Clinical Assessment of ACS Flashcards

1
Q

Thrombolysis in myocardial infarction (TIMI) risk score

A

1 point is given for each of the following: 65 or older, three or more risk factors for CAD, prior coronary stenosis 50% or greater, ST deviation on ECG, two or more anginal events in previous 24 hours, aspirin use in previous 7 days, and elevated cardiac biomarkers

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2
Q

TIMI score assessment

A

Risk of mortality, new or recurrent MI, or severe recurrent ischemia through 14 days; 0–2 is low risk, 3 is intermediate risk, and 4 or more is high risk

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3
Q

NSTE-ACS UA objective findings

A

ST-segment depression, T-wave inversion, or transient or nonspecific ECG changes
No positive biomarkers for cardiac necrosis

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4
Q

NSTEMI objective findings

A

ST-segment depression, T-wave inversion, or transient or nonspecific ECG changes
Positive biomarkers (troponin I or T elevation) - myocardial injury

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5
Q

STEMI objective findings

A

ST-segment elevation > 1 mm above baseline on ECG in two or more contiguous leads
Positive biomarkers (troponin I or T elevation) -myocardial necrosis

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6
Q

Fibrinolytic therapy indication

A

If PCI cannot be done within 120 minutes, performance measure for lytic administration includes a door-to-needle time of 30 minutes

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7
Q

Early invasive strategy indication

A

NSTE-ACS who have refractory angina or hemodynamic or electrical instability or those with high risk on the basis of clinical findings

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8
Q

Ischemia-guided therapy indication

A

Recommended for patients with a low risk score (TIMI 0 or 1, GRACE less than 109); acute chest pain with a low likelihood of ACS who are troponin negative (preferred for low-risk women)

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9
Q

Initial Therapies for ACS

A

Morphine
Oxygen
Nitroglycerin
ASA
Beta Blocker

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10
Q

Nitroglycerin contraindications

A

Sildenafil or vardenafil (use within 24 hr) or tadalafil (use within 48 hr); SBP < 90 mm Hg or ≥ 30 mm Hg below baseline, HR < 50 beats/min, HR > 100 beats/min in absence of symptomatic HF; right ventricular infarction

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11
Q

Oral Beta blocker initiation

A

within 24 hr in patients who do not have signs of HF, evidence of low-output state, increased risk of cardiogenic shock, or other contraindications to β blockade (e.g., PR interval > 0.24 s, second- or third-degree heart block, active asthma, or reactive airway disease)

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