Individual pharmacometric analysis for sugammadex reversal and re-administration of neuromuscular blockade
Sugammadex is an innovative reversal agent for neuromuscular blockade (NMB) induced by rocuronium. Although there is a case that re-paralysis is necessary after sugammadex administration, limited reports can be found on the sugammadex dosage for reversal from profound paralysis after induction and i...
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Veröffentlicht in: | Journal of anesthesia 2020-10, Vol.34 (5), p.786-789 |
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description | Sugammadex is an innovative reversal agent for neuromuscular blockade (NMB) induced by rocuronium. Although there is a case that re-paralysis is necessary after sugammadex administration, limited reports can be found on the sugammadex dosage for reversal from profound paralysis after induction and immediate re-paralysis following such reversal in detail. We experienced a case in which NMB reversal was required in a short period after paralysis for induction due to the discovery of anisocoria. We successfully re-induced general anesthesia with tracheal intubation soon after. To examine the validity of the dosing, we performed a pharmacometric analysis. A pharmacokinetic-pharmacodynamic model was developed for the patient based on a published pharmacokinetic-pharmacodynamic model for rocuronium and sugammadex. The developed model appropriately describes the train of four ratio observed. In this case, the dose of approximately 8 mg/kg sugammadex but not the conventional dose of 16 mg/kg would be enough for immediate reversal after induction. For the re-paralysis 30 min after NMB reversal, not 1.4 mg/kg but 2.2 mg/kg rocuronium was an adequate dose. Taking individual differences including given dose and time intervals in consideration, NMB monitoring should be used to determine the necessary dose of rocuronium and sugammadex in such situations. |
doi_str_mv | 10.1007/s00540-020-02824-5 |
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Although there is a case that re-paralysis is necessary after sugammadex administration, limited reports can be found on the sugammadex dosage for reversal from profound paralysis after induction and immediate re-paralysis following such reversal in detail. We experienced a case in which NMB reversal was required in a short period after paralysis for induction due to the discovery of anisocoria. We successfully re-induced general anesthesia with tracheal intubation soon after. To examine the validity of the dosing, we performed a pharmacometric analysis. A pharmacokinetic-pharmacodynamic model was developed for the patient based on a published pharmacokinetic-pharmacodynamic model for rocuronium and sugammadex. The developed model appropriately describes the train of four ratio observed. In this case, the dose of approximately 8 mg/kg sugammadex but not the conventional dose of 16 mg/kg would be enough for immediate reversal after induction. For the re-paralysis 30 min after NMB reversal, not 1.4 mg/kg but 2.2 mg/kg rocuronium was an adequate dose. Taking individual differences including given dose and time intervals in consideration, NMB monitoring should be used to determine the necessary dose of rocuronium and sugammadex in such situations.</description><identifier>ISSN: 0913-8668</identifier><identifier>EISSN: 1438-8359</identifier><identifier>DOI: 10.1007/s00540-020-02824-5</identifier><identifier>PMID: 32656687</identifier><language>eng</language><publisher>Singapore: Springer Singapore</publisher><subject>Androstanols ; Anesthesiology ; Clinical Report ; Critical Care Medicine ; Emergency Medicine ; gamma-Cyclodextrins ; Humans ; Intensive ; Medicine ; Medicine & Public Health ; Neuromuscular Blockade ; Neuromuscular Nondepolarizing Agents ; Pain Medicine ; Paralysis ; Remifentanil ; Sugammadex ; Time Factors ; Vecuronium</subject><ispartof>Journal of anesthesia, 2020-10, Vol.34 (5), p.786-789</ispartof><rights>Japanese Society of Anesthesiologists 2020</rights><rights>COPYRIGHT 2020 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-b3af7c07f9d731326622c33c1c15af3d7fd2aadaef967b942de924223a32d29e3</citedby><cites>FETCH-LOGICAL-c476t-b3af7c07f9d731326622c33c1c15af3d7fd2aadaef967b942de924223a32d29e3</cites><orcidid>0000-0003-4702-9874</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00540-020-02824-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00540-020-02824-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32656687$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kashima, Yuki</creatorcontrib><creatorcontrib>Masui, Kenichi</creatorcontrib><title>Individual pharmacometric analysis for sugammadex reversal and re-administration of neuromuscular blockade</title><title>Journal of anesthesia</title><addtitle>J Anesth</addtitle><addtitle>J Anesth</addtitle><description>Sugammadex is an innovative reversal agent for neuromuscular blockade (NMB) induced by rocuronium. Although there is a case that re-paralysis is necessary after sugammadex administration, limited reports can be found on the sugammadex dosage for reversal from profound paralysis after induction and immediate re-paralysis following such reversal in detail. We experienced a case in which NMB reversal was required in a short period after paralysis for induction due to the discovery of anisocoria. We successfully re-induced general anesthesia with tracheal intubation soon after. To examine the validity of the dosing, we performed a pharmacometric analysis. A pharmacokinetic-pharmacodynamic model was developed for the patient based on a published pharmacokinetic-pharmacodynamic model for rocuronium and sugammadex. The developed model appropriately describes the train of four ratio observed. In this case, the dose of approximately 8 mg/kg sugammadex but not the conventional dose of 16 mg/kg would be enough for immediate reversal after induction. For the re-paralysis 30 min after NMB reversal, not 1.4 mg/kg but 2.2 mg/kg rocuronium was an adequate dose. Taking individual differences including given dose and time intervals in consideration, NMB monitoring should be used to determine the necessary dose of rocuronium and sugammadex in such situations.</description><subject>Androstanols</subject><subject>Anesthesiology</subject><subject>Clinical Report</subject><subject>Critical Care Medicine</subject><subject>Emergency Medicine</subject><subject>gamma-Cyclodextrins</subject><subject>Humans</subject><subject>Intensive</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neuromuscular Blockade</subject><subject>Neuromuscular Nondepolarizing Agents</subject><subject>Pain Medicine</subject><subject>Paralysis</subject><subject>Remifentanil</subject><subject>Sugammadex</subject><subject>Time Factors</subject><subject>Vecuronium</subject><issn>0913-8668</issn><issn>1438-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kV1rFDEUhoModlv9A17IgDfeTM3HzGTmshS1hYI3eh3OJidr1kmyJpPS_nuzThWERUIIOXneQw4PIW8YvWSUyg-Z0r6jLeXHPfKu7Z-RDevE2I6in56TDZ2YaMdhGM_Iec57SunAmHhJzgQf-lqWG7K_DcbdO1Ngbg7fIXnQ0eOSnG4gwPyYXW5sTE0uO_AeDD40Ce8x5cpDMPXSgvEuuLwkWFwMTbRNwJKiL1mXGVKznaP-UZOvyAsLc8bXT-cF-fbp49frm_buy-fb66u7VndyWNqtACs1lXYyUrD604FzLYRmmvVghZHWcAADaKdBbqeOG5x4x7kAwQ2fUFyQ92vfQ4o_C-ZFeZc1zjMEjCWrCoue9YzJir5b0R3MqFywsU6hj7i6GkRdYye6SrUnqB0GTDDHgNbV8j_85Qm-LoPe6ZMBvgZ0ijkntOqQnIf0qBhVR9VqVa2qavVbtepr6O3TmGXr0fyN_HFbAbECuT6FHSa1jyVVqfl_bX8B5L20uA</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Kashima, Yuki</creator><creator>Masui, Kenichi</creator><general>Springer Singapore</general><general>Springer</general><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><orcidid>https://orcid.org/0000-0003-4702-9874</orcidid></search><sort><creationdate>20201001</creationdate><title>Individual pharmacometric analysis for sugammadex reversal and re-administration of neuromuscular blockade</title><author>Kashima, Yuki ; Masui, Kenichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-b3af7c07f9d731326622c33c1c15af3d7fd2aadaef967b942de924223a32d29e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Androstanols</topic><topic>Anesthesiology</topic><topic>Clinical Report</topic><topic>Critical Care Medicine</topic><topic>Emergency Medicine</topic><topic>gamma-Cyclodextrins</topic><topic>Humans</topic><topic>Intensive</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neuromuscular Blockade</topic><topic>Neuromuscular Nondepolarizing Agents</topic><topic>Pain Medicine</topic><topic>Paralysis</topic><topic>Remifentanil</topic><topic>Sugammadex</topic><topic>Time Factors</topic><topic>Vecuronium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kashima, Yuki</creatorcontrib><creatorcontrib>Masui, Kenichi</creatorcontrib><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>Journal of anesthesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kashima, Yuki</au><au>Masui, Kenichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Individual pharmacometric analysis for sugammadex reversal and re-administration of neuromuscular blockade</atitle><jtitle>Journal of anesthesia</jtitle><stitle>J Anesth</stitle><addtitle>J Anesth</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>34</volume><issue>5</issue><spage>786</spage><epage>789</epage><pages>786-789</pages><issn>0913-8668</issn><eissn>1438-8359</eissn><abstract>Sugammadex is an innovative reversal agent for neuromuscular blockade (NMB) induced by rocuronium. Although there is a case that re-paralysis is necessary after sugammadex administration, limited reports can be found on the sugammadex dosage for reversal from profound paralysis after induction and immediate re-paralysis following such reversal in detail. We experienced a case in which NMB reversal was required in a short period after paralysis for induction due to the discovery of anisocoria. We successfully re-induced general anesthesia with tracheal intubation soon after. To examine the validity of the dosing, we performed a pharmacometric analysis. A pharmacokinetic-pharmacodynamic model was developed for the patient based on a published pharmacokinetic-pharmacodynamic model for rocuronium and sugammadex. The developed model appropriately describes the train of four ratio observed. In this case, the dose of approximately 8 mg/kg sugammadex but not the conventional dose of 16 mg/kg would be enough for immediate reversal after induction. For the re-paralysis 30 min after NMB reversal, not 1.4 mg/kg but 2.2 mg/kg rocuronium was an adequate dose. Taking individual differences including given dose and time intervals in consideration, NMB monitoring should be used to determine the necessary dose of rocuronium and sugammadex in such situations.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><pmid>32656687</pmid><doi>10.1007/s00540-020-02824-5</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0003-4702-9874</orcidid></addata></record> |
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subjects | Androstanols Anesthesiology Clinical Report Critical Care Medicine Emergency Medicine gamma-Cyclodextrins Humans Intensive Medicine Medicine & Public Health Neuromuscular Blockade Neuromuscular Nondepolarizing Agents Pain Medicine Paralysis Remifentanil Sugammadex Time Factors Vecuronium |
title | Individual pharmacometric analysis for sugammadex reversal and re-administration of neuromuscular blockade |
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