New England Journal of Medicine · 2000 · 879 citations · 23 references
MedicineInternal MedicineClinical CardiologyCardiovascular Disease
BACKGROUND: Lymphocytic myocarditis causes left ventricular dysfunction that may be persistent or reversible. There are no clinical criteria that predict which patients will recover ventricular function and which cases will progress to dilated cardiomyopathy. We hypothesized that patients with fulminant myocarditis may have a better long-term prognosis than those with acute (nonfulminant) myocarditis. METHODS: We identified 147 patients considered to have myocarditis according to the findings on endomyocardial biopsy and the Dallas histopathological criteria. Fulminant myocarditis was diagnosed on the basis of clinical features at presentation, including the presence of severe hemodynamic compromise, rapid onset of symptoms, and fever. Patients with acute myocarditis did not have these features. The incidence of the end point of this study, death or heart transplantation, was ascertained by contact with the patient or the patient's family or by a search of the National Death Index. The average period of follow-up was 5.6 years. RESULTS: A total of 15 patients met the criteria for fulminant myocarditis, and 132 met the criteria for acute myocarditis. Among the patients with fulminant myocarditis, 93 percent were alive without having received a heart transplant 11 years after biopsy (95 percent confidence interval, 59 to 99 percent), as compared with only 45 percent of those with acute myocarditis (95 percent confidence interval, 30 to 58 percent; P=0.05 by the log-rank test). Fulminant myocarditis was an independent predictor of survival after adjustments were made for age, histopathological findings, and hemodynamic variables. The rate of transplantation-free survival did not differ significantly between the patients considered to have borderline myocarditis and those considered to have active myocarditis according to the Dallas histopathological criteria. CONCLUSIONS: Fulminant myocarditis is a distinct clinical entity with an excellent long-term prognosis. Aggressive hemodynamic support is warranted for patients with this condition.
23
Myocarditis. A histopathologic definition and classification.
H T Aretz, Margaret E. Billingham, W. D. Edwards et al. · PubMed · 1987 · 1.3K citations
Medicine, Cardiology, Pathology +8
A Clinical Trial of Immunosuppressive Therapy for Myocarditis
Jay W. Mason, John B. OʼConnell, Ahvie Herskowitz et al. · New England Journal of Medicine · 1995 · 1.3K citations · Full text
Woodruff Jf · PubMed · 1980 · 804 citations · Full text
Active Myocarditis in the Spectrum of Acute Dilated Cardiomyopathies
GW Dec, Igor F. Palacios, John T. Fallon et al. · New England Journal of Medicine · 1985 · 567 citations