Oral analgesia in the treatment of post-cesarean pain

被引:35
作者
Jakobi, P [1 ]
Weiner, Z [1 ]
Solt, I [1 ]
Alpert, I [1 ]
Itskovitz-Eldor, J [1 ]
Zimmer, EZ [1 ]
机构
[1] Rambam Med Ctr, Dept Obstet & Gynecol, IL-31096 Haifa, Israel
来源
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY | 2000年 / 93卷 / 01期
关键词
surgery; cesarean section; analgesics; dipyrone; morphine; pain; postoperative; pain measurement;
D O I
10.1016/S0301-2115(00)00256-6
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Cesarean section is one of the most common operations. The new technologies of postoperative pain treatment such as patient-controlled analgesia, are expensive and may limit women caring for their newborns shortly after delivery. The present study assessed patient satisfaction with oral analgesia following cesarean section. Study: design: An open prospective study was conducted on all women who had a cesarean section with epidural analgesia, during two consecutive periods of 3 months each. In the first group of 109 women, an oral solution of I g dipyrone was allowed every 4 h, upon patient request. Patients requesting additional analgesia were administered a tablet of 30 mg immediate-release morphine sulfate. Tn the second group of 90 women, the same protocol was used; however, oral morphine was the drug of choice and dipyrone was used for rescue analgesia. Pain intensity and satisfaction were self-evaluated by patients using a visual analog scale. Results: The results of each study period were independently evaluated. The demographic and obstetrical variables were similar in both groups. The duration of analgesic effect of dipyrone was 6.5 h and the satisfaction score was 90. The duration of analgesic effect of oral morphine was 5.05 h and the satisfaction score was 83.7. Overall, patients in both groups requested only 25% of the permissible dosage of analgesia. Conclusions: Oral analgesia following cesarean section provides satisfactory pain relief, is easily administered, and is a substantially less costly alternative to the new pain treatment technologies currently in use. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:61 / 64
页数:4
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