Antecedent hypertension and the effect of captopril on the risk of adverse cardiovascular outcomes after acute myocardial infarction with left ventricular systolic dysfunction: Insights from the Survival and Ventricular Enlargement Trial Journal Article


Authors: Kenchaiah, S.; Davis, B. R.; Braunwald, E.; Rouleau, J. L.; Dagenais, G. R.; Sussex, B.; Steingart, R. M.; Brown, E. J. Jr; Lamas, G. A.; Gordon, D.; Bernstein, V.; Pfeffer, M. A.
Article Title: Antecedent hypertension and the effect of captopril on the risk of adverse cardiovascular outcomes after acute myocardial infarction with left ventricular systolic dysfunction: Insights from the Survival and Ventricular Enlargement Trial
Abstract: Background Hypertension is a well-established risk factor for myocardial infarction (MI), but its prognostic importance in survivors of an acute MI is less clear. Methods We used Cox proportional hazards models to examine the risk of any major cardiovascular event (cardiovascular death, heart failure, recurrent MI, or stroke) - combined or individual components - and all-cause death and evaluate the efficacy of captopril in 906 patients with hypertension and 1325 patients without hypertension in the Survival and Ventricular Enlargement (SAVE) clinical trial. All patients had survived an acute MI with resultant left ventricular (LV) systolic dysfunction, but without overt heart failure, and were randomized within 3 to 16 days after the index MI to receive either captopril or placebo. The mean (± SD) follow-up period was 42 ± 10 months. Results After adjustment for known risk factors, medication use at enrollment, and baseline systolic blood pressure, patients with hypertension had a significant increase in the risk of experiencing a combined cardiovascular event (47.7% vs 31.3%; hazard ratio [HR], 1.49; 95% CI, 1.28-1.74), cardiovascular death (23.4% vs 15.9%; HR, 1.40; 95% CI, 1.12-1.74), heart failure (27.7% vs 15.5%; HR, 1.64; 95% CI, 1.34-2.02), and all-cause death (27.4 vs 19.3%; HR, 1.25; 95% CI, 1.02-1.53), and a similar but statistically non-significant increase in the risk of non-fatal or fatal recurrent MI (17.4% vs 10.9%; HR, 1.27; 95% CI, 0.98-1.65), and non-fatal or fatal stroke (5.0% vs 3.6%; HR, 1.31; 95% CI, 0.81-2.09). Captopril resulted in similar benefits for both patients with and patients without hypertension. The number of combined cardiovascular events prevented for every 100 patients treated with captopril was 7.0 (95% CI, 0.5-13.5) in patients with hypertension and 7.5 (95% CI, 2.6-12.5) in patients without hypertension. Conclusions In survivors of an acute MI with LV systolic dysfunction, antecedent hypertension was associated with a greater risk of subsequent adverse cardiovascular events, not directly explained by elevated blood pressure levels. Captopril use was beneficial in both patients with and patients without hypertenson.
Keywords: adult; controlled study; treatment outcome; aged; middle aged; survival rate; major clinical study; drug efficacy; heart left ventricle failure; hypertension; follow up; proportional hazards models; risk factors; drug effect; risk assessment; survivors; cause of death; cardiovascular disease; cardiovascular risk; heart death; heart failure; heart infarction; stroke; cardiovascular diseases; acute heart infarction; recurrent disease; antihypertensive agent; systolic blood pressure; blood pressure; randomization; analysis of variance; statistical model; captopril; myocardial infarction; ventricular dysfunction, left; angiotensin-converting enzyme inhibitors; humans; human; male; female; priority journal; article
Journal Title: American Heart Journal
Volume: 148
Issue: 2
ISSN: 0002-8703
Publisher: Mosby Elsevier  
Date Published: 2004-08-01
Start Page: 356
End Page: 364
Language: English
DOI: 10.1016/j.ahj.2004.02.011
PROVIDER: scopus
PUBMED: 15309009
DOI/URL:
Notes: Am. Heart J. -- Cited By (since 1996):18 -- Export Date: 16 June 2014 -- CODEN: AHJOA -- Source: Scopus
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  1. Richard M Steingart
    175 Steingart