Hyperinflammatory syndrome in children during the coronavirus disease 2019 pandemic in sub-Himalayan region

Abstract

To the editor, Hyperinflammatory syndromes are life-threatening disorders caused by overwhelming host immune responses often resulting from defects in negative feedback mechanisms. These include Kawasaki disease (KD) and other serious pediatric inflammatory conditions, such as toxic shock syndrome (TSS) and macrophage activation syndrome (MAS). During the coronavirus disease 2019 (COVID-19) pandemic, a national alert was issued in the United Kingdom and North America in mid-April 2020, as they reported a cluster of children with a multisystem inflammatory condition with multiorgan involvement who required intensive unit care.1,2) They presented with some features similar to KD, TSS, and MAS, with laboratory profiles revealing marked hyperinflammation. The World Health Organisation is calling it multisystem inflammatory syndrome.3) However, the association between hyperinflammatory syndrome in children and COVID-19 is still not known. We are describing a case series of 10 patients with hyperinflammatory syndrome, highlighting clinical presentations, laboratory profiles, management, and outcome during this COVID-19 pandemic, to raise awareness among pediatricians. This retrospective study was conducted in a tertiary care centre in North India from April through May 2020. The Institutional ethical committee approved the study. Patients of age between 1 month to <19 years with clinical features of persistent fever, inflammation, hypotension, and multiple organ failure, who were admitted in pediatric intensive care unit were included. We collected demographic data, past medical history, physical examination findings, chest x-ray, echocardiography (if done), and laboratory findings, including complete blood count with differential count, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), coagulation profile, ferritin, liver enzymes, lactate dehydrogenase, triglyceride, and D-dimer, performed at presentation and throughout the hospital stay. All patients had reverse-transcriptase polymerase chain reaction (RT-PCR) tests for COVID 19. Ten patients with features of hyperinflammation and multiorgan failure were admitted during the study period, whereas only 2 such patients were reported in last 6 months before COVID-19 pandemic in our centre. All these patients were of Indian origin. The median age was 13.5 years (9–17 years). Seven out of 10 patients (70%) were male. These patients were critically sick with muco cutaneous manifestations, such as nonpurulent conjunctivitis, cracked lips, edema of hands or feet, and skin rash. All of these patients were partially fulfilling the diagnostic criteria for KD by 2017 American Heart Association guidelines. They had hypotension at presentation, and their clinical features were consistent with KD shock syndrome.4) We also considered MAS, which is a potentially life-threatening complication of KD. We suspected MAS in 9 out of 10 patients (90%) on the basis of clinical criteria.5) In clinical profile, all patients presented with multiorgan failure with shock (Table 1). Two of our patients presented with decreased limb movement with absent deep tendon reflexes and axonal neuropathy on a nerve conduction study. Only 2 out of 10 patients (20%) had gastrointestinal manifestations in the form of loose stools and vomiting. Blood test results showed raised inflammatory markers; raised CRP in 10 (100%), raised ESR in 9 (90%), hyperferritinemia in 9 (90%), and raised D-dimer in 2 patients (20%) (Table 1). All of 10 patients (100%) had thrombocytopenia, and 5 patients (50%) had lymphopenia. Coagulopathy was found in 7 patients (70%). Chest x-ray was done in 9 patients, and was abnormal in 5 (50%); bilateral infiltrates in 4 and pleural effusion in 1. Echocardiography showed aortic valve regurgitation in 1 patient (10%). Reverse transcription-polymerase chain reaction (RTPCR) test for COVID-19 was done in all patients, and turned out to be negative. All of the patients required some levels of respiratory support, and 8 (80%) required mechanical ventilation. All patients were treated with broad-spectrum antibiotics. As all of the patients presented with shock, they were managed with inotropes/vasopressors. Six patients (60%) received intravenous methylprednisolone, and 3 (30%) received intravenous immunoglobulin (IVIG) along with corticosteroids. Seven patients (70%) died, and 3 (30%) were discharged. KD is a pediatric disease showing acute systemic vasculitis, and is a major cause of acquired heart disease in children; approximately 25% of KD patients may develop chronic coronary artery lesions, if not treated early in the course of the disease.6) The clinical manifestations of KD are various, and patients may not completely fulfil the diagnostic criteria of KD, called “incomplete or atypical” KD.7) Despite uncommon, KD patients may also present with hypotension; a severe form of KD known as KD shock syndrome (KDSS), which is associated with markedly raised inflammatory markers and considerable risk of cardiac involvement. These patients are pretty resistant to IVIG therapy, so often require additional anti-inflammatory treatments.4) The