Abstract
The National Psoriasis Foundation conducts a cross-sectional study of the psoriatic patient community using an online survey conducted annually. Using survey data from 2019 – 2021, this study sought to understanding of health disparities among patients with psoriasis. Survey participants provided demographic information and provider diagnosis of psoriasis (PsO), psoriatic arthritis (PsA) or both. Severity was assessed using the Patient Reported Extent of Psoriasis Involvement (PREPI) for patients with PsO and established cut points for the Psoriatic Arthritis Impact of Disease (PsAID-9) for those with PsA.
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