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What pathways and factors are measured by APTT
intrinsic and common pathways - XII, XI, IX, VIII, X, V, II, I, HMWK, Prekallikrein
Which factors aren’t tested for by APTT
Factor XIII and VII
What is APTT most sensitve to
VIII and IX deficiencies - Hemophilia - sever fibrinogen deficiencies
What does prolonged APTT mean
factor deficiency
WHat is the purpose of ordering an APTT
monitoring heparin therapy - test of choice to screen factor deficience of intrinsic and common - detects phospholipid inhibitors
What is the specimen collected for APTT
NaCitrate - Platelet poor plasma
WHat is in the reagent for APTT
partial thromboplastin and CaCL2
What is within the Controls of APTT
commercial - lyophilized or frozen - normal and abnormal
What is partial thromboplastin within the reagent
composed of phospholipid (platelet of source or substitute) and activator
WHat does an activator do in the partail thromboplastin reagent
maximum activation of the contact factors is accomplished and speeds up the reaction
What is the CaCl2 in the reagent
supplies Ca for the cascade - sodium citrate binds to calcium to prevent coagulation - we need to supply it for coagulation to occur
WHat is the procedure of APTT
PPD is added to citrate - APTT reagent is added and mixture is incubated at 37 degrees - after incubation period, add warmed calcium chloride and start timer - when clot is detected, timer is stopped
WHat is the APTT reference range? What is the critical range?
25-40 seconds - Critical >150 seconds
What causes prolonged APTT
Factor Deficiency - acquired antibody to a specific factor - aquired inhibitor (inhibio=tor to phospholipid - severe liver disease - heparin therapy
What is the criteria for a factor to be deficient
factor is less than 50% of normal
What causes a shortened APTT
high levels of Factor VII - acute phase reactant
What are the most common single factor deficiences
VIII - Hemophilia A, IX - Hemophilia B, XI - Hemophilia C
What is heparin
produced naturally in body in mast cells and basophils - commercial preparations are glycosaminoglycans with molecular weights - effect of heparin depends on the patients amount of antithrombin
What is antithrombin
coagulation inhibitor - main target of inhibitation are IIa and Xa (forms complex with them and inhibits their action) - Also inhibits IXa, XIa, XIIa, plasmin, and kallikrein - does not inhibit VIIa
What is the relationship between heparin and AT
AT is heparin’s cofactor - heparin accelerates AT action, heparin prevents clot from forming
what happens when there is no heparin
AT neutralizes thrombin and Xa forming 1:1 complex in several minutes
What does therapeutic heparin do
same thing as natural heparin
WHat is high molecular wight heparin (unfractionated heparin
most common heparin treatment - has a short half life so requires frequent administration - IV - enhances AT activit against thrombin and Xa
What is unfractionated heparin used in preventionand treatment of:
venous thromboembolism, unstable angina, during and after coronary angioplasty, during cardiovascular surgery
What are therapeutic levels -
1.5-2x the patients - results vary depending on reagent - standardization of results has not yet been achieved
How does the admnistration of heparin work
small amounts of heparin are given until therapeutic levels have been reached - monitored every 6-24 hours - levels should be reached within 24 hours
WHat does long term heparin therapy do
decrease AT which can be dangerous - switch to different anticoagulant once stabilized on heparin
What is Heparin Induced Thrombocytopenia
IgG antibodies cause platelet consumption by the spleen = decrease PLT - may also affect formation of thrombi = life threatening = we must monitor platelet counts as heparin induced thrombocytopenia may occur
What should be monitored on HIT
APTT and Platelets - if platelets drop below 50% of baseline, stop heparin