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dc.contributor.author김교상-
dc.date.accessioned2018-03-12T00:42:27Z-
dc.date.available2018-03-12T00:42:27Z-
dc.date.issued2013-12-
dc.identifier.citationKorean Journal of Anesthesiology, 2013, 65(6), P.501-507en_US
dc.identifier.issn2005-7563-
dc.identifier.urihttps://ekja.org/journal/view.php?doi=10.4097/kjae.2013.65.6.501-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/45024-
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.en_US
dc.description.sponsorshipThis study was sponsored by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ, USA. Assistance with the design and execution of the study was provided by Joris de Bie (Merck Sharp & Dohme Corp., Whitehouse Station, NJ, USA). Additional statistical support was provided by Henk Rietbergen (MSD, Oss, The Netherlands). Medical writing support was provided by Neil Venn from Prime Medica (Knutsford, Cheshire, UK) during the preparation of this manuscript, supported by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ, USA. Responsibility for opinions, conclusions, and interpretation of the data lies with the authors. Disclosures: Tiffany Woo and Phillip Phiri are employees of Merck Sharp & Dohme Corp., Whitehouse Station, NJ.en_US
dc.language.isoenen_US
dc.publisher대한마취통증의학회en_US
dc.subjectCaucasianen_US
dc.subjectNeostigmineen_US
dc.subjectNeuromuscular blockadeen_US
dc.subjectRocuroniumen_US
dc.subjectSugammadexen_US
dc.titleSugammadex versus neostigmine reversal of moderate rocuronium-induced neuromuscular blockade in Korean patientsen_US
dc.typeArticleen_US
dc.relation.no6-
dc.relation.volume65-
dc.identifier.doi10.4097/kjae.2013.65.6.501-
dc.relation.page501-507-
dc.relation.journal대한마취과학회지-
dc.contributor.googleauthorWoo, Tiffany-
dc.contributor.googleauthorPhiri, Phillip-
dc.contributor.googleauthor심연희-
dc.contributor.googleauthor김미경-
dc.contributor.googleauthor임영진-
dc.contributor.googleauthor양홍석-
dc.contributor.googleauthor전진영-
dc.contributor.googleauthor윤석민-
dc.contributor.googleauthor김교상-
dc.relation.code2012212374-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidkimks-
dc.identifier.researcherID35214912700-
dc.identifier.orcid0000-0002-2186-3484-
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COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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