口服可乐定可减少冠心病非心脏手术患者心肌缺血。

Acta anaesthesiologica Sinica Pub Date : 2002-12-01
Young-Chen Yin, Lok-Hi Chow, Cheng-Ming Tsao, Chi-Chun Chu, Mei-Yung Tsou, Kwok-Hon Chan, Shen-Kou Tsai
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引用次数: 0

摘要

背景:探讨可乐定对有冠心病史的非心脏手术患者减少心肌缺血事件的临床效果。方法:60例ASA III级冠心病患者在一项前瞻性双盲研究中随机分为两组,在到达手术室前90分钟接受可乐定(3微克/公斤)或安慰剂(对照组)。术前(术前深夜起)、术中及术后早期(总监测时间= 24小时)连续心电图监测(霍尔特监护),分析II导联、V2导联、V5导联ST段。记录心肌缺血发作,定义为ST段下降幅度至少1mm,发生在J点后60ms,持续3分钟以上。围手术期血流动力学资料采用重复测量的双因素方差分析。非配对数据的学生t检验用于人口统计学分析。ST段变化采用卡方检验。结果以均数+/- SD表示,P < 0.05为有统计学意义。结果:对照组术前出现缺血9例(30%),术中出现缺血7例(23.3%),术后出现缺血12例(40%)。术后早期心肌缺血发生率最高(P < 0.05)。相反,可乐定组术前出现缺血发作10例(33.3%),术中出现缺血发作3例(10%),术后出现缺血发作5例(16.7%)。可乐定组术中、术后心肌缺血发生率均显著低于安慰剂组。部分患者围手术期平均动脉压明显降低(P < 0.05)。可乐定组术后出现嗜睡的患者较多,占66.7% (P < 0.05),但易被唤醒。在口干、恶心、呕吐方面,可乐定组与对照组差异无统计学意义(P > 0.05)。可乐定组杜冷丁消耗量(43.7 +/- 4.6 mg)显著低于对照组(76.3 +/- 3.7 mg, P < 0.05)。结论:术前口服可乐定可显著降低冠心病非心脏手术患者围手术期心肌缺血的发生率。围手术期心肌缺血发生率较高,值得我们格外注意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral clonidine reduces myocardial ischemia in patients with coronary artery disease undergoing noncardiac surgery.

Background: To access the clinical effect of clonidine on reduction of myocardial ischemia events in patients with history of coronary artery disease undergoing noncardiac surgeries.

Methods: Sixty ASA class III patients with coronary artery disease were allotted at random to two groups in a prospective, double-blind study to receive either clonidine (3 micrograms/kg) or placebo (control group) 90 minutes before arrival at the operating room. Continuous EKG monitoring (Holter monitor) was performed to analyze the ST segment in lead II, V2 and V5 during the preoperative (since late hours the night before operation), intraoperative and early postoperative periods (total monitoring time = 24 hours). The episode of myocardial ischemia defined as the magnitude of ST segment depression of at least 1 mm, occurring 60 ms after the J point and persisting for three minutes or more was recorded. Perioperative hemodynamic data were analyzed with two-way ANOVA with repeated measures. Student's t-test for unpaired data was used for analysis of demographics. Chi-square test was used for ST segment changes. Results are expressed as mean +/- SD and P < 0.05 was considered to be statistically significant.

Results: In the control group, 9 patients (30%) were noted to have episodes of ischemia preoperatively, 7 patients (23.3%) intraoperatively, and 12 patients (40%) postoperatively. The occurrence of myocardial ischemia peaked in the early postoperative period (P < 0.05). On the contrary, in the clonidine group, 10 patients (33.3%) saw ischemic episodes preoperatively, 3 patients (10%) intraoperatively and 5 patients (16.7%) postoperatively. The incidence of myocardial ischemia in clonidine group was significantly lower than that in placebo group in intraoperative and postoperative periods. The mean arterial pressure was significantly lower in some clonidine-treated patients during perioperative periods (P < 0.05). A number of patients in clonidine group suffered from drowsiness (66.7%) after operation (P < 0.05), but they could be easily aroused. In regard to dryness of mouth, nausea and vomiting clonidine and control groups did not differ much (P > 0.05). Demerol consumption was significantly lower in clonidine group (43.7 +/- 4.6 mg) than in control group (76.3 +/- 3.7 mg, P < 0.05).

Conclusions: We conclude that premedication with oral clonidine can significantly reduce the incidence of perioperative myocardial ischemia in patients with CAD undergoing noncardiac surgeries. The incidence of myocardial ischemia in these patients is rather high during perioperative period, which deserves our exceptional caution.

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