Essential components of an effective transition from paediatric to adult neurologist care for adolescents with Duchenne muscular dystrophy; a consensus derived using the Delphi methodology in Eastern Europe, Greece and Israel
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
PubMed
38982500
PubMed Central
PMC11234532
DOI
10.1186/s13023-024-03270-2
PII: 10.1186/s13023-024-03270-2
Knihovny.cz E-zdroje
- Klíčová slova
- Adolescents, DMD, Delphi, Duchenne muscular dystrophy, Life expectancy, Transition,
- MeSH
- delfská metoda * MeSH
- dítě MeSH
- dospělí MeSH
- Duchennova muskulární dystrofie * terapie MeSH
- konsensus MeSH
- lidé MeSH
- mladiství MeSH
- neurologové MeSH
- přechod k lékaři pro dospělé MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Evropa MeSH
- Izrael MeSH
- Řecko MeSH
PURPOSE: An increasing number of patients with Duchenne muscular dystrophy (DMD) now have access to improved standard of care and disease modifying treatments, which improve the clinical course of DMD and extend life expectancy beyond 30 years of age. A key issue for adolescent DMD patients is the transition from paediatric- to adult-oriented healthcare. Adolescents and adults with DMD have unique but highly complex healthcare needs associated with long-term steroid use, orthopaedic, respiratory, cardiac, psychological, and gastrointestinal problems meaning that a comprehensive transition process is required. A sub-optimal transition into adult care can have disruptive and deleterious consequences for a patient's long-term care. This paper details the results of a consensus amongst clinicians on transitioning adolescent DMD patients from paediatric to adult neurologists that can act as a guide to best practice to ensure patients have continuous comprehensive care at every stage of their journey. METHODS: The consensus was derived using the Delphi methodology. Fifty-three statements were developed by a Steering Group (the authors of this paper) covering seven topics: Define the goals of transition, Preparing the patient, carers/parents and the adult centre, The transition process at the paediatric centre, The multidisciplinary transition summary - Principles, The multidisciplinary transition summary - Content, First visit in the adult centre, Evaluation of transition. The statements were shared with paediatric and adult neurologists across Central Eastern Europe (CEE) as a survey requesting their level of agreement with each statement. RESULTS: Data from 60 responders (54 full responses and six partial responses) were included in the data set analysis. A consensus was agreed across 100% of the statements. CONCLUSIONS: It is hoped that the findings of this survey which sets out agreed best practice statements, and the transfer template documents developed, will be widely used and so facilitate an effective transition from paediatric to adult care for adolescents with DMD.
1st Department of Neurology University of Athens Athens Greece
Department of Cognitive Science and Psychology New Bulgarian University Sofia Bulgaria
Department of Neurology University Hospital Aleksandrovska Medical University Sofia Bulgaria
Department of Pediatric Neurology University Hospital Brno Brno Czech Republic
Director of Institute of Genomic Medicine and Rare Disorders Semmelweis University Budapest Hungary
Pediatric Center Semmelweis University Budapest Hungary
Pediatric Neurology Department SHATPD Prof Dr Ivan Mitev Sofia Bulgaria
Pediatric Neurology Unit Hadassah University Hospital Jerusalem Israel
Sheba Medical Center at Tel Hashomer Neurology Clinic Ramat Gan Israel
University Emergency Hospital Bucharest Bucharest Romania
University of Medicine and Pharmacy Bucharest Bucharest Romania
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