Article ID Journal Published Year Pages File Type
3306719 Gastrointestinal Endoscopy 2008 9 Pages PDF
Abstract

BackgroundPropofol is an accepted method of sedation for an ERCP and generally achieves deep sedation rather than conscious sedation, and dexmedetomidine has sedative properties of equivalent efficacy.ObjectiveTo examine the hypothesis that dexmedetomidine is as effective as propofol combined with fentanyl for providing conscious sedation during an ERCP.Design and SettingRandomized, blind, double-dummy clinical trial.PatientsTwenty-six adults, American Society of Anesthesiologists status I to III, underwent an ERCP.InterventionsPatients were randomized to receive either propofol (n = 14) (target plasma concentration range 2-4 μg/mL) combined with fentanyl 1 μg/kg, or dexmedetomidine (n = 12) 1 μg/kg for 10 minutes, followed by 0.2 to 0.5 μg/kg/min. Additional sedatives were used if adequate sedation was not achieved at the maximum dose allowed.Main Outcomes MeasurementsThe sedation level was assessed by the Richmond alertness-sedation scale and the demand for additional sedatives. Furthermore, heart rate, blood pressure, oxygen saturation, and respiratory rate were continuously assessed.ResultsThe relative risk (RR) was 2.71 (95% CI, 1.31-5.61) and the number of patients that needed to be treated (NNT) was 1.85 (95% CI, 1.19-4.21) to observe one additional patient with drowsiness 15 minutes after sedation in the dexmedetomidine group. Also, the RR was 9.42 (95% CI, 1.41-62.80), and the NNT was 1.42 (95% CI, 1.0-2.29) to require additional analgesic. However, there was also a greater reduction in blood pressure, a lower heart rate, and greater sedation after the procedure.ConclusionsDexmedetomidine alone was not as effective as propofol combined with fentanyl for providing conscious sedation during an ERCP. Furthermore, dexmedetomidine was associated with greater hemodynamic instability and a prolonged recovery.

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