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一种用于1至2节段开放性腰椎融合术的新型多模式术后疼痛方案:一项回顾性队列研究。

A Novel Multimodal Postoperative Pain Protocol for 1- to 2-Level Open Lumbar Fusions: A Retrospective Cohort Study.

作者信息

Markowitz Michael, Woods Barrett, Schroeder Gregory, Kepler Christopher, Kaye David, Kurd Mark, Armstrong Joshua, Vaccaro Alexander, Radcliff Kris

机构信息

Rowan University School of Osteopathic Medicine Orthopedic Surgery, Stratford, NJ, USA.

The Rothman Institute at Thomas Jefferson University Hospital, Philadelphia, PA, USA.

出版信息

Int J Spine Surg. 2023 Dec 26;17(6):828-834. doi: 10.14444/8484.

Abstract

BACKGROUND

There has been increased interest in exploring methods to reduce postoperative pain without opioid medications. In 2015, a multimodal analgesia protocol was used involving the perioperative use of celecoxib, gabapentin, intravenous acetaminophen, lidocaine, and liposomal bupivacaine. Overall, the goal was to reduce the utilization of scheduled opioids in favor of nonopioid pain management.

METHODS

The results of a consecutive series of 1- to 2-level open primary lumbar fusions were compared to a cohort of patients after the implementation the perioperative multimodal pain management protocol. Primary endpoints included patient-reported pain scores and secondary endpoints included length of stay.

RESULTS

There were 87 patients in the preprotocol cohort and 184 in the protocol cohort. Comparing protocol and preprotocol patients, there were no significant differences in patient demographics. There was significantly average lower pain in the protocol group on postoperative day (POD) 1 (4.50 vs 5.00, < 0.02) and POD2 (4.42 vs 5.50, < 0.03). There was a lower pain score on POD0 (4.80 vs 5.00), but it was only clinically significant. There was a correlation between pain and duration of surgery in the preprotocol patients (POD0 = 0.23, POD1 = 0.02, POD2 = 0.38), but not in the protocol patients (POD0 = -0.05, POD1 = -0.08, POD2 = -0.04). There was a shorter length of stay in the protocol cohort (2.0 vs 3.0, < 0.01). Finally, there was an approximately 35% reduction in morphine milligram equivalents of opioids in the protocol vs preprotocol cohorts (36.2 vs 57.0, < 0.05).

CONCLUSION

Our novel multimodal pain management protocol significantly reduced postoperative pain, length of stay, and opioid consumption in this patient cohort. Opioid usage correlated to pain in the protocol patients, while the preprotocol patients had no correlation between opioid use and pain medication.

CLINICAL RELEVANCE

In this study, we demonstrated that preoperative and intraoperative analgesia can reduce postoperative pain medication requirements. Furthermore, we introduced a novel concept of a correlation of pain with opioid consumption as a marker of effective pain management of breakthrough pain.

摘要

背景

人们对探索不使用阿片类药物减轻术后疼痛的方法越来越感兴趣。2015年,采用了一种多模式镇痛方案,围手术期使用塞来昔布、加巴喷丁、静脉注射对乙酰氨基酚、利多卡因和脂质体布比卡因。总体目标是减少常规阿片类药物的使用,转而采用非阿片类疼痛管理方法。

方法

将连续一系列1至2节段开放式原发性腰椎融合手术的结果与实施围手术期多模式疼痛管理方案后的一组患者进行比较。主要终点包括患者报告的疼痛评分,次要终点包括住院时间。

结果

方案实施前队列中有87例患者,方案队列中有184例患者。比较方案组和方案实施前组患者,患者人口统计学特征无显著差异。方案组术后第1天(POD1)(4.50对5.00,P<0.02)和第2天(POD2)(4.42对5.50,P<0.03)的平均疼痛明显较低。POD0时疼痛评分较低(4.80对5.00),但仅具有临床意义。方案实施前患者的疼痛与手术持续时间之间存在相关性(POD0 = 0.23,POD1 = 0.02,POD2 = 0.38),但方案组患者不存在相关性(POD0 = -0.05,POD1 = -0.08,POD2 = -0.04)。方案队列的住院时间较短(2.0对3.0,P<0.01)。最后,与方案实施前队列相比,方案队列中阿片类药物的吗啡毫克当量减少了约35%(36.2对57.0,P<0.05)。

结论

我们新的多模式疼痛管理方案显著降低了该患者队列的术后疼痛、住院时间和阿片类药物消耗量。方案组患者中阿片类药物的使用与疼痛相关,而方案实施前组患者阿片类药物使用与止痛药物之间无相关性。

临床意义

在本研究中,我们证明术前和术中镇痛可减少术后止痛药物需求。此外,我们引入了一个新的概念,即疼痛与阿片类药物消耗量的相关性可作为突破性疼痛有效疼痛管理的一个指标。

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