Exam 2- hematologic Flashcards

(46 cards)

1
Q

Anticoagulants and Antiplatelets (MOA and type of modification)

A
  • prevention of clot formation
  • inhibition of specific clotting factors
  • inhibition of platelet actions
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2
Q

Heparin- type/class

A

anticoagulant/Indirect Thrombin Inhibitor

- Heparin is the traditional drug of choice for rapid anticoagulation.

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3
Q

Heparin MOA

A

Prevents clotting by activating antithrombin III, thus indirectly inactivating both thrombin and factor Xa. This inhibits fibrin formation

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4
Q

Heparin- Nursing implications (antidote, risks, labs)

A
  • Not absorbed by the intestinal tract and must be given by subcutaneous injection or IV infusion (Do not give IM)
  • Antidote: Protamine Sulfate
  • Risks: Bleeding, Heparin Induced Thrombocytopenia (HIT) (monitor platelets too)
  • Monitored through parital thromboplastin time (aPTT)
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5
Q

Heparin black box warning

A

Spinal/ epidural bleeding with epidural or Lumbar Puncture

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6
Q

Enoxaparin (Lovenox) class/type

A
  • Anticoagulants

- Low molecular weight heparin

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7
Q

Enoxaparin vs. Heparin (6)

A
  • More predictable anticoagulant response than heparin
  • Does not require laboratory monitoring
  • HIT less likely, but higher risk in someone who has had HIT from Heparin
  • Given subcutaneously
  • Can be administered at home
  • same antidote (protamine sulfate)
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8
Q

Warfarin (Coumadin) class/type

A
  • Vitamin K antagonist

- Anticoagulant

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9
Q

Warfarin (Coumadin) MOA

A

Inhibits Vitamin K, thereby preventing the synthesis of four coagulation factors (factor VII, IX, X, and prothrombin.)

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10
Q

Warfarin (Coumadin) Nursing implications/education

A
  • Given orally only
  • Monitored by prothrombin time (PT) and INR (PT-INR) (must be monitored closely)
  • Antidote: Vitamin K
  • Foods high in vitamin K may decrease anticoagulant effects
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11
Q

Warfarin (Coumadin) CI (1)

A
  • Do not use in pregnancy or lactation
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12
Q

Warfarin (Coumadin) Heparin bridge therapy

A
  • Warfarin effects may take 8 to 12 hr, and full therapeutic effect is not achieved for 3 to 5 days.
  • For clients in the hospital setting, explain the need for continued heparin infusion when starting oral warfarin
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13
Q

Dabigatran (Pradaxa) class/type

A

Direct Thrombin Inhibitor

Anticoagulant

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14
Q

Dabigatran (Pradaxa) MOA

A

Work by directly inhibiting thrombin, thus preventing a thrombus from developing.

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15
Q

Dabigatran (Pradaxa) Nursing Implications/Antidote

A
  • Stop 1-6 days prior to surgery
  • antidote- Praxibind
  • Take with food
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16
Q

Dabigatran (Pradaxa) Side effects (4)

A
  • GI discomfort
  • nausea, vomiting
  • esophageal reflux
  • ulcer formation
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17
Q

Dabigatran (Pradaxa) black box warning

A
  • Premature discontinuation INCREASES risk of thrombotic events
  • Epidural/spinal hematoma
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18
Q

Aspirin (ASA) goal/type

A
  • prevent initial clot formation

- antiplatelet

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19
Q

Aspirin (ASA) MOA

A
  • MOA: Blocks thromboxane
  • Result is a “slippery” platelet
  • Because platelets are slippery they do not clump together (aggregate)
  • If things aren’t sticking together, clotting is reduced
  • Irreversibly bound- once platelet bound to ASA it is done
20
Q

Aspirin (ASA) indications

A
  • 81mg “baby aspirin” used in prevention of MI and stroke
  • This low dose affects mostly platelets and will not have as much of an effect on COX-2 pain/fever
  • Lower dose thought to have lower side effects
  • In acute MI
  • chew Aspirin for faster absorption and take a higher dose (325mg)
21
Q

CLOPidogrel (Plavix) goal/class/type

A
  • ADP Receptor Blocker
  • prevent initial clot formation
  • antiplatelet
  • prevents CLots, an Oral Platelet Inhibitor (CLOPI).
22
Q

CLOPidogrel (Plavix) MOA

A
  • Blocks the adenosine diphosphate (ADP) receptor on the platelet membrane, preventing the platelet from “connecting” with other platelets.
  • slippery platelets
23
Q

Thrombolytics goals/indications/risks

A
  • Break down existing clots
  • Extreme risk of bleeding
  • Only used for life-threatening illnesses
  • Dissolve existing intravascular clots in MI and Stroke
  • Risk of bleeding with thrombolytics may outweigh benefits.
    (In patients greater than age 75- research shows do not decrease mortality)
24
Q

Alteplase (Activase) class

25
Alteplase (Activase) MOA
- Activate plasminogen and convert it to plasmin, which can dissolves fibrin clots - Reestablish blood flow so that viable tissue may be reperfused and not be destroyed
26
Alteplase (Activase) Key points
- Should be given within 6 hours of MI symptom onset or 3 hours of thrombotic stroke (60 minute max preferred) - With stroke, must rule out intracranial hemorrhage
27
Alteplase (Activase) Nursing implications (5)
- Follow strict manufacturer’s guidelines for preparation and administration - Monitor IV sites for bleeding, redness, pain - Monitor for bleeding from gums, mucous membranes, nose, injection sites - Observe for signs of internal bleeding (decreased BP, restlessness, increased pulse) - Hold pressure to puncture sites for at least 30 minutes
28
Aminocaproic acid (Amicar) class
hemostatics
29
Aminocaproic acid (Amicar) Use/specific indications (3)
- Hemostatics are used to promote the formation of clots. - Hemophilia - Post Op Cardiac Surgery - Aplastic anemia
30
Aminocaproic acid (Amicar) MOA
Occupies binding sites on plasminogen and plasmin | Prevents breakdown of fibrin clots by plasmin
31
Aminocaproic acid (Amicar) side effects (5)
- Muscle wasting and weakness  rhabdomyolysis - Formation of abnormal clots - Pulmonary thrombus or embolus - Hypotension (with rapid IV administration) - Bradycardia (with rapid IV administration)
32
Aminocaproic acid (Amicar) CI/cautions (4)
- History of CVA in last 3 months - Other thrombotic events - Severe HTN - Bleeding in the Urinary Tract
33
Aminocaproic acid (Amicar) Nursing implications (4)
- Check IV site - Monitor labs * Observe for signs of thrombosis/embolism - Chest pain - Leg pain - Difficulty breathing * Monitor urine - Color - Difficulty urinating
34
Epoetin alfa (Epogen) class
Erythropoietin/Hematopoietic growth factor
35
Epoetin alfa (Epogen) MOA
- Stimulates the division and differentiation of stem cells in the bone marrow - Promotes the synthesis of hemoglobin and causes a shift of marrow reticulocytes into the circulation
36
Epoetin alfa (Epogen) indications
- Treatment of anemia associated with renal failure | - Anemia associated with cancers
37
Epoetin alfa (Epogen) CI/cautions
- Hemoglobin above 12 g/dL | - Bone marrow malignancies
38
Epoetin alfa (Epogen) Black box warning (4)
- Thromboembolic events - Transient ischemic attack - Myocardial infarction - Hypertension
39
Epoetin alfa (Epogen) Nursing implications
- Assess labs closely - Watch vital signs - Monitor for thromboembolic events
40
Epoetin alfa (Epogen) Blood doping
- Elevating red blood cells in athletes bloodstream - Increasing the amount of red cells increase the amount of oxygen delivered to the muscles allowing them to work more efficiently - After 2-4 weeks of treatment effects can be seen - Athlete can then stop taking and benefit from effects during this window without continuing to take it - Epoetin can be metabolized within days making it difficult to detect, especially if it was stopped weeks prior - Difficult to detect Epoetin vs Naturally occurring erythropoietin
41
Filgrastim (Neupogen) class
Colony-stimulating factor
42
Filgrastim (Neupogen) MOA
- Increase in neutrophil production in the bone marrow | - Enhance the phagocytic and cytotoxic functions of existing neutrophils
43
Filgrastim (Neupogen) Side effects (8)
- Nausea and Vomiting very common - Fever/chills - Bone pain - Spleen rupture - Leukocytosis (too many neutrophils) - Respiratory failure - Retinal hemorrhage - MI
44
Filgrastim (Neupogen) indications
- Receiving chemotherapy or radiation therapy - Receiving bone marrow transplants - Chronic neutropenia - Immunosuppressive AIDS - Severe infections
45
Filgrastim (Neupogen) CI/cautions
- Sickle-cell disease - Pre-existing cardiac disease - Sensitivity to e.coli (used to produce drug)
46
Filgrastim (Neupogen) Drug interactions (2 and why)
* Not administered until at least 24 hours after a chemotherapy session - Chemo and Neupogen have opposite actions * Lithium - Lithium promotes neutrophil release increasing risk for leukocytosis