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 |
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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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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.</description><identifier>ISSN: 1155-5645</identifier><identifier>EISSN: 1460-9592</identifier><identifier>DOI: 10.1046/j.1460-9592.1996.d01-8.x</identifier><identifier>PMID: 8880817</identifier><language>eng</language><publisher>Oxford BSL: Blackwell Science Ltd</publisher><subject>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</subject><ispartof>Pediatric anesthesia, 1996-01, Vol.6 (5), p.373-378</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4014-66127dc767f2b8f4cf14f1b3c66c34df36aa32ee1c5b191ce77acebe96d3b7213</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1460-9592.1996.d01-8.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1460-9592.1996.d01-8.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8880817$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MERETOJA, O.A.</creatorcontrib><creatorcontrib>TAIVAINEN, T.</creatorcontrib><creatorcontrib>WIRTAVUORI, K.</creatorcontrib><title>Cisatracurium during halothane and balanced anaesthesia in children</title><title>Pediatric anesthesia</title><addtitle>Paediatr Anaesth</addtitle><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.</description><subject>Anesthesia</subject><subject>Anesthesia, Inhalation</subject><subject>Anesthetics, Combined</subject><subject>Anesthetics, Inhalation</subject><subject>Atracurium - administration & dosage</subject><subject>Atracurium - analogs & 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 & 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 & dosage</topic><topic>Atracurium - analogs & 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 & 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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