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

Molnar, Maria Judit [Molnár, Mária Judit (Neurológia), author] Genomic Medicine and the Institute of Rare Dise... (SU / FM / I); Szabó, Léna [Szabó, Léna (Gyermekgyógyászat), author] Department of Pediatrics (SU / FM / C); Vladacenco, Oana Aurelia; Cobzaru, Ana Maria; Dor, Talya; Dori, Amir; Papadimas, Georgios; Juříková, Lenka; Litvinenko, Ivan; Tournev, Ivailo; Dixon, Craig ✉

English Article (Journal Article) Scientific
Published: ORPHANET JOURNAL OF RARE DISEASES 1750-1172 1750-1172 19 (1) Paper: 260 , 13 p. 2024
  • SJR Scopus - Genetics (clinical): Q1
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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.
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2026-10-13 14:52