TY - JOUR
T1 - Comparison of short and long half-life benzodiazepine hypnotics
T2 - Triazolam and quazepam
AU - Kales, Anthony
AU - Bixler, Edward O.
AU - Vela-Bueno, Antonio
AU - Soldatos, Constantin R.
AU - Niklaus, Douglas E.
AU - Manfredi, Rocco L.
PY - 1986/10
Y1 - 1986/10
N2 - Two benzodiampine hypnotics, triazolam, 0.25 mg, with a short elimination t 1 2, and quazepam, 15 mg, with a long t 1 2 were evaluated in 22-night sleep laboratory studies. Quazepam improved sleep significantly during both short- and intermediate-term use. Daytime sleepiness, which decreased with continued use, was the side effect most often associated with quazepam dosing. In contrast, triazolam dosing did not significantly improve any of the major sleep efficiency parameters, and there was a rapid development of tolerance for the drug's slight initial effectiveness. In addition, there were a number of behavioral side effects including amnesia, confusion, and disinhibition. Withdrawal of triazolam was associated with sleep and mood disturbances (rebound insomnia and rebound anxiety), whereas quazepam exerted carryover effectiveness. Thus the data in this study show that the 0.25 mg dose of triazolam, which is being prescribed increasingly, has a profile of side effects that is similar to that of the 0.5 mg dose.
AB - Two benzodiampine hypnotics, triazolam, 0.25 mg, with a short elimination t 1 2, and quazepam, 15 mg, with a long t 1 2 were evaluated in 22-night sleep laboratory studies. Quazepam improved sleep significantly during both short- and intermediate-term use. Daytime sleepiness, which decreased with continued use, was the side effect most often associated with quazepam dosing. In contrast, triazolam dosing did not significantly improve any of the major sleep efficiency parameters, and there was a rapid development of tolerance for the drug's slight initial effectiveness. In addition, there were a number of behavioral side effects including amnesia, confusion, and disinhibition. Withdrawal of triazolam was associated with sleep and mood disturbances (rebound insomnia and rebound anxiety), whereas quazepam exerted carryover effectiveness. Thus the data in this study show that the 0.25 mg dose of triazolam, which is being prescribed increasingly, has a profile of side effects that is similar to that of the 0.5 mg dose.
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U2 - 10.1038/clpt.1986.194
DO - 10.1038/clpt.1986.194
M3 - Article
C2 - 3530586
AN - SCOPUS:0022480832
SN - 0009-9236
VL - 40
SP - 378
EP - 386
JO - Clinical pharmacology and therapeutics
JF - Clinical pharmacology and therapeutics
IS - 4
ER -