Peripheral Arterial Disease Flashcards

1
Q

What is the most common for of PAD?

A

progressive narrowing of arteries due to atherosclerosis

Plaque formation in the arteries, resulting in decreased blood flow to the legs

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2
Q

PAD is associated with elevated risk of ________ morbidity and mortality even in the absence of prior hx of AMI (acute myocardial infarction), or stroke.

A

cardiovascular disease

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3
Q

What are the treatment goals for PAD?

A
  • improving quality of life
  • controlling comorbid conditions contributing to PAD
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4
Q

What are some comorbid conditions contributing to PAD?

A
  • HTN
  • Hyperlipidemia
  • Diabetes
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5
Q

Will patients in the early stages of PAD show signs of symptoms?

A

NO

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6
Q

What are the 2 most common characteristics of PAD?

A
  • intermittent claudication
  • pain @ rest in the lower extremities
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7
Q

What is the primary indicator in PAD?

A

Intermittent Claudication

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8
Q

What are some descriptors patient use to explain PAD?

A

Fatigue, discomfort, cramping, pain or numbness in buttock, thigh ot calf during exercise and resolves within a few minutes with rest.

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9
Q

What would a physical examination of PAD reveal?

A
  • cool skin temperature
  • thickened toenails
  • lack of hair on calf, feet, toes
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10
Q

T/F: There are no laboratory tests you woud run for PAD

A

TRUE

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11
Q

What is the main diagnostic test you would perform?

A

Ankle Brachial Index: highly sensitive and specific

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12
Q

Fontaine Stage I: Pt is…

A

asymptomatic

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13
Q

Fontaine Stage II: Pt presents w/

A

mild claudication & limb symptoms but NO limitation walking

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14
Q

Fontaine Stage IIa: pt presents w/

A

moderate claudication/limb symptoms

can walk >2 blocks without stopping

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15
Q

Fontaine Stage IIb: pt presents w/

A

severe claudication

can only walk <2 blocks w/o stopping

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16
Q

Fontaine Stage III: pt presents w/

A

Ischemic rest pain

17
Q

Fontaine Stage IV: pt presents w/

A

ischemic ulceration or ischemic gangrene

18
Q

Treatments for PAD

A
  • smoking cessation
  • exercise
  • Percutaneous transluminal angioplasty (PTA) or stent placement
  • Drug therapy
19
Q

What will drug therapy control?

A
  • cholesterol
  • blood pressure
  • blood sugar
  • prevent blood clots
  • provide symptom relief
20
Q

Which drug is this the Mechanism of Action for:

Irreversibly inhibits prostaglanding cyclooxygenase in plateles

Prevents formation of thromboxane A2

21
Q

Which drug has the following side effects?

GI upset/bleeding

22
Q

Which drug has the following contraindications:

active bleeding, hemophilia, thrombocytopenia, deficiency of platelets

23
Q

What is synthesized from Arachidonic Acid via the COX pathway and plays a role in Aspirin MOA?

  • powerful vasconstrictor
  • platelet agonist
A

Thromboxane Az (TXA2)

24
Q

MOA: inhibits binding of ADP analogues to its platelet receptor (P2YI2) causing ireversible inhibition of plateles

A

Clopidogrel and Ticlodipine

25
**Side effects:** chest pain, **purpura,** generalized pain, rash **Contraindications:** active pathologic bleeding **(peptic ulcer, intracranial hemorrhage)** **\*\*Recommend this over no antiplatelet therapy**
Clopidogrel
26
**Side Effects:** leuko**penia**, rash, thrombocyto**penia**, neutro**penia**, agranulocytosis, aplastic anemia. **Contraindications:** active bleeding, hemophilia, thrombocytopenia
Ticlodipine
27
**T/F:** Ticlodipine is recommended over clopidogrel
**False:** clopidogrel is recommended over ticlodipine
28
**MOA:** inhibits activity of **adenosine and phosphodiesterase**, increasing **cyclic AMP**, leading to inhibition of platelet aggregation. Stimulates **PGD2**, resulting in **vasodilation**
**Dipyridamole** and **cliostazol**
29
**Side effects:** angina, dyspnea, hypotension, headache, dizziness **Contraindications:** active bleeding, CAD (coronary steal syndrome)
Dipyridamole
30
**Side Effects:** fever, infections, tachycardia **Contraindications:** **All CHF patients (decreased survival)**
Cliostazol
31
**MOA:** Alters **RBC flexibility**, decreases **platelet adhesion**, reduces **blood viscosity**, decreases **fibrinogen concentration**
Pentoxifylline
32
**Side effects:** dyspnea, nausea, vomiting, headache, dizziness **Contraindications:** recent **retinal/cerebral hemorrhage**; active bleeding
Pentoxifylline
33
**MOA: PAR-1** (Protease-activated receptor-1) **antagonist.** Long half life — effectively irreversible: **lasts 4 weeks after stopping**
Vorapaxar
34
**Side Effects:** **\>10% bleeding** 1-10%: depression, rash, **iron deficiency**, retinopathy Monitor signs of bleeding, H&H **Contraindications:** **\*\*US Box warning: Hx of stroke, TIA, intracranial hemorrhage, active bleeding** **- concern for use in patients with hepatic or renal impairment due to increased risk of bleeding**
**Vorapaxar**
35
**T/F:** No RCTs that state that ASA, or other antiplatelet therapies can actually prevent or delay the progression of PAD
True
36