Abstract
Psoriasis can have significant impact on several aspects of patients’ lives. It causes tremendous quality of life consequences in addition to treatments causing significant financial burden. Dermatologists often focus on achieving minimal disease activity based on their assessment. Dermatologists must understand the disease’s enormous impact on daily routines and quality of life to grasp the unique value of capturing patient-reported outcomes. We conducted five mixed focus groups and ten semistructured interviews with psoriasis patients (n = 25) and their family members (n = 11) seeking to understand their daily struggles with this chronic skin condition.
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