-Author name in bold denotes the presenting author
-Asterisk * with author name denotes a Non-ASH member
Clinically Relevant Abstract denotes an abstract that is clinically relevant.

PhD Trainee denotes that this is a recommended PHD Trainee Session.

Ticketed Session denotes that this is a ticketed session.

Recent Insights into Efficacy of Red Blood Cells in Transfusions and Physiology

PhD Trainee
Sponsor: Scientific Committee on Transfusion Medicine
Program: Scientific Program
Saturday, December 5, 2015: 9:30 AM-11:00 AM
W414AB, Level 4 (Orange County Convention Center)
Saturday, December 5, 2015: 4:00 PM-5:30 PM
W331, Level 3 (Orange County Convention Center)

Description:

Over the past decade there has been intense debate regarding potential adverse effects of stored RBC transfusions on clinical outcomes. Some studies, primarily observational, found associations between transfusions of RBCs stored for longer durations and increased morbidity and mortality. However, recent randomized controlled trials do not demonstrate differences in outcomes following transfusions of RBCs stored for short (<7-10 days) vs standard (oldest available compatible blood) periods in several at-risk patient populations. Recent research has also led to new insights into mechanisms underlying deleterious effects of storage hemolysis and other storage-induced RBC damage, including genetic polymorphisms which result in abnormal expression or varying function of RBC proteins. Recent studies also identified roles for RBCs in clot contraction, which imply a new role for RBCs in hemostasis, and suggest that they could be a marker for thromboembolic disease.

Dr. Glynn has focused the NHLBI agenda for transfusion medicine on better understanding the RBC storage lesion and the clinical effect of transfused RBC stored for different periods. She will review recent developments in the field with attention to the results of recently-published randomized clinical trials.

Dr. Spitalnik has a long-standing interest in the pathophysiological consequences of acute RBC clearance, whether the RBCs are antibody coated, malaria infected, or damaged by refrigerated storage. He will describe the real and potential effects of genetically-encoded RBC polymorphisms on the RBC storage lesion and on the consequences of transfusing these storage-damaged cells.

Dr. Weisel will discuss compression of RBCs during clot contraction to comprise a tightly packed array of polyhedra with platelets and fibrin on the outside, forming a tight seal to stem bleeding that may be especially important in venous hemostasis. He will also present findings on prevalence of these polyhedrocytes in thrombi and pulmonary emboli, suggesting that they may also be a marker for thrombosis.

Chair:
Michael P. Busch, MD, PhD, Blood Systems Research Institute

Disclosures:
No relevant conflicts of interest to declare.

Simone A Glynn, MD1, Darrell J Triulzi, MD2, John Roback, MD, PhD3 and Harvey G. Klein, MD4

1Division of Blood Diseases and Resources, NHLBI, Bethesda, MD
2Institute for Transfusion Medicine, Pittsburgh, PA
3Department of Pathology and Laboratory Medicine, Emory University, Atlanta, GA
4Clinical Center, NIH, Bethesda, MD

Steven L Spitalnik, MD

Department of Pathology & Cell Biology, Columbia University, New York, NY

John W. Weisel, PhD

Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, PA

See more of: Scientific Program