Agarwal Sandhya, Aggarwal Ritu, Gupta Praveen
Department of Anesthesiology and Critical Care, Deen Dayal Upadhyay Hospital, New Delhi, India.
Department of Anesthesiology, Medanta the Medicity Hospital, Gurgaon, Haryana, India.
J Anaesthesiol Clin Pharmacol. 2014 Jan;30(1):36-40. doi: 10.4103/0970-9185.125701.
We compared the effects of adding dexmedetomidine to a 30 ml solution of 0.325% bupivacaine in supraclavicular brachial plexus block. Onset and duration of sensory and motor block along with the duration of analgesia were the primary endpoints.
Fifty patients posted for upper limb surgeries were enrolled for a prospective, randomized, double-blind, placebo-controlled trial. Patients were divided into two groups, the control group S and the study group SD. In group S (n = 25), 30 ml of 0.325% bupivacaine + 1 ml normal saline; and in group SD (n = 25), 30 ml of 0.325% bupivacaine + 1 ml (100 μg) dexmedetomidine were given for supraclavicular brachial plexus block using the peripheral nerve stimulator. Onset and duration of sensory and motor blocks were assessed along with the duration of analgesia, sedation, and adverse effects, if any. Hemodynamic parameters, like heart rate (HR), systolic arterial blood pressure (SBP), and diastolic arterial blood pressure (DBP) were also monitored.
Demographic data and surgical characteristics were comparable in both the groups. The onset times for sensory and motor blocks were significantly shorter in SD than S group (P < 0.001), while the duration of blocks was significantly longer (P < 0.001) in SD group. Except for the initial recordings (at 0, 5, 10, and 15 min), heart rate levels in group SD were significantly lower (P < 0.001). SBP and DBP levels in SD group at 15, 30, 45, 60, 90 and 120 min were significantly lower than in S group (P < 0.001). In fact, when the percentage changes in HR/SBP/DBP were compared from 0-5/0-10/0-15/0-30/0-45/0-60/0-90/0-120 min in SD with S group, they came out to be highly significant (P < 0.001) in group SD. The duration of analgesia (DOA) was significantly longer in SD group than S group (P < 0.001). Except that, bradycardia was observed in one patient in the group SD, no other adverse effects were observed in either of the groups.
Dexmedetomidine added as an adjuvant to bupivacaine for supraclavicular brachial plexus block significantly shortens the onset time and prolongs the duration of sensory and motor blocks and duration of analgesia. Patients in group SD were adequately sedated (modified Ramsay Sedation Score, RSS = 2/6 or 3/6) with no adverse effects except bradycardia in one patient of group SD.
我们比较了在0.325%布比卡因30毫升溶液中添加右美托咪定用于锁骨上臂丛神经阻滞的效果。感觉和运动阻滞的起效时间、持续时间以及镇痛持续时间是主要终点。
五十例拟行上肢手术的患者纳入一项前瞻性、随机、双盲、安慰剂对照试验。患者分为两组,对照组S和研究组SD。在S组(n = 25),给予30毫升0.325%布比卡因 + 1毫升生理盐水;在SD组(n = 25),给予30毫升0.325%布比卡因 + 1毫升(100微克)右美托咪定,使用外周神经刺激器进行锁骨上臂丛神经阻滞。评估感觉和运动阻滞的起效时间、持续时间以及镇痛、镇静持续时间和不良反应(如有)。还监测了血流动力学参数,如心率(HR)、收缩动脉血压(SBP)和舒张动脉血压(DBP)。
两组的人口统计学数据和手术特征具有可比性。SD组感觉和运动阻滞的起效时间明显短于S组(P < 0.001),而SD组阻滞持续时间明显更长(P < 0.001)。除初始记录(0、5、10和15分钟时)外,SD组心率水平明显更低(P < 0.001)。SD组在15、30、45、60、90和120分钟时的SBP和DBP水平明显低于S组(P < 0.001)。实际上,当比较SD组与S组在0 - 5/0 - 10/0 - 15/0 - 30/0 - 45/0 - 60/0 - 90/0 - 120分钟时HR/SBP/DBP的百分比变化时,SD组差异具有高度显著性(P < 0.001)。SD组的镇痛持续时间(DOA)明显长于S组(P < 0.001)。除此之外,SD组有一名患者出现心动过缓,两组均未观察到其他不良反应。
在布比卡因中添加右美托咪定作为锁骨上臂丛神经阻滞的辅助药物可显著缩短起效时间,延长感觉和运动阻滞持续时间以及镇痛持续时间。SD组患者镇静充分(改良拉姆齐镇静评分,RSS = 2/6或3/6),除SD组有一名患者出现心动过缓外无不良反应。