Abstract | OBJECTIVE: To study postoperative pain relief in major gynaecological surgery by perioperative parecoxib administration in Thammasat University Hospital. MATERIAL AND METHOD: This double-blind randomized controlled clinical trial was conducted in Thammasat University Hospital, Pathumthani, Thailand from October 2013 to May 2014. One hundred and twenty patients who underwent elective gynaecological surgery were randomized assigned to study and control groups. Study group (n = 60) received 40 mg parecoxib and control group (n = 60) received placebo at 1 hour before surgery. The postoperative visual analog scale (VAS) at 3, 6, 12 and 24 hours, frequency of meperidine consumption in 24 hours and side effects of parecoxib were recorded. RESULTS: VAS of study group after operation at 3, 6, 12 and 24 hours was significantly lower than control group. Meperidine consumption in placebo group was significantly higher than study group (27.50 ± 19.36 and 48.75 ± 28.15 mg, respectively; p < 0.001). There was no side effect from parecoxib in this study. CONCLUSION:
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Authors | Pawat Arponrat, Densak Pongrojpaw, Chamnan Tanprasertkul, Komsun Suwannarurk, Kornkarn Bhamarapravatana |
Journal | Journal of the Medical Association of Thailand = Chotmaihet thangphaet
(J Med Assoc Thai)
Vol. 98
Issue 7
Pg. 636-42
(Jul 2015)
ISSN: 0125-2208 [Print] Thailand |
PMID | 26267984
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cyclooxygenase 2 Inhibitors
- Isoxazoles
- Meperidine
- parecoxib
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Topics |
- Adult
- Aged
- Cyclooxygenase 2 Inhibitors
(administration & dosage, therapeutic use)
- Double-Blind Method
- Female
- Gynecologic Surgical Procedures
(methods)
- Hospitals, University
- Humans
- Injections, Intravenous
- Isoxazoles
(administration & dosage, therapeutic use)
- Meperidine
(therapeutic use)
- Middle Aged
- Pain Measurement
- Pain, Postoperative
(drug therapy)
- Prospective Studies
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