Abstract | BACKGROUND: OBJECTIVES: PATIENTS AND METHODS: In a randomized, double-blind, and placebo-controlled clinical trial, 90 parturients, ASA class I and II, aged 20-30 years, who undergone spinal anesthesia for cesarean section were randomly allocated to one of three groups receiving midazolam (1 mg bolus and 0.1 mg/kg/hr, n=30), propofol (20 mg bolus and 0.1 mg/kg/hr, n = 30), and placebo (saline, n=30) intravenously (IV) immediately after umbilical cord clamping. Bupivacaine hydrochloride (10 mg) was used for induction of the anesthesia. Patients' hemodynamics was monitored at 3-minute intervals. Furthermore, intraoperative and post-delivery emetic episodes, severity of emesis, scores of sedation and ephedrine consumption were recorded. RESULTS: CONCLUSIONS:
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Authors | Sousan Rasooli, Farnaz Moslemi, Arash Khaki |
Journal | Anesthesiology and pain medicine
(Anesth Pain Med)
Vol. 4
Issue 4
Pg. e19384
(Oct 2014)
ISSN: 2228-7523 [Print] Netherlands |
PMID | 25346896
(Publication Type: Journal Article)
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