Begec Z, Toprak H I, Demirbilek S, Erdil F, Onal D, Ersoy M O
Department of Anaesthesiology and Reanimation, Inonu University, School of Medicine, Malatya, Turkey.
Acta Anaesthesiol Scand. 2008 Feb;52(2):302-6. doi: 10.1111/j.1399-6576.2007.01462.x. Epub 2007 Nov 1.
This study was designed to evaluate the effect of dexmedetomidine on the acute hyperdynamic response, duration of seizure activity and recovery times in patients undergoing electroconvulsive therapy (ECT).
Fourteen patients underwent a total of 84 ECT sessions as a crossover design. Patients were randomly allocated to receive either dexmedetomidine (1 mug/kg IV over a period of 10 min) or saline (control). Anaesthesia was induced with propofol 1 mg/kg, and then succinylcholine 0.5 mg/kg IV was administered. Arterial blood pressure and heart rate (HR) were recorded during the study period.
HR in the dexmedetomidine group was lower than that in the control group at 5 and 10 min after the start of study drug infusion, and at 1, 3 and 10 min after the seizure ended (P<0.05). Peak HR was lower in the dexmedetomidine group compared with that in the control group (P<0.05). The mean arterial pressure (MAP) values in the dexmedetomidine group were lower at 0, 1, 3 and 10 min after the seizure ended compared with the control group (P<0.05). Both motor and electroencephalography (EEG) seizure duration in the control group (35.65 +/- 14.89 and 49.07 +/- 9.94 s, respectively) were similar to that in the dexmedetomidine group (33.30 +/- 12.01 and 45.15 +/- 17.79 s, respectively) (P>0.05). Time to spontaneous breathing, eye opening and obeying commands were not different between the groups.
A dexmedetomidine dose of 1 mug/kg IV administered over 10 min before the induction of anaesthesia with propofol may be useful in preventing the acute hyperdynamic responses to ECT without altering the duration of seizure activity and recovery time.
本研究旨在评估右美托咪定对接受电休克治疗(ECT)患者的急性高动力反应、癫痫发作持续时间及恢复时间的影响。
14例患者采用交叉设计共接受84次ECT治疗。患者被随机分配接受右美托咪定(1μg/kg静脉注射,持续10分钟)或生理盐水(对照组)。用1mg/kg丙泊酚诱导麻醉,然后静脉注射0.5mg/kg琥珀酰胆碱。在研究期间记录动脉血压和心率(HR)。
在输注研究药物开始后5分钟和10分钟以及癫痫发作结束后1分钟、3分钟和10分钟时,右美托咪定组的HR低于对照组(P<0.05)。右美托咪定组的HR峰值低于对照组(P<0.05)。与对照组相比,右美托咪定组在癫痫发作结束后0分钟、1分钟、3分钟和10分钟时的平均动脉压(MAP)值较低(P<0.05)。对照组的运动和脑电图(EEG)癫痫发作持续时间(分别为35.65±14.89秒和49.07±9.94秒)与右美托咪定组(分别为33.30±12.01秒和45.15±17.79秒)相似(P>0.05)。两组间自主呼吸、睁眼和服从指令的时间无差异。
在使用丙泊酚诱导麻醉前10分钟静脉注射1μg/kg右美托咪定,可能有助于预防ECT的急性高动力反应,而不改变癫痫发作持续时间和恢复时间。