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多学科过渡性疼痛服务在脊柱手术患者中减少阿片类药物使用和改善围手术期结局的可行性:一项质量改进研究。

Feasibility of a multidisciplinary Transitional Pain Service in spine surgery patients to minimise opioid use and improve perioperative outcomes: a quality improvement study.

机构信息

Department of Anesthesiology and Pain Medicine, University of Ottawa, Ottawa, Ontario, Canada

Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

出版信息

BMJ Open Qual. 2023 Jun;12(2). doi: 10.1136/bmjoq-2023-002278.

Abstract

INTRODUCTION

Spine surgery patients have high rates of perioperative opioid consumption, with a chronic opioid use prevalence of 20%. A proposed solution is the implementation of a Transitional Pain Service (TPS), which provides patient-tailored multidisciplinary care. Its feasibility has not been demonstrated in spine surgery. The main objective of this study was to evaluate the feasibility of a TPS programme in patients undergoing spine surgery.

METHODS

Patients were recruited between July 2020 and November 2021 at a single, tertiary care academic centre. Success of our study was defined as: (1) enrolment: ability to enrol ≥80% of eligible patients, (2) data collection: ability to collect data for ≥80% of participants, including effectiveness measures (oral morphine equivalent (OME) and Visual Analogue Scale (VAS)-perceived analgesic management and overall health) and programme resource requirements measures (appointment attendance, 60-day return to emergency and length of stay), and (3) efficacy: estimate potential programme effectiveness defined as ≥80% of patients weaned back to their intake OME requirements at programme discharge.

RESULTS

Thirty out of 36 (83.3%) eligible patients were enrolled and 26 completed the TPS programme. The main programme outcomes and resource measures were successfully tracked for >80% of patients. All 26 patients had the same or lower OME at programme discharge than at intake (intake 38.75 mg vs discharge 12.50 mg; p<0.001). At TPS discharge, patients reported similar overall health VAS (pre 60.0 vs post 70.0; p=0.14), improved scores for VAS-perceived analgesic management (pre 47.6 vs post 75.6; p<0.001) and improved Brief Pain Inventory pain intensity (pre 39.1 vs post 25.0; p=0.02).

CONCLUSION

Our feasibility study successfully met or exceeded our three main objectives. Based on this success and the defined clinical need for a TPS programme, we plan to expand our TPS care model to include other surgical procedures at our centre.

摘要

简介

脊柱手术患者围手术期阿片类药物的使用率很高,慢性阿片类药物使用率为 20%。一种可行的解决方案是实施过渡性疼痛服务(TPS),该服务提供患者定制的多学科护理。在脊柱手术中,其可行性尚未得到证实。本研究的主要目的是评估 TPS 方案在脊柱手术患者中的可行性。

方法

患者于 2020 年 7 月至 2021 年 11 月在一家单中心、三级学术中心招募。我们研究的成功定义为:(1)入组:有能力招募≥80%的合格患者,(2)数据收集:能够收集≥80%参与者的数据,包括有效性措施(口服吗啡当量(OME)和视觉模拟量表(VAS)-感知镇痛管理和整体健康)和方案资源需求措施(预约出勤率、60 天内返回急诊和住院时间),以及(3)疗效:估计方案的潜在疗效,定义为≥80%的患者在方案出院时可逐渐减少至其 OME 需求。

结果

36 名符合条件的患者中有 30 名(83.3%)入组,26 名完成了 TPS 方案。主要方案结果和资源措施成功地跟踪了超过 80%的患者。所有 26 名患者在 TPS 出院时的 OME 与入院时相同或更低(入院时 38.75mg 与出院时 12.50mg;p<0.001)。在 TPS 出院时,患者报告了相似的整体健康 VAS(术前 60.0 与术后 70.0;p=0.14),VAS-感知镇痛管理评分有所改善(术前 47.6 与术后 75.6;p<0.001),简明疼痛量表疼痛强度也有所改善(术前 39.1 与术后 25.0;p=0.02)。

结论

我们的可行性研究成功地满足或超过了我们的三个主要目标。基于这一成功以及 TPS 方案的临床需求,我们计划在我们的中心将 TPS 护理模式扩展到其他手术程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d439/10314708/a3705aa8f988/bmjoq-2023-002278f01.jpg

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