The effectiveness of cupping therapy on low back pain: A systematic review and meta-analysis of randomized control trials

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-01-05 DOI:10.1016/j.ctim.2024.103013
Zixin Zhang , Mahesh Pasapula , Zelu Wang , Kimberley Edwards , Alan Norrish
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The methodological quality of the included studies was evaluated independently by two reviewers using an adapted tool. Change-from-baseline outcomes were treated as continuous variables and calculated according to the Cochrane Handbook. Data were extracted and pooled into the meta-analysis by Review Manager software (version 5.4, Nordic Cochrane Centre).</p></div><div><h3>Results</h3><p>Eleven trials involving 921 participants were included. Five studies were assessed as being at low risk of bias, and six studies were of acceptable quality. High-quality evidence demonstrated cupping significantly improves pain at 2–8 weeks endpoint intervention (d=1.09, 95% CI: [0.35–1.83], p = 0.004). There was no continuous pain improvement observed at one month (d=0.11, 95% CI: [−1.02–1.23], p = 0.85) and 3–6 months (d=0.39, 95% CI: [−0.09–0.87], p = 0.11). Dry cupping did not improve pain (d=1.06, 95% CI: [−0.34, 2.45], p = 0.14) compared with wet cupping (d=1.5, 95% CI: [0.39–2.6], p = 0.008) at the endpoint intervention. There was no evidence indicating the association between pain reduction and different types of cupping (p = 0.2). Moderate- to low-quality evidence showed that cupping did not reduce chronic low back pain (d=0.74, 95% CI: [−0.67–2.15], p = 0.30) and non-specific chronic low back pain (d=0.27, 95% CI: [−1.69–2.24], p = 0.78) at the endpoint intervention. Cupping on acupoints showed a significant improvement in pain (d=1.29, 95% CI: [0.63–1.94], p &lt; 0.01) compared with the lower back area (d=0.35, 95% CI: [−0.29–0.99], p = 0.29). A potential association between pain reduction and different cupping locations (p = 0.05) was found. Meta-analysis showed a significant effect on pain improvement compared to medication therapy (n = 8; d=1.8 [95% CI: 1.22 – 2.39], p &lt; 0.001) and usual care (n = 5; d=1.07 [95% CI: 0.21- 1.93], p = 0.01). Two studies demonstrated that cupping significantly mediated sensory and emotional pain immediately, after 24 h, and 2 weeks post-intervention (d= 5.49, 95% CI [4.13–6.84], p &lt; 0.001). Moderate evidence suggested that cupping improved disability at the 1–6 months follow-up (d=0.67, 95% CI: [0.06–1.28], p = 0.03). There was no immediate effect observed at the 2–8 weeks endpoint (d=0.40, 95% CI: [−0.51–1.30], p = 0.39). A high degree of heterogeneity was noted in the subgroup analysis (I<sup>2</sup> &gt;50%).</p></div><div><h3>Conclusion</h3><p>High- to moderate-quality evidence indicates that cupping significantly improves pain and disability. The effectiveness of cupping for LBP varies based on treatment durations, cupping types, treatment locations, and LBP classifications. 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Abstract

Objectives

This study aims to investigate the effectiveness of cupping therapy on low back pain (LBP).

Methods

Medline, Embase, Scopus and WANFANG databases were searched for relevant cupping RCTs on low back pain articles up to 2023. A complementary search was manually made on 27 September for update screening. Full-text English and Chinese articles on all ethnic adults with LBP of cupping management were included in this study. Studies looking at acute low back pain only were excluded. Two independent reviewers screened and extracted data, with any disagreement resolved through consensus by a third reviewer. The methodological quality of the included studies was evaluated independently by two reviewers using an adapted tool. Change-from-baseline outcomes were treated as continuous variables and calculated according to the Cochrane Handbook. Data were extracted and pooled into the meta-analysis by Review Manager software (version 5.4, Nordic Cochrane Centre).

Results

Eleven trials involving 921 participants were included. Five studies were assessed as being at low risk of bias, and six studies were of acceptable quality. High-quality evidence demonstrated cupping significantly improves pain at 2–8 weeks endpoint intervention (d=1.09, 95% CI: [0.35–1.83], p = 0.004). There was no continuous pain improvement observed at one month (d=0.11, 95% CI: [−1.02–1.23], p = 0.85) and 3–6 months (d=0.39, 95% CI: [−0.09–0.87], p = 0.11). Dry cupping did not improve pain (d=1.06, 95% CI: [−0.34, 2.45], p = 0.14) compared with wet cupping (d=1.5, 95% CI: [0.39–2.6], p = 0.008) at the endpoint intervention. There was no evidence indicating the association between pain reduction and different types of cupping (p = 0.2). Moderate- to low-quality evidence showed that cupping did not reduce chronic low back pain (d=0.74, 95% CI: [−0.67–2.15], p = 0.30) and non-specific chronic low back pain (d=0.27, 95% CI: [−1.69–2.24], p = 0.78) at the endpoint intervention. Cupping on acupoints showed a significant improvement in pain (d=1.29, 95% CI: [0.63–1.94], p < 0.01) compared with the lower back area (d=0.35, 95% CI: [−0.29–0.99], p = 0.29). A potential association between pain reduction and different cupping locations (p = 0.05) was found. Meta-analysis showed a significant effect on pain improvement compared to medication therapy (n = 8; d=1.8 [95% CI: 1.22 – 2.39], p < 0.001) and usual care (n = 5; d=1.07 [95% CI: 0.21- 1.93], p = 0.01). Two studies demonstrated that cupping significantly mediated sensory and emotional pain immediately, after 24 h, and 2 weeks post-intervention (d= 5.49, 95% CI [4.13–6.84], p < 0.001). Moderate evidence suggested that cupping improved disability at the 1–6 months follow-up (d=0.67, 95% CI: [0.06–1.28], p = 0.03). There was no immediate effect observed at the 2–8 weeks endpoint (d=0.40, 95% CI: [−0.51–1.30], p = 0.39). A high degree of heterogeneity was noted in the subgroup analysis (I2 >50%).

Conclusion

High- to moderate-quality evidence indicates that cupping significantly improves pain and disability. The effectiveness of cupping for LBP varies based on treatment durations, cupping types, treatment locations, and LBP classifications. Cupping demonstrated a superior and sustained effect on pain reduction compared with medication and usual care. The notable heterogeneity among studies raises concerns about the certainty of these findings. Further research should be designed with a standardized cupping manipulation that specifies treatment sessions, frequency, cupping types, and treatment locations. The actual therapeutic effects of cupping could be confirmed by using objective pain assessments. Studies with at least six- to twelve-month follow-ups are needed to investigate the long-term efficacy of cupping in managing LBP.

Trial registration

This systematic review was initially registered on PROSPERO with registration code: CRD42021271245 on 08 September 2021.

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拔罐疗法对腰背痛的疗效:随机对照试验的系统回顾和荟萃分析
方法检索Medline、Embase、Scopus和WANFANG数据库中截至2023年关于腰背痛拔罐疗法的相关RCT文章。9 月 27 日进行了人工补充检索,以进行更新筛选。本研究纳入了关于所有族裔成人腰背痛拔罐治疗的英文和中文全文文章。仅针对急性腰背痛的研究被排除在外。两名独立审稿人负责筛选和提取数据,如有任何分歧,由第三名审稿人达成共识后解决。纳入研究的方法学质量由两名审稿人使用改编工具进行独立评估。与基线相比的变化结果被视为连续变量,并根据 Cochrane 手册进行计算。数据由Review Manager软件(5.4版,北欧Cochrane中心)提取并汇总到荟萃分析中。其中五项研究的偏倚风险较低,六项研究的质量可接受。高质量的证据表明,拔罐能显著改善2-8周终点干预时的疼痛(d=1.09,95% CI:[0.35-1.83],p=0.004)。在一个月(d=0.11,95% CI:[-1.02-1.23],p=0.85)和 3-6 个月(d=0.39,95% CI:[-0.09-0.87],p=0.11)时,没有观察到持续的疼痛改善。在终点干预时,干拔罐与湿拔罐(d=1.5,95% CI:[0.39-2.6],p=0.008)相比,没有改善疼痛(d=1.06,95% CI:[-0.34,2.45],p=0.14)。没有证据表明疼痛减轻与不同类型的拔罐有关联(P=0.2)。中低质量的证据显示,在终点干预时,拔罐并未减轻慢性腰背痛(d=0.74,95% CI:[-0.67-2.15],p=0.30)和非特异性慢性腰背痛(d=0.27,95% CI:[-1.69-2.24],p=0.78)。与下背部区域(d=0.35,95% CI:[-0.29-0.99],p=0.29)相比,穴位拔罐对疼痛有显著改善(d=1.29,95% CI:[0.63-1.94],p<0.01)。研究发现,疼痛减轻与不同拔罐位置之间存在潜在联系(P=0.05)。元分析表明,与药物治疗(n=8;d=1.8 [95% CI:1.22 - 2.39],p<0.001)和常规护理(n=5;d=1.07 [95% CI:0.21 - 1.93],p=0.01)相比,拔罐对疼痛的改善有显著效果。两项研究表明,拔罐能显著缓解干预后即刻、24 小时后和 2 周内的感觉和情绪疼痛(d= 5.49,95% CI [4.13-6.84],p<0.001)。中等程度的证据表明,拔罐可在 1-6 个月的随访中改善残疾状况(d=0.67,95% CI:[0.06-1.28],p=0.03)。在2-8周的终点没有观察到立竿见影的效果(d=0.40,95% CI:[-0.51-1.30],p=0.39)。亚组分析中发现了高度异质性(I2 >50%)。结论中高质量的证据表明,拔罐能显著改善疼痛和残疾状况。拔罐治疗腰椎间盘突出症的效果因治疗时间、拔罐类型、治疗部位和腰椎间盘突出症分类而异。与药物治疗和常规护理相比,拔罐在减轻疼痛方面表现出更优越、更持久的效果。不同研究之间存在明显的异质性,令人担忧这些研究结果的确定性。进一步的研究应设计标准化的拔罐操作,规定治疗疗程、频率、拔罐类型和治疗部位。拔罐的真正治疗效果可以通过假设备或客观结果测量来证实。需要进行至少六到十二个月的随访研究,以调查拔罐治疗腰椎间盘突出症的长期疗效:本系统性综述于 2021 年 9 月 8 日在 PROSPERO 上注册,注册代码为 CRD42021271245。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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