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

Published online by Cambridge University Press:  13 April 2020

Stephanie S. Gaydos*
Affiliation:
Division of Pediatric Cardiology, Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA
Shahryar M. Chowdhury
Affiliation:
Division of Pediatric Cardiology, Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA
Rochelle N. Judd
Affiliation:
Division of Cardiology, Department of Medicine, Medical University of South Carolina, Charleston, SC, USA
Kimberly E. McHugh
Affiliation:
Division of Pediatric Cardiology, Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA
*
Author for correspondence: S. S. Gaydos, Division of Pediatric Cardiology, Department of Pediatrics, Medical University of South Carolina, Shawn Jenkins Children’s Hospital, 10 McClellan Banks Drive, MSC 915 Charleston, SC29425, USA. Tel: +843-792-3286; Fax: +843-792-3284. E-mail [email protected]

Abstract

Background:

Children with congenital heart disease (CHD) require lifelong cardiology follow-up. Many experience gaps in care around the age of transition to adult-oriented care with associated comorbidity. We describe the impact of a clinic-based intervention on follow-up rates in this high-risk population.

Methods:

Patients ≥11 years seen in a paediatric outpatient CHD Transition Clinic completed self-assessment questionnaires, underwent focused teaching, and were followed on a clinic registry with assessment of care continuation. The cohort “lost to follow-up” rate, defined as absence from care at least 6 months beyond the recommended timeframe, was compared with a control group. Secondary outcomes included questionnaire scores and adult cardiology referral trends.

Results:

Over 26 months, 53 participants completed an initial Transition Clinic visit; 43% (23/53) underwent a second visit. Median participant age was 18.0 years (interquartile range 16.0, 22.0). The cohort’s “lost to follow-up” rate was 7.3%, which was significantly lower than the control rate (25.9%, p < 0.01). Multivariable regression analyses demonstrated clinic participation as the only factor independently associated with follow-up rates (p = 0.048). Transition readiness was associated with older age (p = 0.01) but not sex, univentricular heart, interventional history, or surgical complexity. One-third of adult participants transferred to adult care.

Conclusions:

A CHD Transition Clinic intervention can improve follow-up rates in adolescents and young adults. Age is an important factor in transition readiness, and retention of adults in paediatric care appears multi-factorial. We postulate that serial assessments of self-management, focused education, and registry utilisation may improve patient outcomes by reducing lapses in care.

Type
Original Article
Copyright
© The Author(s) 2020. Published by Cambridge University Press

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References

Hoffman, JI, Kaplan, S, Liberthson, RR. Prevalence of congenital heart disease. Am Heart J 2004; 147(3): 425439.CrossRefGoogle ScholarPubMed
Warnes, CA, Liberthson, R, Danielson, GK, et al.Task force 1: the changing profile of congenital heart disease in adult life. J Am Coll Cardiol 2001; 37(5): 11701175.10.1016/S0735-1097(01)01272-4CrossRefGoogle ScholarPubMed
Mackie, AS, Ionescu-Ittu, R, Therrien, J, et al.Children and adults with congenital heart disease lost to follow-up: who and when? Circulation 2009; 120(4): 302309.CrossRefGoogle ScholarPubMed
Yeung, E, Kay, J, Roosevelt, GE, et al.Lapse of care as a predictor for morbidity in adults with congenital heart disease. Int J Cardiol 2008; 125(1): 6265.10.1016/j.ijcard.2007.02.023CrossRefGoogle Scholar
Gurvitz, M, Valente, AM, Broberg, C, et al.Prevalence and predictors of gaps in care among adult congenital heart disease patients: HEART-ACHD (The Health, Education, and Access Research Trial). J Am Coll Cardiol 2013; 61(21): 21802184.CrossRefGoogle Scholar
Wacker, A, Kaemmerer, H, Hollweck, R, et al.Outcome of operated and unoperated adults with congenital cardiac disease lost to follow-up for more than five years. Am J Cardiol 2005; 95(6): 776779.CrossRefGoogle ScholarPubMed
de Bono, J, Freeman, LJ. Aortic coarctation repair-- lost and found: the role of local long term specialised care. International Journal of Cardiology 2005; 104(2): 176183.CrossRefGoogle ScholarPubMed
Gurvitz, MZ, Inkelas, M, Lee, M, et al.Changes in hospitalization patterns among patients with congenital heart disease during the transition from adolescence to adulthood. J Am Coll Cardiol 2007; 49(8): 875882.10.1016/j.jacc.2006.09.051CrossRefGoogle Scholar
Sable, C, Foster, E, Uzark, K, et al.Best practices in managing transition to adulthood for adolescents with congenital heart disease: the transition process and medical and psychosocial issues: a scientific statement from the American Heart Association. Circulation 2011; 123(13): 14541485.CrossRefGoogle ScholarPubMed
Health, T.N.A.t.A.A. Got Transition. 2004; Available from: https://www.gottransition.org/index.cfmGoogle Scholar
Mackie, AS, Islam, S, Magill-Evans, J, et al.Healthcare transition for youth with heart disease: a clinical trial. Heart 2014; 100(14): 11131118.CrossRefGoogle ScholarPubMed
Wood, DL, Sawicki, GS, Miller, MD, et al.The Transition Readiness Assessment Questionnaire (TRAQ): its factor structure, reliability, and validity. Acad Pediatr 2014; 14(4): 415422.CrossRefGoogle ScholarPubMed
Sawicki, GS, Lukens-Bull, K, Yin, X, et al.Measuring the transition readiness of youth with special healthcare needs: validation of the TRAQ--Transition Readiness Assessment Questionnaire. J Pediatr Psychol 2011; 36(2): 160171.10.1093/jpepsy/jsp128CrossRefGoogle ScholarPubMed
Uzark, K, Jones, K, Burwinkle, TM, Varni, JW. The Pediatric Quality of Life Inventory in children with heart disease. Progress in Pediatric Cardiology 2003; 18(2): 141149.10.1016/S1058-9813(03)00087-0CrossRefGoogle Scholar
Ladouceur, M, Calderon, J, Traore, M, Cheurfi, R, Pagnon, C, Khraiche, D, Bajolle, F, Bonnet, D. Educational needs of adolescents with congenital heart disease: Impact of a transition inervention programme. Archives of Cardiovascular Diseases 2017; 110(5): 317324.CrossRefGoogle Scholar
Valente, AM, Landzberg, MJ, Gianola, A, et al.Improving heart disease knowledge and research participation in adults with congenital heart disease (the Health, Education and Access Research Trial: HEART-ACHD). Int J Cardiol 2013; 168(4): 32363240.CrossRefGoogle Scholar
Goossens, E, Fieuws, S, Van Deyk, K, et al.Effectiveness of structured education on knowledge and health behaviors in patients with congenital heart disease. J Pediatr 2015; 166(6): 1370–6.e1.CrossRefGoogle ScholarPubMed
Acuña Mora, M, Sparud-Lundin, C, Bratt, E-L, Moons, P. Person-centred transition programme to empower adolescents with congenital heart disease in the transition to adulthood: a study protocol for a hybrid randomised controlled trial (STEPSTONES project). BMJ Open 2017; 7(4).CrossRefGoogle Scholar
Huang, JS, Terrones, L, Tompane, T, et al.Preparing adolescents with chronic disease for transition to adult care: a technology program. Pediatrics 2014; 133(6): e16391646.10.1542/peds.2013-2830CrossRefGoogle ScholarPubMed
Mackie, AS, Rempel, GR, Kovacs, AH, et al.Transition intervention for adolescents with congenital heart disease. J Am Coll Cardiol 2018; 71(16): 17681777.CrossRefGoogle ScholarPubMed
Goossens, E, Stephani, I, Hilderson, D, et al.Transfer of adolescents with congenital heart disease from pediatric cardiology to adult health care: an analysis of transfer destinations. J Am Coll Cardiol 2011; 57(23): 23682374.CrossRefGoogle ScholarPubMed
Fernandes, SM, Khairy, P, Fishman, L, et al.Referral patterns and perceived barriers to adult congenital heart disease care: results of a survey of U.S. pediatric cardiologists. J Am Coll Cardiol 2012; 60(23): 24112418.CrossRefGoogle ScholarPubMed
Marino, BS, Lipkin, PH, Newburger, JW, et al.Neurodevelopmental outcomes in children with congenital heart disease: evaluation and management: a scientific statement from the American Heart Association. Circulation 2012; 126(9): 11431172.CrossRefGoogle ScholarPubMed
Gaynor, JW, Stopp, C, Wypij, D, et al.Neurodevelopmental outcomes after cardiac surgery in infancy. Pediatrics 2015; 135(5): 816825.10.1542/peds.2014-3825CrossRefGoogle ScholarPubMed
Ilardi, D, Ono, KE, McCartney, R, et al.Neurocognitive functioning in adults with congenital heart disease. Congenit Heart Dis 2017; 12(2): 166173.10.1111/chd.12434CrossRefGoogle ScholarPubMed
Oster, ME, Watkins, S, Hill, KD, et al.Academic outcomes in children with congenital heart defects: a population-based cohort study. Circ Cardiovasc Qual Outcomes 2017; 10(2): p. e003074.CrossRefGoogle ScholarPubMed
Zomer, AC, Vaartjes, I, Uiterwaal, CS, et al.Social burden and lifestyle in adults with congenital heart disease. Am J Cardiol 2012; 109(11): 16571663.CrossRefGoogle ScholarPubMed
Karsenty, C, Maury, P, Blot-Souletie, N, et al.The medical history of adults with complex congenital heart disease affects their social development and professional activity. Arch Cardiovasc Dis 2015; 108(11): 589597.CrossRefGoogle ScholarPubMed
Lee, A, Bailey, B, Cullen-Dean, G, et al.Transition of care in congenital heart disease: ensuring the proper handoff. Curr Cardiol Rep 2017; 19(6): 55.CrossRefGoogle ScholarPubMed
Heery, E, Sheehan, AM, While, AE, et al.Experiences and outcomes of transition from pediatric to adult health care services for young people with congenital heart disease: a systematic review. Congenit Heart Dis 2015; 10(5): 413427.CrossRefGoogle ScholarPubMed
Gurvitz, M, Saidi, A. Transition in congenital heart disease: it takes a village. Heart 2014; 100(14): 10751076.CrossRefGoogle Scholar