<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Becker WC</submitter><funding>NCIPC CDC HHS</funding><funding>NCATS NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>HSRD VA</funding><pagination>372-381</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11833656</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>185(4)</volume><pubmed_abstract>&lt;h4>Importance&lt;/h4>Guidelines recommend dose reduction or discontinuation of long-term opioid therapy when harm outweighs benefit, but strategies to help patients do so are limited.&lt;h4>Objective&lt;/h4>To test optionally switching to buprenorphine as a strategy for improving pain and reducing opioids among patients prescribed high-dose, full agonist long-term opioid therapy.&lt;h4>Design, setting, and participants&lt;/h4>In this pragmatic, multisite, 12-month randomized clinical trial with masked outcome assessment, patients treated at Veterans Affairs primary care clinics were recruited from October 2017 to March 2021, with follow-up completed June 2022. Eligible patients had moderate to severe chronic pain despite high-dose opioid therapy (≥70 mg/d for at least 3 months). Patients were randomized</pubmed_abstract><journal>JAMA internal medicine</journal><pubmed_title>Buprenorphine, Pain, and Opioid Use in Patients Taking High-Dose Long-Term Opioids: A Randomized Clinical Trial.</pubmed_title><pmcid>PMC11833656</pmcid><funding_grant_id>R01 CE003668</funding_grant_id><funding_grant_id>I01 HX003411</funding_grant_id><funding_grant_id>K23 DA047475</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><pubmed_authors>Aryal A</pubmed_authors><pubmed_authors>Patel A</pubmed_authors><pubmed_authors>Ugbo E</pubmed_authors><pubmed_authors>Carr M</pubmed_authors><pubmed_authors>Atkins D</pubmed_authors><pubmed_authors>Naylor J</pubmed_authors><pubmed_authors>Svabek K</pubmed_authors><pubmed_authors>Williams B</pubmed_authors><pubmed_authors>Tappainer C</pubmed_authors><pubmed_authors>Kross T</pubmed_authors><pubmed_authors>Carr T</pubmed_authors><pubmed_authors>Allen KD</pubmed_authors><pubmed_authors>Sloan J</pubmed_authors><pubmed_authors>Baskin 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opioids among patients prescribed high-dose, full agonist long-term opioid therapy.&lt;h4>Design, setting, and participants&lt;/h4>In this pragmatic, multisite, 12-month randomized clinical trial with masked outcome assessment, patients treated at Veterans Affairs primary care clinics were recruited from October 2017 to March 2021, with follow-up completed June 2022. Eligible patients had moderate to severe chronic pain despite high-dose opioid therapy (≥70 mg/d for at least 3 months). Patients were randomized</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-07-15T22:11:57.235Z</modification><creation>2026-07-09T10:20:47.641Z</creation></dates><accession>S-EPMC11833656</accession><cross_references><pubmed>39960730</pubmed><doi>10.1001/jamainternmed.2024.8361</doi></cross_references></HashMap>