Miron Oren, Wolff-Sagy Yael, Levin Mark, Lubich Esti, Lewinski Jordan, Shpunt Maya, Abu Ahmad Wiessam, Borochov Ilya, Netzer Doron, Lavie Gil
Branch of Planning and Strategy, Clalit Health Services, Tel Aviv, Israel.
Department of Health Policy and Management, Ben-Gurion University of the Negev, Beer Sheva, Israel.
J Gen Intern Med. 2024 Nov 4. doi: 10.1007/s11606-024-09160-4.
Healthcare organizations attempt to address unwarranted fentanyl use, which often leads to increased risk of addiction and overdose.
To assess the impact of a requirement for a specialist's approval on fentanyl initiation for non-oncological pain.
A retrospective cohort study based on observational data.
All 4.4 million non-oncological members of Clalit Health Services were included, from July 20, 2021, to July 19, 2023.
The rate of fentanyl initiation was assessed before and after the implementation of the requirement for specialist's approval, which was introduced on July 2022, and expanded 6 months later for continued use. A sub-group analysis by age group was performed, and patient characteristics and indications were assessed. We also compared total opioid dispensation in the 6th and 12th months after the implementation with the predicted rate based on pre-implementation rates.
Fentanyl initiation rate in the year before the requirement was 711 per million capita, which decreased following the requirement by - 81% (95% CI: - 77%; - 85%). The decrease attenuated with age. The prevalence of diagnosis with substance abuse disorders at the time of fentanyl initiation decreased from 6 to 3%. In the 6th and 12th months after the requirement was implemented, the morphine milligram equivalent (MME) from dispensation of total opioids was lower than predicted based on pre-implementation rates by 7% and 26%, respectively.
Requiring specialist approval for fentanyl initiation for non-oncological chronic pain was associated with a decrease in fentanyl prescription initiations, especially among non-elderly patients. A decrease also occurred gradually in total opioid dispensations, further decreasing following the extension of the requirement to continuous fentanyl. The requirement for specialist approval upon fentanyl initiation and continuous fentanyl may present an effective tool for limiting the use of fentanyl and total opioids in healthcare systems.
医疗保健机构试图解决不必要的芬太尼使用问题,这种使用往往会增加成瘾和过量用药的风险。
评估非肿瘤性疼痛使用芬太尼起始治疗时要求专科医生批准的影响。
基于观察数据的回顾性队列研究。
纳入了2021年7月20日至2023年7月19日期间Clalit健康服务机构的所有440万非肿瘤性会员。
在2022年7月引入并在6个月后扩大至持续使用的专科医生批准要求实施前后,评估芬太尼起始治疗率。按年龄组进行亚组分析,并评估患者特征和用药指征。我们还将实施后的第6个月和第12个月的总阿片类药物配药量与基于实施前比率预测的比率进行了比较。
在该要求实施前一年,芬太尼起始治疗率为每百万人口711例,实施该要求后下降了-81%(95%置信区间:-77%;-85%)。这种下降随着年龄增长而减弱。芬太尼起始治疗时物质使用障碍的诊断患病率从6%降至3%。在该要求实施后的第6个月和第12个月,总阿片类药物配药量中的吗啡毫克当量(MME)分别比基于实施前比率预测的低7%和26%。
非肿瘤性慢性疼痛使用芬太尼起始治疗要求专科医生批准与芬太尼处方起始量减少有关,尤其是在非老年患者中。总阿片类药物配药量也逐渐减少,在该要求扩展至芬太尼持续使用后进一步下降。芬太尼起始治疗和芬太尼持续使用时要求专科医生批准可能是医疗系统中限制芬太尼和总阿片类药物使用的有效工具。