دورية أكاديمية

Essen transition model for neuromuscular diseases

التفاصيل البيبلوغرافية
العنوان: Essen transition model for neuromuscular diseases
المؤلفون: Michael Fleischer, Bayram Coskun, Benjamin Stolte, Adela Della-Marina, Heike Kölbel, Hildegard Lax, Michael Nonnemacher, Christoph Kleinschnitz, Ulrike Schara-Schmidt, Tim Hagenacker
المصدر: Neurological Research and Practice, Vol 4, Iss 1, Pp 1-7 (2022)
بيانات النشر: BMC, 2022.
سنة النشر: 2022
المجموعة: LCC:Neurosciences. Biological psychiatry. Neuropsychiatry
LCC:Neurology. Diseases of the nervous system
مصطلحات موضوعية: Transition, Neuromuscular diseases, Late-onset Pompe disease, Juvenile myasthenia gravis, Duchenne muscular dystrophy, The concept of care, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurology. Diseases of the nervous system, RC346-429
الوصف: Abstract Background With the optimization of medical care structures and the rapid progress in the development of new therapeutic methods, an increase in life expectancy is observed in patients with neuromuscular diseases. This leads to an expansion of the phenotypic spectrum, whereby new or previously less relevant disease manifestations in different organ systems gain more importance. The care of adolescents and young adults with neuromuscular diseases, therefore, requires increasingly close interdisciplinary collaboration within neuromuscular centers. Research question How can the transition process from pediatric to adult care be structured so that the individual disciplines are efficiently integrated into the complex treatment and care process, and the patients' quality of life is improved? Material and methods A structured transition process was established at the University Hospital in Essen, Germany. Exemplarily, a comparable care concept was developed based on Pompe disease, Duchenne muscular dystrophy, and juvenile myasthenia gravis comprising four elements: (1) With the introduction of cross-department standard operating procedures, the logistical processes, as well as the diagnostic and therapeutic measures, are uniformly coordinated, and the transition process is bindingly defined. (2) To ensure a seamless transition, young patients are seen with their parents during joint consultations before they reach their 17th birthday. This creates an opportunity for patients to get to know the subsequent department structure and build a lasting relationship of trust. (3) A quarterly “transition board” regularly brings together the participating disciplines from pediatric and adult care systems for a case-related interdisciplinary exchange and continuous optimization of the transition process. (4) A cross-department “Transition Database”, in which medical findings and parameters are recorded, was implemented as a common information platform and database. Conclusion The Essen Transition Model aims to close the gap in care for young patients with neuromuscular diseases during the critical transition from pediatric to adult medicine and to create a successful continuation of treatment in adulthood.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2524-3489
Relation: https://doaj.org/toc/2524-3489
DOI: 10.1186/s42466-022-00206-8
URL الوصول: https://doaj.org/article/2d98e2fca23a47679888b8f7380b17e1
رقم الأكسشن: edsdoj.2d98e2fca23a47679888b8f7380b17e1
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:25243489
DOI:10.1186/s42466-022-00206-8