Pediatric multisystem inflammatory syndrome associated with COVID-19: urgent attention required

SUMMARY

OBJECTIVE:

To identify epidemiological and clinical characteristics of multisystemic inflammatory syndrome associated with coronavirus infection as one of the severe forms of COVID-19 involvement in children and adolescents.

METHODS:

review was based on articles published in 2020 in the PubMed, Medline, Scopus, SciELO and Cochrane databases.

SUMMARY:

Multisystemic inflammatory syndrome is a serious clinical disorder that affects children and adolescents and is associated with the detection of previous exposure to SARS-CoV-2. It is characterized by the installation of a shock picture, with a significant increase in inflammatory markers such as presentations of Kawasaki Disease or shock syndrome related to Kawasaki Disease, or even toxic shock syndrome, with the clinical picture being characterized by fever of difficult control, rash, conjunctivitis, peripheral edema, generalized pain in the extremities and gastrointestinal symptoms.

CONCLUSIONS:

Although the vast majority of children with COVID-19 have mild symptoms, it is necessary to consider that some have a hyperinflammatory response. It is essential that health professionals receive information that can assist in the recognition of this clinical condition, differentiating it from other diagnoses, so that early and appropriate treatment is instituted.

KEYWORDS:
Betacoronavirus; Coronavirus infections; Child; Systemic inflammatory response syndrome; Mucocutaneous lymph node syndrome

INTRODUCTION

The first case of a disease with significant pulmonary impairment caused by a new species of coronavirus (SARS-CoV-2) was reported In China, in December 2019. Due to its high transmissibility, it was quickly declared a pandemic, responsible for more than 19 million confirmed cases and over 728,000 deaths worldwide by August 10^th, 2020¹. Its incidence among children and adolescents can reach 5% of all cases² and mortality is probably low³, but children under one year of age are more likely to have complications of the disease⁴. Obese children are also at risk for serious manifestations⁵, including higher risk of multisystem inflammatory syndrome⁶.

On the other hand, adults with comorbidities and older adults represent the main risk groups; the majority of affected children and adolescents are asymptomatic or have mild airway infection or gastrointestinal symptoms, abdominal pain, vomiting, and diarrhea⁷. However, in view of clinical peculiarities manifested during the evolution of some cases, a group of children who had severe forms of a systemic inflammatory disease could be identified, similar to Kawasaki Disease (KD), which was called multisystemic inflammatory syndrome in children (MIS-C) due to coronavirus infection⁸. KD is a febrile and acute vasculitis that affects young children, primarily not belonging to any specific risk group⁹. Given this syndrome does not yet have adequately defined etiological factors, it becomes even more challenging to understand its overlapping with MIS-C^10,11,12 and its relation with COVID-19, as well as its causes and prognosis, which are still being better studied. Due to its severity, different scientific societies have sought to create criteria for defining cases and treatment, and alert health professionals about the disease^13,14,15,16.

This article seeks to review current knowledge about MIS-C, with the main objective of providing health professionals with the necessary knowledge so that they can make the diagnosis and implement the treatment of this condition in face of the COVID-19 pandemic.

MULTISYSTEMIC INFLAMMATORY SYNDROME IN CHILDREN ASSOCIATED WITH SARS-COV-2 (MIS-C)

Case series

MIS-C refers to a new and serious clinical disorder, first described in April 2020 by Riphagen et al.¹⁷, affecting previously healthy children. They studied eight cases in England, and all patients evolved with circulatory shock refractory to volumetric expansion, requiring use of vasoactive drugs for hemodynamic support; pleural, pericardial effusions and ascites were common findings; ventricular dysfunctions were observed in most patients, and an eight-year-old child developed significant coronary dilation. Most children did not have significant respiratory involvement, although ventilatory support was required in seven (87.5%) of the eight patients. An obese 14-year-old patient died, secondary to extensive cerebral infarction. During hospitalization, everyone tested negative for SARS-CoV-2 in bronchoalveolar lavage or nasopharyngeal aspirates. However, four children had previously known family exposure to COVID-19¹⁷.

After this initial report, others were published. In an American series with 186 children and adolescents under 21 years of age (mean 8.3 years) with MIS-C, 70% of the individuals were positive for SARS-CoV-2 (RT-PCR or antibodies); 40% had symptoms that met the criteria for KD, and 15%, coronary aneurysms. A total of 92% had a significant increase in at least four inflammation markers, and four patients died⁸. In another series, 90% of 21 patients under 18 years of age (mean 7.9 years) with MIS-C treated at a hospital in Paris, presented evidence of infection by SARS-CoV-2; 57% manifested signs and symptoms of shock syndrome associated with KD, and 76%, myocarditis. No patient died, but 24% had coronary dilation and significant increase in inflammation markers¹⁸. Among individuals in whom the presence of previous symptoms related to COVID-19 could be identified, the time interval between the onset of those symptoms and the onset of MIS-C was 25 days in American and 45 days in French series.

As to the features of the case series already described, some conclusions can be drawn: the syndrome has been manifested in children and adolescents about four weeks after contact with SARS-CoV-2. It appears to affect patients aged between four and 14 years old and is associated with detection of previous exposure to SARS-CoV-2. Children present with shock and increase in inflammatory markers, as seen in KD¹⁷, however, the age range in the MIS-C seems to be more advanced (average age of 10 years compared to two years for KD) and respiratory, gastrointestinal and neurological symptoms are more frequent¹⁹. The clinical condition of MIS-C can be characterized by difficulty to control fever, rash, conjunctivitis, peripheral edema, generalized pain in the extremities, and gastrointestinal symptoms¹⁷. Affected children show marked lymphopenia and thrombocytopenia, coagulopathy, increased cardiac enzymes (troponin and cerebral natriuretic peptide, brain natriuretic peptide), hyponatremia, hypoalbuminemia, and increased serum lactate dehydrogenase and ferritin²⁰.

Diagnostic criteria and classification

Recently, the American Centers for Disease Control and Prevention (CDC) proposed a criteria for screening MIS-C, which has been adopted in the United States to notify new cases (Figure 1). They also suggested a classification into three classes (Figure 2), aiming to better identify the most common presentations of the disease⁶. Both definitions were based on a series of 570 patients diagnosed with MIS-C in 40 states in the U.S., between March 2 and July 18, 2020. These patients had median age of eight years, 55.4% were male, and 40% were Hispanic/Latino. Two thirds were previous healthy, and 25.6% were obese. Regarding organ system, 86% had four or more involved. The majority were admitted at intensive care units (63.9%) and had severe complications: cardiac dysfunction (40.6%), shock (35.4%), myocarditis (22.8%), coronary artery dilatation or aneurysm (18.6%), and acute kidney injury (18.4%)⁶. The World Health Organization (WHO)²¹ also proposed a diagnostic criteria for preliminary case definition of MIS-C (Figure 1).

Figure 1
Case definition for multisystemic inflammatory syndrome in children, according to the centers for disease control and the World Health Organization.

MIS-C: multisystemic inflammatory syndrome in children; CDC: centers for disease control; WHO: World Health Organization.

Figure 2
Classification in accordance with the centers for disease control, of 570 patients affected by multisystemic inflammatory syndrome.

These CDC data also show that 99% (n=565) of confirmed MIS-C cases in the United States tested positive for SARS-CoV-2²². Although available data suggest that MIS-C is an uncommon complication of SARS-CoV-2 infection in children and adolescents⁸, current evidence does not support the conclusion that SARS-CoV-2 infection is the cause of MIS-C, with only a temporal relation being established. It should be noted that some cases may have a different underlying cause, such as toxic shock associated with other viruses^23,24. In addition, several cases of MIS-C have been identified at hospitals units, so the results are not generalizable beyond the surveillance population. Seen that, in the absence of a comparison group, caution is warranted when interpreting data to infer risk factors for MIS-C.

Treatment

In the screening of patients with clinical and epidemiological symptoms of COVID-19, initial ambulatory evaluation may be considered. A preliminary laboratory workup is necessary, including complete blood count with differential, liver function tests, urinalysis, electrolytes, erythrocyte sedimentation rate, C-reactive protein, and tests for SARS-CoV-2. Patients who are in good general condition, with stable vital signs, can be followed up on an outpatient basis. Hospital admissions are indicated for patients under investigation for MIS-C with the following symptoms or conditions^13,25:

• Abnormal vital signs (tachycardia, tachypnea);

• Respiratory distress of any severity;

• Neurologic deficits or change in mental status (including subtle manifestations);

• Even mild renal or hepatic injury;

• Severe abdominal pain, uncontrollable vomiting, inability to eat;

• Dehydration;

• KD disease-like features (partial or complete);

• Markedly elevated inflammatory markers;

• Abnormal EKG, BNP, or troponin T;

• Shock;

• Comorbidities (lung diseases, chronic heart diseases, immunodeficiencies, neoplasms, and autoimmune diseases);

• Impossibility of outpatient follow-up.

The need for admission to the intensive care unit will depend on the severity of the signs and symptoms of each patient²⁵. As MIS-C is a post-infectious and immune-mediated disease, the need for isolation must be based on positive RT-PCR or serological tests for SARS-CoV-2²⁵. During hospitalization, patients under investigation for MIS-C must be followed by a multidisciplinary team, which includes pediatric rheumatologist, cardiologist, immunologist, infectious disease specialist, hematologist, and intensive care pediatrician^13,26.

In addition to supportive care, treatment consists primarily of addressing the underlying systemic inflammatory state of the syndrome and its consequent complications. Figure 3 shows the basis of current proposed treatment^13,25,26.

Figure 3
Basis of current proposed treatment for multisystemic inflammatory syndrome in children.

FINAL CONSIDERATIONS

Since the beginning of the COVID-19 pandemic, much has been discussed and reported in the scientific community. Unlike adults, the vast majority of children with COVID-19 have mild symptoms. However, there are reported cases of children who present conditions related to a hyperinflammatory response, similar to that observed in adults. The full spectrum of MIS-C is not yet clear, as well as it is not clear yet if geographic distribution in North America and Europe reflects a true pattern or if the condition has simply not been recognized elsewhere. Therefore, there is an urgent need to collect standardized data describing clinical presentations, severity, outcomes, and epidemiology²¹. Until further robust data on the etiology of MIS-C is available, pediatricians should be alert to the rapid recognition of these cases, enabling appropriate management in emergency services, hospital wards, and intensive care units (ICUs).

Health professionals must receive information that can assist in the recognition of the MIS-C diagnosis. Common clinical features of MIS-C include fever and other clinical signs, such as findings of rash, conjunctivitis, hands and feet edema, red and / or chapped lips, “strawberry” tongue, myocardial dysfunction, cardiac conduction abnormalities, shock, gastrointestinal symptoms, and lymphadenopathy, as well as neurological changes. However, these findings can occur both in other infectious and in non-infectious diseases. Thus, the diagnostic evaluation must include other differential diagnoses more common in pediatric population and relate clinical presentation to the high prevalence of COVID-19 cases with patient’s geographic region. Distinguishing patients with MIS-C from those with acute COVID-19 and other hyperinflammatory conditions is essential for early diagnosis and appropriate treatment.

• Funding: none.

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Publication Dates

• Publication in this collection
  13 Aug 2021
• Date of issue
  2021

History

• Received
  22 Sept 2020
• Accepted
  21 Oct 2020