Mentzer Robert M, Oz Mehmet C, Sladen Robert N, Graeve Allen H, Hebeler Robert F, Luber John M, Smedira Nicholas G
Division of Cardiothoracic Surgery, Department of Surgery, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.
J Am Coll Cardiol. 2007 Feb 13;49(6):716-26. doi: 10.1016/j.jacc.2006.10.048. Epub 2006 Dec 11.
The purpose of this study was to determine the role nesiritide might play in patients with left ventricular dysfunction undergoing coronary artery bypass grafting (CABG) using cardiopulmonary bypass (CPB).
Given the hemodynamic, neurohormonal, and renal effects of natriuretic peptides, nesiritide might be useful in the management of patients undergoing cardiac surgery.
This prospective, double-blind, exploratory evaluation randomly assigned patients with ejection fraction </=40% who were undergoing CABG with anticipated use of CPB to receive either nesiritide or placebo, in addition to usual care, for 24 to 96 h after induction of anesthesia. Postoperative renal function, hemodynamics, and drug use (primary end points) were assessed in patients who underwent CABG using CPB; mortality and safety (secondary end points) were assessed in all patients who received the study drug.
Of 303 randomized patients, 279 received the study drug and 272 underwent CABG using CPB. Compared with placebo, nesiritide was associated with a significantly attenuated peak increase in serum creatinine (0.15 +/- 0.29 mg/dl vs. 0.34 +/- 0.48 mg/dl; p < 0.001) and a smaller fall in glomerular filtration rate (-10.8 +/- 19.3 ml/min/1.73 m(2) vs. -17.2 +/- 21.9 ml/min/1.73 m(2); p = 0.001) during hospital stay or by study day 14, and a greater urine output (2,926 +/- 1,179 ml vs. 2,350 +/- 1,066 ml; p < 0.001) during the initial 24 h after surgery. In addition, nesiritide-treated patients had a shorter hospital stay (p = 0.043) and lower 180-day mortality (p = 0.046).
Nesiritide in the setting of CABG with CPB is associated with improved postoperative renal function and possibly enhanced survival. (The NAPA Trial; ; ).
本研究旨在确定奈西立肽在接受体外循环冠状动脉搭桥术(CABG)的左心室功能不全患者中可能发挥的作用。
鉴于利钠肽的血流动力学、神经激素和肾脏效应,奈西立肽可能对心脏手术患者的管理有用。
这项前瞻性、双盲、探索性评估将预期接受体外循环CABG且射血分数≤40%的患者随机分为两组,除常规治疗外,在麻醉诱导后24至96小时接受奈西立肽或安慰剂治疗。对接受体外循环CABG的患者评估术后肾功能、血流动力学和药物使用情况(主要终点);对所有接受研究药物的患者评估死亡率和安全性(次要终点)。
303例随机分组患者中,279例接受了研究药物,272例接受了体外循环CABG。与安慰剂相比,奈西立肽与住院期间或研究第14天时血清肌酐峰值升高显著减轻相关(0.15±0.29mg/dl对0.34±0.48mg/dl;p<0.001),肾小球滤过率下降幅度较小(-10.8±19.3ml/min/1.73m²对-17.2±21.9ml/min/1.73m²;p=0.001),且术后最初24小时尿量更多(2926±1179ml对2350±1066ml;p<0.001)。此外,接受奈西立肽治疗的患者住院时间较短(p=0.043),180天死亡率较低(p=0.046)。
在体外循环CABG中使用奈西立肽与术后肾功能改善及可能提高生存率相关。(NAPA试验;;)