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血红蛋白拉非默(Hemolink)在择期冠状动脉搭桥手术中的II期剂量反应研究。

A phase II dose-response study of hemoglobin raffimer (Hemolink) in elective coronary artery bypass surgery.

作者信息

Cheng D C H, Mazer C D, Martineau R, Ralph-Edwards A, Karski J, Robblee J, Finegan B, Hall R I, Latimer R, Vuylsteke A

机构信息

London Health Sciences Center, University of Western Ontario, London, Canada.

出版信息

J Thorac Cardiovasc Surg. 2004 Jan;127(1):79-86. doi: 10.1016/j.jtcvs.2003.08.024.

Abstract

BACKGROUND

We performed this study to determine the dose-response of hemoglobin raffimer administered in conjunction with intraoperative autologous donation in patients undergoing coronary artery bypass grafting surgery. A secondary objective was to evaluate hemoglobin raffimer for reducing the incidence of allogeneic red blood cell transfusions.

METHODS

This was a phase II, single-blind, multicenter, placebo-controlled, open-label study. Patients undergoing coronary artery bypass grafting with cardiopulmonary bypass and intraoperative autologous donation were randomized to receive a single dose of hemoglobin raffimer or control (10% pentastarch). Patients were sequentially enrolled in a dose block of 250, 500, 750, and 1000 mL.

RESULTS

Sixty patients received hemoglobin raffimer (n = 30) or control (n = 30). Hemoglobin raffimer was well tolerated. Most (98%) adverse events were mild or moderate in severity. There was an expected dose-dependent increase in the incidence of blood pressure increases and jaundice in hemoglobin raffimer-treated patients. In a dose-pooled analysis of hemoglobin raffimer versus control, increased blood pressure (43% vs 17%), nausea (37% vs 33%), and atrial fibrillation (37% vs 17%) were the most frequently reported adverse events. All serious adverse events were considered unrelated or unlikely to be related to study drug. No hemoglobin raffimer-treated patient required an intraoperative allogeneic red blood cell transfusion, compared with 5 (17%) pentastarch-treated patients (P =.052). This advantage of hemoglobin raffimer was maintained at 24 hours after surgery (7% vs 37%; P =.010) and up to 5 days after surgery (10% vs 47%; P =.0034).

CONCLUSIONS

Hemoglobin raffimer was not associated with any serious adverse events in patients undergoing primary coronary artery bypass grafting with cardiopulmonary bypass and intraoperative autologous donation in a dose-response study up to 1000 mL. Hemoglobin raffimer was effective in facilitating decreased exposure or avoidance of allogeneic red blood cell transfusions when used in conjunction with intraoperative autologous donation.

摘要

背景

我们开展这项研究,以确定在接受冠状动脉搭桥手术的患者中,与术中自体献血联合使用时,血红蛋白拉非默的剂量反应。次要目标是评估血红蛋白拉非默降低异体红细胞输血发生率的效果。

方法

这是一项II期、单盲、多中心、安慰剂对照、开放标签研究。接受体外循环和术中自体献血的冠状动脉搭桥手术患者被随机分配接受单剂量的血红蛋白拉非默或对照(10% 羟乙基淀粉)。患者按250、500、750和1000 mL的剂量组依次入组。

结果

60例患者接受了血红蛋白拉非默(n = 30)或对照(n = 30)。血红蛋白拉非默耐受性良好。大多数(98%)不良事件的严重程度为轻度或中度。在接受血红蛋白拉非默治疗的患者中,血压升高和黄疸的发生率出现预期的剂量依赖性增加。在血红蛋白拉非默与对照的剂量汇总分析中,血压升高(43% 对17%)、恶心(37% 对33%)和心房颤动(37% 对17%)是最常报告的不良事件。所有严重不良事件均被认为与研究药物无关或不太可能相关。与5例(17%)接受羟乙基淀粉治疗的患者相比,接受血红蛋白拉非默治疗的患者术中均无需异体红细胞输血(P = 0.052)。血红蛋白拉非默的这一优势在术后24小时(7% 对37%;P = 0.010)以及术后长达5天(10% 对47%;P = 0.0034)时均得以维持。

结论

在一项高达1000 mL的剂量反应研究中,对于接受体外循环和术中自体献血的初次冠状动脉搭桥手术患者,血红蛋白拉非默未出现任何严重不良事件。血红蛋白拉非默与术中自体献血联合使用时,可有效减少异体红细胞输血的暴露或避免异体红细胞输血

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