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Sugammadex versus neostigmine reversal of moderate rocuronium-induced neuromuscular blockade in Korean patients

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dc.contributor.authorWoo, T.-
dc.contributor.authorKim, K.S.-
dc.contributor.authorShim, Y.H.-
dc.contributor.authorKim, M.K.-
dc.contributor.authorYoon, S.M.-
dc.contributor.authorLim, Y.J.-
dc.contributor.authorYang, H.S.-
dc.contributor.authorPhiri, P.-
dc.contributor.authorChon, J.Y.-
dc.date.accessioned2021-09-05T15:53:32Z-
dc.date.available2021-09-05T15:53:32Z-
dc.date.created2021-06-17-
dc.date.issued2014-
dc.identifier.issn2005-6419-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/100696-
dc.description.abstractBackground: Rapid and complete reversal of neuromuscular blockade (NMB) is desirable at the end of surgery. Sugammadex reverses rocuronium-induced NMB by encapsulation. It is well tolerated in Caucasian patients, providing rapid reversal of moderate (reappearance of T2) rocuronium-induced NMB. We investigated the efficacy and safety of sugammadex versus neostigmine in Korean patients. Methods: This randomized, safety assessor-blinded trial (NCT01050543) included Korean patients undergoing general anesthesia. Rocuronium 0.6 mg/kg was given prior to intubation with maintenance doses of 0.1-0.2 mg/kg as required. Patients received sugammadex 2.0 mg/kg or neostigmine 50 μg/kg with glycopyrrolate 10 μg/kg to reverse the NMB at the reappearance of T2, after the last rocuronium dose. The primary efficacy endpoint was the time from sugammadex or neostigmine administration to recovery of the train-of-four (TOF) ratio to 0.9. The safety of these medications was also assessed. Results: Of 128 randomized patients, 118 had evaluable data (n = 59 in each group). The geometric mean (95% confidence interval) time to recovery of the TOF ratio to 0.9 was 1.8 (1.6, 2.0) minutes in the sugammadex group and 14.8 (12.4, 17.6) minutes in the neostigmine group (P < 0.0001). Sugammadex was generally well tolerated, with no evidence of residual or recurrence of NMB; four patients in the neostigmine group reported adverse events possibly indicative of inadequate NMB reversal. Conclusions: Sugammadex was well tolerated and provided rapid reversal of moderate rocuronium-induced NMB in Korean patients, with a recovery time 8.1 times faster than neostigmine. These results are consistent with those reported for Caucasian patients. © the Korean Society of Anesthesiologists, 2013.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKorean Society of Anesthesiologists-
dc.subjectneostigmine-
dc.subjectrocuronium-
dc.subjectsugammadex-
dc.subjectadult-
dc.subjectarticle-
dc.subjectclinical trial-
dc.subjectcomparative study-
dc.subjectcoughing-
dc.subjectdizziness-
dc.subjectdrug efficacy-
dc.subjectdrug safety-
dc.subjectdrug tolerability-
dc.subjectendotracheal intubation-
dc.subjectfemale-
dc.subjectfever-
dc.subjectheadache-
dc.subjecthuman-
dc.subjectmajor clinical study-
dc.subjectmale-
dc.subjectnausea-
dc.subjectneuromuscular blocking-
dc.subjectneuromuscular monitoring-
dc.subjectoutcome assessment-
dc.subjectpain-
dc.subjectpostoperative nausea and vomiting-
dc.subjectrandomization-
dc.subjectrandomized controlled trial-
dc.subjectrhinorrhea-
dc.subjectrisk factor-
dc.subjectsensitivity analysis-
dc.subjectsingle drug dose-
dc.subjectwound complication-
dc.titleSugammadex versus neostigmine reversal of moderate rocuronium-induced neuromuscular blockade in Korean patients-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoon, S.M.-
dc.identifier.doi10.4097/kjae.2013.65.6.501-
dc.identifier.scopusid2-s2.0-84891889204-
dc.identifier.bibliographicCitationKorean Journal of Anesthesiology, v.65, no.6, pp.501 - 507-
dc.relation.isPartOfKorean Journal of Anesthesiology-
dc.citation.titleKorean Journal of Anesthesiology-
dc.citation.volume65-
dc.citation.number6-
dc.citation.startPage501-
dc.citation.endPage507-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordPlusneostigmine-
dc.subject.keywordPlusrocuronium-
dc.subject.keywordPlussugammadex-
dc.subject.keywordPlusadult-
dc.subject.keywordPlusarticle-
dc.subject.keywordPlusclinical trial-
dc.subject.keywordPluscomparative study-
dc.subject.keywordPluscoughing-
dc.subject.keywordPlusdizziness-
dc.subject.keywordPlusdrug efficacy-
dc.subject.keywordPlusdrug safety-
dc.subject.keywordPlusdrug tolerability-
dc.subject.keywordPlusendotracheal intubation-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlusfever-
dc.subject.keywordPlusheadache-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusmajor clinical study-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusnausea-
dc.subject.keywordPlusneuromuscular blocking-
dc.subject.keywordPlusneuromuscular monitoring-
dc.subject.keywordPlusoutcome assessment-
dc.subject.keywordPluspain-
dc.subject.keywordPluspostoperative nausea and vomiting-
dc.subject.keywordPlusrandomization-
dc.subject.keywordPlusrandomized controlled trial-
dc.subject.keywordPlusrhinorrhea-
dc.subject.keywordPlusrisk factor-
dc.subject.keywordPlussensitivity analysis-
dc.subject.keywordPlussingle drug dose-
dc.subject.keywordPluswound complication-
dc.subject.keywordAuthorCaucasian-
dc.subject.keywordAuthorKorean-
dc.subject.keywordAuthorNeostigmine-
dc.subject.keywordAuthorNeuromuscular blockade-
dc.subject.keywordAuthorRocuronium-
dc.subject.keywordAuthorSugammadex-
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