Key result
Combined temporary mechanical circulatory support and immunoregulatory therapy was associated with significantly lower in-hospital mortality (4.2% vs 52.4%; adjusted OR 0.11) in fulminant myocarditis.
Why the study?
Fulminant myocarditis carries high mortality and Chinese scientific statements proposed extensive use of temporary mechanical circulatory support combined with immunoregulatory therapy, but formal trials are lacking.
Does temporary mechanical circulatory support combined with immunoregulatory therapy reduce in-hospital mortality in patients with fulminant myocarditis?
Cohort (n=138)
Yes
Does temporary mechanical circulatory support combined with immunoregulatory therapy reduce in-hospital mortality in patients with fulminant myocarditis?
Odds Ratio: 0.11 (95% CI 0.09–0.46)
Absolute Event Rate: 4.2% vs 52.4%
p-value: p=0.001
The combined use of temporary mechanical circulatory support and immunomodulation therapy is associated with a significant reduction in in-hospital mortality among patients with fulminant myocarditis.
Supports combined t-MCS and immunoregulatory therapy in fulminant myocarditis; hypothesis-generating pending randomized confirmation.
Patients presenting with acute myocarditis and sudden hemodynamic instability (termed fulminant myocarditis [FM]) still have a high mortality and need for heart transplantation, up to 28% at 60 days. 1 , 2 , 3 Recent scientific statements and expert opinion consensus suggests early use of temporary mechanical circulatory supports (t-MCS). 3 , 4 Specifically, Chinese scientific statement proposed an extensive use of t-MCS combined with immunoregulatory therapy (IT), 4 although formal trials are lacking. We present a multicenter, retrospective study to compare the outcome of patients who were treated with t-MCS and IT vs. patients who didn’t receive these treatments. We included patients with the diagnosis of FM based on the presence of viral prodromal signs/symptoms followed by acute onset of severe heart failure (HF) without other relevant differential diagnosis or pre-existing cardiac disorders. Patients who received both t-MCS and IT during hospitalization were classified as t-MCS+IT group. T-MCS used were intra-aortic balloon pulsation (IABP) (median duration 7 days, first to third quartile [Q1–Q3, 4–8]) or venous-arterial extracorporeal membrane oxygenation (VA-ECMO) (median duration 5 days [Q1–Q3, 5–7], or both. IT included methylprednisolone (200–400 mg) or dexamethasone (20–40 mg), qd for 3–5 days of intravenous (IV) and then gradually down titrated and weaned in 7–10 days, and IV immunoglobulin (10–20 g qd for the 3–5 days and then 10 g for another 3–5 days). Patients who didn’t receive both t-MCS and IT were classified as non-t-MCS+IT 3 group. Statistical differences were analyzed using the Mann–Whitney U test for continuous variables. Categorical variables were compared using Fisher’s exact test or χ 2 test.
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Zhou et al. (2021) conducted a cohort in Fulminant myocarditis (n=138). Temporary mechanical circulatory support (t-MCS) and immunoregulatory therapy (IT) vs. Non-t-MCS+IT (did not receive both treatments) was evaluated on In-hospital mortality (adjusted OR 0.11, 95% CI 0.09-0.46, p=0.001). Combined temporary mechanical circulatory support and immunoregulatory therapy was associated with significantly lower in-hospital mortality (4.2% vs 52.4%; adjusted OR 0.11) in fulminant myocarditis.
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