Wijeysundera Duminda N, Karkouti Keyvan, Rao Vivek, Granton John T, Chan Christopher T, Raban Roshan, Carroll Jo, Poonawala Humara, Beattie W Scott
Department of Anesthesia, Toronto General Hospital and University of Toronto, Toronto, Ontario, Canada.
Crit Care Med. 2009 Jun;37(6):1929-34. doi: 10.1097/CCM.0b013e31819ffed4.
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.
Blinded (patients, caregivers, outcome assessors) placebo-controlled parallel group randomized trial (www.ClinicalTrials.gov ID NCT00188630).
Tertiary care hospital in Toronto, Ontario, Canada (September 2003 to October 2005).
A total of 177 patients with preexisting moderate renal insufficiency (estimated glomerular filtration rate <or=60 mL/min) and undergoing cardiac surgery.
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.
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).
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.
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。
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)。
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)。
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。
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。
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)。
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。