2010, Number S1
<< Back Next >>
Rev Mex Med Transfus 2010; 3 (S1)
Clinical use of plasma and plasmatic derivated
Paredes AR
Language: Spanish
References: 18
Page: 87-91
PDF size: 147.69 Kb.
ABSTRACT
Plasma and plasma fractions have specific, limited indications and should not be used indiscriminately. Specific coagulation defects should be treated with specific plasma fractions, not FFP. FFP is not indicated for volume replacement. FFP and cryoprecipitate should not be used for prophylaxis or for abnormal coagulations test in the abscense of bleeding. Large-scale, prospective, randomized trials are needed to clarify the efficacy of plasma and plasma products in many clinical settings. An inexpensive means of pathogen elimination is needed. Expanded knowledge of the interactions between coagulation factors and the endothelial cell surface will help focus future clinical research.
REFERENCES
Spence RK. Clinical use of plasma and plasma fractions. Best Practice and Research Clinical Haematology 2006; 19: 83-96.
Kakaiya RM, Morse EE, Panek S. Labile coagulation factors in thawed fresh frozen plasma prepared by two 0methods. Vox Sang 1984; 46: 44-46.
Novis DA, Renner S, Friedberg RC et al. Quality indicators of fresh frozen plasma and platelet utilization. Arch Pathol Lab Med 2002; 126: 527-532.
Solheim BG, Flesland O, Brosstad F et al. Improved preservation of coagulation factors after pre-storage leukocyte depletion of whole blood. Transfus Apheresis Sci 2003; 29: 133-139.
Hoots WK, Abrams C, Tankersley D. The food and drug administration’s perspective on plasma safety. Transfus Med Rev 2001; 15: 20-26.
Williamson LM, Allain JP. Virally inactivated fresh frozen plasma. Vox Sang 1995; 69: 159-165.
Fischer G, Hoots WK, Abrams C. Viral reduction techniques: types and purpose. Transfus Med Rev 2001; 15: 27-39.
Hilfenhaus J, Groner A, Novak T, Weiner T. Analysis of human plasma products: Polymerase chain reaction does not discriminate between live and inactivated viruses. Transfusion 1997; 37: 935-940.
Beek H, Hellstern P. In vitro characterization of solvent/detergent-treated plasma and of quarantine fresh frozen plasma. Vox Sang 1998; 74: 219-223.
Hellstern P, Haubelt H. Manufacture and composition of fresh frozen plasma and Virus-inactivated therapeutic plasma preparations: correlation between composition and therapeutic efficacy. Thromb Res 2002; 107: 53-58.
Wieding JU, Hellstern P, Kohler M. Inactivation of viruses in fresh frozen plasma. Ann Hematol 1993; 67: 259-266.
Doyle S, O’Brien P, Murphy K et al. Coagulation factor content of solvent/detergent plasma compared with fresh frozen plasma. Blood Coag Fibrinolysis 2003; 14: 283-287.
Suontaka AM, Blomback M, Chapman J. Changes in functional activities of plasma fibrinogen after treatment with methylene blue and red light. Transfusion 2003; 43: 568-575.
AuBuchon JP, Birkmeyer JD. Safety and cost-effectiveness of solvent/detergent-treated plasma. In search of a zero-risk blood supply. JAMA 1994; 272: 1210-1214.
Standworth SJ. The evidence-based use of FFP and cryoprecipitate for abnormalities of coagulation tests and clinical coagulopathy. American Society of Hematology. Education Program book 2007: 179-186.
Segal JB, Dzik WH. Paucity of studies to support that abnormal coagulation test results predict bleeding in the setting of invasive procedures: an evidence-based review. Transfusion 2005; 45: 1413-1425.
Peterson GA. Does systematic anticoagulation increase the risk of internal yugular vein cannulation? (letter) Anesthesiology 1991; 75: 1124.
Ewe K. Bleeding after liver biopsy does not correlate with indices of pertipheral coagulation. Dig Dis Sci 1981; 26: 388-393.