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N-乙酰半胱氨酸与心脏手术期间出血量增加及血液制品使用增多有关。

N-acetylcysteine is associated with increased blood loss and blood product utilization during cardiac surgery.

作者信息

Wijeysundera Duminda N, Karkouti Keyvan, Rao Vivek, Granton John T, Chan Christopher T, Raban Roshan, Carroll Jo, Poonawala Humara, Beattie W Scott

机构信息

Department of Anesthesia, Toronto General Hospital and University of Toronto, Toronto, Ontario, Canada.

出版信息

Crit Care Med. 2009 Jun;37(6):1929-34. doi: 10.1097/CCM.0b013e31819ffed4.

Abstract

OBJECTIVE

When used to prevent perioperative inflammation and ischemia-reperfusion injury, N-acetylcysteine may inadvertently impair hemostasis. We, therefore, performed a post hoc analysis of a recent randomized controlled trial in cardiac surgery to determine whether N-acetylcysteine was associated with increased blood loss and blood product transfusion.

DESIGN

Blinded (patients, caregivers, outcome assessors) placebo-controlled parallel group randomized trial (www.ClinicalTrials.gov ID NCT00188630).

SETTING

Tertiary care hospital in Toronto, Ontario, Canada (September 2003 to October 2005).

PATIENTS

A total of 177 patients with preexisting moderate renal insufficiency (estimated glomerular filtration rate <or=60 mL/min) and undergoing cardiac surgery.

INTERVENTIONS

Eighty-nine patients were randomized to receive intravenous N-acetylcysteine (100 mg/kg bolus; 20 mg.kg.hr infusion until 4 hours after cardiopulmonary bypass), and 88 were randomized to receive placebo.

MEASUREMENTS AND MAIN RESULTS

We used laboratory markers (hemoglobin, platelets, coagulation), chest-tube blood loss, and blood product transfusion to evaluate hemostasis. Compared with placebo, patients who received N-acetylcysteine arm experienced a mean 24-hour chest-tube blood loss that was 261 mL higher (95% confidence interval [CI] 93-488 mL, p = 0.008), and were transfused 1.6 more units of red blood cells (95% CI 0.4-3.1 units, p = 0.02) during hospitalization. The risk of receiving >or=5 units of red blood cells within 24 hours of surgery was significantly higher with N-acetylcysteine (relative risk 1.85, 95% CI 1.06-3.21, p = 0.03; adjusted relative risk 2.09, 95% CI 1.24-3.83, p = 0.005).

CONCLUSIONS

In patients who have preexisting moderate renal insufficiency and are undergoing cardiac surgery, N-acetylcysteine was associated with important effects on blood loss and blood product transfusion. Clinicians and researchers should, therefore, consider the potential for impaired hemostasis when using N-acetylcysteine in the perioperative setting. Further research is needed to elucidate mechanisms by which N-acetylcysteine may impair hemostasis, and the risk-benefit profile of N-acetylcysteine for perioperative organ protection.

摘要

目的

当用于预防围手术期炎症和缺血再灌注损伤时,N - 乙酰半胱氨酸可能会意外损害止血功能。因此,我们对近期一项心脏手术的随机对照试验进行了事后分析,以确定N - 乙酰半胱氨酸是否与失血增加和血液制品输注有关。

设计

双盲(患者、护理人员、结果评估者)安慰剂对照平行组随机试验(www.ClinicalTrials.gov标识符NCT00188630)。

地点

加拿大安大略省多伦多的三级护理医院(2003年9月至2005年10月)。

患者

共有177例存在中度肾功能不全(估计肾小球滤过率≤60 mL/分钟)且接受心脏手术的患者。

干预措施

89例患者随机接受静脉注射N - 乙酰半胱氨酸(100 mg/kg推注;20 mg·kg·小时输注直至体外循环后4小时),88例患者随机接受安慰剂。

测量指标及主要结果

我们使用实验室指标(血红蛋白、血小板、凝血指标)、胸管失血量和血液制品输注情况来评估止血功能。与安慰剂组相比,接受N - 乙酰半胱氨酸组的患者24小时平均胸管失血量多261 mL(95%置信区间[CI] 93 - 488 mL,p = 0.008),住院期间多输注1.6个单位的红细胞(95% CI 0.4 - 3.1单位,p = 0.02)。在手术后24小时内接受≥5个单位红细胞输注的风险,N - 乙酰半胱氨酸组显著更高(相对风险1.85,95% CI 1.06 - 3.21,p = 0.03;调整后相对风险2.09,95% CI 1.24 - 3.83,p = 0.005)。

结论

在存在中度肾功能不全且接受心脏手术的患者中,N - 乙酰半胱氨酸与失血和血液制品输注有重要关联。因此,临床医生和研究人员在围手术期使用N - 乙酰半胱氨酸时应考虑其损害止血功能的可能性。需要进一步研究以阐明N - 乙酰半胱氨酸可能损害止血功能的机制,以及N - 乙酰半胱氨酸用于围手术期器官保护的风险效益情况。

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