02Oct 2022
Recurrent Respiratory Papillomatosis: Quality of Life Data from an International Patient Registry

Recurrent Respiratory Papillomatosis: Quality of Life Data from an International Patient Registry

Quality-of-life studies in recurrent respiratory papillomatosis (RRP) have traditionally relied upon clinician‐designed survey instruments. This study aims to report quality of life outcomes from a patient‐designed questionnaire. Patients who provided health information and completed a quality-of-life questionnaire were identified from the RRPF‐CoRDS patient registry. Due to their RRP, 65.7% reported missing at least five work days each month. Social anxiety was reported in 79.5% of patients, though only 28.8% of the cohort reported utilizing mental health services. The median (range) lifetime number of surgeries received was 20 (1 ‐ 3). Most patients (57.5%) reported paying at least 5% of their annual income towards RRP‐related medical care. RRP presents a high mental and fiscal burden.

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