RESUMEN
Introducción
La leishmaniasis visceral (LV) es una enfermedad infecciosa causada por protozoos del género Leishmania; predomina en las regiones tropicales, subtropicales y templadas.
Objetivo
Caracterizar una serie de casos de LV en pacientes mayores de 18 años atendidos en un hospital de referencia del norte de Minas Gerais, así como describir la ocurrencia de casos, según la caracterización climatológica, y correlacionar la distribución de los casos con la lluvia y la temperatura ambiente.
Métodos
El diseño del estudio fue una serie de casos recopilados entre 1999 y 2016. Los datos se extrajeron de historias clínicas seleccionadas cronológicamente. La información climática se recopiló en el Centro de estudios del Semiárido de la Universidad Federal de Montes Claros (Unimontes).
Resultados
Hubo un ligero predominio del sexo masculino (54,4%) y de edades comprendidas entre uno y cuatro años (42,9%). El tiempo de evolución de las manifestaciones clínicas hasta el momento de la hospitalización osciló entre cinco y 120 días, siendo la duración más frecuente entre 16 y 30 días (34,4%). Hepatomegalia, esplenomegalia, palidez cutánea y fiebre fueron manifestaciones presentes en más del 90% de los pacientes al ingreso. El diagnóstico se realizó por métodos serológicos en la mayoría de los casos (85,9%). La mayor parte de los ingresos duró entre 16 y 30 días (44%) y el alta hospitalaria con orientación para el control ambulatorio fue el resultado más frecuente de los ingresos. El porcentaje de muertes fue del 2%.
Conclusión
Las características predominantes son niños varones de 1 a 4 años, que acudió al servicio de salud con la clásica tríada LV: hepatoesplenomegalia, palidez y fiebre prolongada. En este estudio no hubo asociación estadísticamente significativa entre temperatura, precipitación y número de casos, sin embargo, existen matices en los factores ambientales que influyen en la dinámica de transmisión de LV, los cuales varían de región a otra.
Palabras clave
leishmaniasis visceral; distribución temporal; epidemiología.
INTRODUCTION
Visceral leishmaniasis (VL) is an infectious disease caused by the protozoa of the genus Leishmania; it is predominant in tropical, subtropical, and temperate regions, with an estimated worldwide incidence of 200 to 400,000 new cases each year(11 Alvar J, Vélez ID, Bern C, et al. Leishmaniasis worldwide and global estimates of its incidence. PLoS One. 2012; 7(5): e35671. doi:10.1371/journal.pone.0035671.
https://doi.org/10.1371/journal.pone.003...
). It is a disease most commonly seen in children and is characterized by prolonged fever, hepatosplenomegaly, and pancytopenia; however, it has a wide clinical presentation, which ranges from asymptomatic to very severe cases(22 Belo VS, Werneck GL, Barbosa DS, et al. Factors associated with visceral leishmaniasis in the americas: a systematic review and meta-analysis. PLoS Negl Trop Dis. 2013; 25: e2182.,33 Herwaldt BL. Leishmaniasis. Lancet. 1999; 354: 1191–99.). In countries where VL is more prevalent, it mainly affects the socially less favored population, with a more notable incidence in rural and peri-urban areas(44 Alvar J, Yactoyo S, Bern C. Leishmaniasis and poverty. Trends Parasitol. 2006; 22(12): 552–7.,55 Misha J, Carpenter S, Singh S. Low serum zinc levels in na endemic area of visceral leishmaniasis in Bihar, India. Indian J Med Res. 2010; 793–98.). The distribution on the planet concentrates 90% of cases in just six countries: Brazil, India, Bangladesh, Sudan, Ethiopia, and Nepal – regions known to have a tropical and subtropical climate. Mortality is around 50,000 individuals/year, as VL may be fatal if not diagnosed and treated promptly(11 Alvar J, Vélez ID, Bern C, et al. Leishmaniasis worldwide and global estimates of its incidence. PLoS One. 2012; 7(5): e35671. doi:10.1371/journal.pone.0035671.
https://doi.org/10.1371/journal.pone.003...
,66 Yared S, Deribe K, Gebreselassie A, et al. Risk factors of visceral leishmaniasis: a case control study in north-western Ethiopia. Parasites & Vectors. 2014; 7: 470.). Some more recent studies highlight a change in the epidemiological picture of the disease, from the increase in cases among adults and the increase in the incidence of cases in peri-urban areas, possibly due to vector and natural reservoirs urbanization(77 Cardim MFM, Rodas LAC, Dibo MR, et al. Introdução e expansão da leishmaniose visceral americana em humanos no Estado de São Paulo, 1999-2011. Rev Saúde Pública. 2013; 47(4): 691–700.–99 Gontijo CMF, Melo MN. Leishmaniose visceral no Brasil: quadro atual, desafios e perspectivas. Rev Bras Epidemiol. 2004; 7(3): 338–49.).
The north of Minas Gerais is one of the endemic regions of VL in Brazil(1010 Silva TAM, Coura-Vital W, Barbosa DS, et al. Spatial and temporal trends of visceral leishmaniasis by mesoregion in a Southeastern state of Brazil, 2002-2013. PLoS Negl Trop Dis. 2017; 11(10): e0005950.). It is an area of great territorial extension in the state, with approximately 130 thousand square kilometers (an area larger than that of many Brazilian states), comprising 89 municipalities, with a resident population of almost two million inhabitants. It is a transition region between the South/Southeast and the Northeast of the country, with a dry and hot climate and low rainfall. It also stands out for being one of the poorest regions in the country, with low human development indicators(1111 Instituto Brasileiro de Geografia e Estatítica [internet homepage]. Latitude média dos municípios brasileiros. Available at: http:www.ibge.gov.br/latitudes. [Accessed on: Jun 2, 2018].
http:www.ibge.gov.br/latitudes...
). For the entire region, there is only one referral hospital for VL treatment, located in the city of Montes Claros, the region’s hub: The University Hospital Clemente Faria (HUCF).
Considering that VL often leads to hospitalization, the survey of the profile of hospital admissions over time, as well as the climatic characterization of the same period, has the potential to reveal important characteristics of the disease, enabling the development of preventive and control actions more effectively. The present study aimed to characterize the series of VL cases treated at a referral hospital in the north of Minas Gerais over 18 years, in addition to describing the occurrence of these cases, according to the climatic characterization, and correlating their distribution with rainfall and environmental temperature.
METHODS
Descriptive case series study, whose data were collected at the HUCF, State University of Montes Claros (Unimontes), the only referral institution for healthcare delivery to patients with VL in the region. Data were collected directly from the medical records of patients who had a diagnosis of VL on admission or during the hospital stay, from 1999 to 2016.
For data collection in the medical records, a specific form was used developed by the researchers, covering the patient’s demographic, epidemiological and clinical characteristics, laboratory features, and clinical outcomes. A team of four specially trained medical students made a thorough reading of the medical records for data collection. Quality control was carried out through random access to the medical records of patients with VL to check the data collected in the forms.
The inclusion criteria were defined as all medical records that presented a diagnosis of VL defined by clinical, immunological, histological, or epidemiological parameters, or even the association between these criteria. Exclusion criteria were: illegible and inaccessible medical records (not found after an extensive search), and other types of leishmaniasis.
Information about the monthly average rainfall in cubic millimeters and the monthly average temperature in degrees Celsius were obtained from the Center for Coexistence with the Semiarid Studies [Centro de Estudos de Convivência com o Semiárido (CECS)], Unimontes’ virtual platform. Spearman correlations were investigated between monthly rainfall average and monthly temperature average and the average of the numbers of hospitalized cases at a referral hospital over the years studied.
To characterize the case series, a descriptive analysis was performed, with the presentation of absolute and relative values, measures of central tendency, and amplitude. Spearman’s correlation was verified between the average of monthly numbers of LV cases and the mean of average temperature, and also between the averages of monthly numbers of VL cases and the averages of local rainfall from 1999 to 2016. The collected data were processed using the Statistical Package for the Social Science – SPSS 20.0.
The research project was approved by the institution’s administrative board and by the Research Ethics Committee, under opinion 1.471.595.
RESULTS
Over the period studied, 967 medical records were identified and located. The main characteristics of the patients are shown in Table 1. A slight predominance of males (54.4%) and in the age group from 1 to 4 years (42.9%) was verified. The evolution time of clinical manifestations until the time of admission ranged from five to 120 days, and the length between 16 and 30 days was more frequent (34.4%).
Demographic, clinical, and evolution data of hospitalized patients with a diagnosis of VL at the Hospital Universitário Clemente Faria, Montes Claros, Minas Gerais, Brazil, in the period 1999-2016
Hepatomegaly, splenomegaly, skin pallor, and fever were manifestations present in more than 90% of patients at admission. The diagnosis was performed by serological methods in most cases (85.9%). The largest portion of admissions lasted between 16 and 30 days (44%), and hospital discharge with guidance for outpatient control was the most frequent outcome of admissions. The percentage of deaths was 2%.
The distribution of assisted cases, according to the origin of the patients, is shown in Figure 1.
Distribution of VL cases admitted to a referral hospital in the north of Minas Gerais, according to place of origin (1999-2016)
The monthly distribution of cases is listed in Figures 2 (1999 to 2007) and 3 (2008 to 2016), which include graphs that also show the monthly average of temperatures and rainfall.
Monthly distribution of VL cases admitted to a referral hospital in the north of Minas Gerais, in addition to monthly averages of average temperature and monthly rainfall, 1999-2007
Table 2 shows the results of Spearman’s correlation between the average of monthly numbers of LV cases and the mean of average temperatures (p = 0.292), and between the average numbers of monthly VL cases and average local rainfall (p = 0.214), over the years 1999 to 2016.
Monthly distribution of VL cases admitted to a referral hospital in the north of Minas Gerais, in addition to monthly averages of average temperature and monthly rainfall, 2007-2016
Spearman’s correlation between monthly averages of number of VL cases, average temperature, and rainfall, between 1999 and 2016; HUCF, Montes Claros, Minas Gerais, Brazil
DISCUSSION
This study provided a detailed characterization of a series of VL cases treated at a reference hospital in an endemic area over 18 years, identifying that, in the aforementioned period, children were the main victims of the disease, with a predominance of cases in urban areas. The data reinforce the process of urbanization of the disease, as reported in other studies(1212 Campos Jr D. Características clínico-epidemiológicas do Calazar na criança. Estudo de 75 casos. J Pediatr, Rio Janeiro. 1995; 71(5): 261–5.–1616 Oliveira IBB, Batista HL, Peluzi JM, et al. Aspectos epidemiológicos e ambientais da leishmaniose visceral em menores de 15 anos, no período de 2007 a 2012, no município de Araguaína, Tocantins, Brasil. Rev Soc Bras Med Trop. 2014; 4(47).).
The clinical findings recorded over the study period confirm the predominance of cases in children, and the classic condition of hepatosplenomegaly, skin and mucous pallor, and fever. The triad of fever, increased abdominal volume, and skin pallor – the most prevalent findings reported on admission to the hospital –is still the main reason for patients to seek health care. Similar results have been presented in other studies(1414 Rey LC, Martins CV, Ribeiro HB, et al. American visceral leishmaniasis (kala-azar) in hospitalized children from an endemic area. J Pediatr, Rio Janeiro. 2005; 81(1): 73–78.,1515 Oliveira JM, Fernandes AC, Dorval MEC, et al. Mortalidade por leishmaniose visceral: aspectos clínicos e laboratoriais. Rev Soc Bras Med Trop. 2010; 43(2): 188–193.,1717 Xavier-Gomes LM, Costa WB, Prado, PF, Oliveira-Campos M, Leite MTS. Características clínicas e epidemiológicas da leishmaniose visceral em crianças internadas em um hospital universitário de referência no norte de Minas Gerais, Brasil. Rev Bras Epidemiol. 2009; 123(4): 549–55.,1818 Rigo RS, Rigo L, Honer MR. Aspectos clínicos e laboratoriais na leishmaniose visceral americana. J Bras Nefrol. 2009; 31(1): 48–5.).
Observations regarding the time of evolution of VL, considering the appearance of signs and symptoms until hospital admission, revealed that most patients were admitted for hospital treatment within 30 days of manifestations of the disease. In another study(1313 Queiroz MJA, Alves JGB, Correia JB. Leishmaniose visceral: características clínico-epidemiológicas em crianças de área endêmica. J Pediatric. 2004; 80(2).), this interval ranged from 1 to 365 days, and the average reached 42.7 days, with 88.7% of cases manifesting symptoms for a period longer than 30 days. In another study(1313 Queiroz MJA, Alves JGB, Correia JB. Leishmaniose visceral: características clínico-epidemiológicas em crianças de área endêmica. J Pediatric. 2004; 80(2).), although the interval variation was the same as found by Queiroz et al. (2004)(1313 Queiroz MJA, Alves JGB, Correia JB. Leishmaniose visceral: características clínico-epidemiológicas em crianças de área endêmica. J Pediatric. 2004; 80(2).), the average reached 78.2 days, and 60% of cases evolved for more than 30 and less than 60 days. In the present study, as the municipality of Montes Claros is an endemic area with a referral hospital for leishmaniasis, this seems to justify the shorter time interval between the onset of symptoms and seeking medical care. However, there is still a considerable number of patients with disease evolution for more than 30 days, which suggests a late diagnosis and/or difficulties in accessing specialized health services(1515 Oliveira JM, Fernandes AC, Dorval MEC, et al. Mortalidade por leishmaniose visceral: aspectos clínicos e laboratoriais. Rev Soc Bras Med Trop. 2010; 43(2): 188–193.).
The diagnostic confirmation, according to the analysis of the medical records, is mainly by serology, either by the indirect immunofluorescence method, immunoenzymatic test (Elisa), or rK39 antibody, or even the direct agglutination test. Although the gold standard is the identification of the protozoan in organic tissues, that is, the parasitological method, as observed in other studies(1212 Campos Jr D. Características clínico-epidemiológicas do Calazar na criança. Estudo de 75 casos. J Pediatr, Rio Janeiro. 1995; 71(5): 261–5.–1515 Oliveira JM, Fernandes AC, Dorval MEC, et al. Mortalidade por leishmaniose visceral: aspectos clínicos e laboratoriais. Rev Soc Bras Med Trop. 2010; 43(2): 188–193.), serological diagnosis and/or association with epidemiological and clinical issues have been widely used(1919 Diro E, Lynen L, Gebregziabiher B, et al. Clinical aspects of paediatric visceral leishmaniasis in North-west Ethiopia. Trop Med Int Health. 2015; 20(1): 8–16.). It is important to highlight the association of methods for the conclusion of the diagnosis and the timely implementation of therapy.
The length of stay is a significant variable, as the patient’s long stay in the hospital can be a complication for hospital- acquired infections(2020 Souza GAAD, Garcial LM, Rocha SS, Maciel APF. Perfil microbiológico de infecções de pele e partes moles em pacientes internos de um hospital universitário. Rev Epidemiologia Controle de Infecção, Santa Cruz do Sul. 2016; 6(1): 33–36. Available at: https://online.unisc.br/seer/index.php/epidemiologia/article/view/5901/5057. [Accessed on: March 10, 2018].
https://online.unisc.br/seer/index.php/e...
). In individuals undergoing treatment for VL, this aspect takes on even greater importance, as concomitant infections represent a worse prognosis(2121 Costa DL. Fatores de prognóstico na leishmaniose visceral: alterações clínicas e laboratoriais associadas à resposta imune, aos distúrbios da coagulação e à morte. [thesis]. Programa de Pós-Graduação da Universidade Federal de Minas Gerais; 2009.). In this study, the average length of stay was 39.8 days and the longest time interval recorded was between 16 and 30 days. In the literature, the length of stay ranged from 11.2 to 46 days, with an average of 25.2 days(1212 Campos Jr D. Características clínico-epidemiológicas do Calazar na criança. Estudo de 75 casos. J Pediatr, Rio Janeiro. 1995; 71(5): 261–5.–1515 Oliveira JM, Fernandes AC, Dorval MEC, et al. Mortalidade por leishmaniose visceral: aspectos clínicos e laboratoriais. Rev Soc Bras Med Trop. 2010; 43(2): 188–193.).
In general, after the introduction of adequate treatment, the level of death significantly reduces. In this study, 19 cases (2%) evolved to death. Oliveira et al. (2010)(1515 Oliveira JM, Fernandes AC, Dorval MEC, et al. Mortalidade por leishmaniose visceral: aspectos clínicos e laboratoriais. Rev Soc Bras Med Trop. 2010; 43(2): 188–193.) had 14.5% of death, while Xavier-Gomes et al. (2009)(1717 Xavier-Gomes LM, Costa WB, Prado, PF, Oliveira-Campos M, Leite MTS. Características clínicas e epidemiológicas da leishmaniose visceral em crianças internadas em um hospital universitário de referência no norte de Minas Gerais, Brasil. Rev Bras Epidemiol. 2009; 123(4): 549–55.) and Diro et al. (2015)(1919 Diro E, Lynen L, Gebregziabiher B, et al. Clinical aspects of paediatric visceral leishmaniasis in North-west Ethiopia. Trop Med Int Health. 2015; 20(1): 8–16.) reported less than 10%, a value closer to that found in our study. The Brazilian Ministry of Health evaluated the lethality caused by VL in the last two decades and observed an increase of more than 67%, that is, increased from 3.4% in 1994 to 5.7% in 2009(2222!Brasil. Ministério da Saúde. Secretaria de Vigilância em Saúde. Departamento de Vigilância Epidemiológica. Leishmaniose visceral: recomendações clínicas para redução da letalidade. Série A. Normas e manuais técnicos. Brasília: Ministério da Saúde; 2011.). This problem is due to drug resistance, the toxicity of first-line drugs, complications from the infection itself, and late diagnosis(2222!Brasil. Ministério da Saúde. Secretaria de Vigilância em Saúde. Departamento de Vigilância Epidemiológica. Leishmaniose visceral: recomendações clínicas para redução da letalidade. Série A. Normas e manuais técnicos. Brasília: Ministério da Saúde; 2011.,2323 Aguiar PF, Rodrigues RK. Leishmaniose visceral no Brasil: artigo de revisão. Unimontes Científica. 2017; 19(1): 191–204.).
In this study, there was no statistically significant association between environmental variables, temperature, and rainfall, and an increase in the number of cases over the period analyzed. Although the influence of the environment on the increase in the number of cases of certain diseases has been the object of study by several authors, physical factors are reported as intervening in the chain of transmission of zoonotic diseases. Rainfall, temperature variation, humidity, light intensity, presence of organic matter in household and peridomestic areas, altitude, among other factors, are highlighted within this perspective, since they can affect reproduction and nutrient availability for vectors and/or hosts, thus favoring disease transmissibility(1616 Oliveira IBB, Batista HL, Peluzi JM, et al. Aspectos epidemiológicos e ambientais da leishmaniose visceral em menores de 15 anos, no período de 2007 a 2012, no município de Araguaína, Tocantins, Brasil. Rev Soc Bras Med Trop. 2014; 4(47).,2424 Dias ES, França-Silva JC, Silva JC, et al. Flebotomíneos (Diptera: Psychodidae) de um foco de leishmaniose tegumentar no Estado de Minas Gerais. Rev Soc Bras Med Trop. 2007; 40(1): 49–52.).
A study on the distribution of VL in the city of Belo Horizonte, Minas Gerais, based on a spatial analysis, showed that the variable altitude was associated with an increase in the number of human and canine cases; 71.9% and 67.5%, respectively, were in a range between 780 and 880 meters above sea level. In this region, the highest vector density of the sandfly fauna was identified(2525 Monteiro EM, França JC, Costa RT, et al. Leishmaniose visceral: estudo de flebotomíneos e infecção canina em Montes Claros, Minas Gerais. Rev Soc Bras Med Trop. 2005; 38(2): 147–152.). The municipality of Montes Claros, the highest number of cases (399) recorded in this study has an average altitude of 678 meters above sea level; the other municipalities that registered higher rates, according to data from the Brazilian Institute of Geography and Statistics [Instituto Brasileiro de Geografia e Estatística (IBGE)](1111 Instituto Brasileiro de Geografia e Estatítica [internet homepage]. Latitude média dos municípios brasileiros. Available at: http:www.ibge.gov.br/latitudes. [Accessed on: Jun 2, 2018].
http:www.ibge.gov.br/latitudes...
), were: Janaúba (53) with 510 m, Porteirinha (48) with 556 m, São Francisco (42) with 786 m, and Matias Cardoso (38) with 500 m. Although most of these cities are below the levels observed in the study mentioned above, it is important to highlight that there are other factors involved in the maintenance of the sandfly fauna, such as temperature, humidity, and the presence of organic matter.
This scenario greatly influences the available prophylactic measures, as well as their observance over time. The presence of the sandfly is inherent to the ecosystem of tropical and subtropical regions. The use of residual insecticide is a mandatory resource in maintaining low levels of sandfly population density, and its application is an elementary care before and after the period of greatest rainfall, although the abiotic factor of temperature is more correlated with the VL distribution in the environment. Considering the tropical bands with the highest solar incidence, it would be a difficult factor to control(2525 Monteiro EM, França JC, Costa RT, et al. Leishmaniose visceral: estudo de flebotomíneos e infecção canina em Montes Claros, Minas Gerais. Rev Soc Bras Med Trop. 2005; 38(2): 147–152.).
A statistically significant association was found between annual average temperature and the number of VL cases. In this study, the temperature varied between 25.3°C in the dry season and 26.3°C in the rainy season. Presumably, the temperature directly affects the VL incidence coefficient; therefore, milder temperatures can increase the number of cases of the disease(1616 Oliveira IBB, Batista HL, Peluzi JM, et al. Aspectos epidemiológicos e ambientais da leishmaniose visceral em menores de 15 anos, no período de 2007 a 2012, no município de Araguaína, Tocantins, Brasil. Rev Soc Bras Med Trop. 2014; 4(47).).
Furthermore, other environmental aspects favor the proliferation of the vector and, consequently, the risk of contracting the disease, such as afforestation, accumulation of organic matter, and population displacement, which end up generating anthropic action on the environment(1616 Oliveira IBB, Batista HL, Peluzi JM, et al. Aspectos epidemiológicos e ambientais da leishmaniose visceral em menores de 15 anos, no período de 2007 a 2012, no município de Araguaína, Tocantins, Brasil. Rev Soc Bras Med Trop. 2014; 4(47).). A study carried out in Ethiopia on risk factors for VL discusses the concept of anthropic action by presenting variables with a strong statistical association, such as raising animals around the house, houses with cracks in the walls, larger families, and the number of days spent in the farm field(66 Yared S, Deribe K, Gebreselassie A, et al. Risk factors of visceral leishmaniasis: a case control study in north-western Ethiopia. Parasites & Vectors. 2014; 7: 470.). These aspects have not yet been studied in Brazil.
In this study, the relationship between confirmed VL cases and accessibility/availability to health services was not evaluated. It is worth noting that the municipality of Montes Claros has 133 teams of the family health strategy (100% population coverage), a referral center for infectious parasitic diseases for the city and the entire northern region of Minas Gerais, and a hospital with a referral infectious parasitic disease outpatient clinic(2626 Barbosa MN, Guimarães EAA, Luz ZMP. Avaliação de estratégia de organização de serviços de saúde para prevenção e controle da leishmaniose visceral. Epidemiol Serv Saúde [Internet]. 2016; 25(3): 563–574 [quoted on March 31,2020]. Available at: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S223796222016000300563&lng=en.
http://www.scielo.br/scielo.php?script=s...
). Moreover, the city is a university center in several areas of the health sciences, which, theoretically, combined with the epidemiological surveillance service, would make the organization of the service more sensitive to case detection.
Further works need to be developed in the region to verify other environmental aspects, such as those proposed in the studies selected for discussion. The altitude and the presence/ quantity of organic matter in the peridomicile and the households, for example, would be elements to be included in understanding the dynamics of fluctuation in the number of cases throughout the year.
The results of the present study must be considered in light of some limitations. Secondary data from patient records were used. In similar situations, there is not always uniformity in recording information. Over the years considered in this study, the hospital’s medical file service underwent important structural changes, especially in 2015, with the introduction of the electronic health record. The physical space of the service has also changed. These processes led to data loss, even respecting the 20-year interval for archiving the physical record, as provided by the Brazilian Federal Council of Medicine. Despite thelimitations,theperiodandnumberofcasesevaluatedmakethe study relevant, which should support further research in the area.
REFERENCES
-
1Alvar J, Vélez ID, Bern C, et al. Leishmaniasis worldwide and global estimates of its incidence. PLoS One. 2012; 7(5): e35671. doi:10.1371/journal.pone.0035671.
» https://doi.org/10.1371/journal.pone.0035671 -
2Belo VS, Werneck GL, Barbosa DS, et al. Factors associated with visceral leishmaniasis in the americas: a systematic review and meta-analysis. PLoS Negl Trop Dis. 2013; 25: e2182.
-
3Herwaldt BL. Leishmaniasis. Lancet. 1999; 354: 1191–99.
-
4Alvar J, Yactoyo S, Bern C. Leishmaniasis and poverty. Trends Parasitol. 2006; 22(12): 552–7.
-
5Misha J, Carpenter S, Singh S. Low serum zinc levels in na endemic area of visceral leishmaniasis in Bihar, India. Indian J Med Res. 2010; 793–98.
-
6Yared S, Deribe K, Gebreselassie A, et al. Risk factors of visceral leishmaniasis: a case control study in north-western Ethiopia. Parasites & Vectors. 2014; 7: 470.
-
7Cardim MFM, Rodas LAC, Dibo MR, et al. Introdução e expansão da leishmaniose visceral americana em humanos no Estado de São Paulo, 1999-2011. Rev Saúde Pública. 2013; 47(4): 691–700.
-
8Werneck GL. Expansão geográfica da leishmaniose visceral no Brasil. Cad de Saúde Pública. 2010; 26(4): 644–45.
-
9Gontijo CMF, Melo MN. Leishmaniose visceral no Brasil: quadro atual, desafios e perspectivas. Rev Bras Epidemiol. 2004; 7(3): 338–49.
-
10Silva TAM, Coura-Vital W, Barbosa DS, et al. Spatial and temporal trends of visceral leishmaniasis by mesoregion in a Southeastern state of Brazil, 2002-2013. PLoS Negl Trop Dis. 2017; 11(10): e0005950.
-
11Instituto Brasileiro de Geografia e Estatítica [internet homepage]. Latitude média dos municípios brasileiros. Available at: http:www.ibge.gov.br/latitudes [Accessed on: Jun 2, 2018].
» http:www.ibge.gov.br/latitudes -
12Campos Jr D. Características clínico-epidemiológicas do Calazar na criança. Estudo de 75 casos. J Pediatr, Rio Janeiro. 1995; 71(5): 261–5.
-
13Queiroz MJA, Alves JGB, Correia JB. Leishmaniose visceral: características clínico-epidemiológicas em crianças de área endêmica. J Pediatric. 2004; 80(2).
-
14Rey LC, Martins CV, Ribeiro HB, et al. American visceral leishmaniasis (kala-azar) in hospitalized children from an endemic area. J Pediatr, Rio Janeiro. 2005; 81(1): 73–78.
-
15Oliveira JM, Fernandes AC, Dorval MEC, et al. Mortalidade por leishmaniose visceral: aspectos clínicos e laboratoriais. Rev Soc Bras Med Trop. 2010; 43(2): 188–193.
-
16Oliveira IBB, Batista HL, Peluzi JM, et al. Aspectos epidemiológicos e ambientais da leishmaniose visceral em menores de 15 anos, no período de 2007 a 2012, no município de Araguaína, Tocantins, Brasil. Rev Soc Bras Med Trop. 2014; 4(47).
-
17Xavier-Gomes LM, Costa WB, Prado, PF, Oliveira-Campos M, Leite MTS. Características clínicas e epidemiológicas da leishmaniose visceral em crianças internadas em um hospital universitário de referência no norte de Minas Gerais, Brasil. Rev Bras Epidemiol. 2009; 123(4): 549–55.
-
18Rigo RS, Rigo L, Honer MR. Aspectos clínicos e laboratoriais na leishmaniose visceral americana. J Bras Nefrol. 2009; 31(1): 48–5.
-
19Diro E, Lynen L, Gebregziabiher B, et al. Clinical aspects of paediatric visceral leishmaniasis in North-west Ethiopia. Trop Med Int Health. 2015; 20(1): 8–16.
-
20Souza GAAD, Garcial LM, Rocha SS, Maciel APF. Perfil microbiológico de infecções de pele e partes moles em pacientes internos de um hospital universitário. Rev Epidemiologia Controle de Infecção, Santa Cruz do Sul. 2016; 6(1): 33–36. Available at: https://online.unisc.br/seer/index.php/epidemiologia/article/view/5901/5057 [Accessed on: March 10, 2018].
» https://online.unisc.br/seer/index.php/epidemiologia/article/view/5901/5057 -
21Costa DL. Fatores de prognóstico na leishmaniose visceral: alterações clínicas e laboratoriais associadas à resposta imune, aos distúrbios da coagulação e à morte. [thesis]. Programa de Pós-Graduação da Universidade Federal de Minas Gerais; 2009.
-
22!Brasil. Ministério da Saúde. Secretaria de Vigilância em Saúde. Departamento de Vigilância Epidemiológica. Leishmaniose visceral: recomendações clínicas para redução da letalidade. Série A. Normas e manuais técnicos. Brasília: Ministério da Saúde; 2011.
-
23Aguiar PF, Rodrigues RK. Leishmaniose visceral no Brasil: artigo de revisão. Unimontes Científica. 2017; 19(1): 191–204.
-
24Dias ES, França-Silva JC, Silva JC, et al. Flebotomíneos (Diptera: Psychodidae) de um foco de leishmaniose tegumentar no Estado de Minas Gerais. Rev Soc Bras Med Trop. 2007; 40(1): 49–52.
-
25Monteiro EM, França JC, Costa RT, et al. Leishmaniose visceral: estudo de flebotomíneos e infecção canina em Montes Claros, Minas Gerais. Rev Soc Bras Med Trop. 2005; 38(2): 147–152.
-
26Barbosa MN, Guimarães EAA, Luz ZMP. Avaliação de estratégia de organização de serviços de saúde para prevenção e controle da leishmaniose visceral. Epidemiol Serv Saúde [Internet]. 2016; 25(3): 563–574 [quoted on March 31,2020]. Available at: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S223796222016000300563&lng=en
» http://www.scielo.br/scielo.php?script=sci_arttext&pid=S223796222016000300563&lng=en
Publication Dates
-
Publication in this collection
29 Nov 2021 -
Date of issue
2021
History
-
Received
11 Feb 2020 -
Reviewed
11 Feb 2020 -
Accepted
23 Apr 2020