Superiority of propolis and honey over topical acyclovir for herpes simplex: A meta-analysis.
- 2026-01-06
- International journal of STD & AIDS 37(5)
- Nurdjannah Jane Niode
- Paulus Mario Christopher
- Trina Ekawati Tallei
- PubMed: 41496519
- DOI: 10.1177/09564624251413431
Study Design
- Type
- Meta-Analysis
- Methods
- Systematic search of PubMed, Scopus, Europe PMC, and the Cochrane Library to identify studies comparing topical propolis and/or honey with 5% acyclovir for herpes simplex lesions. Clinical outcomes were synthesized using random-effects models.
Research Insights
more patients reporting being symptom-free by day 3
- Effect
- Beneficial
- Effect size
- Moderate
higher healing rates by day 7 (OR: 4.71; 95% CI: 2.70-8.25; p < 0.00001)
- Effect
- Beneficial
- Effect size
- Large
No significant difference was observed in the number of aborted attacks (p = 0.66)
- Effect
- Neutral
- Effect size
- Small
Treatment with propolis and/or honey was associated with quicker lesion resolution (MD: -1.87 days; 95% CI: -2.73 to -1.01; p < 0.0001)
- Effect
- Beneficial
- Effect size
- Moderate
Propolis and/or honey also reported reduced pain duration (MD: -0.96 days; p = 0.03)
- Effect
- Beneficial
- Effect size
- Small
pain intensity (MD: -6.53; p = 0.0002)
- Effect
- Beneficial
- Effect size
- Moderate
more patients reporting being symptom-free by day 3
- Effect
- Beneficial
- Effect size
- Moderate
higher healing rates by day 7 (OR: 4.71; 95% CI: 2.70-8.25; p < 0.00001)
- Effect
- Beneficial
- Effect size
- Large
No significant difference was observed in the number of aborted attacks (p = 0.66)
- Effect
- Neutral
- Effect size
- Small
Treatment with propolis and/or honey was associated with quicker lesion resolution (MD: -1.87 days; 95% CI: -2.73 to -1.01; p < 0.0001)
- Effect
- Beneficial
- Effect size
- Moderate
Propolis and/or honey also reported reduced pain duration (MD: -0.96 days; p = 0.03)
- Effect
- Beneficial
- Effect size
- Small
pain intensity (MD: -6.53; p = 0.0002)
- Effect
- Beneficial
- Effect size
- Moderate
Adverse Events Reported
No significant difference was observed in adverse events (AEs) rates between the natural therapy and acyclovir groups.
- Finding
- No significant difference
No significant difference was observed in adverse events (AEs) rates between the natural therapy and acyclovir groups.
- Finding
- No significant difference