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Opioids & SU

The Literature Collection contains over 11,000 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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11248 Results
7161
Patient experience of an integrated care model in a family practice clinic & FQHC
Type: Journal Article
Authors: A. N. Koehler, L. E. Sudano, E. Ip, S. W. Davis, G. S. Marion, J. K. Kirk
Year: 2020
Publication Place: United States
Abstract:

In order to investigate the patient experience of integrated behavioral health care in primary care settings, we implemented a patient cohort model from a combined site sample (N = 727) consisting of a family practice clinic and a Federally Qualified Health Center. Patient experience was measured using 12 questions from a validated measure, the Agency for Healthcare Research and Quality's Consumer Assessment of Health Care Providers and Systems (CAHPS®), Home and Community Based Services version, and six additional questions about interactions with an integrated behavioral health care team. We assessed bivariate relationships between satisfaction with integration and the clinic practice and self-reported physical health or self-reported mental/emotional health. We also utilized multiple regression to evaluate this relationship. Our analyses showed a statistically significant and small to moderate direct correlation between patients' self-reported health (both physical and mental/emotional health) and their ratings of the practice as a whole (p = .0003), such that patients who rated their physical and/or mental/emotional health as better were more likely to rate their overall satisfaction with the practice higher. The results of this study suggest that primary care patients with only mild to moderate health conditions (physical and/or mental/emotional) may experience greater satisfaction with integrated behavioral health care than patients with multiple and/or severe health conditions. In contrast, patients with multiple and/or severe health conditions may experience lower satisfaction with integrated behavioral health care and may be better served through higher levels of care.

Topic(s):
Education & Workforce See topic collection
,
Healthcare Disparities See topic collection
,
Measures See topic collection
7163
Patient experiences in behavioral health integrated primary care settings: the role of stigma in shaping patient outcomes over time
Type: Journal Article
Authors: Royal Kenton, L. Broffman, K. Jones, Albrecht Mcmenamin, M. Weller, K. Brown, J. Currier, B. Wright
Year: 2019
Publication Place: England
Abstract: Behavioral health integration (BHI) models seek to improve patient experience and outcomes by bridging physical and behavioral health services. Past BHI research has not focused on stigma in these settings, which has been previously found to impact patient engagement and outcomes. We surveyed patients over a two year period at 12 integrated clinics in Oregon using measures developed by a Patient Advisory Team. Over a quarter of respondents reported stigmatization (26.81%). Compared to non-stigmatized patients, those who reported stigma had five times the odds of reporting unmet health needs (OR=5.14, p<0.0001), three times the odds reporting issues accessing care (OR=2.93, p<0.0001), six times the odds reporting hassle to get care (OR=6.49, p<0.0001), and three times the odds of reporting poor communication between providers (OR=3.45, p<0.0001). After examining the interaction between stigmatization and time, we found that stigmatized patients had lower odds at year two of reporting unmet health needs (OR=0.68, p=0.0034), issues accessing care (OR=0.77, p=0.0400), hassle getting care (OR=0.57, p=0.0001), and poor provider communication (OR=0.77, p=0.0544). We found that stigma remained prevalent for patients seeking care in the integrated clinics studied despite integration. Systems should consider integration efforts and reducing stigmatizing experiences in tandem to truly improve patient outcomes.
Topic(s):
General Literature See topic collection
7164
Patient experiences of COVID-19-induced changes to methadone treatment in a large community-based opioid treatment program in Baltimore
Type: Journal Article
Authors: T. M. Abidogun, T. O. Cole, E. Massey, M. Kleinman, A. D. Greenblatt, C. J. Seitz-Brown, J. F. Magidson, A. M. Belcher
Year: 2023
7165
Patient experiences of methadone treatment changes during the first wave of COVID-19: a national community-driven survey
Type: Journal Article
Authors: S. Brothers, A. Palayew, C. Simon, A. Coulter, K. Strichartz, N. Voyles, L. Vincent
Year: 2023
Topic(s):
Opioids & Substance Use See topic collection
,
Financing & Sustainability See topic collection
7166
Patient experiences with a primary care medical home tailored for people with serious mental illness
Type: Journal Article
Authors: A. A. Bergman, E. T. Chang, A. N. Cohen, S. Hovsepian, R. S. Oberman, M. Vinzon, A. S. Young
Year: 2023
Topic(s):
Healthcare Disparities See topic collection
,
Medical Home See topic collection
7167
Patient Health Questionnaire (PHQ-9)
Type: Report
Year: 2005
Publication Place: Washington, D.C.
Topic(s):
Grey Literature See topic collection
Disclaimer:

This grey literature reference is included in the Academy's Literature Collection in keeping with our mission to gather all sources of information on integration. Grey literature is comprised of materials that are not made available through traditional publishing avenues. Often, the information from unpublished resources can be limited and the risk of bias cannot be determined.

7168
Patient Health Questionnaire Modified for Teens (PHQ-9)
Type: Report
Authors: R. L. Spitzer, K. Kroenke, J. B. W. Williams
Year: 2010
Publication Place: Columbia University
Topic(s):
Grey Literature See topic collection
Disclaimer:

This grey literature reference is included in the Academy's Literature Collection in keeping with our mission to gather all sources of information on integration. Grey literature is comprised of materials that are not made available through traditional publishing avenues. Often, the information from unpublished resources can be limited and the risk of bias cannot be determined.

7169
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
7170
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
7171
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
7172
Patient navigation models for mental health of parents expecting or caring for an infant or young child: A systematic review
Type: Journal Article
Authors: S. A. Harris, M. Harrison, K. Hazell-Raine, C. Wade, V. Eapen, J. Kohlhoff
Year: 2023
Topic(s):
Healthcare Disparities See topic collection
7173
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
7175
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
7176
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
7177
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
7178
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
7180
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