Srinivas Chaitra, Tiwari Tanmay, Prakash Ravi, Prabha Rati, Raman Rajesh, Arshad Zia
Anesthesiology, King George's Medical University, Lucknow, IND.
Cureus. 2023 Apr 30;15(4):e38322. doi: 10.7759/cureus.38322. eCollection 2023 Apr.
Introduction Awake fibreoptic intubation is a technique used to secure the airway of patients who are having predicted difficult intubation. We compared two routes, intravenous and nebulized, for administering a combination of ketamine and dexmedetomidine to patients requiring sedation for fibreoptic intubation. Methods and materials After approval of the institutional ethics committee, 64 patients between 18 and 60 years belonging to the American Society of Anesthesiologists physical status I or II and having predicted difficult airway were randomized to receive study medications through either intravenous (group I, n = 32) or nebulized (group N, n = 32) routes. Group I patients were given a combination of ketamine and dexmedetomidine through intravenous route. Group N patients were nebulized with a combination of ketamine and dexmedetomidine. The time required for awake fiberoptic intubation was the primary outcome variable. In addition, sedation score, cough severity, patient tolerance, intubating condition, hemodynamic changes, recall of events and discomfort during intubation, and any adverse events in the perioperative period were also compared. Results Compared to group N, the time needed to intubate the patients was significantly less in group I (75.69 ± 10.83 versus 49.19 ± 3.60 seconds, p < 0.001). Observer assessment sedation/alertness score (p < 0.001), cough severity (p < 0.001), patient tolerance (p < 0.001), and intubating condition (p = 0.001) were statistically significant, all conditions being better in group I. Patient discomfort and recall of the procedure were statistically similar between the groups. Conclusions The efficacy of a combination of dexmedetomidine and ketamine through the intravenous route is better than the nebulized route for patients undergoing awake fibreoptic intubation.
引言
清醒纤维光导喉镜引导插管是一种用于确保预计插管困难患者气道安全的技术。我们比较了静脉注射和雾化吸入两种途径,用于为需要清醒纤维光导喉镜引导插管镇静的患者联合使用氯胺酮和右美托咪定。
方法和材料
经机构伦理委员会批准,64例年龄在18至60岁之间、美国麻醉医师协会身体状况分级为I或II级且预计气道困难的患者被随机分为两组,分别通过静脉注射(I组,n = 32)或雾化吸入(N组,n = 32)途径接受研究药物。I组患者通过静脉途径给予氯胺酮和右美托咪定联合用药。N组患者用氯胺酮和右美托咪定联合雾化吸入。清醒纤维光导喉镜引导插管所需时间是主要结局变量。此外,还比较了镇静评分、咳嗽严重程度、患者耐受性、插管条件、血流动力学变化、对插管过程的回忆和不适,以及围手术期的任何不良事件。
结果
与N组相比,I组患者插管所需时间显著更短(75.69 ± 10.83秒对49.19 ± 3.60秒,p < 0.001)。观察者评估的镇静/警觉评分(p < 0.001)、咳嗽严重程度(p < 0.001)、患者耐受性(p < 0.001)和插管条件(p = 0.001)差异均有统计学意义,所有情况I组均更好。两组间患者不适和对操作的回忆在统计学上相似。
结论
对于接受清醒纤维光导喉镜引导插管的患者,通过静脉途径联合使用右美托咪定和氯胺酮的效果优于雾化吸入途径。