Background
The common cold is a viral disease that typically resolves naturally but causes inconvenience in daily life, and acupuncture treatment has been actively studied for improving symptoms and shortening the duration of the illness.
Objectives
T...
Background
The common cold is a viral disease that typically resolves naturally but causes inconvenience in daily life, and acupuncture treatment has been actively studied for improving symptoms and shortening the duration of the illness.
Objectives
To systematically evaluate the efficacy and safety of acupuncture in the treatment of the common cold.
Methods
Randomized controlled trials (RCTs) on acupuncture treatment for the common cold were identified from nine databases without language restrictions (from inception to October 14, 2024). Two reviewers independently performed study selection, data extraction, and risk of bias assessment using the Cochrane Risk of Bias tool version 2 (RoB 2). Meta-analysis was conducted using RevMan 9.8.2, and the certainty of evidence was evaluated using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach.
Results
Seven randomized controlled trials involving 751 patients with the common cold were included. Meta-analysis showed that acupuncture significantly improved the total effective rate compared to conventional Western medication alone, with no observed heterogeneity (RR 1.07, 95% CI 1.02–1.12). Acupuncture also relieved fever score more than conventional treatment (SMD = -0.29, 95% CI -0.51 to -0.07), and shortened the time to reduce body temperature by 0.5℃ (SMD = -0.42, 95% CI -0.72 to -0.13). Furthermore, acupuncture significantly reduced the total symptom Score at 24 hours post-treatment (SMD = -0.69, 95% CI -0.91 to -0.47). Three studies explicitly reported adverse events, with no adverse reactions observed in the acupuncture groups. Overall, acupuncture demonstrated favorable efficacy and safety with moderate certainty of evidence.
Conclusion
Acupuncture may be effective in alleviating common cold symptoms and shortening fever duration with a favorable safety profile, suggesting it as a viable clinical option for the common cold. However, due to study heterogeneity and risk of bias, further high-quality multicenter clinical trials with standardized outcome measures and longer follow-up are needed.