Abstract | BACKGROUND AND OBJECTIVES: METHODS: RESULTS: There was a significant prolongation of analgesia in the tenoxicam group (365 +/- 91.1 minutes versus 305 +/- 53.2 minutes in control group, P < .001). Supplementary analgesic requirements were significantly decreased by intravenous tenoxicam (1.55 +/- 0.70 versus 2.25 +/- 0.68). Adverse side effects did not differ between groups and few complaints of phlebitis were noted. Apgar scores and blood gas analyses were similar in neonates from both groups. CONCLUSIONS:
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Authors | S D Belzarena |
Journal | Regional anesthesia
(Reg Anesth)
1994 Nov-Dec
Vol. 19
Issue 6
Pg. 408-11
ISSN: 0146-521X [Print] United States |
PMID | 7848951
(Publication Type: Clinical Trial, Controlled Clinical Trial, Journal Article)
|
Chemical References |
- Anti-Inflammatory Agents, Non-Steroidal
- Piroxicam
- Carbon Dioxide
- Oxygen
- Bupivacaine
- tenoxicam
|
Topics |
- Adult
- Analgesia, Obstetrical
- Anesthesia, Obstetrical
- Anesthesia, Spinal
- Anti-Inflammatory Agents, Non-Steroidal
(administration & dosage, adverse effects)
- Apgar Score
- Bupivacaine
(administration & dosage)
- Carbon Dioxide
(blood)
- Cesarean Section
(adverse effects)
- Drug Evaluation
- Female
- Fetal Blood
(chemistry)
- Humans
- Infant, Newborn
- Injections, Intravenous
- Oxygen
(blood)
- Pain, Postoperative
(prevention & control)
- Piroxicam
(administration & dosage, adverse effects, analogs & derivatives)
- Pregnancy
- Premedication
- Time Factors
|