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Serum sodium levels and related treatment-emergent adverse events during eslicarbazepine acetate use in adults with epilepsy.
Wechsler, Robert T; Radtke, Rodney A; Smith, Michael; Vossler, David G; Strom, Laura; Trinka, Eugen; Cheng, Hailong; Grinnell, Todd; Blum, David; Vieira, Mariana; Moreira, Joana; Rocha, Francisco.
  • Wechsler RT; Idaho Comprehensive Epilepsy Center, Boise, Idaho.
  • Radtke RA; Duke University School of Medicine, Durham, North Carolina.
  • Smith M; Rush University Medical Center, Chicago, Illinois.
  • Vossler DG; University of Washington, Valley Medical Center, Renton, Washington.
  • Strom L; University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Trinka E; Uniklinikum Salzburg, Christian-Doppler-Klinik, Salzburg, Austria.
  • Cheng H; Sunovion Pharmaceuticals, Inc., Marlborough, Massachusetts.
  • Grinnell T; Sunovion Pharmaceuticals, Inc., Marlborough, Massachusetts.
  • Blum D; Sunovion Pharmaceuticals, Inc., Marlborough, Massachusetts.
  • Vieira M; BIAL - Portela & Cª., S.A., Coronado (S. Romão e S. Mamede), Portugal.
  • Moreira J; BIAL - Portela & Cª., S.A., Coronado (S. Romão e S. Mamede), Portugal.
  • Rocha F; BIAL - Portela & Cª., S.A., Coronado (S. Romão e S. Mamede), Portugal.
Epilepsia ; 60(7): 1341-1352, 2019 07.
Article en En | MEDLINE | ID: mdl-31260089
ABSTRACT

OBJECTIVE:

To examine the frequency of hyponatremia and potentially related symptoms in clinical trials of eslicarbazepine acetate (ESL) in adults with focal- (partial-) onset seizures.

METHODS:

This post hoc, exploratory analysis included data from three controlled phase 3 trials of adjunctive ESL (400-1200 mg once daily), two phase 3 trials of ESL monotherapy (1200-1600 mg once daily), and their open-label extension studies. Exploratory endpoints included clinical laboratory measurements of serum sodium concentrations ([Na+ ]), incidences of hyponatremia-related treatment-emergent adverse events (TEAEs), and incidences of TEAEs that are potential symptoms of hyponatremia.

RESULTS:

The controlled trials of adjunctive ESL and ESL monotherapy included 1447 (placebo, n = 426; ESL, n = 1021) and 365 (ESL, n = 365) patients, respectively; 639 and 274 patients continued onto uncontrolled, open-label extensions. In the controlled and uncontrolled trials ≤3.3% of patients taking ESL had a minimum postdose [Na+ ] measurement ≤125 mEq/L, <9% had a >10 mEq/L decrease in [Na+ ] from baseline, <6% had a hyponatremia-related TEAE, and <2% discontinued the controlled trials due to a hyponatremia-related TEAE. Hyponatremia appeared to be more frequent in the monotherapy (vs adjunctive therapy) trials; in the controlled trials of adjunctive ESL and ESL monotherapy, incidence generally increased with increasing ESL dose. The majority of patients with an investigator-reported TEAE of "hyponatremia" or "blood sodium decreased" did not have a corresponding laboratory [Na+ ] measurement ≤125 mEq/L. Some symptoms potentially related to hyponatremia (including nausea and vomiting) were more frequent in patients with a minimum postdose [Na+ ] measurement ≤125 mEq/L.

SIGNIFICANCE:

Reductions in serum sodium concentrations and hyponatremia-related TEAEs occurred in a small number of patients taking ESL. Suspected hyponatremia should be confirmed and monitored via [Na+ ] measurements.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sodio / Dibenzazepinas / Epilepsia / Hiponatremia / Anticonvulsivantes Tipo de estudio: Clinical_trials Límite: Adolescent / Adult / Aged / Humans / Middle aged Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sodio / Dibenzazepinas / Epilepsia / Hiponatremia / Anticonvulsivantes Tipo de estudio: Clinical_trials Límite: Adolescent / Adult / Aged / Humans / Middle aged Idioma: En Año: 2019 Tipo del documento: Article