首页> 外文期刊>The New England journal of medicine >Intravenous nesiritide, a natriuretic peptide, in the treatment of decompensated congestive heart failure. Nesiritide Study Group.
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Intravenous nesiritide, a natriuretic peptide, in the treatment of decompensated congestive heart failure. Nesiritide Study Group.

机译:静脉注射奈西立肽,一种利钠肽,用于治疗代偿性充血性心力衰竭。奈西立肽研究组。

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BACKGROUND: Intravenous infusion of nesiritide, a brain (B-type) natriuretic peptide, has beneficial hemodynamic effects in patients with decompensated congestive heart failure. We investigated the clinical use of nesiritide in such patients. METHODS: Patients hospitalized because of symptomatic congestive heart failure were enrolled in either an efficacy trial or a comparative trial. In the efficacy trial, which required the placement of a Swan-Ganz catheter, 127 patients with a pulmonary-capillary wedge pressure of 18 mm Hg or higher and a cardiac index of 2.7 liters per minute per square meter of body-surface area or less were randomly assigned to double-blind treatment with placebo or nesiritide (infused at a rate of 0.015 or 0.030 microg per kilogram of body weight per minute) for six hours. In the comparative trial, which did not require hemodynamic monitoring, 305 patients were randomly assigned to open-label therapy with standard agents or nesiritide for up to seven days. RESULTS: In the efficacy trial, at six hours, nesiritide infusion at rates of 0.015 and 0.030 microg per kilogram per minute decreased pulmonary-capillary wedge pressure by 6.0 and 9.6 mm Hg, respectively (as compared with an increase of 2.0 mm Hg with placebo, P<0.001), resulted in improvements in global clinical status in 60 percent and 67 percent of the patients (as compared with 14 percent of those receiving placebo, P<0.001), reduced dyspnea in 57 percent and 53 percent of the patients (as compared with 12 percent of those receiving placebo, P<0.001), and reduced fatigue in 32 percent and 38 percent of the patients (as compared with 5 percent of those receiving placebo, P<0.001). In the comparative trial, the improvements in global clinical status, dyspnea, and fatigue were sustained with nesiritide therapy for up to seven days and were similar to those observed with standard intravenous therapy for heart failure. The most common side effect was dose-related hypotension, which was usually asymptomatic. CONCLUSIONS: In patients hospitalized with decompensated congestive heart failure, nesiritide improves hemodynamic function and clinical status. Nesiritide is useful for the treatment of decompensated congestive heart failure.
机译:背景:脑内(B型)利尿钠肽奈西立肽的静脉输注对失代偿性充血性心力衰竭患者具有有益的血液动力学作用。我们调查了奈西立肽在此类患者中的临床使用。方法:因症状性充血性心力衰竭住院的患者参加了一项功效试验或一项比较试验。在需要放置Swan-Ganz导管的功效试验中,有127名患者的肺毛细血管楔压为18 mm Hg或更高,心脏指数为每分钟每平方米表面积2.7升每分钟随机分配安慰剂或奈西立肽(以每公斤体重每分钟0.015或0.030微克的速度输注)进行双盲治疗6小时。在一项不需要血液动力学监测的比较试验中,将305名患者随机分配到使用标准药物或奈西立肽的开放标签治疗中,长达7天。结果:在功效试验中,在六个小时时,以每公斤每分钟0.015和0.030微克的速度输注奈西立肽,分别使肺毛细血管楔压降低了6.0和9.6 mm Hg(与之相比,安慰剂增加了2.0 mm Hg ,P <0.001)改善了60%和67%的患者的整体临床状况(相比之下,接受安慰剂的患者为14%,P <0.001),减少了57%和53%的患者的呼吸困难(与接受安慰剂的患者的12%相比,P <0.001),以及32%和38%的患者的疲劳减轻(与接受安慰剂的患者5%相比,P <0.001)。在该比较试验中,奈西立肽治疗可维持长达7天的总体临床状态,呼吸困难和疲劳改善,与标准心力衰竭静脉注射治疗相似。最常见的副作用是与剂量有关的低血压,通常无症状。结论:对于失代偿性充血性心力衰竭住院的患者,奈西立肽可改善血液动力学功能和临床状况。奈西立肽可用于治疗代偿性充血性心力衰竭。

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