Kumar Miriyala Pavan, Patro Madhusmita, Panigrahy Sasmita, Samal Soumya, Kartheek B Sai
Department of Anaesthesiology and Critical Care, IMS and SUM Hospital, Bhubaneswar, Odisha, India.
Anesth Essays Res. 2021 Apr-Jun;15(2):213-219. doi: 10.4103/aer.aer_73_21. Epub 2021 Dec 16.
Awake fiber-optic bronchoscopy-guided intubation is the method of choice in difficult airway which requires effective airway anesthesia to ensure patient comfort and acceptance.
This study was conducted to assess the quality of airway anesthesia, patient comfort during intubation, and postoperative satisfaction of patients.
Patients posted for surgeries under general anesthesia with Mallampati Grade I and II in a medical college. Patients were followed in the operation theater and postoperative ward.
This was a prospective randomized single-blind study.
Group D received intravenous (i.v.) dexmedetomidine 1 μg.kg i.v. over 10 min and 3 ml of 4% lignocaine spray as you go (SAYGo). Group F received i.v. fentanyl 2 μg.kg over 10 min and transtracheal injection 3 ml of 4% lignocaine. Parameters assessed were endoscopic time, intubating condition, vocal cord position, cough severity, comfort during intubation, postoperative patient satisfaction, and any adverse effects such as sore throat, hoarseness, unpleasant memories, and hemodynamic response during intubation.
Independent Student's -test, Mann-Whitney, Chi-squared test, or Fisher's exact test were used. ≤ 0.05 was considered statistically significant.
Intubating conditions, vocal cord position, cough severity, comfort during intubation, and postoperative patient satisfaction were statistically significant ( ≤ 0.05) in favor of Group D though endoscopic time was longer.
IV dexmedetomidine with SAYGo is effective than IV fentanyl with transtracheal block for awake fiber-optic videoscopic intubation in terms of intubating conditions, vocal cord position, cough severity, comfort during intubation, and postoperative satisfaction of patients with significant attenuation of postintubation hemodynamic response and better preservation of respiration though endoscopic time is more.
清醒纤维支气管镜引导插管是困难气道的首选方法,这需要有效的气道麻醉以确保患者的舒适度和接受度。
本研究旨在评估气道麻醉质量、插管过程中患者的舒适度以及患者术后满意度。
在一所医学院,为全身麻醉下进行手术的马兰帕蒂分级为Ⅰ级和Ⅱ级的患者实施手术。在手术室和术后病房对患者进行随访。
这是一项前瞻性随机单盲研究。
D组在10分钟内静脉注射(i.v.)右美托咪定1μg/kg,同时逐段喷雾3ml 4%利多卡因(边走边喷[SAYGo])。F组在10分钟内静脉注射芬太尼2μg/kg,并经气管注射3ml 4%利多卡因。评估的参数包括内镜检查时间、插管条件、声带位置、咳嗽严重程度、插管过程中的舒适度、术后患者满意度以及任何不良反应,如咽痛、声音嘶哑、不愉快记忆和插管过程中的血流动力学反应。
使用独立样本t检验、曼-惠特尼检验、卡方检验或费舍尔精确检验。P≤0.05被认为具有统计学意义。
尽管内镜检查时间较长,但在插管条件、声带位置、咳嗽严重程度、插管过程中的舒适度和术后患者满意度方面,D组具有统计学显著性差异(P≤0.05)。
就插管条件、声带位置、咳嗽严重程度、插管过程中的舒适度以及患者术后满意度而言,静脉注射右美托咪定联合边走边喷利多卡因用于清醒纤维支气管镜视频插管比静脉注射芬太尼联合经气管阻滞更有效,插管后血流动力学反应显著减弱,呼吸功能得到更好的保留,尽管内镜检查时间更长。