<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>46</viewCount><searchCount>0</searchCount></scores><additional><submitter>Murphy SM</submitter><funding>NIDA NIH HHS</funding><pagination>90-98</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6581635</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>170(2)</volume><pubmed_abstract>Background:Not enough evidence exists to compare buprenorphine-naloxone with extended-release naltrexone for treating opioid use disorder. Objective:To evaluate the cost-effectiveness of buprenorphine-naloxone versus extended-release naltrexone. Design:Cost-effectiveness analysis alongside a previously reported randomized clinical trial of 570 adults in 8 U.S. inpatient or residential treatment programs. Data Sources:Study instruments. Target Population:Adults with opioid use disorder. Time Horizon:24-week intervention with an additional 12 weeks of observation. Perspective:Health care sector and societal. Interventions:Buprenorphine-naloxone and extended-release naltrexone. Outcome Measures:Incremental costs combined with incremental quality-adjusted life-years (QALYs) and incremental time abstinent from opioids. Results of Base-Case Analysis:Use of the health care sector perspective and a willingness-to-pay threshold of $100 000 per QALY showed buprenorphine-naloxone to be preferable to extended-release naltrexone in 97% of bootstrap replications at 24 weeks and in 85% at 36 weeks. Similar results were obtained with incremental time abstinent from opioids as an outcome and with use of the societal perspective. Results of Sensitivity Analysis:The base-case results were sensitive to the cost of the 2 treatments and the success of randomized treatment initiation. Limitation:Relatively short follow-up for a chronic condition, substantial missing data, no information on patient out-of-pocket and social service costs. Conclusion:Buprenorphine-naloxone is preferred to extended-release naltrexone as first-line treatment when both options are clinically appropriate and patients require detoxification before initiating extended-release naltrexone. Primary Funding Source:National Institute on Drug Abuse, National Institutes of Health.</pubmed_abstract><journal>Annals of internal medicine</journal><pubmed_title>Cost-Effectiveness of Buprenorphine-Naloxone Versus Extended-Release Naltrexone to Prevent Opioid Relapse.</pubmed_title><pmcid>PMC6581635</pmcid><funding_grant_id>UG1 DA013035</funding_grant_id><funding_grant_id>U10 DA013732</funding_grant_id><funding_grant_id>K24 DA022412</funding_grant_id><funding_grant_id>U10 DA013720</funding_grant_id><funding_grant_id>R01 DA035808</funding_grant_id><funding_grant_id>U10 DA015833</funding_grant_id><funding_grant_id>UG1 DA013034</funding_grant_id><funding_grant_id>U10 DA013035</funding_grant_id><funding_grant_id>U10 DA013046</funding_grant_id><funding_grant_id>U10 DA013045</funding_grant_id><funding_grant_id>U10 DA013034</funding_grant_id><funding_grant_id>U10 DA015831</funding_grant_id><funding_grant_id>HHSN271201500065C</funding_grant_id><funding_grant_id>HHSN271201200017C</funding_grant_id><funding_grant_id>UG1 DA013714</funding_grant_id><funding_grant_id>U10 DA013714</funding_grant_id><funding_grant_id>UG1 DA013732</funding_grant_id><funding_grant_id>P30 DA040500</funding_grant_id><funding_grant_id>UG1 DA015831</funding_grant_id><funding_grant_id>UG1 DA013720</funding_grant_id><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Leff JA</pubmed_authors><pubmed_authors>Nunes EV</pubmed_authors><pubmed_authors>Schackman BR</pubmed_authors><pubmed_authors>Jeng PJ</pubmed_authors><pubmed_authors>Lee JD</pubmed_authors><pubmed_authors>McCollister KE</pubmed_authors><pubmed_authors>Murphy SM</pubmed_authors><pubmed_authors>Novo P</pubmed_authors><pubmed_authors>Rotrosen J</pubmed_authors><view_count>46</view_count></additional><is_claimable>false</is_claimable><name>Cost-Effectiveness of Buprenorphine-Naloxone Versus Extended-Release Naltrexone to Prevent Opioid Relapse.</name><description>Background:Not enough evidence exists to compare buprenorphine-naloxone with extended-release naltrexone for treating opioid use disorder. Objective:To evaluate the cost-effectiveness of buprenorphine-naloxone versus extended-release naltrexone. Design:Cost-effectiveness analysis alongside a previously reported randomized clinical trial of 570 adults in 8 U.S. inpatient or residential treatment programs. Data Sources:Study instruments. Target Population:Adults with opioid use disorder. Time Horizon:24-week intervention with an additional 12 weeks of observation. Perspective:Health care sector and societal. Interventions:Buprenorphine-naloxone and extended-release naltrexone. Outcome Measures:Incremental costs combined with incremental quality-adjusted life-years (QALYs) and incremental time abstinent from opioids. Results of Base-Case Analysis:Use of the health care sector perspective and a willingness-to-pay threshold of $100 000 per QALY showed buprenorphine-naloxone to be preferable to extended-release naltrexone in 97% of bootstrap replications at 24 weeks and in 85% at 36 weeks. Similar results were obtained with incremental time abstinent from opioids as an outcome and with use of the societal perspective. Results of Sensitivity Analysis:The base-case results were sensitive to the cost of the 2 treatments and the success of randomized treatment initiation. Limitation:Relatively short follow-up for a chronic condition, substantial missing data, no information on patient out-of-pocket and social service costs. Conclusion:Buprenorphine-naloxone is preferred to extended-release naltrexone as first-line treatment when both options are clinically appropriate and patients require detoxification before initiating extended-release naltrexone. Primary Funding Source:National Institute on Drug Abuse, National Institutes of Health.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2024-02-15T07:56:02.806Z</modification><creation>2019-09-14T07:03:03Z</creation></dates><accession>S-EPMC6581635</accession><cross_references><pubmed>30557443</pubmed><doi>10.7326/M18-0227</doi><doi>10.7326/m18-0227</doi></cross_references></HashMap>