Patient Perspectives on Adapting Collaborative Care for Opioid Use Disorder With Depression and/or Post-traumatic Stress Disorder

被引:0
|
作者
Leamon, Isabel M. [1 ]
Jacobsohn, Vanessa [2 ]
Dopp, Alex R. [1 ]
Hindmarch, Grace [1 ]
Ceballos, Venice [2 ]
Komaromy, Miriam [3 ]
Watkins, Katherine E. [1 ]
Osilla, Karen Chan [4 ]
机构
[1] RAND, Santa Monica, CA USA
[2] Univ New Mexico, Dept Psychiat & Behav Sci, Sch Med, Albuquerque, NM USA
[3] Boston Univ, Grayken Ctr Addict, Boston Med Ctr, Boston, MA USA
[4] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, 401 Quarry Rd, Palo Alto, CA 94305 USA
关键词
Community health research; Community-based participatory research; Opioid use disorder; Patient partners; Collaborative care; Primary care; ALCOHOL-USE DISORDERS; QUALITY IMPROVEMENT; SUBSTANCE USE; MINORITY PATIENTS; IMPROVING CARE; MEDICAL-CARE; LOW-INCOME; VETERANS; PEOPLE; INTERVENTIONS;
D O I
10.1353/cpr.2024.a937390
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Individuals with opioid use disorder and cooccurring mental health concerns experience heightened consequences and lower rates of treatment access. Engaging patients as research partners alongside health systems is critical for tailoring care for this population. Collaborative care is promising for the treatment of co-occurring disorders Objectives: We used a community-participatory partnered research1 1 approach to partner with patients, providers, and clinic administrators to adapt and implement a collaborative care intervention for co-occurring disorders in primary care. Methods: We conducted qualitative interviews with patients to assess their feedback on the proposed collaborative care model before intervention implementation. A first round of interviews was conducted to obtain patient feedback on our adaptation ideas (n = 11). The team then incorporated these suggestions, beta-tested the intervention with participants (n = 9), and assessed participant feedback. Data were analyzed using rapid content analysis and then implemented by health systems. Results: Patient feedback underscored the need for the care coordinator (CC) to be trained in patient engagement and stigma reduction and to provide assistance around socioeconomic barriers and relapse. Patients shared that it was helpful to have the CC address co-occurring disorders, emphasized the need for the CC to be flexible, and expressed that telehealth was acceptable. Patient feedback was integrated in subsequent CC training with health systems. Conclusions: The present research demonstrates the feasibility and usefulness of incorporating patient perspectives into treatment design and implementation in health systems using community-participatory partnered research .
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页数:14
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