Feldman A M, Bristow M R, Parmley W W, Carson P E, Pepine C J, Gilbert E M, Strobeck J E, Hendrix G H, Powers E R, Bain R P
Peter Belfer Cardiac Laboratories, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
N Engl J Med. 1993 Jul 15;329(3):149-55. doi: 10.1056/NEJM199307153290301.
Inotropic therapy, other than with digitalis glycosides, has had limited success in patients with chronic congestive heart failure. We investigated whether vesnarinone, a new positive inotropic agent, reduces morbidity and mortality and improves the quality of life of patients with symptomatic heart failure.
Patients receiving concomitant therapy with digoxin (87 percent) and an angiotensin-converting-enzyme inhibitor (90 percent) who had ejection fractions of 30 percent or less were randomly assigned to receive double-blinded therapy with 60 mg of vesnarinone per day, 120 mg of vesnarinone per day, or placebo. Afer 253 patients had been enrolled, randomization to the 120-mg vesnarinone group had to be stopped because of a significant increase in early mortality in this group. Thereafter, patients were randomly assigned only to 60 mg of vesnarinone per day (a total of 239 patients) or placebo (a total of 238 patients).
Significantly fewer patients in the group receiving 60 mg of vesnarinone than in the group receiving placebo (26 vs. 50 patients; P = 0.003) died or had worsening heart failure during the six-month study period. The reduction in risk was 50 percent (95 percent confidence interval, 20 to 69 percent). Similarly, there was a 62 percent reduction (95 percent confidence interval, 28 to 80 percent) in the risk of dying from any cause among the patients receiving vesnarinone. Furthermore, quality of life improved to a greater extent in the vesnarinone group than in the placebo group over 12 weeks (P = 0.008). The principal side effect associated with vesnarinone was reversible neutropenia, which occurred in 2.5 percent of the patients.
Six months of therapy with 60 mg of vesnarinone per day resulted in lower morbidity and mortality and improved the quality of life of patients with congestive heart failure. However, a higher dose of vesnarinone (120 mg per day) increased mortality, suggesting that this drug has a narrow therapeutic range; the long-term effects of vesnarinone are unknown.
除洋地黄糖苷外,强心治疗在慢性充血性心力衰竭患者中的成效有限。我们研究了新型正性肌力药物维司力农是否能降低有症状心力衰竭患者的发病率和死亡率,并改善其生活质量。
正在接受地高辛(87%)和血管紧张素转换酶抑制剂(90%)联合治疗、射血分数在30%及以下的患者被随机分配接受双盲治疗,分别为每日60毫克维司力农、每日120毫克维司力农或安慰剂。在253名患者入组后,由于每日120毫克维司力农组早期死亡率显著增加,该组随机分组不得不停止。此后,患者仅被随机分配至每日60毫克维司力农组(共239名患者)或安慰剂组(共238名患者)。
在为期6个月的研究期间,接受60毫克维司力农治疗的患者中死亡或心力衰竭恶化的人数显著少于接受安慰剂治疗的患者(分别为26例和50例;P = 0.003)。风险降低了50%(95%置信区间为20%至69%)。同样,接受维司力农治疗的患者中任何原因导致的死亡风险降低了62%(95%置信区间为28%至80%)。此外,在12周内,维司力农组的生活质量改善程度大于安慰剂组(P = 0.008)。与维司力农相关的主要副作用是可逆性中性粒细胞减少,发生率为2.5%。
每日60毫克维司力农治疗6个月可降低充血性心力衰竭患者的发病率和死亡率,并改善其生活质量。然而,更高剂量的维司力农(每日120毫克)会增加死亡率,表明该药物的治疗范围较窄;维司力农的长期影响尚不清楚。