Single-Blinded, Randomised Preliminary Study Evaluating the Effects of 2 hz Electroacupuncture for Postoperative Pain in Patients with Total Knee Arthroplasty

Author:

Tzeng Chung-Yuh12,Chang Shih-Liang3,Wu Chih-Cheng45,Chang Chu-Ling2,Chen Wen-Gii6,Tong Kwok-Man1,Huang Kui-Chou1,Hsieh Ching-Liang678

Affiliation:

1. Department of Orthopedic Surgery, Taichung Veterans General Hospital, Taichung, Taiwan

2. Department of Nursing, Hung Kuang University, Taiwan

3. Department of Medicinal Botanicals and Health Care, Da-Yeh University, Chunghwa, Taiwan

4. Department of Anesthesia, Taichung Veterans General Hospital, Taichung, Taiwan

5. Department of Financial and Computational Mathematics, Providence University, Taichung, Taiwan

6. Graduate Institute of Integrated Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan

7. Department of Chinese Medicine, China Medical University Hospital, Taichung, Taiwan

8. Research Center for Chinese Medicine and Acupuncture, China Medical University, Taichung, Taiwan

Abstract

Objective To explore the point-specific clinical effect of 2 Hz electroacupuncture (EA) in treating postoperative pain in patients undergoing total knee arthroplasty (TKA), Methods In a randomised, partially single-blinded preliminary study, 47patients with TKA were randomly divided into three groups: control group (CG, n=17) using only patient-controlled analgesia (PCA); EA group (EAG, n=16) with 2 Hz EA applied at ST36 ( Zusanli) and GB34 ( Yanglingquan) contralateral to the operated leg for 30 min on the first two postoperative days, also receiving PCA; and non-point group (NPG, n=14), with EA identical to the EAG except given 1 cm lateral to both ST36 and GB34. The Mann–Whitney test was used to show the difference between two groups and the Kruskal–Wallis test to show the difference between the three groups. Results The time until patients first required PCA in the CG was 34.1±22.0 min, which was significantly shorter than the 92.0±82.7 min in the EAG (p<0.001) and 90.7±94.8 min in the NPG (p<0.001); there was no difference between the EAG and NPG groups (p>0.05). The total dosage of PCA solution given was 4.6±0.9 mL/kg body weight in the CG, 4.2±1.0 mL/kg in the EAG and 4.5±1.0 mL/kg in the NPG; there were no significant differences (p>0.05) among the three groups. Conclusions In this small preliminary study, EA retarded the first demand for PCA in comparison with no EA. No effect was seen on the total dosage of PCA required and no point-specific effect was seen.

Publisher

SAGE Publications

Subject

Clinical Neurology,Complementary and alternative medicine,General Medicine

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