针灸联合非甾体抗炎药(NSAIDs)与单独针灸或非甾体抗炎药治疗慢性颈部疼痛:一项评估盲随机对照试验研究

Jae-Heung Cho, Dong-Hyun Nam, Ki-Tack Kim, Jun-Hwan Lee
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引用次数: 15

摘要

目的:探讨针灸联合非甾体抗炎药(NSAIDs)治疗慢性颈部疼痛与单独针灸或非甾体抗炎药(NSAIDs)治疗的有效性的可行性和所需样本量。方法:对45例慢性颈部疼痛患者进行研究。针刺联合非甾体抗炎药治疗组每日服用非甾体抗炎药(zaltoprofen, 80 mg),针刺治疗组每周3次。针刺治疗组每周治疗3次,非甾体抗炎药治疗组每日服用。主要结果是确定可行性和计算样本量。作为次要结局,测量慢性颈部疼痛的疼痛强度和疼痛相关症状。结果:在入组率和退组率方面,88.2%的患者同意加入试验,15.6%的参与者失去了随访。全面试验的样本量估计为120名患者。虽然是初步的,但在所有组中,颈部疼痛强度的视觉模拟量表(VAS)在基线测量和每个评估点之间都有显著变化。然而,三组之间的VAS评分没有差异。结论:本初步研究为针灸联合非甾体抗炎药治疗慢性颈部疼痛与单独针灸或非甾体抗炎药治疗相比的全面试验提供了可行性和样本量。针刺与非甾体抗炎药的疗效有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Acupuncture with non-steroidal anti-inflammatory drugs (NSAIDs) versus acupuncture or NSAIDs alone for the treatment of chronic neck pain: an assessor-blinded randomised controlled pilot study.

Acupuncture with non-steroidal anti-inflammatory drugs (NSAIDs) versus acupuncture or NSAIDs alone for the treatment of chronic neck pain: an assessor-blinded randomised controlled pilot study.

Acupuncture with non-steroidal anti-inflammatory drugs (NSAIDs) versus acupuncture or NSAIDs alone for the treatment of chronic neck pain: an assessor-blinded randomised controlled pilot study.

Objective: To investigate the feasibility and sample size required for a full-scale randomised controlled trial of the effectiveness of acupuncture with non-steroidal anti-inflammatory drugs (NSAIDs) for chronic neck pain compared with acupuncture or NSAID treatment alone.

Methods: A total of 45 patients with chronic neck pain participated in the study. For 3 weeks the acupuncture with NSAIDs treatment group took NSAIDs (zaltoprofen, 80 mg) daily while receiving acupuncture treatment three times a week. The acupuncture treatment group received treatment three times a week and the NSAID treatment group took NSAIDs daily. The primary outcomes were to determine the feasibility and to calculate the sample size. As secondary outcomes, pain intensity and pain-related symptoms for chronic neck pain were measured.

Results: With regard to enrolment and dropout rates, 88.2% of patients consented to be recruited to the trial and 15.6% of participants were lost to follow-up. The sample size for a full-scale trial was estimated to be 120 patients. Although preliminary, there was a significant change in the visual analogue scale (VAS) for neck pain intensity between the baseline measurement and each point of assessment in all groups. However, there was no difference in VAS scores between the three groups.

Conclusions: This pilot study has provided the feasibility and sample size for a full-scale trial of acupuncture with NSAIDs for chronic neck pain compared with acupuncture or NSAID treatment alone. Further research is needed to validate the effects of acupuncture with NSAIDs.

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