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Idiopathic hypersomnia years after the diagnosis
K. Šonka, E. Feketeová, S. Nevšímalová, EM. Horvat, I. Příhodová, S. Dostálová, K. Galušková, M. Milata, J. Bušková, M. Susta
Language English Country England, Great Britain
Document type Journal Article
Grant support
Charles University Cooperatio program in neuroscience
NU20-04-00088
Ministry of Health of the Czech Republic
PubMed
37572055
DOI
10.1111/jsr.14011
Knihovny.cz E-resources
- MeSH
- Adult MeSH
- Idiopathic Hypersomnia * diagnosis epidemiology drug therapy MeSH
- Comorbidity MeSH
- Middle Aged MeSH
- Humans MeSH
- Narcolepsy * diagnosis epidemiology MeSH
- Disorders of Excessive Somnolence * diagnosis epidemiology complications MeSH
- Attention MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
Little attention has been paid to the long-term development of idiopathic hypersomnia symptoms and idiopathic hypersomnia comorbidities. The aim of this study was to describe the general health of patients with idiopathic hypersomnia years after the initial diagnosis, focusing on current subjective hypersomnolence and the presence of its other possible causes. Adult patients diagnosed with idiopathic hypersomnia ≥ 3 years ago at sleep centres in Prague and Kosice were invited to participate in this study. A total of 60 patients were examined (age 47.3 ± SD = 13.2 years, 66.7% women). In all participants, their hypersomnolence could not be explained by any other cause but idiopathic hypersomnia at the time of diagnosis. The mean duration of follow-up was 9.8 + 8.0 years. Fifty patients (83%) reported persisting hypersomnolence, but only 33 (55%) had no other disease that could also explain the patient's excessive daytime sleepiness and/or prolonged sleep. In two patients (3%), the diagnosis in the meantime had changed to narcolepsy type 2, and 15 patients (25%) had developed a disease or diseases potentially causing hypersomnolence since the initial diagnosis. Complete hypersomnolence resolution without stimulant treatment lasting longer than 6 months was reported by 10 patients (17%). To conclude, in a longer interval from the diagnosis of idiopathic hypersomnia, hypersomnolence may disappear or may theoretically be explained by another newly developed disease, or the diagnosis may be changed to narcolepsy type 2. Thus, after 9.8 years, only 55% of the examined patients with idiopathic hypersomnia had a typical clinical picture of idiopathic hypersomnia without doubts about the cause of the current hypersomnolence.
References provided by Crossref.org
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