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Treatment Patterns in Pediatric Hidradenitis Suppurativa: Time to Treatment Initiation, Initial Treatment, and Time
Shaliz Aflatooni1, Andrea Ure2, Kimberly Smart3
1USF Morsani College of Medicine, Tampa, Florida, USA.
Insights
Pediatric hidradenitis suppurativa (HS) treatment shows delayed escalation and antibiotic-heavy initial therapy. Treatment initiation varies by demographics, with non-White children starting sooner than White children.
Area of Science:
- Dermatology
- Pediatric Health
- Real-world Evidence
Background:
- Hidradenitis suppurativa (HS) significantly impacts children's quality of life.
- Current understanding of pediatric HS treatment patterns across diverse demographics is limited.
Purpose of the Study:
- To analyze treatment initiation time, initial therapies, and treatment switching in pediatric HS.
- To investigate demographic variations (sex, race, ethnicity) in pediatric HS treatment patterns.
Main Methods:
- Retrospective cohort study using a large U.S. electronic health record database (2005-2025).
- Included patients under 18 years with an HS diagnosis.
- Categorized treatments within one year of diagnosis: systemic antibiotics, topicals, hormonal therapies, retinoids, biologics, procedures.
Main Results:
- The cohort comprised 6659 children (mean age 12.8 years, 74.9% female).
- Average time to treatment initiation was 15 days; common initial therapy was systemic antibiotics plus topicals.
- Girls received more treatments (including biologics) than boys; non-White children initiated treatment faster than White children (1 vs. 17 days).
- Most children stayed on initial therapy for approximately one year before switching.
Conclusions:
- Pediatric HS management is marked by delayed treatment escalation.
- Initial HS therapy is predominantly antibiotic-based.
- Significant demographic variations exist in pediatric HS treatment initiation timing.
Background:
Hidradenitis suppurativa (HS) causes significant morbidity in children. Treatment patterns across sex, race, and ethnicity in pediatric HS have not been thoroughly evaluated. We aim to characterize treatment patterns in pediatric HS, including (1) time to treatment initiation, (2) first prescribed HS treatment, and (3) time to switching following initial therapy across demographic factors.
Methods:
We conducted a real-world, retrospective cohort study of patients < 18 years with a HS diagnosis, using a large U.S. national electronic health record database (2005-2025). Treatments prescribed within 1 year after HS diagnosis were categorized as systemic antibiotics, topicals, hormonal therapies, retinoids, biologics, or procedures.
Results:
The cohort included 6659 children with HS (mean age 12.8 ± 2.8 years at diagnosis), 74.9% female, 37.7% White, and 56.5% non-Hispanic/Latino. Overall, 3.2% of children received biologics. Following HS diagnosis, the mean time to treatment initiation was 15 days. The most common initial treatment was systemic antibiotics plus topical therapies. The mean time on the initial treatment regimen prior to switching was 386 days. Multivariable analyses demonstrated that girls were more likely than boys to receive any treatments, including biologics, except major procedures. Non-White children initiated treatment sooner than White children (1 vs. 17 days, p < 0.0001). Regardless of demographic subgroup, most children remained on their initial HS treatment for a mean duration of approximately a year before switching therapies.
Conclusion:
Pediatric HS care is characterized by delayed treatment escalation, antibiotic-dominant initial therapy, and variation in treatment initiation timing across demographic groups.
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