Research AppraisalSystematic Review

The effectiveness of dry needling at myofascial trigger points for knee disorders: A quantitative synthesis of randomized controlled trials

PloS oneHu, Xin, Lei, Ting, Liu, Zheng et al.DOI

Clinical Snapshot

85CEBM
Evidence: ModerateSystematic Review

PICO Framework

P — PopulationAdults with knee disorders (knee osteoarthritis and patellofemoral pain syndrome), mean age 22-69 years
I — InterventionDry needling targeting myofascial trigger points
C — ComparatorSham dry needling, no intervention, or other active treatments
O — OutcomesPain intensity (VAS, NPRS, WOMAC pain), functional status (WOMAC functional subscale, Kujala Patellofemoral Score)

Bottom Line

This well-conducted meta-analysis of 20 RCTs (n=1,234) demonstrates that dry needling targeting myofascial trigger points provides statistically significant short-term pain relief and functional improvement in knee osteoarthritis and patellofemoral pain syndrome. The overall pain reduction of 1.25 points approaches the minimal clinically important difference, with moderate certainty evidence. However, substantial heterogeneity between studies (I² = 74.7%), blinding limitations, and short follow-up periods necessitate cautious interpretation. While the intervention appears safe and effective for short-term symptom management, clinicians should consider it as part of a multimodal approach rather than standalone treatment. The evidence supports dry needling as a reasonable adjunctive therapy for patients with knee disorders who have not responded adequately to first-line treatments, particularly when delivered by appropriately trained practitioners. Long-term effectiveness and optimal treatment protocols require further investigation through high-quality RCTs with extended follow-up periods.

Evidence: Moderate

Key Findings

  • P Value: Statistically significant (p < 0.001 based on confidence intervals)

  • Effect Size: Small to moderate effect size approaching clinically important difference

  • Primary Outcome: Overall pooled pain reduction WMD = -1.25 (95% CI: -1.58 to -0.92)

  • Nnt Or Sensitivity: Pain reduction approaching minimal clinically important difference of 1.5 points on 0-10 scale

  • Confidence Interval: 95% CI: -1.58 to -0.92 for overall pain reduction

Clinical Application

Requires trained practitioners in dry needling technique, readily available in physiotherapy and sports medicine settings Dry needling practiced by physiotherapists under AHPRA registration, not currently PBS subsidized, aligns with RACGP recommendations for non-pharmacological knee OA management Adults with knee osteoarthritis and patellofemoral pain syndrome seeking non-pharmacological pain management

Abstract

PURPOSE: Dry needling (DN) targeting myofascial trigger points (MTrPs) has been proposed as a treatment for knee disorders, including knee osteoarthritis (KOA) and patellofemoral pain syndrome (PFPS). This meta-analysis evaluated the effectiveness of DN in improving pain and function in patients with knee disorders. METHODS: This meta-analysis was conducted in accordance with PRISMA 2020 guidelines and was prospectively registered in PROSPERO (CRD420261294603). Systematic searches were performed in PubMed, Embase, Web of Science, Cochrane CENTRAL, CNKI, Wanfang, and VIP databases from inception to December 2025 for randomized controlled trials (RCTs) comparing DN targeting MTrPs with sham DN, no intervention, or other active treatments for knee disorders. Primary outcomes were pain intensity measured by the Visual Analog Scale (VAS) and Numeric Pain Rating Scale (NPRS). Secondary outcomes included functional status assessed by the WOMAC functional subscale and the Kujala Patellofemoral Score. Weighted mean differences (WMDs) were calculated using random-effects models. Risk of bias was assessed using the Cochrane Risk of Bias 2 (RoB 2) tool, and certainty of evidence was evaluated using the GRADE framework. RESULTS: Twenty RCTs (n = 1,234; mean age range: 22-69 years) met the inclusion criteria. Compared with controls, DN significantly reduced knee pain across all pain measures: NPRS (WMD = -1.00, 95% CI: -1.25 to -0.76; I² = 0.0%), VAS (WMD = -1.19, 95% CI: -1.73 to -0.66; I² = 80.4%), and WOMAC Pain subscale (WMD = -1.76, 95% CI: -2.57 to -0.95; I² = 67.6%), with an overall pooled pain reduction of WMD = -1.25 (95% CI: -1.58 to -0.92; I² = 74.7%). DN also significantly improved knee function as measured by the WOMAC functional subscale (WMD = -6.59, 95% CI: -8.88 to -4.29; I² = 61.6%) and the Kujala Patellofemoral Score (WMD = 6.39, 95% CI: 4.64 to 8.14; I² = 30.1%). Pre-specified sensitivity analyses using standardized mean differences confirmed the robustness of these findings. The overall risk of bias was moderate, with concerns primarily related to inadequate blinding of participants and outcome assessors. The GRADE certainty of evidence was rated as moderate for all primary outcomes. CONCLUSION: DN targeting MTrPs provides significant short-term pain relief and functional improvement in KOA and PFPS, with pain reductions approaching clinically important thresholds. However, substantial heterogeneity, blinding limitations, and short follow-up necessitate cautious interpretation, and high-quality long-term RCTs are needed.

References

  1. 1.Hu, X., Lei, T., Liu, Z., Xu, Z., & Zhu, G. (2026). The effectiveness of dry needling at myofascial trigger points for knee disorders: A quantitative synthesis of randomized controlled trials. PLoS One. https://doi.org/10.1371/journal.pone.0346129
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