More Efficient Exchange of Sickle Red Blood Cells can be Achieved by Exchanging the Densest Red Blood Cells

Similar documents
Snapshot. Make sure you have your Blood and its cells packet - you will need notes on blood cells to play a game

34 th Annual Meeting of ASFA, May 22-25, 2013, Denver, CO

A PRIMER ON APHERESIS MEDICINE

FILE / SICKLE CELL ANEMIA AND MALARIA EBOOK

What are the four parts of blood and what are their main functions?

Emergency Medical Training Services Emergency Medical Technician Paramedic Program Outlines Outline Topic: HEMATOLOGY Revised: 11/2013

RENAL & HEMATOLOGY EMERGENCIES JEFF SIMONS B.S. F-PC

Circulation and Blood

Hydroxyurea Treatment for Sickle Cell Disease

Complete Blood Count (CBC) Assist.Prof. Filiz BAKAR ATEŞ

Step 2. Common Blood Tests, and the Coulter Counter Readout

Anemia s. Troy Lund MSMS PhD MD

Ding Wen Wu, Rachel Friedmann, Joan Uehlinger, Sadiqa Karim, Etan Marks, Angie Bonzon-Adelson, Kala Mohandas, Evan Himchak, Ronald Walsh.

Changes to CBC Reference Ranges

Collect and label sample according to standard protocols. Gently invert tube 8-10 times immediately after draw. DO NOT SHAKE. Do not centrifuge.

CASE STUDIES IN CLINICAL APPLICATIONS OF THERAPEUTIC PLASMA EXCHANGE

Hydroxyurea Treatment for Sickle Cell Disease

2/2/2011. Blood Components and Transfusions. Why Blood Transfusion?

Hydroxyurea and Transfusion Therapy for the Treatment of Sickle Cell Disease

Sickle Cell Disease and impact on the society

Lifeblood Lab Activity

Instructor s Manual Chapter 26 Hematological Alterations. 1. A man and woman both test positive for the sickle cell trait. The couple asks the

Below are the sections of the DNA sequences of a normal hemoglobin gene and the mutated gene that causes sickle cell disease.

M. Velizarova, T. Yacheva and K. Tzatchev Department of Clinical Laboratory and Clinical Immunology, MU Sofia

AN OVERVIEW OF CELLULAR THERAPY

Preferred Clinical Services for Leading Age Florida August 26-27, 2015

6.1 Extended family screening

HEMOLYTIC ANEMIA DUE TO ABNORMAL HEMOGLOBIN SYNTHESIS

SICKLE CELL DISEASE. Dr. MUBARAK ABDELRAHMAN MD PEDIATRICS AND CHILD HEALTH. Assistant Professor FACULTY OF MEDICINE -JAZAN

DIC. Disseminated intravascular coagulation, is a life threatening pathological process in which clotting factors are abnormally activated.

Sickle Cell Disease 101. Objectives. What is SCD? 4/20/2016. Discuss the pathophysiology & genetics of Sickle Cell Disease (SCD).

American University of Beirut Faculty of Health Sciences Medical Laboratory Sciences Program

American University of Beirut Faculty of Health Sciences Medical Laboratory Sciences Program

Hematological profile among Sudanese patients with sickle cell anemia

EDUCATIONAL COMMENTARY MORPHOLOGIC CHANGES IN PERIPHERAL BLOOD CELLS

Other labs 4/24/2012. N 24: Pediatric Hematological Alterations & Cancer Intro. Cabrillo College ADN Program C. Madsen RN, MSN 1.

Name: Per: Date: Unit 9a: Blood (Composition/Types/Inheritance)

Genetics of Thalassemia

A closer look at BLOOD Lab

Understanding Blood Tests

ASFA 2015 Consensus Conference: RBC Exchange in Sickle Cell Disease

The % of blood consisting of packed RBCs is known as the hematocrit. Blood s color ranges from scarlet (oxygen-rich) to dark red (oxygen poor).

APHERESIS PROCEDURES. Worldwide implemented nowadays. Most of Asian Countries also involved. The usage of this procedure varies between countries.

Blood Components & Indications for Transfusion. Neda Kalhor

Hematocrit. Hematocrit = using a centrifuge to separate out the parts of blood. Plasma Formed elements:

Natural Selection In Humans (Sickle Cell Anemia)

Case Study 1: Red Cell Exchange

Congenital Haemoglobinopathies

Erythrocyte sedimentation rate. Hemolysis. Blood groups. Erythrocyte sedimentation rate (ESR)

Complete Blood Count (CBC)

Thinking outside of the box Perfusion management and myocardial protection strategy for a patient with sickle cell disease

Hydroxurea: A Novel Approach to Optimizing the Health of Pediatric Patients with Sickle Cell Disease. Maa Ohui Quarmyne September 9 th, 2017

Components of Blood. N26 Blood Administration 4/24/2012. Cabrillo College ADN/C. Madsen RN, MSN 1. Formed elements Cells. Plasma. What can we give?

Haemoglobin BY: MUHAMMAD RADWAN WISSAM MUHAMMAD

Anemia In the Insurance Applicant What do the numbers mean?

Medical Surgical Review Handout- Hematology/Oncology 2016

Discloser. Objectives LETTING GO OF THE RULES OF 3. I am receiving an honorarium from Sysmex for this presentation

DONE BY : RaSHA RAKAN & Bushra Saleem

Interpreting the CBC. Robert Miller PA Assistant Professor of Clinical Pediatrics and Family Medicine USC Keck School of Medicine Retired

SICKLE CELL AWARENESS. The Sickle Cell Society has produced the following information leaflets available at sicklecellsociety.org

A sickle in a pickle! by Julie Kirkegaard, MT(ASCP)SBB Community Blood Center, KC, MO and Elizabeth Jones, MT(ASCP)BB Saint Luke s Hospital, KC, MO

Hydroxyurea in Pediatric Patients With Sickle Cell Disease: What Nurses Need to Know

Efficacy of the AGRO-JET MIT-II NEEDLE-LESS JET INJECTOR for Iron Dextran Administration in Piglets

, Manu S nejana Dro. afe b,c. nca d, V. Ost

Outline. What is aplastic anemia? 9/19/2012. Aplastic Anemia Current Thinking on the Disease, Diagnosis, and Non-Transplant Treatment Options

Transfusion Practices and Creation of a Registry for Patients with Sickle Cell Disease within the Atlanta Sickle Cell Consortium

MECHANISMS OF HUMAN DISEASE: LABORATORY SESSIONS LYMPHOMA. April 16, 2008

Hematology & Coagulation Practicum Objectives CLS - 647

Sickle Cell Anemia. Sickle cell anemia is an inherited disorder of the blood which occurs when just one base pair substitution

Whole Blood. Lab 29A. Blood. Plasma. Whole Blood. Formed Elements. Plasma: Fluid component. Formed elements: Cells and fragments

Comparison of Spectra Optia and COBE Spectra apheresis systems performances for Red Blood Cell Exchange procedures

SICKLE CELL BROCHURE

Erythrocytapheresis vs continuous Manual Exchange Transfusion to treat cerebral macrovasculopathy in children with sickle cell anemia

Sickle Cell Anemia A Fictional Reconstruction Answer Key

A Lawyer s Perspective on Genetic Screening Performed by Cryobanks

Friday, January 4. Bell Work:

7.03 Lecture 26 11/14/01

Jovona Powelson, B.S. MLT (ASCP) Director of Laboratories

Pediatric Red Cell Exchange Indications, Benefits, Barriers. View from California Saturday May 9 th ASFA 2015

NM-96: A Small Molecule For The! Treatment of Acute Sickle Crisis!! Life Science Summit 10/29/14! Steven Isaacman, Ph.D.!

Optimal RBC products for RBC exchange for patients with sickle cell disease

Susan Stegman, MD Medical Director AXA Equitable Life May 3, 2016

A Prospective & Multicentric Study of RBC Parameters in Patients of Sickle Cell Disorder

Selected blood test. Danil Hammoudi.MD

Icd code for cbc with differential/ platelet

Evaluation of a Microcurrent Device in the Treatment of Malaria

20/01/1439. Prof. M. Rushdi. Prof. Mahmoud Rushdi Faculty of Veterinary Medicine Assiut University Egypt.

Human Genetic Disorders

Rationale for RBC Transfusion in SCD

Approach to Hemolysis

YEREVAN STATE MEDICAL UNIVERSITY DEPARTMENT OF HEMATOLOGY COURSE DESCRIPTION HEMATOLOGY

Sickle Cell Disease Why Is A Simple Genetic Disorder So Hard To Treat And How Are We Doing?

Blood CHAPTER. Lesson Objectives. Lesson Vocabulary. Introduction. Structure and Functions of Blood. Chapter 1. Blood

JMSCR Vol 04 Issue 12 Pages December 2016

8/28/2015. ACP Toolbox SYSMEX CLINICAL SUPPORT TEAM SYSMEX CUSTOMER RESOURCE CENTER. Maggie Fischer BSN, RN, MS Carolyn Williams, BSN, RN, CRNI

CORD BLOOD TESTING AND HDFN A CASE STUDY. Eric Rosa, MLS (ASCP) CM University of Kansas Hospital April 20, 2016

Regulatory Challenges in Apheresis Global Perspectives - Cell Therapy

KCI Cotransport Activity in Light versus Dense Transferrin Receptor-positive

8/28/2018. Disclosures. Objectives. None. Automation to PreciseType and Everything in Between

Automation to PreciseType and Everything in Between. Jessie Singer MT(ASCP) Transfusion Medicine Children s Hospital Los Angeles

Transcription:

More Efficient Exchange of Sickle Red Blood Cells can be Achieved by Exchanging the Densest Red Blood Cells Thibodeaux, SR, Jamensky, L, Schell K, Irwin L, O Doherty U Hospital of the University of Pennsylvania Department of Pathology and Laboratory Medicine Division of Transfusion Medicine and Therapeutic Pathology

Sickle Cell Disease Prevalence in the USA 100,000 people affected 1/365 Black or African- American births 1/13 have sickle cell trait Pathogenesis Autosomal recessive disease Point mutation causes glutamic acid valine http://www.cdc.gov/ncbddd/sicklecell/data.html http://sgugenetics.pbworks.com/f/1353132747/8.jpg

Sickle Cell Disease has Major Health Implications Complications Acute Chronic Cost 2004 - cost for hospital stays due to SCD complications ~$488 million http://www.sickle-thal.nwlh.nhs.uk/images/clinicalimplicationscomplicationsscd.png http://www.cdc.gov/ncbddd/sicklecell/data.html

Increased quantity, but what about quality of life? https://www.washingtonpost.com/national/health-science/unbearable-pain-not-enough-doctors-just-another-day-as-an-adult-with-sickle-cell/2016/03/21/f6598a5c-e655-11e5-a6f3-21ccdbc5f74e_story.html http://www.nhlbi.nih.gov/sites/www.nhlbi.nih.gov/files/images_561

Sickled Red Blood Cells are Denser than non-sickled Red Blood Cells Erythrocyte dehydration K+ efflux from the red blood cell Decreased intracellular water content Increased mean corpuscular hemoglobin concentration (MCHC) Can we capitalize on this density difference? Dense, Dehydrated Red Blood Cells (DRBCs) defined as having a density exceeding 1.120 Increased rigidity, decreased stability Include a variable fraction of irreversibly sickled cells Non-sickle cell patient Sickle cell patient N Engl J Med. 1997 Sep 11;337(11):762-9. Microcirculation (2004) 11, 209 225 Blood. 2012;120(15):3136-3141

Experimental Approach Control RCE Experimental RCE Waste Donor Plasma WBCs Patient Plasma WBCs RBCs RBCs Control settings (current practice) exchange the entire RBC layer based on the patient s hematocrit Patient RCE exchange waste product Donor therapeutic phlebotomy waste Waste Waste from this exchange Experimental settings exchanges the bottom half of the RBC layer based on the patient s hematocrit

Initial Findings support that targeting the densest RBCs leads to lower HgbS Control settings Experiment al settings Pre- RCE Percent Hgb S Reduction 23.2% Control Experimental Hgb S 23.7% 76.7% 94.5% Post- RCE Hgb S 5.4% Hgb S 1.3%

Better Reduction in Hemoglobin S is Reproducible

However, Reproducibility was not 100% In three experiments, there was no improvement by exchanging the bottom half of the hematocrit

Unexpected hurdles: Age of product tested Age of patient blood stored before exchange Density of RBCs may re-equilibrate with time due to K+ flux The experiments that did not work all used aged patient product MCHC s decrease over time in stored products Fresh product Old product (37 days old) Percent Decrease in HgbS 83.02 72.09

Unexpected hurdles: RBC depletion Hematocrit loss with experimental settings Taking more RBCs than we give back Average Percent Reduction 25% More than 50% of the RBCs are in the bottom half of the RBC layer J. Cell. Mol. Med. Vol 15, No 12, 2011 pp. 2634-2642

Conclusions More effective red cell exchange in sickle cell anemia patients is possible by taking advantage the density gradient between sickled RBCs and normal RBCs Goals and applicability to patients 1) achieve a higher reduction in hemoglobin S in patients or 2) achieve the previous levels of reduction using fewer donor units Hurdles Hematocrit loss with experimental settings Patient variability in RBC density may lead to difficulty in identifying patients that will most benefit from the procedure and leads to difficulty in correcting the patient final hematocrit

Acknowledgements The nurses in apheresis Especially Clarice Dixon for saving donor units The Blood Bank Staff Especially Rachel Hauser for the training to make donor units and type blood The Stem Cell Lab Staff For measuring CBCs The hematology lab For Hemoglobin S measurements And our fine colleagues Nicole Aqui, Eric Russell, Carlos Villa