Oren Miron, Yael Wolff Sagy, Mark Levin, Esti Lubich, Jordan Lewinski, Maya Shpunt, Wiessam Abu Ahmad, Ilya Borochov, Doron Netzer, Gil Lavie
{"title":"Fentanyl initiation rate following the requirement for specialist approval","authors":"Oren Miron, Yael Wolff Sagy, Mark Levin, Esti Lubich, Jordan Lewinski, Maya Shpunt, Wiessam Abu Ahmad, Ilya Borochov, Doron Netzer, Gil Lavie","doi":"10.1101/2024.03.13.24304188","DOIUrl":null,"url":null,"abstract":"Importance Healthcare organizations are exploring tools to address unwarranted fentanyl use which often leads to increased risk of addiction and overdose. Objective To assess the impact of a requirement for a specialist's approval on fentanyl initiation for non-oncological pain.\nDesign, Settings and Participants Retrospective cohort examination of fentanyl initiations and opioid dispensations for 4.4 million members of Clalit Health Services following a requirement for specialist's approval for fentanyl initiation on July 2022, which was expanded 6 months later for continued use.\nMain Outcomes and Measures We analyzed the change in initiations of fentanyl in the year before and after the implementation and 95% confidence interval, with a sub-group analysis by age group. We also compared total opioid dispensation, fentanyl, and non-fentanyl in the 6th and 12th month after the implementation with the predicted rate based on pre-implementation rates. Results The fentanyl initiation rate in the year before the requirement was 711/1,000,000 capita, which decreased following the requirement by -81% (95% confidence interval:-77%; -85%). The decrease attenuated with age: at ages 0-17 years -100% (16%; -216%), at ages 18-39 years -88% (-78%; -97%), at ages 40-64 years -89% (-83%; -95%) and at ages 65 years and above -73% (-68%; -79%). In the 6th month after the requirement was implemented the morphine milligram equivalent from dispensation of total opioids and fentanyl was lower than predicted by 7% and 12% respectively, while non-fentanyl opioids dispensation was 3% higher than predicted. In the 12th month after the initiation requirement, the dispensation of total opioids and fentanyl was lower than predicted by 26% and 39% respectively, while in non-fentanyl opioids it was 4% higher than predicted.\nConclusions and Relevance Our results indicate that 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. These findings suggest that requiring specialist approval for non-oncological fentanyl initiations is likely an effective strategy to be considered by other healthcare providers.","PeriodicalId":501282,"journal":{"name":"medRxiv - Addiction Medicine","volume":"56 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv - Addiction Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.03.13.24304188","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Importance Healthcare organizations are exploring tools to address unwarranted fentanyl use which often leads to increased risk of addiction and overdose. Objective To assess the impact of a requirement for a specialist's approval on fentanyl initiation for non-oncological pain.
Design, Settings and Participants Retrospective cohort examination of fentanyl initiations and opioid dispensations for 4.4 million members of Clalit Health Services following a requirement for specialist's approval for fentanyl initiation on July 2022, which was expanded 6 months later for continued use.
Main Outcomes and Measures We analyzed the change in initiations of fentanyl in the year before and after the implementation and 95% confidence interval, with a sub-group analysis by age group. We also compared total opioid dispensation, fentanyl, and non-fentanyl in the 6th and 12th month after the implementation with the predicted rate based on pre-implementation rates. Results The fentanyl initiation rate in the year before the requirement was 711/1,000,000 capita, which decreased following the requirement by -81% (95% confidence interval:-77%; -85%). The decrease attenuated with age: at ages 0-17 years -100% (16%; -216%), at ages 18-39 years -88% (-78%; -97%), at ages 40-64 years -89% (-83%; -95%) and at ages 65 years and above -73% (-68%; -79%). In the 6th month after the requirement was implemented the morphine milligram equivalent from dispensation of total opioids and fentanyl was lower than predicted by 7% and 12% respectively, while non-fentanyl opioids dispensation was 3% higher than predicted. In the 12th month after the initiation requirement, the dispensation of total opioids and fentanyl was lower than predicted by 26% and 39% respectively, while in non-fentanyl opioids it was 4% higher than predicted.
Conclusions and Relevance Our results indicate that 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. These findings suggest that requiring specialist approval for non-oncological fentanyl initiations is likely an effective strategy to be considered by other healthcare providers.