Transcutaneous Electrical Acupoint Stimulation (TEAS) Facilitates Postoperative Recovery in Day Lung Cancer Surgery: A Randomized Controlled Trial

被引:0
作者
Wu, Siyin [1 ]
Lou, Jieqiong [2 ]
Zou, Houdong [3 ]
Wang, Wei [1 ]
Zhang, Yunyun [1 ]
Xu, Yunhua [4 ]
Hou, Xumin [2 ]
Wu, Jingxiang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Sch Med, Dept Anesthesiol, 241 West Huaihai Rd, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Sch Med, Presidents Off, Shanghai, Peoples R China
[3] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Sci & Educ, Sch Med, Shanghai, Peoples R China
[4] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Shanghai Lung Canc Ctr, Sch Med, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
transcutaneous electrical acupoint stimulation; postoperative pain; day surgery; lung cancer; enhanced recovery after surgery; THORACIC-SURGERY; ANESTHESIA; NAUSEA; LOBECTOMY; QUALITY; PAIN;
D O I
10.2147/JPR.S529193
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Day thoracic surgery requires effective analgesia and a rapid recovery. This study evaluated whether Transcutaneous Electrical Acupoint Stimulation (TEAS) reduces postoperative pain and analgesic use in lung cancer surgery. Methods: In this randomized, sham-controlled trial at a tertiary hospital in Shanghai, 100 patients (18-70 years old, ASA I-II) who underwent day lung cancer surgery (video-assisted thoracoscopic pulmonary wedge resection) were enrolled. Participants were randomized to receive either TEAS or sham TEAS in the Post-Anesthesia Care Unit. The TEAS group received 30 minutes of stimulation at Hegu (LI4) and Neiguan (PC6), whereas the sham group received electrode placement without stimulation. Primary outcome was pain intensity 24 h after surgery, measured using the visual analog scale (VAS). Secondary outcomes were VAS scores at 1 h and 12 h post-surgery, analgesic consumption, incidence of moderate-to-severe pain (VAS score >4), incidence of postoperative nausea and vomiting (PONV), Quality of Recovery (QoR-15) scores, and safety events. Results: The TEAS group had significantly lower VAS scores at 1 hour (0.94 vs 1.84, p = 0.006), 12 hours (2.00 vs 5.40, p < 0.001), and 24 hours (1.72 vs 4.02, p < 0.001). The incidence of moderate-to-severe pain within 12 hours was reduced (12.0% vs 74.0%, p < 0.001). Analgesic consumption was lower in the TEAS group. The QoR-15 scores at 24 h were higher in the TEAS group (130.8 vs 115.9, p < 0.001). No significant differences were observed in PONV, length of hospital stay, or adverse events. Conclusion: TEAS reduces postoperative pain and analgesic use, improves the recovery quality in lung cancer surgery, and supports its integration into ERAS protocols. Trial Registration: ChiCTR2200066600. https://www.chictr.org.cn/showproj.html?proj=187035.
引用
收藏
页码:3017 / 3026
页数:10
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