Caverni Valentina, Rosa Giovanni, Pinto Giovanni, Tordiglione Paolo, Favaro Roberto
Department of Anesthesiology and Resuscitation, Umberto I Polyclinic, La Sapienza University, Rome, Italy.
J Craniofac Surg. 2005 Jul;16(4):531-6. doi: 10.1097/01.scs.0000159084.60049.e6.
The aim of our study was to compare three different anesthesiological techniques with regard to hemodynamics, recovery, and postoperative morbidity, for craniofacial surgery. One hundred twenty patients with American Society of Anesthesiologists (ASA) classification of I or II patients, 18 to 32 years old, and undergoing maxillary and mandibular osteotomies were randomly assigned to receive anesthesia with propofol-remifentanil (group P), desflurane-remifentanil (group D), or sevoflurane-remifentanil (group S). All patients were given premedication: midazolam 0.03 mg/kg, atropine 0.007 mg/kg, desametasone 0.1 mg/kg, NaCl 0.9% 100 mL + 2 mg/kg ketoprofene + 1.5 mg/kg ranitidine + 1 microg/kg clonidine. Anesthesia was induced by O2/air (FiO2 0.5), remifentanil 0.5 microg/kg/min, propofol 2 mg/kg, rocuronium 0.6 mg/kg. Maintenance group P received O2/air (FiO2 0.5), remifentanil 0.25 to 1.5 microg/kg/min, propofol 6 to 10 mg/kg/h; groups D and S received O2/air (FiO2 0.5), remifentanil 0.25 to 1.5 microg/kg/min, and respectively, sevoflurane or desflurane 0.5 minimum alveolar anesthetic concentration. The dosage of propofol, desflurane, and sevoflurane, obtained with a value of bispectral index (BIS) 40, was kept unchanged throughout the course, and remifentanil was titrated to maintain controlled hypotension: systolic arterial blood pressure 70 to 90 mmHg and mean arterial blood pressure 50 to 65 mmHg. A 24-hour elastomeric infusion system (ketoprofene 320 mg) was started 60 minutes before induction and cloridrat ondansetron 0.1 mg/kg was administered 30 minutes before the end of surgery. Hypotension was successfully obtained in all three groups with a bloodless surgical field, and there was no need for additional use of a potent hypotensive agent. Early and late recovery were faster and more complete in the D group; P < 0.05. Postoperative morbidity (nausea, vomiting, shivering, pain, and edema) was slight and did not significantly differ among the groups.
我们研究的目的是比较三种不同麻醉技术在颅面外科手术中的血流动力学、恢复情况及术后发病率。120例美国麻醉医师协会(ASA)分级为I或II级、年龄在18至32岁、接受上颌骨和下颌骨截骨术的患者被随机分配接受丙泊酚-瑞芬太尼麻醉(P组)、地氟烷-瑞芬太尼麻醉(D组)或七氟烷-瑞芬太尼麻醉(S组)。所有患者均接受术前用药:咪达唑仑0.03mg/kg、阿托品0.007mg/kg、地塞米松0.1mg/kg、0.9%氯化钠100mL + 2mg/kg酮洛芬 + 1.5mg/kg雷尼替丁 + 1μg/kg可乐定。通过O₂/空气(吸入氧浓度0.5)、瑞芬太尼0.5μg/kg/min、丙泊酚2mg/kg、罗库溴铵0.6mg/kg诱导麻醉。P组维持麻醉时接受O₂/空气(吸入氧浓度0.5)、瑞芬太尼0.25至1.5μg/kg/min、丙泊酚6至10mg/kg/h;D组和S组接受O₂/空气(吸入氧浓度0.5)、瑞芬太尼0.25至1.5μg/kg/min,分别给予七氟烷或地氟烷0.5最低肺泡有效浓度。在整个过程中,以脑电双频指数(BIS)值40获得的丙泊酚、地氟烷和七氟烷剂量保持不变,瑞芬太尼进行滴定以维持控制性低血压:收缩压70至90mmHg,平均动脉压50至65mmHg。在诱导前60分钟开始使用24小时弹性输注系统(酮洛芬320mg),在手术结束前30分钟给予昂丹司琼0.1mg/kg。所有三组均成功获得低血压,术野无血,无需额外使用强效降压药。D组的早期和晚期恢复更快且更完全;P < 0.05。术后发病率(恶心、呕吐、寒战、疼痛和水肿)轻微,各组间无显著差异。