Literature Collection

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Grey Literature

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Opioids & SU

The Literature Collection contains over 10,000 references for published and grey literature on the integration of behavioral health and primary care. Learn More

Use the Search feature below to find references for your terms across the entire Literature Collection, or limit your searches by Authors, Keywords, or Titles and by Year, Type, or Topic. View your search results as displayed, or use the options to: Show more references per page; Sort references by Title or Date; and Refine your search criteria. Expand an individual reference to View Details. Full-text access to the literature may be available through a link to PubMed, a DOI, or a URL. References may also be exported for use in bibliographic software (e.g., EndNote, RefWorks, Zotero).

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6901
Patient involvement in developing a patient‐targeted feedback intervention after depression screening in primary care within the randomized controlled trial GET.FEEDBACK.GP
Type: Journal Article
Authors: Tharanya Seeralan, Martin Härter, Cornelia Koschnitzke, Michael Scholl, Sebastian Kohlmann, Marco Lehmann, Marion Eisele, Lea‐Elena Braunschneider, Gabriella Marx, Martin Scherer, Bernd Lowe, Julia Luise Magaard, Anna Levke Brütt
Year: 2021
Topic(s):
Education & Workforce See topic collection
,
Measures See topic collection
6902
Patient navigation for pregnant individuals with opioid use disorder: Results of a randomized multi-site pilot trial
Type: Journal Article
Authors: G. Cochran, M. C. Smid, E. E. Krans, Z. Yu, K. Carlston, A. White, W. Abdulla, J. Baylis, E. Charron, A. Okifugi, A. J. Gordon, B. Lundahl, J. Silipigni, N. Seliski, B. Haaland, R. Tarter
Year: 2024
Topic(s):
Opioids & Substance Use See topic collection
,
Healthcare Disparities See topic collection
6903
Patient navigation for pregnant individuals with opioid use disorder: Results of a randomized multi‐site pilot trial
Type: Journal Article
Authors: Gerald Cochran, Marcela C. Smid, Elizabeth E. Krans, Ziji Yu, Kristi Carlston, Ashley White, Walitta Abdulla, Jacob Baylis, Elizabeth Charron, Akiko Okifugi, Adam J. Gordon, Brad Lundahl, John Silipigni, Natasha Seliski, Benjamin Haaland, Ralph Tarter
Year: 2024
Topic(s):
Healthcare Disparities See topic collection
6904
Patient outcomes associated with primary care behavioral health services: A systematic review
Type: Journal Article
Authors: K. Possemato, E. M. Johnson, G. P. Beehler, R. L. Shepardson, P. King, C. L. Vair, J. S. Funderburk, S. A. Maisto, L. O. Wray
Year: 2018
Publication Place: United States
Abstract: OBJECTIVE: This systematic review focused on Primary Care Behavioral Health (PCBH) services delivered under normal clinic conditions that included the patient outcomes of: 1) access/utilization of behavioral health services, 2) health status, and 3) satisfaction. METHOD: Following PRISMA guidelines, comprehensive database searches and rigorous coding procedures rendered 36 articles meeting inclusion criteria. The principle summary measures of odd ratios or Cohen's d effect sizes were reported. RESULTS: Due to significant limitations in the methodological rigor of reviewed studies, robust findings only emerged for healthcare utilization: PCBH is associated with shorter wait-times for treatment, higher likelihood of engaging in care, and attending a greater number of visits. Several small, uncontrolled studies report emerging evidence that functioning, depression, and anxiety improve overtime. There was no evidence of greater improvement in patient health status when PCBH was compared to other active treatments. The limited available evidence supports that patient satisfaction with PCBH services is high. CONCLUSIONS: The implementation of PCBH services is ahead of the science supporting the usefulness of these services. Patient outcomes for PCBH are weaker than outcomes for Collaborative Care. More rigorous investigations of patient outcomes associated with PCBH are needed to allow for optimization of services.
Topic(s):
General Literature See topic collection
6906
Patient outcomes at 26 months in the patient-centered medical home National Demonstration Project
Type: Journal Article
Authors: C. R. Jaen, R. L. Ferrer, W. L. Miller, R. F. Palmer, R. Wood, M. Davila, E. E. Stewart, B. F. Crabtree, P. A. Nutting, K. C. Stange
Year: 2010
Publication Place: United States
Abstract: PURPOSE: The purpose of this study was to evaluate patient outcomes in the National Demonstration Project (NDP) of practices' transition to patient-centered medical homes (PCMHs). METHODS: In 2006, a total of 36 family practices were randomized to facilitated or self-directed intervention groups. Progress toward the PCMH was measured by independent assessments of how many of 39 predominantly technological NDP model components the practices adopted. We evaluated 2 types of patient outcomes with repeated cross-sectional surveys and medical record audits at baseline, 9 months, and 26 months: patient-rated outcomes and condition-specific quality of care outcomes. Patient-rated outcomes included core primary care attributes, patient empowerment, general health status, and satisfaction with the service relationship. Condition-specific outcomes were measures of the quality of care from the Ambulatory Care Quality Alliance (ACQA) Starter Set and measures of delivery of clinical preventive services and chronic disease care. RESULTS: Practices adopted substantial numbers of NDP components over 26 months. Facilitated practices adopted more new components on average than self-directed practices (10.7 components vs 7.7 components, P=.005). ACQA scores improved over time in both groups (by 8.3% in the facilitated group and by 9.1% in the self-directed group, P <.0001) as did chronic care scores (by 5.2% in the facilitated group and by 5.0% in the self-directed group, P=.002), with no significant differences between groups. There were no improvements in patient-rated outcomes. Adoption of PCMH components was associated with improved access (standardized beta [Sbeta]=0.32, P = .04) and better prevention scores (Sbeta=0.42, P=.001), ACQA scores (Sbeta=0.45, P = .007), and chronic care scores (Sbeta=0.25, P =.08). CONCLUSIONS: After slightly more than 2 years, implementation of PCMH components, whether by facilitation or practice self-direction, was associated with small improvements in condition-specific quality of care but not patient experience. PCMH models that call for practice change without altering the broader delivery system may not achieve their intended results, at least in the short term.
Topic(s):
Medical Home See topic collection
6907
Patient Outcomes Following Opioid Dose Reduction Among Patients with Chronic Opioid Therapy
Type: Journal Article
Authors: S. Hallvik, El Ibrahimi, K. Johnston, J. Gedes, G. Leichtling, P. T. Korthuis, D. Hartung
Year: 2020
Publication Place: Chicago
Topic(s):
Education & Workforce See topic collection
,
Financing & Sustainability See topic collection
,
Healthcare Disparities See topic collection
,
Opioids & Substance Use See topic collection
6908
Patient outcomes from a student-led interprofessional clinic in primary care
Type: Journal Article
Authors: Fiona Kent
Year: 2013
Topic(s):
Education & Workforce See topic collection
6909
Patient Perceptions of Integrating Meditation-based Interventions in Office-based Opioid Treatment with Buprenorphine: A Mixed-methods Survey
Type: Journal Article
Authors: B. Tofighi, C. Marini, J. D. Lee, E. L. Garland
Year: 2023
Topic(s):
Opioids & Substance Use See topic collection
6911
Patient perspectives of an integrated program of medical care and substance use treatment
Type: Journal Article
Authors: M. L. Drainoni, C. Farrell, A. Sorensen-Alawad, J. N. Palmisano, C. Chaisson, A . Y. Walley
Year: 2014
Publication Place: United States
Abstract: The benefits of integrating primary care and substance use disorder treatment are well known, yet true integration is difficult. We developed and evaluated a team-based model of integrated care within the primary care setting for HIV-infected substance users and substance users at risk for contracting HIV. Qualitative data were gathered via focus groups and satisfaction surveys to assess patients' views of the program, evaluate key elements for success, and provide recommendations for other programs. Key themes related to preferences for the convenience and efficiency of integrated care; support for a team-based model of care; a feeling that the program requirements offered needed structure; the importance of counseling and education; and how provision of concrete services improved overall well-being and quality of life. For patients who received buprenorphine/naloxone for opioid dependence, this was viewed as a major benefit. Our results support other studies that theorize integrated care could be of significant value for hard-to-reach populations and indicate that having a clinical team dedicated to providing substance use disorder treatment, HIV risk reduction, and case management services integrated into primary care clinics has the potential to greatly enhance the ability to serve a challenging population with unmet treatment needs.
Topic(s):
General Literature See topic collection
6912
Patient perspectives of barriers to naloxone obtainment and use in a primary care, underserved setting: A qualitative study
Type: Journal Article
Authors: Jennifer Ko, Emily Chan, Shadi Doroudgar
Year: 2021
Publication Place: Philadelphia, Pennsylvania
Topic(s):
Education & Workforce See topic collection
,
Healthcare Disparities See topic collection
,
Opioids & Substance Use See topic collection
6913
Patient perspectives on alcohol use disorder pharmacotherapy and integration of treatment into primary care settings
Type: Journal Article
Authors: S. J. Haley, E. A. Pinsker, H. Gerould, J. P. Wisdom, H. J. Hagedorn
Year: 2019
Publication Place: United States
Abstract: BACKGROUND: Evidence-based pharmacotherapies for alcohol use disorders (AUDs) are underutilized. This mixed-methods study reports supplementary findings from the alcohol use disorder pharmacotherapy and treatment in primary care (ADaPT-PC) implementation study at 3 Veterans Health Administration (VHA) hospital sites to understand why prescription rates did not increase following the ADaPT-PC intervention. METHODS: Qualitative interviews (N = 30) were conducted in advance of the ADaPT-PC intervention to understand patients' pharmacotherapy attitudes among those in AUD treatment, with previous treatment experience, or who needed assistance with their alcohol use. Following the ADaPT-PC intervention, chart reviews from a random sample of patients with AUD or a most recent Alcohol Use Disorders Identification Test consumption questions (AUDIT-C) score >8, and no active AUD prescription, were conducted to determine the frequency of alcohol-related conversations (N = 455). RESULTS: Most interviewed patients welcomed a discussion about their alcohol use and pharmacotherapy. Of the 15 medication-naive patients interviewed, 6 stated that they would be willing to try pharmacotherapy, 5 stated that they were unlikely, 2 identified reservations, 1 said no, and 1 was not asked. Fifteen patients were either currently taking medications (n = 10) or had taken medication in the past (n = 7; 2 patients had past and current experience). Chart reviews indicated that although 66% of charts (n = 299) documented a discussion of their alcohol use with the provider, only 7.5% (n = 22) of individuals with an AUD diagnosis had a documented discussion of AUD pharmacotherapy, and only 5 received pharmacotherapy. CONCLUSION: Most interviewed patients were open to discussing AUD treatment, including discussions of pharmacotherapy, with their provider. From documented conversations about alcohol use to treatment options, medical records suggests a continuous narrowing of the number of patients engaged in alcohol-related consultations. Although some interviewed patients expressed reticence about initiating pharmacotherapy, these findings suggest that the treatment cascade may have a greater influence on the number of pharmacotherapy prescriptions than patients' preferences.
Topic(s):
Opioids & Substance Use See topic collection
6914
Patient perspectives on an opioid overdose education and naloxone distribution program in the U.S. Department of Veterans Affairs
Type: Journal Article
Authors: E. M. Oliva, A. Nevedal, E. T. Lewis, M. D. McCaa, M. F. Cochran, P. E. Konicki, C. S. Davis, C. Wilder
Year: 2016
Publication Place: United States
Abstract: BACKGROUND: In an effort to prevent opioid overdose mortality among Veterans, Department of Veterans Affairs (VA) facilities began implementing opioid overdose education and naloxone distribution (OEND) in 2013 and a national program began in 2014. VA is the first national health care system to implement OEND. The goal of this study is to examine patient perceptions of OEND training and naloxone kits. METHODS: Four focus groups were conducted between December 2014 and February 2015 with 21 patients trained in OEND. Participants were recruited from a VA residential facility in California with a substance use disorder treatment program (mandatory OEND training) and a homeless program (optional OEND training). Data were analyzed using matrices and open and closed coding approaches to identify participants' perspectives on OEND training including benefits, concerns, differing opinions, and suggestions for improvement. RESULTS: Veterans thought OEND training was interesting, novel, and empowering, and that naloxone kits will save lives. Some veterans expressed concern about using syringes in the kits. A few patients who never used opioids were not interested in receiving kits. Veterans had differing opinions about legal and liability issues, whether naloxone kits might contribute to relapse, and whether and how to involve family in training. Some veterans expressed uncertainty about the effects of naloxone. Suggested improvements included active learning approaches, enhanced training materials, and increased advertisement. CONCLUSIONS: OEND training was generally well received among study participants, including those with no indication for a naloxone kit. Patients described a need for OEND and believed it could save lives. Patient feedback on OEND training benefits, concerns, opinions, and suggestions provides important insights to inform future OEND training programs both within VA and in other health care settings. Training is critical to maximizing the potential for OEND to save lives, and this study includes specific suggestions for improving the effectiveness and acceptability of training.
Topic(s):
Opioids & Substance Use See topic collection
6915
Patient perspectives on buprenorphine/naloxone: A qualitative study of retention during the Starting Treatment with Agonist Replacement Therapies (START) Study.
Type: Journal Article
Authors: Cheryl Teruya, Robert P. Schwartz, Shannon Gwin Mitchell, Albert L. Hasson, Christie Thomas, Samantha H. Buoncristiani, Yih-Ing Hser, Katharina Wiest, Allan J. Cohen, Naomi Glick, Petra Jacobs, Paul McLaughlin, Walter Ling
Year: 2014
Topic(s):
Opioids & Substance Use See topic collection
6916
Patient perspectives on community pharmacy administered and dispensing of methadone treatment for opioid use disorder: A qualitative study in the U.S
Type: Journal Article
Authors: Li-Tzy Wu, William S. John, Paolo Mannelli, Eric D. Morse, Alyssa Anderson, Robert P. Schwartz
Year: 2023
Topic(s):
Education & Workforce See topic collection
6917
Patient perspectives on quality of care for depression and anxiety in primary health care teams: A qualitative study
Type: Journal Article
Authors: Rachelle Ashcroft, Matthew Menear, Andrea Greenblatt, Jose Silveira, Simone Dahrouge, Nadiya Sunderji, Monica Emode, Jocelyn Booton, Marvelous Muchenje, Rachel Cooper, Asante Haughton, Kwame McKenzie
Year: 2021
Topic(s):
Education & Workforce See topic collection
6919
Patient predictors and utilization of health services within a medical home for homeless persons
Type: Journal Article
Authors: A. L. Jones, R. Thomas, D. O. Hedayati, S. K. Saba, J. Conley, A. J. Gordon
Year: 2018
Publication Place: United States
Topic(s):
Healthcare Disparities See topic collection
,
Medical Home See topic collection
6920
Patient Preferences for Discussing Childhood Trauma in Primary Care
Type: Journal Article
Authors: E. Goldstein, N. Athale, A. F. Sciolla, S. L. Catz
Year: 2017
Publication Place: United States
Abstract: CONTEXT: Exposure to traumatic events is common in primary care patients, yet health care professionals may be hesitant to assess and address the impact of childhood trauma in their patients. OBJECTIVE: To assess patient preferences for discussing traumatic experiences and posttraumatic stress disorder (PTSD) with clinicians in underserved, predominantly Latino primary care patients. DESIGN: Cross-sectional study. MAIN OUTCOME MEASURE: We evaluated patients with a questionnaire assessing comfort to discuss trauma exposure and symptoms using the Adverse Childhood Experiences (ACE) Study questionnaire and the Primary Care-PTSD screen. The questionnaire also assessed patients' confidence in their clinicians' ability to help with trauma-related issues. Surveys were collected at an integrated medical and behavioral health care clinic. RESULTS: Of 178 adult patients asked, 152 (83%) agreed to participate. Among participants, 37% screened positive for PTSD, 42% reported 4 or more ACEs, and 26% had elevated scores on both measures. Primary Care-PTSD and ACE scores were strongly positively correlated (r = 0.57, p < 0.001). Most patients agreed they were comfortable being asked about trauma directly or through screening questionnaires and did not oppose the inclusion of trauma-related information in their medical record. In addition, most patients perceived their clinician as comfortable asking questions about childhood trauma and able to address trauma-related problems. CONCLUSION: Screening is acceptable to most primary care patients regardless of trauma exposure or positive PTSD screening. Findings may aid primary care clinicians to consider screening regularly for ACEs and PTSD to better serve the health care needs of trauma-exposed patients.
Topic(s):
Education & Workforce See topic collection