key: cord-0860912-eo2ukw2h
authors: Bajaj, Retesh; Sinclair, Hannah C; Patel, Kush; Low, Ben; Pericao, Ana; Manisty, Charlotte; Guttmann, Oliver; Zemrak, Filip; Miller, Owen; Longhi, Paula; Proudfoot, Alastair; Lams, Boris; Agarwal, Sangita; Marelli-Berg, Federica M; Tiberi, Simon; Cutino-Moguel, Teresa; Carr-White, Gerry; Mohiddin, Saidi A
title: Delayed-onset myocarditis following COVID-19
date: 2021-02-19
journal: Lancet Respir Med
DOI: 10.1016/s2213-2600(21)00085-0
sha: 5160e3a66ecac95e2862dccd6f5211fe64aa0470
doc_id: 860912
cord_uid: eo2ukw2h

nan

A multisystem inflammatory syndrome occurring several weeks after SARS-CoV-2 infection and that can include severe acute heart failure has been reported in children (MIS-C). 1,2 In adults with acute severe heart failure, we have identified a similar syndrome (MIS-A) and describe presenting characteristics, diagnostic features, and early outcomes. Our data also complement reports of MIS-A. 3 The recognition that three patients presenting with fulminant myocarditis also had clinical features of COVID-19, but were negative for SARS-CoV-2 on RT-PCR, was made during recruitment for a study of patients with cardiac injury associated with SARS-CoV-2. To identify implications for patient care, we audited digital records to identify similar presentations to Barts Health National Health Service (NHS) Trust, London, UK, and Guy's and St Thomas' NHS Trust, London, between March 1, and Sept 30, 2020. As a formal service evaluation, as defined by the UK NHS Health Research Authority, this study did not require review by the Research Ethics Committee. All participants had stored serum for antibody testing, and included nine patients (cases 1-9) with acute cardiac decompensation, negative RT-PCR for SARS-CoV-2, markedly increased serum troponin, and substantially raised inflammatory markers. We also studied three controls (cases 10-12) with acute heart failure and SARS-CoV-2 antibodies, but without all the other features.

Patients Patients deteriorated rapidly after admission, including eight (89%) transferring into the tertiary cardiac intensive care unit (ICU) at a mean of 2·9 days after admission (range 1-6 days); one patient (case 5) was transferred to the local ICU 1 day after admission. We suggest that this series describes cardiogenic shock due to a MIS-A after COVID-19. Similarities with patients with MIS-C include frequent gastrointestinal involvement, pulmonary infiltrates, mucocutaneous involvement, and significantly increased inflammatory markers. 1,2 Detectable antibody and RNA absence is consistent with recent recovery following SARS-CoV-2 infection in London before March, 2020. Not all patients had detectable SARS-CoV-2 antibody, another feature that is common to MIS-C, and one with important clinical implications. Case 5* Case 6 Case 7

Case 8* Case 9* Case 10 Case 11* Case 12

Red lines indicate patients (cases 1-9) and blue lines indicate controls (cases 10-12). Panels A, C, and E show biochemical markers. Day 0 represents the timepoint when corticosteroids were administered, or ICU admission for the patients who did not receive steroids. Data from a previous acute COVID-19 admission were available for two cases (cases 2 and 11). Panels B and D show imaging features in patients. Echocardiography was obtained at ICU admission, CMR1 at a mean of 11 days (range 3-24) after ICU admission, and CMR2 103 days (48-155) following CMR1. For echocardiography (B), the median value is used whenever ejection fraction was reported within a range. The highest T1 (left-sided y-axis) and T2 (right-sided y-axis) values reported for each patient are plotted (D). CMR1=acute cardiac MRI. CMR2=convalescent MRI. ICU=intensive care unit. *Patients 5,8, and 9, and control 11 did not receive immunomodulatory therapy. or delayed seroconversion, or early declines in antibody concentrations. Alternatively, initiating events other than SARS-CoV-2 might be responsible. However, the primary purpose of this Correspondence is to highlight a novel clinical presentation of a multisystem disorder that can have life-threatening features, yet might respond adroitly to therapy. Potential factors responsible for the delay in identifying this syndrome in adults or diagnosing individual patients include:

(1) severe cardiac involvement is likely to be rare, (2) negative RT-PCR testing at the time of the cardiac presentation, (3) limited diagnostic role for antibody testing (unavailable early in the pandemic and poor specificity subsequently), (4) attribution of systolic impairment to pre-existing cardiac disease, (5) high frequency of COVID-19-related acute myocardial injury and multiplicity of its causes (up to 40% of hospitalised patients have increased troponin concentrations 4 ), and (6) difficulties obtaining complex or invasive diagnostic investigations in ICU patients during the pandemic. Finally, as MIS-C is a wide-spectrum disorder, including variable severity and involving multiple systems, 2 adult practitioners should also be alert to the likelihood that MIS-A will be heterogenous and might not include cardiac involvement.

We declare no competing interests. RB and HCS contributed equally. This study was not externally funded. An associated study (ROAD-COVID19, A preponderance of male patients and patients from minority ethnic groups in the UK mark another similarity with MIS-C. As is similar in patients with MIS-C, a rapid and profound improvement in cardiac function closely followed initiation of supportive, antimicrobial, or immunomodulatory therapy.

The three controls helped define the key features of cardiogenic shock in patients with MIS-A, and illustrate diagnostic challenges arising from the heterogeneous causes of acutely presenting heart failure. Presenting within weeks of SARS-CoV-2 infection, none showed extreme increases in inflammatory markers, gastrointestinal symptoms, or mucocutaneous features. Only one control (case 12) had greatly increased cardiac troponin concentration, and had lymphocytic myocarditis with parvovirus on biopsy. With increasing population seropositivity, the control findings also emphasise that anti-SARS-CoV-2 IgG will make little contribution to the diagnosis of MIS-A.

Our study's limitations include selection bias. Notably, lethal and milder cases of MIS-A were not represented. All therapeutic interventions were uncontrolled and causality was not inferred. Two patients were negative for SARS-CoV-2 antibodies, consistent with seropositivity prevalence in patients with MIS-C. 1,2 This finding might reflect test sensitivity, failed

Hyperinflammatory shock in children during COVID-19 pandemic

Acute cardiovascular manifestations in 286 children with multisystem inflammatory syndrome associated with COVID-19 infection in Europe

case series of multisystem inflammatory syndrome in adults associated with SARS-CoV-2 infection-United Kingdom and United States

COVID-19 and the cardiovascular system: implications for risk assessment, diagnosis, and treatment options