904. Outcomes Research: Hemoglobinopathies: Poster I

Caregiver and Provider Reports of Symptom Severity, Functionality, and Quality of Life Lack Congruence with Patient Reports in Pediatric Sickle Cell Disease

Delayed Physical Growth and Related Factors in Pediatric Patients with Transfusion-Dependent Thalassemia

High Concordance between Investigator-Verified Diagnosis and Manual Data Abstraction for Sickle Cell Diagnosis Type: An ASH Research Collaborative Data Hub Validation Study

Intersection of Pain-Related Healthcare Utilization with Neighborhood Factorsin Adults Living with Sickle Cell Disease

Opioid Overdose in Patients with Sickle Cell Disease, Outcomes Among Hospitalized Patients in the United States: A Nationwide Analysis

Pain-Specific Patient-Reported Outcomes Are Worse in Adults Compared to Children with Sickle Cell Disease

Pre-Transplant Liver Fibrosis Predicts Poor Overall Survival Following Hematopoietic Stem Cell Transplantation for Sickle Cell Disease

Prevalence of Pulmonary Hypertension in Patients Hospitalized with Sickle Cell Crisis

Thalassemia Scenario in Brazil: A Descriptive Study

Voxelotor Therapy Reduces Whole Blood Adhesion to VCAM-1 and P-Selectin, and Shows Modest Improvements in Self-Reported Pain in a Real-World Clinical Setting in a Multi-Center Retrospective Analysis