129 Management of Acute Coronary Syndromes Flashcards

1
Q

ST segment elevation myocardial infarction

A

usually associated with: Total obstruction without good residual flow and a large degree of heart damage

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2
Q

Spectrum of CAD

A
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3
Q

Platelet activation in vascular injury/ACS

A
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4
Q

Mechanisms of oral antiplatelet therapies

A
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5
Q

Intersection of anti-platelet and anti-coagulation cascade drugs for ACS

A
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6
Q

New Classification of MI

A
  • 1 Spontaneous MI related to ischemia due to a primary coronary event, such as plaque erosion and/or rupture, fissuring, or dissection
  • 2 MI secondary to ischemia due to an imbalance of O2 supply and demand, as from coronary spasm or embolism, anemia, arrhythmias, hypertension, or hypotension
  • 3 Sudden unexpected cardiac death, including cardiac arrest, often with symptoms suggesting ischemia with new ST-segment elevation; new left bundle branch block; or pathologic or angiographic evidence of fresh coronary thrombus—in the absence of reliable biomarker findings
  • 4a MI associated with PCI
  • 4b MI associated with documented in-stent thrombosis
  • 5 MI associated with CABG surgery
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7
Q

Time course of MI enzyme markers

A

Re-establishemnt of blood flow makes the enzyme markers peak earlier

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8
Q

STEMI Guidelines:
Acute Medical Therapy

A
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9
Q

“Wavefront” Phenomenon

A
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10
Q

Fibrinolytic Reperfusion—Pros and Cons

A
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11
Q

Currently Available Fibrinolytics

A
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12
Q

Risk Score for UA/NSTEMI (7)

A
  1. Age ≥65 y
  2. ≥3 CAD risk factors (high cholesterol, family history, hypertension, diabetes, smoking)
  3. Prior coronary stenosis ≥50%
  4. Aspirin in last 7 days
  5. ≥2 anginal events ≤24 h
  6. ST-segment deviation

7.Elevated cardiac markers
(CK-MB or troponin)

N-STEMI:

  • Reinfarction occurs more frequently than following STEMI
  • There is less of an urgency to perform PTCA within 90 minutes of presentation
  • Discharge medications are identical to patients with STEMI
  • The incidence of mortality at one year is similar to patients with STEMI
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13
Q

Risk Stratification
to Target Therapies in UA/NSTEMI

A

*Aspirin super effective*, clopidogrel on top of aspirin increased benefit, with or without PCI benefit of GP2b3a inhibitor FOR PATIENTS WITH POSITIVE TROPONINS

•Four classes of anticoagulants are available

–Unfractionated heparin (UFH)

–Low-molecular-weight heparins (LMWH)

–Direct thrombin inhibitors

–Factor Xa inhibitors

  • Current guidelines support use of UFH and LMWH with enoxaparin preferred over UFH (Class IIa)
  • Recent studies suggest direct thrombin inhibitors (bivalirudin) and factor Xa inhibitors (fondaparinux) may be appropriate new options for anticoagulation but in limited patient populations
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14
Q

Medications at Discharge for NSTEMI

A
  • •Antiplatelet therapy (aspirin/ADP antagonist such as clopidogrel/prasugrel/ticagrelor and for some—vorapaxar)
  • •Beta blocker
  • •Angiotensin converting enzyme inhibitor/angiotensin receptor blocker
  • •Statin
  • •Reduction of cardiac risk
    • –Control BP: 130/80
    • –Stop smoking
    • –Increase activity
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15
Q

In-hospital mortality rate for ACS

A

4.8%

Hospitals that follow guidelines for therapy better have lower rates of mortality (5.95%–>4.16%)

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