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Sleep. 2003 Feb 1;26(1):31-5.

A 12-month, open-label, multicenter extension trial of orally administered sodium oxybate for the treatment of narcolepsy.

[No authors listed]

Abstract

OBJECTIVES:

To evaluate the long-term safety and efficacy of nightly sodium oxybate for the treatment of narcolepsy.

DESIGN:

A multicenter, 12-month, open-label trial.

PARTICIPANTS:

118 narcolepsy patients previously enrolled in a 4-week double-blind sodium oxybate trial.

INTERVENTIONS:

Patients were administered 6 g sodium oxybate nightly, taken in equally divided doses at bedtime and 2.5 to 4 hours later. The study protocol permitted the dose to be increased or decreased in 1.5-g increments at 2-week intervals based on efficacy response or adverse experiences but staying within the range of 3 to 9 g nightly.

MEASURES:

Narcolepsy symptoms and adverse events were recorded in daily diaries. Safety measures included physical and laboratory examinations repeated at 6 and 12 months. The primary efficacy measure was the change in weekly cataplexy attacks from baseline. Secondary measures included daytime sleepiness using the Epworth Sleepiness Scale (ESS), inadvertent naps/sleep attacks, nighttime awakenings, and the overall change in disease severity as rated by the investigators (Clinical Global Impression of Change; CGI-c).

RESULTS:

Sodium oxybate, in doses of 3 to 9 g nightly, produced overall improvements in narcolepsy symptoms, which were significant at 4 weeks and maximal after 8 weeks. Reported improvements included a significant decrease in frequency of cataplexy attacks (p < 0.001); diminished daytime sleepiness (p < 0.001); and patient descriptions of nocturnal sleep quality, level of alertness, and ability to concentrate (for each p < 0.001). Adverse events were generally mild and patients showed no evidence of tolerance.

CONCLUSION:

Sodium oxybate is an effective and well-tolerated treatment for narcolepsy.

PMID:
12627729
[PubMed - indexed for MEDLINE]
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