Torri G, Casati A, Comotti L, Bignami E, Santorsola R, Scarioni M
Department of Anesthesiology, IRCCS H. San Raffaele, Vita-Salute University of Milan, Milan, Italy.
Minerva Anestesiol. 2002 Jun;68(6):523-7.
The aim of this prospective, randomized study is to compare sevoflurane and isoflurane pharmacokinetics in morbidly obese patients.
With Ethical Committee approval and written informed consent, 14 obese patients (BMI >35 kg/m2), ASA physical status II, undergoing laparoscopic, silicone-adjustable gastric banding were randomly allocated to receive either sevoflurane (n=7) or isoflurane (n=7) as main anesthetic agents. General anesthesia was induced with 1 mg x kg-1 fentanyl, 6 mg x kg-1 sodium thiopental, and 1 mg x kg-1 succinylcholine followed by 0.4 mg kg-1 x h-1 atracurium bromide (doses were referred to ideal body weight). Intermittent positive pressure ventilation (IPPV) was applied using a Servo-900C ventilator with a nonrebreathing circuit and a 15 l x min-1 fresh gas flow (tidal volume: of 10 ml x kg-1; respiratory rate: 12 breaths/min; inspiratory to expiratory time ratio of 1:2) using an oxygen/air mixture (FiO2=50%), while supplemental boluses of thiopental or fentanyl were given as indicated in order to maintain blood pressure and heart rate values within +/-20% from baseline. After adequate placement of tracheal tube and stabilization of the ventilation parameters, 2% sevoflurane or 1.2% isoflurane was given for 30 min via a nonrebreathing circuit. End-tidal samples were collected at 1, 5, 10, 15, 20, 25 and 30 min, and measured using a calibrated infrared gas analyzer. General anesthesia was then maintained with the same inhalational agents, while supplemental fentanyl was given as indicated. After the last skin suture the inhalational agents were suspended, and the end tidal samples were collected at 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, and 5 min. Then the lungs were manually ventilated until extubation.
No differences in age, gender and body mass index were reported between the two groups. Surgical procedure required 91+/-13 in the sevoflurane group and 83+/-32 min in the isoflurane group. The FA/FI ratio was higher in the sevoflurane group from the 5th to the 30th min. Also the washout curve was faster in the sevoflurane group during the observation period; however, the observed differences were statistically significant only 30 and 60 sec after discontinuation of the inhalational agents.
The results of this prospective, randomized study confirmed that sevoflurane provides more rapid wash-in and wash-out curves than isoflurane also in the morbid obese patient.
这项前瞻性随机研究的目的是比较七氟醚和异氟醚在病态肥胖患者中的药代动力学。
经伦理委员会批准并获得书面知情同意后,14例肥胖患者(BMI>35 kg/m2),美国麻醉医师协会(ASA)身体状况分级为II级,接受腹腔镜可调节硅酮胃束带手术,被随机分配接受七氟醚(n = 7)或异氟醚(n = 7)作为主要麻醉剂。全身麻醉诱导采用1 mg/kg芬太尼、6 mg/kg硫喷妥钠和1 mg/kg琥珀酰胆碱,随后给予0.4 mg·kg-1·h-1阿曲库铵(剂量参照理想体重)。使用Servo - 900C呼吸机通过无重复吸入回路和15 l/min新鲜气流进行间歇正压通气(IPPV)(潮气量:10 ml/kg;呼吸频率:12次/分钟;吸呼比为1:2),使用氧气/空气混合气体(FiO2 = 50%),同时根据需要给予硫喷妥钠或芬太尼补充推注,以维持血压和心率值在基线值的±20%范围内。在气管导管妥善放置且通气参数稳定后,通过无重复吸入回路给予2%七氟醚或1.2%异氟醚30分钟。在第1、5、10、15、20、25和30分钟采集呼气末样本,并用校准的红外气体分析仪进行测量。然后用相同的吸入麻醉剂维持全身麻醉,同时根据需要给予芬太尼补充。最后一针皮肤缝合后停止吸入麻醉剂,在0.5、1、1.5、2、2.5、3、3.5、4、4.5和5分钟采集呼气末样本。然后手动通气直至拔管。
两组在年龄、性别和体重指数方面无差异。七氟醚组手术时间为91±13分钟,异氟醚组为83±32分钟。从第5分钟至第30分钟,七氟醚组的FA/FI比值更高。在观察期内,七氟醚组的洗出曲线也更快;然而,仅在停止吸入麻醉剂后30秒和60秒观察到的差异具有统计学意义。
这项前瞻性随机研究的结果证实,在病态肥胖患者中,七氟醚比异氟醚具有更快的吸入和洗出曲线。