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Published on: May 16, 2020
The natural history of acute dilated cardiomyopathy
1Boston, Massachusetts.
Insights
Acute dilated cardiomyopathy (ADCM) treatment has improved significantly, with higher survival rates in contemporary patients compared to earlier eras. Aggressive therapies like ACE-I/ARBs and beta-blockers enhance left ventricular ejection fraction (LVEF) and transplantation-free survival.
Area of Science:
- Cardiology
- Internal Medicine
Background:
- Acute dilated cardiomyopathy (ADCM) is a significant cause for cardiac transplant referral.
- The prognosis and natural history of ADCM on current therapies are not well-established.
Purpose of the Study:
- To evaluate the natural history and prognosis of ADCM in contemporary patients treated with modern pharmacologic therapy.
- To compare current outcomes with historical data from 1975-2000.
Main Methods:
- The Multicenter Intervention in Myocarditis and Acute Cardiomyopathy (IMAC)-2 trial enrolled 373 patients with ADCM (LVEF ≤ 40%, heart failure symptoms < 6 months).
- Historical data was gathered from a MEDLINE search of observational studies published between 1975 and 2000.
Main Results:
- Mean LVEF improved from 24% to 40% with ACE-I/ARB and beta-blocker therapy.
- Transplantation-free survival at 1, 2, and 4 years was 94%, 92%, and 86%, respectively, significantly higher than in the prior era.
- Smaller LV dimension and higher systolic blood pressure predicted LVEF improvement, while black race and higher NYHA class were associated with lower final LVEF.
Conclusions:
- Contemporary diagnosis and aggressive pharmacologic therapy have led to improved prognosis in ADCM.
- Earlier intervention and advanced treatments contribute to better outcomes and higher survival rates.
Introduction:
Acute dilated cardiomyopathy (ADCM) is a frequent cause for referral for cardiac transplantation yet its prognosis and natural history on contemporary therapy remain uncertain.
Methods:
The Multicenter Intervention in Myocarditis and Acute Cardiomyopathy (IMAC)-2 trial enrolled 373 patients at 12 academic medical centers with left ventricular ejection fraction (LVEF) ≤ 40%, heart failure symptoms < 6 months duration, and a diagnostic evaluation consistent with idiopathic cardiomyopathy or acute myocarditis. The natural history of ADCM in an earlier era (1975-2000) was also examined via a MEDLINE search of published observational studies.
Results:
Mean age of the IMAC-2 study cohort was 45 ± 4 years and 38% were female. Mean initial LVEF was 24% ± 8% and increased to 40% ± 12% during treatment with ACE-I/ARB (82%), and a beta-blocker (94%). Transplantation-free survival at 1, 2, and 4 years was 94%, 92%, and 86%, respectively. This survival rate was substantially higher than the prior era. Multivariate predictors of improvement in LVEF were smaller LV dimension and higher systolic blood pressure whereas black race and higher initial New York Heart Association functional class were associated with lower final LVEF. Genotypic variation did not correlate with response to pharmacological therapy.
Conclusion:
Earlier diagnosis and aggressive pharmacologic and device-based therapy of ADCM has led to improved prognosis.
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Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy I: Introduction and Classification
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