Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institute, Yonsei University College of Medicine, Gangnam Severance Hospital, Seoul, Republic of Korea.
Department of Anesthesiology and Pain Medicine, Seoul National University College of Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul, Republic of Korea.
Can J Anaesth. 2024 Jul;71(7):978-986. doi: 10.1007/s12630-024-02743-z. Epub 2024 Mar 28.
We sought to compare three intubation methods using different intubation techniques/tube materials for tube advancement from the nasal cavity into the oral cavity during nasotracheal intubation.
We conducted a randomized clinical trial with adult patients scheduled to undergo elective surgery requiring nasotracheal intubation for general anesthesia. Participants were randomly allocated to a polyvinyl chloride (PVC) tube group (group P), PVC tube attached to a rubber catheter group (group PR), or velvet-soft PVC tube group (group V). Tracheal intubation was then performed based on group allocation. The primary outcome was the first-attempt success rate of tube advancement into the oral cavity; secondary outcomes included the time required for tube advancement into the oral cavity, total intubation time, and the incidence of epistaxis.
A total of 149 patients were included in the study. The first-attempt success rate in group V (90%) was significantly higher than that in group P (58%) (odds ratio, 6.5; 95% confidence interval [CI], 2.2 to 19.2), but similar to that in group PR (100%). The mean (standard deviation) time required for tube advancement into the oral cavity was significantly shorter in group V (16 [13] sec) than in group PR [40 (10) sec; 95% CI of mean difference, 17 to 30] and group P (26 [16] sec; 95% CI of mean difference, 3 to 16). Total intubation time was longest in group PR. Epistaxis occurred the least in group V.
Among the three intubation techniques/tube materials for nasotracheal intubation, the velvet-soft PVC tube provided the highest first-attempt success rate, most expeditious advancement into the oral cavity, and lowest incidence of epistaxis.
ClinicalTrials.gov (NCT04695444); first submitted 30 December 2020.
我们旨在比较三种不同插管方法/管材料,以推进经鼻腔至口腔的气管内插管。
我们进行了一项随机临床试验,纳入了计划接受全身麻醉下择期手术且需要经鼻气管插管的成年患者。参与者被随机分配到聚氯乙烯(PVC)管组(P 组)、PVC 管连接橡胶导管组(PR 组)或天鹅绒软 PVC 管组(V 组)。然后根据分组进行气管插管。主要结局是将管推进口腔的首次尝试成功率;次要结局包括将管推进口腔的时间、总插管时间和鼻出血的发生率。
共有 149 例患者纳入研究。V 组(90%)的首次尝试成功率明显高于 P 组(58%)(优势比,6.5;95%置信区间[CI],2.2 至 19.2),但与 PR 组(100%)相似。V 组(16 [13] 秒)将管推进口腔所需的平均(标准差)时间明显短于 PR 组[40(10)秒;95%CI 的均数差,17 至 30]和 P 组[26(16)秒;95%CI 的均数差,3 至 16]。PR 组的总插管时间最长。V 组的鼻出血发生率最低。
在三种经鼻气管插管技术/管材料中,天鹅绒软 PVC 管提供了最高的首次尝试成功率、最快的推进口腔的速度和最低的鼻出血发生率。
ClinicalTrials.gov(NCT04695444);首次提交日期 2020 年 12 月 30 日。