Comparison of Clinical Outcomes Between Adult and Pediatric Patients (pts) with Sickle Cell Disease (SCD): 3-Year (y) Follow-up in a Prospective, Longitudinal, Noninterventional Registry Trial

Introduction: Although advances in care have allowed individuals with SCD to live further into adulthood, treatment of adult SCD pts is challenging due to increased rates of comorbidities and complications. Here we present clinical outcomes and treatment patterns from a prospective registry of pediatric and adult pts with SCD at 3 y to better characterize disease and treatment patterns in adult pts.