Literature DB >> 29914755

Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M).

B Chabrol1, P Jacquin2, L Francois2, P Broué3, D Dobbelaere4, C Douillard4, S Dubois5, F Feillet6, A Perrier7, A Fouilhoux8, F Labarthe8, D Lamireau9, K Mazodier10, F Maillot8, F Mochel11, M Schiff2, N Belmatoug12.   

Abstract

Inherited metabolic diseases (IMD) form a heterogeneous group of genetic disorders that surface primarily during childhood and result in significant morbidity and mortality. A prevalence of 1 in 2500-5000 live births is often reported. The transfer of adolescents from pediatric care to adult health facilities is often difficult for patients and their families and can lead to a breakdown in medical follow-up and therefore serious complications. Existing recommendations for the successful transition of patients with chronic disorders do not specifically address patients with IMDs associated with dietary treatment. Here, the French network for rare inherited metabolic diseases (G2M) presents its reflections and recommendations for a successful transition. Preparations for the transfer must be made well in advance. The transfer must aim for adolescents gaining autonomy by making them responsible and providing them with the knowledge that will enable them to manage their care themselves, know how to react appropriately if there is any change in their condition, and move comfortably within the adult healthcare system. This requires the active participation of the patient, his or her family, and pediatric and adult care teams. It involves multidisciplinary management plus the production and maintenance of an educational therapy program. Finally, the identification of physicians and dietitians trained in IMDs, relevant subspecialists, and even expert patients could improve the continuum of complete and appropriate care for these patients within adult medicine.
Copyright © 2018. Published by Elsevier Masson SAS.

Entities:  

Keywords:  Hereditary metabolic diseases; Pediatric care; Transition

Year:  2018        PMID: 29914755     DOI: 10.1016/j.arcped.2018.05.009

Source DB:  PubMed          Journal:  Arch Pediatr        ISSN: 0929-693X            Impact factor:   1.180


  4 in total

1.  Implementing a Transition Program from Paediatric to Adult Services in Phenylketonuria: Results After Two Years of Follow-Up with an Adult Team.

Authors:  Maria Peres; Manuela F Almeida; Élia J Pinto; Carla Carmona; Sara Rocha; Arlindo Guimas; Rosa Ribeiro; Esmeralda Martins; Anabela Bandeira; Anita MacDonald; Júlio C Rocha
Journal:  Nutrients       Date:  2021-02-28       Impact factor: 5.717

2.  Transition from child to adult health care for patients with lysosomal storage diseases in France: current status and priorities-the TENALYS study, a patient perspective survey.

Authors:  Delphine Genevaz; Armelle Arnoux; Catherine Marcel; Anaïs Brassier; Samia Pichard; François Feillet; François Labarthe; Brigitte Chabrol; Marc Berger; Anne-Sophie Lapointe; Yvann Frigout; Bénédicte Héron; Gilles Chatellier; Nadia Belmatoug
Journal:  Orphanet J Rare Dis       Date:  2022-02-21       Impact factor: 4.123

3.  The Epidemiology of Transition into Adulthood of Rare Diseases Patients: Results from a Population-Based Registry.

Authors:  Monica Mazzucato; Laura Visonà Dalla Pozza; Cinzia Minichiello; Silvia Manea; Sara Barbieri; Ema Toto; Andrea Vianello; Paola Facchin
Journal:  Int J Environ Res Public Health       Date:  2018-10-10       Impact factor: 3.390

Review 4.  Healthcare transition from childhood to adulthood in Tuberous Sclerosis Complex.

Authors:  Angela Peron; Maria Paola Canevini; Filippo Ghelma; Fabiano Di Marco; Aglaia Vignoli
Journal:  Am J Med Genet C Semin Med Genet       Date:  2018-09-25       Impact factor: 3.908

  4 in total

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