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重组人心房利钠肽治疗缺血性急性肾衰竭:一项随机安慰剂对照试验

Recombinant human atrial natriuretic peptide in ischemic acute renal failure: a randomized placebo-controlled trial.

作者信息

Swärd Kristina, Valsson Felix, Odencrants Per, Samuelsson Ola, Ricksten Sven-Erik

机构信息

Department of Cardiothoracic Anesthesia and Intensive Care, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

Crit Care Med. 2004 Jun;32(6):1310-5. doi: 10.1097/01.ccm.0000128560.57111.cd.

Abstract

OBJECTIVE

Acute renal failure is associated with significant morbidity and mortality rates. Need for dialysis is an independent risk factor for early mortality after complicated cardiac surgery. Human atrial natriuretic peptide (h-ANP) is a potent endogenous natriuretic and diuretic substance. Exogenous administration of h-ANP increases glomerular filtration rate and renal blood flow in clinical acute renal failure. We have studied the effects of h-ANP on renal outcome in ischemic acute renal failure.

DESIGN

A prospective, double-blind, randomized, placebo-controlled study.

SETTING

Cardiothoracic intensive care units of two tertiary care centers.

PATIENTS

Sixty-one patients with normal preoperative renal function suffering from postcardiac surgical heart failure requiring significant inotropic and vasoactive support.

INTERVENTIONS

The patients were randomized to receive a continuous infusion of either recombinant h-ANP (50 ng.kg(-1).min(-1)) or placebo when serum creatinine increased by >50% from baseline. The treatment with h-ANP/placebo continued until serum creatinine decreased below the trigger value for inclusion or the patients fulfilled predefined criteria for dialysis.

MEASUREMENTS AND MAIN RESULTS

The primary outcome variable was dialysis on or before day 21 after the start of treatment. Secondary renal outcome variables were dialysis-free survival at day 21 and creatinine clearance. Twenty-nine patients were assigned h-ANP and 30 placebo. Six (21%) patients in the h-ANP group compared with 14 (47%) in the placebo group needed dialysis before or at day 21 (hazard ratio, 0.28; 95% confidence interval, 0.10-0.73; p =.009). Eight (28%) patients in the h-ANP group compared with 17 (57%) in the placebo group suffered from the combined end point dialysis or death before or at day 21 (hazard ratio, 0.35; 95% confidence interval, 0.14-0.82; p =.017). h-ANP improved creatinine clearance in contrast to placebo (p =.040).

CONCLUSIONS

Infusion of h-ANP at a rate of 50 ng.kg(-1).min(-1) enhances renal excretory function, decreases the probability of dialysis, and improves dialysis-free survival in early, ischemic acute renal dysfunction after complicated cardiac surgery.

摘要

目的

急性肾衰竭与显著的发病率和死亡率相关。需要透析是心脏直视手术后早期死亡的独立危险因素。人心房利钠肽(h-ANP)是一种有效的内源性利钠和利尿物质。在临床急性肾衰竭中,外源性给予h-ANP可增加肾小球滤过率和肾血流量。我们研究了h-ANP对缺血性急性肾衰竭肾脏结局的影响。

设计

一项前瞻性、双盲、随机、安慰剂对照研究。

地点

两个三级医疗中心的心胸重症监护病房。

患者

61例术前肾功能正常、术后因心力衰竭需要大量使用正性肌力药物和血管活性药物支持的患者。

干预措施

当血清肌酐较基线水平升高>50%时,将患者随机分为两组,分别持续输注重组h-ANP(50 ng·kg⁻¹·min⁻¹)或安慰剂。h-ANP/安慰剂治疗持续至血清肌酐降至纳入触发值以下或患者符合预先定义的透析标准。

测量指标及主要结果

主要结局变量为治疗开始后21天内或第21天进行透析。次要肾脏结局变量为第21天无透析生存和肌酐清除率。29例患者被分配接受h-ANP治疗,30例接受安慰剂治疗。h-ANP组6例(21%)患者与安慰剂组14例(47%)患者在第21天之前或当天需要透析(风险比,0.28;95%置信区间,0.10 - 0.73;p = 0.009)。h-ANP组8例(28%)患者与安慰剂组17例(57%)患者在第21天之前或当天出现透析或死亡的联合终点(风险比,0.35;95%置信区间,0.14 - 0.82;p = 0.017)。与安慰剂相比,h-ANP改善了肌酐清除率(p = 0.040)。

结论

以50 ng·kg⁻¹·min⁻¹的速率输注h-ANP可增强肾脏排泄功能,降低透析概率,并改善心脏直视手术后早期缺血性急性肾功能不全患者的无透析生存率。

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