Dexmedetomidine sedation for endobronchial ultrasound-guided transbronchial needle aspiration, a randomised controlled trial

Ting-Yu Lin, Yu-Chen Huang, Chih-Hsi Kuo, Fu-Tsai Chung, Yu-Ting Lin, Tsai-Yu Wang, Shu-Min Lin, Yu-Lun Lo, Ting-Yu Lin, Yu-Chen Huang, Chih-Hsi Kuo, Fu-Tsai Chung, Yu-Ting Lin, Tsai-Yu Wang, Shu-Min Lin, Yu-Lun Lo

Abstract

Background and aim: Appropriate sedation is important to the success of endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA). Dexmedetomidine is a sedative agent that operates via the α2 adrenergic agonist, which provides sleep-like sedation with little respiratory suppression. This study compared the efficacy and safety of dexmedetomidine sedation with propofol in cases of EBUS-TBNA.

Methods: Patients requiring EBUS-TBNA were randomly assigned dexmedetomidine sedation (D, n=25) or propofol sedation (P, n=25). Vital signs, diagnostic yield and the bispectral index (BIS) were recorded throughout the bronchoscopic procedure and recovery period. The tolerance and cooperation of the patients were evaluated using questionnaires.

Measurements and results: The lowest mean arterial blood pressure in group D (79.2±9.9 versus 72.5±12.9 mmHg, p=0.049) exceeded that in group P, the lowest heart rate was lower (60.9±10.2 versus 71.4±11.8 beats·min-1, p=0.006) and the mean BIS during sedation was significantly higher (84.1±8.3 versus 73.6±5.7, p<0.001). Patients in group D were more likely to report perceiving procedure-related symptoms and express an unwillingness to undergo the bronchoscopy again, if indicated (41.1 versus 83.3%, p=0.007). One subject in group D aborted EBUS-TBNA due to intolerance. Many of the variables in the two groups were similar, including the proportion of hypoxaemic events, recovery times, patient cooperation and diagnostic yield.

Conclusions: The effects of dexmedetomidine on haemodynamics were in line with its pharmacodynamic features. Patients who received dexmedetomidine were more likely than those who received propofol to perceive the procedures. Overall, dexmedetomidine did not prove inferior to propofol sedation in terms of patient cooperation or diagnostic yield.

Conflict of interest statement

Conflict of interest: T-Y. Lin has nothing to disclose. Conflict of interest: Y-C. Huang has nothing to disclose. Conflict of interest: C-H. Kuo has nothing to disclose. Conflict of interest: F-T. Chung has nothing to disclose. Conflict of interest: Y-T. Lin has nothing to disclose. Conflict of interest: T-Y. Wang has nothing to disclose. Conflict of interest: S-M. Lin has nothing to disclose. Conflict of interest: Y-L. Lo has nothing to disclose.

Copyright ©ERS 2020.

Figures

FIGURE 1
FIGURE 1
Wakefulness during sedation. Following recovery, patients were asked if they had seen or heard anything during the bronchoscopic procedure. One subject in each group refused to answer the questionnaire.
FIGURE 2
FIGURE 2
a) Patient tolerance for procedure-related symptoms. Following recovery, subjects answered a questionnaire on procedure-related symptoms, including reactions to nebulised xylocaine inhalation, stimulation caused by scope insertion through the mouth, coughing, dyspnoea, pain and global tolerance to the entire procedure. Note that one subject in each group refused to answer the questionnaire. b) Patient cooperation during the bronchoscopic procedure. Bronchoscopist answered a questionnaire on the ease of scope insertion and biopsy, coughing by the patient and global cooperation during the procedure. The design of the questionnaire was based on a 100-mm visual analogue scale (VAS, 0: no bother, 100: worst intolerable/uncooperative).
FIGURE 3
FIGURE 3
Willingness to undergo repeated bronchoscopic procedure. Following recovery, patients were queried about their willingness to undergo the procedure again if indicated clinically (definitely not, possibly not, not sure, possibly yes and definitely yes). One subject in each group refused to answer the questionnaire.

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Source: PubMed

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