Acquired Blood dys Flashcards

1
Q

what 3 things are required for clotting

A

platelets, vessel wall, clotting factors

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2
Q

what happens to clotting in massive blood loss

A

RBC’s can’t push platelets to vessel wall so they can’t adhere

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3
Q

describe what PT measures in clotting

A

prothrombin time - measures factors 2, 5, 7, 10 and fibrinogen which is the extrinsic pathway
time in seconds from exposure to clot formation

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4
Q

what is the only test that measures factor VII

A

prothrombin time

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5
Q

what are causes of prolonged PT test

A

deficiency in 2, 5, 7, 10 or fibrinogen (vit K deficiency) - they are on warfarin or have liver disease

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6
Q

what clotting tests give evidence of early liver disease

A

isolated prolonged PT but normal APTT

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7
Q

which clotting factor has the shortest half life

A

VII

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8
Q

what is an APTT and what does is measure

A

activated partial thromboplastin time

measure 2, 5, 8, 9, 10, 12, kallikrein, HMWK and fibrinogen

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9
Q

what can make a APTT test be abnormal without having bleeding problems

A

deficiencies in kallikrein, HMWK and factor 12

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10
Q

what can cause isolated APTT

A

UFH, lupus anticoagulant, haemophilia or deficiencies sin APTT clotting factors

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11
Q

what are common things that cause prolonged PT and APTT

A

deficiency in 2, 5, 10 or fibrinogen, DIC, HMWK, kallikrein deficiency

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12
Q

what does the thrombin time TT measure

A

function and amount of function of fibrinogen

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13
Q

what causes prolonged TT

A

dysfibrinogenaemia - none
low fibrinogen
heparin
DIC

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14
Q

what is LAC in coagulation

A

lupus anticoagulant - IgG/M autoantibody which prolongs the APTT

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15
Q

what type of drug is heparin

A

anticoagulant

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16
Q

what is the mode of action of heparin and its subtypes

A

wraps around antithrombin - inhibits factor X
LMWH - inhibits factor Xa
UFH - inhibits Xa and thrombin to switch of coagulation cascade

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17
Q

what is the efficacy ratio of LMWH

A

higher ratio of anti Xa compared to anti LLa (thrombin)

18
Q

what are the two benefits of using LMWH

A

better bioavailability and longer half life

19
Q

why do you want to avoid using UFH and what is it monitored using

A

badly monitored but with APTT

can be hard to anticoagulate in infants

20
Q

what are some complications of heparin treatment

A

HIT - heparin induced thrombocytopenia

skin / allergic reactions and bleeding

21
Q

what is given for patients with too much UFH from bleeding

A

protamine sulphate - derived from fish sperm - may have allergies

22
Q

what is the mechanism of action of warfarin

A

inhibits vit K epoxide reducatase - prevents activation of vit K factors 2, 7, 9, 10 and protein C/S

another anticoagulant

23
Q

what do you monitor treatment of warfarin

A

INR

24
Q

how do you treat excessive bleeding on warfarin

A

stop warfarin
give prothrombin complex conc
vit K

25
Q

what are DOAC’s used for and give examples

A

inhibitors of factor Xa (drugs that end in xaban)

drugs that inhibit thrombin IIa - dabigatran

26
Q

what is fondaparinux

A

similar to heparin

anti-Xa

27
Q

give examples of two types of anti-platelet agents

A

aspirin - inactivates platelet cyclooxyrgenase

P2Y12 antagonists - clopidogrel

28
Q

what factors are inactive in VIT k deficiency and what is the treatment / cause

A
def in factor 2, 7, 9, 10 
causes - obstructive jaundice, neonates 
treat with oral vit K
29
Q

what is another name for bleeding in the liver

A

cirrhotic coagulopathy

30
Q

in cirrhotic coagulopathy which factor is not deficient

A

VIII

31
Q

what are the clinical features of cirrhotic caoguloppathy

A

impaired homeostasis
platelet dysfunction
excessive plasmin activity

32
Q

what is the treatment for bleeding in the liver ie cirrhotic coagulopathy

A

platelet transfusion

prothrombin complex concentrate

33
Q

what are the clinical features of bleeding with renal disease and what is the risk with hypertension

A

bruising, gum bleeding, nose bleeds

risk of intracerebral haemorrhage

34
Q

what are the causes and features of bleeding with renal disease

A

anaemia - decreased platelet interaction with lining
penecillin blocking platelets
uraemia - disrupts platelet interactions and impaired binding

35
Q

how to you prevent bleeding in renal disease

A

EPO and transfusion

desmopressin (stimulates vWF release)

36
Q

in a major haemorrhage how much blood is needed for transfusion

A

equal to patients total blood volume in less than 24 hours

with HR greater than 110 and BP less than 90

37
Q

what can massive haemorrhages lead to with clotting factors

A

DIC - become over active

38
Q

what is DIC in bleeding

A

disseminated intravascular coagulation - overactive clotting leading to fibrin clots = organ failure

39
Q

what is the pathogenesis and causes of DIC

A

excess thrombin generation - reduced natural anticoagulant activity and decreased fibrinolysis

acute cause - sepsis, trauma, acute liver haemolysis, live disease

chronic cause - malignancy

40
Q

what test results signify DIC

A

low platelet, elevated d dimer, prolonged PT low fibrinogen

41
Q

what is the management of `DIC

A

treatunderlying cause ie chemo, antibiotics

folic acid and VK supplementation