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Patient-Reported Outcome Measures in Adult Patients Diagnosed with Epilepsy Being Treated with Perampanel.
Moseley, Brian D; Gupta, Shaloo; Way, Nate; Wright, Jonathon; Rowland, John C; Barghout, Victoria E; Frech, Feride; Plauschinat, Craig.
Affiliation
  • Moseley BD; Department of Neurology and Rehabilitation Medicine, University of Cincinnati, Cincinnati, OH, 45267, USA.
  • Gupta S; Real World Evidence, Cerner Enviza, Malvern, PA, 19355, USA.
  • Way N; Real World Evidence, Cerner Enviza, Malvern, PA, 19355, USA.
  • Wright J; Real World Evidence, Cerner Enviza, Malvern, PA, 19355, USA.
  • Rowland JC; Real World Evidence, Cerner Enviza, Malvern, PA, 19355, USA.
  • Barghout VE; VEB HealthCare LLC, Morristown, NJ, 07960, USA.
  • Frech F; Health Economics, Outcomes Research, and Real World Evidence, Eisai Inc., Nutley, NJ, 07110, USA.
  • Plauschinat C; Health Economics, Outcomes Research, and Real World Evidence, Eisai Inc., Nutley, NJ, 07110, USA.
Patient Relat Outcome Meas ; 13: 39-52, 2022.
Article in En | MEDLINE | ID: mdl-35173501
ABSTRACT

BACKGROUND:

Epilepsy is a complex disorder that can affect patients' medical, psychological, and social well-being. The purpose of this study was to evaluate the patient-reported outcome (PRO) measures of health-related quality of life (HRQoL), satisfaction, and adherence in adult patients diagnosed with epilepsy treated with perampanel in the United States (US).

METHODS:

A US-based, multicenter, observational cross-sectional survey was completed by 61 patients taking perampanel with or without other antiseizure medications (ASMs). Respondents were ≥18 years old, had a physician-confirmed diagnosis of epilepsy, used perampanel for ≥4 months, and provided informed consent. Patients responded to questions concerning their demographic characteristics, treatment history, experiences before perampanel, experiences while taking perampanel, HRQoL, treatment satisfaction, and medication adherence.

RESULTS:

Patients (N=61) were 42.8 years old on average; majority were female (63.9%) and white (75.4%). Mean time on perampanel was 2.5 years, with sodium channel blockers often (55.7%) used concomitantly with perampanel. Patients reported, on average, 5.5 (standard deviation [SD]=13.2) seizures/month after initiating perampanel, whereas these same patients reported experiencing 20.4 (SD=60.0) seizures/month prior to perampanel. When comparing their experience on perampanel with their experience with previous ASMs, more patients "strongly agreed" that perampanel allowed them to live a more normal life (36.1% vs 27.5%) and worked as intended if they missed taking a dose (16.4% vs 7.8%). Average satisfaction scores were high, with ratings of 71.8 for effectiveness, 84.0 for convenience, and 71.9 for global satisfaction (0-100 scores). Perampanel use was associated with improvements in HRQoL and fewer symptoms of depression and anxiety. The majority of patients were adherent (62.3%) to perampanel.

DISCUSSION:

Perampanel use was associated with reductions in number of seizures, better HRQoL, and high adherence rates. These results provide initial evidence that perampanel can be an effective, tolerable, and valid option for patients with epilepsy in the real world.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Diagnostic_studies / Risk_factors_studies Aspects: Patient_preference Language: En Journal: Patient Relat Outcome Meas Year: 2022 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Diagnostic_studies / Risk_factors_studies Aspects: Patient_preference Language: En Journal: Patient Relat Outcome Meas Year: 2022 Document type: Article Affiliation country: Estados Unidos