Samantaray Aloka, Rao Mangu Hanumantha, Chandra Abha
Department of Anaesthesiology & Critical Care, Sri Venkateswara Institute of Medical Sciences, SVIMS University, Tirupati, Andhra Pradesh, India.
Indian J Anaesth. 2012 Jul;56(4):359-64. doi: 10.4103/0019-5049.100817.
Treatment of acute post-thoracotomy pain is particularly important not only to keep the patient comfortable but also to minimize pulmonary complications.
This study was designed to test the effect of pre-induction administration of clonidine, given as a single intravenous dose, on post-operative pain scores and fentanyl consumption in patients after thoracic surgery.
Tertiary referral centre. Prospective, randomised, double-blind, placebo-controlled trial.
Sixty patients were randomly allocated to receive clonidine (3 mcg/kg) or saline pre-operatively before induction of anaesthesia. The primary endpoint was pain on coughing (visual analogue scale (VAS) 0-100 mm) 120 min after surgery, time to first analgesic injection in the post-anaesthesia care unit (PACU) and 24-h fentanyl consumption.
For between-group comparisons, t-test and U-test were used as appropriate after checking normality of distribution. The incidence of complications between the groups was compared by Fisher's exact test.
The post-operative VAS for the first 120 min and the fentanyl consumption at 24 h was significantly greater in the placebo group compared with the clonidine group (P<0.05). The sedation score was increased in the clonidine group during study drug infusion, but did not differ significantly on admission to the PACU.
A single intravenous dose of clonidine (3 mcg/kg) given before induction of anaesthesia significantly reduced the post-operative VAS score in the initial period and fentanyl consumption during 24 h after thoracic surgery.
开胸术后急性疼痛的治疗尤为重要,这不仅能让患者保持舒适,还能将肺部并发症降至最低。
本研究旨在测试术前单次静脉注射可乐定对胸外科手术后患者术后疼痛评分和芬太尼用量的影响。
三级转诊中心。前瞻性、随机、双盲、安慰剂对照试验。
60例患者在麻醉诱导前随机分为两组,分别接受可乐定(3微克/千克)或生理盐水预处理。主要终点指标为术后120分钟咳嗽时的疼痛程度(视觉模拟评分法(VAS)0 - 100毫米)、麻醉后护理单元(PACU)首次注射镇痛药的时间以及24小时内芬太尼的用量。
在检查分布正态性后,组间比较分别采用t检验和U检验。两组间并发症的发生率采用Fisher精确检验进行比较。
与可乐定组相比,安慰剂组术后前120分钟的VAS评分及24小时芬太尼用量显著更高(P<0.05)。在输注研究药物期间,可乐定组的镇静评分有所升高,但进入PACU时两组无显著差异。
麻醉诱导前单次静脉注射可乐定(3微克/千克)可显著降低胸外科手术后初期的VAS评分及24小时内的芬太尼用量。