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Pain: Original Article

Postoperative analgesic requirements after subarachnoid or epidural anesthesia with ropivacaine 0.75% in cesarean section. A double-blind randomized trial

, , , &
Pages 1497-1504 | Accepted 17 Aug 2012, Published online: 02 Sep 2012
 

Abstract

Objective:

Postoperative analgesic requirements and pain scores were compared after subarachnoid versus epidural anesthesia with plain ropivacaine 0.75% for elective cesarean section.

Study design:

Ropivacaine 0.75% was randomly administered for subarachnoid or epidural anesthesia in 108 parturients, scheduled for cesarean section. Times for the sensory block to reach T4 level and to regress to T6 level were recorded. At 2, 4, 8 and 24 h postoperatively, pain scores at rest and cough, morphine consumption as well as patient satisfaction, incidence of headache, nausea and/or vomiting were measured.

Results:

Median (min–max) time for the sensory block to reach T4 was 7 (3–0) min versus 24 (16–73) min and to regress to T6 was 126 (70–332) min versus 200 (98–439) min in the subarachnoid and epidural groups, respectively (p = 0.001). Although the subarachnoid had more analgesic consumption than the epidural group at 2 and 4 h postoperatively (7.3 ± 4.7 vs. 1.8 ± 2.4 mg, p = 0.001 and 9 ± 5.7 vs. 3.3 ± 3.8 mg, p = 0.001, respectively) no difference was observed at 8 or 24 h postoperatively (p = 0.14 and p = 0.38, respectively). VAS scores at rest and after cough (p = 0.56, p = 0.35, respectively), patient satisfaction (p = 0.61), incidence of headache (p = 1.0), nausea and/or vomiting (p = 0.78) did not differ between the two groups.

Conclusions:

Postoperative pain, analgesic requirements, patient satisfaction and adverse effects did not differ when subarachnoid or epidural anesthesia with ropivacaine 0.75% was used for elective cesarean section. Nevertheless, subarachnoid provides faster onset and offset of the block, compared to epidural anesthesia. The key limitation of this study is the lack of postoperative serum ropivacaine measurements taken with concurrent pain score measurements.

Transparency

Declaration of funding

There was no financial support for this study outside institutional sources.

Declaration of financial/other interest

The authors of this study have disclosed that they have no relevant financial relationships involving this study. CMRO peer reviewers on this manuscript have no relevant financial relationships to disclose.

Acknowledgments

The authors thank the statisticians, Ms Katerina Dimitriou (BSc) and Mr Vasili Nikolaou (MSc) for their invaluable help in the statistical analysis of the data. Financial support for their analyses was provided solely from institutional sources.

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