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PMID: 3400411 Published · ppublish English Clinical Trial Controlled Clinical Trial Journal Article

Efficacy of lorazepam oral fast dissolving drug formulation (FDDF) in anesthesia premedication in adults: a double-blind placebo controlled comparison.

Acta anaesthesiologica Belgica ·Vol. 39 ·No. 2 ·1988-00-00 ·Pages 95-100

Van de Velde A, Camu F

Abstract

Lorazepam 4 mg oral fast dissolving drug formulation was compared to placebo in a double-blind study as premedicant in adult anesthesia. Lorazepam induced in this trial a marked relief of anxiety after 60 minutes without changes in vital parameters nor in reflex activity or muscle tonus. Anterograde amnesia was present in about 60 percent of the patients. The clinical anesthetists rated the quality of premedication as satisfactory or better in 77 percent of lorazepam treated patients. The rating as "good" or "excellent" by patients reached 93 percent. The incidence of side effects was low. Postoperative residual effects on attention, cognitive, somatic and visceral functions were present till 5 hours postmedication. Lorazepam FDDF (fast dissolving drug formulation) appeared to be an effective and clinically safe premedicant for its good anxiolytic and amnestic effect and its high acceptance by the patients. Its use is not recommended for outpatient anesthesia because it prolongs recovery from anesthesia.

MeSH Terms
Absorption Administration, Oral Adult Aged Anxiety Double-Blind Method Female Humans Lorazepam/administration & dosage,adverse effects,metabolism Male Mental Processes/drug effects Middle Aged Preanesthetic Medication
Chemicals
Lorazepam
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Van de Velde A
Department of Anesthesiology, Flemish Free University of Brussels, School of Medicine, University Medical Center, Belgium.
Camu F
Article Info
Journal
Acta anaesthesiologica Belgica
Abbr.
Acta Anaesthesiol Belg
ISSN
0001-5164
Published
1988-00-00
Pages
95-100
Language
English
Region
Belgium
NLM ID
0421022
Subset
IM
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