Abou Nafeh Nancy G, Aouad Marie T, Khalili Amro F, Serhan Fatima G, Sokhn Anthony M, Kaddoum Roland N
From the Department of Anesthesiology and Pain Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Department of Chemistry, Lebanese American University, Beirut, Lebanon.
Anesth Analg. 2025 Apr 1;140(4):931-937. doi: 10.1213/ANE.0000000000007199. Epub 2024 Oct 4.
After an induction dose of rocuronium, sugammadex in a dose of 16 mg.kg -1 has been shown to provide early reversal of the neuromuscular blockade. However, the use of sugammadex to rescue a "cannot intubate, cannot ventilate" (CICV) scenario remains controversial. The aim of this systematic review was to discuss case reports describing the use of sugammadex as a rescue reversal in CICV scenarios and analyze the influencing factors potentially shaping the outcome of such reversal. The study has been registered on International Prospective Register of Systematic Reviews (PROSPERO) (CRD42024514255). We conducted a systematic review of the literature using PubMed, Medline, and Embase. Records were included if they were case reports or case series published in peer-reviewed journals, describing the administration of sugammadex as a rescue reversal in CICV scenarios, and including clinical outcomes and details of the management. Sources were last searched on November 30, 2023. The articles selected were initially screened based on their titles and abstracts, and then complete articles were examined to determine their eligibility and compliance with the inclusion criteria. Two independent authors evaluated the quality of the individual studies using the Joanna Briggs Institute Critical Appraisal Checklist for Case Reports. Eight articles were included in our review. In all patients, CICV scenarios were declared minutes following induction. In 6/8 cases (75%), adequate spontaneous ventilation was restored after the administration of sugammadex. In the remaining 2 cases, sugammadex administration resulted in an obstructed pattern of breathing, and surgical airway was the successful rescue technique. There was wide variability in the sugammadex dose with a median (range) of 14 (5-16) mg.kg -1 and median timing (range) from rocuronium administration of 6 (2-10) minutes. This case-report-based review is susceptible to reporting bias and may not encompass all pertinent data and adverse events. Also, cases with both favorable and unfavorable outcomes may have not been published, and the heterogeneity of cases limits the ability to draw definitive conclusions. In summary, although these case reports suggest that sugammadex might be helpful in CICV scenarios, further research is needed to confirm its effectiveness. However, due to the rare occurrence of CICV events, gathering sufficient data for conclusive evidence may be challenging.
给予诱导剂量的罗库溴铵后,已证明剂量为16mg·kg-1的舒更葡糖能使神经肌肉阻滞早期逆转。然而,在“无法插管、无法通气”(CICV)情况下使用舒更葡糖进行抢救仍存在争议。本系统评价的目的是讨论描述在CICV情况下使用舒更葡糖进行抢救逆转的病例报告,并分析可能影响此类逆转结果的因素。该研究已在国际系统评价前瞻性注册库(PROSPERO)(CRD42024514255)上注册。我们使用PubMed、Medline和Embase对文献进行了系统评价。如果记录是发表在同行评审期刊上的病例报告或病例系列,描述了在CICV情况下使用舒更葡糖进行抢救逆转,并包括临床结果和管理细节,则纳入记录。检索来源的最后时间为2023年11月30日。所选文章首先根据标题和摘要进行筛选,然后检查全文以确定其是否符合纳入标准。两名独立作者使用乔安娜·布里格斯研究所病例报告关键评价清单评估了个体研究的质量。我们的评价纳入了8篇文章。在所有患者中,诱导后数分钟宣布出现CICV情况。在6/8例(75%)患者中,给予舒更葡糖后恢复了充分的自主通气。在其余2例患者中,给予舒更葡糖后出现呼吸梗阻模式,手术气道是成功的抢救技术。舒更葡糖剂量差异很大,中位数(范围)为14(5-16)mg·kg-1,从给予罗库溴铵到使用舒更葡糖的中位时间(范围)为6(2-10)分钟。这种基于病例报告的评价容易受到报告偏倚的影响,可能未涵盖所有相关数据和不良事件。此外,可能未发表有良好和不良结果的病例,病例的异质性限制了得出明确结论的能力。总之,尽管这些病例报告表明舒更葡糖在CICV情况下可能有用,但需要进一步研究来证实其有效性。然而,由于CICV事件罕见,收集足够的数据以获得确凿证据可能具有挑战性。