Faculty of Medicine and Health, School of Pharmacy, The University of Sydney, Sydney, NSW, Australia.
Department of Pharmacy, Prince of Wales Hospital, Randwick, NWS, Australia.
Anaesthesia. 2023 Oct;78(10):1237-1248. doi: 10.1111/anae.16070. Epub 2023 Jun 26.
Modified-release opioids are often prescribed for the management of moderate to severe acute pain following total hip and knee arthroplasty, despite recommendations against their use due to increasing concerns regarding harm. The primary objective of this multicentre study was to examine the impact of modified-release opioid use on the incidence of opioid-related adverse events compared with immediate-release opioid use, among adult inpatients following total hip or knee arthroplasty. Data for total hip and knee arthroplasty inpatients receiving an opioid analgesic for postoperative analgesia during hospitalisation were collected from electronic medical records of three tertiary metropolitan hospitals in Australia. The primary outcome was the incidence of opioid-related adverse events during hospital admission. Patients who received modified with or without immediate-release opioids were matched to those receiving immediate-release opioids only (1:1) using nearest neighbour propensity score matching with patient and clinical characteristics as covariates. This included total opioid dose received. In the matched cohorts, patients given modified-release opioids (n = 347) experienced a higher incidence of opioid-related adverse events overall, compared with those given immediate-release opioids only (20.5%, 71/347 vs. 12.7%, 44/347; difference in proportions 7.8% [95%CI 2.3-13.3%]). Modified-release opioid use was associated with an increased risk of harm when used for acute pain during hospitalisation after total hip or knee arthroplasty.
尽管由于对危害的担忧不断增加,建议不要使用,但改良型阿片类药物仍常被用于治疗全髋关节和膝关节置换术后的中重度急性疼痛。这项多中心研究的主要目的是,与使用即释型阿片类药物相比,评估全髋关节或膝关节置换术后成年住院患者使用改良型阿片类药物对阿片类药物相关不良事件发生率的影响。从澳大利亚 3 家三级大都市医院的电子病历中收集了接受阿片类镇痛药进行术后镇痛的全髋关节和膝关节置换术住院患者的改良型和即释型阿片类药物使用数据。主要结局是住院期间阿片类药物相关不良事件的发生率。接受改良型阿片类药物联合或不联合即释型阿片类药物治疗的患者与仅接受即释型阿片类药物治疗的患者(1:1)进行了最近邻倾向评分匹配,以患者和临床特征为协变量。这包括所接受的总阿片类药物剂量。在匹配队列中,与仅接受即释型阿片类药物的患者相比,接受改良型阿片类药物的患者总体上经历了更高的阿片类药物相关不良事件发生率(20.5%,71/347 与 12.7%,44/347;差异比例 7.8%[95%CI 2.3-13.3%])。改良型阿片类药物在全髋关节或膝关节置换术后住院期间用于急性疼痛时,与危害风险增加相关。