Abstract | OBJECTIVE: DESIGN: Prospective, randomized, double-blind study. SETTING: University-affiliated teaching hospital. PATIENTS: Ninety patients (48 females, 42 males) scheduled for middle ear surgery. INTERVENTION: MAIN OUTCOME MEASURE:
Emetic episodes and safety assessment were performed during 2 periods-0 to 3 hours in the postanesthetic care unit and 3 to 24 hours in the ward-after receiving anesthesia. RESULTS: The incidence of patients who were emesis free during the 0- to 3-hour period after receiving anesthesia was 93% for those who received propofol, 73% for those who received droperidol, and 70% for those who received metoclopramide, respectively; the respective corresponding incidence during the 3- to 24-hour period after receiving anesthesia was 90%, 67%, and 60% (P<.05, overall Fisher exact probability test). No clinically adverse events were observed in any of the groups. CONCLUSION:
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Authors | Y Fujii, H Tanaka, N Kobayashi |
Journal | Archives of otolaryngology--head & neck surgery
(Arch Otolaryngol Head Neck Surg)
Vol. 127
Issue 1
Pg. 25-8
(Jan 2001)
ISSN: 0886-4470 [Print] United States |
PMID | 11177010
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial, Retracted Publication)
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Chemical References |
- Antiemetics
- Metoclopramide
- Droperidol
- Propofol
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Topics |
- Adult
- Analysis of Variance
- Antiemetics
(administration & dosage, therapeutic use)
- Dose-Response Relationship, Drug
- Double-Blind Method
- Droperidol
(administration & dosage, therapeutic use)
- Ear, Middle
(surgery)
- Female
- Humans
- Male
- Metoclopramide
(administration & dosage, therapeutic use)
- Middle Aged
- Postoperative Nausea and Vomiting
(prevention & control)
- Propofol
(administration & dosage, therapeutic use)
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