Sleep-Disordered Breathing

نویسندگان

  • Kathleen A. Ferguson
  • Michael J. Strong
  • Dildar Ahmad
  • Charles F. P. George
چکیده

Objective: The purpose of this study was to assess sleep and breathing in patients with amyotrophic lateral sclerosis (ALS) with bulbar muscle involvement. Design: Prospective, controlled study of sleep and breathing measured during polysomnography. Setting: University teaching hospital and referral center. Patients: Patients with definite ALS and healthy age-matched control subjects. Interventions: Eighteen ALS patients and 10 age-matched control subjects underwent one night of polysomnography. Thirteen patients with ALS were studied for a second night. Results: The ALS patients had more arousals per hour (p=0.008), more stage 1 sleep (p=0.01), and a shorter total sleep time (TST) (279±69 vs 331.4±55.9 min, mean±SD, p=0.04) than the control subjects. The ALS patients had mild sleep-disordered breathing with a greater apnea/hypopnea in¬ dex (AHI) than the control subjects (p=0.005). On the second night ofpolysomnography, there was

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تاریخ انتشار 2007