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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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1290 Results
182
Building Mental Health Capacity: Exploring the Role of Adaptive Expertise in the ECHO Virtual Learning Model
Type: Journal Article
Authors: Sanjeev Sockalingam, Thiyake Rajaratnam, Carrol Zhou, Eva Serhal, Allison Crawford, Maria Mylopoulos
Year: 2021
Topic(s):
Education & Workforce See topic collection
,
HIT & Telehealth See topic collection
183
Building Provincial Mental Health Capacity in Primary Care: An Evaluation of a Project ECHO Mental Health Program
Type: Journal Article
Authors: S. Sockalingam, A. Arena, E. Serhal, L. Mohri, J. Alloo, A. Crawford
Year: 2018
Publication Place: United States
Abstract: OBJECTIVE: Project Extension for Community Healthcare Outcomes (Project ECHO(c)) addresses urban-rural disparities in access to specialist care by building primary care provider (PCP) capacity through tele-education. Evidence supporting the use of this model for mental health care is limited. Therefore, this study evaluated a mental health and addictions-focused ECHO program. Primary outcome measures were PCP knowledge and perceived self-efficacy. Secondary objectives included: satisfaction, engagement, and sense of professional isolation. PCP knowledge and self-efficacy were hypothesized to improve with participation. METHODS: Using Moore's evaluation framework, we evaluated the ECHO program on participant engagement, satisfaction, learning, and competence. A pre-post design and weekly questionnaires measured primary and secondary outcomes, respectively. RESULTS: Knowledge test performance and self-efficacy ratings improved post-ECHO (knowledge change was significant, p < 0.001, d = 1.13; self-efficacy approached significance; p = 0.056, d = 0.57). Attrition rate was low (7.7%) and satisfaction ratings were high across all domains, with spokes reporting reduced feelings of isolation. DISCUSSION: This is the first study to report objective mental health outcomes related to Project ECHO. The results indicate high-participant retention is achievable, and provide preliminary evidence for increased knowledge and self-efficacy. These findings suggest this intervention may improve mental health management in primary care.
Topic(s):
Healthcare Disparities See topic collection
,
HIT & Telehealth See topic collection
184
Building Provincial Mental Health Capacity in Primary Care: An Evaluation of a Project ECHO Mental Health Program
Type: Journal Article
Authors: S. Sockalingam, A. Arena, E. Serhal, L. Mohri, J. Alloo, A. Crawford
Year: 2018
Publication Place: United States
Abstract: OBJECTIVE: Project Extension for Community Healthcare Outcomes (Project ECHO(c)) addresses urban-rural disparities in access to specialist care by building primary care provider (PCP) capacity through tele-education. Evidence supporting the use of this model for mental health care is limited. Therefore, this study evaluated a mental health and addictions-focused ECHO program. Primary outcome measures were PCP knowledge and perceived self-efficacy. Secondary objectives included: satisfaction, engagement, and sense of professional isolation. PCP knowledge and self-efficacy were hypothesized to improve with participation. METHODS: Using Moore's evaluation framework, we evaluated the ECHO program on participant engagement, satisfaction, learning, and competence. A pre-post design and weekly questionnaires measured primary and secondary outcomes, respectively. RESULTS: Knowledge test performance and self-efficacy ratings improved post-ECHO (knowledge change was significant, p < 0.001, d = 1.13; self-efficacy approached significance; p = 0.056, d = 0.57). Attrition rate was low (7.7%) and satisfaction ratings were high across all domains, with spokes reporting reduced feelings of isolation. DISCUSSION: This is the first study to report objective mental health outcomes related to Project ECHO. The results indicate high-participant retention is achievable, and provide preliminary evidence for increased knowledge and self-efficacy. These findings suggest this intervention may improve mental health management in primary care.
Topic(s):
Healthcare Disparities See topic collection
,
HIT & Telehealth See topic collection
185
Buprenorphine implementation at syringe service programs following waiver of the Ryan Haight Act in the United States
Type: Journal Article
Authors: Barrot H. Lambdin, Ricky N. Bluthenthal, Hansel E. Tookes, Lynn Wenger, Terry Morris, Paul LaKosky, Alex H. Kral
Year: 2022
Topic(s):
HIT & Telehealth See topic collection
,
Healthcare Policy See topic collection
186
Buprenorphine Induction in a Rural Maryland Detention Center During COVID-19: Implementation and Preliminary Outcomes of a Novel Telemedicine Treatment Program for Incarcerated Individuals With Opioid Use Disorder
Type: Journal Article
Authors: A. M. Belcher, K. Coble, T. O. Cole, C. J. Welsh, A. Whitney, E. Weintraub
Year: 2021
Topic(s):
Healthcare Disparities See topic collection
,
HIT & Telehealth See topic collection
,
Opioids & Substance Use See topic collection
187
Buprenorphine inductions eased by telehealth
Type: Journal Article
Year: 2019
Publication Place: Hoboken, New Jersey
Topic(s):
HIT & Telehealth See topic collection
,
Opioids & Substance Use See topic collection
Reference Links:       
188
CADTH Health Technology Review
Type: Book Chapter
Year: 2025
Publication Place: Ottawa (ON)
Abstract:

WHAT IS ALTERNATE LEVEL OF CARE? • Alternate level of care (ALC) is a designation used and applied by clinical staff to the portion of a patient’s hospital stay when the patient is occupying a bed in a facility (e.g., acute care; mental health; rehabilitation; and chronic, intermediate, or complex continuing care settings) but they no longer require the intensity of resources or services provided in that care setting. WHAT ARE THE CHALLENGES? • In 2022–2023, an estimated 6.2% of hospitalizations in Canada had an ALC component, with a provincial and territorial range of 1.0% to 8.3%. An estimated 17.0% of hospital days were for patients in ALC, with a provincial and territorial range of 6.8% to 26.1%. • Patients with an ALC designation may be more at risk of adverse events, hospital-acquired infections, mental and physical deterioration, and mortality. ALC bed days also contribute to higher hospital costs and system flow issues, including overcapacity, emergency department (ED) and hospital overcrowding, and prolonged wait times. • Patients of any age and any health condition may remain in hospital after their acute care needs have been met; however, the most common group of patients who are in ALC are older adults. • Determining whether a patient’s stay receives an ALC designation requires the application of the ALC definition while considering the individual patient’s context. There are many factors that influence whether a hospital stay will result in an ALC designation, including variations in patients, settings, and circumstances. • The ALC indicator was originally meant to capture unmet needs of patients. It is now predominantly a designation placed on a portion of patients’ hospital stays, and often patients are unaware of their ALC status and what it means. • The variation in ALC definitions and their application, as well as situational contexts such as the demographics of patients, ALC rates, and interventions, make it difficult to compare ALC between jurisdictions. WHAT DID WE DO? • To inform policy and decision-making in support of evidence-informed strategies to reduce the time people spend in ALC, we assess: o.. ALC definitions in Canada and how they are applied across jurisdictions; o.. reasons for ALC designation, including the reasons people with unmet needs receive ALC designation and remain in ALC in acute inpatient care settings and the relevant, related ethical considerations; o.. effectiveness and harms of published interventions to alleviate the ALC burden; o.. other interventions implemented in Canada and internationally that exist to help alleviate the ALC burden; o.. economic and resource considerations associated with ALC interventions to health systems and patients; o.. implementation considerations to identify facilitators of, and barriers to, implementation of ALC interventions. • Interventions were aligned with 3 categories: ALC avoidance (upstream), ALC patient flow (midstream), and ALC patient discharge (downstream). • To supplement findings from the evidence, review and to help describe the ALC landscape across Canada, we also conducted an analysis of real-world data. We developed an interactive dashboard that includes figures that describe ALC data by different provinces and territories in Canada, over time. • To support this work, we engaged people with personal and/or professional experience with ALC, caring for older adults as they age, or health care decision-making in Canada. We searched key information and data sources — including journal databases, trial registers, and websites — and conducted focused internet searches for relevant evidence on initiatives to reduce ALC. WHAT DID WE FIND? • Across the jurisdictions, ALC is defined in alignment with the Canadian Institute for Health Information (CIHI) definition as patients occupying a bed while no longer requiring the services provided by their admitting acute care facility or department as they wait for transfer to more appropriate care settings. Slight differences arise from the designation criteria and the code assignments for patients. • ALC designation involves assigning specific codes or criteria to reflect the change in a patient’s status and reasons for the designation. • ALC days are widely used as a performance indicator across jurisdictions to assess ALC, along with other metrics such as the percentage of hospitalized patients designated as ALC and the number of ALC beds occupied per day. • We found that individual sociodemographic and clinical factors, process and practice factors within and across acute and nonacute care settings, and structural factors contribute to ALC designations. We also found that multiple, intersecting factors that contribute to ALC can raise ethical considerations and present ethical dilemmas for patients, care partners, families, health care providers, and health systems in the context of ALC designations. • We examined evidence on the effectiveness of 6 multicomponent interventions that have been described in comparative studies in the published literature intended to alleviate the ALC burden in acute care hospital settings. Overall, there was very low–certainty evidence of the clinical benefits of these interventions: • The Humber River Health’s Humber’s Elderly Assess and Restore Team (HEART) program (a midstream-downstream intervention) and a step-down intermediate care unit for older patients who are hospitalized plus a 72-hour discharge target (a downstream intervention) may reduce ALC rates compared with usual care, but the evidence is very uncertain due to critical or serious risk of bias and indirectness. • The Sub-Acute Care for Frail Elderly (SAFE) Unit located in a long-term care [LTC] home in Ontario (a downstream intervention), vertical integration of care (a system-level intervention), and urgent and emergency care vanguards (a system-level intervention) may reduce ALC lengths of stay compared with usual care or no intervention, but the evidence is very uncertain due to critical risk of bias and indirectness. • Coordinated care planning based on the Health Links model (a system-level intervention) may make little to no difference on ALC lengths of stay compared to no intervention, but the evidence is very uncertain due to serious risk of bias and serious imprecision. • We also identified 11 noncomparative studies (that were not critically appraised) of the following: o.. six midstream interventions — increased step-down beds, specialized acute care space or service, and enhanced discharge planning; o.. two downstream interventions — transitional care units; o.. three system-level interventions — integrated care for older people and home-first strategies. • From the literature, we identified a total of 19 new and emerging interventions in Canada, 10 international interventions, and 2 international case studies. Interventions intended to help reduce ALC designation of patients, improve patient flow, facilitate patient discharge, and provide educational and practical guidance about ways to alleviate the ALC burden. • Findings from a survey conducted as part of our environmental scanning activities suggested that although most jurisdictions use the CIHI definition of ALC, there is variation in the type of staff who assign ALC codes, the uses of ALC data, and fees associated with ALC designation. Strategies to alleviate the ALC burden most often aim to reduce ALC length of stay, are typically set in hospitals, involve a wide range of clinical and nonclinical staff, and are frequently targeted toward older adults, people awaiting discharge to residential care, and people with complex needs. • Resource impacts should be considered with respect to the implementation of any strategies to alleviate the ALC burden, including those pertaining to set-up, management, and delivery of care, alongside careful consideration of coordination, flow between different strategies, and redistribution implications. We identified 1 Canadian economic evaluation on the cost-effectiveness of the SAFE Unit (a downstream intervention) compared with usual care to alleviate the ALC burden. The overall literature suggests that this and other strategies for alleviating ALC may be less costly, resulting in the opportunity to treat more patients at the required level of care and thus increase efficiency in the use of health care resources. • Key participants in the implementation of ALC interventions include patients, care partners, clinicians, support staff, government, administrators, and communities, suggesting everyone involved plays a role in the successful implementation of these interventions. • Care providers should consider the use of cross-sector integration, enhanced communication, and multidisciplinary collaboration, supported by high-quality data that are integrated with the flow of the patient through their health journey to inform decision-making to aid in successfully implementing of ALC interventions. • Implementation should be approached as a continuum where approaches are tailored to the needs and complexities of the individual patient while assessing the requirements to transition between each step of care. NEXT STEPS: • Our Health Technology Expert Review Panel will use the findings of this report to support deliberations that will result in the development of guidance to inform decisions around evidence-informed strategies and initiatives that could be considered to reduce the time patients spend with an ALC designation.

Topic(s):
HIT & Telehealth See topic collection
189
California primary care, mental health, and substance use services integration policy initiative: Volume II - Working Papers
Type: Government Report
Year: 2009
Publication Place: Sacramento, CA
Topic(s):
Education & Workforce See topic collection
,
Financing & Sustainability See topic collection
,
HIT & Telehealth See topic collection
,
Healthcare Policy See topic collection
,
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.

190
Can the electronic medical record provide reliable indicators of primary care behavioral health fidelity? Comparison of accessibility and productivity indicators assessed through observational coding
Type: Journal Article
Authors: A. R. Dueweke, A. Archer, M. Tolliver, J. Polaha
Year: 2024
Topic(s):
HIT & Telehealth See topic collection
191
Can the electronic medical record provide reliable indicators of primary care behavioral health fidelity? Comparison of accessibility and productivity indicators assessed through observational coding
Type: Journal Article
Authors: Aubrey R. Dueweke, Allen Archer, Matthew Tolliver, Jodi Polaha
Year: 2023
Topic(s):
HIT & Telehealth See topic collection
192
Can you hear me now? Patient perceptions of telehealth in a rural primary care population
Type: Journal Article
Authors: Nithin Charlly, Matthew Swedlund
Year: 2024
Topic(s):
HIT & Telehealth See topic collection
,
Healthcare Disparities See topic collection
193
Capturing Social and Behavioral Domains in Electronic Health Records: Phase 1
Type: Government Report
Authors: Institute of Medicine
Year: 2014
Publication Place: Washington, DC
Abstract:

Substantial empirical evidence of the contribution of social and behavioral factors to functional status and the onset and progression of disease has accumulated over the past few decades. Traditionally, research and interventions on social and behavioral determinants of health have largely been the purview of public health which has focused on disease prevention and maintenance of the public’s health. Health care systems, in contrast, have focused primarily on the treatment of disease in individual patients, and, until recently, social determinants of health have not been linked to clinical practice or health care delivery systems. Electronic health records (EHRs) provide crucial information to providers treating individual patients, to health systems about the health of populations, and to researchers about the determinants of health and the effectiveness of treatments. The Health Information Technology for Economic and Clinical Health Act and the Patient Protection and Affordable Care Act place new importance on the widespread adoption and meaningful use of EHRs.The IOM was asked to form a committee to identify domains and measures that capture the social determinants of health to inform the development of recommendations for meaningful use of EHRs. In its Phase 1 report, the committee identifies the social and behavioral domains that are the best candidates to be considered in all EHRs; specifies criteria that should be used in deciding which domains should be included; and identifies any domains that should be included for specific populations or settings defined by age, socioeconomic status, race/ethnicity, disease, or other characteristics.

Topic(s):
Grey Literature See topic collection
,
HIT & Telehealth 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.

194
Care coordination between rural primary care and telemedicine to expand medication treatment for opioid use disorder: Results from a single‐arm, multisite feasibility study
Type: Journal Article
Authors: Yih‐Ing Hser, Larissa J. Mooney, Laura‐Mae Baldwin, Allison Ober, Lisa A. Marsch, Seth Sherman, Abigail Matthews, Sarah Clingan, Zhe Fei, Yuhui Zhu, Alex Dopp, Megan E. Curtis, Katie P. Osterhage, Emily G. Hichborn, Chunqing Lin, Megan Black, Stacy Calhoun, Caleb C. Holtzer, Noah Nesin, Denise Bouchard
Year: 2023
Topic(s):
Opioids & Substance Use See topic collection
,
Healthcare Disparities See topic collection
,
Education & Workforce See topic collection
,
HIT & Telehealth See topic collection
195
Care Delivery in Community Health Centers Before, During, and After the COVID-19 Pandemic (2019-2022)
Type: Journal Article
Authors: N. Cook, B. M. McGrath, S. M. Navale, S. M. Koroukian, A. R. Templeton, L. C. Crocker, S. J. Zyzanski, W. P. Bensken, K. C. Stange
Year: 2024
Topic(s):
HIT & Telehealth See topic collection
197
CareConnect: Adapting a Virtual Urgent Care Model to Provide Buprenorphine Transitional Care
Type: Journal Article
Authors: Margaret Lowenstein, Nicole O'Donnell, Jasmine Barnes, Kathryn Gallagher, Gilly Gehri, Jon K. Pomeroy, Shoshana Aronowitz, Krisda Chaiyachati, Emily Cubbage, Rachel French, Susan McGinley, Brittany Salerno, Jeanmarie Perrone
Year: 2022
Topic(s):
Opioids & Substance Use See topic collection
,
HIT & Telehealth See topic collection
,
Education & Workforce See topic collection
198
Caring for women with substance use disorders through pregnancy and postpartum during the COVID-19 pandemic: Lessons learned from psychology trainees in an integrated OBGYN/substance use disorder outpatient treatment program
Type: Journal Article
Authors: J. S. Sadicario, A. B. Parlier-Ahmad, J. K. Brechbiel, L. Z. Islam, C. E. Martin
Year: 2021
Topic(s):
Education & Workforce See topic collection
,
Healthcare Disparities See topic collection
,
HIT & Telehealth See topic collection
,
Opioids & Substance Use See topic collection
199
Caring for women with substance use disorders through pregnancy and postpartum during the COVID-19 pandemic: Lessons learned from psychology trainees in an integrated OBGYN/substance use disorder outpatient treatment program
Type: Journal Article
Authors: J. S. Sadicario, A. B. Parlier-Ahmad, J. K. Brechbiel, L. Z. Islam, C. E. Martin
Year: 2020
Topic(s):
Education & Workforce See topic collection
,
Healthcare Disparities See topic collection
,
HIT & Telehealth See topic collection
,
Opioids & Substance Use See topic collection
200
Case management for depression by health care assistants in small primary care practices: a cluster randomized trial
Type: Journal Article
Authors: J. Gensichen, M. Von Korff, M. Peitz, C. Muth, M. Beyer, C. Guthlin, M. Torge, J. J. Petersen, T. Rosemann, J. Konig, F. M. Gerlach, PRoMPT
Year: 2009
Publication Place: United States
Abstract: BACKGROUND: Case management by health care assistants in small primary care practices provides unclear benefit for improving depression symptoms. OBJECTIVE: To determine whether case management provided by health care assistants in small primary care practices is more effective than usual care in improving depression symptoms and process of care for patients with major depression. DESIGN: Cluster randomized, controlled trial. A central automated system generated the randomization scheme, which was stratified by urban and rural practices; allocation sequence was concealed until groups were assigned. SETTING: 74 small primary care practices in Germany from April 2005 to September 2007. PATIENTS: 626 patients age 18 to 80 years with major depression. INTERVENTION: Structured telephone interview to monitor depression symptoms and support for adherence to medication, with feedback to the family physician. MEASUREMENTS: Depression symptoms at 12 months, as measured by the Patient Health Questionnaire-9 (PHQ-9); secondary outcomes were patient assessment of chronic illness care, adherence to medication, and quality of life. RESULTS: A total of 310 patients were randomly assigned to case management and 316 to usual care. At 12 months, 249 intervention recipients and 278 control patients were assessed; 555 patients were included in a modified intention-to-treat-analysis (267 intervention recipients vs. 288 control patients). Compared with control patients, intervention recipients had lower mean PHQ-9 values in depression symptoms (-1.41 [95% CI, -2.49 to -0.33]; P = 0.014), more favorable assessments of care (3.41 vs. 3.11; P = 0.011), and increased treatment adherence (2.70 vs. 2.53; P = 0.042). Quality-of-life scores did not differ between groups. LIMITATION: Patients, health care assistants, family physicians, and researchers were not blinded to group assignment, and 12-month follow-up of patients was incomplete. CONCLUSION: Case management provided by primary care practice-based health care assistants may reduce depression symptoms and improve process of care for patients with major depression more than usual care. PRIMARY FUNDING SOURCE: German Ministry of Education and Research.
Topic(s):
HIT & Telehealth See topic collection