Cisatracurium during halothane and balanced anaesthesia in children

Cisatracurium, 51W89, is one of the ten stereoisomers of Tracrium® which, unlike atracurium, has been reported to have a lack of histamine mediated cardiovascular effects at doses as high as 8×ED95 in adults. We compared the time‐course of neuromuscular effects of 80 μg·kg−1 or 100 μg·kg−1 cisatracu...

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Veröffentlicht in:Pediatric anesthesia 1996-01, Vol.6 (5), p.373-378
Hauptverfasser: MERETOJA, O.A., TAIVAINEN, T., WIRTAVUORI, K.
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WIRTAVUORI, K.
description Cisatracurium, 51W89, is one of the ten stereoisomers of Tracrium® which, unlike atracurium, has been reported to have a lack of histamine mediated cardiovascular effects at doses as high as 8×ED95 in adults. We compared the time‐course of neuromuscular effects of 80 μg·kg−1 or 100 μg·kg−1 cisatracurium during N2O‐O2‐halothane or N2O‐O2‐opioid anaesthesia, respectively, in 32 children 2–12 years old. Neuromuscular function was monitored by evoked adductor pollicis EMG. Even‐numbered patients (n=16) were allowed to obtain full spontaneous recovery of neuromuscular function and odd‐numbered patients (n=16) received neostigmine 45 μg·kg−1 together with glycopyrrolate at the time of 25% EMG recovery. Data are expressed as median with 10th to 90th percentile range. Cisatracurium had an onset time (time from administration to maximal effect) of 2.2 (1.7–3.8) or 2.3 (1.8–4.9) min, a clinical duration (time to 25% EMG recovery) of 34 (22–40) or 27 (24–33) min, and a spontaneous 25–75% recovery time (time from 25 to 75% EMG recovery) of 11 (9–13) or 11 (7–12) min during halothane or balanced anaesthesia, respectively (NS). Train‐of‐four ratio recovered to 0.70 in 2.5 (1.8–3.0) or 3.2 (2.1–4.3) min following neostigmine during halothane or balanced anaesthesia, respectively (NS). Changes in blood pressure or heart rate following cisatracurium were negligible. We regard cisatracurium as a safe and promising intermediate duration muscle relaxant the effects of which can easily be reversed with neostigmine.
doi_str_mv 10.1046/j.1460-9592.1996.d01-8.x
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Train‐of‐four ratio recovered to 0.70 in 2.5 (1.8–3.0) or 3.2 (2.1–4.3) min following neostigmine during halothane or balanced anaesthesia, respectively (NS). Changes in blood pressure or heart rate following cisatracurium were negligible. 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Train‐of‐four ratio recovered to 0.70 in 2.5 (1.8–3.0) or 3.2 (2.1–4.3) min following neostigmine during halothane or balanced anaesthesia, respectively (NS). Changes in blood pressure or heart rate following cisatracurium were negligible. We regard cisatracurium as a safe and promising intermediate duration muscle relaxant the effects of which can easily be reversed with neostigmine.</description><subject>Anesthesia</subject><subject>Anesthesia, Inhalation</subject><subject>Anesthetics, Combined</subject><subject>Anesthetics, Inhalation</subject><subject>Atracurium - administration &amp; dosage</subject><subject>Atracurium - analogs &amp; derivatives</subject><subject>Atracurium - pharmacology</subject><subject>Blood Pressure - drug effects</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Electromyography</subject><subject>Female</subject><subject>Fentanyl</subject><subject>Halothane</subject><subject>Heart Rate - drug effects</subject><subject>Humans</subject><subject>Male</subject><subject>Neostigmine - pharmacology</subject><subject>Neuromuscular Blockade</subject><subject>Neuromuscular Blocking Agents - administration &amp; dosage</subject><subject>Neuromuscular Blocking Agents - pharmacology</subject><subject>Neuromuscular Junction - drug effects</subject><subject>Nitrous Oxide</subject><subject>Thiopental</subject><issn>1155-5645</issn><issn>1460-9592</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMFqGzEQhkVISdO0jxDYU2-71ay0khZyCSZOC0laaEKgl0ErzdZy1utU8lLn7Stj43NPI_HPNzN8jBXAK-BSfVlWIBUv26atK2hbVXkOpam2J-z8GJzmNzRN2SjZvGcfUlpyDqJW9Rk7M8ZwA_qczWYh2U20bophWhU-l_F3sbDDerOwIxV29EVnBzs68vljKW0WlIItwli4RRh8pPEje9fbIdGnQ71gT_Obx9nX8u777bfZ9V3pJAdZKgW19k4r3ded6aXrQfbQCaeUE9L3QlkraiJwTQctONLaOuqoVV50ugZxwT7v577G9Z8pX4KrkBwN-TpaTwm1kUqJ1uRGs290cZ1SpB5fY1jZ-IbAcecPl7jThDtNuPOH2R8a3Gb08rBj6lbkj-BBWM6v9vnfMNDbf8_FH9cPjZQZL_d4SBvaHnEbX1BpoRt8frjFn_Nfz_fivsW5-Ad1AY9V</recordid><startdate>19960101</startdate><enddate>19960101</enddate><creator>MERETOJA, O.A.</creator><creator>TAIVAINEN, T.</creator><creator>WIRTAVUORI, K.</creator><general>Blackwell Science Ltd</general><scope>BSCLL</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><scope>7X8</scope></search><sort><creationdate>19960101</creationdate><title>Cisatracurium during halothane and balanced anaesthesia in children</title><author>MERETOJA, O.A. ; TAIVAINEN, T. ; WIRTAVUORI, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4014-66127dc767f2b8f4cf14f1b3c66c34df36aa32ee1c5b191ce77acebe96d3b7213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Anesthesia</topic><topic>Anesthesia, Inhalation</topic><topic>Anesthetics, Combined</topic><topic>Anesthetics, Inhalation</topic><topic>Atracurium - administration &amp; dosage</topic><topic>Atracurium - analogs &amp; derivatives</topic><topic>Atracurium - pharmacology</topic><topic>Blood Pressure - drug effects</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Electromyography</topic><topic>Female</topic><topic>Fentanyl</topic><topic>Halothane</topic><topic>Heart Rate - drug effects</topic><topic>Humans</topic><topic>Male</topic><topic>Neostigmine - pharmacology</topic><topic>Neuromuscular Blockade</topic><topic>Neuromuscular Blocking Agents - administration &amp; dosage</topic><topic>Neuromuscular Blocking Agents - pharmacology</topic><topic>Neuromuscular Junction - drug effects</topic><topic>Nitrous Oxide</topic><topic>Thiopental</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MERETOJA, O.A.</creatorcontrib><creatorcontrib>TAIVAINEN, T.</creatorcontrib><creatorcontrib>WIRTAVUORI, K.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric anesthesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MERETOJA, O.A.</au><au>TAIVAINEN, T.</au><au>WIRTAVUORI, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cisatracurium during halothane and balanced anaesthesia in children</atitle><jtitle>Pediatric anesthesia</jtitle><addtitle>Paediatr Anaesth</addtitle><date>1996-01-01</date><risdate>1996</risdate><volume>6</volume><issue>5</issue><spage>373</spage><epage>378</epage><pages>373-378</pages><issn>1155-5645</issn><eissn>1460-9592</eissn><abstract>Cisatracurium, 51W89, is one of the ten stereoisomers of Tracrium® which, unlike atracurium, has been reported to have a lack of histamine mediated cardiovascular effects at doses as high as 8×ED95 in adults. We compared the time‐course of neuromuscular effects of 80 μg·kg−1 or 100 μg·kg−1 cisatracurium during N2O‐O2‐halothane or N2O‐O2‐opioid anaesthesia, respectively, in 32 children 2–12 years old. Neuromuscular function was monitored by evoked adductor pollicis EMG. Even‐numbered patients (n=16) were allowed to obtain full spontaneous recovery of neuromuscular function and odd‐numbered patients (n=16) received neostigmine 45 μg·kg−1 together with glycopyrrolate at the time of 25% EMG recovery. Data are expressed as median with 10th to 90th percentile range. Cisatracurium had an onset time (time from administration to maximal effect) of 2.2 (1.7–3.8) or 2.3 (1.8–4.9) min, a clinical duration (time to 25% EMG recovery) of 34 (22–40) or 27 (24–33) min, and a spontaneous 25–75% recovery time (time from 25 to 75% EMG recovery) of 11 (9–13) or 11 (7–12) min during halothane or balanced anaesthesia, respectively (NS). Train‐of‐four ratio recovered to 0.70 in 2.5 (1.8–3.0) or 3.2 (2.1–4.3) min following neostigmine during halothane or balanced anaesthesia, respectively (NS). Changes in blood pressure or heart rate following cisatracurium were negligible. We regard cisatracurium as a safe and promising intermediate duration muscle relaxant the effects of which can easily be reversed with neostigmine.</abstract><cop>Oxford BSL</cop><pub>Blackwell Science Ltd</pub><pmid>8880817</pmid><doi>10.1046/j.1460-9592.1996.d01-8.x</doi><tpages>6</tpages></addata></record>
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subjects Anesthesia
Anesthesia, Inhalation
Anesthetics, Combined
Anesthetics, Inhalation
Atracurium - administration & dosage
Atracurium - analogs & derivatives
Atracurium - pharmacology
Blood Pressure - drug effects
Child
Child, Preschool
Electromyography
Female
Fentanyl
Halothane
Heart Rate - drug effects
Humans
Male
Neostigmine - pharmacology
Neuromuscular Blockade
Neuromuscular Blocking Agents - administration & dosage
Neuromuscular Blocking Agents - pharmacology
Neuromuscular Junction - drug effects
Nitrous Oxide
Thiopental
title Cisatracurium during halothane and balanced anaesthesia in children
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