Modelling the Transference of Paediatric Patients with Inborn Errors of Metabolism to Adult Hospitals: Clinical Experience
Authors:
- Aida DeuderoADAida Deudero
- Esther LasherasELEsther Lasheras
- Roser VenturaRVRoser Ventura
- Cristina Montserrat-CarbonellCMCristina Montserrat-Carbonell
- José César MilisendaJMJosé César Milisenda
- Natalia Juliá-PalaciosNJNatalia Juliá-Palacios
- Ana MatasAna Matas
- María de Talló Forga-VisaMFMaría de Talló Forga-Visa
- Rosa María López-GaleraRLRosa María López-Galera
- Judit García-VilloriaJGJudit García-Villoria
- Mercè PlaceresMPMercè Placeres
- Adriana PanéAPAdriana Pané
Open Access
- 22 December 2025
- journal article
- research article
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 15 (1) , 81
Abstract
Background/Objectives: Inborn errors of metabolism (IEM) are chronic, life-threatening genetic disorders with a significant cumulative prevalence worldwide. Advances in early diagnosis and treatment have significantly increased life expectancy, underscoring the need for specialised adult care units and the establishment of structured transition programmes from paediatric to adult services. We hereby present a functional transition model for IEM patients and share our implementation experience. Methods: Initiated in 2012, the partnership between the paediatric Hospital Sant Joan de Déu (HSJD) and the adult-care centre at Hospital Clinic of Barcelona (HCB) culminated in 2019 with the transference of the first IEM patients under the structured A10! Programme. This model is structured around the transition units of paediatric and adult centres to guarantee communication and functional management. Regular monthly meetings at each centre and joint quarterly sessions allowed for protocol harmonisation and personalised care planning. Coordinated engagement of the multidisciplinary health care teams with patients and families smoothed the transfer process. Results: Between 2019 and 2024, 94 IEM patients were successfully transferred. Diagnoses included intermediary metabolism defects (71.23%), lipid metabolism and transport disorders (4.25%), heterocyclic compound metabolism (2.12%), complex molecules and organelle dysfunction (6.37%), cofactor and mineral metabolism (2.12%), signalling defects (5.31%), and unclassified cases (8.51% of rare disorders, maybe non-IEM). Transition formats included 21 in-person joint visits in HSJD, 37 remote transitions during the COVID-19 pandemic, and 36 streamlined transfers via standardised protocols. Sessions, trainings, and meetings allowed the exchange of patients’ needs and protocols. Conclusions: The successful transference of IEM patients requires structured programmes with interdisciplinary paediatric and adult teams, joining efforts with the patient, families, and caregivers. Communication between paediatric and adult transition units is essential to promote continuity of care and patient empowerment. While constantly updated, this model has proven effective, gaining positive evaluations from healthcare professionals and patients alike, representing a scalable framework for lifelong management of IEM in adult care settings.Keywords
Funding Information
- Generalitat de Catalunya (2021SGR01423)
This publication has 44 references indexed in Scilit:
- Incidence and genetic variants of inborn errors of metabolism identified through newborn screening: A 7‐year study in eastern coastal areas of ChinaMolecular Genetics & Genomic Medicine, 2023
- An international classification of inherited metabolic disorders (ICIMD)Journal of Inherited Metabolic Disease, 2020
- Transition and Transfer From Pediatric to Adult Congenital Heart Disease Care in Canada: Call For Strategic ImplementationCanadian Journal of Cardiology, 2019
- Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M)Archives de Pédiatrie, 2018
- Pacientes empoderados para una mayor confianza en el sistema sanitarioRevista de Calidad Asistencial, 2015
- Transition of young adults with phenylketonuria from pediatric to adult careJournal of Inherited Metabolic Disease, 2011
- Transition from pediatric to adult health care: expectations of adolescents with chronic disorders and their parentsEuropean Journal of Pediatrics, 2010
- The truth of treating patients with phenylketonuria after childhood: The need for a new guidelineJournal of Inherited Metabolic Disease, 2008
- Erwachsene mit angeborenen StoffwechselkrankheitenMedizinische Klinik, 2005
- Transition to adult health care: Setting the stageJournal of Adolescent Health, 1995