PREAMI Trial shows that perindopril significantly improves outcome for elderly survivors of myocardial infarction who have preserved left ventricular function
Perindopril significantly reduces the risk
of death, hospitalization for heart failure, and cardiac remodeling
in elderly survivors of myocardial infarction with preserved left
ventricular function, according to a presentation at the annual
meeting of the European Society of Cardiology.
The PREAMI (Perindopril Remodelling in Elderly
with Acute Myocardial Infarction) study is the first to evaluate
an angiotensin-converting enzyme inhibitor in this elderly population,
which is widely represented in clinical practice.
The beneficial effect of perindopril was
due to a highly significant 46-percent reduction in cardiac remodeling
compared with placebo. Previous studies had demonstrated the beneficial
effect of this drug class in younger patients with decreased left
ventricular function.
"The PREAMI findings fill a gap in our
knowledge of the effect of ACE inhibitors in post-myocardial infarction
patients," said Professor R. Ferrari from Santa Anna Hospital,
University of Ferrara, Italy, and lead investigator of the PREAMI
study.
"PREAMI demonstrated that, even in patients
who survived a heart attack and who have normal left ventricular
function more than 10 days after acute phase, progressive cardiac
remodeling silently appears. The good news is that perindopril can
significantly prevent this cardiac decline and could be of benefit
to millions of post-myocardial infarction elderly patients."
The multinational, double-blind, randomized,
parallel, multi-center study compared perindopril (8 mg/day with
placebo in 1,252 elderly (average age, 73 years) post-myocardial
infarction patients with a left ventricular ejection fraction of
40 percent or more.
Patients received recommended usual therapy
(anti-thrombotics, beta-blockers, and angiotensin-converting enzyme
inhibitors). The 1,252 patients with preserved left ventricular
function were randomized 11 +/- 4 days after infarction to the additional
therapy of 4 mg/day perindopril or placebo for the first month of
treatment, followed by 8 mg/day perindopril or placebo for the remaining
11 months of the trial.
Perindopril was associated with a highly
significant relative risk reduction of 38 percent in the combined
primary end point (death, hospitalization for heart failure, cardiac
remodeling). The results showed significantly less left ventricular
remodeling in the perindopril group compared with the placebo group
(28 versus 51 percent).
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