Care Models to Improve Pain and Reduce Opioids Among Patients Prescribed Long-Term Opioid Therapy: The VOICE Randomized Clinical Trial
IMPORTANCE: Patients prescribed long-term opioid therapy for chronic pain often experience unrelieved pain, poor quality of life, and serious adverse events. OBJECTIVE: To compare the effects of integrated pain team (IPT) vs pharmacist collaborative management (PCM) on pain and opioid dosage. DESIGN...
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creator | Krebs, Erin E Becker, William C Nelson, David B DeRonne, Beth M Jensen, Agnes C Kats, Allyson M Morasco, Benjamin J Frank, Joseph W Makris, Una E Allen, Kelli D Naylor, Jennifer C Mixon, Amanda S Bohnert, Amy Reznik, Thomas E Painter, Jacob T Hudson, Teresa J Hagedorn, Hildi J Manuel, Jennifer K Borsari, Brian Purcell, Natalie Hammett, Patrick Amundson, Erin C Kerns, Robert D Barbosa, Monica R Garvey, Caitlin Jones, Elzie J Noh, Maureen Y Okere, Jennifer B Bhushan, Sujata Pinsonnault, John Williams, Beth E Herbst, Ellen Lagisetty, Pooja Librodo, Sara Mapara, Payal S Son, Elizabeth Tat, Christina Marraffa, Rebecca A Seys, Randy L Baxley, Catherine Seal, Karen H |
description | IMPORTANCE: Patients prescribed long-term opioid therapy for chronic pain often experience unrelieved pain, poor quality of life, and serious adverse events. OBJECTIVE: To compare the effects of integrated pain team (IPT) vs pharmacist collaborative management (PCM) on pain and opioid dosage. DESIGN, SETTING, AND PARTICIPANTS: This study was a pragmatic multisite 12-month randomized comparative effectiveness trial with masked outcome assessment. Patients were recruited from October 2017 to March 2021; follow-up was completed June 2022. The study sites were Veterans Affairs primary care clinics. Eligible patients had moderate to severe chronic pain despite long-term opioid therapy (≥20 mg/d for at least 3 months). INTERVENTIONS: IPT involved interdisciplinary pain care planning, visits throughout 12 months with medical and mental health clinicians, and emphasis on nondrug therapies and motivational interviewing. PCM was a collaborative care intervention involving visits throughout 12 months with a clinical pharmacist care manager who conducted structured monitoring and medication optimization. Both interventions provided individualized pain care and opioid tapering recommendations to patients. MAIN OUTCOMES AND MEASURES: The primary outcome was pain response (≥30% decrease in Brief Pain Inventory total score) at 12 months. The main secondary outcome was 50% or greater reduction in opioid daily dosage at 12 months. RESULTS: A total of 820 patients were randomized to IPT (n = 411) or PCM (n = 409). Participants’ mean (SD) age was 62.2 (10.6) years, and 709 (86.5%) were male. A pain response was achieved in 58/350 patients in the IPT group (16.4%) vs 54/362 patients in the PCM group (14.9%) (odds ratio, 1.11 [95% CI, 0.74-1.67]; P = .61). A 50% opioid dose reduction was achieved in 102/403 patients in the IPT group (25.3%) vs 98/399 patients in the PCM group (24.6%) (odds ratio, 1.03 [95% CI, 0.75-1.42]; P = .85). Over 12 months, the mean (SD) Brief Pain Inventory total score improved from 6.7 (1.5) points to 6.1 (1.8) points (P |
doi_str_mv | 10.1001/jamainternmed.2024.6683 |
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OBJECTIVE: To compare the effects of integrated pain team (IPT) vs pharmacist collaborative management (PCM) on pain and opioid dosage. DESIGN, SETTING, AND PARTICIPANTS: This study was a pragmatic multisite 12-month randomized comparative effectiveness trial with masked outcome assessment. Patients were recruited from October 2017 to March 2021; follow-up was completed June 2022. The study sites were Veterans Affairs primary care clinics. Eligible patients had moderate to severe chronic pain despite long-term opioid therapy (≥20 mg/d for at least 3 months). INTERVENTIONS: IPT involved interdisciplinary pain care planning, visits throughout 12 months with medical and mental health clinicians, and emphasis on nondrug therapies and motivational interviewing. PCM was a collaborative care intervention involving visits throughout 12 months with a clinical pharmacist care manager who conducted structured monitoring and medication optimization. Both interventions provided individualized pain care and opioid tapering recommendations to patients. MAIN OUTCOMES AND MEASURES: The primary outcome was pain response (≥30% decrease in Brief Pain Inventory total score) at 12 months. The main secondary outcome was 50% or greater reduction in opioid daily dosage at 12 months. RESULTS: A total of 820 patients were randomized to IPT (n = 411) or PCM (n = 409). Participants’ mean (SD) age was 62.2 (10.6) years, and 709 (86.5%) were male. A pain response was achieved in 58/350 patients in the IPT group (16.4%) vs 54/362 patients in the PCM group (14.9%) (odds ratio, 1.11 [95% CI, 0.74-1.67]; P = .61). A 50% opioid dose reduction was achieved in 102/403 patients in the IPT group (25.3%) vs 98/399 patients in the PCM group (24.6%) (odds ratio, 1.03 [95% CI, 0.75-1.42]; P = .85). Over 12 months, the mean (SD) Brief Pain Inventory total score improved from 6.7 (1.5) points to 6.1 (1.8) points (P < .001) in IPT and from 6.6 (1.6) points to 6.0 (1.9) points (P < .001) in PCM (between-group P = .82). Over 12 months, mean (SD) opioid daily dosage decreased from 80.8 (74.2) mg/d to 54.2 (65.0) mg/d in IPT (P < .001) and from 74.5 (56.9) mg/d to 52.8 (51.9) mg/d (P < .001) in PCM (between-group P = .22). CONCLUSIONS AND RELEVANCE: Outcomes in this randomized clinical trial did not differ between groups; both had small improvements in pain and substantial reductions in opioid dosage. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03026790</description><identifier>ISSN: 2168-6106</identifier><identifier>ISSN: 2168-6114</identifier><identifier>EISSN: 2168-6114</identifier><identifier>DOI: 10.1001/jamainternmed.2024.6683</identifier><identifier>PMID: 39652356</identifier><language>eng</language><publisher>United States: American Medical Association</publisher><ispartof>JAMA internal medicine, 2024-12</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a1236-341b91f1599bf0428ef3a2e7aaf9d3198df88871215a9e27353730dba2fdae3e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jamanetwork.com/journals/jamainternalmedicine/articlepdf/10.1001/jamainternmed.2024.6683$$EPDF$$P50$$Gama$$H</linktopdf><linktohtml>$$Uhttps://jamanetwork.com/journals/jamainternalmedicine/fullarticle/10.1001/jamainternmed.2024.6683$$EHTML$$P50$$Gama$$H</linktohtml><link.rule.ids>64,314,777,781,3327,27905,27906,76238,76241</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39652356$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krebs, Erin E</creatorcontrib><creatorcontrib>Becker, William C</creatorcontrib><creatorcontrib>Nelson, David B</creatorcontrib><creatorcontrib>DeRonne, Beth M</creatorcontrib><creatorcontrib>Jensen, Agnes C</creatorcontrib><creatorcontrib>Kats, Allyson M</creatorcontrib><creatorcontrib>Morasco, Benjamin J</creatorcontrib><creatorcontrib>Frank, Joseph W</creatorcontrib><creatorcontrib>Makris, Una E</creatorcontrib><creatorcontrib>Allen, Kelli D</creatorcontrib><creatorcontrib>Naylor, Jennifer C</creatorcontrib><creatorcontrib>Mixon, Amanda S</creatorcontrib><creatorcontrib>Bohnert, Amy</creatorcontrib><creatorcontrib>Reznik, Thomas E</creatorcontrib><creatorcontrib>Painter, Jacob T</creatorcontrib><creatorcontrib>Hudson, Teresa J</creatorcontrib><creatorcontrib>Hagedorn, Hildi J</creatorcontrib><creatorcontrib>Manuel, Jennifer K</creatorcontrib><creatorcontrib>Borsari, Brian</creatorcontrib><creatorcontrib>Purcell, Natalie</creatorcontrib><creatorcontrib>Hammett, Patrick</creatorcontrib><creatorcontrib>Amundson, Erin C</creatorcontrib><creatorcontrib>Kerns, Robert D</creatorcontrib><creatorcontrib>Barbosa, Monica R</creatorcontrib><creatorcontrib>Garvey, Caitlin</creatorcontrib><creatorcontrib>Jones, Elzie J</creatorcontrib><creatorcontrib>Noh, Maureen Y</creatorcontrib><creatorcontrib>Okere, Jennifer B</creatorcontrib><creatorcontrib>Bhushan, Sujata</creatorcontrib><creatorcontrib>Pinsonnault, John</creatorcontrib><creatorcontrib>Williams, Beth E</creatorcontrib><creatorcontrib>Herbst, Ellen</creatorcontrib><creatorcontrib>Lagisetty, Pooja</creatorcontrib><creatorcontrib>Librodo, Sara</creatorcontrib><creatorcontrib>Mapara, Payal S</creatorcontrib><creatorcontrib>Son, Elizabeth</creatorcontrib><creatorcontrib>Tat, Christina</creatorcontrib><creatorcontrib>Marraffa, Rebecca A</creatorcontrib><creatorcontrib>Seys, Randy L</creatorcontrib><creatorcontrib>Baxley, Catherine</creatorcontrib><creatorcontrib>Seal, Karen H</creatorcontrib><creatorcontrib>VOICE Study Group</creatorcontrib><title>Care Models to Improve Pain and Reduce Opioids Among Patients Prescribed Long-Term Opioid Therapy: The VOICE Randomized Clinical Trial</title><title>JAMA internal medicine</title><addtitle>JAMA Intern Med</addtitle><description>IMPORTANCE: Patients prescribed long-term opioid therapy for chronic pain often experience unrelieved pain, poor quality of life, and serious adverse events. OBJECTIVE: To compare the effects of integrated pain team (IPT) vs pharmacist collaborative management (PCM) on pain and opioid dosage. DESIGN, SETTING, AND PARTICIPANTS: This study was a pragmatic multisite 12-month randomized comparative effectiveness trial with masked outcome assessment. Patients were recruited from October 2017 to March 2021; follow-up was completed June 2022. The study sites were Veterans Affairs primary care clinics. Eligible patients had moderate to severe chronic pain despite long-term opioid therapy (≥20 mg/d for at least 3 months). INTERVENTIONS: IPT involved interdisciplinary pain care planning, visits throughout 12 months with medical and mental health clinicians, and emphasis on nondrug therapies and motivational interviewing. PCM was a collaborative care intervention involving visits throughout 12 months with a clinical pharmacist care manager who conducted structured monitoring and medication optimization. Both interventions provided individualized pain care and opioid tapering recommendations to patients. MAIN OUTCOMES AND MEASURES: The primary outcome was pain response (≥30% decrease in Brief Pain Inventory total score) at 12 months. The main secondary outcome was 50% or greater reduction in opioid daily dosage at 12 months. RESULTS: A total of 820 patients were randomized to IPT (n = 411) or PCM (n = 409). Participants’ mean (SD) age was 62.2 (10.6) years, and 709 (86.5%) were male. A pain response was achieved in 58/350 patients in the IPT group (16.4%) vs 54/362 patients in the PCM group (14.9%) (odds ratio, 1.11 [95% CI, 0.74-1.67]; P = .61). A 50% opioid dose reduction was achieved in 102/403 patients in the IPT group (25.3%) vs 98/399 patients in the PCM group (24.6%) (odds ratio, 1.03 [95% CI, 0.75-1.42]; P = .85). Over 12 months, the mean (SD) Brief Pain Inventory total score improved from 6.7 (1.5) points to 6.1 (1.8) points (P < .001) in IPT and from 6.6 (1.6) points to 6.0 (1.9) points (P < .001) in PCM (between-group P = .82). Over 12 months, mean (SD) opioid daily dosage decreased from 80.8 (74.2) mg/d to 54.2 (65.0) mg/d in IPT (P < .001) and from 74.5 (56.9) mg/d to 52.8 (51.9) mg/d (P < .001) in PCM (between-group P = .22). CONCLUSIONS AND RELEVANCE: Outcomes in this randomized clinical trial did not differ between groups; both had small improvements in pain and substantial reductions in opioid dosage. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03026790</description><issn>2168-6106</issn><issn>2168-6114</issn><issn>2168-6114</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpVkc9q3DAQxkVJaUKSF-ih1TEXbySNLcu9BbNtFjZsCNtezdgatwr-s5W8gfQB-tyR2U0gc5mB7zffIH2MfZViIYWQ14_Yoxsm8kNPdqGEShdaG_jAzpTUJtFSpidvs9Cn7DKERxHLCJECfGKnUOhMQabP2P8SPfG70VIX-DTyVb_z4xPx-3iB42D5A9l9Q3yzc6Ozgd_04_A7qpOjYQr83lNovKvJ8nUUki35_sjy7R_yuHv-Ng_812ZVLvlDdBx79y_iZecG12DHt95hd8E-ttgFujz2c_bz-3Jb3ibrzY9VebNOUCrQCaSyLmQrs6KoW5EqQy2gohyxLSzIwtjWGJNLJTMsSOWQQQ7C1qhaiwQE5-zq4Btf-XdPYap6FxrqOhxo3IcKZKq1yLWREc0PaOPHEDy11c67Hv1zJUU151C9y6Gac6jmHOLml-ORfT0rr3uvvx6BzwcgGrypyqhcg4YXxEqQCg</recordid><startdate>20241209</startdate><enddate>20241209</enddate><creator>Krebs, Erin E</creator><creator>Becker, William C</creator><creator>Nelson, David B</creator><creator>DeRonne, Beth M</creator><creator>Jensen, Agnes C</creator><creator>Kats, Allyson M</creator><creator>Morasco, Benjamin J</creator><creator>Frank, Joseph W</creator><creator>Makris, Una E</creator><creator>Allen, Kelli D</creator><creator>Naylor, Jennifer C</creator><creator>Mixon, Amanda S</creator><creator>Bohnert, Amy</creator><creator>Reznik, Thomas E</creator><creator>Painter, Jacob T</creator><creator>Hudson, Teresa J</creator><creator>Hagedorn, Hildi J</creator><creator>Manuel, Jennifer K</creator><creator>Borsari, Brian</creator><creator>Purcell, Natalie</creator><creator>Hammett, Patrick</creator><creator>Amundson, Erin C</creator><creator>Kerns, Robert D</creator><creator>Barbosa, Monica R</creator><creator>Garvey, Caitlin</creator><creator>Jones, Elzie J</creator><creator>Noh, Maureen Y</creator><creator>Okere, Jennifer B</creator><creator>Bhushan, Sujata</creator><creator>Pinsonnault, John</creator><creator>Williams, Beth E</creator><creator>Herbst, Ellen</creator><creator>Lagisetty, Pooja</creator><creator>Librodo, Sara</creator><creator>Mapara, Payal S</creator><creator>Son, Elizabeth</creator><creator>Tat, Christina</creator><creator>Marraffa, Rebecca A</creator><creator>Seys, Randy L</creator><creator>Baxley, Catherine</creator><creator>Seal, Karen H</creator><general>American Medical Association</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20241209</creationdate><title>Care Models to Improve Pain and Reduce Opioids Among Patients Prescribed Long-Term Opioid Therapy: The VOICE Randomized Clinical Trial</title><author>Krebs, Erin E ; 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OBJECTIVE: To compare the effects of integrated pain team (IPT) vs pharmacist collaborative management (PCM) on pain and opioid dosage. DESIGN, SETTING, AND PARTICIPANTS: This study was a pragmatic multisite 12-month randomized comparative effectiveness trial with masked outcome assessment. Patients were recruited from October 2017 to March 2021; follow-up was completed June 2022. The study sites were Veterans Affairs primary care clinics. Eligible patients had moderate to severe chronic pain despite long-term opioid therapy (≥20 mg/d for at least 3 months). INTERVENTIONS: IPT involved interdisciplinary pain care planning, visits throughout 12 months with medical and mental health clinicians, and emphasis on nondrug therapies and motivational interviewing. PCM was a collaborative care intervention involving visits throughout 12 months with a clinical pharmacist care manager who conducted structured monitoring and medication optimization. Both interventions provided individualized pain care and opioid tapering recommendations to patients. MAIN OUTCOMES AND MEASURES: The primary outcome was pain response (≥30% decrease in Brief Pain Inventory total score) at 12 months. The main secondary outcome was 50% or greater reduction in opioid daily dosage at 12 months. RESULTS: A total of 820 patients were randomized to IPT (n = 411) or PCM (n = 409). Participants’ mean (SD) age was 62.2 (10.6) years, and 709 (86.5%) were male. A pain response was achieved in 58/350 patients in the IPT group (16.4%) vs 54/362 patients in the PCM group (14.9%) (odds ratio, 1.11 [95% CI, 0.74-1.67]; P = .61). A 50% opioid dose reduction was achieved in 102/403 patients in the IPT group (25.3%) vs 98/399 patients in the PCM group (24.6%) (odds ratio, 1.03 [95% CI, 0.75-1.42]; P = .85). Over 12 months, the mean (SD) Brief Pain Inventory total score improved from 6.7 (1.5) points to 6.1 (1.8) points (P < .001) in IPT and from 6.6 (1.6) points to 6.0 (1.9) points (P < .001) in PCM (between-group P = .82). Over 12 months, mean (SD) opioid daily dosage decreased from 80.8 (74.2) mg/d to 54.2 (65.0) mg/d in IPT (P < .001) and from 74.5 (56.9) mg/d to 52.8 (51.9) mg/d (P < .001) in PCM (between-group P = .22). CONCLUSIONS AND RELEVANCE: Outcomes in this randomized clinical trial did not differ between groups; both had small improvements in pain and substantial reductions in opioid dosage. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03026790</abstract><cop>United States</cop><pub>American Medical Association</pub><pmid>39652356</pmid><doi>10.1001/jamainternmed.2024.6683</doi></addata></record> |
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ispartof | JAMA internal medicine, 2024-12 |
issn | 2168-6106 2168-6114 2168-6114 |
language | eng |
recordid | cdi_pubmed_primary_39652356 |
source | American Medical Association Journals |
title | Care Models to Improve Pain and Reduce Opioids Among Patients Prescribed Long-Term Opioid Therapy: The VOICE Randomized Clinical Trial |
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