Quality of life, anxiety and depression in adult patients after add-on of levetiracetam and conversion to levetiracetam monotherapy

Anne Hagemann, Theodor W. May, Esther Nieder, Karin Witte-Bölt, Bernd Pohlmann-Eden, Christian E. Elger, Frithjof Tergau, Andreas Schulze-Bonhage, Hans Beatus Straub, Stephan Arnold, Christian Brandt

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

15 Citas (Scopus)

Resumen

The aim of this study was to investigate the change of health related quality of life (HRQoL), anxiety and depression in adult patients in whom an adjunctive treatment with levetiracetam (LEV) was converted to a LEV monotherapy. A prospective, open, investigator initiated multicenter study enrolled 140 patients in whom LEV was added to the existing antiepileptic medication. A total of 65 patients who benefited from the 16-week add-on treatment with LEV (≥50% seizure reduction) were converted to LEV monotherapy (16-week follow-up). In LEV responders, HRQoL, anxiety and depression improved after add-on of LEV. The subsequent conversion to LEV monotherapy did not lead to a significant change in HRQoL, anxiety and depression. However, comparing baseline with LEV monotherapy, the improvements remained significant for most dimensions of HRQoL and for anxiety and depression. Patients' ratings of efficacy of LEV were related with their HRQoL after the conversion to monotherapy. Add-on therapy of LEV improved HRQoL, anxiety and depression in LEV responders. Conversion to a LEV monotherapy did not inevitably improve HRQoL in LEV responders, but the positive effect was maintained in the majority of the patients. The effects were highly related to seizure reduction.

Idioma originalEnglish
Páginas (desde-hasta)140-150
Número de páginas11
PublicaciónEpilepsy Research
Volumen104
N.º1-2
DOI
EstadoPublished - mar. 2013

Nota bibliográfica

Funding Information:
This investigator-initiated study was supported by UCB.

Funding Information:
CB, FT have received support from, and/or have served as a paid consultant for UCB, Pfizer, Eisai, Novartis, GSK, Janssen-Cilag, and Desitin. EN has received support from Sanofi Pasteur MSD. BP received research grants and honoraria from Desitin Germany, Eisai Canada, Pfizer, and UCB. CE received speaker honoraria from Desitin, Pfizer, UCB, GSK and grants from the Deutsche Forschungsgemeinschaft. AS has received support from and/or has received honoraria from Desitin, Eisai, GSK, Pfitzer, UCB. HS received research grants and honoraria from UCB, Eisai, Pfizer, Glaxo-Smith-Kline and Desitin. SA has participated in research projects of UCB/Schwarz BioSciences, Eisai, Novartis and Valeant. He also has served as a paid consultant for UCB and Janssen-Cilag, and received honorarium as a speaker for UCB, Janssen-Cilag and Eisai. TM has participated in research projects with unrestricted grants from Desitin, Eisai, GSK, Janssen-Cilag, Pfizer, Sanofi-Aventis and UCB. AH, KW have declared no conflicts of interest.

ASJC Scopus Subject Areas

  • Neurology
  • Clinical Neurology

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