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.
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