Skip to main content

Impact of atopic dermatitis lesion locations and extent on patient burden: A real-world study

Publication ,  Journal Article
Simpson, E; Lio, P; Pierce, E; Cronin, A; McLean, RR; Eckmann, T; Atwater, AR; Dawson, Z; Silverberg, JI
Published in: JEADV Clinical Practice
September 1, 2024

Background: Atopic dermatitis (AD) is associated with patient burden, but few studies describe the anatomic distribution of the disease or the impact of number of lesion locations. Objectives: To describe lesion locations and assess the relationship between the number of lesion locations (disease extent) and disease burden in patients with AD. Methods: This cross-sectional study included adults with dermatologist- or dermatology practitioner-diagnosed AD enroled in the CorEvitas AD Registry (2020–2021) who initiated systemic therapy within 12 months prior to or at enrolment or had moderate-to-severe AD (vIGA-AD® ≥3 and EASI ≥12) at enrolment. Thirteen areas of lesion involvement were assessed using a body map, and numbers of lesion locations were categorised as: 0, 1, 2–3, 4–6 and ≥7. Demographics, disease characteristics, PROs by number of lesion locations were descriptively compared using effect sizes (ES). The ES thresholds for small, medium, and large differences, respectively, were 0.10, 0.30, and 0.50 for phi (categorical outcomes) and 0.10, 0.25 and 0.40 for Cohen's f (continuous outcomes). Results: Among 1211 patients, lesion involvement was most frequent on the arms (69.5%) and lower limbs (61.7%). A total of 10.6%, 9.3%, 20.1%, 26.3% and 33.8% of patients had 0, 1, 2–3, 4–6 and ≥7 lesion locations, respectively. Current use of systemic (≥81.2%) and topical (≥74.7%) therapies was common, irrespective of lesion location. Disease severity increased with number of lesion locations: mean total BSA (ES = 1.17), EASI (ES = 1.11), and SCORAD (ES = 1.21). vIGA-AD ≥3 was observed in 28.3%, 45.3%, 78.0%, and 93.9% of patients with 1, 2–3, 4–6 and ≥7 locations, respectively (ES = 0.63). Greater number of lesion locations was associated with worse PROs: mean POEM (ES = 0.57), sleep loss (ES = 0.41), peak pruritus (ES = 0.50), DLQI (ES = 0.40), and ADCT (ES = 0.53). Uncontrolled AD (ADCT ≥7) was observed in 48.2%, 52.9%, 70.4%, 81.6% of patients with 1, 2–3, 4–6 and ≥7 locations, respectively (ES = 0.42). Conclusions: AD lesions were reported for each body area assessed. Greater number of lesion locations was associated with increased disease severity, poor disease control, and decreased quality of life. Patients experienced substantial disease burden regardless of number of lesion locations involved.

Duke Scholars

Published In

JEADV Clinical Practice

DOI

EISSN

2768-6566

Publication Date

September 1, 2024

Volume

3

Issue

4

Start / End Page

1061 / 1075
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Simpson, E., Lio, P., Pierce, E., Cronin, A., McLean, R. R., Eckmann, T., … Silverberg, J. I. (2024). Impact of atopic dermatitis lesion locations and extent on patient burden: A real-world study. JEADV Clinical Practice, 3(4), 1061–1075. https://doi.org/10.1002/jvc2.413
Simpson, E., P. Lio, E. Pierce, A. Cronin, R. R. McLean, T. Eckmann, A. R. Atwater, Z. Dawson, and J. I. Silverberg. “Impact of atopic dermatitis lesion locations and extent on patient burden: A real-world study.” JEADV Clinical Practice 3, no. 4 (September 1, 2024): 1061–75. https://doi.org/10.1002/jvc2.413.
Simpson E, Lio P, Pierce E, Cronin A, McLean RR, Eckmann T, et al. Impact of atopic dermatitis lesion locations and extent on patient burden: A real-world study. JEADV Clinical Practice. 2024 Sep 1;3(4):1061–75.
Simpson, E., et al. “Impact of atopic dermatitis lesion locations and extent on patient burden: A real-world study.” JEADV Clinical Practice, vol. 3, no. 4, Sept. 2024, pp. 1061–75. Scopus, doi:10.1002/jvc2.413.
Simpson E, Lio P, Pierce E, Cronin A, McLean RR, Eckmann T, Atwater AR, Dawson Z, Silverberg JI. Impact of atopic dermatitis lesion locations and extent on patient burden: A real-world study. JEADV Clinical Practice. 2024 Sep 1;3(4):1061–1075.

Published In

JEADV Clinical Practice

DOI

EISSN

2768-6566

Publication Date

September 1, 2024

Volume

3

Issue

4

Start / End Page

1061 / 1075