Literature Collection

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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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12581 Results
8161
Patient, Program, and System Barriers and Facilitators to Detoxification Services in the U.S. Veterans Health Administration: A Qualitative Study of Provider Perspectives
Type: Journal Article
Authors: Nicole R. Schultz, Rociel Martinez, Michael A. Cucciare, Christine Timko
Year: 2016
Publication Place: New York
Topic(s):
Healthcare Disparities See topic collection
,
Opioids & Substance Use See topic collection
8162
Patients Charting the Course: Citizen Engagement and the Learning Health System: Workshop Summary
Type: Government Report
Authors: Institute of Medicine, LeighAnne Olsen, Robert S. Saunders, Michael McGinnis
Year: 2011
Publication Place: Washington, DC
Abstract: As past, current, or future patients, the public should be the health care system's unwavering focus and serve as change agents in its care. Taking this into account, the quality of health care should be judged not only by whether clinical decisions are informed by the best available scientific evidence, but also by whether care is tailored to a patient's individual needs and perspectives. However, too often it is provider preference and convenience, rather than those of the patient, that drive what care is delivered. As part of its Learning Health System series of workshops, the Roundtable on Value & Science-Driven Health Care hosted a workshop to assess the prospects for improving health and lowering costs by advancing patient involvement in the elements of a learning health system.
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.

8163
Patients use the internet to enter the medical home
Type: Journal Article
Authors: J. H. Wasson, R. Benjamin, D. Johnson, L. G. Moore, T. Mackenzie
Year: 2011
Publication Place: United States
Abstract: There is a large gap between the promise of patient-centered medical home (PCMH) and our current capacity to define and measure it. The purpose of this article is to describe the findings of "real-time" patient-reported data about constructs of the PCMH and to demonstrate how an Internet-based method can be useful for obtaining patient report about the PCMH. We find that patients' Internet ratings seem stable and demonstrate relationships that fit constructs and models for the PCMH. We also find that current PCMH performance across this sample of 69 clinical settings is highly variable and still leaves a great deal of room for improvement.
Topic(s):
Medical Home See topic collection
8164
Patients who somatize in primary care: a longitudinal study of cognitive and social characteristics
Type: Journal Article
Authors: L. J. Kirmayer, J. M. Robbins
Year: 1996
Topic(s):
Medically Unexplained Symptoms See topic collection
8166
Patients With Mental Health Needs Are Engaged In Asking Questions, But Physicians' Responses Vary
Type: Journal Article
Authors: M. Tai-Seale, P. K. Foo, C. D. Stults
Year: 2013
Topic(s):
Education & Workforce See topic collection
8167
Patients With OUD Are Patients
Type: Web Resource
Year: 2018
Topic(s):
Grey Literature See topic collection
,
Opioids & Substance Use 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.

8168
Patients with persistent medically unexplained symptoms in general practice: characteristics and quality of care
Type: Journal Article
Authors: A. J. Dirkzwager, P. F. Verhaak
Year: 2007
Publication Place: England
Abstract: BACKGROUND: Medically unexplained physical symptoms (MUPS) are common in general practice (GP), and are even more problematic as they become persistent. The present study examines the relationship between persistent MUPS in general practice on the one hand and quality of life, social conditions, and coping on the other hand. Additionally, it is examined how patients with persistent MUPS evaluate the quality of GP-care. METHODS: Data were used from a representative survey of morbidity in Dutch general practice, in which data from the electronic medical records were extracted. A random sample of patients participated in an extensive health interview and completed self-reported measures on social isolation, coping and the quality of GP-care. Patients with persistent MUPS (N = 192) were compared with general practice patients not meeting the criteria for persistent MUPS (N = 7.314), and with a group of patients that visited the GP in comparable rates for medical diagnoses (N = 2.265). Multiple logistic regression analyses were used to control for relevant socio-demographic variables and chronic diseases. RESULTS: After adjustment for demographics and chronic diseases, patients with persistent MUPS reported more psychological distress, more functional impairment, more social isolation, and they evaluated the quality of GP-care less positive than the other two patient groups. Although the majority of MUPS patients were positive about the quality of GP-care, they more often felt that they were not taken seriously or not involved in treatment decisions, and more often reported that the GP did not take sufficient time. The three groups did not differ with respect to the statement that the GP unnecessarily explains physical problems as psychological ones. CONCLUSION: Strengthening MUPS patients' social network and encouraging social activities may be a meaningful intervention in which the GP may play a stimulating role. To further improve MUPS patients' satisfaction with GP-care, GPs may pay extra attention to taking sufficient time when treating MUPS patients, taking the problems seriously, and involving them in treatment decisions.
Topic(s):
Medically Unexplained Symptoms See topic collection
8169
Patients, Providers, And Systems Need To Acquire A Specific Set Of Competencies To Achieve Truly Patient-Centered Care
Type: Journal Article
Authors: E. Bernabeo, E. S. Holmboe
Year: 2013
Topic(s):
General Literature See topic collection
8170
Patients' and Therapists' Views of Integrated Online CBT for Depression
Type: Journal Article
Authors: F. Fox, N. Wiles, D. Kessler, D. Tallon, L. Thomas, C. Williams, R. Shafran, P. Lanham, K. Turner
Year: 2024
Topic(s):
HIT & Telehealth See topic collection
8171
Patients' experience of being triaged directly to a psychologist in primary care: a qualitative study
Type: Journal Article
Authors: L. Dahlof, A. Simonsson, J. Thorn, M. E. Larsson
Year: 2014
Publication Place: England
Abstract: BACKGROUND: In a primary health-care centre (PHCC) situated in a segregated area with low socio-economic status, 'primary care triage' has increased efficiency and accessibility. In the primary-care triage, the nurse sorts the patient to the appropriate PHCC profession according to described symptoms. Aim The aim of this study was to examine the patients' experience of being triaged directly to a psychologist for assessment. METHOD: Interviews were conducted with 20 patients and then analysed using qualitative content analysis. FINDINGS: The results show that patients contacting the PHCC for mental health issues often are active agents with their own intent to see a psychologist, not a doctor, as a first-hand choice when contacting the PHCC. Seeking help for mental health issues is described as a sensitive issue that demands building up strength before contacting. The quick access to the preferred health-care professional is appreciated. The nurse was perceived as a caring facilitator rather than a decision maker. It is the patient's wish rather than the symptoms that directs the sorting. The patients' expectations when meeting the psychologist were wide and diverse. The structured assessment sometimes collided and sometimes united with these expectations, yielding different outcome satisfaction. The results could be seen in line with the present goal to increase patients' choice in the health-care system. The improved accessibility to the psychologist seems to meet community expectations. The results also indicate a need for providing more prior information about the assessment and potential outcomes.
Topic(s):
Education & Workforce See topic collection
,
Healthcare Disparities See topic collection
8172
Patients' experience of being triaged directly to a psychologist in primary care: A qualitative study.
Type: Journal Article
Authors: Linda Dahlof, Anna Simonsson, Jorgen Thorn, Maria EH Larsson
Year: 2014
Topic(s):
Healthcare Disparities See topic collection
,
Education & Workforce See topic collection
8173
Patients' experiences of seeking help for emotional concerns in primary care: doctor as drug, detective and collaborator
Type: Journal Article
Authors: Daisy Parker, Richard Byng, Chris Dickens, Rose McCabe
Year: 2020
Topic(s):
Education & Workforce See topic collection
,
Healthcare Disparities See topic collection
8175
Patients' perspectives of barriers and facilitators to accessing support through primary care for common mental health problems in England: A systematic review
Type: Journal Article
Authors: A. Tunks, C. Berry, C. Strauss, P. Nyikavaranda, E. Ford
Year: 2023
Topic(s):
Healthcare Disparities See topic collection
8176
Patients' readiness to receive psychosocial care during nurse-led routine diabetes consultations in primary care: A mixed methods study
Type: Journal Article
Authors: Anneke van Dijk- de Vries, Marloes A. van Bokhoven, Sabine de Jong, Job F. M. Metsemakers, Peter F. M. Verhaak, der Weijden van, Jacques Th. M. van Eijk
Year: 2016
Publication Place: Philadelphia, Pennsylvania
Topic(s):
General Literature See topic collection
8177
Patients' reasons for declining a primary care trial online therapy: a mixed methods study
Type: Journal Article
Authors: F. Fox, D. Tallon, R. Shafran, P. Lanham, C. Williams, B. Jude, N. Wiles, D. Kessler, K. Turner
Year: 2025
Abstract:

BACKGROUND: Integrating therapist-led sessions and Cognitive Behavioural Therapy (CBT) materials within one online platform may be effective for people with depression. A trial evaluating this mode of delivering CBT is being conducted. To maximize future trial recruitment and understand patients' views of health interventions, it is important to explore reasons for declining to participate. AIM: To explore patients' reasons for declining to participate in a trial of integrated online CBT for depression. DESIGN & SETTING: A mixed methods study collecting data from patients via questionnaires and telephone interviews at the three UK trial sites. METHOD: Individuals completed a short questionnaire about their reasons for not taking part in the trial. Telephone interviews further explored these reasons with a sub-group. Quantitative data were summarized using descriptive statistics. Qualitative interviews were analysed thematically. RESULTS: Of 1799 patients who responded to an invitation to participate in the trial, 40.3% declined contact. The most common reasons were not wanting: to take part in research (n=387); therapy provided online (n=284); to receive CBT (n=262). Qualitative interviews with 15 'decliners' highlighted that decisions related to perceptions of eligibility, previous experiences of CBT and uncertainty about receiving CBT online. Personal circumstances, depressive symptoms or other mental health issues were also barriers to participation. CONCLUSION: Reasons given by primary care patients for not taking part in a trial of integrated online CBT suggest that, at the point of recruitment, it is important to discuss the patient's perceptions of their eligibility and whether they would accept the intervention being evaluated.

Topic(s):
HIT & Telehealth See topic collection
8178
Patients’ expectations for and experiences with primary healthcare services received from a patient centered medical home
Type: Journal Article
Authors: Janet Reis, Dawn Juker, Molly Volk, Chelsea Stevenson
Year: 2020
Topic(s):
Medical Home See topic collection
8180
Patterns and correlates of polysubstance use among US youth aged 15-17 years: wave 1 of the Population Assessment of Tobacco and Health (PATH) Study
Type: Journal Article
Authors: M. L. Silveira, V. R. Green, R. Iannaccone, H. L. Kimmel, K. P. Conway
Year: 2019
Abstract:

BACKGROUND AND AIMS: Youth aged 15-17 years are at high risk of tobacco, alcohol and drug use. Given the changing landscape with respect to availability, use of emerging products and regulatory environments, we examined patterns and correlates of polysubstance use among US youth aged 15-17 years. DESIGN: Cross-sectional self-reported data. SETTING: United States. PARTICIPANTS: A total of 6127 US youth aged 15-17 years from wave 1 (2013-14) of the nationally representative Population Assessment of Tobacco and Health (PATH) Study. MEASUREMENTS: Latent class analysis was used to identify subgroups of polysubstance use, including 12 tobacco products, alcohol, marijuana, prescription drugs and other drugs. Socio-demographic characteristics, residence in urban area, sensation-seeking, sexual orientation and internalizing and externalizing problems were examined as correlates. FINDINGS: Approximately 43.5% of 15-17-year-olds had used at least one substance in the past 12 months. A 5-class model was identified: class 1 'abstainers' (67.3%), class 2 'alcohol users' (19.2%), class 3 'alcohol, marijuana and tobacco (AMT(predominant AM) ) users' (8.2%), class 4 'alcohol, marijuana and tobacco (AMT(predominant T) ) users' (3.9%) and class 5 'alcohol, marijuana, tobacco and other drug (AMTOD) users' (1.4%). Abstainers were considered the reference class. Higher sensation-seeking scores, higher age and lower academic grades were each associated with greater likelihood of membership in all user classes. Gender, race/ethnicity, parents/guardians' education, residence in non-urban areas and sexual minority groups were associated with membership in some, but not all, user classes. Compared with no/low/moderate severity, high severity internalizing problems were associated with membership in classes 2, 3 and 5, whereas high severity externalizing problems were associated with membership in classes 3 and 5 only. CONCLUSIONS: There appear to be three heterogeneous polysubstance use classes among US youth aged 15-17 years. Correlates of substance use among US youth include higher sensation-seeking, poor academic performance, non-urban residence, minority sexual orientation and mental health problems.

Topic(s):
Healthcare Disparities See topic collection
,
Opioids & Substance Use See topic collection