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少尿型急性肾衰竭中的心房利钠因子。阿那利肽急性肾衰竭研究组。

Atrial natriuretic factor in oliguric acute renal failure. Anaritide Acute Renal Failure Study Group.

作者信息

Lewis J, Salem M M, Chertow G M, Weisberg L S, McGrew F, Marbury T C, Allgren R L

机构信息

Division of Nephrology, Vanderbilt University Medical Center, Nashville, TN, USA.

出版信息

Am J Kidney Dis. 2000 Oct;36(4):767-74. doi: 10.1053/ajkd.2000.17659.

Abstract

Atrial natriuretic peptide (ANP), an endogenous hormone synthesized by the cardiac atria, has been shown to improve renal function in multiple animal models of acute renal failure. In a recent multicenter clinical trial of 504 patients with acute tubular necrosis (oliguric and nonoliguric), ANP decreased the need for dialysis only in the oliguric patients. In the present study, 222 patients with oliguric acute renal failure were enrolled into a multicenter, randomized, double-blind, placebo-controlled trial designed to assess prospectively the safety and efficacy of ANP compared with placebo. Subjects were randomized to treatment with a 24-hour infusion of ANP (anaritide, 0.2 microgram/kg/min; synthetic form of human ANP) or placebo. Dialysis and mortality status were followed up for 60 days. The primary efficacy end point was dialysis-free survival through day 21. Dialysis-free survival rates were 21% in the ANP group and 15% in the placebo group (P = 0.22). By day 14 of the study, 64% and 77% of the ANP and placebo groups had undergone dialysis, respectively (P = 0.054), and 9 additional patients (7 patients, ANP group; 2 patients, placebo group) needed dialysis but did not receive it. Although a trend was present, there was no statistically significant beneficial effect of ANP in dialysis-free survival or reduction in dialysis in these subjects with oliguric acute renal failure. Mortality rates through day 60 were 60% versus 56% in the ANP and placebo groups, respectively (P = 0.541). One hundred two of 108 (95%) versus 63 of 114 (55%) patients in the ANP and placebo groups had systolic blood pressures less than 90 mm Hg during the study-drug infusion (P < 0.001). The maximal absolute decrease in systolic blood pressure was significantly greater in the anaritide group than placebo group (33.6 versus 23.9 mm Hg; P < 0.001). This well-characterized population with oliguric acute renal failure had an overall high morbidity and mortality.

摘要

心房利钠肽(ANP)是一种由心脏心房合成的内源性激素,已证实在多种急性肾衰竭动物模型中可改善肾功能。在一项针对504例急性肾小管坏死患者(少尿型和非少尿型)的近期多中心临床试验中,ANP仅在少尿型患者中减少了透析需求。在本研究中,222例少尿型急性肾衰竭患者被纳入一项多中心、随机、双盲、安慰剂对照试验,旨在前瞻性评估ANP与安慰剂相比的安全性和有效性。受试者被随机分为接受24小时输注ANP(阿那立肽,0.2微克/千克/分钟;人ANP的合成形式)治疗或安慰剂治疗。对透析和死亡状况进行了60天的随访。主要疗效终点是至第21天的无透析生存期。ANP组的无透析生存率为21%,安慰剂组为15%(P = 0.22)。在研究的第14天,ANP组和安慰剂组分别有64%和77%的患者接受了透析(P = 0.054),另有9例患者(ANP组7例;安慰剂组2例)需要透析但未接受透析。尽管存在一种趋势,但ANP在这些少尿型急性肾衰竭受试者的无透析生存期或减少透析方面没有统计学上的显著有益效果。至第60天的死亡率在ANP组和安慰剂组分别为60%和56%(P = 0.541)。在研究药物输注期间,ANP组108例患者中有102例(95%),安慰剂组114例患者中有63例(55%)收缩压低于90毫米汞柱(P < 0.001)。阿那立肽组收缩压的最大绝对下降幅度显著大于安慰剂组(33.6对23.9毫米汞柱;P < 0.001)。这群特征明确的少尿型急性肾衰竭患者总体发病率和死亡率较高。

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