Two Transcutaneous Stimulation Techniques in Shoulder Pain: Transcutaneous Pulsed Radiofrequency (TPRF) versus Transcutaneous Electrical Nerve Stimulation (TENS): A Comparative Pilot Study

被引:5
|
作者
Lin, Mu-Lien [1 ,2 ]
Chiu, Hung-Wei [3 ]
Shih, Zao-Ming [4 ,5 ]
Lee, Po-Ying [3 ]
Li, Pei-Zhi [3 ]
Guo, Chin-Hong [3 ]
Luo, Yuan-Jie [3 ]
Lin, Shen-Chieh [6 ]
Lin, Kwan-Yu [2 ]
Hsu, Yu-Ming [3 ]
Pang, Angela [7 ]
Pang, Weiwu [8 ]
机构
[1] Natl Yang Ming Univ, Dept Anesthesiol, Taipei, Taiwan
[2] Taipei City Hosp, Dept Anesthesiol, Zhongxing Branch, Taipei, Taiwan
[3] Natl Taipei Univ Technol, Dept Elect Engn, Taipei, Taiwan
[4] Feng Chia Univ, Taichung, Taiwan
[5] Kuang Tien Gen Hosp, Dept Emergency & Crit Care Med, 117 Shatian Rd, Taichung 433, Taiwan
[6] Natl Taiwan Univ Hosp, Dept Surg, Taipei, Taiwan
[7] Univ Florida, Psychol & English, 8257 Via Vivaldi, Orlando, FL USA
[8] Kuang Tien Gen Hosp, 117 Shatian Rd, Taichung 433, Taiwan
来源
PAIN RESEARCH & MANAGEMENT | 2019年 / 2019卷
关键词
INTENSITY; TENDON;
D O I
10.1155/2019/2823401
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective. To compare the safety and efficacy of 2 transcutaneous stimulation techniques, transcutaneous pulsed radiofrequency (TPRF) versus transcutaneous electrical nerve stimulation (TENS), in chronic shoulder tendonitis. Design. A prospective, randomized, and double-blind clinical trial. Setting. Academic pain service of a city hospital. Subjects. Fifty patients with sonography-confirmed shoulder tendonitis. Methods. Fifty patients were randomly allocated into two groups for electrical stimulation treatment with 3-month follow-ups: Group 1 (n = 25), TENS and Group 2 (n = 25), TPRF. Both groups underwent either treatment for 15 minutes every other day, three times total. Our primary goals were to find any treatment comfort level, adverse event, and changes in Constant-Murley shoulder (CMS) scores. The secondary goals were finding the changes in pain, enjoyment of life, and general activity (PEG) scores. Results. For primary goals, no adverse events were noted throughout this study. No differences were found between groups for treatment tolerability (3.20 + 0.87 vs. 2.16 + 0.75). Statistically significant lower PEG scores were noticeable with the TPRF group after the course (12.73 + 5.79 vs. 24.53 + 10.21, p = 0.013). Their statistical significance lasted for 3 months although the difference gap diminished after 1 month. CMS scores were significantly higher in the TPRF group (70.84 + 6.74 vs. 59.56 + 9.49, p = 0.007) right after treatment course but the significance did not last. Conclusions. In treating chronic shoulder tendinitis using two transcutaneous stimulation techniques, both TPRF and TENS are safe and effective. TPRF is superior to TENS.
引用
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页数:9
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