Stigmatization and Mental Health Impact of Chronic Pediatric Skin Disorders

JAMA Dermatology
Open Access

Clinical Summary

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What was studied

Cross-sectional, single-visit study at 32 pediatric dermatology centers in the US and Canada (2018–2021) of 1671 children aged 8–17 with chronic skin disease and a parent. Stigma (PROMIS Stigma‑Skin) was examined by physician/child/proxy-rated visibility and severity, and its associations with quality of life (Skindex‑Teen), depression, anxiety, and peer relationships.

Key findings

Only 27.0% had minimal/no stigma (T<40) and 43.8% had at least moderate stigma (T≥45); stigma differed by visibility and severity and correlated with lower QOL (ρ=0.73), higher depression (ρ=0.61), higher anxiety (ρ=0.54), and poorer peer relations (ρ=−0.49). Bullying was reported by 29.4% of parents and was linked to higher stigma (Cohen d≈0.79), girls reported more stigma than boys (d=0.26), and stigma strongly predicted worse Skindex‑Teen total (estimate 1.05; 95% CI, 0.96–1.13).

Study limitations

Cross-sectional, single-visit design limits causal inference. Conducted in specialty pediatric dermatology centers with small samples for some diagnoses (e.g., hyperhidrosis n=18; hidradenitis suppurativa n=22), which may affect generalizability and subgroup estimates.

Clinical implications

Do not rely solely on physician-rated severity or visibility to gauge impact. Routinely identify stigmatization and bullying and track change with validated tools to guide medical and psychosocial care.