Approximately 20 million units of blood components are transfused in the United States each year. Transfusion-associated acute lung injury (TRALI) is increasingly recognized as an important cause of transfusion-induced adverse events. The incidence and mechanisms of severe TRALI will be studied in Project 1. In addition to severe TRALI, recent studies suggest that mild to moderate lung injury (TRALI) is also caused by transfusions of blood products, especially in patients with underlying medical and surgical disorders. The lack of well-designed prospective studies has limited progress in evaluating mild to moderate TRALI. Therefore, the goals of this project are (1) to determine if TRALI exists as a spectrum of pulmonary dysfunction, rather than exclusively as a severe form of lung injury; (2) to determine the influence of elevated concentrations of cytokines and lyso-phosphatidyl choline in the plasma of stored red cells or platelets on pulmonary function; and (3) and to determine if an event prior to transfusion (""""""""first event"""""""") is necessary before transfusion results in pulmonary dysfunction.
These aims will be accomplished by prospective randomized clinical studies in humans with a wide range of risk for pulmonary dysfunction, using sensitive measures of lung injury including normal controls, patients undergoing major surgery, and critically ill patients who require mechanical ventilation. Data from these prospective, randomized studies will generate valuable new information regarding the scope and etiology of TRALI in humans, and will thereby provide important guidelines regarding preparation and administration of blood product transfusions hi several patient populations.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
5P50HL081027-04
Application #
7686155
Study Section
Special Emphasis Panel (ZHL1)
Project Start
Project End
Budget Start
2008-09-01
Budget End
2009-08-31
Support Year
4
Fiscal Year
2008
Total Cost
$355,971
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Toy, Pearl; Kleinman, Steven H; Looney, Mark R (2017) Proposed revised nomenclature for transfusion-related acute lung injury. Transfusion 57:709-713
Roubinian, Nareg H; Looney, Mark R; Keating, Sheila et al. (2017) Differentiating pulmonary transfusion reactions using recipient and transfusion factors. Transfusion 57:1684-1690
Roubinian, Nareg H; Looney, Mark R; Kor, Daryl J et al. (2015) Cytokines and clinical predictors in distinguishing pulmonary transfusion reactions. Transfusion 55:1838-46
Toy, Pearl; Bacchetti, Peter; Grimes, Barbara et al. (2015) Recipient clinical risk factors predominate in possible transfusion-related acute lung injury. Transfusion 55:947-52
Feiner, John R; Gropper, Michael A; Toy, Pearl et al. (2015) A Clinical Trial to Detect Subclinical Transfusion-induced Lung Injury during Surgery. Anesthesiology 123:126-35
Looney, Mark R; Roubinian, Nareg; Gajic, Ognjen et al. (2014) Prospective study on the clinical course and outcomes in transfusion-related acute lung injury*. Crit Care Med 42:1676-87
Murphy, Edward L; Kwaan, Nicholas; Looney, Mark R et al. (2013) Risk factors and outcomes in transfusion-associated circulatory overload. Am J Med 126:357.e29-38
Gandhi, Manish J; Carrick, Danielle M; Jenkins, Sarah et al. (2013) Lot-to-lot variability in HLA antibody screening using a multiplexed bead-based assay. Transfusion 53:1940-7
Rollins, Mark D; Molofsky, Ari B; Nambiar, Ashok et al. (2012) Two septic transfusion reactions presenting as transfusion-related acute lung injury from a split plateletpheresis unit. Crit Care Med 40:2488-91
Kor, Daryl J; Kashyap, Rahul; Weiskopf, Richard B et al. (2012) Fresh red blood cell transfusion and short-term pulmonary, immunologic, and coagulation status: a randomized clinical trial. Am J Respir Crit Care Med 185:842-50

Showing the most recent 10 out of 26 publications