Exam 2 Flashcards

1
Q

What protein prevents clot formation?

A

Anti-thrombin III

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2
Q

What is heparin used for?

A

Prophylaxis and treatment of thromboembolic events
Prevents formation of new clots and prevents enlargement of existing clots

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3
Q

What route and frequency is heparin usually given for PROPHYLACTIC anticoagulation?

A

subcutaneous, q8-12hrs

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4
Q

What route is heparin given for THERAPEUTIC anticoagulation?

A

Intermittent or continuous IV infusion

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5
Q

What is the dosing of heparin based on when used for therapeutic anticoagulation?

A

weight-based dosing, and a bolus (loading dose) is given first

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6
Q

What lab needs to be monitored when giving heparin for therapeutic anticoagulation?

A

aPTT

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7
Q

What does Activated Partial Thromboplastin Time (aPTT) measure?

A

Time, in seconds, it takes for a clot to form

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8
Q

What is the normal range for aPTT?

A

30-40 seconds

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9
Q

What is the therapeutic range for aPTT? What value would be concering?

A

Therapeutic range 1.5-2.5x the control
Concerning if greater than 70 seconds

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10
Q

How often is aPTT drawn for an INTERMITTENT infusion?

A

aPTT drawn 30 min before each dose initial therapy and then periodically

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11
Q

How often is aPTT monitored for continuous infusions? What do you do if aPTT is above theraputic?

A

q4-6 hrs
If above therapeutic stop heparin for 1 hr and redraw aPTT

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12
Q

What type of heparin is Heparin-Induced Thrombocytopenia (HIT-Type I) common with?

A

Unfractionated heparin (UFH) rather than enoxaparin (low-molecular-weight heparin, LMWH)

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13
Q

What is the onset time for HIT-Type 1?

A

Within 2 days of starting Heparin

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14
Q

What happens to the platelet count in HIT-Type 1?

A

Drops slightly but normalizes on its own

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15
Q

What is the management for HIT-Type 1?

A

Heparin therapy can continue, as this form is not dangerous.

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16
Q

What is the cause of HIT-Type 2?

A

It is an immune reaction where heparin binds to platelet factor, triggering antibody formation

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17
Q

What is the onset time for HIT-Type 2?

A

Develops 5-14 days after starting heparin

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18
Q

What are the effects of HIT-Type 2?

A

Hypercoagulable state - increased risk of blood clots despite low platelet count.
Increased platelet activation - antibody coated platelets become overactive, leading to clot formation.
Macrophages remove platelets.
Thrombotic complications.

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19
Q

What is the management of HIT-Type 2?

A

Stop heparin immediately.
Use a non-heparin anticoagulant.

20
Q

What is enoxaparin (Lovenox) used for?

A

VTE prophylaxis or Tx of DVT/PE
“Bridge therapy”

21
Q

What is the MOA of enoxaparin?

A

inhibits factor 10a

22
Q

What should you assess for when giving enoxaparin?

A

Thrombocytopenia and bleeding

23
Q

What is the dose and frequency of enoxaparin when given prophylacticly?

A

30-40mg daily or q12 h

24
Q

What is the dose for enoxaparin when given for the Tx of DVT or PE?

A

1mg/kg q12h or 1.5mg/kg q24hr (weight based)

25
Q

What are the nursing implications for Heparin and enoxaparin (Lovenox)?

A

Never use heparin and enoxaparin concurrently.
Assess for signs of bleeding, and stop medication if found.
Contraindicated w hemorrhagic stroke and uncontrolled HTN.
Monitor platelet count for thrombocytopenia (more critical with heparin).
D-D interactions: NSAIDS, antiplatetes
Herbal products such as, ginger, ginko, green tea, ginseng, increase risk of bleeding

26
Q

What is the antidote for Heparin?

A

protamine sulfate IV

27
Q

What is the primary function of neutrohils?

A

Neutrophils respond to bacterial infections and have phagocytic fuction

28
Q

How long do neutrophils live?

29
Q

What do neutrophil granules contain?

A

Granules contain antimicrobial proteins that help kill bacteria

30
Q

When are band cells (immature neutrophils) produced and what is their function?

A

The body stimulates band cells (immature neutrophils) during a severe inflammatory response. Band cells are capable of phagocytosis.

31
Q

What does an increased number of band cells indicate?

A

An increase in band cells is called a “left shift,” which suggests an active infection or inflammation.

32
Q

What is the normal range for band cells?

A

Band cells normally range from 0-5%

33
Q

What is the primary function of lymphocytes?

A

Lymphocytes provide immunity against pathogens and help destroy invading viruses and some bacteria.

34
Q

What are the functions of monocytes?

A

Migrate into tissues and transform into macrophages
Phagocytic cells
Ingest bacteria, debris, and old/defective RBCs

35
Q

What is the role of C-reactive protein (CRP)?

A

CRP is a non-specific inflammatory marker that is present in tissue injury & acute inflammation.

36
Q

When does CRP appear after an inflammatory response? When does CRP peak?

A

CRP appears 6-10 hours after inflammation begins.
CRP peaks 48-72 hours after the start of inflammation.

37
Q

What conditions can elevate CRP levels?

A

CRP may be elevated with hypertension (HTN), smoking, and cardiovascular disease (CVD).

38
Q

What is the normal CRP level?

A

Less than 3 mg/dL.

39
Q

What are non-modifiable risk factors for CAD?

A

Age and gender - greater than 45 years for males and greater than 55 years for females
Ethnicity - African Americans, Native Americans
Genetic predisposition and family hx

40
Q

What are the modifiable risk factors for CAD?

A

Abnormal cholesterol & lipid levels
HTN
DM
Tobacco use
Physical inactivity
Obesity

41
Q

What contributes to high triglycerides?

A

Excess sugars and calories

42
Q

Where are triglycerides stored in the body?

A

in adipose tissue

43
Q

How is cholesterol produced?

A

It is made by the liver and comes from animal dietary sources

44
Q

How does excess cholesterol affect health?

A

Excess cholesterol contributes to atherosclerosis

45
Q

When is cholesterol biosynthesis higher?

A

Cholesterol biosynthesis is higher in the evening

46
Q

What are the indications for the use of Penicillin (PCN)?

A

empiric therapy, respiratory therapy, intra-abdominal infection

47
Q

What are the adverse effects with Penicillin?

A

cross-reactivity with cephalosporins allergy