Dierking G, Duedahl T H, Rasmussen M L, Fomsgaard J S, Møiniche S, Rømsing J, Dahl J B
Department of Anaesthesiology, Glostrup University Hospital, Glostrup, Denmark.
Acta Anaesthesiol Scand. 2004 Mar;48(3):322-7. doi: 10.1111/j.0001-5172.2004.0329.x.
Preliminary clinical studies have suggested that gabapentin may produce analgesia and reduce the need for opioids in postoperative patients. The aim of the present study was to investigate the opioid-sparing and analgesic effects of gabapentin administered during the first 24 h after abdominal hysterectomy.
In a randomized, double-blind study, 80 patients received oral gabapentin 1200 mg or placebo 1 h before surgery, followed by oral gabapentin 600 mg or placebo 8, 16 and 24 h after the initial dose. Patients received patient-controlled analgesia with morphine at doses of 2.5 mg with a lock-out time of 10 min for 24 h postoperatively. Pain was assessed on a visual analogue scale (VAS) at rest and during mobilization, nausea, somnolence and dizziness on a four-point verbal scale, and vomiting as present/not present at 2, 4, 22 and 24 h postoperatively.
Thirty-nine patients in the gabapentin group, and 32 patients in the placebo group completed the study. Gabapentin reduced total morphine consumption from median 63 (interquartile range 53-88) mg to 43 (28-60) mg (P < 0.001). We observed a significant inverse association between plasma levels of gabapentin at 2 h postoperatively, and morphine usage from 0 to 2 h, and from 0 to 4 h postoperatively (R2 = 0.30, P = 0.003 and R2 = 0.24 P = 0.008, respectively). No significant differences in pain at rest or during mobilization, or in side-effects, were observed between groups.
Gabapentin in a total dose of 3000 mg, administered before and during the first 24 h after abdominal hysterectomy, reduced morphine consumption with 32%, without significant effects on pain scores. No significant differences in side-effects were observed between study-groups.
初步临床研究表明,加巴喷丁可能产生镇痛作用,并减少术后患者对阿片类药物的需求。本研究的目的是调查腹部子宫切除术后24小时内给予加巴喷丁的阿片类药物节省和镇痛效果。
在一项随机双盲研究中,80例患者在手术前1小时口服加巴喷丁1200毫克或安慰剂,初始剂量后8、16和24小时口服加巴喷丁600毫克或安慰剂。患者术后24小时接受患者自控镇痛,吗啡剂量为2.5毫克,锁定时间为10分钟。在静息和活动时用视觉模拟量表(VAS)评估疼痛,用四点言语量表评估恶心、嗜睡和头晕,并在术后2、4、22和24小时评估呕吐情况(存在/不存在)。
加巴喷丁组39例患者和安慰剂组32例患者完成了研究。加巴喷丁将吗啡总消耗量从中位数63(四分位间距53 - 88)毫克降至43(28 - 60)毫克(P < 0.001)。我们观察到术后2小时加巴喷丁血浆水平与术后0至2小时以及0至4小时的吗啡用量之间存在显著负相关(R2 = 0.30,P = 0.003和R2 = 0.24,P = 0.008)。两组之间在静息或活动时的疼痛或副作用方面未观察到显著差异。
腹部子宫切除术前及术后24小时内给予总量为3000毫克的加巴喷丁,可使吗啡消耗量减少32%,对疼痛评分无显著影响。研究组之间在副作用方面未观察到显著差异。