Objective:
To evaluate the effectiveness of oral antihistamines in treating atopic dermatitis severity and itch in pediatric and adult patients.
Approach:
- Study Design: Systematic review and network meta-analysis of 47 randomized trials involving 6,230 patients.
- Data Sources: Data was collected from Medline, Embase, CENTRAL, and regulatory databases from inception through May 5, 2025.
- Analysis Method: Bayesian random-effects network meta-analyses were conducted, assessing treatment effects and certainty using the Grading of Recommendations Assessment, Development, and Evaluation approach.
Key Findings:
- Second-generation H1 antihistamines reduced Scoring Atopic Dermatitis scores by approximately 2 points compared to placebo, which is below the minimal important difference.
- First-generation H1 antihistamines did not produce a clinically important difference in disease severity or itch.
- Increasing antihistamine doses may not improve itch, with very uncertain evidence.
- First-generation H1 antihistamines likely increased cognitive impairment, with an estimated 66 additional events of cognitive impairment per 1,000 patients.
- No significant difference in serious adverse events between antihistamines and placebo.
Interpretation:
The review found moderate and high certainty evidence of harms and no clinically important benefit of oral antihistamines added to placebo with or without background topical treatments.
Limitations:
- Trial populations differed in baseline disease severity.
- Subgroup analyses may have been limited by small sample sizes.
- Some crossover trials reported outcomes across the entire trial rather than by crossover period.
Conclusion:
The findings indicate the need for updated clinical practice guidelines regarding the use of oral antihistamines in atopic dermatitis treatment.
Sources:
This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.
