Blood Products and Coagulation Flashcards
What acid/base abnormality can occur with massive blood transfusion? What electrolyte abnormalities?
Metabolic alkalosis
Hypocalcemia and Hyperkalemia (sometimes hypokalemia secondary to the alkalosis)
What causes the reaction seen in febrile nonhemolytic reaction?
cytokines (IL-1, IL-6, TNF)
What causes transfusion related lung injury? What is it similar to clinically? How does it differ?
pulmonary agglutinin reaction
ARDS
resolves in usually 4 days
What are the treatments for TTP?
plasmapharesis, exchange transfusions, antiplatelet agents, and rarely splenectomy
DO NOT TRANSFUSE PLATEMENTS
What are the treatments for ITP?
steroids and splenectomy
How long does the platelet effect of ASA last?
10 days i.e. the life of the platelet
Which coagulation pathway affects PTT?
intrinsic
Which coagulation pathway affects PT?
extrinsic
What components make up the intrinsic pathway?
XII, XI, iX w/ VIII followed by the shared pathway
What components make up the extrinsic pathway?
Tissue thromboplastin, VII followed by the shared pathway
What is the shared pathway for intrinsic and extrinsic coagulation cascades?
X (w/ V) II Thrombin I (Fibrinogen) Fibrin (w/ XII) Stabilized fibrin
What coagulation lab measures are affected by DIC?
elevated PT, PTT, and bleeding time
What is the treatment for DIC?
- treat the causative agent
- heparin
- cryoprecipitate
- platelets
- whole blood
What are the vitamin K dependent coagulation factors?
protein C and S, factors VIII. IX. X. II
Hemophilia B is caused by what factor deficiency? What is the genetic inheritance? What are the abnormal lab values? What’s the treatment?
factor IX
X-linked recessive
increased PTT, normal PT, normal bleeding time
FFP
What is the genetic inheritance of factor VIII deficiency? What’s it called? What is the treatment?
X-linked recessive
Hemophilia A
Cryoprecipitate
What is the treatment for vWF disease? What’s the treatment?
autosomal dominant
cryoprecipitate
What coagulation factor deficiencies causes hypercoagulablity? What are the clinical manifestations?
protein C, S, and antithrombin III
venous thrombosis
What is the mechanism of action for heparin?
increases the action of antithrombin III
What is the reversal agent for heparin?
protamine sulfate