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Transcutaneous electrical acupoint stimulation benefits postoperative pain relief of oocyte retrieval: A randomized controlled trial

医学 随机对照试验 刺激 麻醉 止痛 针灸科 卵母细胞 物理疗法 外科 替代医学 内科学 生物 胚胎 细胞生物学 病理
作者
Liying Liu,Yang Su,Rongrong Wang,Yuan‐Yuan Lai,Lei Huang,LI Yi-ting,Xin-yue Tao,Meng-hua Su,Xiaoyan Zheng,Shi-chen Huang,Yong-Na Wu,Siyi Yu,Fanrong Liang,Jie Yang
出处
期刊:Journal of Integrative Medicine [Elsevier BV]
卷期号:22 (1): 32-38 被引量:2
标识
DOI:10.1016/j.joim.2024.01.005
摘要

Transvaginal oocyte retrieval is frequently followed by adverse events related to anesthesia and the procedure. Some research showed that transcutaneous electrical acupoint stimulation (TEAS) can relieve intraoperative pain and postoperative nausea. This study examined whether TEAS can alleviate pain and relieve adverse symptoms after oocyte retrieval. Design, setting, participants and interventions: Altogether 128 patients were randomly divided into the TEAS group and the mock TEAS group. The two groups received a 30-minute-long TEAS or mock TEAS treatment that began 30 min after oocyte retrieval. Main outcome measures: The primary outcome was the visual analog scale (VAS) pain score. Secondary outcomes were pressure pain threshold, McGill score, pain rating index (PRI), present pain intensity (PPI), VAS stress score, VAS anxiety score, and postoperative adverse symptoms. The baseline characteristics of the two groups were comparable (P > 0.05). The VAS pain scores of the TEAS group were lower than those of the mock TEAS group at 60 and 90 min after oocyte retrieval (P < 0.05). The McGill score, PRI and PPI in the TEAS group were significantly lower than those in the control group at 60 min after oocyte retrieval (P < 0.05). However, the two groups had equivalent beneficial effects regarding the negative emotions, such as nervousness and anxiety (P > 0.05). The TEAS group was superior to the mock TEAS group for relieving postoperative adverse symptoms (P < 0.05). TEAS treatment can relieve postoperative pain and postoperative adverse symptoms for patients undergoing oocyte retrieval. Trial registration number: ChiCTR2100050153.
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