rated patient anatomy as at high risk of migration or development of Ia endoleaks. In total, 78.3 percent of patients enrolled met the criteria for hostile neck. The technical success rate was 95.2 percent. At 14 months follow-up there were no ruptures, migration, or conversion to open surgery. In patients submitted to control CT, 1.5 percent had type Ia endoleaks. Aneurysm sac > 0.5 cm decreased in 42.9 percent of patients, while it increased in 1.6 percent. Major limitations in this registry were incomplete follow-up and the absence of a control group.¹⁵⁵

Physician modified endografts

Several techniques may be used for bench modifications of conventional endografts, such as creating fenestrations, scallops, or branches to incorporate visceral arteries, establishing a fixation zone in patients with inadequate anatomy for conventional grafts. These techniques have the benefit of obviating the wait time for manufacturing a customized graft, and are usually deployed in emergency situations, in high surgical risk patients, or at institutions where customized grafts are not available, whether in Brazil or abroad.

With the ongoing development of customized grafts, the use of modified devices in elective procedures is increasingly restricted. In their retrospective study, Oderich et al.¹⁵⁶ observed a time shift, where physician-modified endografts (PMEGs) were more widely used in the first years of endovascular treatment for juxtarenal, pararenal or thoracoabdominal aneurysms, while custom-made devices (CMD) were more frequently used in more recent years. In that comparison, patients treated with PMEGs had more comorbidities and larger aneurysms. Technical success was higher with CMD grafts (99.5 versus 98 percent, p = 0.02), and 30-day mortality was higher for the PMEG group (5.5 versus 0 percent, p = 0.0018). At 3-year follow-up, survival and primary and secondary branch vessel patency were similar for both groups.¹⁵⁶ More recently, a large case series with 5-year follow-up published by a group with extensive experience in PMEGs found good patency and branch stability levels.¹⁵⁷

Fenestrated and branched endografts

Technical progress and increased experience in endovascular repair have enabled physicians to extend the proximal fixation zone for endografts, incorporating visceral and renal arteries to repair juxtarenal and pararenal aneurysms⁶¹⁶¹. The greatest advantage of fenestrated/branched endovascular repair (FEVAR/BrEVAR) compared to open surgery is that it does not require aortic clamping, avoiding the subsequent risk of renal dysfunction. They also have lower surgical trauma and faster recovery times, which may benefit high surgical risk patients. FEVAR and BrEVAR are challenging techniques. They should be performed at specialty centers, by expert and experienced surgical teams.⁶

Systematic reviews show the safety and efficacy of FEVAR.¹⁰⁸,¹⁵⁸-¹⁶⁰ In a review of 14 case series including 751 patients,¹⁰⁸ in-hospital or 30-day mortality was 4.1 percent, the prevalence of transient renal failure was 11 percent, and 2 percent of patients required permanent dialysis. The GLOBALSTAR database included 318 patients treated with FEVAR in 14 British centers.¹²⁶ The perioperative mortality rate was 4.1%. Rates of patients free from secondary reintervention were 90, 86, and 70 percent at 1, 2, and 3 years, respectively.

Single and multicenter series on fenestrated and branched endografts have shown promising results.¹⁶¹,¹⁶² When performed by experienced surgeons, technical success was achieved in a large majority of cases (92 to 99.6 percent), with low perioperative mortality rates. At 1-year follow-up, visceral branch vessel patency was also good (96 to 98 percent), and at 3 years, 91 percent of patients were free of aneurysm-related mortality, with a global survival rate of 57 percent.¹⁶³

Recent observational studies have tried to compare the outcomes of open surgery and FEVAR for complex aortic aneurysms. Varkevisser et al.¹⁶⁴ compared FEVAR, OS for complex aortic aneurysm and EVAR and found a higher risk of death within 30 days for open repair compared to endovascular repair (OR, 4,9; 95% CI 1.4-1.9), and mortality rates comparable to EVAR.¹⁶⁴ One should also keep in mind that candidates for complex aortic repair such as FEVAR or BrEVAR have also been selected for good to moderate risk, since very frail or very high risk patients might not survive neither open nor endovascular repair.

However, the late reintervention rate is higher after FEVAR compared to open surgery,¹⁰⁸,¹⁶⁵ as well as persistent kidney injury, and 3-year mortality (excluding perioperative deaths) (HR 1.7; 95% CI 1.1-2.6).¹⁶⁵ Like for infrarenal endovascular repair, the available data show similar findings, with an initial benefit for survival rates, but diminishing advantages over time and higher reintervention rates. Therefore, FEVAR may be more beneficial for moderate to high surgical risk patients, who are more likely to suffer from perioperative complications.

In addition to branch vessel patency, another critical point for FEVAR/BrEVAR is spinal cord ischemia, especially associated with greater extents of aortic coverage. The manufacturing of customized grafts or modification of off-the-shelf grafts have been described as ways of reducing the length of aortic coverage.¹⁶⁶,¹⁶⁷ Another critical point is absolutely the manufacturing time for customized grafts, which means that PMEGs and off-the-shelf grafts are likely to retain an important role for emergency cases and symptomatic aneurysms in the near future.¹⁵⁷,¹⁶⁸

Therefore, for young, good surgical risk patients, OS is the recommended alternative, while for moderate to high surgical risk patients, endovascular repair is indicated, preferably FEVAR/BrEVAR, as long as they are anatomically possible. Treatment options should be discussed with patients and family members, taking into consideration the advantages and disadvantages of each technique. In patients who underwent endovascular treatment, rigorous follow-up with annual imaging examinations are required.¹⁶¹

Table 9 summarizes recommendations for endovascular treatment of juxtarenal and pararenal aneurysms.

Table 9
Recommendations for endovascular treatment of juxtarenal and pararenal aortic aneurysms.

Recommendation	Level of evidence
In young patients at low clinical risk, open surgical repair of juxtarenal or pararenal aneurysms greater than 5.5 cm is recommended.	I
In patients at moderate to high surgical risk and symptomatic patients, consider endovascular repair using one of the available techniques.	IIa
In frail and very high surgical risk patients, consider nonsurgical treatment, with open or endovascular repair, using a shared decision-making process.	IIa

POSTOPERATIVE FOLLOW-UP

After treatment of AAAs, the goal of follow-up is to avoid aneurysm-related complications or deaths. After open surgery, the formation of pseudoaneurysms at anastomoses or the dilation and formation of new aortic or iliac artery aneurysms is unusual at initial follow-up, with rates of around 1 percent at 5 years, 6-12 percent at 10 years, and up to 35 percent at 15 years.¹⁶⁹-¹⁷¹

In patients who underwent endovascular treatment, the rate of complications and need for reintervention is significantly higher, and the most frequent complications are endoleaks. Aneurysm sac enlargement without detectable endoleak, endograft migration, and endograft failure may also be found.

Though postoperative follow-up with imaging examinations is recommended from the outset of endovascular repair of AAAs, that plan is rarely followed to the letter, with compliance failures in over 60 percent of cases.¹⁷²,¹⁷³ The rate of late aneurym rupture after endovascular treatment can be as high as 5 percent in 8 years, and it should be stressed that this incidence is closely related to inadequate case selection, especially cases of unfavorable anatomy and noncompliance with device IFUs. These factors may be more relevant than intrinsic failures of endovascular procedures or materials.¹³

Aneurysm sac retraction during follow-up is an important indicator of successful aneurysm exclusion, and has been shown to be a predictor of low risk of complications at 5-year follow-up.¹⁷⁴ On the other hand, no study has been able to show increased survival or lower rupture rates in patients who underwent rigid follow-up protocols.¹⁷⁴

Though there is no consensus among the various health services and publications, recommendations for postoperative follow-up after endovascular treatment are based on CT angiography 30 days after index procedure and, in the absence of leaks and with satisfactory sealing zones, patients should undergo annual CT angiographies. In case of endoleak or aneurysm sac enlargement, examinations should be performed every 6 months.¹⁷⁵,¹⁷⁶

Some authors have shown safety in ultrasound follow-up, either standalone or after an initial CT angiography, showing adequate sealing zones and absence of type I or III endoleak.¹⁷⁵,¹⁷⁷ Contrast ultrasonography is still little used, but has superior sensitivity to CT angiography in identifying endoleaks. It is cheaper, does not use radiation, and has no renal toxicity. Its drawbacks are similar to those of conventional ultrasonography: dependence of examiner experience and limitations related to obesity and abdominal gases.¹⁷⁸ In patients who underwent open surgery, imaging examinations should be performed every 5 years, preferably including CT angiography.¹⁷¹

Recommendations for postoperative follow-up for AAAs treated with OS or EVAR can be found in Table 10.

Table 10
Recommendations for postoperative follow-up for abdominal aneurysms treated with conventional or endovascular procedures.

Recommendation	Level of evidence
CT angiography 30 days after endovascular treatment of abdominal aortic aneurysms is recommended at follow-up.	I
After the initial CT angiography, if there is no endoleak or aneurysm growth, the next examination should be performed at 12 months. This examination may be a CT angiography or Doppler ultrasound, depending on patient and health care service characteristics.	I
If the initial 30-day CT angiography finds a type II endoleak, an imaging examination should be repeated at 6 months. This examination may be a CT angiography or Doppler ultrasound, depending on patient and health care service characteristics.	IIb
If the imaging examination at 12 months finds no endoleak, no aneurysm sac growth, and adequate sealing areas, an imaging examination should be performed annually or at longer intervals no greater than once every 5 years.	IIb
CT scans of the aorta and iliac arteries should be performed every 5 years for patients who underwent open repair of abdominal aortic aneurysms.	IIb

POSTOPERATIVE COMPLICATIONS

Graft infection

Aortic graft infection is an infection of a primary prosthesis. The concept includes both grafts used in OS and endografts used in endovascular repair. The complication is rare: the literature reports a 1 percent rate of incidence,¹⁷⁹,¹⁸⁰ mostly within one year of the procedure. Recent data found no statistically significant difference between patients who underwent OS and those who underwent endovascular repair.¹⁸¹ The primary sources of infection are: contamination during implantation; aortoenteric fistula (AEF) or erosion to adjacent organ (gastrointestinal tract or airways); or, more rarely, hematogenous dissemination.¹⁸²

Early infections (within 3 months of intervention) are frequently associated with fever, abdominal or back pain, and leukocytosis, while in late infections (after 3 months of intervention), symptoms are insidious, such as fatigue, malaise, and weight loss, with or without fever.¹⁷⁹ AEF patients often have more severe symptoms, such as bleeding, sepsis, and hemorrhagic shock.¹⁸³

Initial supplementary diagnostic tests include laboratory tests, blood culture, and imaging examinations, preferably CT angiography. In cases of suspected AEF or hemorrhage, an endoscopy and/or colonoscopy is indicated. The diagnostic criteria proposed by Lyons et al.¹⁸⁴ are especially useful in cases of suspected aortic graft infection. Radiological findings include perigraft fluid ≥ 3 months postimplantation, perigraft gas ≥ 7 months postimplantation or increased gas in serial CT scans, abscess, inflammatory changes, rapid aneurysm growth or pseudoaneurysm.¹⁸³,¹⁸⁴

Conservative treatment is exceptional, and includes percutaneous drainage and long-term antibiotic therapy. It may be initiated for patients in pre-op preparation or for very high surgical risk patients as palliative care.¹⁷⁹,¹⁸⁵,¹⁸⁶

For acceptable surgical risk patients and aortic graft infection, the recommended treatment is complete excision of the prosthesis/endograft and infected tissues as definitive treatment.¹⁷⁹,¹⁸⁷ The choice of arterial reconstruction should be made on an individual basis, taking into account the type of infected graft, surgeon experience, patient status, and available materials.

The techniques available for arterial reconstruction include extra-anatomic or in situ bypass with autologous graft, cryopreserved grafts (not available in Brazil), or rifampin-soaked synthetic grafts. There is no evidence for the superiority of any form of graft, and using any of these options is acceptable for stable patients without extensive infection by multiresistant microorganisms.¹⁷⁹,¹⁸⁸

For patients with extensive perigraft abscesses or infection by multiresistant bacteria, such as methicillin-resistant S. aureus and Pseudomonas, extra-anatomic bypass or in situ femoral vein or allograft reconstruction procedures may offer more time free from reinfection.¹⁸⁹

In situ reconstructions using autologous grafts have lower reinfection rates; however, they are associated with longer operative time, incompatibility with artery size, and venous complications in the legs.¹⁸⁹,¹⁹⁰ Unstable patients requiring rapid proximal vascular control and arterial reconstruction should preferably be treated with allografts (if readily available) or rifampin-soaked synthetic grafts.¹⁸³,¹⁸⁹-¹⁹¹

Endovascular treatment has a role in situations requiring rapid hemorrhage control, and can increase AEF patient survival when used as bridge therapy to definitive treatment. In patients clinically unable to undergo infected graft excision, endovascular repair may be considered as the definitive treatment. In these cases, lifelong antibiotic therapy should be considered.¹⁷⁹,¹⁸³,¹⁹²

Aortic graft infection has a high early mortality rate, ranging from 15 to 22 percent.¹⁷⁹ Despite the progressive increase in the treatment of aortic aneurysms in recent years with the advent of endovascular repair, it remains a rare complication and scientific evidence about its treatment consequently remains limited.

Treatment and follow-up for these patients require a multidisciplinary team, involving infectious disease specialists to establish appropriate antibiotic therapy. Intravenous antibiotic therapy is recommended for a period of 6 weeks, followed by oral antibiotics for 3-6 months, depending on the extent of the infection, associated microorganisms, and type of repair.¹⁸⁹,¹⁹³,¹⁹⁴ Lifelong antibiotic therapy is recommended in select cases, such as patients with extensive infections, resistant microorganisms, in situ reconstructions with grafts or endovascular without full resection of the infected graft.¹⁷⁹,¹⁹²,¹⁹⁵,¹⁹⁶

Follow-up should include imaging examinations and laboratory tests every 3-6 months during the first year, and every 6-12 months afterwards.¹⁷⁹

Endoleak

EVAR is associated with complications that may lead to endograft failure and rupture of the aneurysm sac over time, thus requiring follow-up and monitoring.¹⁹⁷-²⁰⁰ The goal of this section is to provide a critical discussion of major post-EVAR complications associated with endoleaks and their implications in follow-up in order to recognize them and treat them before refilling and pressurization of the aneurysm sac.²⁰⁰,²⁰¹

Post-EVAR complications are found in 16 to 33 percent of patients.²⁰⁰,²⁰¹ A more recent study found a 26 percent complication rate, of which 39.4 percent were observed within the first year.²⁰⁰ The most frightening complication is an aneurysm rupture, which may be the result of endoleaks, pressurization of the aneurysm (endotension), migration, deterioration of endografts or degeneration of the proximal neck caused by aneurysm progression.¹⁹⁸,²⁰⁰

Endoleak refers to the presence of flow in the aneurysm sac outside the endograft after EVAR,²⁰² and is observed in 1/3 of all cases,¹⁹⁹ though prevalence depends on type of endograft used as well as imaging examinations performed during follow-up.¹⁹⁷,²⁰⁰,²⁰¹ Endoleaks are classified as primary/early (present at the time of the repair) or secondary/late (detected postoperatively using prior normal control images),²⁰³ as well as to the cause of the periendograft flow. The presence of an endoleak affects aneurysm sac retraction over time due to the pressurization of the aneurysm sac.¹⁹⁹ Approximately half of all leaks (especially type II leaks) resolve spontaneously, without requiring reintervention.¹⁹⁹ Antiplatelet therapy may increase the risk of endoleaks after EVAR.²⁰⁴ Early detection of the complication, before it becomes clinically relevant, enables its treatment and prevents more severe scenarios. Thus, vascular surgeons should be familiar with existing imaging examinations for post-EVAR follow-up in order to diagnose and better manage potential complications.²⁰⁵

Currently, patients with anatomies not favoring endovascular treatment increasingly undergo this form of therapy, requiring more adjunctive procedures and suffering from higher rates of secondary intervention, despite improvements in materials. Therefore, surgeons who offer the choice of EVAR for patients are expected to be familiarized with these complications and know how to properly utilize studies and preparatory work, accurately classify the type of leak, and indicate the proper moment for a secondary intervention.²⁰⁶

Type I endoleak

A type I endoleak is defined as an inadequate circumferential sealing in the areas of graft fixation to the aortic wall, promoting persistent direct flow in the aneurysm sac.¹⁹⁷,¹⁹⁹,²⁰⁰ It can be further subdivided into type Ia, when the leak comes from proximal fixation (proximal neck); Ib, with the leak in the distal fixation region (iliac axis); and Ic, when the leaks is caused by direct communication between the aorta and the iliac artery after an occluder plug is placed in the iliac artery when using a mono-iliac endograft.²⁰⁷ Since this form of leak involves direct pressurization of the aneurysm sac, often accompanied by aneurysm enlargement and consequently an increased risk of rupture, a type I endoleak should be promptly treated with the aim of excluding the aneurysm from pressurized circulation. Endovascular repair options for type Ia endoleaks include balloon dilation of endograft fixation points with or without stenting or use of endovascular clamps (endoanchors) for endograft tissue fixation to the aortic wall if there was no migration and in the presence of an adequate sealing zone (proximal neck).²⁰⁸ More often, proximal extension of the sealing zone is required, including implantation of a proximal cuff or fenestrated endograft. In type Ib endoleaks, extension to the distal iliac artery is usually enough.²⁰⁸ However, if the disease progresses by distal neck degeneration, involving the iliac bifurcation, the physician should consider extension to the external iliac artery or the use of a bifurcated iliac endograft. If an endovascular option is not available in a timely manner and the patient meets the criteria for open surgery, conversion is recommended and has acceptable outcomes.²⁰⁹

Type II endoleak

A type II endoleak is defined as retrograde blood flow from collateral aortic branches filling the aneurysm sac. The most frequently involved arteries in type II endoleaks are the inferior mesenteric and lumbar arteries.^203205206 In case of aneurysm sac enlargement due to suspected type II endoleak, adequate imaging examinations should be performed to rule out other causes, such as inadequate sealing or type III internal endoleak (connection, integrity of graft or suture holes).²¹⁰ It is classified as type IIa when only one collateral branch is involved and type IIb when two or more branches flow into the aneurysm sac.²¹¹

They are divided into:

21. Early type II, when diagnosed within 30 days post-EVAR;

22. Late type II, when diagnosed between 30 days and 6 months post-EVAR;

23. Persistent type II, when sustained for over 6 months post-EVAR.

In a meta-analysis of 2,367 patients who underwent EVAR, 18 percent had early type II endoleaks that resolved spontaneously, 5 percent had persistent type II endoleaks, and 11 percent had new type II leaks during follow-up.²⁰⁶ Approximately half of all patients with persistent or late endoleaks suffered from sac enlargement, and the reintervention rate was 50 percent within 2 years. Factors associated with persistent or recurring type II endoleaks include internal iniliac artery coil embolization, distal graft extension, age over 80, and anatomic characteristics such as number of patent side branches arising from the aneurysm, thrombus in aneurysm sac, and diameter of lumbar (> 0.2 cm) and inferior mesenteric arteries (> 0.3 cm).²¹²,²¹³ Preoperative embolization of the aneurysm sac in select patients has been suggested to reduce the risk of developing type II endoleaks,²¹⁴,²¹⁵ but the benefit of fewer reinterventions or lower incidence of rupture is still controversial.²¹⁶

The progression of most type II endoleaks seems to be benign, but aneurysm rupture may happen even so.²¹⁷ However, in a systematic review of retrospective studies, fewer than 1 percent of type II endoleaks resulted in ruptures, and reintervention was indicated to repair persistent leaks with aneurysm sac enlargement.²¹⁰,²¹⁸ Though most ruptures appear to be related to aneurysm enlargement, there are also report of ruptures in the absence of aneurysm expansion.²¹¹ Some centers treat type II endoleaks in case of aneurysm sac enlargement > 1 cm, while others use > 0.5 cm; the latter number is the threshold for detecting aneurysm sac enlargement when comparing two imaging examinations using the same technique.²⁰⁶

Endovascular repair may be performed using embolization of the aneurysm sac and/or feedback vessels using transarterial, translumbar, transcaval or transealing (between the iliac branch of the endograft and the native iliac artery wall) approaches, with a wide variety of devices.²¹⁰,²¹⁸ Technical success is achieved in 60 to 80 percent of cases; however, there is no objective definition of indication and management for these cases, which may impact interpretation.²⁰⁶

Surgical treatment options include laparoscopic ligation or open repair of side branches flowing back into the aneurysm sac, suturing of the ostia under direct visualization after opening the aneurysm sac or surgically removing the endograft, with conversion to conventional surgery in cases of failure of endovascular treatment.²⁰⁶,²¹⁰,²¹⁹

Type III endoleak

A type III endoleak can be defined as a secondary leak after a structural failure of the endograft. It is classified as type IIIa if caused by disconnection between components, and type IIIb if caused by manufacturing defects, with the latter further subdivided into those with holes larger or smaller than 0.2 cm. These endoleaks may also be caused by malpositioned endografts with inadequate superposition, proximal or distal endograft migration, or material fatigue.¹⁹⁷,¹⁹⁹,²⁰⁰ It has an incidence rate of 2.1 percent within 4 years post-EVAR, with type IIIa accounting for 56 percent of cases and type IIIb for 44 percent.²²⁰ However, with the use of more modern endografts, the incidence rate can fall to 1 percent.

Similar to type I endoleaks, in type III there is direct pressurization of the aneurysm sac, with subsequent risk of rupture.²¹⁷ Therefore, immediate endovascular repair is recommended; the most widely used options are implantation of iliac extension, coaxial cuff at the leak site, implantation of new bifurcated endograft, or conversion to mono-iliac endograft, followed by revascularization of the controlateral limb using femoral-femoral crossover bypass. Conversion to open surgery is required only if the endovascular measures described are unable to control the leak.²²⁰,²²¹

Type IV endoleak

Type IV endoleaks are very rare in clinical practice, related to graft fabric porosity, and may be related to the use of anticoagulant or antiplatelet therapy. The blood leaks through intact fabric; in the vast majority of cases it is resolved within 30 days of the procedure, and is considered benign.¹⁹⁷,¹⁹⁹,²⁰⁰ According to a review of post-EVAR ruptures reported in the literature until 2008, no cases of ruptures caused by type IV leaks were found.²¹⁷ Type IV leaks are rare for most modern devices and do not require reintervention.

Type V endoleak or endotension

The type V endoleak, also known as endotension, is the presence of sac enlargement without an identifiable endoleak. The incidence rate ranges from 1.5 to 5 percent, and all other types of endoleak must be ruled out before a definitive diagnosis.¹⁹⁷,¹⁹⁹,²⁰⁰ Several possible mechanisms for endotension have been suggested, including endograft permeability, resulting in direct transmission of pressure through endografts to the aortic wall, or the use first-generation polytetrafluoroethylene endografts, which might hinder thrombus organization and fibrinolysis in the aneurysm sac.²²² However, given the definition, cases classified as endotension might be caused by a form of endoleak undeterminable by current imaging technologies.²²² Treatment sis recommended for cases of significant aneurysm sac enlargement (> 1 cm) and consists in open surgery to realign or remove the endograft.²²³

Migration

Conceptually, endograft migration is defined as endograft movement > 1 cm compared to fixed anatomic reference points, checked against the midline of tomographic reconstructions, or any migration resulting in symptoms or reintervention.²²⁴ Endograft migration used to be a common event, and most studies on risk factors for proximal device migration were performed using case series involving first-generation endografts, but the development of suprarenal or infrarenal active fixation in more modern endografts led to decreased prevalence of migration.²²⁵,²²⁶

Migration can result in type I endoleak, disconnection between endograft components, kinking, and branch vessel occlusion. Factors contributing to proximal migration include short proximal fixation, angulated neck, large aneurysms, endograft type,²²⁴,²²⁷,²²⁸ and oversized endografts (> 30 percent); the latter is controversial, but there is evidence that it may also contribute to migration.²²⁹,²³⁰ Disease progression with proximal neck dilation may cause migration, and is related to initial neck diameter.²³¹

Migration may also occur due to changes in aneurysm morphology or aneurysm sac retraction after EVAR. Iliac fixation length (distal neck) of at least > 2 cm, or preferably up to the iliac bifurcation, reduces the risk of endograft migration.²³²,²³³

Table 11 summarizes recommendations for treatment of endoleaks.

Table 11
Recommendations for treatment of endoleaks after endovascular repair of abdominal aortic aneurysms.

Recommendation	Level of evidence
In patients with type I endoleak after endovascular repair of an abdominal aortic aneurysm, early reintervention is recommended to achieve aneurysm sealing and exclusion, preferably via endovascular procedure.	I
Preserving at least one hypogastric artery in case of iliac bifurcation involvement.	I
Reintervention for type II endoleak treatment after endovascular repair for abdominal aortic aneurysm should be considered in the presence of significant aneurysm growth, preferably via endovascular procedure.	IIa
Aneurysm sac diameter growth greater than 1 cm found at follow-up after endovascular repair of abdominal aortic aneurysm, using the same imaging and measurement techniques, may be considered a reasonable criteria to detect significant growth in cases of type II endoleak.	IIb
In patients with type III endoleak after endovascular repair of an abdominal aortic aneurysm, reintervention is recommended, preferably via endovascular procedure.	IIa
Significant aneurysm sac growth after endovascular repair of abdominal aortic aneurysm without endoleak identified in standard imaging examinations requires considering additional diagnostic assessment and possible endograft realignment or explantation.	IIa

RUPTURED ABDOMINAL AORTIC ANEURYSM

A ruptured aortic aneurysm is one of the most dramatic conditions in emergency care patients. It is lethal in the vast majority of cases, if not all, when untreated. The primary factors for rate of rupture are size, morphology, and growth rate.²³⁴ In Brazil, it is estimated that between 2000 and 2016, ruptures were the direct cause of 38,000 deaths, representing 55 percent of all aortic aneurysm-related mortality.⁴ Historically, the in-hospital mortality rate for ruptured aneurysms was 50 percent, but widespread endovascular treatment has led to a drop in mortality, which currently ranges from 20 to 30 percent.²³⁴-²³⁷

The classic symptom triad of ruptured AAAs includes hypotension, abdominal pain, and pulsatile mass. There may be other manifestations, however, such as back pain and groin pain; in case of visceral perforation, there may be gastrointestinal tract bleeding, with subsequent hematemesis or melaena. There is a peculiar form of rupture, i.e., rupture into the inferior vena cava, that manifests as an aortocaval fistula, with abdominal fremitus as its frequent sign, which may be associated with acute and severe heart failure and paradoxical pulmonary embolism.⁶

Anatomically, the rupture site is also associated with prognostic factors. AAA rupture is the most frequent, and there are differences if it occurs in the anterior or posterior aneurysm wall. In the interior wall, it usually also perforates the retroperitoneum and flows into the peritoneal cavity, which hinders tamponading, and many patients in this situation die before they can have access to hospital care. Ruptured aneurysm tamponade is often caused by rupture of the posterior wall, and the spinal column and iliopsoas muscles help contain the bleeding, giving the patient a higher statistical likelihood of arriving at the hospital alive to receive care.

Diagnosis begins with clinical suspicion, and is possibly easier when the patient is aware of a prior diagnosis of AAA. The challenge may be maintain a high degree of suspicion for hypotensive patients with a life-threatening condition, but no apparent cause.

The establishment of protocols and the volume and experience of the health care service are associated with better outcomes and higher chances of survival throughout the world.⁷,²³⁸-²⁴⁰ Both diagnosis and referral for treatment require a pre-established workflow in hospital departments.

Patients with ruptured aneurysms should receive initial care at the emergency room, where large-bore peripheral access should be inserted and the first sample for laboratory tests collected. Volume replacement should be used with the goal of achieving permissive hypotension,⁷,²³⁸ which means keeping the patient conscious and their systolic blood pressure between 70 and 90 mmHg. The stabilization is recommended in case the patient has to be transferred to a center with an aortic team and prepared for both types of therapy, endovascular or conventional repair.

Abdominal ultrasound and chest X-rays are usually widely available in emergency rooms; the first can reveal free fluid in the abdominal cavity or costal recess, while the latter can show opacification of a hemithorax, or increased cardiac area in case of thoracic

However, these tests cannot rule out rupture, because the bleeding may be contained, and the diagnostic examination of choice is a CT angiography of the aorta, which should include planes from the ascending aorta and the arch to the common femoral arteries. Adequate technique is crucial for surgical planning.

CT angiography can find clear or indirect signs of abdominal aortic rupture. These are blurring of the psoas, aortic wall discontinuity, contrast extravasation, crescent sign or thrombus fissuration, and intraperitoneal or retroperitoneal hematoma.²⁴¹

Historically, the treatment of ruptured aneurysms had a high mortality rate, but the advent of endovascular surgery has significantly decreased that rate. After 20 years of consistent endovascular repairs, there is strong evidence, from randomized trials and meta-analyses, that faced with a ruptured aortic aneurysm, endovascular repair is absolutely better than open surgery.⁶,⁷,²³⁴,²³⁶,²³⁷,²⁴²,²⁴³

The better outcome translates into lower medium and long-term mortality as well as lower 30-day mortality rates, in addition to lower complications rates in recovery, such as ostomies and amputations, and better quality of life.²⁴² Therefore, training the team, providing material and operating rooms for open or endovascular repair can directly impact the likelihood that patients survive ruptures.²³⁸

The main limitation to EVAR in cases of ruptured AAA is patient anatomy, more specifically the diameter and proximal neck length of the endograft fixation site. Therefore, in the absence of these conditions or of materials and teams for endovascular treatment, open surgery is required, and the reference center should be ready for both options.

Permissive hypotension and patient preparation for anesthesia with the surgical team in position for intervention may reduce the chance of overcoming the tamponade. Therefore, coordination with the anesthesia team is critical. Volume and blood product replacement are part of an effective therapy.

Both repairs may require supraceliac aortic clamping in case of severe hypovolemic shock. This may be an open procedure, via midline laparotomy, blunt dissection of the lesser curvature of the stomach, and aortic clamping to the spinal cord. It may also be an endovascular procedure, and even performed under local anesthesia, via femoral access by dissection, placement of 12FR introducer sheath and ipsilateral guidewire for the aortic occluding balloon, which can be inflated at the level of the 12th thoracic vertebra.²³⁸ It should be stressed that hemodynamically unstable patients have high mortality rates, and systolic pressure below 70 mmHg is an independent predictor of death. Finally, keep in mind that in cases of this nature, submitting an unstable patient to conventional repair is almost always fatal, and endovascular repair is even more justified in that condition.⁷

EVAR has an additional advantage over conventional treatment of ruptured aneurysms, i.e., the possibility of administering local anesthesia and using sedation only if required²³⁸—current evidence indicates better outcomes for patients treated under local anesthesia, hemodynamics permitting.²⁴⁴-²⁴⁶ In addition, not intubating patients with ruptured aneurysms is associated with a higher likelihood of survival.²³⁴

The choice between bifurcated and mono-iliac endografts has to involve surgeon experience and preferences, since achieving rapid hemostasis is key. The time to catheterization of the contralateral branch vessel should not be extended, but avoiding a femoral-femoral crossover bypass graft also has advantages for the patient. Overall, prioritizing the use of bifurcated endografts seems reasonable as group experience advances.⁶

Recommendations for treatment of ruptured AAAs can be found in Table 12.

Table 12
Recommendations for treatment of ruptured abdominal aortic aneurysms.

Recommendation	Level of evidence
In cases of ruptured abdominal aortic aneurysm, endovascular repair is recommended.	I
If the hospital is unable to offer endovascular repair, transferring the patient to a specialty center is acceptable, as long as their clinical condition and hemodynamics allow it.	IIa
Volume replacement should be used in order to keep the patient conscious and their systolic blood pressure between 70 and 90 mmHg.	I
In patients arriving at the hospital, consider stabilization and thoracoabdominal CT angiography to assist surgical planning.	IIb
The use of bifurcated endografts is preferred, given adequate anatomical conditions.	IIb

INFLAMMATORY ANEURYSM

Inflammatory aortic aneurysms are characterized by a thick layer of inflammatory tissue frequently associated with periaortic and retroperitoneal fibrosis and adherence to neighboring organs and tissues. Exuberant inflammatory infiltrates in the adventitia are among the primary differences between it and an atherosclerotic degenerative aneurysm.²⁴⁷ The condition makes open surgical treatment difficult, and potentially lethal.²⁴⁸ The literature reports incidence rates ranging from 5 to 18 percent.²⁴⁸,²⁴⁹

From a physiopathological perspective, the mechanisms causing the inflammation are still poorly understood. Clinical symptoms, such as back pain, fever, weight loss, and loos of appetite, may be present. Major risk factors identified thus far are male gender, smoking, and genetics^253.255. Unlike other inflammatory or rheumatological diseases, aortic inflammation is most often isolated, with no involvement of other arteries.²⁴⁸

Laboratory tests may be altered, including leukocytes and inflammatory markers, such as C-reactive protein. CT angiography of the aorta reveals signs such as periaortic thickening, which may also include retroperitoneal involvement, and has high diagnostic sensitivity.²⁴⁷ Though they are not as sharp and clear as the images produced by CT angiography, abdominal ultrasounds can often identify a hyperechogenic halo around the aortic wall. Positron emission tomography can also reveal periaortic inflammation.²⁴⁸

OS can be challenging, and possibly lethal, due to adhesions to adjacent organs, such as the inferior vena cava, ureters, and small intestine, which may require enterectomies.²⁴⁷,²⁵⁰ Give this history, endovascular repair is increasingly used to treat inflammatory aneurysms. However, it should be stressed that after analyzing the published data, we still lack randomized and long-term follow-up trials to verify its efficacy and safety.²⁴⁸,²⁵⁰

ANEURYSMS IN WOMEN

AAAs are less common in women compared to men, at a ratio ranging from 1:4 to 1:9 in the literature. There are no randomized clinical trials analyzing AAA in women specifically. However, there are many scientific studies about this important subject. The prevalence of AAAs among people over of 60 is 0.7 percent, and it increases rapidly with age.¹⁰⁰ Operative mortality increases with age, and women have clinically relevant AAA at older ages compared to men. AAA morphology differs significantly between the two: men tend to have larger aortas, iliac arteries, and femoral arteries than women. Women are older and have smaller AAAs at treatment.¹⁹,³⁶,¹⁰⁰,²⁵¹

The EVAR 1, DREAM, OVER, and ACE randomized trials found a significant decrease in mortality among open surgery and endovascular repair patients and similar long-term survival.²⁰⁶ It is not clear that both genders benefited equally. Women had fewer advantages, but since they were only a small part of the trials (0.6 to 9 percent), a more accurate statistical analysis is not possible.

Several theories have been suggested to explain the differences between male and female AAA patients, but there are still no definitive conclusions. A few studies using statistical data stand out: Ulug et al.,¹⁰⁰ in a systematic meta-analysis of nine studies conducted between 2005 and 2016, which included 52,018 men and 11,076 women, found a post-EVAR 30-day mortality rate of 1.4 percent for men and 2.3 percent for women. In open surgery, the numbers were worse: 2.8 percent for men, 5.4 percent for women. Sidloff et al.,²⁵² in their analysis of the UK National Vascular Registry (United Kingdom, 2010-2014), which included 23,245 patients, of which 13 percent were women, found a 30-day post-EVAR mortality rate of 0.7 percent for men and 1.8 percent for women. In open surgery, mortality numbers were worse: 4 percent for men, 6.9 percent for women. Deery et al., in their analysis of the American College of Surgeons National Surgical Improvement Program (2011-2014), found a 30-day mortality rate of 1.2 percent for men and 3.2 percent for women post-EVAR. In open surgery, the numbers were worse: 4 percent for men, 8 percent for women.²⁵³ Erben et al.²⁵⁴ report a higher rate of complications and reinterventions in women, especially due to arterial thrombosis of the lower limbs.

Though the mortality of AAA treatment decreased exponentially over the last decade, female mortality remains excessively high, especially for open surgery. Wanhainen et al.,⁶ in the Guidelines they organized, found a 6.9 percent mortality rate for women who underwent open repair for AAA, compared to 1.8 percent after endoluminal repair. Though not statistically important, statistically significant higher rates of complications and mortality for women still persist. Recent studies, such as Tumer et al.,²⁵⁵ Corsi et al.,²⁵⁶ Ilyas et al.,²⁵⁷ Tedjawirja et al.²⁵⁸ continue to find higher mortality for women.

The causes are multifactorial: even though they have fewer AAAs, women have them at more advanced ages, with more comorbidities, and are generally underdiagnosed. In particular, AAA at advanced ages are more often associated with occlusive arterial disease, which represents a more challenging anatomy for endovascular treatment. For these reasons, women have higher rates of complications and postoperative mortality, both for open surgery and for endovascular treatment. In short, they have worse prognoses. For better prognoses, their AAAs should be treated more often once they reach 4 cm in diameter³⁶,¹⁰⁰,²⁵¹-²⁵⁹

In women, AAAs rupture at smaller diameters than men. Solberg et al.²⁶⁰ showed that AAAs grow faster in women compared to men. In terms of risk of rupture, a 4.5 cm AAA in women has the same risk as a 5.5 cm one in men. With a diameter of 5 cm, women are at risk of rupture in 1/30 of cases (3.3 percent). It is also known that with identical diameters, the risk of rupture is 4 times greater for women than for men.¹⁹,³⁶,²⁵¹,²⁵⁹ The causes may also be multifactorial, but in absolute values, the most important one is that women's arteries are approximately 1/3 smaller than men's in diameter, meaning AAA diameter is proportionally much larger in women, which makes ruptures easier. We also cannot compare anatomical data from English-speaking countries, where most population studies about AAA are conducted, with data for Brazilians, who tend to be smaller, especially women. The data for Asian populations, more similar to Brazilians in size, has been very well analyzed.²⁶¹ Therefore, in recent years, many publications have indicated treating AAA starting at 4.5 cm in diamater in women, and especially not letting it grow past 5 cm, in elective cases.²⁵²,²⁵⁴,²⁵⁷-²⁶³ The surgical risk for endovascular treatment in several studies is under 2 percent. Therefore, it would be logical to recommend this effective form of treatment prophylactically for women with AAA when the diameter is greater than 4.5 cm.

Women are known to often have aortoiliac morphology unfavorable to EVAR—short and angulated necks and smaller iliac and femoral arteries, frequently incompatible with endograft introducer system diameters. Sweet et al.²⁶⁴ report that 70 percent of men, but only 40 percent of women, had anatomies compatible with instructions for use for the endografts available in 2011. In previous decades, the situation was even worse. At the moment, there are no endografts designed specifically for women. However, the challenges specific to female anatomy have recently become the topic of specific studies, and adequate devices are being developed to expand indications for EVAR in women. This would also decrease complication rates. Recent data suggests poor historical outcomes may be related to technical problems rather to gender differences themselves. There are three ultra-low profile endograft systems: Incraft^®, Ovation^®, and Altura^®. Others are currently in development. There are long term studies about the first two systems, and they compare favorably to historical results for AAA treatment in women.²⁶⁵-²⁶⁷

Women with AAA are treated at older ages, with more comorbidities, and have proportionally larger aneurysms. They frequently have anatomies hostile to EVAR, with small-caliber aortas, iliac arteries, and femoral arteries, as well as more advanced atherothrombotic disease. These situations require specific devices to overcome these challenges. In women, low profile and high flexibility endografts have had better outcomes in terms of technical success and mortality, reducing the complications associated with the procedure.

Improvements in materials, reductions in profile without loss of resistance, and accuracy of implantation should help narrow the gap between outcomes for men and women. Larger patient numbers and more multicenter trials studying the new devices to verify their long-term efficacy and durability are required before a definitive position about the subject can be established.

Recommendations for treatment of AAAs in women can be found in Table 13.

Table 13
Recommendations for treatment of abdominal aortic aneurysms in women.

Recommendation	Level of evidence
Women with abdominal aortic aneurysms with aortic diameter of 4 cm should undergo aneurysm control semiannually.	IIa
Elective treatment of abdominal aortic aneurysms in women with aortic diameter of 5 cm or larger is recommended.	IIa
For endovascular treatment of abdominal aortic aneurysms in women, a device with delivery system dimensions compatible with patient anatomy should be found. Low-profile endografts should be considered, if required.	IIb

• How to cite:
  Mulatti GC, Joviliano EE, Pereira AH, et al. Brazilian Society for Angiology and Vascular Surgery guidelines on abdominal aortic aneurysm. J Vasc Bras. 2023;22:e20230040. https://doi.org/10.1590/1677-5449.202300402
• Financial support:
  None.
• The study was carried out at Sociedade Brasileira de Angiologia e Cirurgia Vascular (SBACV), São Paulo, SP, Brasil.
• Ethics committee approval:
  CAAE number 62177722.2.0000.0068.

REFERENCES

• ¹ Nobre MRC, Bernardo WM. Diretrizes AMB/CFM. Rev Assoc Med Bras. 2002;48(4):290. http://dx.doi.org/10.1590/S0104-42302002000400027
  » http://dx.doi.org/10.1590/S0104-42302002000400027
• ² Migowski A, Stein AT, Da M, Santos S, Ferreira DM. Diretrizes metodológicas: elaboração de diretrizes clínicas [Internet]. Brasília: Ministério da Saúde; 2016 [cited 2023 Mar 13]. https://www.researchgate.net/publication/303564633
  » https://www.researchgate.net/publication/303564633
• ³ Kent KC, Zwolak RM, Egorova NN, et al. Analysis of risk factors for abdominal aortic aneurysm in a cohort of more than 3 million individuals. J Vasc Surg. 2010;52(3):539-48. http://dx.doi.org/10.1016/j.jvs.2010.05.090 PMid:20630687.
  » http://dx.doi.org/10.1016/j.jvs.2010.05.090
• ⁴ Santo AH, Puech-Leão P, Krutman M. Trends in abdominal aortic aneurysm-related mortality in Brazil, 2000-2016: a multiple-cause-of-death study. Clinics. 2021;76:e2388. http://dx.doi.org/10.6061/clinics/2021/e2388 PMid:33503194.
  » http://dx.doi.org/10.6061/clinics/2021/e2388
• ⁵ von Ristow A, Estensoro AE, Corrêa MP, Presti C. Aneurismas da aorta abdominal: diagnóstico e tratamento. São Paulo: SBACV; 2015.
• ⁶ Wanhainen A, Verzini F, van Herzeele I, et al. European Society for Vascular Surgery (ESVS) 2019 clinical practice guidelines on the management of abdominal aorto-iliac artery aneurysms. Eur J Vasc Endovasc Surg. 2019;57(1):8-93. http://dx.doi.org/10.1016/j.ejvs.2018.09.020 PMid:30528142.
  » http://dx.doi.org/10.1016/j.ejvs.2018.09.020
• ⁷ Chaikof EL, Dalman RL, Eskandari MK, et al. The Society for Vascular Surgery practice guidelines on the care of patients with an abdominal aortic aneurysm. J Vasc Surg. 2018;67(1):2-77.e2. http://dx.doi.org/10.1016/j.jvs.2017.10.044 PMid:29268916.
  » http://dx.doi.org/10.1016/j.jvs.2017.10.044
• ⁸ Sterne JAC, Savović J, Page MJ, et al. RoB 2: a revised tool for assessing risk of bias in randomised trials. BMJ. 2019;366:l4898. http://dx.doi.org/10.1136/bmj.l4898
  » http://dx.doi.org/10.1136/bmj.l4898
• ⁹ Wells G, Shea B, O’Connel D. The Newcastle-Ottawa scale (NOS) for assessing the quailty of nonrandomised studies in meta-analyses [Internet]. Ottawa: Ottawa Hospital Research Institute; 2009 [cited 2023 Mar 13]. https://www.ohri.ca/programs/clinical_epidemiology/oxford.asp
  » https://www.ohri.ca/programs/clinical_epidemiology/oxford.asp
• ¹⁰ Tan KHM, Salim S, Machin M, et al. Abdominal aortic aneurysm clinical practice guidelines: a methodological assessment using the AGREE II instrument. BMJ Open. 2022;12(1):e056750. http://dx.doi.org/10.1136/bmjopen-2021-056750 PMid:35058266.
  » http://dx.doi.org/10.1136/bmjopen-2021-056750
• ¹¹ Erbel R, Aboyans V, Boileau C, et al. 2014 ESC guidelines on the diagnosis and treatment of aortic diseases. Eur Heart J. 2014;35(41):2873-926. http://dx.doi.org/10.1093/eurheartj/ehu281 PMid:25173340.
  » http://dx.doi.org/10.1093/eurheartj/ehu281
• ¹² Bradbury AW, Davies AH, Dhesi JK, et al. Recommendations on the use of open surgical and endovascular aneurysm repair for the management of unruptured abdominal aortic aneurysm from the guideline development committee appointed by the UK National Institute for Health and Care Excellence. Eur J Vasc Endovasc Surg. 2021;61(6):877-80. http://dx.doi.org/10.1016/j.ejvs.2021.01.047 PMid:33685761.
  » http://dx.doi.org/10.1016/j.ejvs.2021.01.047
• ¹³ Schanzer A, Greenberg RK, Hevelone N, et al. Predictors of abdominal aortic aneurysm sac enlargement after endovascular repair. Circulation. 2011;123(24):2848-55. http://dx.doi.org/10.1161/CIRCULATIONAHA.110.014902 PMid:21478500.
  » http://dx.doi.org/10.1161/CIRCULATIONAHA.110.014902
• ¹⁴ Chisci E, Kristmundsson T, de Donato G, et al. The AAA with a challenging neck: outcome of open versus endovascular repair with standard and fenestrated stent-grafts. J Endovasc Ther. 2009;16(2):137-46. http://dx.doi.org/10.1583/08-2531.1 PMid:19456190.
  » http://dx.doi.org/10.1583/08-2531.1
• ¹⁵ Svensjö S, Björck M, Gürtelschmid M, Djavani Gidlund K, Hellberg A, Wanhainen A. Low prevalence of abdominal aortic aneurysm among 65-year-old swedish men indicates a change in the epidemiology of the disease. Circulation. 2011;124(10):1118-23. http://dx.doi.org/10.1161/CIRCULATIONAHA.111.030379 PMid:21844079.
  » http://dx.doi.org/10.1161/CIRCULATIONAHA.111.030379
• ¹⁶ Jacomelli J, Summers L, Stevenson A, Lees T, Earnshaw JJ. Impact of the first 5 years of a national abdominal aortic aneurysm screening programme. Br J Surg. 2016;103(9):1125-31. http://dx.doi.org/10.1002/bjs.10173 PMid:27270466.
  » http://dx.doi.org/10.1002/bjs.10173
• ¹⁷ Grøndal N, Søgaard R, Lindholt JS. Baseline prevalence of abdominal aortic aneurysm, peripheral arterial disease and hypertension in men aged 65-74 years from a population screening study (VIVA trial). Br J Surg. 2015;102(8):902-6. http://dx.doi.org/10.1002/bjs.9825 PMid:25923784.
  » http://dx.doi.org/10.1002/bjs.9825
• ¹⁸ Lee ES, Pickett E, Hedayati N, Dawson DL, Pevec WC. Implementation of an aortic screening program in clinical practice: implications for the Screen for Abdominal Aortic Aneurysms Very Efficiently (SAAAVE) act. J Vasc Surg. 2009;49(5):1107-11. http://dx.doi.org/10.1016/j.jvs.2008.12.008 PMid:19307082.
  » http://dx.doi.org/10.1016/j.jvs.2008.12.008
• ¹⁹ Ulug P, Powell JT, Sweeting MJ, et al. Meta-analysis of the current prevalence of screen-detected abdominal aortic aneurysm in women. Br J Surg. 2016;103(9):1097-104. http://dx.doi.org/10.1002/bjs.10225 PMid:27346306.
  » http://dx.doi.org/10.1002/bjs.10225
• ²⁰ Ullery BW, Hallett RL, Fleischmann D. Epidemiology and contemporary management of abdominal aortic aneurysms. Abdom Radiol. 2018;43(5):1032-43. http://dx.doi.org/10.1007/s00261-017-1450-7 PMid:29313113.
  » http://dx.doi.org/10.1007/s00261-017-1450-7
• ²¹ Sampson UKA, Norman PE, Fowkes FGR, et al. Estimation of global and regional incidence and prevalence of abdominal aortic aneurysms 1990 to 2010. Glob Heart. 2014;9(1):159-70. http://dx.doi.org/10.1016/j.gheart.2013.12.009 PMid:25432125.
  » http://dx.doi.org/10.1016/j.gheart.2013.12.009
• ²² Sidloff D, Stather P, Dattani N, et al. Aneurysm global epidemiology study: public health measures can further reduce abdominal aortic aneurysm mortality. Circulation. 2014;129(7):747-53. http://dx.doi.org/10.1161/CIRCULATIONAHA.113.005457 PMid:24249717.
  » http://dx.doi.org/10.1161/CIRCULATIONAHA.113.005457
• ²³ Lindholt JS, Juul S, Fasting H, Henneberg EW. Screening for abdominal aortic aneurysms: single centre randomised controlled trial. BMJ. 2005;330(7494):750. http://dx.doi.org/10.1136/bmj.38369.620162.82 PMid:15757960.
  » http://dx.doi.org/10.1136/bmj.38369.620162.82
• ²⁴ Ashton HA, Buxton MJ, Day NE, et al. The Multicentre Aneurysm Screening Study (MASS) into the effect of abdominal aortic aneurysm screening on mortality in men: a randomised controlled trial. Lancet. 2002;360(9345):1531-9. http://dx.doi.org/10.1016/S0140-6736(02)11522-4 PMid:12443589.
  » http://dx.doi.org/10.1016/S0140-6736(02)11522-4
• ²⁵ Norman PE, Jamrozik K, Lawrence-Brown M, et al. Population based randomised controlled trial on impact of screening on mortality from abdominal aortic aneurysm. BMJ. 2004;329(7477):1259. http://dx.doi.org/10.1136/bmj.38272.478438.55 PMid:15545293.
  » http://dx.doi.org/10.1136/bmj.38272.478438.55
• ²⁶ Scott RAP, Wilson NM, Ashton HA, Kay DN. Influence of screening on the incidence of ruptured abdominal aortic aneurysm: 5-year results of a randomized controlled study. Br J Surg. 1995;82(8):1066-70. http://dx.doi.org/10.1002/bjs.1800820821 PMid:7648155.
  » http://dx.doi.org/10.1002/bjs.1800820821
• ²⁷ Thompson SG, Ashton HA, Gao L, Scott RAP. Screening men for abdominal aortic aneurysm: 10 year mortality and cost effectiveness results from the randomised Multicentre Aneurysm Screening Study. BMJ. 2009;338:b2307. http://dx.doi.org/10.1136/bmj.b2307
  » http://dx.doi.org/10.1136/bmj.b2307
• ²⁸ Cosford PA, Leng GC. Screening for abdominal aortic aneurysm. Cochrane Database Syst Rev. 2007;(2):CD002945. http://dx.doi.org/10.1002/14651858.CD002945.pub2 PMid:17443519.
  » http://dx.doi.org/10.1002/14651858.CD002945.pub2
• ²⁹ Lederle FA. The last (randomized) word on screening for abdominal aortic aneurysms. JAMA Intern Med. 2016;176(12):1767-8. http://dx.doi.org/10.1001/jamainternmed.2016.6663 PMid:27802490.
  » http://dx.doi.org/10.1001/jamainternmed.2016.6663
• ³⁰ Wanhainen A, Hultgren R, Linné A, et al. Outcome of the Swedish Nationwide Abdominal Aortic Aneurysm Screening Program. Circulation. 2016;134(16):1141-8. http://dx.doi.org/10.1161/CIRCULATIONAHA.116.022305 PMid:27630132.
  » http://dx.doi.org/10.1161/CIRCULATIONAHA.116.022305
• ³¹ LeFevre ML. Screening for abdominal aortic aneurysm: U.S. preventive services task force recommendation statement. Ann Intern Med. 2014;161(4):281-90. http://dx.doi.org/10.7326/M14-1204 PMid:24957320.
  » http://dx.doi.org/10.7326/M14-1204
• ³² Wanhainen A, Lundkvist J, Bergqvist D, Björck M. Cost-effectiveness of different screening strategies for abdominal aortic aneurysm. J Vasc Surg. 2005;41(5):741-51. http://dx.doi.org/10.1016/j.jvs.2005.01.055 PMid:15886653.
  » http://dx.doi.org/10.1016/j.jvs.2005.01.055
• ³³ Akai A, Watanabe Y, Hoshina K, et al. Family history of aortic aneurysm is an independent risk factor for more rapid growth of small abdominal aortic aneurysms in Japan. J Vasc Surg. 2015;61(2):287-90. http://dx.doi.org/10.1016/j.jvs.2014.07.007 PMid:25175636.
  » http://dx.doi.org/10.1016/j.jvs.2014.07.007
• ³⁴ Verloes A, Sakalihasan N, Koulischer L, Limet R. Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees. J Vasc Surg. 1995;21(4):646-55. http://dx.doi.org/10.1016/S0741-5214(95)70196-6 PMid:7707569.
  » http://dx.doi.org/10.1016/S0741-5214(95)70196-6
• ³⁵ Ravn H, Wanhainen A, Björck M. Risk of new aneurysms after surgery for popliteal artery aneurysm. Br J Surg. 2008;95(5):571-5. http://dx.doi.org/10.1002/bjs.6074 PMid:18306151.
  » http://dx.doi.org/10.1002/bjs.6074
• ³⁶ Bown MJ, Sweeting MJ, Brown LC, Powell JT, Thompson SG. Surveillance intervals for small abdominal aortic aneurysms. JAMA. 2013;309(8):806-13. http://dx.doi.org/10.1001/jama.2013.950 PMid:23443444.
  » http://dx.doi.org/10.1001/jama.2013.950
• ³⁷ Hamel C, Ghannad M, McInnes MDF, et al. Potential benefits and harms of offering ultrasound surveillance to men aged 65 years and older with a subaneurysmal (2.5-2.9 cm) infrarenal aorta. J Vasc Surg. 2018;67(4):1298-307. http://dx.doi.org/10.1016/j.jvs.2017.11.074 PMid:29477237.
  » http://dx.doi.org/10.1016/j.jvs.2017.11.074
• ³⁸ Moll FL, Powell JT, Fraedrich G, et al. Management of Abdominal aortic aneurysms clinical practice guidelines of the European Society for Vascular Surgery. Eur J Vasc Endovasc Surg. 2011;41(Suppl 1):S1-58. http://dx.doi.org/10.1016/j.ejvs.2010.09.011 PMid:21215940.
  » http://dx.doi.org/10.1016/j.ejvs.2010.09.011
• ³⁹ Stather PW, Sidloff DA, Dattani N, et al. Meta-analysis and meta-regression analysis of biomarkers for abdominal aortic aneurysm. Br J Surg. 2014;101(11):1358-72. http://dx.doi.org/10.1002/bjs.9593 PMid:25131707.
  » http://dx.doi.org/10.1002/bjs.9593
• ⁴⁰ Krumholz HM, Keenan PS, Brush JE Jr, et al. Standards for measures used for public reporting of efficiency in health care. J Am Coll Cardiol. 2008;52(18):1518-26. http://dx.doi.org/10.1016/j.jacc.2008.09.004 PMid:19017522.
  » http://dx.doi.org/10.1016/j.jacc.2008.09.004
• ⁴¹ Makrygiannis G, Labalue P, Erpicum M, et al. Extending abdominal aortic aneurysm detection to older age groups: preliminary results from the Liège Screening Programme. Ann Vasc Surg. 2016;36:55-63. http://dx.doi.org/10.1016/j.avsg.2016.02.034 PMid:27364735.
  » http://dx.doi.org/10.1016/j.avsg.2016.02.034
• ⁴² Krohn CD, Kullmann G, Kvernebo K, Rosén L, Kroese A. Ultrasonographic screening for abdominal aortic aneurysm. Eur J Surg. 1992;158(10):527-30. PMid:1360823.
• ⁴³ Chun KC, Schmidt AS, Bains S, et al. Surveillance outcomes of small abdominal aortic aneurysms identified from a large screening program. J Vasc Surg. 2016;63(1):55-61. http://dx.doi.org/10.1016/j.jvs.2015.08.059 PMid:26474507.
  » http://dx.doi.org/10.1016/j.jvs.2015.08.059
• ⁴⁴ Owens DK, Davidson KW, Krist AH, et al. Screening for abdominal aortic aneurysm: US preventive services task force recommendation statement. JAMA. 2019;322(22):2211-8. http://dx.doi.org/10.1001/jama.2019.18928 PMid:31821437.
  » http://dx.doi.org/10.1001/jama.2019.18928
• ⁴⁵ Thijssen CGE, Bons LR, Gökalp AL, et al. Exercise and sports participation in patients with thoracic aortic disease: a review. Expert Rev Cardiovasc Ther. 2019;17(4):251-66. http://dx.doi.org/10.1080/14779072.2019.1585807 PMid:30887852.
  » http://dx.doi.org/10.1080/14779072.2019.1585807
• ⁴⁶ Hornsby WE, Norton EL, Fink S, et al. Cardiopulmonary exercise testing following open repair for a proximal thoracic aortic aneurysm or dissection. J Cardiopulm Rehabil Prev. 2020;40(2):108-15. http://dx.doi.org/10.1097/HCR.0000000000000446 PMid:31478921.
  » http://dx.doi.org/10.1097/HCR.0000000000000446
• ⁴⁷ Chaddha A, Eagle KA, Braverman AC, et al. Exercise and physical activity for the post-aortic dissection patient: the clinician’s Conundrum. Clin Cardiol. 2015;38(11):647-51. http://dx.doi.org/10.1002/clc.22481 PMid:26769698.
  » http://dx.doi.org/10.1002/clc.22481
• ⁴⁸ Wahlgren CM, Larsson E, Magnusson PKE, Hultgren R, Swedenborg J. Genetic and environmental contributions to abdominal aortic aneurysm development in a twin population. J Vasc Surg. 2010;51(1):3-7. http://dx.doi.org/10.1016/j.jvs.2009.08.036 PMid:19939604.
  » http://dx.doi.org/10.1016/j.jvs.2009.08.036
• ⁴⁹ Shalhub S, Wallace S, Okunbor O, Newhall K. Genetic aortic disease epidemiology, management principles, and disparities in care. Semin Vasc Surg. 2021;34(1):79-88. http://dx.doi.org/10.1053/j.semvascsurg.2021.02.012 PMid:33757640.
  » http://dx.doi.org/10.1053/j.semvascsurg.2021.02.012
• ⁵⁰ Larsson E, Granath F, Swedenborg J, Hultgren R. A population-based case-control study of the familial risk of abdominal aortic aneurysm. J Vasc Surg. 2009;49(1):47-50. http://dx.doi.org/10.1016/j.jvs.2008.08.012 PMid:19028058.
  » http://dx.doi.org/10.1016/j.jvs.2008.08.012
• ⁵¹ Ogata T, MacKean GL, Cole CW, et al. The lifetime prevalence of abdominal aortic aneurysms among siblings of aneurysm patients is eightfold higher than among siblings of spouses: An analysis of 187 aneurysm families in Nova Scotia, Canada. J Vasc Surg. 2005;42(5):891-7. http://dx.doi.org/10.1016/j.jvs.2005.08.002 PMid:16275443.
  » http://dx.doi.org/10.1016/j.jvs.2005.08.002
• ⁵² Jones GT, Hill BG, Curtis N, et al. Comparison of three targeted approaches to screening for abdominal aortic aneurysm based on cardiovascular risk. Br J Surg. 2016;103(9):1139-46. http://dx.doi.org/10.1002/bjs.10224 PMid:27426269.
  » http://dx.doi.org/10.1002/bjs.10224
• ⁵³ Sakalihasan N, Defraigne JO, Kerstenne MA, et al. Family members of patients with abdominal aortic aneurysms are at increased risk for aneurysms: analysis of 618 probands and their families from the Liège AAA family study. Ann Vasc Surg. 2014;28(4):787-97. http://dx.doi.org/10.1016/j.avsg.2013.11.005 PMid:24365082.
  » http://dx.doi.org/10.1016/j.avsg.2013.11.005
• ⁵⁴ van de Luijtgaarden KM, Bastos Gonçalves F, Hoeks SE, et al. Familial abdominal aortic aneurysm is associated with more complications after endovascular aneurysm repair. J Vasc Surg. 2014;59(2):275-82. http://dx.doi.org/10.1016/j.jvs.2013.08.029 PMid:24139982.
  » http://dx.doi.org/10.1016/j.jvs.2013.08.029
• ⁵⁵ Gomez D, Swiatlowska P, Owens GK. Epigenetic control of smooth muscle cell identity and lineage memory. Arterioscler Thromb Vasc Biol. 2015;35(12):2508-16. http://dx.doi.org/10.1161/ATVBAHA.115.305044 PMid:26449751.
  » http://dx.doi.org/10.1161/ATVBAHA.115.305044
• ⁵⁶ Hof FNG, Ruigrok YM, Lee CH. Shared genetic risk factors of intracranial, abdominal, and thoracic aneurysms. J Am Heart Assoc. 2018;7(3):e004150. http://dx.doi.org/10.1161/JAHA.117.004150 PMid:29420217.
  » http://dx.doi.org/10.1161/JAHA.117.004150
• ⁵⁷ Helgadottir A, Thorleifsson G, Magnusson KP, et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet. 2008;40(2):217-24. http://dx.doi.org/10.1038/ng.72 PMid:18176561.
  » http://dx.doi.org/10.1038/ng.72
• ⁵⁸ Weintraub NL. Understanding abdominal aortic aneurysm. N Engl J Med. 2009;361(11):1114-6. http://dx.doi.org/10.1056/NEJMcibr0905244 PMid:19741234.
  » http://dx.doi.org/10.1056/NEJMcibr0905244
• ⁵⁹ Cowan JA Jr, Dimick JB, Henke PK, Rectenwald J, Stanley JC, Upchurch GR Jr. Epidemiology of aortic aneurysm repair in the United States from 1993 to 2003. Ann N Y Acad Sci. 2006;1085(1):1-10. http://dx.doi.org/10.1196/annals.1383.030
  » http://dx.doi.org/10.1196/annals.1383.030
• ⁶⁰ Wanhainen A, Mani K, Golledge J. Surrogate markers of abdominal aortic aneurysm progression. Arterioscler Thromb Vasc Biol. 2016;36(2):236-44. http://dx.doi.org/10.1161/ATVBAHA.115.306538 PMid:26715680.
  » http://dx.doi.org/10.1161/ATVBAHA.115.306538
• ⁶¹ Albornoz G, Coady MA, Roberts M, et al. Familial thoracic aortic aneurysms and dissections: incidence, modes of inheritance, and phenotypic patterns. Ann Thorac Surg. 2006;82(4):1400-5. http://dx.doi.org/10.1016/j.athoracsur.2006.04.098 PMid:16996941.
  » http://dx.doi.org/10.1016/j.athoracsur.2006.04.098
• ⁶² Dietz HC, Cutting CR, Pyeritz RE, et al. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature. 1991;352(6333):337-9. http://dx.doi.org/10.1038/352337a0 PMid:1852208.
  » http://dx.doi.org/10.1038/352337a0
• ⁶³ Faivre L, Masurel-Paulet A, Collod-Béroud G, et al. Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 Probands with pathogenic FBN1 mutations. Pediatrics. 2009;123(1):391-8. http://dx.doi.org/10.1542/peds.2008-0703 PMid:19117906.
  » http://dx.doi.org/10.1542/peds.2008-0703
• ⁶⁴ LeMaire SA, McDonald MLN, Guo DC, et al. Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1. Nat Genet. 2011;43(10):996-1000. http://dx.doi.org/10.1038/ng.934 PMid:21909107.
  » http://dx.doi.org/10.1038/ng.934
• ⁶⁵ Collod-Béroud G, le Bourdelles S, Ades L, et al. Update of the UMD- FBN1 mutation database and creation of an FBN1 polymorphism database. Hum Mutat. 2003;22(3):199-208. http://dx.doi.org/10.1002/humu.10249 PMid:12938084.
  » http://dx.doi.org/10.1002/humu.10249
• ⁶⁶ Loeys BL, Chen J, Neptune ER, et al. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. Nat Genet. 2005;37(3):275-81. http://dx.doi.org/10.1038/ng1511 PMid:15731757.
  » http://dx.doi.org/10.1038/ng1511
• ⁶⁷ Baas AF, Medic J, van ’t Slot R, et al. Association of the TGF-β receptor genes with abdominal aortic aneurysm. Eur J Hum Genet. 2010;18(2):240-4. http://dx.doi.org/10.1038/ejhg.2009.141 PMid:19672284.
  » http://dx.doi.org/10.1038/ejhg.2009.141
• ⁶⁸ Kim HW, Stansfield BK. Genetic and Epigenetic Regulation of Aortic Aneurysms. BioMed Res Int. 2017;2017:7268521. http://dx.doi.org/10.1155/2017/7268521 PMid:28116311.
  » http://dx.doi.org/10.1155/2017/7268521
• ⁶⁹ Gurung R, Choong AM, Woo CC, Foo R, Sorokin V. Genetic and epigenetic mechanisms underlying vascular smooth muscle cell phenotypic modulation in abdominal aortic aneurysm. Int J Mol Sci. 2020;21(17):6334. http://dx.doi.org/10.3390/ijms21176334 PMid:32878347.
  » http://dx.doi.org/10.3390/ijms21176334
• ⁷⁰ Altobelli E, Rapacchietta L, Profeta V, Fagnano R. Risk factors for abdominal aortic aneurysm in population-based studies: a systematic review and meta-analysis. Int J Environ Res Public Health. 2018;15(12):2805. http://dx.doi.org/10.3390/ijerph15122805 PMid:30544688.
  » http://dx.doi.org/10.3390/ijerph15122805
• ⁷¹ Karkos C, Mukhopadhyay U, Papakostas I, Ghosh J, Thomson G, Hughes R. Abdominal aortic aneurysm: the role of clinical examination and opportunistic detection. Eur J Vasc Endovasc Surg. 2000;19(3):299-303. http://dx.doi.org/10.1053/ejvs.1999.1002 PMid:10753695.
  » http://dx.doi.org/10.1053/ejvs.1999.1002
• ⁷² Beede SD, Ballard DJ, James EM, Ilstrup DM, Hallet JW Jr. Positive predictive value of clinical suspicion of abdominal aortic aneurysm. Implications for efficient use of abdominal ultrasonography. Arch Intern Med. 1990;150(3):549-51. http://dx.doi.org/10.1001/archinte.1990.00390150053010 PMid:2106847.
  » http://dx.doi.org/10.1001/archinte.1990.00390150053010
• ⁷³ Fink HA, Lederle FA, Roth CS, Bowles CA, Nelson DB, Haas MA. The accuracy of physical examination to detect abdominal aortic aneurysm. Arch Intern Med. 2000;160(6):833-6. http://dx.doi.org/10.1001/archinte.160.6.833 PMid:10737283.
  » http://dx.doi.org/10.1001/archinte.160.6.833
• ⁷⁴ Lederle FA, Simel DL. The rational clinical examination. Does this patient have abdominal aortic aneurysm? JAMA. 1999;281(1):77-82. http://dx.doi.org/10.1001/jama.281.1.77 PMid:9892455.
  » http://dx.doi.org/10.1001/jama.281.1.77
• ⁷⁵ Long A, Rouet L, Lindholt JS, Allaire E. Measuring the maximum diameter of native abdominal aortic aneurysms: review and critical analysis. Eur J Vasc Endovasc Surg. 2012;43(5):515-24. http://dx.doi.org/10.1016/j.ejvs.2012.01.018 PMid:22336051.
  » http://dx.doi.org/10.1016/j.ejvs.2012.01.018
• ⁷⁶ Rubano E, Mehta N, Caputo W, Paladino L, Sinert R. Systematic review: emergency department bedside ultrasonography for diagnosing suspected abdominal aortic aneurysm. Acad Emerg Med. 2013;20(2):128-38. http://dx.doi.org/10.1111/acem.12080 PMid:23406071.
  » http://dx.doi.org/10.1111/acem.12080
• ⁷⁷ Mora C, Marcus C, Barbe C, Ecarnot F, Long A. Measurement of maximum diameter of native abdominal aortic aneurysm by angio-CT: reproducibility is better with the semi-automated method. Eur J Vasc Endovasc Surg. 2014;47(2):139-50. http://dx.doi.org/10.1016/j.ejvs.2013.10.013 PMid:24268793.
  » http://dx.doi.org/10.1016/j.ejvs.2013.10.013
• ⁷⁸ Engellau L, Albrechtsson U, Dahlström N, Norgren L, Persson A, Larsson EM. Measurements before endovascular repair of abdominal aortic aneurysms. MR imaging with MRA vs. angiography and CT. Acta Radiol. 2003;44(2):177-84. http://dx.doi.org/10.1034/j.1600-0455.2003.00029.x PMid:12694105.
  » http://dx.doi.org/10.1034/j.1600-0455.2003.00029.x
• ⁷⁹ Murakami M, Morikage N, Samura M, Yamashita O, Suehiro K, Hamano K. Fluorine-18-fluorodeoxyglucose positron emission tomography-computed tomography for diagnosis of infected aortic aneurysms. Ann Vasc Surg. 2014;28(3):575-8. http://dx.doi.org/10.1016/j.avsg.2013.04.013 PMid:24200128.
  » http://dx.doi.org/10.1016/j.avsg.2013.04.013
• ⁸⁰ Isselbacher EM, Preventza O, Black JH, et al. 2022 ACC/AHA guideline for the diagnosis and management of aortic disease: a report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines. Circulation. 2022;146(24):e334-482. http://dx.doi.org/10.1161/CIR.0000000000001106 PMid:36322642.
  » http://dx.doi.org/10.1161/CIR.0000000000001106
• ⁸¹ Lewington S, Clarke R, Qizilbash N, Peto R, Collins R. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies. Lancet. 2002;360(9349):1903-13. http://dx.doi.org/10.1016/S0140-6736(02)11911-8 PMid:12493255.
  » http://dx.doi.org/10.1016/S0140-6736(02)11911-8
• ⁸² Ogden LG, He J, Lydick E, Whelton PK. Long-term absolute benefit of lowering blood pressure in hypertensive patients according to the JNC VI risk stratification. Hypertension. 2000;35(2):539-43. http://dx.doi.org/10.1161/01.HYP.35.2.539 PMid:10679494.
  » http://dx.doi.org/10.1161/01.HYP.35.2.539
• ⁸³ Wright JT Jr, Williamson JD, Whelton PK, et al. A randomized trial of intensive versus standard blood-pressure control. N Engl J Med. 2015;373(22):2103-16. http://dx.doi.org/10.1056/NEJMoa1511939 PMid:26551272.
  » http://dx.doi.org/10.1056/NEJMoa1511939
• ⁸⁴ Vaduganathan M, Claggett BL, Juraschek SP, Solomon SD. Assessment of long-term benefit of intensive blood pressure control on residual life Span. JAMA Cardiol. 2020;5(5):576-81. http://dx.doi.org/10.1001/jamacardio.2019.6192 PMid:32101262.
  » http://dx.doi.org/10.1001/jamacardio.2019.6192
• ⁸⁵ O’Donnell TFX, Deery SE, Shean KE, et al. Statin therapy is associated with higher long-term but not perioperative survival after abdominal aortic aneurysm repair. J Vasc Surg. 2018;68(2):392-9. http://dx.doi.org/10.1016/j.jvs.2017.11.084 PMid:29580855.
  » http://dx.doi.org/10.1016/j.jvs.2017.11.084
• ⁸⁶ Salata K, Syed M, Hussain MA, et al. Statins reduce abdominal aortic aneurysm growth, rupture, and perioperative mortality: a systematic review and meta‐analysis. J Am Heart Assoc. 2018;7(19):e008657. http://dx.doi.org/10.1161/JAHA.118.008657 PMid:30371297.
  » http://dx.doi.org/10.1161/JAHA.118.008657
• ⁸⁷ Baigent C, Blackwell L, Emberson J, et al. Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170 000 participants in 26 randomised trials. Lancet. 2010;376(9753):1670-81. http://dx.doi.org/10.1016/S0140-6736(10)61350-5 PMid:21067804.
  » http://dx.doi.org/10.1016/S0140-6736(10)61350-5
• ⁸⁸ Grundy SM, Stone NJ, Bailey AL, et al. AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA guideline on the management of blood cholesterol: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation. 2019;139(25):e1082-143. http://dx.doi.org/10.1161/CIR.0000000000000625 PMid:30586774.
  » http://dx.doi.org/10.1161/CIR.0000000000000625
• ⁸⁹ Whelton PK, Carey RM, Aronow WS, et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA guideline for the prevention, detection, evaluation, and management of high blood pressure in adults: executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Hypertension. 2018;71(6):1269-324. http://dx.doi.org/10.1161/HYP.0000000000000066 PMid:29133354.
  » http://dx.doi.org/10.1161/HYP.0000000000000066
• ⁹⁰ Katz DA, Holman JE, Nugent AS, et al. The Emergency Department Action in Smoking Cessation (EDASC) trial: impact on cessation outcomes. Nicotine Tob Res. 2013;15(6):1032-43. http://dx.doi.org/10.1093/ntr/nts219 PMid:23125437.
  » http://dx.doi.org/10.1093/ntr/nts219
• ⁹¹ Fiore MC, Jaén CR, Baker TB. Treating tobacco use and dependence: 2008 update: tobacco use and dependence guideline panel. Rockville: US Department of Health and Human Services; 2008.
• ⁹² Berry KM, Reynolds LM, Collins JM, et al. E-cigarette initiation and associated changes in smoking cessation and reduction: the population assessment of tobacco and health study, 2013-2015. Tob Control. 2019;28(1):42-9. http://dx.doi.org/10.1136/tobaccocontrol-2017-054108
  » http://dx.doi.org/10.1136/tobaccocontrol-2017-054108
• ⁹³ Smith SC Jr, Allen J, Blair SN, et al. AHA/ACC guidelines for secondary prevention for patients with coronary and other atherosclerotic vascular disease: 2006 update. J Am Coll Cardiol. 2006;47(10):2130-9. http://dx.doi.org/10.1016/j.jacc.2006.04.026 PMid:16697342.
  » http://dx.doi.org/10.1016/j.jacc.2006.04.026
• ⁹⁴ Wemmelund H, Jørgensen TMM, Høgh A, Behr-Rasmussen C, Johnsen SP, Lindholt JS. Low-dose aspirin and rupture of abdominal aortic aneurysm. J Vasc Surg. 2017;65(3):616-625.e4. http://dx.doi.org/10.1016/j.jvs.2016.04.061 PMid:27460909.
  » http://dx.doi.org/10.1016/j.jvs.2016.04.061
• ⁹⁵ Lederle FA, Johnson GR, Wilson SE, et al. Yield of repeated screening for abdominal aortic aneurysm after a 4-year interval. Arch Intern Med. 2000;160(8):1117-21. http://dx.doi.org/10.1001/archinte.160.8.1117 PMid:10789604.
  » http://dx.doi.org/10.1001/archinte.160.8.1117
• ⁹⁶ Cao P, Rango P, Verzini F, Parlani G, Romano L, Cieri E. Comparison of Surveillance Versus Aortic Endografting for Small Aneurysm Repair (CAESAR): Results from a Randomised Trial. Eur J Vasc Endovasc Surg. 2011;41(1):13-25. http://dx.doi.org/10.1016/j.ejvs.2010.08.026 PMid:20869890.
  » http://dx.doi.org/10.1016/j.ejvs.2010.08.026
• ⁹⁷ Powell JT, Brady AR, Brown LC, et al. Long-term outcomes of immediate repair compared with surveillance of small abdominal aortic aneurysms. N Engl J Med. 2002;346(19):1445-52. http://dx.doi.org/10.1056/NEJMoa013527 PMid:12000814.
  » http://dx.doi.org/10.1056/NEJMoa013527
• ⁹⁸ United Kingdom Small Aneurysm Trial Participants. Mortality results for randomised controlled trial of early elective surgery or ultrasonographic surveillance for small abdominal aortic aneurysms. Lancet. 1998;352(9141):1649-55. http://dx.doi.org/10.1016/S0140-6736(98)10137-X PMid:9853436.
  » http://dx.doi.org/10.1016/S0140-6736(98)10137-X
• ⁹⁹ Ouriel K, Clair DG, Kent KC, Zarins CK. Endovascular repair compared with surveillance for patients with small abdominal aortic aneurysms. J Vasc Surg. 2010;51(5):1081-7. http://dx.doi.org/10.1016/j.jvs.2009.10.113 PMid:20304589.
  » http://dx.doi.org/10.1016/j.jvs.2009.10.113
• ¹⁰⁰ Ulug P, Powell JT, Martinez MAM, Ballard DJ, Filardo G. Surgery for small asymptomatic abdominal aortic aneurysms. Cochrane Database Syst Rev. 2020;7(7):CD001835. http://dx.doi.org/10.1002/14651858.CD001835.pub5 PMid:32609382.
  » http://dx.doi.org/10.1002/14651858.CD001835.pub5
• ¹⁰¹ Nevitt MP, Ballard DJ, Hallett JW Jr. Prognosis of abdominal aortic aneurysms: a population-based study. N Engl J Med. 1989;321(15):1009-14. http://dx.doi.org/10.1056/NEJM198910123211504 PMid:2674715.
  » http://dx.doi.org/10.1056/NEJM198910123211504
• ¹⁰² Brown PM, Zelt DT, Sobolev B. The risk of rupture in untreated aneurysms: the impact of size, gender, and expansion rate. J Vasc Surg. 2003;37(2):280-4. http://dx.doi.org/10.1067/mva.2003.119 PMid:12563196.
  » http://dx.doi.org/10.1067/mva.2003.119
• ¹⁰³ Cronenwett JL, Murphy TF, Zelenock GB, et al. Actuarial analysis of variables associated with rupture of small abdominal aortic aneurysms. Surgery. 1985;98(3):472-83. PMid:3898453.
• ¹⁰⁴ Hoffman M, Avellone JC, Plecha FR, et al. Operation for ruptured abdominal aortic aneurysms: a community-wide experience. Surgery. 1982;91(5):597-602. PMid:7071748.
• ¹⁰⁵ Shang EK, Nathan DP, Boonn WW, et al. A modern experience with saccular aortic aneurysms. J Vasc Surg. 2013;57(1):84-8. http://dx.doi.org/10.1016/j.jvs.2012.07.002 PMid:23127980.
  » http://dx.doi.org/10.1016/j.jvs.2012.07.002
• ¹⁰⁶ Karthaus EG, Tong TML, Vahl A, Hamming JF. Saccular abdominal aortic aneurysms: patient characteristics, clinical presentation, treatment, and outcomes in the Netherland. Ann Surg. 2019;270(5):852-8. http://dx.doi.org/10.1097/SLA.0000000000003529 PMid:31498185.
  » http://dx.doi.org/10.1097/SLA.0000000000003529
• ¹⁰⁷ De Bruin JL, Baas AF, Buth J, et al. Long-term outcome of open or endovascular repair of abdominal aortic aneurysm. N Engl J Med. 2010;362(20):1881-9. http://dx.doi.org/10.1056/NEJMoa0909499 PMid:20484396.
  » http://dx.doi.org/10.1056/NEJMoa0909499
• ¹⁰⁸ Rao R, Lane TRA, Franklin IJ, Davies AH. Open repair versus fenestrated endovascular aneurysm repair of juxtarenal aneurysms. J Vasc Surg. 2015;61(1):242-255. http://dx.doi.org/10.1016/j.jvs.2014.08.068 PMid:25240242.
  » http://dx.doi.org/10.1016/j.jvs.2014.08.068
• ¹⁰⁹ Magliano C, Senna K, Santos M, Tura BR, Santos B, Lassance M. Diretriz brasileira para o tratamento do aneurisma de aorta abdominal. Brasília: Ministério da Saúde; 2017.
• ¹¹⁰ Sampram ESK, Karafa MT, Mascha EJ, et al. Nature, frequency, and predictors of secondary procedures after endovascular repair of abdominal aortic aneurysm. J Vasc Surg. 2003;37(5):930-7. http://dx.doi.org/10.1067/mva.2003.281 PMid:12756335.
  » http://dx.doi.org/10.1067/mva.2003.281
• ¹¹¹ Johnston KW. Multicenter prospective study of nonruptured abdominal aortic aneurysm. Part II. Variables predicting morbidity and mortality. J Vasc Surg. 1989;9(3):437. http://dx.doi.org/10.1016/S0741-5214(89)70007-0 PMid:2646460.
  » http://dx.doi.org/10.1016/S0741-5214(89)70007-0
• ¹¹² Mitchell KM, Valentine JR. Inferior mesenteric artery reimplantation does not guarantee colon viability in aortic surgery. J Am Coll Surg. 2002;194(2):151-5. http://dx.doi.org/10.1016/S1072-7515(01)01151-6 PMid:11848633.
  » http://dx.doi.org/10.1016/S1072-7515(01)01151-6
• ¹¹³ Becquemin JP, Majewski M, Fermani N, et al. Colon ischemia following abdominal aortic aneurysm repair in the era of endovascular abdominal aortic repair. J Vasc Surg. 2008;47(2):258-63. http://dx.doi.org/10.1016/j.jvs.2007.10.001 PMid:18241745.
  » http://dx.doi.org/10.1016/j.jvs.2007.10.001
• ¹¹⁴ Senekowitsch C, Assadian A, Assadian O, Hartleb H, Ptakovsky H, Hagmüller GW. Replanting the inferior mesentery artery during infrarenal aortic aneurysm repair: Influence on postoperative colon ischemia. J Vasc Surg. 2006;43(4):689-94. http://dx.doi.org/10.1016/j.jvs.2005.12.016 PMid:16616221.
  » http://dx.doi.org/10.1016/j.jvs.2005.12.016
• ¹¹⁵ Fassiadis N, Roidl M, Hennig M, South LM, Andrews SM. Randomized clinical trial of vertical or transverse laparotomy for abdominal aortic aneurysm repair. Br J Surg. 2005;92(10):1208-11. http://dx.doi.org/10.1002/bjs.5140 PMid:16175532.
  » http://dx.doi.org/10.1002/bjs.5140
• ¹¹⁶ Sieunarine K, Lawrence-Brown MM, Goodman MA. Comparison of transperitoneal and retroperitoneal approaches for infrarenal aortic surgery: early and late results. Cardiovasc Surg. 1997;5(1):71-6. http://dx.doi.org/10.1016/S0967-2109(96)00035-X PMid:9158126.
  » http://dx.doi.org/10.1016/S0967-2109(96)00035-X
• ¹¹⁷ Sicard GA, Reilly JM, Rubin BG, et al. Transabdominal versus retroperitoneal incision for abdominal aortic surgery: report of a prospective randomized trial. J Vasc Surg. 1995;21(2):174-81. http://dx.doi.org/10.1016/S0741-5214(95)70260-1 PMid:7853592.
  » http://dx.doi.org/10.1016/S0741-5214(95)70260-1
• ¹¹⁸ Cambria RP, Brewster DC, Abbott WM, et al. Transperitoneal versus retroperitoneal approach for aortic reconstruction: a randomized prospective study. J Vasc Surg. 1990;11(2):314-24. http://dx.doi.org/10.1016/0741-5214(90)90275-F PMid:2405200.
  » http://dx.doi.org/10.1016/0741-5214(90)90275-F
• ¹¹⁹ Caradu C, Ammollo RP, Dari L, et al. Management of inflammatory aortic aneurysms: a scoping review. Eur J Vasc Endovasc Surg. 2023;65(4):493-502. http://dx.doi.org/10.1016/j.ejvs.2023.01.003 PMid:36623764.
  » http://dx.doi.org/10.1016/j.ejvs.2023.01.003
• ¹²⁰ Jairam AP, Timmermans L, Eker HH, et al. Prevention of incisional hernia with prophylactic onlay and sublay mesh reinforcement versus primary suture only in midline laparotomies (PRIMA): 2-year follow-up of a multicentre, double-blind, randomised controlled trial. Lancet. 2017;390(10094):567-76. http://dx.doi.org/10.1016/S0140-6736(17)31332-6 PMid:28641875.
  » http://dx.doi.org/10.1016/S0140-6736(17)31332-6
• ¹²¹ Indrakusuma R, Jalalzadeh H, van der Meij JE, Balm R, Koelemay MJW. Prophylactic mesh reinforcement versus sutured closure to prevent incisional hernias after open abdominal aortic aneurysm repair via midline laparotomy: a systematic review and meta-analysis. Eur J Vasc Endovasc Surg. 2018;56(1):120-8. http://dx.doi.org/10.1016/j.ejvs.2018.03.021 PMid:29685678.
  » http://dx.doi.org/10.1016/j.ejvs.2018.03.021
• ¹²² Knott AW, Kalra M, Duncan AA, et al. Open repair of juxtarenal aortic aneurysms (JAA) remains a safe option in the era of fenestrated endografts. J Vasc Surg. 2008;47(4):695-701. http://dx.doi.org/10.1016/j.jvs.2007.12.007 PMid:18272317.
  » http://dx.doi.org/10.1016/j.jvs.2007.12.007
• ¹²³ Jongkind V, Yeung KK, Akkersdijk GJM, et al. Juxtarenal aortic aneurysm repair. J Vasc Surg. 2010;52(3):760-7. http://dx.doi.org/10.1016/j.jvs.2010.01.049 PMid:20382492.
  » http://dx.doi.org/10.1016/j.jvs.2010.01.049
• ¹²⁴ Chaufour X, Segal J, Soler R, et al. Durability of open repair of juxtarenal abdominal aortic aneurysms: a multicentre retrospective study in five French academic centres. Eur J Vasc Endovasc Surg. 2020;59(1):40-9. http://dx.doi.org/10.1016/j.ejvs.2019.05.010 PMid:31530501.
  » http://dx.doi.org/10.1016/j.ejvs.2019.05.010
• ¹²⁵ Greenberg RK, Haulon S, O’Neill S, Lyden S, Ouriel K. Primary endovascular repair of juxtarenal aneurysms with fenestrated endovascular grafting. Eur J Vasc Endovasc Surg. 2004;27(5):484-91. http://dx.doi.org/10.1016/j.ejvs.2004.02.015 PMid:15079770.
  » http://dx.doi.org/10.1016/j.ejvs.2004.02.015
• ¹²⁶ Ambler G, Boyle JR, Cousins C, et al. Early results of fenestrated endovascular repair of juxtarenal aortic aneurysms in the United Kingdom. Circulation. 2012;125(22):2707-15. http://dx.doi.org/10.1161/CIRCULATIONAHA.111.070334 PMid:22665884.
  » http://dx.doi.org/10.1161/CIRCULATIONAHA.111.070334
• ¹²⁷ Wu H, Zhang L, Li M, Wei S, Zhang C, Bai H. Systematic review and meta-analysis of published studies on endovascular repair of abdominal aortic aneurysm with the p-Branch. Front Surg. 2022;9:879682. http://dx.doi.org/10.3389/fsurg.2022.879682 PMid:35574550.
  » http://dx.doi.org/10.3389/fsurg.2022.879682
• ¹²⁸ Doonan RJ, Girsowicz E, Dubois L, Gill HL. A systematic review and meta-analysis of endovascular juxtarenal aortic aneurysm repair demonstrates lower perioperative mortality compared with open repair. J Vasc Surg. 2019;70(6):2054-2064.e3. http://dx.doi.org/10.1016/j.jvs.2019.04.464 PMid:31327612.
  » http://dx.doi.org/10.1016/j.jvs.2019.04.464
• ¹²⁹ Patel SR, Ormesher DC, Griffin R, Jackson RJ, Lip GYH, Vallabhaneni SR. Comparison of open, standard, and complex endovascular aortic repair treatments for juxtarenal/short neck aneurysms: a systematic review and network meta-analysis. Eur J Vasc Endovasc Surg. 2022;63(5):696-706. http://dx.doi.org/10.1016/j.ejvs.2021.12.042 PMid:35221243.
  » http://dx.doi.org/10.1016/j.ejvs.2021.12.042
• ¹³⁰ Rosenfeld ES, Macsata RA, Lala S, et al. Open surgical repair of juxtarenal abdominal aortic aneurysms in the elderly is not associated with increased thirty-day mortality compared with fenestrated endovascular grafting. J Vasc Surg. 2021;73(4):1139-47. http://dx.doi.org/10.1016/j.jvs.2020.08.121 PMid:32919026.
  » http://dx.doi.org/10.1016/j.jvs.2020.08.121
• ¹³¹ Zettervall SL, Schermerhorn ML, Soden PA, et al. The effect of surgeon and hospital volume on mortality after open and endovascular repair of abdominal aortic aneurysms. J Vasc Surg. 2017;65(3):626-34. http://dx.doi.org/10.1016/j.jvs.2016.09.036 PMid:27988158.
  » http://dx.doi.org/10.1016/j.jvs.2016.09.036
• ¹³² Greenhalgh RM, Brown LC, Kwong GPS, Powell JT, Thompson SG. Comparison of endovascular aneurysm repair with open repair in patients with abdominal aortic aneurysm (EVAR trial 1), 30-day operative mortality results: randomised controlled trial. Lancet. 2004;364(9437):843-8. http://dx.doi.org/10.1016/S0140-6736(04)16979-1 PMid:15351191.
  » http://dx.doi.org/10.1016/S0140-6736(04)16979-1
• ¹³³ EVAR Trial Participants. Endovascular aneurysm repair and outcome in patients unfit for open repair of abdominal aortic aneurysm (EVAR trial 2): randomised controlled trial. Lancet. 2005;365(9478):2187-92. http://dx.doi.org/10.1016/S0140-6736(05)66628-7 PMid:15978926.
  » http://dx.doi.org/10.1016/S0140-6736(05)66628-7
• ¹³⁴ Prinssen M, Verhoeven ELG, Buth J, et al. A Randomized Trial Comparing Conventional and Endovascular Repair of Abdominal Aortic Aneurysms. N Engl J Med. 2004;351(16):1607-18. http://dx.doi.org/10.1056/NEJMoa042002 PMid:15483279.
  » http://dx.doi.org/10.1056/NEJMoa042002
• ¹³⁵ Becquemin JP, Pillet JC, Lescalie F, et al. A randomized controlled trial of endovascular aneurysm repair versus open surgery for abdominal aortic aneurysms in low- to moderate-risk patients. J Vasc Surg. 2011;53(5):1167-1173.e1. http://dx.doi.org/10.1016/j.jvs.2010.10.124 PMid:21276681.
  » http://dx.doi.org/10.1016/j.jvs.2010.10.124
• ¹³⁶ Lederle FA, Freischlag JA, Kyriakides TC, et al. Long-term comparison of endovascular and open repair of abdominal aortic aneurysm. N Engl J Med. 2012;367(21):1988-97. http://dx.doi.org/10.1056/NEJMoa1207481 PMid:23171095.
  » http://dx.doi.org/10.1056/NEJMoa1207481
• ¹³⁷ Lovegrove RE, Javid M, Magee TR, Galland RB. A meta-analysis of 21 178 patients undergoing open or endovascular repair of abdominal aortic aneurysm. Br J Surg. 2008;95(6):677-84. http://dx.doi.org/10.1002/bjs.6240 PMid:18446774.
  » http://dx.doi.org/10.1002/bjs.6240
• ¹³⁸ Sajid MS, Desai M, Haider Z, Baker DM, Hamilton G. Endovascular Aortic Aneurysm Repair (EVAR) has significantly lower perioperative mortality in comparison to open repair: a systematic review. Asian J Surg. 2008;31(3):119-23. http://dx.doi.org/10.1016/S1015-9584(08)60071-8 PMid:18658009.
  » http://dx.doi.org/10.1016/S1015-9584(08)60071-8
• ¹³⁹ Paravastu SCV, Jayarajasingam R, Cottam R, Palfreyman SJ, Michaels JA, Thomas SM. Endovascular repair of abdominal aortic aneurysm. Cochrane Database Syst Rev. 2014;(1):CD004178. http://dx.doi.org/10.1002/14651858.CD004178.pub2 PMid:24453068.
  » http://dx.doi.org/10.1002/14651858.CD004178.pub2
• ¹⁴⁰ Nelson PR, Kracjer Z, Kansal N, et al. A multicenter, randomized, controlled trial of totally percutaneous access versus open femoral exposure for endovascular aortic aneurysm repair (the PEVAR trial). J Vasc Surg. 2014;59(5):1181-93. http://dx.doi.org/10.1016/j.jvs.2013.10.101 PMid:24440678.
  » http://dx.doi.org/10.1016/j.jvs.2013.10.101
• ¹⁴¹ Vierhout BP, Pol RA, Ott MA, et al. Randomized multicenter trial on percutaneous versus open access in endovascular aneurysm repair (PiERO). J Vasc Surg. 2019;69(5):1429-36. http://dx.doi.org/10.1016/j.jvs.2018.07.052 PMid:30292613.
  » http://dx.doi.org/10.1016/j.jvs.2018.07.052
• ¹⁴² Kalish J, Eslami M, Gillespie D, et al. Routine use of ultrasound guidance in femoral arterial access for peripheral vascular intervention decreases groin hematoma rates. J Vasc Surg. 2015;61(5):1231-8. http://dx.doi.org/10.1016/j.jvs.2014.12.003 PMid:25595399.
  » http://dx.doi.org/10.1016/j.jvs.2014.12.003
• ¹⁴³ Greenhalgh RM, Brown LC, Powell JT, Thompson SG, Epstein D, Sculpher MJ. Endovascular versus open repair of abdominal aortic aneurysm. N Engl J Med. 2010;362(20):1863-71. http://dx.doi.org/10.1056/NEJMoa0909305 PMid:20382983.
  » http://dx.doi.org/10.1056/NEJMoa0909305
• ¹⁴⁴ Carpenter JP, Baum RA, Barker CF, et al. Impact of exclusion criteria on patient selection for endovascular abdominal aortic aneurysm repair. J Vasc Surg. 2001;34(6):1050-4. http://dx.doi.org/10.1067/mva.2001.120037 PMid:11743559.
  » http://dx.doi.org/10.1067/mva.2001.120037
• ¹⁴⁵ Antoniou GA, Georgiadis GS, Antoniou SA, Kuhan G, Murray D. A meta-analysis of outcomes of endovascular abdominal aortic aneurysm repair in patients with hostile and friendly neck anatomy. J Vasc Surg. 2013;57(2):527-38. http://dx.doi.org/10.1016/j.jvs.2012.09.050 PMid:23265584.
  » http://dx.doi.org/10.1016/j.jvs.2012.09.050
• ¹⁴⁶ Speziale F, Sirignano P, Setacci F, et al. Immediate and two-year outcomes after EVAR in “on-label” and “off-label” neck anatomies using different commercially available devices: analysis of the experience of two Italian vascular centers. Ann Vasc Surg. 2014;28(8):1892-900. http://dx.doi.org/10.1016/j.avsg.2014.06.057 PMid:25011083.
  » http://dx.doi.org/10.1016/j.avsg.2014.06.057
• ¹⁴⁷ Lindblad B, Bin Jabr A, Holst J, Malina M. Chimney grafts in aortic stent grafting: hazardous or useful technique? Systematic review of current data. Eur J Vasc Endovasc Surg. 2015;50(6):722-31. http://dx.doi.org/10.1016/j.ejvs.2015.07.038 PMid:26371416.
  » http://dx.doi.org/10.1016/j.ejvs.2015.07.038
• ¹⁴⁸ Lobato AC, Camacho-Lobato L. Endovascular treatment of complex aortic aneurysms using the sandwich technique. J Endovasc Ther. 2012;19(6):691-706. http://dx.doi.org/10.1583/JEVT-12-4023R.1 PMid:23210864.
  » http://dx.doi.org/10.1583/JEVT-12-4023R.1
• ¹⁴⁹ Schwierz E, Kolvenbach RR, Yoshida R, Yoshida W, Alpaslan A, Karmeli R. Experience with the sandwich technique in endovascular thoracoabdominal aortic aneurysm repair. J Vasc Surg. 2014;59(6):1562-9. http://dx.doi.org/10.1016/j.jvs.2013.12.044 PMid:24613690.
  » http://dx.doi.org/10.1016/j.jvs.2013.12.044
• ¹⁵⁰ Donas KP, Lee JT, Lachat M, Torsello G, Veith FJ. Collected world experience about the performance of the snorkel/chimney endovascular technique in the treatment of complex aortic pathologies: the PERICLES registry. Ann Surg. 2015;262(3):546-53. http://dx.doi.org/10.1097/SLA.0000000000001405 PMid:26258324.
  » http://dx.doi.org/10.1097/SLA.0000000000001405
• ¹⁵¹ Li Y, Hu Z, Bai C, et al. Fenestrated and chimney technique for juxtarenal aortic aneurysm: a systematic review and pooled data analysis. Sci Rep. 2016;6(1):20497. http://dx.doi.org/10.1038/srep20497 PMid:26869488.
  » http://dx.doi.org/10.1038/srep20497
• ¹⁵² Mestres G, Yugueros X, Apodaka A, et al. The best in vitro conditions for two and three parallel stenting during endovascular aneurysm repair. J Vasc Surg. 2017;66(4):1227-35. http://dx.doi.org/10.1016/j.jvs.2016.09.046 PMid:28662925.
  » http://dx.doi.org/10.1016/j.jvs.2016.09.046
• ¹⁵³ Melas N, Perdikides T, Saratzis A, Saratzis N, Kiskinis D, Deaton DH. Helical EndoStaples enhance endograft fixation in an experimental model using human cadaveric aortas. J Vasc Surg. 2012;55(6):1726-33. http://dx.doi.org/10.1016/j.jvs.2011.11.048 PMid:22322119.
  » http://dx.doi.org/10.1016/j.jvs.2011.11.048
• ¹⁵⁴ Arko FR 3rd, Stanley GA, Pearce BJ, et al. Endosuture aneurysm repair in patients treated with Endurant II/IIs in conjunction with Heli-FX EndoAnchor implants for short-neck abdominal aortic aneurysm. J Vasc Surg. 2019;70(3):732-40. http://dx.doi.org/10.1016/j.jvs.2018.11.033 PMid:30850297.
  » http://dx.doi.org/10.1016/j.jvs.2018.11.033
• ¹⁵⁵ Jordan WD Jr, de Vries JPPM, Ouriel K, et al. Midterm outcome of endoanchors for the prevention of endoleak and stent-graft migration in patients with challenging proximal aortic neck anatomy. J Endovasc Ther. 2015;22(2):163-70. http://dx.doi.org/10.1177/1526602815574685 PMid:25809354.
  » http://dx.doi.org/10.1177/1526602815574685
• ¹⁵⁶ Oderich GS, Ribeiro MS, Sandri GA, et al. Evolution from physician-modified to company-manufactured fenestrated-branched endografts to treat pararenal and thoracoabdominal aortic aneurysms. J Vasc Surg. 2019;70(1):31-42.e7. http://dx.doi.org/10.1016/j.jvs.2018.09.063 PMid:30583902.
  » http://dx.doi.org/10.1016/j.jvs.2018.09.063
• ¹⁵⁷ Chait J, Tenorio ER, Hofer JM, DeMartino RR, Oderich GS, Mendes BC. Five-year outcomes of physician-modified endografts for repair of complex abdominal and thoracoabdominal aortic aneurysms. J Vasc Surg. 2023;77(2):374-385.e4. http://dx.doi.org/10.1016/j.jvs.2022.09.019 PMid:36356675.
  » http://dx.doi.org/10.1016/j.jvs.2022.09.019
• ¹⁵⁸ Linsen MAM, Jongkind V, Nio D, Hoksbergen AWJ, Wisselink W. Pararenal aortic aneurysm repair using fenestrated endografts. J Vasc Surg. 2012;56(1):238-46. http://dx.doi.org/10.1016/j.jvs.2011.10.092 PMid:22264696.
  » http://dx.doi.org/10.1016/j.jvs.2011.10.092
• ¹⁵⁹ Katsargyris A, Oikonomou K, Klonaris C, Töpel I, Verhoeven ELG. Comparison of Outcomes with open, fenestrated, and chimney graft repair of juxtarenal aneurysms: are we ready for a paradigm shift? J Endovasc Ther. 2013;20(2):159-69. http://dx.doi.org/10.1583/1545-1550-20.2.159 PMid:23581756.
  » http://dx.doi.org/10.1583/1545-1550-20.2.159
• ¹⁶⁰ Katsargyris A, Yazar O, Oikonomou K, Bekkema F, Tielliu I, Verhoeven ELG. Fenestrated stent-grafts for salvage of prior endovascular abdominal aortic aneurysm repair. Eur J Vasc Endovasc Surg. 2013;46(1):49-56. http://dx.doi.org/10.1016/j.ejvs.2013.03.028 PMid:23642523.
  » http://dx.doi.org/10.1016/j.ejvs.2013.03.028
• ¹⁶¹ Tenorio ER, Balachandran PW, Marcondes GB, et al. Incidence, predictive factors, and outcomes of intraprocedure adverse events during fenestrated-branched endovascular aortic repair of complex abdominal and thoracoabdominal aortic aneurysms. J Vasc Surg. 2022;75(3):783-793.e4. http://dx.doi.org/10.1016/j.jvs.2021.10.026 PMid:34742884.
  » http://dx.doi.org/10.1016/j.jvs.2021.10.026
• ¹⁶² Oderich GS, Farber MA, Silveira PG, et al. Technical aspects and 30-day outcomes of the prospective early feasibility study of the GORE EXCLUDER Thoracoabdominal Branched Endoprosthesis (TAMBE) to treat pararenal and extent IV thoracoabdominal aortic aneurysms. J Vasc Surg. 2019;70(2):358-368.e6. http://dx.doi.org/10.1016/j.jvs.2018.10.103 PMid:30612825.
  » http://dx.doi.org/10.1016/j.jvs.2018.10.103
• ¹⁶³ Eagleton MJ, Follansbee M, Wolski K, Mastracci T, Kuramochi Y. Fenestrated and branched endovascular aneurysm repair outcomes for type II and III thoracoabdominal aortic aneurysms. J Vasc Surg. 2016;63(4):930-42. http://dx.doi.org/10.1016/j.jvs.2015.10.095 PMid:26792544.
  » http://dx.doi.org/10.1016/j.jvs.2015.10.095
• ¹⁶⁴ Varkevisser RRB, O’Donnell TFX, Swerdlow NJ, et al. Fenestrated endovascular aneurysm repair is associated with lower perioperative morbidity and mortality compared with open repair for complex abdominal aortic aneurysms. J Vasc Surg. 2019;69(6):1670-8. http://dx.doi.org/10.1016/j.jvs.2018.08.192 PMid:30553730.
  » http://dx.doi.org/10.1016/j.jvs.2018.08.192
• ¹⁶⁵ Jones AD, Waduud MA, Walker P, Stocken D, Bailey MA, Scott DJA. Meta‐analysis of fenestrated endovascular aneurysm repair versus open surgical repair of juxtarenal abdominal aortic aneurysms over the last 10 years. BJS Open. 2019;3(5):572-84. http://dx.doi.org/10.1002/bjs5.50178 PMid:31592091.
  » http://dx.doi.org/10.1002/bjs5.50178
• ¹⁶⁶ Oderich GS, Farber MA, Schneider D, et al. Final 5-year results of the United States Zenith Fenestrated prospective multicenter study for juxtarenal abdominal aortic aneurysms. J Vasc Surg. 2021;73(4):1128-1138.e2. http://dx.doi.org/10.1016/j.jvs.2020.08.128 PMid:32891806.
  » http://dx.doi.org/10.1016/j.jvs.2020.08.128
• ¹⁶⁷ Ferreira M, Mannarino M, Cunha R, Ferreira D, Capotorto LF, Oderich GS. Stent Graft Modification to Preserve Intercostal Arteries Using Thoracoabdominal Off-the-Shelf Multibranched (t-Branch) Endograft. J Endovasc Ther. 2021;28(3):382-7. http://dx.doi.org/10.1177/1526602821996718 PMid:33759610.
  » http://dx.doi.org/10.1177/1526602821996718
• ¹⁶⁸ Kölbel T, Spanos K, Jama K, et al. Early outcomes of the t-Branch off-the-shelf multi-branched stent graft in 542 patients for elective and urgent aortic pathologies: a retrospective observational study. J Vasc Surg. 2021;74(6):1817-24. http://dx.doi.org/10.1016/j.jvs.2021.05.041 PMid:34171424.
  » http://dx.doi.org/10.1016/j.jvs.2021.05.041
• ¹⁶⁹ Biancari F, Ylönen K, Anttila V, et al. Durability of open repair of infrarenal abdominal aortic aneurysm: a 15-year follow-up study. J Vasc Surg. 2002;35(1):87-93. http://dx.doi.org/10.1016/S0741-5214(02)42909-6 PMid:11802137.
  » http://dx.doi.org/10.1016/S0741-5214(02)42909-6
• ¹⁷⁰ Conrad MF, Crawford RS, Pedraza JD, et al. Long-term durability of open abdominal aortic aneurysm repair. J Vasc Surg. 2007;46(4):669-75. http://dx.doi.org/10.1016/j.jvs.2007.05.046 PMid:17903647.
  » http://dx.doi.org/10.1016/j.jvs.2007.05.046
• ¹⁷¹ Mii S, Mori A, Sakata H, Kawazoe N. Para-anastomotic aneurysms: incidence, risk factors, treatment and prognosis. J Cardiovasc Surg. 1998;39(3):259-66. PMid:9678544.
• ¹⁷² Garg T, Baker LC, Mell MW. Adherence to postoperative surveillance guidelines after endovascular aortic aneurysm repair among Medicare beneficiaries. J Vasc Surg. 2015;61(1):23-7. http://dx.doi.org/10.1016/j.jvs.2014.07.003 PMid:25088738.
  » http://dx.doi.org/10.1016/j.jvs.2014.07.003
• ¹⁷³ Schanzer A, Messina LM, Ghosh K, et al. Follow-up compliance after endovascular abdominal aortic aneurysm repair in Medicare beneficiaries. J Vasc Surg. 2015;61(1):16-22.e1. http://dx.doi.org/10.1016/j.jvs.2014.06.006 PMid:25441010.
  » http://dx.doi.org/10.1016/j.jvs.2014.06.006
• ¹⁷⁴ Houbballah R, Majewski M, Becquemin JP. Significant sac retraction after endovascular aneurysm repair is a robust indicator of durable treatment success. J Vasc Surg. 2010;52(4):878-83. http://dx.doi.org/10.1016/j.jvs.2010.04.069 PMid:20638230.
  » http://dx.doi.org/10.1016/j.jvs.2010.04.069
• ¹⁷⁵ Go MR, Barbato JE, Rhee RY, Makaroun MS. What is the clinical utility of a 6-month computed tomography in the follow-up of endovascular aneurysm repair patients? J Vasc Surg. 2008;47(6):1181-6. http://dx.doi.org/10.1016/j.jvs.2008.01.056 PMid:18514835.
  » http://dx.doi.org/10.1016/j.jvs.2008.01.056
• ¹⁷⁶ Sternbergh WC 3rd, Greenberg RK, Chuter TAM, Tonnessen BH. Redefining postoperative surveillance after endovascular aneurysm repair: recommendations based on 5-year follow-up in the US Zenith multicenter trial. J Vasc Surg. 2008;48(2):278-84. http://dx.doi.org/10.1016/j.jvs.2008.02.075 PMid:18572368.
  » http://dx.doi.org/10.1016/j.jvs.2008.02.075
• ¹⁷⁷ Nyheim T, Staxrud LE, Rosen L, Slagsvold CE, Sandbæk G, Jørgensen JJ. Review of postoperative CT and ultrasound for endovascular aneurysm repair using Talent stent graft: Can we simplify the surveillance protocol and reduce the number of CT scans? Acta Radiol. 2013;54(1):54-8. http://dx.doi.org/10.1258/ar.2012.110291 PMid:23377874.
  » http://dx.doi.org/10.1258/ar.2012.110291
• ¹⁷⁸ Abbas A, Hansrani V, Sedgwick N, Ghosh J, McCollum CN. 3D contrast enhanced ultrasound for detecting endoleak following Endovascular Aneurysm Repair (EVAR). Eur J Vasc Endovasc Surg. 2014;47(5):487-92. http://dx.doi.org/10.1016/j.ejvs.2014.02.002 PMid:24618331.
  » http://dx.doi.org/10.1016/j.ejvs.2014.02.002
• ¹⁷⁹ Chakfé N, Diener H, Lejay A, et al. European Society for Vascular Surgery (ESVS) 2020 clinical practice guidelines on the management of vascular graft and endograft infections. Eur J Vasc Endovasc Surg. 2020;59(3):339-84. http://dx.doi.org/10.1016/j.ejvs.2019.10.016 PMid:32035742.
  » http://dx.doi.org/10.1016/j.ejvs.2019.10.016
• ¹⁸⁰ Argyriou C, Georgiadis GS, Lazarides MK, Georgakarakos E, Antoniou GA. Endograft infection after endovascular abdominal aortic aneurysm repair: a systematic review and meta-analysis. J Endovasc Ther. 2017;24(5):688-97. http://dx.doi.org/10.1177/1526602817722018 PMid:28756719.
  » http://dx.doi.org/10.1177/1526602817722018
• ¹⁸¹ Vogel TR, Symons R, Flum DR. The incidence and factors associated with graft infection after aortic aneurysm repair. J Vasc Surg. 2008;47(2):264-9. http://dx.doi.org/10.1016/j.jvs.2007.10.030 PMid:18241747.
  » http://dx.doi.org/10.1016/j.jvs.2007.10.030
• ¹⁸² Wilson W, Taubert KA, Gewitz M, et al. Prevention of Infective endocarditis: a guideline from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee, Council on Cardiovascular Disease in the Young, and the Council on Clinical Cardiology, Council on Cardiovascular Surgery and Anesthesia, and the Quality of Care and Outcomes Research Interdisciplinary Working Group. Circulation. 2007;116(15):1736-54. http://dx.doi.org/10.1161/CIRCULATIONAHA.106.183095 PMid:17446442.
  » http://dx.doi.org/10.1161/CIRCULATIONAHA.106.183095
• ¹⁸³ Kakkos SK, Bicknell CD, Tsolakis IA, Bergqvist D. Management of secondary aorto-enteric and other abdominal arterio-enteric fistulas: a review and pooled data analysis. Eur J Vasc Endovasc Surg. 2016;52(6):770-86. http://dx.doi.org/10.1016/j.ejvs.2016.09.014 PMid:27838156.
  » http://dx.doi.org/10.1016/j.ejvs.2016.09.014
• ¹⁸⁴ Lyons OTA, Baguneid M, Barwick TD, et al. Diagnosis of aortic graft infection: a case definition by the Management of Aortic Graft Infection Collaboration (MAGIC). Eur J Vasc Endovasc Surg. 2016;52(6):758-63. http://dx.doi.org/10.1016/j.ejvs.2016.09.007 PMid:27771318.
  » http://dx.doi.org/10.1016/j.ejvs.2016.09.007
• ¹⁸⁵ Calligaro KD, Veith FJ, Yuan JG, Gargiulo NJ, Dougherty MJ. Intra-abdominal aortic graft infection: complete or partial graft preservation in patients at very high risk. J Vasc Surg. 2003;38(6):1199-205. http://dx.doi.org/10.1016/S0741-5214(03)01043-7 PMid:14681612.
  » http://dx.doi.org/10.1016/S0741-5214(03)01043-7
• ¹⁸⁶ Berard X, Brizzi V. Current management of aortic endograft infection: prepare your team for this new challenge. Eur J Vasc Endovasc Surg. 2019;58(4):624-5. http://dx.doi.org/10.1016/j.ejvs.2019.05.016 PMid:31350133.
  » http://dx.doi.org/10.1016/j.ejvs.2019.05.016
• ¹⁸⁷ Batt M, Feugier P, Camou F, et al. A meta-analysis of outcomes after in situ reconstructions for aortic graft infection. Angiology. 2018;69(5):370-9. http://dx.doi.org/10.1177/0003319717710114 PMid:28578619.
  » http://dx.doi.org/10.1177/0003319717710114
• ¹⁸⁸ Janko MR, Woo K, Hacker RI, et al. In situ bypass and extra-anatomic bypass procedures result in similar survival in patients with secondary aortoenteric fistulas. J Vasc Surg. 2021;73(1):210-221.e1. http://dx.doi.org/10.1016/j.jvs.2020.04.515 PMid:32445832.
  » http://dx.doi.org/10.1016/j.jvs.2020.04.515
• ¹⁸⁹ O’Connor S, Andrew P, Batt M, Becquemin JP. A systematic review and meta-analysis of treatments for aortic graft infection. J Vasc Surg. 2006;44(1):38-45. http://dx.doi.org/10.1016/j.jvs.2006.02.053 PMid:16828424.
  » http://dx.doi.org/10.1016/j.jvs.2006.02.053
• ¹⁹⁰ Clagett GP, Valentine RJ, Hagino RT. Autogenous aortoiliac/femoral reconstruction from superficial femoral-popliteal veins: feasibility and durability. J Vasc Surg. 1997;25(2):255-66. http://dx.doi.org/10.1016/S0741-5214(97)70347-1 PMid:9052560.
  » http://dx.doi.org/10.1016/S0741-5214(97)70347-1
• ¹⁹¹ Oderich GS, Bower TC, Hofer J, et al. In situ rifampin-soaked grafts with omental coverage and antibiotic suppression are durable with low reinfection rates in patients with aortic graft enteric erosion or fistula. J Vasc Surg. 2011;53(1):99-107. http://dx.doi.org/10.1016/j.jvs.2010.08.018 PMid:21184932.
  » http://dx.doi.org/10.1016/j.jvs.2010.08.018
• ¹⁹² Plotkin A, Magee GA, Elsayed RS, et al. Methicillin-resistant Staphylococcus aureus portends a poor prognosis after endovascular repair of mycotic aortic aneurysms and aortic graft infections. J Vasc Surg. 2020;72(1):276-85. http://dx.doi.org/10.1016/j.jvs.2019.08.274 PMid:31843303.
  » http://dx.doi.org/10.1016/j.jvs.2019.08.274
• ¹⁹³ Baddour LM, Wilson WR, Bayer AS, et al. Infective endocarditis in adults: diagnosis, antimicrobial therapy, and management of complications: a scientific statement for healthcare professionals from the American Heart Association. Circulation. 2015;132(15):1435-86. http://dx.doi.org/10.1161/CIR.0000000000000296 PMid:26373316.
  » http://dx.doi.org/10.1161/CIR.0000000000000296
• ¹⁹⁴ Kieffer E, Gomes D, Chiche L, Fléron MH, Koskas F, Bahnini A. Allograft replacement for infrarenal aortic graft infection: early and late results in 179 patients. J Vasc Surg. 2004;39(5):1009-17. http://dx.doi.org/10.1016/j.jvs.2003.12.040 PMid:15111853.
  » http://dx.doi.org/10.1016/j.jvs.2003.12.040
• ¹⁹⁵ Haidar GM, Hicks TD, Strosberg DS, El-Sayed HF, Davies MG. “In situ” endografting in the treatment of arterial and graft infections. J Vasc Surg. 2017;65(6):1824-9. http://dx.doi.org/10.1016/j.jvs.2016.12.134 PMid:28359717.
  » http://dx.doi.org/10.1016/j.jvs.2016.12.134
• ¹⁹⁶ Antonello RM, D’Oria M, Cavallaro M, et al. Management of abdominal aortic prosthetic graft and endograft infections: a multidisciplinary update. J Infect Chemother. 2019;25(9):669-80. http://dx.doi.org/10.1016/j.jiac.2019.05.013 PMid:31182331.
  » http://dx.doi.org/10.1016/j.jiac.2019.05.013
• ¹⁹⁷ Li B, Khan S, Salata K, et al. A systematic review and meta-analysis of the long-term outcomes of endovascular versus open repair of abdominal aortic aneurysm. J Vasc Surg. 2019;70(3):954-969.e30. http://dx.doi.org/10.1016/j.jvs.2019.01.076 PMid:31147117.
  » http://dx.doi.org/10.1016/j.jvs.2019.01.076
• ¹⁹⁸ Stather PW, Sidloff D, Dattani N, Choke E, Bown MJ, Sayers RD. Systematic review and meta-analysis of the early and late outcomes of open and endovascular repair of abdominal aortic aneurysm. Br J Surg. 2013;100(7):863-72. http://dx.doi.org/10.1002/bjs.9101 PMid:23475697.
  » http://dx.doi.org/10.1002/bjs.9101
• ¹⁹⁹ Lal BK, Zhou W, Li Z, et al. Predictors and outcomes of endoleaks in the Veterans Affairs Open Versus Endovascular Repair (OVER) Trial of Abdominal Aortic Aneurysms. J Vasc Surg. 2015;62(6):1394-404. http://dx.doi.org/10.1016/j.jvs.2015.02.003 PMid:26598115.
  » http://dx.doi.org/10.1016/j.jvs.2015.02.003
• ²⁰⁰ Baderkhan H, Wanhainen A, Haller O, Björck M, Mani K. Detection of late complications after endovascular abdominal aortic aneurysm repair and implications for follow up based on retrospective assessment of a two centre cohort. Eur J Vasc Endovasc Surg. 2020;60(2):171-9. http://dx.doi.org/10.1016/j.ejvs.2020.02.021 PMid:32209282.
  » http://dx.doi.org/10.1016/j.ejvs.2020.02.021
• ²⁰¹ Patel SR, Allen C, Grima MJ, et al. A Systematic Review of Predictors of Reintervention After EVAR: Guidance for Risk-Stratified Surveillance. Vasc Endovascular Surg. 2017;51(6):417-28. http://dx.doi.org/10.1177/1538574417712648 PMid:28656809.
  » http://dx.doi.org/10.1177/1538574417712648
• ²⁰² White GH, May J, Waugh RC, Chaufour X, Yu W. Type III and type IV endoleak: toward a complete definition of blood flow in the sac after endoluminal AAA repair. J Endovasc Surg. 1998;5(4):305-9. http://dx.doi.org/10.1583/1074-6218(1998)005<0305:TIATIE>2.0.CO;2 PMid:9867318.
  » http://dx.doi.org/10.1583/1074-6218(1998)005<0305:TIATIE>2.0.CO;2
• ²⁰³ Ameli-Renani S, Pavlidis V, Morgan RA. Secondary endoleak management following TEVAR and EVAR. Cardiovasc Intervent Radiol. 2020;43(12):1839-54. http://dx.doi.org/10.1007/s00270-020-02572-9 PMid:32778905.
  » http://dx.doi.org/10.1007/s00270-020-02572-9
• ²⁰⁴ Bobadilla JL, Hoch JR, Leverson GE, Tefera G. The effect of warfarin therapy on endoleak development after endovascular aneurysm repair (EVAR) of the abdominal aorta. J Vasc Surg. 2010;52(2):267-71. http://dx.doi.org/10.1016/j.jvs.2010.02.290 PMid:20591602.
  » http://dx.doi.org/10.1016/j.jvs.2010.02.290
• ²⁰⁵ Kapetanios D, Kontopodis N, Mavridis D, McWilliams RG, Giannoukas AD, Antoniou GA. Meta-analysis of the accuracy of contrast-enhanced ultrasound for the detection of endoleak after endovascular aneurysm repair. J Vasc Surg. 2019;69(1):280-294.e6. http://dx.doi.org/10.1016/j.jvs.2018.07.044 PMid:30385149.
  » http://dx.doi.org/10.1016/j.jvs.2018.07.044
• ²⁰⁶ Powell JT, Sweeting MJ, Ulug P, et al. Meta-analysis of individual-patient data from EVAR-1, DREAM, OVER and ACE trials comparing outcomes of endovascular or open repair for abdominal aortic aneurysm over 5 years. Br J Surg. 2017;104(3):166-78. http://dx.doi.org/10.1002/bjs.10430 PMid:28160528.
  » http://dx.doi.org/10.1002/bjs.10430
• ²⁰⁷ Spanos K, Rohlffs F, Panuccio G, Eleshra A, Tsilimparis N, Kölbel T. Outcomes of endovascular treatment of endoleak type Ia after EVAR: a systematic review of the literature. J Cardiovasc Surg. 2019;60(2):175-85. http://dx.doi.org/10.23736/S0021-9509.19.10854-3 PMid:30650961.
  » http://dx.doi.org/10.23736/S0021-9509.19.10854-3
• ²⁰⁸ Qamhawi Z, Barge TF, Makris GC, et al. Systematic review of the use of endoanchors in endovascular aortic aneurysm repair. Eur J Vasc Endovasc Surg. 2020;59(5):748-56. http://dx.doi.org/10.1016/j.ejvs.2020.02.008 PMid:32192844.
  » http://dx.doi.org/10.1016/j.ejvs.2020.02.008
• ²⁰⁹ Scali ST, McNally MM, Feezor RJ, et al. Elective endovascular aortic repair conversion for type Ia endoleak is not associated with increased morbidity or mortality compared with primary juxtarenal aneurysm repair. J Vasc Surg. 2014;60(2):286-294.e1. http://dx.doi.org/10.1016/j.jvs.2014.02.046 PMid:24684769.
  » http://dx.doi.org/10.1016/j.jvs.2014.02.046
• ²¹⁰ Ultee KHJ, Büttner S, Huurman R, et al. Systematic review and meta-analysis of the outcome of treatment for type ii endoleak following endovascular aneurysm repair. Eur J Vasc Endovasc Surg. 2018;56(6):794-807. http://dx.doi.org/10.1016/j.ejvs.2018.06.009 PMid:30104089.
  » http://dx.doi.org/10.1016/j.ejvs.2018.06.009
• ²¹¹ Sidloff DA, Stather PW, Choke E, Bown MJ, Sayers RD. Type II endoleak after endovascular aneurysm repair. Br J Surg. 2013;100(10):1262-70. http://dx.doi.org/10.1002/bjs.9181 PMid:23939840.
  » http://dx.doi.org/10.1002/bjs.9181
• ²¹² Lo RC, Buck DB, Herrmann J, et al. Risk factors and consequences of persistent type II endoleaks. J Vasc Surg. 2016;63(4):895-901. http://dx.doi.org/10.1016/j.jvs.2015.10.088 PMid:26796291.
  » http://dx.doi.org/10.1016/j.jvs.2015.10.088
• ²¹³ Couchet G, Pereira B, Carrieres C, et al. Predictive factors for type II endoleaks after treatment of abdominal aortic aneurysm by conventional endovascular aneurysm repair. Ann Vasc Surg. 2015;29(8):1673-9. http://dx.doi.org/10.1016/j.avsg.2015.07.007 PMid:26303269.
  » http://dx.doi.org/10.1016/j.avsg.2015.07.007
• ²¹⁴ Piazza M, Frigatti P, Scrivere P, et al. Role of aneurysm sac embolization during endovascular aneurysm repair in the prevention of type II endoleak-related complications. J Vasc Surg. 2013;57(4):934-41. http://dx.doi.org/10.1016/j.jvs.2012.10.078 PMid:23384494.
  » http://dx.doi.org/10.1016/j.jvs.2012.10.078
• ²¹⁵ Samura M, Morikage N, Otsuka R, et al. Endovascular aneurysm repair with inferior mesenteric artery embolization for preventing type II endoleak. Ann Surg. 2020;271(2):238-44. http://dx.doi.org/10.1097/SLA.0000000000003299 PMid:30946077.
  » http://dx.doi.org/10.1097/SLA.0000000000003299
• ²¹⁶ Mulay S, Geraedts ACM, Koelemay MJW, et al. Type 2 endoleak with or without intervention and survival after endovascular aneurysm repair. Eur J Vasc Endovasc Surg. 2021;61(5):779-86. http://dx.doi.org/10.1016/j.ejvs.2021.01.017 PMid:33632609.
  » http://dx.doi.org/10.1016/j.ejvs.2021.01.017
• ²¹⁷ Schlösser FJV, Gusberg RJ, Dardik A, et al. Aneurysm Rupture after EVAR: Can the Ultimate Failure be Predicted? Eur J Vasc Endovasc Surg. 2009;37(1):15-22. http://dx.doi.org/10.1016/j.ejvs.2008.10.011 PMid:19008129.
  » http://dx.doi.org/10.1016/j.ejvs.2008.10.011
• ²¹⁸ Guo Q, Zhao J, Ma Y, et al. A meta-analysis of translumbar embolization versus transarterial embolization for type II endoleak after endovascular repair of abdominal aortic aneurysm. J Vasc Surg. 2020;71(3):1029-1034.e1. http://dx.doi.org/10.1016/j.jvs.2019.05.074 PMid:31677943.
  » http://dx.doi.org/10.1016/j.jvs.2019.05.074
• ²¹⁹ Yu H, Desai H, Isaacson AJ, Dixon RG, Farber MA, Burke CT. Comparison of type ii endoleak embolizations: embolization of endoleak nidus only versus embolization of endoleak nidus and branch vessels. J Vasc Interv Radiol. 2017;28(2):176-84. http://dx.doi.org/10.1016/j.jvir.2016.10.002 PMid:27993503.
  » http://dx.doi.org/10.1016/j.jvir.2016.10.002
• ²²⁰ Maleux G, Poorteman L, Laenen A, et al. Incidence, etiology, and management of type III endoleak after endovascular aortic repair. J Vasc Surg. 2017;66(4):1056-64. http://dx.doi.org/10.1016/j.jvs.2017.01.056 PMid:28434700.
  » http://dx.doi.org/10.1016/j.jvs.2017.01.056
• ²²¹ Zoethout AC, Ketting S, Zeebregts CJ, et al. An international, multicenter retrospective observational study to assess technical success and clinical outcomes of patients treated with an endovascular aneurysm sealing device for type III endoleak. J Endovasc Ther. 2022;29(1):57-65. http://dx.doi.org/10.1177/15266028211031933 PMid:34342235.
  » http://dx.doi.org/10.1177/15266028211031933
• ²²² Bussmann A, Heim F, Delay C, et al. Textile aging characterization on new generations of explanted commercial endoprostheses: a preliminary study. Eur J Vasc Endovasc Surg. 2017;54(3):378-86. http://dx.doi.org/10.1016/j.ejvs.2017.06.004 PMid:28716448.
  » http://dx.doi.org/10.1016/j.ejvs.2017.06.004
• ²²³ Turney EJ, Steenberge SP, Lyden SP, et al. Late graft explants in endovascular aneurysm repair. J Vasc Surg. 2014;59(4):886-93. http://dx.doi.org/10.1016/j.jvs.2013.10.079 PMid:24377945.
  » http://dx.doi.org/10.1016/j.jvs.2013.10.079
• ²²⁴ Cao P, Verzini F, Zannetti S, et al. Device migration after endoluminal abdominal aortic aneurysm repair: Analysis of 113 cases with a minimum follow-up period of 2 years. J Vasc Surg. 2002;35(2):229-35. http://dx.doi.org/10.1067/mva.2002.120045 PMid:11854719.
  » http://dx.doi.org/10.1067/mva.2002.120045
• ²²⁵ Bastos Goncalves F, Hoeks SE, Teijink JA, et al. Risk factors for proximal neck complications after endovascular aneurysm repair using the endurant stentgraft. Eur J Vasc Endovasc Surg. 2015;49(2):156-62. http://dx.doi.org/10.1016/j.ejvs.2014.10.003 PMid:25458435.
  » http://dx.doi.org/10.1016/j.ejvs.2014.10.003
• ²²⁶ van Marrewijk CJ, Leurs LJ, Vallabhaneni SR, Harris PL, Buth J, Laheij RJF. Risk-adjusted outcome analysis of endovascular abdominal aortic aneurysm repair in a large population: how do stent-grafts compare? J Endovasc Ther. 2005;12(4):417-29. http://dx.doi.org/10.1583/05-1530R.1 PMid:16048373.
  » http://dx.doi.org/10.1583/05-1530R.1
• ²²⁷ Albertini JN, Kalliafas S, Travis S, et al. Anatomical risk factors for proximal perigraft endoleak and graft migration following endovascular repair of abdominal aortic aneurysms. Eur J Vasc Endovasc Surg. 2000;19(3):308-12. http://dx.doi.org/10.1053/ejvs.1999.1045 PMid:10753697.
  » http://dx.doi.org/10.1053/ejvs.1999.1045
• ²²⁸ Pintoux D, Chaillou P, Azema L, et al. Long-term influence of suprarenal or infrarenal fixation on proximal neck dilatation and stentgraft migration after EVAR. Ann Vasc Surg. 2011;25(8):1012-9. http://dx.doi.org/10.1016/j.avsg.2010.08.013 PMid:22023937.
  » http://dx.doi.org/10.1016/j.avsg.2010.08.013
• ²²⁹ Sternbergh WC 3rd, Money SR, Greenberg RK, Chuter TAM. Influence of endograft oversizing on device migration, endoleak, aneurysm shrinkage, and aortic neck dilation: results from the zenith multicenter trial. J Vasc Surg. 2004;39(1):20-6. http://dx.doi.org/10.1016/j.jvs.2003.09.022 PMid:14718806.
  » http://dx.doi.org/10.1016/j.jvs.2003.09.022
• ²³⁰ van Prehn J, Schlösser FJV, Muhs BE, Verhagen HJM, Moll FL, van Herwaarden JA. Oversizing of aortic stent grafts for abdominal aneurysm repair: a systematic review of the benefits and risks. Eur J Vasc Endovasc Surg. 2009;38(1):42-53. http://dx.doi.org/10.1016/j.ejvs.2009.03.025 PMid:19428273.
  » http://dx.doi.org/10.1016/j.ejvs.2009.03.025
• ²³¹ Cao P, Verzini F, Parlani G, et al. Predictive factors and clinical consequences of proximal aortic neck dilatation in 230 patients undergoing abdominal aorta aneurysm repair with self-expandable stent-grafts. J Vasc Surg. 2003;37(6):1200-5. http://dx.doi.org/10.1016/S0741-5214(02)75340-8 PMid:12764265.
  » http://dx.doi.org/10.1016/S0741-5214(02)75340-8
• ²³² Bastos Gonçalves F, Oliveira NF, Josee van Rijn M, et al. Iliac seal zone dynamics and clinical consequences after endovascular aneurysm repair. Eur J Vasc Endovasc Surg. 2017;53(2):185-92. http://dx.doi.org/10.1016/j.ejvs.2016.11.003 PMid:28027890.
  » http://dx.doi.org/10.1016/j.ejvs.2016.11.003
• ²³³ Waasdorp EJ, de Vries JPPM, Sterkenburg A, et al. The association between iliac fixation and proximal stent-graft migration during EVAR follow-up: mid-term results of 154 talent devices. Eur J Vasc Endovasc Surg. 2009;37(6):681-7. http://dx.doi.org/10.1016/j.ejvs.2009.03.001 PMid:19345632.
  » http://dx.doi.org/10.1016/j.ejvs.2009.03.001
• ²³⁴ Powell JT, Sweeting MJ, Thompson MM, et al. Endovascular or open repair strategy for ruptured abdominal aortic aneurysm: 30 day outcomes from IMPROVE randomised trial. BMJ. 2014;348(2):f7661. http://dx.doi.org/10.1136/bmj.f7661 PMid:24418950.
  » http://dx.doi.org/10.1136/bmj.f7661
• ²³⁵ Mastracci TM, Garrido-Olivares L, Cinà CS, Clase CM. Endovascular repair of ruptured abdominal aortic aneurysms: a systematic review and meta-analysis. J Vasc Surg. 2008;47(1):214-221. http://dx.doi.org/10.1016/j.jvs.2007.07.052 PMid:18178478.
  » http://dx.doi.org/10.1016/j.jvs.2007.07.052
• ²³⁶ Antoniou GA, Georgiadis GS, Antoniou SA, et al. Endovascular repair for ruptured abdominal aortic aneurysm confers an early survival benefit over open repair. J Vasc Surg. 2013;58(4):1091-105. http://dx.doi.org/10.1016/j.jvs.2013.07.109 PMid:24075109.
  » http://dx.doi.org/10.1016/j.jvs.2013.07.109
• ²³⁷ Kontopodis N, Galanakis N, Antoniou SA, et al. Meta-analysis and meta-regression analysis of outcomes of endovascular and open repair for ruptured abdominal aortic aneurysm. Eur J Vasc Endovasc Surg. 2020;59(3):399-410. http://dx.doi.org/10.1016/j.ejvs.2019.12.023 PMid:31932143.
  » http://dx.doi.org/10.1016/j.ejvs.2019.12.023
• ²³⁸ Queiroz AB, Schneidwind KP, Mulatti GC, et al. Repair of ruptured abdominal aortic aneurysms preferably with bifurcated endografts: a single-center study. Clinics. 2014;69(6):420-5. http://dx.doi.org/10.6061/clinics/2014(06)09 PMid:24964307.
  » http://dx.doi.org/10.6061/clinics/2014(06)09
• ²³⁹ Mehta M. Endovascular aneurysm repair for ruptured abdominal aortic aneurysm: The Albany Vascular Group approach. J Vasc Surg. 2010;52(6):1706-12. http://dx.doi.org/10.1016/j.jvs.2010.06.103 PMid:20724101.
  » http://dx.doi.org/10.1016/j.jvs.2010.06.103
• ²⁴⁰ Kontopodis N, Galanakis N, Akoumianakis E, Ioannou CV, Tsetis D, Antoniou GA. Systematic review and meta-analysis of the impact of institutional and surgeon procedure volume on outcomes after ruptured abdominal aortic aneurysm repair. Eur J Vasc Endovasc Surg. 2021;62(3):388-98. http://dx.doi.org/10.1016/j.ejvs.2021.06.015 PMid:34384687.
  » http://dx.doi.org/10.1016/j.ejvs.2021.06.015
• ²⁴¹ Vu KN, Kaitoukov Y, Morin-Roy F, et al. Rupture signs on computed tomography, treatment, and outcome of abdominal aortic aneurysms. Insights Imaging. 2014;5(3):281-93. http://dx.doi.org/10.1007/s13244-014-0327-3 PMid:24789068.
  » http://dx.doi.org/10.1007/s13244-014-0327-3
• ²⁴² IMPROVE trial investigators. Comparative clinical effectiveness and cost effectiveness of endovascular strategy v open repair for ruptured abdominal aortic aneurysm: three year results of the IMPROVE randomised trial. BMJ. 2017;359:j4859. http://dx.doi.org/10.1136/bmj.j4859 PMid:29138135.
  » http://dx.doi.org/10.1136/bmj.j4859
• ²⁴³ Roosendaal LC, Kramer GM, Wiersema AM, Wisselink W, Jongkind V. Outcome of ruptured abdominal aortic aneurysm repair in octogenarians: a systematic review and meta-analysis. Eur J Vasc Endovasc Surg. 2020;59(1):16-22. http://dx.doi.org/10.1016/j.ejvs.2019.07.014 PMid:31810836.
  » http://dx.doi.org/10.1016/j.ejvs.2019.07.014
• ²⁴⁴ Faizer R, Weinhandl E, el Hag S, et al. Decreased mortality with local versus general anesthesia in endovascular aneurysm repair for ruptured abdominal aortic aneurysm in the Vascular Quality Initiative database. J Vasc Surg. 2019;70(1):92-101.e1. http://dx.doi.org/10.1016/j.jvs.2018.10.090 PMid:30611580.
  » http://dx.doi.org/10.1016/j.jvs.2018.10.090
• ²⁴⁵ Karkos CD, Harkin DW, Giannakou A, Gerassimidis TS. Mortality after endovascular repair of ruptured abdominal aortic aneurysms. Arch Surg. 2009;144(8):770-8. http://dx.doi.org/10.1001/archsurg.2009.132 PMid:19687383.
  » http://dx.doi.org/10.1001/archsurg.2009.132
• ²⁴⁶ Lei J, Pu H, Wu Z, et al. Local versus general anesthesia for endovascular aneurysm repair in ruptured abdominal aortic aneurysm: a systematic review and meta‐analysis. Catheter Cardiovasc Interv. 2022;100(4):679-86. http://dx.doi.org/10.1002/ccd.30326 PMid:35801490.
  » http://dx.doi.org/10.1002/ccd.30326
• ²⁴⁷ Hellmann DB, Grand DJ, Freischlag JA. Inflammatory Abdominal Aortic Aneurysm. JAMA. 2007;297(4):395-400. http://dx.doi.org/10.1001/jama.297.4.395 PMid:17244836.
  » http://dx.doi.org/10.1001/jama.297.4.395
• ²⁴⁸ Capoccia L, Riambau V. Endovascular repair versus open repair for inflammatory abdominal aortic aneurysms. Cochrane Database Syst Rev. 2015;(4):CD010313. http://dx.doi.org/10.1002/14651858.CD010313.pub2 PMid:25879695.
  » http://dx.doi.org/10.1002/14651858.CD010313.pub2
• ²⁴⁹ Rasmussen TE, Hallett JW Jr. Inflammatory aortic aneurysms: a clinical review with new perspectives in pathogenesis.. Ann Surg. 1997;225(2):155-64. http://dx.doi.org/10.1097/00000658-199702000-00003 PMid:9065292.
  » http://dx.doi.org/10.1097/00000658-199702000-00003
• ²⁵⁰ Paravastu SCV, Ghosh J, Murray D, Farquharson FG, Serracino-Inglott F, Walker MG. A systematic review of open versus endovascular repair of inflammatory abdominal aortic aneurysms. Eur J Vasc Endovasc Surg. 2009;38(3):291-7. http://dx.doi.org/10.1016/j.ejvs.2009.05.005 PMid:19541509.
  » http://dx.doi.org/10.1016/j.ejvs.2009.05.005
• ²⁵¹ Joergensen TMM, Christensen K, Lindholt JS, Larsen LA, Green A, Houlind K. High heritability of liability to abdominal aortic aneurysms: a population based twin study. Eur J Vasc Endovasc Surg. 2016;52(1):41-6. http://dx.doi.org/10.1016/j.ejvs.2016.03.012 PMid:27107486.
  » http://dx.doi.org/10.1016/j.ejvs.2016.03.012
• ²⁵² Sidloff DA, Saratzis A, Sweeting MJ, et al. Sex differences in mortality after abdominal aortic aneurysm repair in the UK. Br J Surg. 2017;104(12):1656-64. http://dx.doi.org/10.1002/bjs.10600 PMid:28745403.
  » http://dx.doi.org/10.1002/bjs.10600
• ²⁵³ Deery SE, Schermerhorn ML. Should abdominal aortic aneurysms in women be repaired at a lower diameter threshold? Vasc Endovascular Surg. 2018;52(7):543-7. http://dx.doi.org/10.1177/1538574418773247 PMid:29720046.
  » http://dx.doi.org/10.1177/1538574418773247
• ²⁵⁴ Erben Y, Bews KA, Hanson KT, et al. Female sex is a marker for higher morbidity and mortality after elective endovascular aortic aneurysm repair: a national surgical quality improvement program analysis. Ann Vasc Surg. 2020;69:1-8. http://dx.doi.org/10.1016/j.avsg.2020.06.031 PMid:32599114.
  » http://dx.doi.org/10.1016/j.avsg.2020.06.031
• ²⁵⁵ Tumer NB, Askin G, Akkaya BB, Civelek I, Unal EU, Iscan HZ. Outcomes after EVAR in females are similar to males. BMC Cardiovasc Disord. 2021;21(1):301. http://dx.doi.org/10.1186/s12872-021-02114-2 PMid:34130661.
  » http://dx.doi.org/10.1186/s12872-021-02114-2
• ²⁵⁶ Corsi T, Ciaramella MA, Palte NK, Carlson JP, Rahimi SA, Beckerman WE. Female sex is associated with reintervention and mortality following elective endovascular abdominal aortic aneurysm repair. J Vasc Surg. 2022;76(6):1494-1501.e1. http://dx.doi.org/10.1016/j.jvs.2022.05.011 PMid:35705120.
  » http://dx.doi.org/10.1016/j.jvs.2022.05.011
• ²⁵⁷ Ilyas S, Stone DH, Kang J, et al. Non-guideline-compliant endovascular abdominal aortic aneurysm repair in women is associated with increased mortality and reintervention compared with men. J Vasc Surg. 2022;75(1):118-125.e1. http://dx.doi.org/10.1016/j.jvs.2021.07.109 PMid:34302934.
  » http://dx.doi.org/10.1016/j.jvs.2021.07.109
• ²⁵⁸ Tedjawirja VN, Alberga AJ, Hof MHP, et al. Mortality following elective abdominal aortic aneurysm repair in women. Br J Surg. 2022;109(4):340-5. http://dx.doi.org/10.1093/bjs/znab465 PMid:35237792.
  » http://dx.doi.org/10.1093/bjs/znab465
• ²⁵⁹ Sweeting MJ, Thompson SG, Brown LC, Powell JT. Meta-analysis of individual patient data to examine factors affecting growth and rupture of small abdominal aortic aneurysms. Br J Surg. 2012;99(5):655-65. http://dx.doi.org/10.1002/bjs.8707 PMid:22389113.
  » http://dx.doi.org/10.1002/bjs.8707
• ²⁶⁰ Solberg S, Singh K, Wilsgaard T, Jacobsen BK. Increased growth rate of abdominal aortic aneurysms in women: the Tromsø study. Eur J Vasc Endovasc Surg. 2005;29(2):145-9. http://dx.doi.org/10.1016/j.ejvs.2004.11.015 PMid:15649720.
  » http://dx.doi.org/10.1016/j.ejvs.2004.11.015
• ²⁶¹ Li K, Zhang K, Li T, Zhai S. Primary results of abdominal aortic aneurysm screening in the at-risk residents in middle China. BMC Cardiovasc Disord. 2018;18(1):60. http://dx.doi.org/10.1186/s12872-018-0793-5 PMid:29614976.
  » http://dx.doi.org/10.1186/s12872-018-0793-5
• ²⁶² Vavra AK, Kibbe MR. Part One: for the motion. Evidence supports reducing the threshold diameter to 5 cm for elective interventions in women with abdominal aortic aneurysms. Eur J Vasc Endovasc Surg. 2014;48(6):611-4. http://dx.doi.org/10.1016/j.ejvs.2014.08.014 PMid:25476927.
  » http://dx.doi.org/10.1016/j.ejvs.2014.08.014
• ²⁶³ Norman PE, Powell JT. Abdominal aortic aneurysm: the prognosis in women is worse than in men. Circulation. 2007;115(22):2865-9. http://dx.doi.org/10.1161/CIRCULATIONAHA.106.671859 PMid:17548742.
  » http://dx.doi.org/10.1161/CIRCULATIONAHA.106.671859
• ²⁶⁴ Sweet MP, Fillinger MF, Morrison TM, Abel D. The influence of gender and aortic aneurysm size on eligibility for endovascular abdominal aortic aneurysm repair. J Vasc Surg. 2011;54(4):931-7. http://dx.doi.org/10.1016/j.jvs.2011.02.054 PMid:21658895.
  » http://dx.doi.org/10.1016/j.jvs.2011.02.054
• ²⁶⁵ Mazzaccaro D, Malacrida G, Amato B, Alessio Angileri S, Ierardi AM, Nano G. Preliminary experience with the use of ultra-low profile endografts. Diagn Interv Radiol. 2017;23(6):448-53. http://dx.doi.org/10.5152/dir.2017.16523 PMid:29097346.
  » http://dx.doi.org/10.5152/dir.2017.16523
• ²⁶⁶ Ash J, Chandra V, Rzucidlo E, Vouyouka A, Hunter M. LUCY results show females have equivalent outcomes to males following endovascular abdominal aortic aneurysm repair despite more complex aortic morphology. J Vasc Surg. 2020;72(2):566-575.e4. http://dx.doi.org/10.1016/j.jvs.2019.10.080 PMid:31918999.
  » http://dx.doi.org/10.1016/j.jvs.2019.10.080
• ²⁶⁷ Torsello G, Pratesi G, van der Meulen S, Ouriel K. Aortoiliac remodeling and 5-year outcome of an ultralow-profile endograft. J Vasc Surg. 2019;69(6):1747-57. http://dx.doi.org/10.1016/j.jvs.2018.09.059 PMid:30591290.
  » http://dx.doi.org/10.1016/j.jvs.2018.09.059

Publication Dates

• Publication in this collection
  30 Oct 2023
• Date of issue
  2023

History

• Received
  13 Mar 2023
• Accepted
  15 June 2023