The heart failure drug sacubitril/valsartan did not significantly reduce the rate of heart failure or cardiovascular death following a heart attack compared to ramipril, an angiotensin-converting enzyme(ACE)inhibitor proven effective in improving survival following heart attacks. Findings from the PARADISE-MI trial were presented at the American College of Cardiology’s 70thAnnual Scientific Session.
The study is the first large trial to examine whether sacubitril/valsartan can reduce heart failure and associated hospitalizations and deaths in patients post-heart attack who face a high-risk of developing heart failure. Patients taking sacubitril/valsartan were about10% less likely than those taking ramipril experience the study’s primary endpoint—a composite of cardiovascular death, heart failure hospitalization ordevelopment of symptomatic heart failure—falling short of theprespecified threshold ofa15%reductionrequiredto demonstrate statistically significant improvement.However,according to the researchers, the trial foundsacubitril/valsartanwaswell-tolerated, had a favorable safety profile and was associated with a trend toward improvement in the trial’s secondary endpoints,which included cardiovascular death or heart failure hospitalization; heart failure hospitalization or outpatient treatment for heart failure; cardiovascular death, non-fatal heart attack or non-fatal stroke; cardiovascular death and total hospitalizations for heart failure, heart attack or stroke; and death from any cause.
Although we did not significantly reduce our primary endpoint, there were consistent findings that sacubitril/valsartan could represent an incremental improvement over ramipril. The resultsare encouraging, especially when considering recurrent heart failure events and not just the first heart failure events, but the study is not definitive. We did notice several aspects of heart failure development that were lessened with sacubitril/valsartan but to investigate these observations would require further evaluations.”
Marc Pfeffer, MD, PhD, Study Lead Author, Distinguished Dzau Professor of Medicine at Harvard Medical School, and Cardiologist at Brigham and Women’s Hospital
Heart failure is acondition in which the heart becomes too weak or too stiff to pump blood effectively to the rest of the body, causing fatigue, swelling and shortness of breath. While a heart attack does not always lead to heart failure, heart attack survivors are eight times more likely to develop heart failure than those who have not had a heart attack, which has led to an increased emphasis onpreventingheart failure in these patients.
ThePARADISE-MItrial enrolled 5,669 patients in 41 countries who had survived a heart attack less than a week before enrolling in the study.None of the patients had heart failure,but allwere considered to face a high risk of developing it based on a measure of their heart’s pumping abilityorfluid build up in the lungs as well as at least oneof eight additional risk-enhancing factors. Most patients were already taking medications to reduce heart disease risk before their heart attack, including antiplatelet therapy, blood pressure lowering medications and cholesterol lowering medications.
Half of the participants were randomly assigned to receive sacubitril/valsartan and half received ramipril. Most achieved the full dose of their assigned medication and kept taking it throughout the trial, which had a median follow-up period of 23 months.
The rate of the composite primary endpoint was10% lower in patients taking sacubitril/valsartan compared with those taking ramipril. In an exploratory analysis of the total burden of heart failure including recurrent events, there was a 21% reduction observed with sacubitril/valsartan compared to ramipril.
The rate of adverse events was equivalent in both groups, with no significant differences in the rates ofallergicswellingof the airways (angioedema), abnormal potassium levels, renal impairment or liver abnormalities. Patients taking sacubitril/valsartan showed a slightlyhigher rate of hypotension while patients taking ramipril were slightly more likely to report coughing. These findings offerfurther reassurance thatsacubitril/valsartanis safe to use for patients with heart failure, the indication for which it has been approved, researcherssaid.
“We found sacubitril/valsartan was as safe and well-tolerated as one of the best proven ACE inhibitors, even in an acutely ill population,” Pfeffer said.“This trial may not change guidelines, but it should make physicians even more comfortable using sacubitril/valsartan in their patients with heart failure.”