venous thromboembolism Flashcards

1
Q

how does warfarin (coumarins) work?

A

inhibit vitamin K dependent carboxylation of factors II, VII, IX and X in the liver

causes a relative deficiency of these coagulation factors

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2
Q

how is the dosing of warfarin calculated for patient?

A

monitored by the international normalised ratio (INR) derived from the prothrombin time

takes around 5 days to establish maintenance dosing

loading regimens assist early dosing

individual dose for each patient- ethnicity affected

dietary intake of vitamin K affects warfarin dose

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3
Q

what is the most common side effect?

A

bleeding

major bleeds occur in 1% of patients each year

risk of fatal intracranial haemorrhage 0.25% per annum

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4
Q

how to reverse warfarin in a patient?

A

depends on whether the patient is bleeding

vitamin K: oral or intravenous routes

reverse by administering deficient clotting factors

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5
Q

what are the two methods of venous thrombosis prevention?

A

mechanical: foot pumps, compression stockings
pharmacological: LMWH, UFH, fondaparinux, dabigatran, rivaroxaban, warfarin

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6
Q

what is the difference between UFH and LMWH?

A

UFH binds to plasma proteins so requires monitoring whereas nearly 100% bioavailability means no monitoring required

UFH requires continous IV infusion or twice daily sc administration, LMWH requires once daily dosing

UFH carries greater risk of osteoporosis and HIT

UFH can be reversed by d/c infusion so used when there is a high risk of bleeding whereas LMWH cannot be reversed

LMWH has reliable dose dependent anti coagulation effect

UFH has molecular weight from 3000 to 30,000D whilst LMWH is produced by enzymatic or chemical depolymerisation of UFH with a mean MW of 5000- reduced chain length so reduced capacity to inhibit thrombin

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7
Q

how is UFH monitored?

A

activated partial thromboplastin time (APTT)

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8
Q

what are the two types of heparin and how do they. work?

A

unfractionated

low molecular weight

sulphated glycosaminoglycan, biological product derived from porcine intestine

binds to unique pentasaccharide on antithrombin and potentiates its inhibitory action towards factor Xa and thrombin

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9
Q

what are the two steps of anticoagulant therapy?

A

rapid initial anticoagulation to reduce risk of thrombus extension and fatal pulmonary embolism
- parenteral anticoagulant: heparin, LMWH, fondaparinux, DOAC

extended therapy: orally active anticoagulant: vitamin K antagonist (warfarin), OR DOAC to prevent recurrent thrombosis and chronic complications such as post-phlebitic syndrome

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10
Q

how are DOACS used in management of VTE?

A

dabigatran, rivaroxaban, edoxaban, apixaban licensed in UK for treatment of acute DVT

enables rapid initial anticoagulation orally

continue maintenance dose for 6 months or longer for secondary prevention of VTE

apixaban and rivaroxaban dont need overlap with heparin- big advantage in outpatient setting

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11
Q

what is the traditional management of VTE using heparins?

A

give LMWH or UFH for minimum of 5 days if uncomplicated thrombosis or 7 days or longer if extensive disease

start warfarin therapy on day 1

overlap with LMWH or UFH until IKR is 2 for 2 days

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12
Q

what are the clinical features of lower limb DVT?

A

pain, swelling, increased temperature of limb, dilation of superficial veins

usually unilateral

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13
Q

what is the Well’s pre-test probability score?

A

clinical likelihood of DVT

stratifies patients into low, intermediate or high probability categories

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14
Q

what are the diagnostic tests for DVT?

A

venous ultrasonography: most useful objective test: non-compressibility of common femoral vein or popliteal vein diagnostic of DVT

contrast venography: reference standard for diagnosis of DVT

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15
Q

what are the clinical features of pulmonary embolism?

A

collapse, faintness, crushing central chest pain

pleuritic chest pain

difficulty breathing

haemoptysis

exertional dyspnoea

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