901. Health Services and Quality Improvement - Non-Malignant Conditions: Poster III

High Rate of Attendance at a Young Adult Clinic Embedded in an Adult Sickle Cell Center: If You Build It, They Will Come

Setting Cost-Effective Price Thresholds before FDA Approval: Cost-Effectiveness of Iptacopan Monotherapy Versus Standard-of-Care Anti-C5 Therapy in Tr

Abortions Outcomes of People with Sickle Cell Disease

A Novel Online Decision Support Tool to Determine Practice Patterns and Concordance with Experts in the Treatment of Patients with Immune Thrombocytop

“Advancing a More Inclusive Blood and Transplant System for Marginalized Groups”: Development and Evaluation of a Transfusion Medicine Health Equity a

Improving Treatment Adherence in Patients with Sickle Cell Disease

Underestimation of Venous Thromboembolism Risk: A Common Health Care Quality Deficit

Self-Sustainability with Therapeutic Phlebotomy, a Solution to the National Blood Crisis?

Assessing Pain Severity in Sickle Cell Disease Using Animations and a Graphical Body Image

Cost-Effectiveness of Emicizumab Vs Efanesoctocog Alfa, Standard Half Life (SHL) and Other Extended Half Life (EHL) FVIII Products for Prophylaxis in

Taking Shared Decision Making from Concept to Clinical Practice: What Do Sickle Cell Healthcare Providers Need?

Cost-Effectiveness of Caplacizumab in the Warranty Program in Immune Thrombotic Thrombocytopenic Purpura in the USA

Establishing Mental Wellness Screening As Standard of Care in Pediatric Sickle Cell Patients

Implementation of a Best Practice Alert and Dedicated Hematology Consultation on Hospitalization Outcomes of Patients with Sickle Cell Disease

Disease-Modifying Therapies for Sickle Cell Disease: Decisional Needs and Supports Among Adolescents and Young Adults

Implementation of a Multipronged Intervention to Improvement Inpatient Sickle Cell Disease Care

Standard Risk Assessment Tools Fall Short to Assess Risk in Transplant Patients

Improving Access to Comprehensive Care for Pediatric Sickle Cell Patients through the Creation of Multispecialty Clinics

Assessment of Haemophilia Patients’ and Other Bleeding Disorders Needs of Psychosocial Support and Health Care Needs and Their Utilization in Haemophi

Using a Quality Improvement Activity to Enhance the Knowledge, Competence and Confidence of Clinicians Managing Patients with Cold Agglutinin Disease

Exploring the Utility and Significance of an Adult Academic Non-Cancer Hematology Clinic

Impact of Cancer Diagnosis on Appropriate Use of Antithrombotic Medications in Individuals with Cardiovascular Diseases

Facilitators and Barriers to Accessing Antifibrinolytic and Iron Therapies for Patients Who Menstruate – a Global Healthcare Provider Survey