Effects of an angiotensin-converting-enzyme inhibitor, ramipril, on cardiovascular events in high-risk patients
- PMID: 10639539
- DOI: 10.1056/NEJM200001203420301
Effects of an angiotensin-converting-enzyme inhibitor, ramipril, on cardiovascular events in high-risk patients
Erratum in
- 2000 May 4;342(18):1376
- N Engl J Med 2000 Mar 9;342(10):748
Abstract
Background: Angiotensin-converting-enzyme inhibitors improve the outcome among patients with left ventricular dysfunction, whether or not they have heart failure. We assessed the role of an angiotensin-converting-enzyme inhibitor, ramipril, in patients who were at high risk for cardiovascular events but who did not have left ventricular dysfunction or heart failure.
Methods: A total of 9297 high-risk patients (55 years of age or older) who had evidence of vascular disease or diabetes plus one other cardiovascular risk factor and who were not known to have a low ejection fraction or heart failure were randomly assigned to receive ramipril (10 mg once per day orally) or matching placebo for a mean of five years. The primary outcome was a composite of myocardial infarction, stroke, or death from cardiovascular causes. The trial was a two-by-two factorial study evaluating both ramipril and vitamin E. The effects of vitamin E are reported in a companion paper.
Results: A total of 651 patients who were assigned to receive ramipril (14.0 percent) reached the primary end point, as compared with 826 patients who were assigned to receive placebo (17.8 percent) (relative risk, 0.78; 95 percent confidence interval, 0.70 to 0.86; P<0.001). Treatment with ramipril reduced the rates of death from cardiovascular causes (6.1 percent, as compared with 8.1 percent in the placebo group; relative risk, 0.74; P<0.001), myocardial infarction (9.9 percent vs. 12.3 percent; relative risk, 0.80; P<0.001), stroke (3.4 percent vs. 4.9 percent; relative risk, 0.68; P<0.001), death from any cause (10.4 percent vs. 12.2 percent; relative risk, 0.84; P=0.005), revascularization procedures (16.3 percent vs. 18.8 percent; relative risk, 0.85; P<0.001), cardiac arrest (0.8 percent vs. 1.3 percent; relative risk, 0.62; P=0.02), [corrected] heart failure (9.1 percent vs. 11.6 percent; relative risk, 0.77; P<0.001), and complications related to diabetes (6.4 percent vs. 7.6 percent; relative risk, 0.84; P=0.03).
Conclusions: Ramipril significantly reduces the rates of death, myocardial infarction, and stroke in a broad range of high-risk patients who are not known to have a low ejection fraction or heart failure.
Comment in
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ACE inhibition in cardiovascular disease.N Engl J Med. 2000 Jan 20;342(3):201-2. doi: 10.1056/NEJM200001203420309. N Engl J Med. 2000. PMID: 10639547 No abstract available.
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Effect of ramipril on cardiovascular events in high-risk patients.N Engl J Med. 2000 Jul 6;343(1):64; author reply 66. doi: 10.1056/NEJM200007063430113. N Engl J Med. 2000. PMID: 10896543 No abstract available.
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Effect of ramipril on cardiovascular events in high-risk patients.N Engl J Med. 2000 Jul 6;343(1):64-5; author reply 66. N Engl J Med. 2000. PMID: 10896544 No abstract available.
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Effect of ramipril on cardiovascular events in high-risk patients.N Engl J Med. 2000 Jul 6;343(1):65; author reply 66. N Engl J Med. 2000. PMID: 10896545 No abstract available.
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Myocardial perfusion and ACE inhibition.Rev Cardiovasc Med. 2000 Fall;1(2):75-8. Rev Cardiovasc Med. 2000. PMID: 12506938 No abstract available.
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ACE inhibition in stable coronary artery disease.N Engl J Med. 2005 Mar 3;352(9):937-9; author reply 937-9. doi: 10.1056/NEJM200503033520919. N Engl J Med. 2005. PMID: 15745989 No abstract available.
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