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Structured Abstract
Objective:
To understand the evidence base for care interventions, implementation strategies, and between-provider communication tools among children with special healthcare needs (CSHCN) transitioning from pediatric to adult medical care services.
Data sources:
We searched Ovid MEDLINE®, Ovid Embase®, the Cochrane Central trials (CENTRAL) registry, and CINAHL® to identify studies through September 10, 2021. We conducted grey literature searches to identify additional resources relevant to contextual questions.
Review methods:
Using a mixed-studies review approach, we searched for interventions or implementation strategies for transitioning CSHCN from pediatric to adult services. Two investigators screened abstracts and full-text articles of identified references for eligibility. Eligible studies included randomized controlled trials, quasi-experimental observational studies, and mixed-method studies of CSHCN, their families, caregivers, or healthcare providers. We extracted basic study information from all eligible studies and grouped interventions into categories based on disease conditions. We summarized basic study characteristics for included studies and outcomes for studies assessed as low to medium risk of bias using RoB-2.
Results:
We identified 9,549 unique references, 440 of which represented empirical research; of these, 154 (16 major disease categories) described or examined a care transition intervention with enough detail to potentially be eligible for inclusion in any of the Key Questions. Of these, 96 studies met comparator criteria to undergo risk of bias assessment; however only 9 studies were assessed as low or medium risk of bias and included in our analytic set. Low-strength evidence shows transition clinics may not improve hemoglobin A1C levels either at 12 or 24 months in youth with type 1 diabetes mellitus compared with youth who received usual care. For all other interventions and outcomes, the evidence was insufficient to draw meaningful conclusions because the uncertainty of evidence was too high. Some approaches to addressing barriers include dedicating time and resources to support transition planning, developing a workforce trained to care for the needs of this population, and creating structured processes and tools to facilitate the transition process.
No globally accepted definition for effective transition of care from pediatric to adult services for CSHCN exists; definitions are often drawn from principles for transitions, encompassing a broad set of clinical aspects and other factors that influence care outcomes or promote continuity of care. There is also no single measure or set of measures consistently used to evaluate effectiveness of transitions of care. The literature identifies a limited number of available training and other implementation strategies focused on specific clinical specialties in targeted settings. No eligible studies measured the effectiveness of providing linguistically and culturally competent healthcare for CSHCN. Identified transition care training, and care interventions to prepare pediatric patients and their families for transitioning from CSHCN to adult care, varied considerably.
Conclusions:
Little rigorous evidence exists to inform care interventions and implementation strategies. Significant barriers impede implementation of interventions, tools, and trainings to transition CSHCN, which may be reduced in future intervention development. This review highlights the need for more rigorous studies across the diverse populations of CSHCN in order to provide clearer answers for CSHCN, their families, caregivers, providers, funders, and policymakers.
Contents
- Preface
- Acknowledgments
- Technical Expert Panel
- Peer Reviewers
- Executive Summary
- Chapter 1. Introduction
- Chapter 2. Methods
- Chapter 3. Search Results
- Chapter 4. Care Interventions for Transition
- Chapter 5. Implementation Strategies and Communication Tools
- Chapter 6. Barriers and Facilitators for Implementing Interventions and Tools
- Chapter 7. Definitions and Measures for Transitions of Care
- Chapter 8. Training and Implementation Strategies To Prepare Pediatric and Adult Medical Providers
- Chapter 9. Training Available for Linguistically and Culturally Competent Care
- Chapter 10. Training, Implementation Strategies, and Interventions To Prepare Pediatric Patients and Families
- Chapter 11. Strategies To Increase Availability of Adult Providers
- Chapter 12. Discussion
- References
- Abbreviations and Acronyms
- Appendixes
- Appendix A. Methods
- Appendix B. Excluded Studies at Full Text
- Appendix C. Expanded Eligible Studies Bibliography
- Appendix D. Evidence Tables and Evidence Maps for Care Interventions for Transition From Pediatric to Adult Medical Services (Chapter 4)
- Appendix E. Evidence Tables and Evidence Maps for Implementation Strategies and Communication Tools for Care Interventions for Transition, Including Provider-Related Training (Chapter 5)
- Appendix F. Study Sources for Barriers and Facilitators for Implementing Effective Interventions and Tools for Transition From Pediatric to Adult Medical Services
- Appendix G. Measures Used To Evaluate the Effectiveness of Transitions of Care From Pediatric to Adult Services for Children With Special Healthcare Needs
- Appendix H. References for Evidence Tables
Suggested citation:
Parsons HM, Abdi HI, Nelson VA, Claussen A, Wagner BL, Sadak KT, Scal PB, Wilt TJ, Butler M. Transitions of Care From Pediatric to Adult Services for Children With Special Healthcare Needs. Comparative Effectiveness Review No. 255. (Prepared by the Minnesota Evidence-based Practice Center under Contract No. 75Q80120D00008.) AHRQ Publication No. 22-EHC027. Rockville, MD: Agency for Healthcare Research and Quality; May 2022. DOI: https://doi.org/10.23970/AHRQEPCCER255. Posted final reports are located on the Effective Health Care Program search page.
This report is based on research conducted by the Minnesota Evidence-based Practice Center (EPC) under contract to the Agency for Healthcare Research and Quality (AHRQ), Rockville, MD (Contract No. 75Q80120D00008). The National Cancer Institute (NCI) of the National Institutes of Health (NIH) funded the report. The findings and conclusions in this document are those of the authors, who are responsible for its contents; the findings and conclusions do not necessarily represent the views of AHRQ or NCI/NIH. Therefore, no statement in this report should be construed as an official position of AHRQ, NCI/NIH, or the U.S. Department of Health and Human Services.
None of the investigators have any affiliations or financial involvement that conflicts with the material presented in this report.
The information in this report is intended to help healthcare decision makers—patients and clinicians, health system leaders, and policymakers, among others—make well-informed decisions and thereby improve the quality of healthcare services. This report is not intended to be a substitute for the application of clinical judgment. Anyone who makes decisions concerning the provision of clinical care should consider this report in the same way as any medical reference and in conjunction with all other pertinent information, i.e., in the context of available resources and circumstances presented by individual patients.
This report is made available to the public under the terms of a licensing agreement between the author and the Agency for Healthcare Research and Quality. Most AHRQ documents are publicly available to use for noncommercial purposes (research, clinical or patient education, quality improvement projects) in the United States, and do not need specific permission to be reprinted and used unless they contain material that is copyrighted by others. Specific written permission is needed for commercial use (reprinting for sale, incorporation into software, incorporation into for-profit training courses) or for use outside of the United States. If organizational policies require permission to adapt or use these materials, AHRQ will provide such permission in writing.
AHRQ or U.S. Department of Health and Human Services endorsement of any derivative products that may be developed from this report, such as clinical practice guidelines, other quality enhancement tools, or reimbursement or coverage policies, may not be stated or implied.
A representative from AHRQ served as a Contracting Officer’s Representative and reviewed the contract deliverables for adherence to contract requirements and quality. AHRQ did not directly participate in the literature search, determination of study eligibility criteria, data analysis or interpretation, or preparation or drafting of this report.
AHRQ appreciates appropriate acknowledgment and citation of its work. Suggested language for acknowledgment: This work was based on an evidence report, Transitions of Care From Pediatric to Adult Services for Children With Special Healthcare Needs, by the Evidence-based Practice Center Program at the Agency for Healthcare Research and Quality (AHRQ).
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