阿片类药物安全措施的实施:退伍军人健康管理局患者不良后果的学术细节影响。

Emily C. Williams, Madeline C. Frost, M. Bounthavong, Amy T. Edmonds, Marcos K. Lau, E. J. Edelman, Michael A. Harvey, M. Christopher
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引用次数: 0

摘要

背景退伍军人健康管理局(VA)实施了学术细化(AD),以支持更安全的阿片类药物处方和过量预防措施。方法每月从退伍军人健康管理局的电子健康记录中提取患者级别的数据,以评估在长期开具阿片类药物处方(在给定月份前 6 个月阿片类药物的供应量≥45 天,且处方间隔时间≤15 天)的患者观察队列中,AD 的实施是否与全因死亡率、阿片类药物中毒住院人数和阿片类药物中毒急诊科(ED)就诊人数的变化有关。使用分段逻辑回归对死亡率进行单组间断时间序列分析,使用泊松回归对住院人数和急诊室就诊人数进行单组间断时间序列分析,以确定这些结果的水平和斜率是否因实施 AD 而发生变化。结果在 955 376 名患者(19 431 241 人月)中,有 53 369 人死亡(AD 实施前 29 025 人;AD 实施后 24 344 人),1927 名阿片类药物中毒住院患者(AD 实施前 610 人;AD 实施后 1317 人)和 408 名阿片类药物中毒急诊就诊者(AD 实施前 207 人;AD 实施后 201 人)。AD 实施后,全因死亡率降低了 5.8%(95% 置信区间 [CI]:0.897, 0.990)。然而,在刚实施 AD 后,患者因阿片类药物中毒住院的发生率明显增加(发生率比 = 1.523;95% 置信区间:1.118, 2.077)。结论 在长期服用阿片类药物的患者中,阿片类药物滥用与全因死亡率下降有关,但与阿片类药物中毒住院率上升有关。应探讨 AD 影响阿片类药物相关结果的机制。
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Implementation of Opioid Safety Efforts: Influence of Academic Detailing on Adverse Outcomes Among Patients in the Veterans Health Administration.
BACKGROUND The Veterans Health Administration (VA) implemented academic detailing (AD) to support safer opioid prescribing and overdose prevention initiatives. METHODS Patient-level data were extracted monthly from VA's electronic health record to evaluate whether AD implementation was associated with changes in all-cause mortality, opioid poisoning inpatient admissions, and opioid poisoning emergency department (ED) visits in an observational cohort of patients with long-term opioid prescriptions (≥45-day supply of opioids 6 months prior to a given month with ≤15 days between prescriptions). A single-group interrupted time series analysis using segmented logistic regression for mortality and Poisson regression for counts of inpatient admissions and ED visits was used to identify whether the level and slope of these outcomes changed in response to AD implementation. RESULTS Among 955 376 unique patients (19 431 241 person-months), there were 53 369 deaths (29 025 pre-AD; 24 344 post-AD), 1927 opioid poisoning inpatient admissions (610 pre-AD; 1317 post-AD), and 408 opioid poisoning ED visits (207 pre-AD; 201 post-AD). Immediately after AD implementation, there was a 5.8% reduction in the odds of all-cause mortality (95% confidence interval [CI]: 0.897, 0.990). However, patients had a significantly increased incidence rate of inpatient admissions for opioid poisoning immediately after AD implementation (incidence rate ratio = 1.523; 95% CI: 1.118, 2.077). No significant differences in ED visits for opioid poisoning were observed. CONCLUSIONS AD was associated with decreased all-cause mortality but increased inpatient hospitalization for opioid poisoning among patients prescribed long-term opioids. Mechanisms via which AD's efforts influenced opioid-related outcomes should be explored.
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Study Protocol for the Healing Opioid Misuse and Pain Through Engagement Trial: Integrated Treatment for Individuals With Co-occurring Chronic Pain and Opioid Use Disorder. Pain Care at Home to Amplify Function: Protocol Article. Addressing the Intersections of Chronic Pain and OUD: Integrative Management of Chronic Pain and OUD for Whole Recovery (IMPOWR) Research Network. Connecting Chronic Pain and Opioid Use Disorder Clinical Trials Through Data Harmonization: Wake Forest IMPOWR Dissemination, Education, and Coordination Center (IDEA-CC). The IMPOWR Network Divided or Single Exposure Study (DOSE) Protocol: A Randomized Controlled Comparison of Once Versus Split Dosing of Methadone for the Treatment of Comorbid Chronic Pain and Opioid Use Disorder.
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