Comparison of the Simple Patient-Centric Atopic Dermatitis Scoring System PEST with SCORAD in Young Children Using a

Mark Jean-Ann Koh1, Yoke Chin Giam2, Hui Min Liew1

  • 1KK Women's and Children's Hospital, Bukit Timah, Singapore, Singapore.

Insights

The Patient Eczema Severity Time (PEST) score shows a moderate correlation with the SCORAD scale in children with atopic dermatitis. PEST may be more sensitive in detecting changes in eczema severity over time.

Area of Science:

  • Dermatology
  • Clinical Trials
  • Patient-Reported Outcomes

Background:

  • Atopic dermatitis (AD) management often relies on clinician-assessed scales like SCORAD.
  • Patient Eczema Severity Time (PEST) is a novel patient-reported outcome measure for AD.
  • PEST aims to capture daily eczema experience, enhancing patient engagement and treatment adherence.

Purpose of the Study:

  • To evaluate the correlation between carer-assessed PEST and clinician-assessed SCORAD in pediatric AD patients.
  • To assess the efficacy and safety of a ceramide-dominant moisturizer over 12 weeks.
  • To determine the responsiveness of PEST compared to SCORAD in measuring AD severity changes.

Main Methods:

  • A prospective, open-label, multi-center study involving 58 children (6 months to 6 years) with mild-to-moderate AD.
  • Patients used a ceramide-dominant therapeutic moisturizer twice daily for 12 weeks.
  • Correlation between 7-day averaged PEST and SCORAD scores was analyzed using a general linear model.

Main Results:

  • A moderate correlation (r=0.51) was observed between PEST and SCORAD scores at 12 weeks.
  • Both SCORAD and PEST scores showed significant improvement from baseline (p<0.0001).
  • PEST demonstrated higher responsiveness to change (33.3% of scale) compared to SCORAD (13.8% of scale).

Conclusions:

  • PEST scores correlate well with SCORAD scores in pediatric AD.
  • PEST may offer improved sensitivity for detecting AD severity fluctuations.
  • The ceramide-dominant moisturizer proved safe and effective for managing pediatric AD.
Abstract