Anesth Analg 1999;89:1453
© 1999 International Anesthesia Research Society
OBSTETRIC ANESTHESIA
Assessing Platelet and Fibrinogen Contribution to Clot Strength Using Modified Thromboelastography in Pregnant Women
Vijaya N. R. Gottumukkala, MD, FRCA,
Shiv K. Sharma, MD, FRCA, and
John Philip, MD
Department of Anesthesiology and Pain Management, Obstetric Anesthesia Division, University of Texas Southwestern Medical School, Dallas, Texas
Address correspondence and reprint requests to Dr. Shiv K. Sharma, Department of Anesthesiology and Pain Management, University of Texas Southwestern Medical School, 5323 Harry Hines Blvd., Dallas, TX 75235-9068. Address e-mail to shiv.sharm{at}email.swmed.edu
The monoclonal antibody fragment c7E3 Fab (ReoPro®), by binding to platelet surface fibrinogen receptors (glycoprotein, GPIIb/IIIa), inhibits platelet aggregation and its interaction with fibrinogen. In this study, we used thromboelastography with ReoPro® to evaluate the independent contribution of fibrinogen and platelets to clot strength. Thromboelastography was performed in 21 healthy, term parturients scheduled for elective cesarean delivery with 360 µL of celite-activated whole blood and with 5 µL of (2 mg/mL) ReoPro® added to 355 µL of celite-activated whole blood. The contribution of platelets to clot strength (MAplt) was derived by subtracting MAfib (maximal amplitude with ReoPro®) from MAwb (maximal amplitude with whole blood). Thus, MAwb - MAfib = MAplt. The value for MAwb (mean ± SD) was 73 ± 4 mm, for MAfib it was 33 ± 5 mm, and for MAplt it was 40 ± 3 mm. The contribution of fibrinogen and platelets to the MAplt was 45% and 55%, respectively. Modified thromboelastography using ReoPro® in healthy parturients can be used to determine the contribution of fibrinogen and platelets to blood clot strength.
Implications: Determining the independent contribution of platelets and fibrinogen to the maximal amplitude of thromboelastography using c7E3 Fab may further improve the use of thromboelastography in detecting and treating coagulation defects.
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