Department of Emergency Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.
JAMA Netw Open. 2024 Jul 1;7(7):e2423954. doi: 10.1001/jamanetworkopen.2024.23954.
Hospitalizations related to opioid use disorder (OUD) represent an opportunity to initiate medication for OUD (MOUD).
To assess whether starting MOUD after a hospitalization or emergency department (ED) visit is associated with the odds of fatal and nonfatal opioid overdose at 6 and 12 months.
DESIGN, SETTING, AND PARTICIPANTS: This population-based cohort study used data from the Oregon Comprehensive Opioid Risk Registry, which links all payer claims data to other administrative health datasets, for individuals aged 18 years or older who had diagnosis codes related to OUD recorded at an index ED visit or hospitalization from January 2017 to December 2019. Data were analyzed between May 2023 and January 2024.
Receipt of MOUD within the 7 days after an OUD-related hospital visit.
The primary outcome was fatal or nonfatal overdose at 6 and 12 months after discharge. Sample characteristics, including age, sex, insurance plan, number of comorbidities, and opioid-related overdose events, were stratified by receipt or nonreceipt of MOUD within 7 days after an OUD-related hospital visit. A logistic regression model was used to investigate the association between receipt of MOUD and having an opioid overdose event.
The study included 22 235 patients (53.1% female; 25.0% aged 25-39 years) who had an OUD-related hospital visit during the study period. Overall, 1184 patients (5.3%) received MOUD within 7 days of their ED visit or hospitalization. Of these patients, 683 (57.7%) received buprenorphine, 463 (39.1%) received methadone, and 46 (3.9%) received long-acting injectable naltrexone. Patients who received MOUD within 7 days after discharge had lower adjusted odds of fatal or nonfatal overdose at 6 months compared with those who did not (adjusted odds ratio [AOR], 0.63; 95% CI, 0.41-0.97). At 12 months, there was no difference in adjusted odds of fatal or nonfatal overdose between these groups (AOR, 0.79; 95% CI, 0.58-1.08). Patients had a lower risk of fatal or nonfatal overdose at 6 months associated with buprenorphine use (AOR, 0.50; 95% CI, 0.27-0.95) but not with methadone use (AOR, 0.57; 95% CI, 0.28-1.17).
In this cohort study of individuals with an OUD-related hospital visit, initiation of MOUD was associated with reduced odds of opioid-related overdose at 6 months. Hospitals should consider implementing programs and protocols to offer initiation of MOUD to patients with OUD who present for care.
与阿片类药物使用障碍(OUD)相关的住院治疗代表了开始 OUD 药物治疗(MOUD)的机会。
评估在住院或急诊(ED)就诊后开始 MOUD 是否与 6 个月和 12 个月时致命和非致命阿片类药物过量的几率相关。
设计、地点和参与者:这项基于人群的队列研究使用了俄勒冈综合阿片类药物风险登记处的数据,该登记处将所有支付者的索赔数据与其他行政健康数据集联系起来,针对的是在 2017 年 1 月至 2019 年 12 月期间在索引 ED 就诊或住院期间有 OUD 相关诊断代码记录的年龄在 18 岁或以上的个人。数据在 2023 年 5 月至 2024 年 1 月之间进行分析。
在 OUD 相关住院治疗后的 7 天内接受 MOUD。
主要结果是出院后 6 个月和 12 个月时的致命或非致命过量。根据在 OUD 相关住院治疗后的 7 天内是否接受 MOUD,按接受或未接受 MOUD 分层,样本特征包括年龄、性别、保险计划、合并症数量和阿片类药物相关的过量事件。使用逻辑回归模型调查接受 MOUD 与发生阿片类药物过量事件之间的关联。
该研究纳入了 22235 名患者(53.1%为女性;25.0%年龄在 25-39 岁),在研究期间有 OUD 相关的住院治疗。总体而言,1184 名患者(5.3%)在 ED 就诊或住院后 7 天内接受了 MOUD。其中,683 名(57.7%)接受了丁丙诺啡,463 名(39.1%)接受了美沙酮,46 名(3.9%)接受了长效纳曲酮。与未接受 MOUD 的患者相比,出院后 7 天内接受 MOUD 的患者在 6 个月时致命或非致命过量的调整后几率较低(调整后的比值比 [AOR],0.63;95%CI,0.41-0.97)。在 12 个月时,这些组之间在致命或非致命过量的调整后几率没有差异(AOR,0.79;95%CI,0.58-1.08)。与丁丙诺啡使用相关,患者在 6 个月时致命或非致命过量的风险较低(AOR,0.50;95%CI,0.27-0.95),但与美沙酮使用无关(AOR,0.57;95%CI,0.28-1.17)。
在这项对有 OUD 相关住院治疗的患者进行的队列研究中,开始 MOUD 与降低 6 个月时阿片类药物相关过量的几率相关。医院应考虑实施方案和协议,为就诊的 OUD 患者提供 MOUD 的启动。