Literature DB >> 34286896

Transition care continuity promotes long-term retention in adult care among young adults with sickle cell disease.

Kristen E Howell1,2, Anjelica C Saulsberry-Abate1,3, Joacy G Mathias1,2,4, Jerlym S Porter5, Jason R Hodges1, Kenneth I Ataga6, Sheila Anderson1, Vikki Nolan2, Jane S Hankins1.   

Abstract

BACKGROUND/
OBJECTIVES: Care continuity prevents increased health care utilization and mortality during transition from pediatric to adult care. Our program employs a co-located care delivery model, in which pediatric provider involvement continues during young adulthood. We tested the hypothesis that individuals who participated in the co-located model have greater retention in adult care compared to those who only received pediatric transition services.
METHODS: This study consisted of 311 youth with SCD (51.4% male; 63.0% HbSS/HbSβ0 -thalassemia) who transferred to adult care from 2007 to 2017. Retention was defined as continuation with an adult provider for ≥12 or ≥24 months post-pediatric care. Logistic regression estimated the association between co-location status and retention at 12 and 24 months. Logistic regression and t-tests were used to evaluate potential predictors of retention in adult care.
RESULTS: Individuals who participated in the co-location model were 1.9 times more likely to remain in adult care 12 (95% CI: 1.01, 3.47) and 24 (95% CI: 1.01, 3.70) months post-pediatric care compared to those who did not participate. Individuals with HbSS/HbSβ0 -thalassemia were 1.9 times more likely to be retained at 12 months compared to those with HbSC/HbSβ+ -thalassemia/HbS/HPFH (95% CI: 1.12, 3.09). For every clinic encounter in the last 2 years of pediatric care, the odds of being retained at least 24 months after initiating adult care increased 1.1 times (95% CI: 1.02, 1.13).
CONCLUSIONS: Continuity of providers from pediatric to adult care may increase long-term retention in adult care. Longitudinal monitoring of adult outcomes is critical to identifying the efficacy of transition services.
© 2021 Wiley Periodicals LLC.

Entities:  

Keywords:  adult care retention; care continuity; health care transition; sickle cell disease; transition to adult care

Mesh:

Substances:

Year:  2021        PMID: 34286896      PMCID: PMC9084595          DOI: 10.1002/pbc.29209

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.838


  19 in total

1.  A consensus statement on health care transitions for young adults with special health care needs.

Authors: 
Journal:  Pediatrics       Date:  2002-12       Impact factor: 7.124

Review 2.  Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years.

Authors:  Shruti Chaturvedi; Michael R DeBaun
Journal:  Am J Hematol       Date:  2016-01       Impact factor: 10.047

3.  Pediatric to adult care co-location transitional model for youth with sickle cell disease.

Authors:  Vikki G Nolan; Sheila M Anderson; Matthew P Smeltzer; Jerlym S Porter; Yvonne M Carroll; Ian M Brooks; Nada Elmagboul; James G Gurney; Jane S Hankins
Journal:  Am J Hematol       Date:  2017-11-10       Impact factor: 10.047

Review 4.  Preventing morbidity and mortality from sickle cell disease. A public health perspective.

Authors:  R S Olney
Journal:  Am J Prev Med       Date:  1999-02       Impact factor: 5.043

5.  Transition of care provided for adolescents with special health care needs. American Academy of Pediatrics Committee on Children with Disabilities and Committee on Adolescence.

Authors: 
Journal:  Pediatrics       Date:  1996-12       Impact factor: 7.124

6.  Age-Related Emergency Department Reliance in Patients with Sickle Cell Disease.

Authors:  Morey A Blinder; Mei Sheng Duh; Medha Sasane; Alex Trahey; Carole Paley; Francis Vekeman
Journal:  J Emerg Med       Date:  2015-04-21       Impact factor: 1.484

7.  High mortality among children with sickle cell anemia and overt stroke who discontinue blood transfusion after transition to an adult program.

Authors:  Joseph F McLaughlin; Samir K Ballas
Journal:  Transfusion       Date:  2015-11-23       Impact factor: 3.157

8.  Transition to adult care in sickle cell disease: A longitudinal study of clinical characteristics and disease severity.

Authors:  Mariam Kayle; Sharron L Docherty; Richard Sloane; Paula Tanabe; Gary Maslow; Wei Pan; Nirmish Shah
Journal:  Pediatr Blood Cancer       Date:  2018-09-24       Impact factor: 3.167

9.  Risk factors for mortality in adult patients with sickle cell disease: a meta-analysis of studies in North America and Europe.

Authors:  Poulami Maitra; Melissa Caughey; Laura Robinson; Payal C Desai; Susan Jones; Mehdi Nouraie; Mark T Gladwin; Alan Hinderliter; Jianwen Cai; Kenneth I Ataga
Journal:  Haematologica       Date:  2017-01-19       Impact factor: 9.941

Review 10.  Transition to adulthood and adult health care for patients with sickle cell disease or cystic fibrosis: Current practices and research priorities.

Authors:  Sophie Lanzkron; Gregory S Sawicki; Kathryn L Hassell; Michael W Konstan; Robert I Liem; Susanna A McColley
Journal:  J Clin Transl Sci       Date:  2018-10
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