Effectiveness and feasibility of acupuncture for knee osteoarthritis: a pilot randomized controlled trial

医学 沃马克 骨关节炎 针灸科 随机对照试验 物理疗法 样本量测定 生活质量(医疗保健) 不利影响 外科 内科学 替代医学 数学 统计 病理 护理部
作者
Lu‐Lu Lin,Yongting Li,Jian‐Feng Tu,Jing‐Wen Yang,Ning Sun,Shuai Zhang,Tianqi Wang,Guang‐Xia Shi,Yi Du,Jingjie Zhao,Da-Chang Xiong,Hai-Kun Hou,Cun‐Zhi Liu
出处
期刊:Clinical Rehabilitation [SAGE Publishing]
卷期号:32 (12): 1666-1675 被引量:31
标识
DOI:10.1177/0269215518790632
摘要

Objective: To evaluate the effectiveness of acupuncture for pain relief and function improvement in patients with knee osteoarthritis and to determine the feasibility of an eight-week acupuncture intervention. Design: Pilot randomized controlled trial. Setting: Three teaching hospitals in China. Subjects: Patients with knee osteoarthritis (Kellgren grade II or III). Interventions: Patients were randomly assigned to an eight-week (three sessions per week) intervention of either traditional Chinese acupuncture or sham acupuncture. Main measures: The primary outcome was response rate—the proportion of patients achieving score ⩾36% decrease in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain and function at week 8 compared with baseline. Secondary outcomes included pain, function and quality of life. Results: Of 42 patients randomized, 36 (85.7%) completed the study. There was no significant difference in response rate between the traditional Chinese acupuncture and control groups: 61.9% (13 of 21) versus 42.9% (9 of 21) achieved score ⩾36% decrease in WOMAC pain and function at week 8 ( P = 0.217). The sum of WOMAC pain and function scores at week 8 was 11.6 (9.1) in the traditional Chinese acupuncture group compared with 16.3 (10.9) in the control group ( P = 0.183). There was no significant difference between groups. Three adverse events were recorded and were classified as mild. Conclusion: It showed that three sessions per week acupuncture intervention of knee osteoarthritis was feasible and safe. No difference was observed between groups due to small sample size. Larger (sample size ⩾ 296) randomized controlled trials of this intervention appear justified.
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