1983
DOI: 10.1159/000137924
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Zopiclone to Geriatric Patients

Abstract: Zopiclone was given for 14 nights to 68 geriatric patients (mean age 81 years) with sleep problems. The patients were randomly allocated to four treatment groups: 3.75 mg, 5.0, 7.5, or 10.0 mg of zopiclone. Sleep quantity and quality, side effects, and influence on psychomotor performance (digit symbol substitution and letter cancellation test) were studied before treatment, during active treatment, and after withdrawal of the drug. All patients slept better on zopiclone compared to placebo. There were only sl… Show more

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Cited by 12 publications
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“…However, in a recent systematic review, assessments on older adults using zolpidem during night time and/or next-morning awakening pointed to minimal or no losses in psychometric and/or psychomotor performance [68]. Likewise, the literature also presents evidence that cognitive and psychomotor functions as well as alertness on waking do not appear to be substantially impacted by the use of zopiclone [54,[69][70][71]. Despite of (or owing to) the controversy, zopiclone and zolpidem present pharmacological issues regarding tolerability and safety that cannot be neglected and deserve further investigation, being so far comparable in frequency and intensity to those of BZDs as evidenced by studies elsewhere [72][73][74], and with use of all these drug classes intended to be personalized, implemented with caution, and under watchful surveillance.…”
Section: Discussionmentioning
confidence: 99%
“…However, in a recent systematic review, assessments on older adults using zolpidem during night time and/or next-morning awakening pointed to minimal or no losses in psychometric and/or psychomotor performance [68]. Likewise, the literature also presents evidence that cognitive and psychomotor functions as well as alertness on waking do not appear to be substantially impacted by the use of zopiclone [54,[69][70][71]. Despite of (or owing to) the controversy, zopiclone and zolpidem present pharmacological issues regarding tolerability and safety that cannot be neglected and deserve further investigation, being so far comparable in frequency and intensity to those of BZDs as evidenced by studies elsewhere [72][73][74], and with use of all these drug classes intended to be personalized, implemented with caution, and under watchful surveillance.…”
Section: Discussionmentioning
confidence: 99%