摘要：First-person accounts of COVID-19 illness and treatment can complement and enrich data derived from electronic medical or public health records . With patient-reported data, it is uniquely possible to ascertain in-depth contextual information as well as behavioral and emotional responses to illness . The Novel Coronavirus Illness Patient Report (NCIPR) dataset includes complete survey responses from 1,584 confrmed COVID-19 patients ages 18 to 98. NCIPR survey questions address symptoms, medical complications, home and hospital treatments, lasting efects, anxiety about illness, employment impacts, quarantine behaviors, vaccine-related behaviors and efects, and illness of other family/ household members . Additional questions address fnancial security, perceived discrimination, pandemic impacts (relationship, social, stress, sleep), health history, and coping strategies . Detailed patient reports of illness, environment, and psychosocial impact, proximal to timing of infection and considerate of demographic variation, is meaningful for understanding pandemic-related public health from the perspective of those that contracted the disease .
