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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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101
Lexicon for Behavioral Health and Primary Care Integration
Type: Government Report
Authors: C. J. Peek, National Integration Academy Council
Year: 2013
Publication Place: Rockville, MD
Topic(s):
Healthcare Policy See topic collection
,
Key & Foundational See topic collection
,
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 Often, the information from unpublished resources can be limited and the risk of bias cannot be determined.

102
Lexicon for Behavioral Health and Primary Care Integration: Executive Summary
Type: Government Report
Authors: C. J. Peek, National Integration Academy Council
Year: 2013
Publication Place: Rockville, MD
Topic(s):
Healthcare Policy See topic collection
,
Key & Foundational See topic collection
,
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 Often, the information from unpublished resources can be limited and the risk of bias cannot be determined.

103
Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Results from the National Comorbidity Survey
Type: Journal Article
Authors: R. C. Kessler, K. A. McGonagle, S. Zhao, C. B. Nelson, M. Hughes, S. Eshleman, H. U. Wittchen, K. S. Kendler
Year: 1994
Publication Place: UNITED STATES
Abstract: BACKGROUND: This study presents estimates of lifetime and 12-month prevalence of 14 DSM-III-R psychiatric disorders from the National Comorbidity Survey, the first survey to administer a structured psychiatric interview to a national probability sample in the United States. METHODS: The DSM-III-R psychiatric disorders among persons aged 15 to 54 years in the noninstitutionalized civilian population of the United States were assessed with data collected by lay interviewers using a revised version of the Composite International Diagnostic Interview. RESULTS: Nearly 50% of respondents reported at least one lifetime disorder, and close to 30% reported at least one 12-month disorder. The most common disorders were major depressive episode, alcohol dependence, social phobia, and simple phobia. More than half of all lifetime disorders occurred in the 14% of the population who had a history of three or more comorbid disorders. These highly comorbid people also included the vast majority of people with severe disorders. Less than 40% of those with a lifetime disorder had ever received professional treatment, and less than 20% of those with a recent disorder had been in treatment during the past 12 months. Consistent with previous risk factor research, it was found that women had elevated rates of affective disorders and anxiety disorders, that men had elevated rates of substance use disorders and antisocial personality disorder, and that most disorders declined with age and with higher socioeconomic status. CONCLUSIONS: The prevalence of psychiatric disorders is greater than previously thought to be the case. Furthermore, this morbidity is more highly concentrated than previously recognized in roughly one sixth of the population who have a history of three or more comorbid disorders. This suggests that the causes and consequences of high comorbidity should be the focus of research attention. The majority of people with psychiatric disorders fail to obtain professional treatment. Even among people with a lifetime history of three or more comorbid disorders, the proportion who ever obtain specialty sector mental health treatment is less than 50%. These results argue for the importance of more outreach and more research on barriers to professional help-seeking.
Topic(s):
Key & Foundational See topic collection
104
Long-term cost effects of collaborative care for late-life depression
Type: Journal Article
Authors: J. Unutzer, W. J. Katon, M . Y. Fan, M. C. Schoenbaum, E. H. Lin, R. D. Della Penna, D. Powers
Year: 2008
Publication Place: United States
Abstract: OBJECTIVE: To determine the long-term effects on total healthcare costs of the Improving Mood: Promoting Access to Collaborative Treatment (IMPACT) program for late-life depression compared with usual care. STUDY DESIGN: Randomized controlled trial with enrollment from July 1999 through August 2001. The IMPACT trial, conducted in primary care practices in 8 delivery organizations across the United States, enrolled 1801 depressed primary care patients 60 years or older. Data are from the 2 IMPACT sites for which 4-year cost data were available. Trial enrollment across these 2 health maintenance organizations was 551 patients. METHODS: Participants were randomly assigned to the IMPACT intervention (n = 279) or to usual primary care (n = 272). Intervention patients had access to a depression care manager who provided education, behavioral activation, support of antidepressant medication management prescribed by their regular primary care provider, and problem-solving treatment in primary care for up to 12 months. Care managers were supervised by a psychiatrist and a primary care provider. The main outcome measures were healthcare costs during 4 years. RESULTS: IMPACT participants had lower mean total healthcare costs ($29 422; 95% confidence interval, $26 479-$32 365) than usual care patients ($32 785; 95% confidence interval, $27 648-$37 921) during 4 years. Results of a bootstrap analysis suggested an 87% probability that the IMPACT program was associated with lower healthcare costs than usual care. CONCLUSION: Compared with usual primary care, the IMPACT program is associated with a high probability of lower total healthcare costs during a 4-year period.
Topic(s):
Financing & Sustainability See topic collection
,
Key & Foundational See topic collection
105
Making room for mental health in the medical home
Type: Journal Article
Authors: M. F. Hogan, L. I. Sederer, T. E. Smith, I. R. Nossel
Year: 2010
Publication Place: United States
Abstract: Discussions of health care reform emphasize the need for coordinated care, and evidence supports the effectiveness of medical home and integrated delivery system models. However, mental health often is left out of the discussion. Early intervention approaches for children and adolescents in primary care are important given the increased rates of detection of mental illness in youth. Most adults also receive treatment for mental illness from nonspecialists, underscoring the role for mental health in medical home models. Flexible models for coordinated care are needed for people with serious mental illness, who have high rates of comorbid medical problems. Programs implemented in the New York State public mental health system are examples of efforts to better coordinate medical and mental health services.
Topic(s):
Key & Foundational See topic collection
,
Medical Home See topic collection
,
Healthcare Policy See topic collection
106
Mass. report finds integrated care crucial to federal HC reform
Type: Journal Article
Year: 2011
Topic(s):
Healthcare Policy See topic collection
,
Key & Foundational See topic collection
107
Measuring integrated care
Type: Journal Article
Authors: M. Strandberg-Larsen
Year: 2011
Publication Place: Denmark
Abstract: The positive outcomes of coordination of healthcare services are to an increasing extent becoming clear. However the complexity of the field is an inhibiting factor for vigorously designed trial studies. Conceptual clarity and a consistent theoretical frame-work are thus needed. While researchers respond to these needs, patients and providers face the multiple challenges of today's healthcare environment. Decision makers, planners and managers need evidence based policy options and information on the scope of the integrated care challenges they are facing. The US managed care organization Kaiser Permanente has been put forward as an example for European healthcare systems to follow, although the evidence base is far from conclusive. The thesis has five objectives: 1) To contribute to the understanding of the concept of integration in healthcare systems and to identify measurement methods to capture the multi-dimensional aspects of integrated healthcare delivery. 2) To assess the level of integration of the Danish healthcare system. 3) To assess the use of joint health plans as a tool for coordination between the regional and local level in the Danish healthcare system. 4) To compare the inputs and performance of the Danish healthcare system and the managed care organization Kaiser Permanente, California, US. 5) To compare primary care clinicians' perception of clinical integration in two healthcare systems: Kaiser Permanente, Northern California and the Danish healthcare system. Further to examine the associations between specific organizational factors and clinical integration within each system. The literature was systematically searched to identify methods for measurement of integrated healthcare delivery. A national cross-sectional survey was conducted among major professional stake-holders at five different levels of the Danish healthcare system. The survey data were used to allow for analysis of the level of integration achieved. Data from the survey were additionally used to investigate the use of joint health planning as a tool for coordination of regional-local healthcare delivery. Analysis of secondary data from the Danish healthcare system and Kaiser Permanente, California were used to compare population characteristics, professional staff, delivery structure, utilisation, quality measures and direct costs. A cross-sectional survey among primary care clinicians in Denmark and in Kaiser Permanente, Northern California was completed to allow for comparison of clinical integration in the two systems and system specific associated factors. In this thesis a conceptual framework and a model for assessment of the conditions for integrations as an intermediate healthcare system outcome are presented. Furthermore, the results show that integrated healthcare delivery can be measured: 24 methods are available and some are highly developed. However, the field is still in its early phase and guidelines for how to proceed are devised. It was confirmed on a national level that integration of care is a widespread challenge, and that only half or less than half of patients in need of integrated services receive such care. Options for decision makers and managers are discussed. From a theoretical perspective joint health plans as applied in Denmark do not match the degree of complexity in the healthcare system. It was therefore in agreement with the theoretical findings when major stakeholders agreed that the joint health plans had not been effective as a tool for coordination. Joint health planning processes should actively engage all stakeholders and a high degree of recurrent feedback are warranted. When comparing Kaiser Permanente, California with the Danish healthcare system, our study suggest that Kaiser Permanente has a population with more documented disease and higher operating costs, and performs better than the Danish healthcare system on the observed quality measures. Substantial differences were found in the perception of clinical integration in the two settings. More primary care clinicians in the Northern California region of Kaiser Permanente reported being part of a clinical integrated environment than did Danish general practitioners. By measuring the level of clinical integration in Kaiser Permanente using the Danish healthcare system as a point of reference our findings support the literature that points to the importance of integrated healthcare delivery as a driver for the performance results of Kaiser Permanente. However caution must be advised before making concrete conclusions due to the complexity of the matter and until more studies have been conducted. With this thesis an initial step has been taken into a new research field. Ongoing research will make it possible to deliver the evidence needed by decision makers, planners and managers - ultimately to benefit the patients.
Topic(s):
HIT & Telehealth See topic collection
,
Key & Foundational See topic collection
108
Medications for Opioid Use Disorder Save Lives
Type: Report
Authors: National Academies of Sciences, Engineering, and Medicine
Year: 2019
Topic(s):
Grey Literature See topic collection
,
Key & Foundational 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.

109
Mending Missouri's safety net: Transforming systems of care by integrating primary and behavioral health care
Type: Journal Article
Authors: Dorn Schuffman, Benjamin G. Druss, Joseph J. Parks
Year: 2009
Publication Place: US: American Psychiatric Assn
Topic(s):
Financing & Sustainability See topic collection
,
Key & Foundational See topic collection
110
Mental Health: A report of the Surgeon General
Type: Government Report
Authors: U.S. Department of Health and Human Services
Year: 1999
Publication Place: Rockville, MD
Topic(s):
Grey Literature See topic collection
,
Key & Foundational 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.

111
Mental Health: Culture, race, and ethnicity. A supplement to mental health: A report to the surgeon general
Type: Government Report
Authors: U.S. Department of Health and Human Services
Year: 2001
Publication Place: Rockville, MD
Topic(s):
Grey Literature See topic collection
,
Healthcare Disparities See topic collection
,
Key & Foundational 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.

112
Mental healthcare in the primary care setting: A paradigm problem
Type: Journal Article
Authors: Frank V. deGruy
Year: 1997
Publication Place: Inc.; Systems, & Health
Topic(s):
Key & Foundational See topic collection
,
Healthcare Policy See topic collection
113
MHIP - The Clinical Model
Type: Web Resource
Authors: Mental Health Integration Program
Year: 2009
Topic(s):
Key & Foundational See topic collection
,
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.

114
Models of integrated care
Type: Journal Article
Authors: L. R. Wulsin, W. Sollner, H. A. Pincus
Year: 2006
Topic(s):
Key & Foundational See topic collection
115
National Models of Integrated Healthcare: The Four Quadrant Model In Washtenaw County, Michigan
Type: Web Resource
Authors: K. Reynolds
Year: 2008
Topic(s):
Key & Foundational See topic collection
,
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.

116
No-show rates in partially integrated models of behavioral health care in a primary care setting
Type: Journal Article
Authors: T. P. Guck, A. J. Guck, A. B. Brack, D. R. Frey
Year: 2007
Publication Place: URL
Topic(s):
Financing & Sustainability See topic collection
,
Key & Foundational See topic collection
119
Patient-centered health care : achieving co-ordination, communication and innovation
Type: Book
Authors: Mary Keating, Aoife McDermott, Kathleen Montgomery
Year: 2013
Abstract: There are four core themes developed in "Patient-Centred Health Care" which deal with critical issues, models, theories and frameworks (both theoretical and empirical) that expound understandings of patient centred care and the processes, practices and behaviours supporting its attainment: 1. Conceptions and cultures of patient-centred care 2. Coordinating for care 3. Communicating for care 4. Innovations in patient centred care and the patient experience. Section 1 of this book sets out the origins of the approach of patient centredness, allowing the reader to recognise what this means and looks like, institutionally and educationally, as well as recognising the implications of its absence. Section 2 concentrates on the process of team working itself which may be patient centred but is also involved with co-operation and co-ordination across professional and organisational boundaries. Section 3 focuses on communication within, between and across patients and teams, and Section 4 highlights the innovations in patient centred care that will enable further progress in the field. In each section,the editors illuminate key issues through a case-study of a relevant intervention to support patient-centred care.; Conceptions and Cultures of Patient-Centred Care -- 1. Developments in conceptions of patient-centred care: implementation challenges in the context of high-risk therapy -- 2. The Continuum of Resident Centered Care in U.S. Nursing Homes -- 3. Reconceptualising institutional abuse: Formulating problems and solutions in residential care. -- 4. The place of patient-centred care in medical professional culture: a qualitative study -- Coordinating for Patient centred Care -- 5. Capacity for care: meta-ethnography of acute care nurses' experiences of the nurse-patient relationship -- 6. Creating an enriched environment of care for older people, staff and family carers: Relational practice and organisational culture change in health and social care -- 7. Promoting patient-centred healthcare: an empirically-derived organisational model of interprofessional collaboration -- 8. From a project team to a community of practice? An exploration of boundary and identity in the context of healthcare collaboration -- Communication in Patient-Centred Care -- 9. Is poor quality of care built into the system? 'Routinising' clinician communication as an essential element of care quality. -- 10. Giving Voice in a Multi-voiced Environment: The challenges of palliative care policy implementation in acute care -- 11. Rejections of treatment recommendations through humour -- 12. An expanded shared decision-making model for interprofessional settings -- Innovations in Patient Centred Care -- 13. Testing accelerated experience-based co-design: using a national archive of patient experience narrative interviews to promote rapid patient-centred service improvement. -- 14. Shared Decision Making and Decision Aid Implementation: Stakeholder Views -- 15. Coordination of care in emergency departments: A comparative international ethnography -- 16. Models of user involvement in mental health.
Topic(s):
Grey Literature See topic collection
,
Education & Workforce See topic collection
,
Key & Foundational 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.

120
Persons with chronic conditions. Their prevalence and costs
Type: Journal Article
Authors: C. Hoffman, D. Rice, H . Y. Sung
Year: 1996
Publication Place: UNITED STATES
Abstract: OBJECTIVES: To determine (1) the number and proportion of Americans living with chronic conditions, and (2) the magnitude of their costs, including direct costs (annual personal health expenditures) and indirect costs to society (lost productivity due to chronic conditions and premature death). DESIGN: Analysis of the 1987 National Medical Expenditure Survey for prevalence and direct health care costs; indirect costs based on the 1990 National Health Interview Survey and Vital Statistics of the United States. SETTING: US population. PARTICIPANTS: For the estimate of prevalence and direct costs, the National Medical Expenditure Survey sample of persons who reported health conditions associated with (1) use of health services or supplies or (2) periods of disability. INTERVENTIONS: None. MAIN OUTCOME MEASURES: The number of persons with chronic conditions, their annual direct health care costs, and indirect costs from lost productivity and premature deaths. RESULTS: In 1987, 90 million Americans were living with chronic conditions, 39 million of whom were living with more than 1 chronic condition. Over 45% of noninstitutionalized Americans have 1 or more chronic conditions and their direct health care costs account for three fourths of US health care expenditures. Total costs projected to 1990 for people with chronic conditions amounted to $659 billion--$425 billion for direct health care costs and $234 billion in indirect costs. CONCLUSIONS: The prevalence and costs of chronic conditions as a whole have rarely been estimated. Because the number of persons with limitations due to chronic conditions is more regularly reported in the literature, the total prevalence of chronic conditions has perhaps been minimized. The majority of persons with chronic conditions are not disabled, nor are they elderly. Chronic conditions affect all ages. Because persons with chronic conditions have greater health needs at any age, their costs are disproportionately high.
Topic(s):
Financing & Sustainability See topic collection
,
Key & Foundational See topic collection