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Verfasst von:Maltseva, Margarita [VerfasserIn]   i
 Schubert-Bast, Susanne [VerfasserIn]   i
 Zöllner, Johann Philipp [VerfasserIn]   i
 Bast, Thomas [VerfasserIn]   i
 Mayer, Thomas [VerfasserIn]   i
 von Spiczak, Sarah [VerfasserIn]   i
 Ruf, Susanne [VerfasserIn]   i
 Trollmann, Regina [VerfasserIn]   i
 Wolff, Markus [VerfasserIn]   i
 Hornemann, Frauke [VerfasserIn]   i
 Klotz, Kerstin A. [VerfasserIn]   i
 Jacobs-LeVan, Julia [VerfasserIn]   i
 Kurlemann, Gerhard [VerfasserIn]   i
 Neubauer, Bernd A. [VerfasserIn]   i
 Polster, Tilman [VerfasserIn]   i
 Syrbe, Steffen [VerfasserIn]   i
 Bertsche, Astrid [VerfasserIn]   i
 Bettendorf, Ulrich [VerfasserIn]   i
 Kluger, Gerhard [VerfasserIn]   i
 Flege, Silke [VerfasserIn]   i
 Rosenow, Felix [VerfasserIn]   i
 Kay, Lara [VerfasserIn]   i
 Strzelczyk, Adam [VerfasserIn]   i
Titel:Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome
Titelzusatz:a prospective multicenter study in Germany
Verf.angabe:Margarita Maltseva, Susanne Schubert-Bast, Johann Philipp Zöllner, Thomas Bast, Thomas Mayer, Sarah von Spiczak, Susanne Ruf, Regina Trollmann, Markus Wolff, Frauke Hornemann, Kerstin A. Klotz, Julia Jacobs, Gerhard Kurlemann, Bernd A. Neubauer, Tilman Polster, Steffen Syrbe, Astrid Bertsche, Ulrich Bettendorf, Gerhard Kluger, Silke Flege, Felix Rosenow, Lara Kay and Adam Strzelczyk
E-Jahr:2023
Jahr:29 April 2023
Umfang:14 S.
Fussnoten:Gesehen am 07.07.2023
Titel Quelle:Enthalten in: Orphanet journal of rare diseases
Ort Quelle:London : BioMed Central, 2006
Jahr Quelle:2023
Band/Heft Quelle:18(2023) vom: Apr., Artikel-ID 98, Seite 1-14
ISSN Quelle:1750-1172
Abstract:Background: This study measured sleep quality among caregivers of patients with Dravet syndrome (DS) and assessed the impacts of mental health problems and caregiver burden on sleep quality. Methods: This multicenter, cross-sectional study of patients with DS and their caregivers throughout Germany consisted of a questionnaire and a prospective 4-week diary querying disease characteristics, demographic data, living conditions, nocturnal supervision, and caregivers’ work situations. Sleep quality was assessed using the Pittsburgh Sleeping Quality Index (PSQI). The Hospital Anxiety and Depression Scale (HADS) and the Burden Scale for Family Caregivers (BSFC) were used to measure anxiety, symptoms of depression, and caregiver burden. Results: Our analysis included 108 questionnaires and 82 four-week diaries. Patients with DS were 49.1% male (n = 53), with a mean age of 13.5 ± 10.0 years. Caregivers were 92.6% (n = 100) female, with a mean age of 44.7 ± 10.6 years. The overall mean PSQI score was 8.7 ± 3.5, with 76.9% of participants (n = 83) scoring 6 or higher, indicating abnormal sleep quality. The HADS for anxiety and depression had overall mean scores of 9.3 ± 4.3 and 7.9 ± 3.7, respectively; 61.8% and 50.9% of participants scored above the cutoff value of 8 for anxiety and depression, respectively. Statistical analyses revealed caregiver anxiety levels and patients’ sleep disturbances as major factors influencing PSQI scores. The overall mean BSFC score of 41.7 ± 11.7 indicates a moderate burden, with 45.3% of caregivers scoring 42 or higher. Conclusions: Sleep quality is severely affected among caregivers of patients with DS, correlating with anxiety, comorbidities, and patients’ sleep disturbances. A holistic therapeutic approach should be implemented for patients with DS and their caregivers, focusing on the sleep quality and mental health of caregivers. Trial registration: German Clinical Trials Register (DRKS), DRKS00016967. Registered 27 May 2019, http://www.drks.de/DRKS00016967
DOI:doi:10.1186/s13023-023-02697-3
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.1186/s13023-023-02697-3
 DOI: https://doi.org/10.1186/s13023-023-02697-3
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Encephalopathy
 Epilepsy
 Quality of life
 Seizure
K10plus-PPN:185216140X
Verknüpfungen:→ Zeitschrift

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