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29 Terms

1
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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

2
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Which factors aren’t tested for by APTT

Factor XIII and VII

3
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What is APTT most sensitve to

VIII and IX deficiencies - Hemophilia - sever fibrinogen deficiencies

4
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What does prolonged APTT mean

factor deficiency

5
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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

6
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What is the specimen collected for APTT

NaCitrate - Platelet poor plasma

7
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WHat is in the reagent for APTT

partial thromboplastin and CaCL2

8
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What is within the Controls of APTT

commercial - lyophilized or frozen - normal and abnormal

9
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What is partial thromboplastin within the reagent

composed of phospholipid (platelet of source or substitute) and activator

10
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WHat does an activator do in the partail thromboplastin reagent

maximum activation of the contact factors is accomplished and speeds up the reaction

11
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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

12
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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

13
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WHat is the APTT reference range? What is the critical range?

25-40 seconds - Critical >150 seconds

14
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What causes prolonged APTT

Factor Deficiency - acquired antibody to a specific factor - aquired inhibitor (inhibio=tor to phospholipid - severe liver disease - heparin therapy

15
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What is the criteria for a factor to be deficient

factor is less than 50% of normal

16
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What causes a shortened APTT

high levels of Factor VII - acute phase reactant

17
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What are the most common single factor deficiences

VIII - Hemophilia A, IX - Hemophilia B, XI - Hemophilia C

18
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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

19
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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

20
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What is the relationship between heparin and AT

AT is heparin’s cofactor - heparin accelerates AT action, heparin prevents clot from forming

21
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what happens when there is no heparin

AT neutralizes thrombin and Xa forming 1:1 complex in several minutes

22
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What does therapeutic heparin do

same thing as natural heparin

23
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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

24
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What is unfractionated heparin used in preventionand treatment of:

venous thromboembolism, unstable angina, during and after coronary angioplasty, during cardiovascular surgery

25
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What are therapeutic levels -

1.5-2x the patients - results vary depending on reagent - standardization of results has not yet been achieved

26
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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

27
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WHat does long term heparin therapy do

decrease AT which can be dangerous - switch to different anticoagulant once stabilized on heparin

28
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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

29
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What should be monitored on HIT

APTT and Platelets - if platelets drop below 50% of baseline, stop heparin