Anticoagulant drugs Flashcards

(28 cards)

1
Q

thrombotic events- arterial

A

coronary, cerebral, peripheral= antiplatlet drugs

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2
Q

thrombotic events- venous

A

dvt, pe= anticoagulant drugs

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3
Q

indications anticoagulant drugs (2)

A

venous thrombosis

atrial fibrillation- 85%

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4
Q

anticoagulant drug targets

A

formation of fibrin clot

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5
Q

venous thrombosis (3)

A

low pressure system

platlets not activated

activates coagulation cascade - rich in fibrin clot

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6
Q

naturally occurring anticoagulants

A
  1. serine protease inhibitors
    antithrombin natural defence
    - thrombin key to haemostasis =fibrinogen to fibrin
  2. protein c + s= switch off clotting factors 5 + 8 - reduces chance thrombosis
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7
Q

heparin (3)

A

potentiates antithrombin

immediate effect

2 forms= unfractionated + LWMH

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8
Q

Unfractionated

A

prolongs aptt prothrombin time

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9
Q

LWMH

A

antithrombin bind to thrombin or activated factor 10 and that complex switch sit off, heparin wraps round it

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10
Q

heparin monitoring (2)

A

unfractionated- Activated partial thromboplastin time (APTT)

LWMH- Anti-Xa assay but usually no monitoring required- unless renal failure

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11
Q

heparin complications (3)

A

bleeding​

heparin induced thrombocytopenia (with thrombosis) HITT - monitor FBC in patients on heparin​

osteoporosis with long term use​

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12
Q

heparin reversal (5)

A

stop the heparin (short t1/2)​

in severe bleeding -​
=protamine sulphate​
=reverses antithrombin effect​
=complete reversal for unfractionated​
=partial reversal for LMWH​

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13
Q

coumarin anticoagulants - mech of action

A

inhibition of vitamin K

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14
Q

coumarin anticoagulants - drugs (4)

A

warfarin​!

phenindione​

acenocoumarin​

phenprocoumon​

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15
Q

vitamin K (4)

A

fat soluble vitamin​

absorbed upper intestine​

requires bile salts for absorption​

final carboxylation of clotting factors II, VII, IX and X​

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16
Q

vit K dependent factors (3)

A

factors II (prothrombin), VII, IX & X​
=protein C and protein S​

synthesised in liver​

require vitamin K for final carboxylation step essential for function​

17
Q

warfarin- mech of action

18
Q

warfarin therapy (4)

A

initiation​=
-rapid​
-slow​

stabilisation​

maintenance​
=dose should be taken at same time every day (6pm recommended)​

narrow therapeutic window - need to monitor therapy

19
Q

warfarin monitoring

A

INR
(INR = PTRISI​)

20
Q

warfarin: major adverse effect - haemorrhage (6)

A

factors that may influence bleeding risk:=
-intensity of anticoagulation​
-concomitant clinical disorders​
-concomitant use of other medications ​
-BEWARE DRUG INTERACTIONS​
-quality of management​

21
Q

INR

A

Patient’s PT in Seconds​ /
Mean Normal PT in Seconds​

22
Q

bleeding complications from warfarin (6)

A

mild=
-skin bruising, epistaxis, haematuria

severe=
-gastro, intracerebral, drop in Hb

23
Q

warfarin reversal (5)

A
  1. no action
  2. omit warfarin dose(s)
  3. administer oral vit K
  4. administer clotting factors
  5. ​clinical + lab assessment of response​
24
Q

management of bleeding (6)

A

dependant on= sev of bleeding​ + INR​

speed of action=
vitamin K - 6 hours​
clotting factors - immediate​

25
new anticoagulants- direct activated factor X inhibitors (3)
-apixaban -edoxaban -rivaroxaban
26
new anticoagulants- direct thrombin inhibitors
dabigatran
27
new anticoagulants- benefits (3)
Oral and no monitoring required​ Less drug interactions​ Recently developed specific antidotes for reversal​
28
new anticoagulants- when used ? (3)
initially used instead of LMWH as prophylaxis in elective hip and knee replacement surgery​ used for treatment of DVT/PE​ introduced for stroke prevention in atrial fibrillation for new patients​ ​