Mosher Hilary J, Hadlandsmyth Katherine, Alexander Bruce, Lund Brian C
Center for Comprehensive Access and Delivery Research and Evaluation (CADRE), Iowa City VA Healthcare System, Iowa City, IA, USA.
Department of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
J Gen Intern Med. 2024 Feb;39(2):207-213. doi: 10.1007/s11606-023-08420-z. Epub 2023 Sep 26.
Inpatient hospitalization has the potential to disrupt buprenorphine therapy.
Among patients receiving outpatient buprenorphine prior to admission, we determined the rate of discontinuation during medical and surgical admissions to VA hospitals and its association with subsequent post-discharge continuation of buprenorphine therapy.
We conducted an observational study using Veterans Administration data from 10/1/2018 to 3/31/2020 for all medical and surgical admissions where Veterans had active buprenorphine prescriptions at the time of admission. Pre-admission buprenorphine prescriptions were categorized as either sublingual (presumed indication for opioid use disorder (OUD)) or buccal/topical (presumed indication for pain). The primary measure of post-discharge buprenorphine receipt was any outpatient buprenorphine prescription dispensed between 1 day prior to discharge and 60 days following discharge.
A total of 830 unique inpatient hospitalizations to medical or surgical services occurred among Veterans receiving sublingual (48.3%) or buccal/topical (51.7%) buprenorphine prior to admission. Fewer than half (43.9%) of these patients received buprenorphine at some point during the medical or surgical portion of their hospital stay. Among the 766 patients discharged from a medical or surgical unit, 74.3% received an outpatient buprenorphine prescription within the 60 days following discharge (80.2% sublingual and 69.1% buccal/topical). Among patients who had received buprenorphine during the final 36 h prior to discharge, subsequent outpatient buprenorphine receipt was observed in 94.0%, compared to only 63.7% among those not receiving buprenorphine during the final 36 h (χ = 83.5, p < 0.001).
Inpatient buprenorphine administrations near the time of discharge were highly predictive of continued outpatient therapy and a significant subset of patients did not continue or reinitiate buprenorphine therapy following discharge. As recommendations for perioperative and inpatient management of buprenorphine coalescence around continuation, efforts are needed to optimize hospital-based buprenorphine practices.
住院治疗可能会中断丁丙诺啡治疗。
在入院前接受门诊丁丙诺啡治疗的患者中,我们确定了退伍军人事务部(VA)医院内科和外科住院期间的停药率及其与出院后丁丙诺啡治疗持续情况的关联。
我们进行了一项观察性研究,使用2018年10月1日至2020年3月31日退伍军人事务部的数据,涵盖所有入院时持有有效丁丙诺啡处方的内科和外科住院患者。入院前的丁丙诺啡处方分为舌下含服(推测用于阿片类物质使用障碍(OUD))或颊部/局部用药(推测用于疼痛)。出院后丁丙诺啡接受情况的主要测量指标是出院前1天至出院后60天内开具的任何门诊丁丙诺啡处方。
共有830例独特的内科或外科住院患者,他们在入院前接受舌下含服(48.3%)或颊部/局部用药(51.7%)丁丙诺啡治疗。这些患者中不到一半(43.9%)在住院期间的内科或外科治疗阶段的某个时间接受了丁丙诺啡治疗。在766例从内科或外科病房出院的患者中,74.3%在出院后60天内接受了门诊丁丙诺啡处方(舌下含服80.2%,颊部/局部用药69.1%)。在出院前最后36小时内接受丁丙诺啡治疗的患者中,94.0%随后接受了门诊丁丙诺啡治疗,而在最后36小时内未接受丁丙诺啡治疗的患者中这一比例仅为63.7%(χ=83.5,p<0.001)。
出院时附近的住院丁丙诺啡给药对持续门诊治疗具有高度预测性,并且有相当一部分患者在出院后没有继续或重新开始丁丙诺啡治疗。由于围绕持续用药的丁丙诺啡围手术期和住院管理建议趋于一致,因此需要努力优化基于医院的丁丙诺啡治疗方案。