Rates and predictors of opioid deprescribing after fracture: A retrospective study of Medicare fee-for-service claims.

Kevin T Pritchard, Chun-Ting Yang, Qiaoxi Chen, Yichi Zhang, James M Wilkins, Dae Hyun Kim, Kueiyu Joshua Lin
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Abstract

Background: Adults with Alzheimer's disease and Alzheimer's disease related dementias (ADRD) or frailty are susceptible to fractures. Opioid analgesics are frequently prescribed after fractures. Documenting post-fracture opioid discontinuation rates and predictors of discontinuation among adults with ADRD or frailty can inform clinical practice, identify potential disparities, and improve pain management guidelines. The objective of this paper was to investigate opioid discontinuation in opioid-naïve older adults who used opioids after an acute fracture.

Methods: This retrospective cohort study included opioid-naïve Medicare fee-for-service beneficiaries (N = 33,027) ≥65 years of age who filled an opioid prescription within 30 days of a vertebral, lower extremity, or upper extremity fracture from 2013 to 2018. Beneficiaries were classified according to ADRD (yes/no) and frailty (yes/no) status using validated claims-based algorithms. The primary outcome was opioid discontinuation, defined as a 30-day supply gap. We estimated discontinuation rates with the Kaplan-Meier method and identified predictors of opioid discontinuation using Cox proportional hazards regression.

Results: The 30-day opioid discontinuation rate was similar among non-frail beneficiaries without ADRD (81% [95% CI, 80%-81%]) and those who were non-frail with ADRD (83% [81%-84%]). Comparatively, 30-day discontinuation rates were lower among those with frailty and ADRD (76% [75%-77%]) and those with frailty alone (77% [75%-78%]). After adjusting for sociodemographic characteristics, health status, healthcare utilization, and calendar year, beneficiaries with both ADRD and frailty (HR, 0.90 [0.87-0.93]) and those with frailty alone (HR, 0.85 [0.82-0.89]), but not those with ADRD alone (HR, 1.06 [1.01-1.10]), were less likely to discontinue opioids compared with those without ADRD or frailty.

Conclusions and relevance: Our findings suggest that frailty, but not ADRD, was associated with a lower likelihood of opioid discontinuation among older adults who initiated opioids after an acute fracture. Further research is needed to understand how opioid deprescribing practices depend on patient and provider preferences.

骨折后阿片类药物处方的比率和预测因素:一项针对医疗服务收费索赔的回顾性研究。
背景:患有阿尔茨海默病和阿尔茨海默病相关痴呆(ADRD)或身体虚弱的成年人易发生骨折。阿片类镇痛药常在骨折后使用。记录成人ADRD或体弱者骨折后阿片类药物停药率和停药预测因素可以为临床实践提供信息,识别潜在的差异,并改进疼痛管理指南。本文的目的是调查opioid-naïve老年人在急性骨折后使用阿片类药物的阿片类药物停药。方法:本回顾性队列研究纳入opioid-naïve医疗保险服务收费受益人(N = 33,027)≥65岁,在2013年至2018年椎体、下肢或上肢骨折后30天内服用阿片类药物处方的患者。受益人根据ADRD(是/否)和虚弱(是/否)状态使用有效的基于索赔的算法进行分类。主要结局是阿片类药物停药,定义为30天的供应缺口。我们使用Kaplan-Meier方法估计停药率,并使用Cox比例风险回归确定阿片类药物停药的预测因素。结果:无ADRD的非体弱受益人(81% [95% CI, 80%-81%])和无ADRD的非体弱受益人(83%[81%-84%])30天阿片类药物停药率相似。相比之下,虚弱合并ADRD的患者(76%[75%-77%])和单纯虚弱患者(77%[75%-78%])的30天停药率较低。在调整了社会人口统计学特征、健康状况、医疗保健利用和日历年之后,同时患有ADRD和虚弱的受益人(HR, 0.90[0.87-0.93])和仅患有ADRD的受益人(HR, 0.85[0.82-0.89]),而非仅患有ADRD的受益人(HR, 1.06[1.01-1.10])与没有ADRD或虚弱的受益人相比,停止阿片类药物的可能性更小。结论和相关性:我们的研究结果表明,在急性骨折后开始使用阿片类药物的老年人中,虚弱(而不是ADRD)与阿片类药物停药的可能性较低有关。需要进一步的研究来了解阿片类药物处方如何取决于患者和提供者的偏好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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