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Sugammadex-Associated Hypotension, Bradycardia, Asystole, and Death

机译:Sugammadex相关的低血压,Bradycardia,Asystole和死亡

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On December 16, 2015, the Food and Drug Administration (FDA) in the United States approved sugammadex (Bridion, Merck and Co), a modified gamma-cyclodextrin, to be used as a reversal agent. It is a first and unique selective nondepolarizing steroidal muscle relaxant (NDSMR) binding agent with a great affinity for rocuronium and vecuronium. However, there have been several recently published case reports of bradycardia and asystole immediately after sugammadex administration for the reversal. This report presents a case of sugammadex administration followed by rapidly progressing bradycardia leading to asystole and subsequent death. The family has provided the written consent to share this case report.
机译:2015年12月16日,美国的食品和药物管理局(FDA)在美国批准的Sugammadex(Brition,Merck和Co),改性γ-环糊精,用作逆转剂。它是一种独特的选择性Nondepolarization甾体肌肉松弛剂(NDSMR)粘合剂,对罗冬季和脉尼铵具有很大的亲和力。然而,最近发表了几个关于逆转的辛德克萨克斯管理后立即发表的Bradycardia和Asystole的病例报告。本报告提出了一种急性X次疗法,随后迅速进展前进,导致Asystole和随后的死亡。该家庭提供了书面同意,分享本案报告。

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