Hemolytic Reactions | Reaction | Response | Treatment |
Acute Hemolytic Transfusion Reaction | Antibody reaction + Complement fixation to rbc A, B, Kell, Kidd, Duffy and Ss antigens | Hemolysis, acute renal failure, hypotension, bronchospasm, DIC | Supportive measures: inotropes and vasopressors to prevent shock, maintain intravascular volume and urine output with IVF and diuretics |
Delayed Hemolytic Reactions
| Prior sensitization to donor antigens (kidd, kell, Rh) – low levels of antibodies over time such that they are not detected on routine screening. Transfusion exposure causes an anamnestic response. | Usually rbc destruction occurs extravascularly and symptoms are less severe than AHTR. Low grade fever, ↑ indirect bilirubin, jaundice, anemia | Supportive, hydration and transfusion of compatible rbc as necessary
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Nonhemolytic reactions |
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Minor Allergic Reactions | Allergic reaction to donor plasma proteins | Rash, pruritus, swelling | Diphenhydramine, Steroids |
Anaphylactic Reactions | Prior sensitization in a patient with IgA deficiency and subsequent exposure to IgA containing product | Dyspnea, bronchospasm, angioedema, hypotension | Steroids, epinephrine |
Febrile reactions | Antibody reactions to donor leukocytes. | Typically >1◦C rise in temperature within 4 hours of transfusion plus chills, myalgia, nausea, non-productive cough, respiratory distress | Acetaminophen. Usually defervesce in 48 hours.
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Transfusion-Related Acute Lung Injury (TRALI)
| Anti- HLA antibodies in the donor interacts with recipients leukocytes causing aggregation in the pulmonary circulation | Fever, chills, non-cardiogenic pulmonary edema, bilateral pulmonary infiltrates and severe pulmonary insufficiency | Supportive. Usually resolves in 24-48 hours with supportive care |
Graft-Versus-Host Disease (GVHD) | Donor lymphocytes may not be rejected in immunosuppressed patients. They can proliferate and establish an immune response against the recipient. Typically with transfusion of cellular products, less with FFP and cryoprecipitate. | Rapid pancytopenia | Irradiation of blood products is the only proven preventive measure. |
Driving Pressure and Survival in the Acute Respiratory Distress Syndrome Marcelo B.P. Amato, M.D., Maureen O. Meade, M.D., Arthur S. Slutsky, M.D., Laurent Brochard, M.D., Eduardo L.V. Costa, M.D., David A. Schoenfeld, Ph.D., Thomas E. Stewart, M.D., Matthias Briel, M.D., Daniel Talmor, M.D., M.P.H., Alain Mercat, M.D., Jean-Christophe M. Richard, M.D., Carlos R.R. Carvalho, M.D., and Roy G. Brower, M.D. N Engl J Med 2015; 372:747-755 February 19, 2015 DOI: 10.1056/NEJMsa1410639 BACKGROUND Mechanical-ventilation strategies that use lower end-inspiratory (plateau) airway pressures, lower tidal volumes (V T ), and higher positive end-expiratory pressures (PEEPs) can improve survival in patients with the acute respiratory distress syndrome (ARDS), but the relative importance of each of these components is uncertain. Because respiratory-system compliance (C RS ) is strongly related to the volume of aerated remaining functional lung during disease (termed functional lung size)...
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