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Tytuł pozycji:

Comparative abuse liability of intravenously administered remifentanil and fentanyl.

Tytuł:
Comparative abuse liability of intravenously administered remifentanil and fentanyl.
Autorzy:
Baylon GJ; Department of Pharmacology, and Centre for Research in Women's Health, University of Toronto, Ontario, Canada.
Kaplan HL
Somer G
Busto UE
Sellers EM
Źródło:
Journal of clinical psychopharmacology [J Clin Psychopharmacol] 2000 Dec; Vol. 20 (6), pp. 597-606.
Typ publikacji:
Clinical Trial; Journal Article; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Publication: Baltimore Md : Williams And Wilkins
Original Publication: Baltimore, Md. : Williams & Wilkins, [c1981-
MeSH Terms:
Affect/*drug effects
Analgesics, Opioid/*administration & dosage
Fentanyl/*administration & dosage
Piperidines/*administration & dosage
Pupil/*drug effects
Adult ; Affect/physiology ; Analgesics, Opioid/pharmacology ; Analysis of Variance ; Area Under Curve ; Cross-Over Studies ; Double-Blind Method ; Fentanyl/pharmacology ; Humans ; Infusion Pumps/psychology ; Infusions, Intravenous ; Male ; Middle Aged ; Piperidines/pharmacology ; Pupil/physiology ; Remifentanil ; Substance-Related Disorders/psychology
Substance Nomenclature:
0 (Analgesics, Opioid)
0 (Piperidines)
P10582JYYK (Remifentanil)
UF599785JZ (Fentanyl)
Entry Date(s):
Date Created: 20001206 Date Completed: 20010531 Latest Revision: 20190910
Update Code:
20240104
DOI:
10.1097/00004714-200012000-00002
PMID:
11106130
Czasopismo naukowe
Remifentanil is a short-acting, esterase-metabolized opioid analgesic. This study compared the abuse liability of remifentanil with that of fentanyl and placebo in a randomized, double-blind, crossover study. Twelve recreational users of opioids received increasing doses of remifentanil (0.6, 1.2, 1.8, 2.4, and 3.0 microg/kg), fentanyl (0.4, 0.8, 1.3, 2.0, 3.0, and 4.5 microg/kg) and placebo via an intravenous infusion pump. Subjective measures (Cole/Addiction Research Center Inventory [ARCI] scales and visual analog scale [VAS] items such as "High" and "Good Effects") and physiologic variables (blood pressure, O2 saturation, pupil diameter) were recorded. For each measure, the differences from baseline were reduced to an area under the response curve (AUC) and a peak, and each subject's response to the maximum tolerable dose for each of the two active drug classes and mean response to several placebo infusions were entered into a 12 x 3 analysis of variance. All differences in drug versus placebo effects were significant. Although a majority of the peak effects that were measurable within 4 minutes after drug infusion reflected greater remifentanil effects, only one, High VAS, was statistically significant. In contrast, observations that could only be made > or = 5 minutes after drug infusion predominantly indicated significantly greater fentanyl peak effects, including High VAS, Liking VAS, Good Effects VAS, and Cole/ARCI Abuse Potential. Fentanyl AUCs were generally significantly larger than the corresponding remifentanil AUCs. A drug abuser seeking longer-lasting drug effects might select fentanyl over remifentanil, but these data do not completely rule out remifentanil abuse by some individuals with access to both the drug and the infusion equipment or by those who prefer briefer, repeated effects.

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