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Efficacy and Safety of Dexmedetomidine Nasal Spray as a Premedication in Patients Undergoing Fiberoptic Bronchoscopy Under Sedation: A Randomized Controlled Trial

右美托咪定 医学 术前用药 麻醉 镇静 生理盐水 随机对照试验 鼻腔给药 外科 鼻喷雾剂 不利影响 血流动力学 支气管镜检查 入射(几何) 局部麻醉 临床试验 异丙酚 睫毛膏
作者
Guilin Zhao,Weiyong Qin,Jiangdong Wu,Shen-Qiao Wei,Xiaoqing Jiang,Hang Qiu,Xueke Du,Lini Chen
出处
期刊:Drug Design Development and Therapy [Dove Medical Press]
卷期号:Volume 19: 10735-10749 被引量:1
标识
DOI:10.2147/dddt.s550551
摘要

Background: Fiberoptic bronchoscopy (FB) under sedation can provoke patient discomfort, cough, and hemodynamic fluctuations. This study evaluated the efficacy and safety of dexmedetomidine nasal spray as a premedication compared to intranasal normal saline and lidocaine. Methods: A total of 90 patients scheduled for FB under sedation were randomly assigned to three groups. Group D (dexmedetomidine), Group C (control, normal saline), and Group L (lidocaine) received pre-induction nasal sprays via the same metered-dose aerosolization device. At 10 min post-spray, all patients received standard monitored anesthesia care (MAC) with preserved spontaneous ventilation (respiratory rate, RR ≥ 10 breaths/min; peripheral oxygen saturation, SpO 2 ≥ 95%). Outcomes included hemodynamic parameters (heart rate, HR; mean arterial pressure, MAP) measured at specific time points (T 1 -T 8 ), Modified Observer’s Assessment of Alertness/Sedation (MOAA/S) scores, cough severity and adverse events. Results: Group D demonstrated better overall performance. Hemodynamically, HR in Group D was lower than Group C at T 3 and T 5 , and lower than Group L at T 5 . MAP in Group D was lower than both control groups from T 3 -T 6 . Recovery time in Group D was shorter than in both Group C and Group L. Group D also exhibited superior MOAA/S scores (lower at T 1 , but higher at T 6 -T 8 ), higher bronchoscopist satisfaction, and a lower incidence of both moderate-to-severe cough and postoperative nausea and vomiting (PONV) compared to the other groups. Respiratory rates were comparable, with Group D showing a higher RR than Group C at T 6 . Conclusion: Premedication with dexmedetomidine nasal spray in patients undergoing FB under sedation was associated with more effective suppression of procedure-induced cough, better hemodynamic stability, a lower incidence of PONV, and a faster recovery profile compared to both intranasal saline and lidocaine, without increasing respiratory depression. Consequently, dexmedetomidine nasal spray can effectively and safely enhance patient comfort and safety, and optimize the procedural conditions for the bronchoscopists. Keywords: dexmedetomidine nasal spray, normal saline, lidocaine, fiberoptic bronchoscopy, sedation
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