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在手术室中针对预计困难气道使用清醒纤维光导插管方案:一项随机对照试验的系统评价和荟萃分析。

Awake Fiberoptic Intubation Protocols in the Operating Room for Anticipated Difficult Airway: A Systematic Review and Meta-analysis of Randomized Controlled Trials.

机构信息

From the Department of Anaesthesia and Intensive Care, Istituto di Ricovero e Cura a Carattere Scientifico San Raffaele Scientific Institute, Milan, Italy.

Università Vita-Salute San Raffaele, Milan, Italy.

出版信息

Anesth Analg. 2019 May;128(5):971-980. doi: 10.1213/ANE.0000000000004087.

Abstract

Awake fiberoptic intubation is one of the recommended strategies for surgical patients with anticipated difficult airway, especially when concurrent difficult ventilation is expected. We performed the first systematic review of randomized controlled trials assessing different protocols for awake fiberoptic intubation in anticipated difficult airway, including studies investigating elective awake fiberoptic intubation for scheduled surgery; randomized controlled trials comparing different methods for performing awake fiberoptic intubation; and adult patients with anticipated difficult airway. We excluded studies in the nonoperating theater settings, randomized controlled trials comparing awake fiberoptic intubation with other techniques, and studies based on simulation. Primary outcomes were success rate and death; secondary outcomes were major adverse events. Thirty-seven randomized controlled trials evaluating 2045 patients and 4 areas were identified: premedication, local anesthesia, sedation, and ancillary techniques to facilitate awake fiberoptic intubation. Quality of evidence was moderate-low and based on small-sampled randomized controlled trials. Overall, 12 of 2045 intubation failures (0.59%) and 7 of 2045 severe adverse events (0.34%) occurred, with no permanent consequences or death. All evaluated methods to achieve local anesthesia performed similarly well. No differences were observed in success rate with different sedatives. Dexmedetomidine resulted in fewer desaturation episodes compared to propofol and opioids with or without midazolam (relative risk, 0.51 [95% CI, 0.28-0.95]; P = .03); occurrence of desaturation was similar with remifentanil versus propofol, while incidence of apnoea was lower with sevoflurane versus propofol (relative risk, 0.43 [95% CI, 0.22-0.81]; P = .01). A high degree of efficacy and safety was observed with minimal differences among different protocols; dexmedetomidine might offer a better safety profile compared to other sedatives.

摘要

清醒纤维支气管镜插管是预计存在困难气道的手术患者的推荐策略之一,尤其是当预计同时存在通气困难时。我们对评估不同清醒纤维支气管镜插管方案的随机对照试验进行了首次系统评价,包括对择期手术进行清醒纤维支气管镜插管的研究;比较清醒纤维支气管镜插管不同方法的随机对照试验;以及预计存在困难气道的成年患者。我们排除了非手术室环境中的研究、比较清醒纤维支气管镜插管与其他技术的随机对照试验,以及基于模拟的研究。主要结局为成功率和死亡率;次要结局为主要不良事件。确定了 37 项评估 2045 例患者的随机对照试验和 4 个领域:术前用药、局部麻醉、镇静和辅助技术以促进清醒纤维支气管镜插管。证据质量为中低,基于小样本随机对照试验。总体而言,2045 例插管失败 12 例(0.59%),严重不良事件 7 例(0.34%),无永久性后果或死亡。所有评估的实现局部麻醉的方法效果相似。不同镇静剂的成功率无差异。与丙泊酚和阿片类药物(无论是否合用咪达唑仑)相比,右美托咪定导致的脱氧血症发作更少(相对风险,0.51[95%CI,0.28-0.95];P=0.03);与丙泊酚相比,瑞芬太尼脱氧血症的发生率相似,而与丙泊酚相比,七氟醚呼吸暂停的发生率较低(相对风险,0.43[95%CI,0.22-0.81];P=0.01)。不同方案观察到高度的疗效和安全性,差异极小;与其他镇静剂相比,右美托咪定可能具有更好的安全性。

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