Educating physicians and other healthcare professionals with the most cutting-edge information available related to hemostasis management.
This discussion will describe the hematology of trauma, including the effects of acidosis, hypothermia, and "wash out." The faculty will review the clinical consequences of coagulopathy and anemia in critically ill patients and will present the latest findings regarding transfusion practices in this population. In addition, the faculty will provide insights into the potential clinical consequences of prolonged storage of red blood cells and will discuss the role of hemostatic agents in optimizing blood conservation strategies.
Use of Traditional Blood Products and Novel Hemostatic Agents for the Treatment of Traumatic Bleeding is intended for transfusion medicine specialists interested in learning about hemostasis management during trauma.
After completing this CME activity, participants should be able to:
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It is the policy of the FCG Institute for Continuing Education that all faculty participating in continuing medical education activities are expected to disclose to the program audience (1) any real or apparent conflict(s) of interest related to the content of their presentation and (2) discussion of unlabeled or unapproved uses of drugs or medical devices. Faculty disclosure statements can be found with their biographical sketches.
When individuals in a position to control or influence the development of the content have reported Financial Relationships with one or more commercial interests, The FCG Institute for Continuing Education utilizes a process to identify and resolve potential conflicts to ensure that the content presented is free of commercial bias. The content of this presentation was vetted through The Institute’s process of peer review and content validation and modified as required to meet this standard.
This educational activity may include discussion of drugs or devices or uses of drugs and devices, that have not been approved by the FDA or have been approved by the FDA for specific uses only. It is the responsibility of the physician to determine the FDA clearance status of each drug or device he or she wishes to use in clinical practice. The FCG Institute for Continuing Education is committed to the free exchange of medical education. Inclusion of any product or device discussion, including discussion of investigational or off-label uses, does not imply endorsement by The Institute of the uses, products, or techniques presented.
This CME/CE activity is designed for use by healthcare professionals for educational purposes only. The information and opinions expressed by the faculty are their own and do not necessarily reflect those of The FCG Institute. The FCG Institute for Continuing Education does not define a standard of care, nor does it intend to dictate an exclusive course of management but presents through the educational activities it sponsors recognized methods and techniques of clinical practice for consideration by physicians and other healthcare providers for incorporation into their practices. Participants should use their own clinical judgment before applying information, whether provided here or by others, for any professional use.
Ira A. Shulman, MD
Professor and Vice Chair of Pathology
Director of Transfusion Medicine
University of Southern California
Keck School of Medicine
Los Angeles, CA


The FCG Institute
for Continuing Education and Acumentis gratefully acknowledge an educational
grant from Novo Nordisk Inc. in support of this CME
activity.
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