Hemoglobinopathies

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Developing an Emergency Department Order Set to Treat Acute Pain in Sickle Cell Disease

Reporting in JACEP Open, a multidisciplinary panel of investigators describe how they developed an ED order set for management of acute pain from vaso-occlusive episodes in patients with SCD presenting to the ED in New York City.

JACEP Open

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Hereditary/Acquired Bleeding Disorders

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Hemoglobinopathies

BENIGN HEMATOLOGY BASICS

Benign Hematology Overview

Hereditary and Acquired Bleeding Disorders: Hemophilia

Hereditary and Acquired Bleeding Disorders: von Willebrand Disorders

Autoimmune Cytopenias

Bone Marrow Disorders

Hemoglobinopathies

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Resources

Hemoglobinopathies Neurocognitive Risk in Sickle Cell Disease: Utilizing Neuropsychology Services to Manage Cognitive Symptoms and Functional Limitations

Hemoglobinopathies GRNDaD: Big Data and Sickle Cell Disease

Hemoglobinopathies The Impact of VO and VOCs

Hemoglobinopathies An Overview of Sickle Cell Disease (SCD) and the Impact of Hemoglobin S (Hbs) Polymerization, Anemia, and Hemolysis

Hemoglobinopathies About Sickle Cell Disease

Videos

Hemoglobinopathies Understanding Sickle Cell Disease and the Transition Into Adult Care

Hemoglobinopathies Beta-Thalassemia in Adults

Hemoglobinopathies Collaborative Approaches to the Treatment of Beta-Thalassemia