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Outpatient volumes and medical staf fing resources as predictors for continuity of follow-up care during transfer of adolescents with congenital heart disease
Institute of Health and Care Sciences, University of Gothenburg, Gothenburg, Sweden; Department of Paediatric Cardiology, Queen Silvia's Children's Hospital, Gothenburg, Sweden; KU Leuven Department of Public Health and Primary Care, Leuven, Belgium.
Institute of Health and Care Sciences, University of Gothenburg, Gothenburg, Sweden; KU Leuven Department of Public Health and Primary Care, Leuven, Belgium; Department of Paediatrics and Child Health, University of Cape Town, South Africa.ORCID iD: 0000-0002-8609-4516
Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.ORCID iD: 0000-0003-0976-6910
Department of Paediatric Cardiology, Queen Silvia's Children's Hospital, Gothenburg, Sweden.
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2020 (English)In: International Journal of Cardiology, ISSN 0167-5273, E-ISSN 1874-1754, Vol. 310, p. 51-57Article in journal (Refereed) Published
Abstract [en]

Background: Providing continuous follow-up care to patients with congenital heart disease (CHD) remains a challenge in many settings. Previous studies highlight that patients with CHD experience discontinuation of followup care, but mainly describe a single-centre perspective, neglecting inter-institutional variations. Hospital-related factors above and beyond patient-related factors are believed to affect continuity of care. The present multicentre study therefore investigated (i) proportion of "no follow-up care"; (ii) transfer destinations after leaving paediatric cardiology; (iii) variation in proportions of no follow-up between centres; (iv) the association between no follow-up and outpatient volumes, and (v) its relationship with staffing resources at outpatient clinics.

Methods: An observational, multicentre study was conducted in seven university hospitals. In total, 654 adolescentswith CHD, born between 1991 and 1993, with paediatric outpatient visit at age 14-18 years were included. Transfer status was determined 5 years after the intended transfer to adult care (23y), based on medical files, self-reports and registries.

Results: Overall, 89.7% of patients were receiving adult follow-up care after transfer; 6.6% had no follow-up; and 3.7% were untraceable. Among patients in follow-up care, only one remained in paediatric care and the majority received specialist adult CHD care. Significant variability in proportions of no follow-up were identified across centres. Higher outpatient volumes at paediatric outpatient clinics were associated with better continued follow-up care after transfer (OR = 1.061; 95% CI = 1.001 - 1.124). Medical staffing resources were not found predictive.

Conclusion: Our findings support the theory of hospital-related factors influencing continuity of care, above and beyond patient-related characteristics. (c) 2020 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

Place, publisher, year, edition, pages
Elsevier, 2020. Vol. 310, p. 51-57
Keywords [en]
Adolescent, Continuity of patient care, Heart defects, congenital, Patient transfer, Young adult, Transition to adult care
National Category
Cardiology and Cardiovascular Disease
Identifiers
URN: urn:nbn:se:oru:diva-85062DOI: 10.1016/j.ijcard.2020.01.016ISI: 000552054400012PubMedID: 31959410Scopus ID: 2-s2.0-85077930713OAI: oai:DiVA.org:oru-85062DiVA, id: diva2:1461324
Funder
Swedish Heart Lung FoundationForte, Swedish Research Council for Health, Working Life and Welfare, 2016-07259
Note

Funding Agencies:

Institute of Health and Care Sciences of the University of Gothenburg  

South African Medical Research Council through FORTE  

National Research Foundation - South Africa

Available from: 2020-08-26 Created: 2020-08-26 Last updated: 2025-02-10Bibliographically approved

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Fadl, Shalan

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