Fulminant Versus Acute Nonfulminant Myocarditis in Patients With Left Ventricular Systolic Dysfunction
Open accessAbstract
Background Fulminant myocarditis (FM) is a form of acute myocarditis characterized by severe left ventricular systolic dysfunction requiring inotropes and/or mechanical circulatory support. A single-center study found that a patient with FM had better outcomes than those with acute nonfulminant myocarditis (NFM) presenting with left ventricular systolic dysfunction, but otherwise hemodynamically stable. This was recently challenged, so disagreement still exists. Objectives This study sought to provide additional evidence on the outcome of FM and to ascertain whether patient stratification based on the main histologic subtypes can provide additional prognostic information. Methods A total of 220 patients (median age 42 years, 46.3% female) with histologically proven acute myocarditis (onset of symptoms <30 days) all presenting with left ventricular systolic dysfunction were included in a retrospective, international registry comprising 16 tertiary hospitals in the United States, Europe, and Japan. The main endpoint was the occurrence of cardiac death or heart transplantation within 60 days from admission and at long-term follow-up. Results Patients with FM (n = 165) had significantly higher rates of cardiac death and heart transplantation compared with those with NFM (n = 55), both at 60 days (28.0% vs. 1.8%, p = 0.0001) and at 7-year follow-up (47.7% vs. 10.4%, p < 0.0001). Using Cox multivariate analysis, the histologic subtype emerged as a further variable affecting the outcome in FM patients, with giant cell myocarditis having a significantly worse prognosis compared with eosinophilic and lymphocytic myocarditis. In a subanalysis including only adults with lymphocytic myocarditis, the main endpoints occurred more frequently in FM compared with in NFM both at 60 days (19.5% vs. 0%, p = 0.005) and at 7-year follow up (41.4% vs. 3.1%, p = 0.0004). Conclusions This international registry confirms that patients with FM have higher rates of cardiac death and heart transplantation both in the short- and long-term compared with patients with NFM. Furthermore, we provide evidence that the histologic subtype of FM carries independent prognostic value, highlighting the need for timely endomyocardial biopsy in this condition.
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Lymphocytic myocarditis is characterized by myocardial infiltrates with T lymphocytes and macrophages.
“Lymphocytic myocarditis is characterized by myocardial infiltrates with T lymphocytes and macrophages.”
From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [198]
The Abstract describes myocarditis as an inflammatory disease of the myocardium with inflammatory infiltrates, and the Methods identify lymphocytic myocarditis as a histologic subtype. Our copy does not specify that those infiltrates contain T lymphocytes and macrophages, so the cellular characterization is unsupported. (LLM, conf=0.84)
Experimental — accuracy not yet measuredVarious conditions including infections, drugs, hypersensitivity, and autoimmune factors may be associated with the onset and progress of eosinophilic myocarditis.
“various conditions including infections, drugs, hypersensitivity, and autoimmune factors may be associated with the onset and progress of this disease.”
From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [198]
The introductory passage (indexed under Abstract; page not provided) lists infection, autoimmune disorders, hypersensitivity reactions, and drugs as potential causes of myocarditis generally. Table 5 and its accompanying text report autoimmune disorders among patients with eosinophilic myocarditis. The copy does not establish that all four factors are associated specifically with the onset or progression of eosinophilic myocarditis. (LLM, conf=0.84)
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- Authors
- Ammirati, E., Veronese, G., Brambatti, M., Merlo, M., Cipriani, M., Potena, L., Sormani, P., Aoki, T., Sugimura, K., Sawamura, A., Okumura, T., Pinney, S., Hong, K., Shah, P., Braun, Ö., Van de Heyning, C. M., Montero, S., Petrella, D., Huang, F., Schmidt, M., Raineri, C., Lala, A., Varrenti, M., Foà, A., Leone, O., Gentile, P., Artico, J., Agostini, V., Patel, R., Garascia, A., Van Craenenbroeck, E. M., Hirose, K., Isotani, A., Murohara, T., Arita, Y., Sionis, A., Fabris, E., Hashem, S., Garcia-Hernando, V., Oliva, F., Greenberg, B., Shimokawa, H., Sinagra, G., Adler, E. D., Frigerio, M., & Camici, P. G.
- Affiliations
- Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda (IT)
- University of California San Diego (US)
- University of Trieste (IT)
- IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola (IT)
- Tohoku University (JP)
- Nagoya University (JP)
- Icahn School of Medicine at Mount Sinai (US)
- Inova Health System (US)
- Universitat Autònoma de Barcelona (ES)
- Sorbonne Université (FR)
- Kokura Memorial Hospital (JP)
- Osaka Hospital (JP)
- Vita-Salute San Raffaele University (IT)
- Corresponding author
- Ammirati, Enrico
- ORCID
- Ammirati, Enrico
- Veronese, Giacomo
- Brambatti, Michela
- Merlo, Marco
- Cipriani, Manlio
- Potena, Luciano
- Aoki, Tatsuo
- Sugimura, Koichiro
- Sawamura, Akinori
- Okumura, Takahiro
- Pinney, Sean
- Hong, Kimberly
- Shah, Palak
- Montero, Santiago
- Huang, Florent
- Schmidt, Matthieu
- Raineri, Claudia
- Lala, Anuradha
- Varrenti, Marisa
- Foà, Alberto
- Leone, Ornella
- Gentile, Piero
- Artico, Jessica
- Agostini, Valentina
- Garascia, Andrea
- Isotani, Akihiro
- Murohara, Toyoaki
- Arita, Yoh
- Fabris, Enrico
- Hashem, Sherin
- Oliva, Fabrizio
- Greenberg, Barry
- Shimokawa, Hiroaki
- Sinagra, Gianfranco
- Adler, Eric D.
- Frigerio, Maria
- Camici, Paolo G.
- Venue
- Journal of the American College of Cardiology
- Publisher
- Elsevier BV
- Published
- 2019-07
- Volume
- 74
- Issue
- 3
- Pages
- 299-311
- ISSN
- 0735-1097 (ISSN-L)
- OpenAlex
- W2959591820
- Cited by
- 279
- References
- 1
- Citations by year
- 2026: 41 · 2025: 52 · 2024: 38 · 2023: 40 · 2022: 49 · 2021: 23 · 2020: 29 · 2019: 7
- FWCI
- 19.52
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of the American College of Cardiology (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- ArTS Archivio della ricerca di Trieste (University of Trieste https://www.units.it/) (submittedVersion)
- BOA (University of Milano-Bicocca) (submittedVersion)
- Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion)
- Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele (submittedVersion)
- Lund University Publications (Lund University) (submittedVersion)
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Viral Infections and Immunology Research
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Takotsubo Cardiomyopathy and Associated Phenomena
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Streptococcal Infections and Treatments
- Keywords
- fulminant myocarditis, left ventricular systolic dysfunction, giant cell myocarditis, eosinophilic myocarditis, lymphocytic myocarditis, histological subtypes, cardiovascular mortality, heart transplantation, prognosis, endomyocardial biopsy, mechanical circulatory support, inotropic agents, long-term outcomes
- MeSH terms
- Acute Disease, Adult, Female, Humans, Male, Middle Aged, Myocarditis, Prognosis, Retrospective Studies, Severity of Illness Index, Ventricular Dysfunction, Left
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