曲马多-扑热息痛治疗脊柱手术后疼痛--一项随机、双盲、安慰剂对照研究。

IF 1.5 Q4 CLINICAL NEUROLOGY
Scandinavian Journal of Pain Pub Date : 2024-05-06 eCollection Date: 2024-01-01 DOI:10.1515/sjpain-2023-0105
Emma Lappalainen, Jukka Huttunen, Hannu Kokki, Petri Toroi, Merja Kokki
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引用次数: 0

摘要

目标:多模式疼痛治疗是促进术后恢复方案的一个组成部分。在此,我们通过随机、双盲、安慰剂对照试验,评估曲马多-扑热息痛对术后急性疼痛的疗效以及脊柱手术后 12 个月的疼痛预后:我们随机选取了120名接受脊柱手术的患者,让他们在术后5天内接受两种曲马多-扑热息痛片(37.5 毫克/325 毫克,n = 61)或安慰剂(n = 59),每天两次。在医院,多模式疼痛治疗包括右酮洛芬和羟考酮。出院后,患者需服用布洛芬 200 毫克,每天最多 1,200 毫克。在手术前、手术后 1 周和 52 周,通过简短疼痛量表问卷对疼痛、镇痛药使用情况和对镇痛药的满意度进行了随访。主要结果是患者术后一周对止痛药的满意度:结果:术后1周,两组患者对止痛药物的满意度相似,安慰剂组为75%[四分位距间,30%],曲马多-扑热息痛组为70%[40%](P = 0.949):0% = 不满意,100% = 完全满意。1周后,安慰剂组的布洛芬剂量为200毫克[1,000],而曲马多-扑热息痛组为800毫克[1,600](p = 0.016)。对羟考酮的抢救需求没有差异。曲马多-扑热息痛组患者在术后第一周发生的与镇痛药相关的不良事件较多(相对风险=1.8,95%置信区间为1.2-2.6):结论:使用曲马多-扑热息痛进行附加止痛治疗并不能提高患者对背部手术后早期疼痛治疗的满意度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tramadol-paracetamol for postoperative pain after spine surgery - A randomized, double-blind, placebo-controlled study.

Objectives: Multimodal pain management is one component in enhanced recovery after surgery protocol. Here we evaluate the efficacy of tramadol-paracetamol in acute postoperative pain and pain outcome at 12 months after spine surgery in randomized, double-blind, placebo-controlled trial.

Methods: We randomized 120 patients undergoing spine surgery to receive, for add-on pain management, two tramadol-paracetamol 37.5 mg/325 mg (n = 61) or placebo tablets (n = 59) twice a day for 5 postoperative days. In the hospital, multimodal pain management consisted of dexketoprofen and oxycodone. After discharge, patients were prescribed ibuprofen 200 mg, maximum 1,200 mg/day. Pain, analgesic use, and satisfaction with pain medication were followed up with the Brief Pain Inventory questionnaire before surgery and at 1 and 52 weeks after surgery. The primary outcome was patients' satisfaction with pain medication 1 week after surgery.

Results: At 1 week after surgery, patients' satisfaction with pain medication was similarly high in the two groups, 75% [interquartile range, 30%] in the placebo group and 70% [40%] in the tramadol-paracetamol group (p = 0.949) on a scale: 0% =  not satisfied, 100% = totally satisfied. At 1 week, ibuprofen dose was lower in the placebo group 200 mg [1,000] compared to the tramadol-paracetamol group, 800 mg [1,600] (p = 0.016). There was no difference in the need for rescue oxycodone. Patients in the tramadol-paracetamol group had more adverse events associated with analgesics during the first postoperative week (relative risk = 1.8, 95% confidence interval, 1.2-2.6).

Conclusion: Add-on pain treatment with tramadol-paracetamol did not enhance patients' satisfaction with early pain management after back surgery.

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来源期刊
Scandinavian Journal of Pain
Scandinavian Journal of Pain CLINICAL NEUROLOGY-
CiteScore
3.30
自引率
6.20%
发文量
73
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