Pawlik Michael T, Hansen Ernil, Waldhauser Daniela, Selig Christoph, Kuehnel Thomas S
Departments of *Anesthesiology and †Otorhinolaryngology, Universitätsklinik Regensburg; and ‡Department of Anesthesiology, Universitätsklinik Ulm, Germany.
Anesth Analg. 2005 Nov;101(5):1374-1380. doi: 10.1213/01.ANE.0000180194.30741.40.
Patients with sleep apnea often present with cardiac diseases and breathing difficulties, with a high risk of postoperative respiratory depression. We conducted a randomized, double-blind, prospective study in 30 adult patients with obstructive sleep apnea, undergoing elective ear-nose-throat surgery. The patients were randomly assigned to receive placebo or clonidine (2 microg/kg oral) the night before and the next morning 2 h before surgery. Spo2, heart rate, mean arterial blood pressure, snoring, and oronasal airflow were monitored for 36 h. A standard anesthesia was used consisting of propofol and remifentanil. Anesthetic drug consumption, postoperative analgesics, and pain score were recorded. In the clonidine group, mean arterial blood pressures were significantly lower during induction, operation, and emergence from anesthesia. Both propofol dose required for induction (190 +/- 32.2 mg) and anesthesia (6.3 +/- 1.3 mg . kg(-1).h(-1)) during surgery were significantly reduced in the clonidine group compared with the placebo group (induction 218 +/- 32.4, anesthesia 7.70 +/- 1.5; P < 0.05). Piritramide consumption (7.4 +/- 5.1 versus 14.2 +/- 8.5 mg; P < 0.05) and analgesia scores were significantly reduced in the clonidine group. Apnea and desaturation index were not different between the groups, whereas the minimal postoperative oxygen saturation on the day of surgery was significantly lower in the placebo than in the clonidine group (76.7% +/- 8.0% versus 82.4% +/- 5.8%; P < 0.05). We conclude that oral clonidine premedication stabilizes hemodynamic variables during induction, maintenance, and emergence from anesthesia and reduces the amount of intraoperative anesthetics and postoperative opioids without deterioration of ventilation.
睡眠呼吸暂停患者常伴有心脏疾病和呼吸困难,术后发生呼吸抑制的风险很高。我们对30例接受择期耳鼻喉手术的成年阻塞性睡眠呼吸暂停患者进行了一项随机、双盲、前瞻性研究。患者被随机分配在手术前一晚及手术当天上午手术前2小时接受安慰剂或可乐定(2微克/千克口服)。连续36小时监测血氧饱和度(Spo2)、心率、平均动脉血压、打鼾情况及口鼻气流。采用丙泊酚和瑞芬太尼组成的标准麻醉方案。记录麻醉药物用量、术后镇痛药使用情况及疼痛评分。在可乐定组,诱导期、手术期及麻醉苏醒期的平均动脉血压显著降低。与安慰剂组相比,可乐定组诱导期所需丙泊酚剂量(190±32.2毫克)及手术期间麻醉维持所需丙泊酚剂量(6.3±1.3毫克·千克-1·小时-1)均显著减少(诱导期:218±32.4,麻醉维持期:7.70±1.5;P<0.05)。可乐定组哌替啶用量(7.4±5.1比14.2±8.5毫克;P<0.05)及镇痛评分显著降低。两组间呼吸暂停和去饱和指数无差异,但安慰剂组术后第一天的最低血氧饱和度显著低于可乐定组(76.7%±8.0%比82.4%±5.8%;P<0.05)。我们得出结论,口服可乐定进行术前用药可在麻醉诱导、维持及苏醒期间稳定血流动力学变量,减少术中麻醉药物及术后阿片类药物用量,且不会使通气功能恶化。