Literature DB >> 21636039

Transfer of adolescents with congenital heart disease from pediatric cardiology to adult health care: an analysis of transfer destinations.

Eva Goossens1, Ine Stephani, Deborah Hilderson, Marc Gewillig, Werner Budts, Kristien Van Deyk, Philip Moons.   

Abstract

OBJECTIVES: The transfer of adolescents with congenital heart disease from pediatric to adult care was examined. The aims were to investigate where these adolescents received adult-centered care, to determine the proportion of patients with no follow-up and with no appropriate follow-up after leaving pediatric cardiology, and to explore the determinants of no follow-up and no appropriate follow-up.
BACKGROUND: Even after successful treatment, many patients require lifelong cardiac surveillance by specialized practitioners. Although guidelines describe the most appropriate level of follow-up, this is not always implemented in practice.
METHODS: A descriptive, observational study was performed, including 794 patients with congenital heart disease examined and/or treated at a tertiary care center.
RESULTS: Overall, 58 of the 794 patients included (7.3%) were not in follow-up. Cessation of follow-up was found in 2 of 74 patients with complex (2.7%), 31 of 448 patients with moderate (6.9%), and 25 of 272 patients with simple (9.2%) heart defects. Moreover, 684 patients (86.1%) remained in specialized follow-up. According to international guidelines, 81 patients (10.2%) did not receive the minimal level of cardiac care. Multivariable logistic regression revealed that male sex and no prior heart surgery were associated with no follow-up. Male sex, no prior heart surgery, and greater complexity of congenital heart disease were associated with no appropriate level of cardiac follow-up.
CONCLUSIONS: The proportion of patients in this study lost to follow-up was substantially lower than in other Western countries. Because only patient-related factors were examined with respect to loss to follow-up, further examination of patient-related, hospital-related, and healthcare-related determinants of lack of follow-up is needed.
Copyright © 2011 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21636039     DOI: 10.1016/j.jacc.2010.11.068

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  20 in total

1.  Readiness for Transition to Adult Health Care for Young Adolescents with Congenital Heart Disease.

Authors:  Kimberly T Stewart; Nita Chahal; Adrienne H Kovacs; Cedric Manlhiot; Ahlexxi Jelen; Tanveer Collins; Brian W McCrindle
Journal:  Pediatr Cardiol       Date:  2017-02-10       Impact factor: 1.655

2.  A Systematic Review of Transition Readiness in Youth with Chronic Disease.

Authors:  Maureen Varty; Lori L Popejoy
Journal:  West J Nurs Res       Date:  2019-09-18       Impact factor: 1.967

3.  A transition clinic intervention to improve follow-up rates in adolescents and young adults with congenital heart disease.

Authors:  Stephanie S Gaydos; Shahryar M Chowdhury; Rochelle N Judd; Kimberly E McHugh
Journal:  Cardiol Young       Date:  2020-04-13       Impact factor: 1.093

Review 4.  Transition of Care in Congenital Heart Disease: Ensuring the Proper Handoff.

Authors:  Angela Lee; Barbara Bailey; Geraldine Cullen-Dean; Sandra Aiello; Joanne Morin; Erwin Oechslin
Journal:  Curr Cardiol Rep       Date:  2017-06       Impact factor: 2.931

5.  Preparing adolescents with heart problems for transition to adult care, 2009-2010 National Survey of Children with Special Health Care Needs.

Authors:  Karrie F Downing; Matthew E Oster; Sherry L Farr
Journal:  Congenit Heart Dis       Date:  2017-05-19       Impact factor: 2.007

Review 6.  So hard to say goodbye: transition from paediatric to adult cardiology care.

Authors:  Adrienne H Kovacs; Brian W McCrindle
Journal:  Nat Rev Cardiol       Date:  2013-11-12       Impact factor: 32.419

7.  Survival data and predictors of functional outcome an average of 15 years after the Fontan procedure: the pediatric heart network Fontan cohort.

Authors:  Andrew M Atz; Victor Zak; Lynn Mahony; Karen Uzark; Peter Shrader; Dianne Gallagher; Stephen M Paridon; Richard V Williams; Roger E Breitbart; Steven D Colan; Jonathan R Kaltman; Renee Margossian; Sara K Pasquali; Kerstin Allen; Wyman W Lai; Rosalind Korsin; Bradley S Marino; Nicole Mirarchi; Brian W McCrindle
Journal:  Congenit Heart Dis       Date:  2014-06-17       Impact factor: 2.007

8.  Proximity to Pediatric Cardiac Surgical Care among Adolescents with Congenital Heart Defects in 11 New York Counties.

Authors:  Kristin M Sommerhalter; Tabassum Z Insaf; Tugba Akkaya-Hocagil; Claire E McGarry; Sherry L Farr; Karrie F Downing; George K Lui; Ali N Zaidi; Alissa R Van Zutphen
Journal:  Birth Defects Res       Date:  2017-11-01       Impact factor: 2.344

9.  Long-term outcomes in children with congenital heart disease: National Health Interview Survey.

Authors:  Hilda Razzaghi; Matthew Oster; Jennita Reefhuis
Journal:  J Pediatr       Date:  2014-10-08       Impact factor: 4.406

10.  Longitudinal Outcomes of Patients With Single Ventricle After the Fontan Procedure.

Authors:  Andrew M Atz; Victor Zak; Lynn Mahony; Karen Uzark; Nicholas D'agincourt; David J Goldberg; Richard V Williams; Roger E Breitbart; Steven D Colan; Kristin M Burns; Renee Margossian; Heather T Henderson; Rosalind Korsin; Bradley S Marino; Kaitlyn Daniels; Brian W McCrindle
Journal:  J Am Coll Cardiol       Date:  2017-06-06       Impact factor: 24.094

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