2012
DOI: 10.1097/00003643-201206001-00105
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Propofol versus dexmedetomidine for sedation in colonoscopy: a prospective, randomized study

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Cited by 6 publications
(4 citation statements)
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“…Although dexmedetomidine has a short half-life (2-3 h) due to its rapid distribution and extensive metabolization by the liver, the recovery time was longer than that of propofol, which has a three times shorter half-life (30-60 min). Many studies have been conducted to evaluate the use of dexmedetomidine as a single agent for sedation of gastrointestinal endoscopic procedures, with better results in terms of hemodynamic stability, sedation efficacy, the incidence of side effects, and endoscopist satisfaction [26][27][28][29][30][31]. However, studies conducted by [32][33][34] revealed that using dexmedetomidine as a single agent for sedation of GIE procedures was ineffective in achieving the required sedation level except by using higher doses of rescue sedation doses, resulting in a significant decrease in hemodynamics with a longer time required for recovery and home discharge.…”
Section: Discussionmentioning
confidence: 99%
“…Although dexmedetomidine has a short half-life (2-3 h) due to its rapid distribution and extensive metabolization by the liver, the recovery time was longer than that of propofol, which has a three times shorter half-life (30-60 min). Many studies have been conducted to evaluate the use of dexmedetomidine as a single agent for sedation of gastrointestinal endoscopic procedures, with better results in terms of hemodynamic stability, sedation efficacy, the incidence of side effects, and endoscopist satisfaction [26][27][28][29][30][31]. However, studies conducted by [32][33][34] revealed that using dexmedetomidine as a single agent for sedation of GIE procedures was ineffective in achieving the required sedation level except by using higher doses of rescue sedation doses, resulting in a significant decrease in hemodynamics with a longer time required for recovery and home discharge.…”
Section: Discussionmentioning
confidence: 99%
“…Many anesthetic drugs such as midazolam, propofol, and/or alfentanil or pethidine combinations, α-agonists, and neuroleptics are frequently administered for this matter. 1,2,3 Conscious sedation-analgesia is aimed to comfort the patients with minimal adverse effects, and the ideal method is the one with fast induction and emergence, which preserves respiration and hemodynamics stability. Several regimens of drugs are being used at this time for this purpose.…”
Section: Introductionmentioning
confidence: 99%
“…Many anesthetic drugs such as midazolam, propofol, and/or alfentanil or pethidine combinations, α-agonists, and neuroleptics are frequently administered for this matter. 1 , 2 , 3 …”
Section: Introductionmentioning
confidence: 99%
“…Dexmedetomidine, the S-enantiomer of medetomidine, a relatively newer alpha-2 adrenoreceptor agonist was first used in 1999 as a sedative during premedication primarily in the Intensive Care Units. [ 1 2 3 ] However, with the passage of time, dexmedetomidine has proved to be a novel drug which is currently used for the purpose of analgesia,[ 4 ] day-care surgeries,[ 5 ] short procedures such as colonoscopies,[ 6 7 ] and as an adjunct to general anesthesia for the purpose of co-induction. [ 8 ] The term co-induction of anesthesia has been applied to the use of two or more drugs to induce anesthesia.…”
Section: Introductionmentioning
confidence: 99%