Hackmann T, Gascoyne R D, Naiman S C, Growe G H, Burchill L D, Jamieson W R, Sheps S B, Schechter M T, Townsend G E
Department of Anesthesia, Vancouver General Hospital, University of British Columbia, Canada.
N Engl J Med. 1989 Nov 23;321(21):1437-43. doi: 10.1056/NEJM198911233212104.
Previous studies have suggested that desmopressin may reduce the bleeding diathesis that often complicates open-heart surgery. To pursue this question further, we performed a double-blind, randomized, placebo-controlled trial to determine whether the previously reported beneficial effect of desmopressin on hemostasis during complex cardiac surgery was applicable to all elective cardiac surgical procedures involving cardiopulmonary bypass. In 150 consecutive patients, most of whom underwent primary coronary-artery bypass grafting, we compared the effects of intravenous desmopressin (0.3 microgram per kilogram of body weight) with those of saline placebo on postoperative blood loss and the need to replace blood products. The median amount of blood lost within the first 24 hours after operation was similar in the desmopressin and placebo groups (865 vs. 738 ml; P = 0.26). The postoperative use of blood replacement products did not differ significantly between the groups (1025 ml [95 percent confidence interval, 300 to 4140 ml] in the desmopressin group and 860 ml [247 to 5346 ml] in the placebo group). Desmopressin is believed to exert its hemostatic effect by releasing von Willebrand factor. The level of ristocetin cofactor, a functional index of the level of von Willebrand factor, was increased approximately twofold from base line in both treatment groups 90 minutes and 24 hours after the administration of medication. Similarly, the levels of von Willebrand factor multimers increased uniformly in both groups. These findings may be consistent with a normal stress response of von Willebrand factor to major surgery and could explain our failure to detect a therapeutic effect of desmopressin. We conclude that the majority of patients who undergo elective cardiac surgery receive no hemostatic benefit from the use of desmopressin.
先前的研究表明,去氨加压素可能会减轻常使心脏直视手术复杂化的出血素质。为了进一步探讨这个问题,我们进行了一项双盲、随机、安慰剂对照试验,以确定先前报道的去氨加压素在复杂心脏手术中对止血的有益作用是否适用于所有涉及体外循环的择期心脏手术。在150例连续患者中,大多数患者接受了初次冠状动脉旁路移植术,我们比较了静脉注射去氨加压素(0.3微克/千克体重)与生理盐水安慰剂对术后失血及血液制品替代需求的影响。去氨加压素组和安慰剂组术后24小时内的中位失血量相似(865 vs. 738毫升;P = 0.26)。两组术后血液制品的使用差异无统计学意义(去氨加压素组为1025毫升[95%置信区间,300至4140毫升],安慰剂组为860毫升[247至5346毫升])。去氨加压素被认为通过释放血管性血友病因子发挥止血作用。血管性血友病因子水平的功能指标瑞斯托霉素辅因子水平在给药后90分钟和24小时,在两个治疗组中均从基线水平升高了约两倍。同样,两组中血管性血友病因子多聚体水平均一致升高。这些发现可能与血管性血友病因子对大手术的正常应激反应一致,并可以解释我们未能检测到去氨加压素的治疗效果。我们得出结论,大多数接受择期心脏手术的患者使用去氨加压素未获得止血益处。