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青少年后路脊柱融合术患者的多模式疼痛控制:一项双盲随机对照试验,以验证加巴喷丁对术后疼痛控制、阿片类药物使用及患者满意度的效果。

Multimodal pain control in adolescent posterior spinal fusion patients: a double-blind, randomized controlled trial to validate the effect of gabapentin on postoperative pain control, opioid use, and patient satisfaction.

作者信息

Anderson Devon E, Duletzke Nicholas T, Pedigo Elizabeth B, Halsey Matthew F

机构信息

Department of Orthopaedics and Rehabilitation, Oregon Health and Science University, 3181 SW Sam Jackson Park Road, OP31, Portland, OR, 97239-3098, USA.

Department of Orthopaedics and Rehabilitation, University of Rochester, 601 Elmwood Ave, Box 665, Rochester, NY, 14642, USA.

出版信息

Spine Deform. 2020 Apr;8(2):177-185. doi: 10.1007/s43390-020-00038-z. Epub 2020 Feb 5.

Abstract

STUDY DESIGN

Prospective double-blind, randomized controlled trial.

OBJECTIVES

The objective of this study was to validate the efficacy of gabapentin as part of a multimodal pain regimen in a double-blind, randomized controlled trial for patients aged 10-19 years with idiopathic scoliosis undergoing posterior spinal fusion. Perioperative pain management represents a challenge for patients undergoing surgical correction of adolescent spinal deformity. Gabapentin has been shown to decrease postoperative pain and opioid use after spine surgery, but it has not yet been investigated as part of a multimodal pain regimen intended to decrease the perioperative use of opioids.

METHODS

Fifty patients were randomized to receive gabapentin or placebo pre- and postoperatively in addition to a standardized medication regime including scheduled ketorolac and as-needed acetaminophen, hydromorphone, and oxycodone. Patients were monitored in the pre-, peri-, and postoperative periods for pain levels, medication dosing, side effects, adverse events, hospitalization length of stay, and parent satisfaction.

RESULTS

There were statistically significant decreases in early postoperative pain scores and opioid use as well as total postoperative opioid use for the treatment group relative to controls. There were no statistically significant differences in adverse events, medication side effects, or hospitalization length. Parents of patients in both groups were very satisfied with the pain control provided to their children.

CONCLUSIONS

This randomized controlled trial demonstrates that pre- and postoperative administration of gabapentin as part of a multimodal pain management protocol significantly decreases both opioid use and visual analog pain scales in the first two postoperative days after posterior spinal fusion for adolescent idiopathic scoliosis. Gabapentin should be considered as a standard medication for perioperative pain control in this patient population.

LEVEL OF EVIDENCE

Level I.

摘要

研究设计

前瞻性双盲随机对照试验。

目的

本研究的目的是在一项双盲随机对照试验中,验证加巴喷丁作为多模式疼痛治疗方案的一部分,对10至19岁特发性脊柱侧凸患者行后路脊柱融合术的疗效。围手术期疼痛管理对接受青少年脊柱畸形手术矫正的患者来说是一项挑战。加巴喷丁已被证明可减少脊柱手术后的术后疼痛和阿片类药物使用,但尚未作为旨在减少围手术期阿片类药物使用的多模式疼痛治疗方案的一部分进行研究。

方法

50例患者被随机分为两组,除了标准化药物治疗方案(包括定期使用酮咯酸以及按需使用对乙酰氨基酚、氢吗啡酮和羟考酮)外,术后分别接受加巴喷丁或安慰剂治疗。在术前、术中及术后对患者进行疼痛水平、药物剂量、副作用、不良事件、住院时间和家长满意度的监测。

结果

与对照组相比,治疗组术后早期疼痛评分、阿片类药物使用量以及术后总阿片类药物使用量均有统计学显著下降。不良事件、药物副作用或住院时间方面无统计学显著差异。两组患者的家长对为其孩子提供的疼痛控制都非常满意。

结论

这项随机对照试验表明,对于青少年特发性脊柱侧凸后路脊柱融合术后的患者,在多模式疼痛管理方案中术前和术后使用加巴喷丁,可在术后前两天显著减少阿片类药物的使用和视觉模拟疼痛量表评分。加巴喷丁应被视为该患者群体围手术期疼痛控制的标准药物。

证据级别

一级。

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