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Effects of solriamfetol on on-the-road driving performance in participants with excessive daytime sleepiness associated with obstructive sleep apnoea.
Vinckenbosch, Frederick; Asin, Jerryll; de Vries, Nicolaas; Vonk, Patty E; Donjacour, Claire E H M; Lammers, Gert Jan; Overeem, Sebastiaan; Janssen, Hennie; Wang, Grace; Chen, Dan; Carter, Lawrence P; Zhou, Kefei; Vermeeren, Annemiek; Ramaekers, Johannes G.
Afiliação
  • Vinckenbosch F; Faculty of Psychology and Neuroscience, Maastricht University, Maastricht, Netherlands.
  • Asin J; Center for Sleep Medicine Amphia, Breda, Netherlands.
  • de Vries N; Faculty of Medicine and Health Sciences, Department of Otorhinolaryngology, Head and Neck Surgery, Antwerp University Hospital, Antwerp, Belgium.
  • Vonk PE; OLVG, Amsterdam, Netherlands.
  • Donjacour CEHM; OLVG, Amsterdam, Netherlands.
  • Lammers GJ; Sleep-Wake Centre SEIN, Netherlands.
  • Overeem S; Sleep-Wake Centre SEIN, Netherlands.
  • Janssen H; Department of Neurology, Leiden University Medical Center, Leiden, Netherlands.
  • Wang G; Sleep Medicine Center Kempenhaeghe, Heeze, Netherlands.
  • Chen D; Department of Electrical Engineering, Biomedical Diagnostics Group, Eindhoven University of Technology, Eindhoven, Netherlands.
  • Carter LP; Sleep Medicine Center Kempenhaeghe, Heeze, Netherlands.
  • Zhou K; Jazz Pharmaceuticals, Palo Alto, California, USA.
  • Vermeeren A; Jazz Pharmaceuticals, Palo Alto, California, USA.
  • Ramaekers JG; Alexza Pharmaceuticals, Inc, Mountain View, California, USA.
Hum Psychopharmacol ; 37(6): e2845, 2022 11.
Article em En | MEDLINE | ID: mdl-35633275
OBJECTIVE: To evaluate the impact of solriamfetol, a dopamine and norepinephrine reuptake inhibitor, on on-the-road driving in participants with excessive daytime sleepiness (EDS) associated with obstructive sleep apnoea (OSA). METHODS: Eligible participants were aged 21-75 years with OSA and EDS (Maintenance of Wakefulness Test mean sleep latency <30 minutes and Epworth Sleepiness Scale score ≥10). Participants were randomised 1:1 to solriamfetol (150 mg/day [3 days], then 300 mg/day [4 days]) or placebo for 7 days, before crossover to the other treatment paradigm. On Day 7 of each period, standardised on-road driving tests occurred (2 and 6 hours postdose). Standard deviation of lateral position (SDLP) was the primary endpoint. RESULTS: Solriamfetol significantly reduced SDLP at 2 (n = 34; least squares mean difference, -1.1 cm; 95% CI, -1.85, -0.32; p = 0.006) and 6 hours postdose (n = 32; least squares mean difference, -0.8 cm; 95% CI, -1.58, -0.03; p = 0.043). Two hours postdose, 4 placebo-treated and 1 solriamfetol-treated participants had incomplete driving tests; 6 hours postdose, 7 and 3 participants, respectively, had incomplete tests. Common treatment-emergent adverse events included headache, nausea, and insomnia. CONCLUSIONS: Solriamfetol 300 mg/day significantly improved on-the-road driving performance in participants with EDS associated with OSA.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Apneia Obstrutiva do Sono / Distúrbios do Sono por Sonolência Excessiva Tipo de estudo: Clinical_trials / Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Hum Psychopharmacol Assunto da revista: PSICOFARMACOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Apneia Obstrutiva do Sono / Distúrbios do Sono por Sonolência Excessiva Tipo de estudo: Clinical_trials / Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Hum Psychopharmacol Assunto da revista: PSICOFARMACOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Holanda