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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; Szabó, Léna; Vladacenco, Oana Aurelia; Cobzaru, Ana Maria; Dor, Talya; Dori, Amir; Papadimas, Georgios; Juríková, Lenka; Litvinenko, Ivan; Tournev, Ivailo; Dixon, Craig.
Afiliação
  • Molnar MJ; Director of Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.
  • Szabó L; Pediatric Center, Semmelweis University, Budapest, Hungary.
  • Vladacenco OA; University of Medicine and Pharmacy Bucharest, Bucharest, Romania.
  • Cobzaru AM; University Emergency Hospital Bucharest, Bucharest, Romania.
  • Dor T; Pediatric Neurology Unit, Hadassah University Hospital, Jerusalem, Israel.
  • Dori A; Sheba Medical Center at Tel-Hashomer, Neurology Clinic, Ramat-Gan, Israel.
  • Papadimas G; First Department of Neurology, University of Athens, Athens, Greece.
  • Juríková L; Department of Pediatric Neurology, University Hospital Brno, Brno, Czech Republic.
  • Litvinenko I; Pediatric Neurology Department, SHATPD "Prof. Dr. Ivan Mitev", Sofia, Bulgaria.
  • Tournev I; Department of Neurology, University Hospital Aleksandrovska, Medical University, Sofia, Bulgaria.
  • Dixon C; Department of Cognitive Science and Psychology, New Bulgarian University, Sofia, Bulgaria.
Orphanet J Rare Dis ; 19(1): 260, 2024 Jul 09.
Article em En | MEDLINE | ID: mdl-38982500
ABSTRACT

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Técnica Delphi / Distrofia Muscular de Duchenne Limite: Adolescent / Adult / Child / Female / Humans / Male País/Região como assunto: Asia / Europa Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Técnica Delphi / Distrofia Muscular de Duchenne Limite: Adolescent / Adult / Child / Female / Humans / Male País/Região como assunto: Asia / Europa Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2024 Tipo de documento: Article