PPT-Sickle Cell Disease: Core Concepts for

the Emergency Physician and Nurse Sickle Cell Pain Carlton Haywood Jr PhD MA Core Faculty the Johns Hopkins Berman Institute of Bioethics Assistant Professor The Johns Hopkins School of Medicine. EXAMINING PREVALENCE OF TOBACCO,. ALCOHOL, ILLICIT DRUG USE IN. ADULTS WITH SICKLE CELL ANEMIA. Catherine A. Seamon, Darlene T. Allen, . James G. Taylor VI, Jonathan Wilson, Gregory J. Kato . Disclosures. &. Intercollegiate Athletics. Sickle Cell Trait. (Hereditary Condition) . Red blood cells (RBC’s) are normally round, circular or disc shaped.. RBC’s have hemoglobin component (helps carry oxygen) and platelets (helps in clotting). Jenny Pham. Protein Structure & Function. Spring 2015. Outline. Normal Adult Hemoglobin (. Hb. A). Function: Deoxygenated v. Oxygenated. Mutation in . Hb. A. Sickle Cell Hemoglobin (. Hb. S). Sickle Cell Anemia. By Jessica Sambo. Drepanocytes . Most common of sickle cell diseases. Autosomal recessive genetic disorder. Hemoglobin S. First in Africa. Discovered in US in 1910. “cells in the shape of sickles”. was developed to create a greater awareness in . the Nashville . community of Sickle Cell Disease and to raise . funds for . patient care, . social services. , and research. . All . proceeds from the event . Gary Strokosch, MD. Jane Litvin, MS. Introduction. History of . sickle cell disease . (SCD). Present in Africa for at least . 5,000. . years. 1910-. . Discovered in US. Walter Clement Noel – dental student from Grenada studying in Chicago. . Presenter: Bridget H. Wilson, Ph.D., MS, RN. Introduction. Sickle cell disease (SCD) pain continues to emerge among adolescents. Over 98,000 individuals are believed to have SCD within the United States. . ANEMIA . SUBJECTS. Kehinde. . M.O. 1. ., . Ogungbemi. S.I. 2. .,. . Anigbogu. C.N. 2. .,. . and . Jaja. . S.I. 2. . . 1. Department . of . Medicine, . 2. Department . of . Physiology, . College . Dr. M. . Sofi. MD; FRCP (London); . FRCPEdin. ; . FRCSEdin. The term . sickle cell disease . (SCD) is generally used to describe all of the conditions associated with the phenomenon of . sickling. , whereas the term . Abeer. . Anwer. Ahmed. Sickle cell disease is a group of . haemoglobin. disorders . resulting from . the inheritance of the sickle β‐. globin. gene. . Sickle cell disease (SCD) is . an. . autosomal. Bimpe Adesina, Assistant Professor, University of WashingtoN, Seattle. Emily Johnston, Assistant Professor, University of Alabama at Birmingham. End-of-Life Healthcare Utilization in Sickle Cell Disease and the. Disease Education 5/17 Care of patients with sickle cell disease for primary care providers and emergency room personnel Table of Contents Chapter 1: Background About Sickle Cell Disease and Making t Dr Doreen Karimi . Mutua. Pediatric Hematologist/Oncologist. Gertrude’s Children’s Hospital. Outline. History. Status of Sickle Cell Disease Care . Rationale of Comprehensive Care in Sickle Cell Disease. October 11, 2023. Jennifer Colozza, PharmD. Clinical Pharmacist. MO HealthNet Division. During . at least one regularly scheduled meeting each calendar year, the advisory council on rare diseases and personalized .