Patient and family burden in pediatric atopic dermatitis and its treatment pattern in Japan

Int J Dermatol. 2024 Nov;63(11):e322-e334. doi: 10.1111/ijd.17256. Epub 2024 May 29.

Abstract

Background: This study evaluated the level of burden in pediatric and adolescent atopic dermatitis (AD) patients in Japan, the associated burden on caregivers/families, and whether this burden varied with age.

Methods: Data were drawn from the Adelphi Pediatric AD Disease Specific Programme (DSP)™, a cross-sectional survey of physicians and their patients conducted in Japan between July and December 2022. Physicians reported patient demographics, clinical characteristics, disease burden, and current/previous therapies. Patients and/or caregivers reported perceived disease severity and impact of AD, including the Children's Dermatology Life Quality Index (CDLQI) and Dermatitis Family Impact questionnaire (DFI).

Results: Overall, 55 physicians provided data for 537 AD patients aged ≤17. Mean (SD) overall scores for CDLQI, POEM, and DFI were 9.3 (6.3), 8.3 (6.8), and 11.7 (7.2), respectively. Age was associated with higher patient and/or caregiver-reported CDLQI scores, which increased by 0.543 points per year of age (P = 0.01). Patients with severe disease reported a more significant impact on quality of life factors compared with mild patients (P < 0.001). Age was associated with higher caregiver-reported burden, with DFI scores increasing by 0.325 per year (P = 0.01). Physician-reported impact on caregivers showed that age was significantly associated with increased burden on sleep, daily activities, work, and mood (P < 0.05), with disease severity associated with impact across all factors (P < 0.01).

Conclusions: Both increasing age and disease severity were associated with the increased impact of AD on patients and their caregivers. Disease control/modification through appropriate therapeutic intervention at a younger age may relieve the burden of pediatric AD on patients and their families.

Keywords: atopic dermatitis; caregivers; cross‐sectional study; dermatology; disease burden; pediatric; quality of life.

MeSH terms

  • Adolescent
  • Age Factors
  • Caregiver Burden / epidemiology
  • Caregiver Burden / psychology
  • Caregivers / psychology
  • Caregivers / statistics & numerical data
  • Child
  • Child, Preschool
  • Cost of Illness*
  • Cross-Sectional Studies
  • Dermatitis, Atopic* / psychology
  • Dermatitis, Atopic* / therapy
  • Female
  • Humans
  • Infant
  • Japan
  • Male
  • Quality of Life*
  • Severity of Illness Index*
  • Surveys and Questionnaires / statistics & numerical data

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