Table 9: Summary of drugs commonly used in the emergency
department to treat patients with symptoms suggestive of unstable
angina
Drug category Clinical When to avoid[1] Usual dose
condition (low-high)
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Aspirin Diagnosis of Hypersensitivity, 324 mg (160-
unstable active bleeding, 324)
angina or severe bleeding
acute MI risk
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Heparin Unstable Active bleeding, 80 units/kg
angina in history of IV bolus with
high-risk heparin-induced constant IV
category and thrombocytopenia, infusion at
some severe bleeding 18
intermediate- risk, recent units/kg/hr
risk patients stroke titrated to
maintain aPTT
between 46
and 70
seconds[2]
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Nitrates Ongoing pain Hypotension Sublingual
or ischemia (1-3
tablets)[3]
IV (5-100
micro-g/min)
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Beta Blockers Diagnosis of PR ECG segment Oral dose
unstable >0.24 seconds, 2 appropriate
angina degrees or 3 for specific
degrees AV drug
block, heart IV metoprolol
rate <60, (1-5 m slow
systolic blood IV every 5
pressure <90 minutes to 15
mmHg shock, left mg total)
ventricular
failure with IV propranolol
CHF, severe 0.5 to 1.0 mg
reactive airway
disease IV atenolol 5
mg every
minutes to 10
mg total
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Narcotics Persistent Hypotension, Morphine
pain respiratory sulfate 2 to
following depression, 5 mg IV
initial confusion,
therapy with obtundation
nitrates and
beta blockers
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[1] Allergy or prior intolerance contraindication for all.
[2] Dose regimen assumes a mean control aPTT of 30 seconds and a
therapeutic goal of 1.5 to 2.5 times control.
[3] Patients with symptoms suggestive of unstable angina and
ongoing pain should be given sublingual NTG 0.3 to 0.4 every 5
minutes until discomfort is relieved, three tablets have been
given, or limiting symptoms or signs develop. If discomfort is
still present after three tablets, IV NTG should be started
promptly at a dose of 5 micro-/min and titrated up to 75 to 100
micro-g/min or limiting side effects.
Note: Some of the recommendations in this guideline suggest the
use of agents for purposes or in doses other than those specified
by the Food and Drug Administration (FDA). Such recommendations
are made after consideration of concerns regarding nonapproved
indications. Where made, such recommendations are based on more
recent clinical trials or expert consensus.