A Dose-Dependent Increase in Mortality with Vesnarinone among Patients with Severe Heart Failure

  • Cohn J
  • Goldstein S
  • Greenberg B
  • et al.
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Abstract

Background Vesnarinone, an inotropic drug, was shown in a short-term placebo-controlled trial to improve survival markedly in patients with severe heart failure when given at a dose of 60 mg per day, but there was a trend toward an adverse effect on survival when the dose was 120 mg per day. In a longer-term study, we evaluated the effects of daily doses of 60 mg or 30 mg of vesnarinone, as compared with placebo, on mortality and morbidity. Methods We enrolled 3833 patients who had symptoms of New York Heart Association class III or IV heart failure and a left ventricular ejection fraction of 30 percent or less despite optimal treatment. The mean follow-up was 286 days. Results There were significantly fewer deaths in the placebo group (242 deaths, or 18.9 percent) than in the 60-mg vesnarinone group (292 deaths, or 22.9 percent) and longer survival (P=0.02). The increase in mortality with vesnarinone was attributed to an increase in sudden death, presumed to be due to arrhythmia. The quality of life had ...

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APA

Cohn, J. N., Goldstein, S. O., Greenberg, B. H., Lorell, B. H., Bourge, R. C., Jaski, B. E., … White, B. G. (1998). A Dose-Dependent Increase in Mortality with Vesnarinone among Patients with Severe Heart Failure. New England Journal of Medicine, 339(25), 1810–1816. https://doi.org/10.1056/nejm199812173392503

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