Antiplatelets/coags/thrombolytics Flashcards

1
Q

Aspirin:

MOA:

A

inhibits thromboxane A2 synthesis by inhibition of COX 1

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2
Q

Aspirin: uses

A

prophylaxis of transient cerebral icchemia, reduce incidence of MI, decrease mortality in pre and post MI patients

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3
Q

aspirin is frequenty used with what?

ADRs:

A

other anticlotting drugs (heparin/clopidogrel)

NSAIDs/acetaminophen inhibit COX1 and can antagoinze platelet inhibition by aspirin

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4
Q

prasugrel, cangrelor, clopidogrel MOA:

A

interfere with binding of ADP to platelet receptors thus inhibiting activtion of GP IIb/IIIa

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5
Q

prasugrel, cangrelor, clopidogrel uses:

A

acute coronary syndrome, recent MI, CVA, PAD, stent insertion during MI

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6
Q

prasugrel, cangrelor, clopidogrel which is not effect by food?

ADRs of these drugs?

A

clopidogrel

prolonged bleeding time with no antidote, thrombocytopenia purpura

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7
Q

prasugrel, cangrelor, clopidogrel which is not effect by food?

ADRs of these drugs?

use caution clopidogrel in pts on what?

A

clopidogrel

prolonged bleeding time with no antidote, thrombocytopenia purpura

inhibit cyp450: interfere with metabolism of phenytoin, tolbutamide, warfarin, fluvastatin, tamoxifen

on PPIs

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8
Q

Ticagrelor: similar to prasugrel, clopidogrel, ticlopidine

prevention of what?

A

thrombiotic events in pts with acute coronary syndrome or MI with ST elevations

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9
Q

Abciximab: MOA?

given with what?

ADRs?

how long do antiplatelet effects last?

A

monoclonal AB directed against GP IIb/IIIa receptors

IV heparin/ASA as adjunct to percutaneous coronary intervention for provention of cardiac ischemic comps

bleeding

24-48 hours

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10
Q

eptifibatie/tirofiban: MOA

use?
effect can last for how long after d/c

major SE?

A

block GP IIb/IIIa receptor

decreases incidence of thrombiotic compls associated with acute coronary syndromes

4 hours

bleeding

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11
Q

Dipyridamole:

MOA?

use?

A

coronary vasodilator, phosphodiesterase inhibitor decreasing thromboxane A2 (inhibits thrombus)

prophylactic used to tx angina pectoris

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12
Q

Varapaxar:

MOA?

indication?

CI?

DDI?

A

protease activated receptor-1 antagonist

(does not effect ADP, collagen or thromboxane aggregation) (does not affect coagulation parameters or bleeding time)

reduction of thrombotic CV events in pts w/history of MI or PAD

hx of CVA, TIA or ICH, or active bleeding

ADR: bleeding

DDI- cyp3A4

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13
Q

Heparin: MOA:

A

binds to antithrombin III and potentiates its inactivation effects on serine proteases (factos IIa and Xa)

LMWH only affects Factor Xa!!

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14
Q

Heaprin uses:

A

DVT, PE, prophylactic to prevent post op VE in elective surgery, MI and a fib

reduced coronary artery rethrombosis, DOC in pregnancy for prosthetic heart valves and VE (doesnt cross placenta)

LMWH: (weight based, predictable effects very useful in outpt)

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15
Q

what is a dose based on for heparin?

A

aPTT

LMWH does not need aPTT

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16
Q

half life of heparin is increased when?

A

pts with cirrhosis, renal insufficiency and is dose related with heparin

17
Q

ADRs of heparin?

A

bleeding (manage by admin of protamine sulfate, hypersensitivity, thrombosis (minimized with low dose), hyperkalemia, THROMBOCYTOPENIA (type 1: immunoloigc occurs within first 5 days, type 2: IgG, degradation of platelets can result in thrombocytpenia and thrombosis, occurs 5-14 days and can range fro mild to life threatening, platelets count can drop more than 50% but this is very rare)

18
Q

CI of heparin:

A

IM injection hematoma, HSN, bleeding, ETOH, brain/eye/spinal cord surgery

19
Q

Danaparoid: MOA?

uses?
ADRs?

A

Anti Factor Xa and antithrombin

prophylaxis of DVT in hip replacement surgery and can tx HIT type II

pork allergy, hemorrhage

20
Q

Fondaparinux:

MOA?

A

synthetic pentasaccharide factor Xa inhibitor

low risk of HIT, renally excreted

21
Q

Direct factor Xa inhibitors:

(rivaroxaban, apixaban, edoxaban, betrixaban)

MOA?

substitute for?

A

act directly on factor X without using antithrombin

vit K antagonists or LMWH

prophylaxis/tx for DVT/PE in adults undergoing hip/knee replacement, long term tx to prevent recurrence, CVA prophylaxis in pts with non valvular afib

22
Q

Direct factor Xa inhibitors:

(rivaroxaban, apixaban, edoxaban, betrixaban)

ADRs:

A

no way to reverse

bleeding, fainting, itching, anemia, muscle spasms

edoxaban not to be used in pts with non valvular afib

23
Q
bivalirudin: 
MOA?
uses? 
half life? 
ADR:
A

direct thrombin inhibitor (potent, reversible)

unstable angina undergoing percutaenous transluminal coronary angioplasty, protein IIb/IIIa inhibitor in percutaenous coronary intervention, pts with or at risk of HIT undergoing percutaneous cocornary intervention

25 min

bleeding, HA, hypotension

24
Q

Argatroban: MOA:

A

direct thrombin inhibitor

IV prophylaxis or tx of throbmosis in pts with HIT

bleeding, dyspnea, hypotension

25
Q

Dabigatran: MOA?

A

direct thrombin inhibitor

reduce risk of CVA and systemic embolism in pts with non valvular a fib

reduce dose in renal impairment

bleeding

26
Q

Idarucizumab:

MOA:

A

human monoclonal AB fragment

indicated in pts tx with dabigatran when reversal of anticoagulant effects is needed!!!!!!!!!!

for emergency procedures in life threatening uncontrolled bleeding

IV-higher affinity than the binding affinity of dabigatran to thrombin

Preacution:

thromboembolic risk, HSN, pts with heredity fructose intolerance

ADR-hypokalemia, deleirum, constipation, pyrexia, pneumonia