Abstract:Objectives: To investigate the efficacy and safety of sedation with dexmedetomidine in upper gastrointestinal endoscopy. Methods: Patients with ASA physical status I-II undergoing elective upper gastrointestinal endoscopy were randomly allocated to receive dexmedetomidine or midazolam for conscious sedation. Continuous peripheral oxygen saturation (SpO 2 ), heart rate, mean arterial pressure (MAP), Ramsay Sedation Scale (RSS) and numeric rating scale pain scores were recorded before, during and after the proce… Show more
“…A further six studies were then excluded because of a lack of control groups ( n = 2), comparison of dexmedetomidine with propofol ( n = 2), and comparison of dexmedetomidine with placebo ( n = 2) . Finally, nine studies were included in the systematic review and meta‐analysis . The characteristics of these studies are summarized in Table .…”
Section: Resultsmentioning
confidence: 99%
“…The study by Wu et al . had potential bias in selective reporting and other aspects because it was a retrospective randomized study …”
Section: Resultsmentioning
confidence: 99%
“…Dexmedetomidine has been reported to facilitate the sedation of patients while maintaining their consciousness and to maintain stable respiration and circulation. Several randomized controlled trials (RCT) have evaluated the efficacy of dexmedetomidine in comparison with midazolam for gastrointestinal endoscopy . Unfortunately, none of these trials enrolled a sufficient number of patients to produce an adequate power in order to detect meaningful differences.…”
This meta-analysis shows that dexmedetomidine is a safe and effective sedative agent for gastrointestinal endoscopy, especially endoscopic retrograde cholangiopancreatography and endoscopic submucosal dissection.
“…A further six studies were then excluded because of a lack of control groups ( n = 2), comparison of dexmedetomidine with propofol ( n = 2), and comparison of dexmedetomidine with placebo ( n = 2) . Finally, nine studies were included in the systematic review and meta‐analysis . The characteristics of these studies are summarized in Table .…”
Section: Resultsmentioning
confidence: 99%
“…The study by Wu et al . had potential bias in selective reporting and other aspects because it was a retrospective randomized study …”
Section: Resultsmentioning
confidence: 99%
“…Dexmedetomidine has been reported to facilitate the sedation of patients while maintaining their consciousness and to maintain stable respiration and circulation. Several randomized controlled trials (RCT) have evaluated the efficacy of dexmedetomidine in comparison with midazolam for gastrointestinal endoscopy . Unfortunately, none of these trials enrolled a sufficient number of patients to produce an adequate power in order to detect meaningful differences.…”
This meta-analysis shows that dexmedetomidine is a safe and effective sedative agent for gastrointestinal endoscopy, especially endoscopic retrograde cholangiopancreatography and endoscopic submucosal dissection.
“…It is correlated with cooperative sedation, which is different from the clouding of consciousness that occurs with drugs that act on GABA receptors, such as propofol or midazolam [17]. In a previous study, dexmedetomidine showed better oxygen saturation and RSS than midazolam [18]. In the present study, dexmedetomidine provided sufficient sedation (0 vs 83.6 ± 40.4 vs 89.9 ± 42.7 min), and the duration did not differ between the D-0.5 and D-1 groups.…”
BackgroundIn this prospective, randomized, double-blind, placebo-controlled trial, we tried to find out appropriate amounts of single-dose dexmedetomidine to prolong the duration of spinal anesthesia in a clinical setting.MethodsSixty patients who were scheduled for unilateral lower limb surgery under spinal anesthesia were randomized into three groups receiving normal saline (control group, n = 20) or 0.5 or 1.0 ug/kg dexmedetomidine (D-0.5 group, n = 20; D-1, n = 20) intravenously prior to spinal anesthesia with 12 mg of bupivacaine. The two-dermatome pinprick sensory regression time, duration of the motor block, Ramsay sedation score (RSS), and side effects of dexmedetomidine were assessed.ResultsThe two-dermatome pinprick sensory regression time (57.6 ± 23.2 vs 86.5 ± 24.3 vs 92.5 ± 30.7, P = 0.0002) and duration of the motor block (98.8 ± 34.1 vs 132.9 ± 43.4 vs 130.4 ± 50.4, P = 0.0261) were significantly increased in the D-0.5 and D-1 groups than in the control group. The RSS were significantly higher in the D-0.5 and D-1 groups than in the control group. However, there were no patients with oxygen desaturation in dexmedetomidine groups. The incidences of hypotension and bradycardia showed no differences among the three groups.ConclusionsBoth 0.5 and 1.0 ug/kg of dexmedetomidine administered as isolated boluses in the absence of maintenance infusions prolonged the duration of spinal anesthesia.
“…Earlier randomized controlled trials evaluating the use of dexmedetomidine alone during small diagnostic and therapeutic procedures showed promising results. However, a potential disadvantage of dexmedetomidine is its hemodynamic side effects, which include hypotension and bradycardia …”
In this study group, dexmedetomidine combined with remifentanil provided a high level of patient satisfaction and comfort, as well as operator comfort, without any clinically relevant adverse events. All patients were highly cooperative and instructable; incident pain needs to be closely monitored.
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