Key result
Multisystemic inflammation in fulminant myocarditis shows no significant 30-day mortality benefit overall.
Why the study?
The effect of multisystemic inflammation on clinically diagnosed non-COVID-19-related fulminant myocarditis regarding age and prognosis remains unclear.
Does the presence of multisystemic inflammation (MSI) at admission improve survival in patients with clinically diagnosed non-COVID-19-related fulminant myocarditis?
Cohort (n=736)
Yes
Does the presence of multisystemic inflammation (MSI) at admission improve survival in patients with clinically diagnosed non-COVID-19-related fulminant myocarditis?
Relative Risk: 0.92 (95% CI 0.69–1.23)
Absolute Event Rate: 25.1% vs 32.1%
p-value: p=0.053
In patients with clinically diagnosed non-COVID-19-related fulminant myocarditis, the presence of multisystemic inflammation at admission is associated with a lower 30-day mortality rate, particularly in younger patients (<50 years).
MSI associated with lower 30-day mortality in non-COVID fulminant myocarditis, especially <50 years; leaves open prognostic role pending prospective studies.
Background: In patients with COVID-19-related fulminant myocarditis (COVID-FM), multisystem inflammatory syndrome (MIS) influences clinical outcomes. Multisystemic inflammation (MSI) based on clinical symptoms correlates with the prognosis of non-COVID-FM diagnosed by endomyocardial biopsy. The effect of MSI on clinically diagnosed non-COVID-FM regarding age and prognosis remains unclear. Methods and Results: This retrospective cohort study included 736 patients clinically diagnosed with non-COVID-FM. MSI was defined by clinical symptoms at admission aligned with MSI criteria. We compared all-cause death according to MSI status. Baseline balance was adjusted using inverse probability treatment weighting (IPTW). Overall, 275 (37.4%) non-COVID-FM patients met the MSI status. The MSI (+) group was younger, with fewer male patients and complications such as hypertension, diabetes, chronic kidney disease, and dyslipidaemia. When stratified per age, MSI was highest in patients aged <50 years (48.7%). Overall, the probability of all-cause death was lower in the MSI (+) group (30-day: 25.1% vs. 32.1%, P=0.053, 3-year: 36.1% vs. 42.5%, P=0.004). After IPTW, the MSI (+) group, especially in patients <50 years, was associated with significantly lower risk difference and risk ratio for 30-day all-cause death compared to the MSI (-) group, but not 3-year all-cause death. Conclusions: In patients with non-COVID-FM, MSI often developed at a younger age, and was associated with lower 30-day mortality rate, particularly in patients <50 years.
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Fukushima et al. (2026) conducted a cohort in Non-COVID-19-related fulminant myocarditis (n=736). Multisystemic inflammation (MSI) vs. No multisystemic inflammation was evaluated on 30-day all-cause death (RR 0.92, 95% CI 0.69-1.23, p=0.053). In patients with non-COVID-19-related fulminant myocarditis, multisystemic inflammation was associated with a lower 30-day mortality rate, particularly in patients under 50 years of age.
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