A Comparative Study between Local Dexmedetomidine and Intravenous Dexmedetomidine during Awake Fiberoptic Nasotracheal Intubation.

Anesthesia, Essays and Researches Pub Date : 2022-07-01 Epub Date: 2022-12-09 DOI:10.4103/aer.aer_140_22
Abhay G Sancheti, Sarita S Swami, Shweta Laxmikant Konnur, Nooh Amin
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引用次数: 1

Abstract

Background: Awake fiberoptic intubation (AFOI) is the gold standard for managing a difficult airway. To make the patient comfortable and cooperative during the procedure, many drugs such as benzodiazepines, opioids, or dexmedetomidine are used. Most of these intravenously given drugs may cause respiratory depression and hypoxia.

Aim: We compared the efficacy of dexmedetomidine through nebulization and transtracheal route with intravenous routes with the primary aim of comparing patient tolerance score (PTS) and secondary objectives of comparing sedation score, cough score, and total duration required for awake fiberoptic nasotracheal intubation.

Settings and design: This study was a prospective randomized double-blind study.

Subjects and methods: Seventy-six patients, scheduled for elective surgery requiring AFOI between 18 and 75 years, were included in the study. They were randomly divided into two groups of 38 each. Group I patients received intravenous dexmedetomidine 1 μg.kg-1 and Group L patients received local dexmedetomidine through nebulization 0.5 μg.kg-1 and transtracheal injection 0.5 μg.kg-1.

Statistical analysis used: Statistical Package for the Social Sciences version 22 was used.

Results: Patients who received dexmedetomidine through nebulization and transtracheal route have significantly better PTSs and less cough scores as compared to patients who received dexmedetomidine by intravenous route (P < 0.05). Hemodynamic parameters and sedation scores between the two groups were statistically insignificant (P > 0.05). The time required for the procedure was significantly less in Group L compared to Group I (P < 0.05).

Conclusion: Dexmedetomidine by nebulization and transtracheal route provides optimal conditions for AFOI with good patient tolerance and less cough score as compared to the intravenous route.

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清醒期纤维鼻气管插管时局部和静脉应用右美托咪定的比较研究。
背景:苏醒纤维光学插管(AFOI)是治疗困难气道的黄金标准。为了使患者在手术过程中感到舒适和配合,使用了许多药物,如苯二氮卓类药物、阿片类药物或右美托咪定。这些静脉注射的药物大多可能导致呼吸抑制和缺氧。目的:我们比较了右美托咪定雾化和经气管途径与静脉途径的疗效,主要目的是比较患者耐受性评分(PTS),次要目的是比较清醒纤维鼻气管插管所需的镇静评分、咳嗽评分和总持续时间。设置和设计:本研究是一项前瞻性随机双盲研究。受试者和方法:76名患者被纳入研究,他们计划在18至75岁之间接受需要AFOI的选择性手术。他们被随机分为两组,每组38人。I组患者静脉注射右美托咪定1μg.kg-1,L组患者通过雾化吸入0.5μg.kg-1和经气管注射0.5μg.g.kg-1局部注射右美托咪定。使用的统计分析:使用社会科学版22的统计软件包。结果:与静脉注射右美托咪定患者相比,雾化和气管内注射右美托咪定患者的PTS和咳嗽评分显著改善(P<0.05)。两组之间的血液动力学参数和镇静评分均无统计学意义(P>0.05)结论:与静脉滴注相比,雾化吸入和气管内给药的右美托咪定为AFOI提供了良好的患者耐受性和较低的咳嗽评分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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