drugs affecting coagulation Flashcards

1
Q

extrinsic pathway

A

cascade of clotting factors in blood that has escaped the vascular system to form a clot on the outside of the vessel

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2
Q

hemostatic agents

A

drugs that stop blood loss usually by blocking the plasminogen mechanism and preventing blood clot dissolution

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3
Q

intrinsic pathway

A

cascade of clotting factors leading to the formation of a clot within an injured vessel

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4
Q

plasminogen

A

natural clot dissolving system; converted to plasmin (fibrinolysin) by many substances to dissolve clots that have formed and to maintain the patency of injured vessels

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5
Q

thrombolytic agents

A

drugs that lyse, or break down, a clot that has formed; these drugs activate the plasminogen mechanism to dissolve fibrin threads

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6
Q

clotting factors

A

substances formed in the liver that react in a cascading manner to cause the formation of thrombin from prothrombin; thrombin breaks down fibrin threads from fibrinogen to form a clot

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7
Q

antiplatelet agents

A

decrease the formation of the platelet plug by decreasing the responsiveness of the platelets to stimuli that would cause them to stick and aggregate on a vessel wall

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8
Q

aspirin

A
antiplatelet medication (book prototype)
indications: reduction of r/o TIA, reduction of death or nonfatal MI in pts with hx of infarction or unstable angina
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9
Q

aspirin pharmacokinetics

A

PO: onset 5-30 min

peak 0.25 - 2h

duration: 3 - 6 hrs

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10
Q

aspirin side effects

A

black box warning for fatal bleeding events

headache
dizziness
weakness
nausea/GI upset
skin rash
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11
Q

arterial thrombosis

A

most common cause of MI, stroke, and gangrene

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12
Q

venous thrombosis

A

leads to pulmonary embolism and postphlebitic syndrome

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13
Q

clopidogrel (Plavix)

A

antiplatelet drug (powerpoint prototype)

used to reduce atherosclerotic events

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14
Q

clopidogrel (Plavix) pharmacokinetics

A

administered PO, metabolized in liver. protein bound,

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15
Q

clopidogrel (Plavix) pharmacodynamics

A

inhibits binding of ADP to its platelet reception and subsequent ADP mediated activation of glycoprotein complex to inhibit platelet aggregation

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16
Q

clopidogrel (Plavix) contraindications

A

hypersensitivity, active bleeding disorders

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17
Q

clopidogrel (Plavix) adverse effects

A

bleeding, GI distress, neutropenia

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18
Q

clopidogrel (Plavix) interactions

A

tamoxifen, tolbutamide, warfarin, torsemide, fluvastatin, many NSAIDs

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19
Q

clopidogrel (Plavix) nursing diagnoses

A

risk for injury: increased risk for bleeding r/t decreased platelet aggregation

risk for nause: r/t adverse effects

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20
Q

clopidogrel (Plavix) planning/interventions

A

max therapeutic effects: ensure it is taken routinely

min adverse effects: take with food to reduce GI distress

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21
Q

alteplase recombinant (Activase)

A

thrombolytic drug (powerpoint prototype)

may be given systemically or at the site of the clot

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22
Q

alteplase recombinant (Activase) indications

A

acute MI
PE
acute ischemic stroke
thromboembolic conditions

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23
Q

alteplase recombinant (Activase) pharmacokinetics

A

given IV; rapidly cleared from plasma

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24
Q

alteplase recombinant (Activase) pharmacodynamics

A

converts plasminogen to plasmin

acts in same way as endogenous tPA

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25
Q

alteplase recombinant (Activase) contraindications

A

hypersensitivity, active internal bleeding

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26
Q

alteplase recombinant (Activase) adverse effects

A

internal or superficial bleeding

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27
Q

alteplase recombinant (Activase) interactions

A

other anticoagulant and antiplatelet drugs

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28
Q

alteplase recombinant (Activase) nursing diagnosis

A

risk for injury: r/t drug induced bleeding

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29
Q

alteplase recombinant (Activase) planning/intervention

A

max therapeutic effect: reconstitute in sterile water for injection without preservatives

min adverse effect: closely monitor for signs of active bleeding, ensure pt connected to cardiac monitor

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30
Q

antihemophilic factor

A

clotting factor (powerpoint prototype)

replaces normal blood clotting factor in event of deficiency

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31
Q

antihemophilic factor indications

A

deficiency of clotting factor VIII

hemophilia A

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32
Q

antihemophilic factor pharmacokinetics

A

given IV

T 1/2: 4-24 hrs

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33
Q

antihemophilic factor pharmacodynamics

A

Factor VIII is an essential component of blood clotting and is required for conversion of prothrombin to thrombin

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34
Q

antihemophilic factor contraindications

A

hypersensitivity to mouse protein

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35
Q

antihemophilic factor adverse effects

A

anaphylaxis
urticaria
nausea
chills

36
Q

antihemophilic factor nursing diagnosis

A

risk for injury: hemorrhage r/t deficiency of clotting factor VIII

37
Q

antihemophilic factor planning/interventions

A

max therapeutic effect: refrigerate AHF until used, warm before reconstitution

min adverse effect: administer AHF within 3 hrs of dilution, administer IV only

38
Q

aminocaproic acid (Amicar)

A

hemostatic drug (powerpoint prototype)

stops blood loss by enhancing coagulation

39
Q

aminocaproic acid (Amicar) indications

A

life threatening hemorrhage

40
Q

aminocaproic acid (Amicar) pharmacokinetics

A

given PO or IV

excreted mostly unchanged in urine

41
Q

aminocaproic acid (Amicar) pharmacodynamics

A

blocks action of plasminogen activators

interferes with binding of active plasmin to fibrin

42
Q

aminocaproic acid (Amicar) contraindcations

A

active intravascular clotting disorders

43
Q

aminocaproic acid (Amicar) adverse effects

A

GI distress (n/v/d), headache, dizziness, seizures, hypotension, arrhythmias, tinnitus, nasal congetsion, abdominal cramps, diuresis

44
Q

aminocaproic acid (Amicar) interactions

A

oral contraceptives or estrogen

45
Q

aminocaproic acid (Amicar) nursing diagnosis

A

risk of altered cardiovascular perfusion: r/t volume loss 2/2 uncontrolled bleeding or thrombophlebitis

46
Q

aminocaproic acid (Amicar) nursing intervention

A

min adverse effects:
monitor vitals prior to and during therapy
administer via IV infusion pump
monitor I&O and neurologic status

47
Q

aminocaproic acid (Amicar) pt education

A

change position slowly

48
Q

parenteral anticoagulants

A

prevent the conversion of fibrinogen to fibrin

49
Q

oral anticoagulants

A

prevent synthesis of factors dependent on vitamin K

50
Q

heparin pharmacotherapeutics

A

prototype
parenteral anticoagulant that interferes with final steps of clotting cascade
safe for pregnant women
occurs naturally in body

51
Q

heparin pharmacokinetics

A

given IV or subQ

metabolized in liver, excreted in urine

52
Q

heparin pharmacodynamics

A

rapidly promotes the inactivation of factor X, which in turn, prevents conversion of prothrombin to thrombin

53
Q

heparin contraindications

A

hypersensitivity

54
Q

heparin adverse effects

A

bleeding, thrombocytopenia

55
Q

heparin nursing diagnosis

A

risk for injury:
hemorrhage r/t drug therapy
thrombocytopenia 2/2 drug therapy

56
Q

heparin planning/intervention

A

max therapeutic effect: monitor lab values, allow heparin to reach steady levels before PTT is measured

min adverse effect: decrease dosage if PTT exceeds desired range

57
Q

heparin antidote

A

protamine sulfate

58
Q

warfarin

A

oral anticoagulant

used prophylactically for pts with long term r/o thrombus formation

59
Q

warfarin pharmacokinetics

A

given PO
highly protein bound
metabolized in liver, excreted through bile

60
Q

warfarin pharmacodynamics

A

competitively blocks vitamin K at sites of action

61
Q

warfarin contraindications

A

active bleeding, bleeding disorders

62
Q

warfarin adverse effects

A

bleeding, hemorrhage

63
Q

warfarin nursing diagnosis

A

risk for injury: r/t adverse effects of warfarin

64
Q

warfarin planning/intervetions

A

max therapeutic effect: dosage should be individualized until PT or INR is in therapeutic range

65
Q

warfarin antidote

A

vitamin K (phytonadione)

66
Q

warfarin pt education

A

take drug at the same time every day

67
Q

warfarin dose

A

titrated based on PT and INR

68
Q

enoxaparin (Lovenox)

A

low molecular weight heparin (powerpoint prototype)
used to prevent thromboembolus (DVT) and ischemic complications in clients with unstable angina/select MIs when combined with aspirin

69
Q

enoxaparin (Lovenox) adverse effects

A

bleeding, anemia, thrombocytopenia, local pain

70
Q

enoxaparin (Lovenox) interactions

A

anticoagulant effect enhanced by digitalis, tetracyclines, nicotine, and antihistamines

71
Q

enoxaparin (Lovenox) contraindications

A

hemorrhage, GI ulceration, hemophilia, thrombocytopenia, liver disease, renal disease, uncontrolled HTN, recent CNS injury or stroke, recent surgery

72
Q

enoxaparin (Lovenox) nursing interventions

A

check PTT prior to administration
avoid injection near scar tissue
use electric shaver

73
Q

enoxaparin (Lovenox) cautions

A

pts with malabsorption disease, chronic diarrhea, and vitamin C deficiency may experience increased anticoagulation effect

74
Q

values to monitor warfarin therapy

A

PT and INR

75
Q

A nurse will use extreme caution when administering heparin to a patient with what conditions?

A

peptic ulcer
liver disease
after surgery

because those patients would have greater risk for hemorrhage or excessive blood loss.

76
Q

priority nursing assessment before administering heparin

A

aPTT

77
Q

patients taking warfarin must monitor intake of

A

vitamin K

78
Q

patients taking warfarin should not have

A

grapefruit juice

chamomile (increased r/o bleeding)

79
Q

A client is being administered heparin IV and has been started on warfarin. The client asks the nurse why she is taking both medications. What is the nurse’s most accurate response?

A

“Warfarin takes 3–5 days to develop anticoagulant effects, and you still need heparin.”

80
Q

how long does warfarin take to be effective?

A

anticoagulant effects do not occur for 3 to 5 days after warfarin is started because clotting factors already in the blood follow their normal pathway of elimination

81
Q

healthy INR for anticoagulant therapy

A

2-3

82
Q

why give LMWH (Lovenox) over heparin?

A

low-molecular-weight heparins are associated with less thrombocytopenia than standard heparin.

83
Q

when to use an antiplatelet agent or an anticoagulant?

A

Anticoagulants are more effective in preventing venous thrombosis.

Antiplatelet drugs are used to prevent arterial thrombosis.

84
Q

for CAD, anticoagulant or antiplatelet?

A

antiplatelet – CAD has an arterial rather than venous etiology.

85
Q

The nurse is concerned that the health care provider does not order routine aPTTs when the client is receiving LMWH for thromboembolism prophylaxis. When the nurse calls the provider with the nurse’s concern, what will be the response?

A

aPTTs are not needed.

Monitoring of aPTT is not necessary with low-dose standard heparin given sub-Q for prophylaxis of thromboembolism or with the LMWHs.