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Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina
Address correspondence and reprint requests to Ashraf S. Habib, MBBCh, MSc, Department of Anesthesiology, Box 3094, Duke University Medical Center, Durham, NC, 27710. Address e-mail to habib001{at}mc.duke.edu.
We randomized 94 patients undergoing cesarean delivery with spinal anesthesia to receive transcutaneous acupoint electrical stimulation using the ReliefBand® at the P6 point (active group) or an active ReliefBand® applied to the dorsum of the wrist (sham control group). The ReliefBand® was applied 3060 min preoperatively and left in place for 24 h. There was no statistically significant difference between the active and sham control groups in the incidence of intraoperative/postoperative nausea (30% versus 43%/23% versus 41%), vomiting (13% versus 9%/26 versus 37%), need for rescue antiemetics (23% versus 18%/34% versus 39%), or complete response (55% versus 57%/51% versus 34%). There was also no difference between the two groups in nausea scores, number of vomiting episodes, or patient satisfaction with postoperative nausea and vomiting management.
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