Comparative abuse liability of intravenously administered remifentanil and fentanyl

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...

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Veröffentlicht in:Journal of clinical psychopharmacology 2000-12, Vol.20 (6), p.597-606
Hauptverfasser: BAYLON, Godofredo J, KAPLAN, Howard L, SOMER, Gail, BUSTO, Usoa E, SELLERS, Edward M
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container_issue 6
container_start_page 597
container_title Journal of clinical psychopharmacology
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creator BAYLON, Godofredo J
KAPLAN, Howard L
SOMER, Gail
BUSTO, Usoa E
SELLERS, Edward M
description 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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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. 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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. 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Drug treatments</subject><subject>Piperidines - administration &amp; dosage</subject><subject>Piperidines - pharmacology</subject><subject>Pupil - drug effects</subject><subject>Pupil - physiology</subject><subject>Remifentanil</subject><subject>Substance-Related Disorders - psychology</subject><issn>0271-0749</issn><issn>1533-712X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLAzEUhYMotlb_ggRcj-YmmUmzlOILCi7swt1wJw-IZGZKMi3Mv3dqq97FfRzOuYuPEArsHphWD2wqqUAWfFrg0IqDxM_IHEohCgX885zMGVdQMCX1jFzl_DVZpeLlJZkBAKtAsDn5WPXtFhMOYe8oNrvsaAzYhBiGkfaehm5IuHddv8txpGjb0IU8uOQsTa4N3nUDdiFS7Cw9HmO8JhceY3Y3p7kgm-enzeq1WL-_vK0e14URQg-F0GgQvJfotHDGypKLxnOpKuBWgWJVBYANt8tSVxqccx4NM7bUtimtFAuyPL41qc85OV9vU2gxjTWw-oCp_sVU_2H6kfgUvT1Gt7umdfY_eOIyGe5OBswGo0_YmZD_fEsQSirxDcQMcVM</recordid><startdate>20001201</startdate><enddate>20001201</enddate><creator>BAYLON, Godofredo J</creator><creator>KAPLAN, Howard L</creator><creator>SOMER, Gail</creator><creator>BUSTO, Usoa E</creator><creator>SELLERS, Edward M</creator><general>Lippincott Williams &amp; Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20001201</creationdate><title>Comparative abuse liability of intravenously administered remifentanil and fentanyl</title><author>BAYLON, Godofredo J ; KAPLAN, Howard L ; SOMER, Gail ; BUSTO, Usoa E ; SELLERS, Edward M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-39aca1ff4ae93ecd4523bf247612d71706611ab2d859691eeefac0cd59db5d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adult</topic><topic>Affect - drug effects</topic><topic>Affect - physiology</topic><topic>Analgesics</topic><topic>Analgesics, Opioid - administration &amp; dosage</topic><topic>Analgesics, Opioid - pharmacology</topic><topic>Analysis of Variance</topic><topic>Area Under Curve</topic><topic>Biological and medical sciences</topic><topic>Cross-Over Studies</topic><topic>Double-Blind Method</topic><topic>Fentanyl - administration &amp; dosage</topic><topic>Fentanyl - pharmacology</topic><topic>Humans</topic><topic>Infusion Pumps - psychology</topic><topic>Infusions, Intravenous</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neuropharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Piperidines - administration &amp; dosage</topic><topic>Piperidines - pharmacology</topic><topic>Pupil - drug effects</topic><topic>Pupil - physiology</topic><topic>Remifentanil</topic><topic>Substance-Related Disorders - psychology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BAYLON, Godofredo J</creatorcontrib><creatorcontrib>KAPLAN, Howard L</creatorcontrib><creatorcontrib>SOMER, Gail</creatorcontrib><creatorcontrib>BUSTO, Usoa E</creatorcontrib><creatorcontrib>SELLERS, Edward M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of clinical psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BAYLON, Godofredo J</au><au>KAPLAN, Howard L</au><au>SOMER, Gail</au><au>BUSTO, Usoa E</au><au>SELLERS, Edward M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative abuse liability of intravenously administered remifentanil and fentanyl</atitle><jtitle>Journal of clinical psychopharmacology</jtitle><addtitle>J Clin Psychopharmacol</addtitle><date>2000-12-01</date><risdate>2000</risdate><volume>20</volume><issue>6</issue><spage>597</spage><epage>606</epage><pages>597-606</pages><issn>0271-0749</issn><eissn>1533-712X</eissn><coden>JCPYDR</coden><abstract>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 &gt; 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.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>11106130</pmid><doi>10.1097/00004714-200012000-00002</doi><tpages>10</tpages></addata></record>
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source MEDLINE; Journals@Ovid Complete
subjects Adult
Affect - drug effects
Affect - physiology
Analgesics
Analgesics, Opioid - administration & dosage
Analgesics, Opioid - pharmacology
Analysis of Variance
Area Under Curve
Biological and medical sciences
Cross-Over Studies
Double-Blind Method
Fentanyl - administration & dosage
Fentanyl - pharmacology
Humans
Infusion Pumps - psychology
Infusions, Intravenous
Male
Medical sciences
Middle Aged
Neuropharmacology
Pharmacology. Drug treatments
Piperidines - administration & dosage
Piperidines - pharmacology
Pupil - drug effects
Pupil - physiology
Remifentanil
Substance-Related Disorders - psychology
title Comparative abuse liability of intravenously administered remifentanil and fentanyl
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