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Nurse Care Management for Opioid Use Disorder Treatment: The PROUD Cluster Randomized Clinical Trial.
Wartko, Paige D; Bobb, Jennifer F; Boudreau, Denise M; Matthews, Abigail G; McCormack, Jennifer; Lee, Amy K; Qiu, Hongxiang; Yu, Onchee; Hyun, Noorie; Idu, Abisola E; Campbell, Cynthia I; Saxon, Andrew J; Liu, David S; Altschuler, Andrea; Samet, Jeffrey H; Labelle, Colleen T; Zare-Mehrjerdi, Mohammad; Stotts, Angela L; Braciszewski, Jordan M; Murphy, Mark T; Dryden, Douglas; Arnsten, Julia H; Cunningham, Chinazo O; Horigian, Viviana E; Szapocznik, José; Glass, Joseph E; Caldeiro, Ryan M; Phillips, Rebecca C; Shea, Mary; Bart, Gavin; Schwartz, Robert P; McNeely, Jennifer; Liebschutz, Jane M; Tsui, Judith I; Merrill, Joseph O; Lapham, Gwen T; Addis, Megan; Bradley, Katharine A; Ghiroli, Megan M; Hamilton, Leah K; Hu, Yong; LaHue, Jennifer S; Loree, Amy M; Murphy, Sean M; Northrup, Thomas F; Shmueli-Blumberg, Dikla; Silva, Angela J; Weinstein, Zoe M; Wong, Mark TinFook; Burganowski, Rachael P.
Afiliación
  • Wartko PD; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Bobb JF; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Boudreau DM; Department of Biostatistics, School of Public Health, University of Washington, Seattle.
  • Matthews AG; Kaiser Permanente Washington Health Research Institute, Seattle.
  • McCormack J; Now with Genentech Inc, South San Francisco, California.
  • Lee AK; The Emmes Company, Rockville, Maryland.
  • Qiu H; The Emmes Company, Rockville, Maryland.
  • Yu O; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Hyun N; Now with Kaiser Permanente Washington, Renton.
  • Idu AE; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Campbell CI; Now with Department of Epidemiology and Biostatistics, Michigan State University, East Lansing.
  • Saxon AJ; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Liu DS; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Altschuler A; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Samet JH; Division of Research, Kaiser Permanente Northern California, Oakland.
  • Labelle CT; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco.
  • Zare-Mehrjerdi M; Center of Excellence in Substance Addiction Treatment and Education, VA Puget Sound Health Care System, Seattle, Washington.
  • Stotts AL; National Institute on Drug Abuse Center for Clinical Trials Network, North Bethesda, Maryland.
  • Braciszewski JM; Division of Research, Kaiser Permanente Northern California, Oakland.
  • Murphy MT; Boston University Schools of Medicine and Public Health, Boston Medical Center, Boston, Massachusetts.
  • Dryden D; Boston University Schools of Medicine and Public Health, Boston Medical Center, Boston, Massachusetts.
  • Arnsten JH; Department of Family and Community Medicine, UTHealth Houston McGovern Medical School, Houston, Texas.
  • Cunningham CO; Department of Family and Community Medicine, UTHealth Houston McGovern Medical School, Houston, Texas.
  • Horigian VE; Center for Health Policy and Health Services Research, Henry Ford Health, Detroit, Michigan.
  • Szapocznik J; MultiCare Health System, Tacoma, Washington.
  • Glass JE; MultiCare Health System, Tacoma, Washington.
  • Caldeiro RM; Now with Mosaic Medical, Bend, Oregon.
  • Phillips RC; Montefiore Medical Center, Bronx, New York.
  • Shea M; Albert Einstein College of Medicine, Bronx, New York.
  • Bart G; Albert Einstein College of Medicine, Bronx, New York.
  • Schwartz RP; Now with New York State Office of Addiction Services and Supports, New York.
  • McNeely J; Department of Public Health Sciences, Miller School of Medicine, University of Miami, Miami, Florida.
  • Liebschutz JM; Department of Public Health Sciences, Miller School of Medicine, University of Miami, Miami, Florida.
  • Tsui JI; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Merrill JO; Mental Health and Wellness Department, Kaiser Permanente Washington, Renton.
  • Lapham GT; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Addis M; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Bradley KA; Department of Medicine, Hennepin Healthcare, Minneapolis, Minnesota.
  • Ghiroli MM; Friends Research Institute, Baltimore, Maryland.
  • Hamilton LK; Department of Population Health, Grossman School of Medicine, New York University, New York.
  • Hu Y; Center for Research on Health Care, Division of General Internal Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • LaHue JS; Division of General Internal Medicine, Department of Medicine, University of Washington School of Medicine, Seattle.
  • Loree AM; Division of General Internal Medicine, Department of Medicine, University of Washington School of Medicine, Seattle.
  • Murphy SM; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Northrup TF; Department of Health Systems and Population Health, School of Public Health, University of Washington, Seattle.
  • Shmueli-Blumberg D; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Silva AJ; Kaiser Permanente Washington Health Research Institute, Seattle.
  • Weinstein ZM; Division of General Internal Medicine, Department of Medicine, University of Washington School of Medicine, Seattle.
  • Wong MT; Kaiser Permanente Bernard J Tyson School of Medicine, Pasadena, California.
JAMA Intern Med ; 183(12): 1343-1354, 2023 Dec 01.
Article en En | MEDLINE | ID: mdl-37902748
ABSTRACT
Importance Few primary care (PC) practices treat patients with medications for opioid use disorder (OUD) despite availability of effective treatments.

Objective:

To assess whether implementation of the Massachusetts model of nurse care management for OUD in PC increases OUD treatment with buprenorphine or extended-release injectable naltrexone and secondarily decreases acute care utilization. Design, Setting, and

Participants:

The Primary Care Opioid Use Disorders Treatment (PROUD) trial was a mixed-methods, implementation-effectiveness cluster randomized clinical trial conducted in 6 diverse health systems across 5 US states (New York, Florida, Michigan, Texas, and Washington). Two PC clinics in each system were randomized to intervention or usual care (UC) stratified by system (5 systems were notified on February 28, 2018, and 1 system with delayed data use agreement on August 31, 2018). Data were obtained from electronic health records and insurance claims. An implementation monitoring team collected qualitative data. Primary care patients were included if they were 16 to 90 years old and visited a participating clinic from up to 3 years before a system's randomization date through 2 years after. Intervention The PROUD intervention included 3 components (1) salary for a full-time OUD nurse care manager; (2) training and technical assistance for nurse care managers; and (3) 3 or more PC clinicians agreeing to prescribe buprenorphine. Main Outcomes and

Measures:

The primary outcome was a clinic-level measure of patient-years of OUD treatment (buprenorphine or extended-release injectable naltrexone) per 10 000 PC patients during the 2 years postrandomization (follow-up). The secondary outcome, among patients with OUD prerandomization, was a patient-level measure of the number of days of acute care utilization during follow-up.

Results:

During the baseline period, a total of 130 623 patients were seen in intervention clinics (mean [SD] age, 48.6 [17.7] years; 59.7% female), and 159 459 patients were seen in UC clinics (mean [SD] age, 47.2 [17.5] years; 63.0% female). Intervention clinics provided 8.2 (95% CI, 5.4-∞) more patient-years of OUD treatment per 10 000 PC patients compared with UC clinics (P = .002). Most of the benefit accrued in 2 health systems and in patients new to clinics (5.8 [95% CI, 1.3-∞] more patient-years) or newly treated for OUD postrandomization (8.3 [95% CI, 4.3-∞] more patient-years). Qualitative data indicated that keys to successful implementation included broad commitment to treat OUD in PC from system leaders and PC teams, full financial coverage for OUD treatment, and straightforward pathways for patients to access nurse care managers. Acute care utilization did not differ between intervention and UC clinics (relative rate, 1.16; 95% CI, 0.47-2.92; P = .70). Conclusions and Relevance The PROUD cluster randomized clinical trial intervention meaningfully increased PC OUD treatment, albeit unevenly across health systems; however, it did not decrease acute care utilization among patients with OUD. Trial Registration ClinicalTrials.gov Identifier NCT03407638.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Buprenorfina / Trastornos Relacionados con Opioides Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Intern Med Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Buprenorfina / Trastornos Relacionados con Opioides Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Intern Med Año: 2023 Tipo del documento: Article