低频或高频穴位电刺激对产妇脊髓麻醉后低血压的影响比较:前瞻性随机对照临床试验》。

IF 1.3 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Journal of Integrative and Complementary Medicine Pub Date : 2024-08-01 Epub Date: 2024-03-28 DOI:10.1089/jicm.2023.0610
Xiaoyu Liu, Zijun Gao, Yongzhou Jiang, Xiaoshuang Tuo, Shan He, Feifei Xu, Zhihong Lu
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引用次数: 0

摘要

目的研究PC6经皮穴位电刺激(TEAS)能否减轻产妇脊髓麻醉(SA)后的低血压,并比较不同频率的TEAS的效果。研究方法从 2023 年 2 月 20 日至 2023 年 8 月 29 日,90 名计划在椎管内麻醉下剖腹产的产妇被随机分配接受无治疗(对照组)、高频率 TEAS(TEAS-HF)或低频率 TEAS(TEAS-LF)。治疗在 SA 后立即开始,持续 30 分钟。主要终点是 SA 后 30 分钟内低血压的发生率。次要终点包括SA后30分钟内的最低收缩压(SBP)、麻黄碱剂量、阿托品剂量、1分钟时的Apgar评分以及不良反应,包括恶心、呕吐、头晕、呼吸困难和胸闷。结果在 TEAS-HF 组,SA 后 30 分钟低血压发生率(13.3%)低于对照组(53.3%,P = 0.001;OR 1.9,95% 置信区间 [CI]:1.2-2.8)和 TEAS-LF 组(40.0%,P = 0.02,OR 1.4,95% CI:1.0-2.0)。与对照组(91.5 ± 16.5 mm Hg)和 TEAS-LF 组(93.9 ± 16.6 mm Hg)相比,TEAS-HF 组在 SA 后 30 分钟内的最低 SBP(100.0 ± 9.4 mm Hg)更高。接受 TEAS 治疗的患者的恶心和呕吐评分较低(均为 p = 0.02)。TEAS-HF 组患者头晕、呼吸困难和胸闷的发生率低于其他两组。阿托品用量和新生儿阿普加评分没有差异。结论PC6时的TEAS-HF降低了产妇SA后的低血压,而TEAS-LF则没有。试验注册:ClinicalTrials.gov (NCT05724095)。
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Comparison of Low-Frequency or High-Frequency Electrical Acupoint Stimulation on Hypotension After Spinal Anesthesia in Parturients: A Prospective Randomized Controlled Clinical Trial.

Objective: To investigate whether transcutaneous electrical acupoint stimulation (TEAS) at PC6 could reduce hypotension after spinal anesthesia (SA) in parturients and to compare the effect of TEAS at different frequencies. Methods: From February 20, 2023, to August 29, 2023, 90 parturients scheduled for c-section under SA were randomly assigned to receive no treatment (Control), TEAS at high frequency (TEAS-HF), or TEAS at low frequency (TEAS-LF). Treatments started immediately after SA and lasted for 30 min. The primary endpoint was incidence of hypotension by 30 min after SA. Secondary endpoints included lowest systolic blood pressure (SBP) during 30 min after SA, dose of ephedrine, dose of atropine, Apgar score at 1 min, and adverse events, including nausea, vomiting, dizziness, dyspnea, and chest congestion. Results: In the TEAS-HF group, the incidence of hypotension by 30 min after SA was lower (13.3%) than in the Control (53.3%, p = 0.001; OR 1.9, 95% confidence interval [CI]: 1.2-2.8) and TEAS-LF group (40.0%, p = 0.02, OR 1.4, 95% CI: 1.0-2.0). The lowest SBP during 30 min after SA was higher in the TEAS-HF group (100.0 ± 9.4 mm Hg) than in the Control group (91.5 ± 16.5 mm Hg) and TEAS-LF group (93.9 ± 16.6 mm Hg). Patients who received TEAS showed a lower score of nausea and vomiting (both p = 0.02). Patients in the group TEAS-HF showed a lower incidence of dizziness, dyspnea, and of chest congestion than those in the other two groups. There was no difference with respect to atropine consumption and neonatal Apgar score. Conclusions: TEAS-HF at PC6 reduced hypotension after SA in parturients, while TEAS-LF did not. Trial registration: ClinicalTrials.gov (NCT05724095).

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