• Medicina · Aug 2020

    Transition from Childhood to Adulthood in Patients with Duchenne Muscular Dystrophy.

    • Eliza Wasilewska, Sylwia Małgorzewicz, Agnieszka Sobierajska-Rek, Joanna Jabłońska-Brudło, Lucyna Górska, Karolina Śledzińska, Joanna Bautembach-Minkowska, and Jolanta Wierzba.
    • Department of Allergology and Pulmonology, Medical University of Gdańsk, 80-211 Gdańsk, Poland.
    • Medicina (Kaunas). 2020 Aug 24; 56 (9).

    AbstractRecently, progress has been observed in the knowledge about Duchenne Muscular Dystrophy (DMD), which is a severe and commonly diagnosed genetic myopathy in childhood, historically resulting in early death. Currently, there are a lot of methods available to improve the clinical course of DMD and extend patients' life expectancy to more than 30 years of age. The key issue for DMD patients is the period between 16-18 years of age, which is described as a transition from pediatric- to adult-oriented healthcare. Adolescents and adults with DMD have highly complex healthcare needs associated with long-term steroid usage, orthopedic, ventilation, cardiac, and gastrointestinal problems. The current paper provides a comprehensive overview of special healthcare needs related to the transfer of a patient with DMD from child-oriented to adult-oriented care. Additionally, the need to organize effective care for adults with DMD is presented.

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