A Clinical Tool to Measure the Components of Health-Care Transition from Pediatric Care to Adult Care: TheUNC TRxANSITION Scale

Renal Failure ◽  
2012 ◽  
Vol 34 (6) ◽  
pp. 744-753 ◽  
Author(s):  
Maria E Ferris ◽  
Donna H Harward ◽  
Kristi Bickford ◽  
J. Bradley Layton ◽  
M. Ted Ferris ◽  
...  
2021 ◽  
Vol 42 (12) ◽  
pp. 684-693
Author(s):  
Lynn F. Davidson ◽  
Maya H. Doyle

Preparing all youth for the transition to adult-oriented care, adulthood itself, and a greater responsibility for their own health and health-care is an essential part of pediatric care. This process, typically described as health-care transition, can occur throughout ongoing pediatric health-care to prepare patients for transfer to an adult clinician and integration into adult care. Gaps remain in practice and in outcomes research regarding health-care transition. This review discusses recent literature, details best practices, and recommends guidance and tools to assist pediatric clinicians in providing a smooth transition process and a successful transfer to adult care for youth with and without special health-care needs.


Author(s):  
Nagib Dahdah ◽  
Samuel C. Kung ◽  
Kevin G. Friedman ◽  
Ariane Marelli ◽  
John B. Gordon ◽  
...  

Background Health care transition (HCT) is a period of high vulnerability for patients with chronic childhood diseases, particularly when patients shift from a pediatric to an adult care setting. An increasing number of patients with Kawasaki disease (KD) who develop medium and large coronary artery aneurysms (classified by the American Heart Association according to maximal internal coronary artery diameter Z‐scores ≥5 and ≥10, respectively) are becoming adults and thus undergoing an HCT. However, a poor transition to an adult provider represents a risk of loss to follow‐up, which can result in increasing morbidity and mortality. Methods and Results This scientific statement provides a summary of available literature and expert opinion pertaining to KD and HCT of children as they reach adulthood. The statement reviews the existing life‐long risks for patients with KD, explains current guidelines for long‐term care of patients with KD, and offers guidance on assessment and preparation of patients with KD for HCT. The key element to a successful HCT, enabling successful transition outcomes, is having a structured intervention that incorporates the components of planning, transfer, and integration into adult care. This structured intervention can be accomplished by using the Six Core Elements approach that is recommended by the American Academy of Pediatrics, the American Academy of Family Physicians, and the American College of Physicians. Conclusions Formal HCT programs for patients with KD who develop aneurysms should be established to ensure a smooth transition with uninterrupted medical care as these youths become adults.


2011 ◽  
Vol 18 (5) ◽  
pp. 384-390 ◽  
Author(s):  
Lorraine E. Bell ◽  
Maria E. Ferris ◽  
Nicole Fenton ◽  
Stephen R. Hooper

Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 5820-5820 ◽  
Author(s):  
Anjelica Christina Saulsberry ◽  
Pradeep S. B. Podila ◽  
Shiela Anderson ◽  
Jason R Hodges ◽  
Jerlym Porter ◽  
...  

Abstract Introduction: Unsuccessful transition from pediatric to adult care among youth with sickle cell disease (SCD) contributes to frequent disease complications and early death. The literature is sparse on longitudinal SCD transition program outcomes. The St. Jude SCD Transition to Adult Care Program started in 2007, is a comprehensive, co-located, and interdisciplinary program embedded in a larger SCD medical home. The objective of this study is to describe transfer rates, time to transfer, and maintenance of adult care over a 9-year period. Methods: With St. Jude IRB approval, we conducted a retrospective review of the rate of matriculation in adult care, the latency time from leaving pediatric care and initiating adult care, and maintenance of engagement in adult care 12 and 24 months later. Eligibility criteria: 1) SCD diagnosis and 2) Completion of pediatric care between 2007 and 2016. Results: Three hundred and sixty participants transferred to adult care over the study period. Mean age at transfer was 18 years. Matriculation in adult care within 6 months from leaving pediatric care substantially increased: 71% in 2007 to 93% in 2016. We observed a progressive reduction in the latency time from pediatric to adult care, from 12 months in 2007 to 1.5 months in 2016. Fifty-five percent (n=198) of youth who transitioned to the partner Methodist Comprehensive Sickle Cell Center (MCSCC) post-pediatric care continued to be followed by our program. Of these, 77% and 57% remained with the MCSCC 12 and 24 months after transfer to adult care, respectively. Conclusions: The St. Jude SCD Transition to Adult Care Program demonstrated a gradual increase in transfer rates and a reduction in length of time-to-adult transfer since its creation. Adult care engagement declined over time and warrants future interventions. Improved health care transition outcomes could potentially translate into improved quality of life and greater longevity. Disclosures Hankins: bluebird bio: Consultancy; NCQA: Consultancy; Novartis: Research Funding; Global Blood Therapeutics: Research Funding.


2021 ◽  
Author(s):  
Lars Pape ◽  
Gundula Ernst

Abstract PurposeFor consistent quality of treatment of young people with chronic health care needs, a structured transition from pediatric medicine to adult medical care is essential. Currently, most countries have no guidelines on health care transition (HCT) based on systematic evidence research. To close this gap guidance to support the transition was developed in Germany.MethodsTwenty-five experts in the management of adolescents and young adults with different chronic conditions were invited to take part in the guideline group. Based on a systematic literature search recommendations for transition were drafted. Where evidence was lacking, recommendations were developed using collective expert consensus. The consensus process was independently moderated using a Delphi approach. The final draft was reviewed and endorsed by all major German medical societies.ResultsThe clinical recommendations provide guidance for all chronic somatic diseases. After assessment of transition readiness, an individualized plan for transition should be drawn up. Key elements here are a responsible coordinator, age-adapted patient education, involvement of parents, web-based interventions, joint visits and a structured summary for the receiving physician. The aim is the gradual transfer of responsibility for disease management to the young person themselves.ConclusionAs only a few randomized controlled studies on HCT are available, evidence-based statements are possible for some but not all areas of transition. However, this guideline may help to develop globally accepted standards. These standards should be established, implemented and financed by individual national health systems to allow appropriate support for young people.


Hematology ◽  
2019 ◽  
Vol 2019 (1) ◽  
pp. 496-504 ◽  
Author(s):  
Anjelica C. Saulsberry ◽  
Jerlym S. Porter ◽  
Jane S. Hankins

Abstract Most children with sickle cell disease (SCD) today survive into adulthood. Among emerging adults, there is a marked increase in acute care utilization and a rise in mortality, which can be exacerbated by not establishing or remaining in adult care. Health care transition programs are therefore essential to prepare, transfer, and integrate emerging adults in the adult care setting. The Six Core Elements of Health Care Transition, created by the Center for Health Care Transition Improvement, define the basic components of health care transition support as follows: (1) transition policy, (2) tracking and monitoring progress, (3) assessing transition readiness, (4) planning for adult care, (5) transferring to adult care, and (6) integrating into adult care. Programs that implement the Six Core Elements have experienced significant declines in care abandonment during adolescence and young adulthood and higher early adult care engagement. Most of the core transition activities are not currently reimbursable, however, posing a challenge to sustain transition programs. Ongoing studies are investigating interventions in comparative effectiveness trials to improve health-related quality of life and reduce acute care utilization among emerging adults with SCD. Although these studies will identify best practices for health care transition, it is also important to define how the transition outcomes will be measured, as no consensus definition exists for successful health care transition in SCD. Future research is needed to define best practices for health care transition, systematically assess transition outcomes, and revise payment models to promote sustainability of health care transition programs.


2010 ◽  
Author(s):  
Cindy L. Buchanan ◽  
Debra Lefkowitz ◽  
Karen McCandless ◽  
Samuel Goldfarb

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