Department of Anesthesiology, Sina Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Department of Otology/Neurotology, Erfan Hospital, Tehran, Iran.
Eur Arch Otorhinolaryngol. 2019 Aug;276(8):2243-2249. doi: 10.1007/s00405-019-05448-y. Epub 2019 May 4.
To evaluate the efficacy of single low dose (75 mg) preoperative pregabalin in reducing post-operative pain of septorhinoplasty.
A double blind single center Randomized controlled trial based on block randomization. In the pregabalin group (PG) 34 participants received 75 mg pregabalin orally one hour before anesthesia induction while in control group (CG) 34 participants received a placebo. Pain and sedation were repeatedly measured with Visual Analouge Scale (VAS) and Riker Sedation-Agitation Scale (RSAS) respectively, 0.5, 1, 2, 6, 24 hours postextubation. Cumulative doses of fentanyl and ibuprofen received in both groups were compared.
Thirty-two of the participants in PG and 33 of the participants in CG completed the study. The Mean VAS pain score was less in PG versus CG 30 min postoperatively (2.30 ± 1.30 vs. 4.85 ± 1.17), one hour (2.28 ± 0.92 vs. 4.27 ± 0.78), two hours (2.11 ± 0.88 vs. 3.60 ± 0.61) and six hours (1.47 0.62 vs. 2.76 ± 0.91) but not 24-hours postoperatively (0.84 ± 0.62 vs. 1.09 ± 0.92). Participants in the PG were less agitated during early post-extubation period (at 10 min: RSAS 3.93 ± 0.43 vs. 4.42 ± 0.50) and more alert during the first hour post-extubation (at 60 min: RSAS 3.90 ± 0.29 vs. 3.36 ± 0.69). The total dose of rescue fentanyl and ibuprofen was lower in the PG compared to the CG.
A single dose of 75 mg pregabalin is very effective for pain control after septorhinoplasty procedure when administered one hour before anesthesia induction. Side effects are rare and opioid sparing was noted.
Clinical trial number: IRCT2017043033706N1.
评估单剂量(75 毫克)术前普瑞巴林用于减少鼻中隔成形术后疼痛的效果。
这是一项基于区组随机化的双盲、单中心随机对照试验。在普瑞巴林组(PG)中,34 名参与者在麻醉诱导前 1 小时口服 75 毫克普瑞巴林,而在对照组(CG)中,34 名参与者给予安慰剂。分别使用视觉模拟量表(VAS)和 Riker 镇静-躁动量表(RSAS)反复测量疼痛和镇静程度,在拔管后 0.5、1、2、6、24 小时进行测量。比较两组中芬太尼和布洛芬的累积剂量。
PG 组有 32 名参与者和 CG 组有 33 名参与者完成了研究。与 CG 组相比,PG 组术后 30 分钟(2.30±1.30 对 4.85±1.17)、1 小时(2.28±0.92 对 4.27±0.78)、2 小时(2.11±0.88 对 3.60±0.61)和 6 小时(1.47±0.62 对 2.76±0.91)的平均 VAS 疼痛评分较低,但 24 小时后(0.84±0.62 对 1.09±0.92)则没有差异。PG 组在拔管后早期(10 分钟:RSAS 3.93±0.43 对 4.42±0.50)期间更加镇静,在拔管后 1 小时期间更加警觉(60 分钟:RSAS 3.90±0.29 对 3.36±0.69)。PG 组的芬太尼和布洛芬补救剂量低于 CG 组。
在麻醉诱导前 1 小时给予 75 毫克普瑞巴林单次剂量对鼻中隔成形术后疼痛控制非常有效。副作用罕见,且具有阿片类药物节约作用。
临床试验编号:IRCT2017043033706N1。