Acute Coronary Syndrome (ACS) : Basic Principles For ACS
Acute Coronary Syndrome (ACS) : Basic Principles For ACS
MARCH
2013
All
All HIGH Probability ACS patients should be transferred to a hospital with interventional
capabilities within 24 hours. This will allow diagnostic catheterization and revascularization
to be performed within the time requirements of national guidelines.
All STEMI and High Probability ACS patients should have evaluation of left ventricular function
performed during their initial hospitalization.
For MODERATE and LOW Probability ACS patients presenting to the ED, initial negative Troponin-I
and ECG are not enough to rule out ACS. Also required are a second set of Troponin-I and
follow-up ECG at 3 hours from ED arrival. In most cases, a negative stress test is also required.
Key References:
OGara PT, Kushner FG, Ascheim DD, et al. 2013 ACCF/AHA Guideline for
the Management of ST-Elevation Myocardial Infarction: Executive Summary:
A Report of the American College of Cardiology Foundation/American
Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol.
2013;61(4):485-510.
Jneid H, Anderson JL, Wright RS, et al. 2012 ACCF/AHA focused update of
the guideline for the management of patients with unstable angina/non-STelevation myocardial infarction (updating the 2007 guideline and replacing
the 2011 focused update): a report of the American College of Cardiology
Foundation/American Heart Association Task Force on Practice Guidelines.
J Am Coll Cardiol. 2012;60(7):645-81.
Use the tables below to guide the diagnosis and management of ACS presenting at Intermountain emergency departments.
Diagnosis: Assign the patient to an ACS-probability category based on signs and symptoms.
HIGH Probability ACS:
STEMI
MODERATE
Probability ACS
Non-ST-Elevation MI (NSTEMI) OR
Definite Unstable Angina
(ST-elevation MI)
LOW
Probability ACS
Symptoms
ECG
ST depression >1 mm OR
Deep T-wave inversion
Troponin-I (cTnI)
Stress test
>2.0 ng/mL
AMI
Increase
<50%
Increase
>50%
Increase
<20%
Increase
>20%
Stress test
AMI
Stress test
AMI
Higher
clinical
risk
0.04 to <0.1
>0.1
Retest at 3 hrs
AMI
<0.1
Early invasive
strategy*
>0.1
High-risk
indicators for
adverse CV event
Note: Presence of risk
indicators may warrant
moving patient to a
higher ACS probability
category.
Anteroseptal MI
Hypotension, cardiogenic shock
ST changes of inferoposterolateral MI
RV infarction
New significant arrhythmia or heart block
Heart failure
Age >75
Elevated troponin
3 traditional risk factors for CAD
3 traditional risk factors for CAD
Hypotension
Prior coronary stenosis >50%
Prior coronary stenosis >50%
Dynamic ECG changes with pain
Use of ASA within past 7 days
Use of ASA within past 7 days
Prolonged ischemic pain or recurrent pain
Recurrence of pain after initial relief
Recurrence of pain after initial relief
after initial relief
>2 anginal events within prior 24 hours
>2 anginal events within the prior 24 hours
New significant arrhythmia or heart block
Heart failure
Heart failure
>2 anginal events within the prior 24 hours Age >75
Age >75
Heart failure
Age >75
If evaluation is negative for ischemia, consider pulmonary embolism, pericarditis, aortic dissection, and GI as potential causes.
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STEMI
Non-ST-Elevation MI (NSTEMI) OR
Definite Unstable Angina
(ST-elevation MI)
Admit Status
Diagnostic and
therapeutic care
Initial medications
and treatment
(unless contraindicated;
see footnotes and
back for notes and
contraindications)
Adjunct care
(unless contraindicated;
see footnotes and
back for notes and
contraindications)
CCU
Immediate Cath/PCI1
( 90 minute door to PCI)
Delayed Cath/PCI
(>90 minutes door to PCI)
URGENT REPERFUSION
Primary PCI (PPCI) in 90
minutes door-to-balloon time
(see STEMI Orders:
Primary PCI)
ECG and Troponin-I at 0, 3
to 6, 12 and 18 hours from
ED arrival
Lipids and BNP
In the ED:
Aspirin, NTG, and O2
Heparin bolus only (see
STEMI UFH Bolus... on back)
Morphine, prn
In the cath lab:
Clopidogrel 600 mg
OR ticagrelor 180 mg OR
prasugrel2 60 mg
PO (load)
Anticoagulant: heparin or
bivalirudin
GPI per cardiologist (eg, for
high clot burden)
In the ED:
Aspirin, NTG, and O2
Clopidogrel:
Age <75, 300 mg by mouth
Age 75, 75 mg by mouth
Enoxaparin (see dosing
on back)
Morphine, prn
(GPI or anticoagulant agent
administered in cath lab per
cardiologist)
In the ED:
Aspirin, NTG, and O2
Heparin (see ACS/NonSTEMI UFH... on back)
Eptifibatide or GPI
per cardiologist (see
dosing on back)
Morphine, prn
In the ED:
Aspirin, NTG, and O2
Enoxaparin (see dosing
on back)
Eptifibatide or GPI per
cardiologist (see dosing
on back)
Morphine, prn
In the cath lab:
In the cath lab:
Clopidogrel 600 mg OR Clopidogrel 600 mg OR
ticagrelor 180 mg OR
ticagrelor 180 mg OR
prasugrel2 60 mg
prasugrel2 60 mg
PO (load) if PCI
PO (load) if PCI
Additional enoxaparin
Heparin or bivalirudin
(per guideline)
MODERATE
Probability ACS
LOW
Probability ACS
ER/Observation
Medications as
Statin
ACEI (or ARB) when BP stable
if EF <40%
Aldosterone blocker if EF <40%
and symptomatic HF or DM
As indicated
indicated
1. Immediate Cath/PCI: On-site cath lab or transferable to interventional center in <60 minutes from ER to receiving hospital cath lab. Refer to STEMI Orders: Primary PCI or STEMI Orders: Fibrinolytic Pathway.
2. Prasugrel: Avoid if CVA or TIA history; increases bleeds in patients >75 years or <60 kg. In patients <60 kg, manufacturer suggests 5 mg daily maintenance dose, but no prospective clinical trial data exist to support this recommendation.
Clopidogrel, prasugrel, and ticagrelor: Consider platelet function testing for all ACS and high-risk elective PCI patients; see Antiplatelet Guidelines.
3. Oral beta blocker (BB) within 24 hours for patients without signs of HF, low-output, risk for cardiogenic shock, or other relative contraindications. Avoid IV BB except in STEMI patients with hypertension or tachyarrythmias and
without signs of HF, low-output, risk for cardiogenic shock, or other relative contraindications.
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4. May discontinue P2Y12 inhibitor earlier, especially for bare metal stent, if patient is at high bleeding risk.
Notes:
Do not give if GPI (GP IIb/IIIa inhibitor) was
given (e.g., abciximab, eptifibatide, or tirofiban).
Dose
30 mg IV bolus over 5 seconds
35 mg IV bolus over 5 seconds
40 mg IV bolus over 5 seconds
45 mg IV bolus over 5 seconds
50 mg IV bolus over 5 seconds
Indications
Contraindications
Previous
hemorrhagic stroke at
any time; other strokes
or cerebrovascular
events within 1 year
Known intracranial
neoplasm
Active internal bleeding
(does not include
menses)
Suspected aortic
dissection
<75
30 mg IV bolus followed
15 min later by 1 mg/kg
subcut every 12 hours
(max 100 mg first 2 doses)
30 mg IV bolus followed
15 min later by 1 mg/kg
subcut once daily (max
100 mg first 2 doses)
1 mg/kg subcut
every 12 hours
1 mg/kg subcut
once daily
75
No bolus. 1 mg/kg
subcut once daily
(max 75 mg first 2 doses)
Contraindications: Hemodialysis; active major bleeding; recent or planned epidural or dural anesthesia; known or
suspected heparin-induced thrombocytopenia (HIT).
Laboratory monitoring: Draw a baseline BMP, aPTT STAT (include CBC, PT/INR if not done in last 24 hours); draw
CBC every other day while hospitalized; monitor BMP if clinical situation suggests risk of decline in renal function.
Cautions: Thrombocytopenia (platelet count less than 100,000/mm3) or known bleeding diathesis; recent internal
bleeding or uncontrollable active bleeding (hospital admission or transfusion in last 30 days); recent (within the
previous 2 weeks) surgery, major trauma, or thrombotic stroke; acute peptic ulcer disease
Less than 46 kg
4652 kg
5361 kg
6270 kg
7180 kg
8190 kg
Over 90 kg
2500 units
3000 units
3500 units
4000 units
5000 units
5500 units
6000 units
Steps (non-STEMI):
1. Draw baseline aPTT
STAT (include CBC,
PT/INR if not done in
last 24 hours).
2. Give initial dosage as
in Table 1 above.
3. Use aPTT testing to
monitor and adjust
dose as per
Table 2 at right.
UFH Contraindications: Active major bleeding; recent or planned epidural anesthesia; known or suspected heparin-induced
thrombocytopenia (HIT). For HIT, DO NOT use heparin or LMWH; use a direct thrombin inhibitor.
Cautions: Thrombocytopenia (platelets less than 100,000/mm3) or bleeding diathesis; recent internal bleeding or
uncontrollable active bleeding (admission or transfusion in past 30 days); recent surgery (within the past 2 weeks), major
trauma or thrombotic stroke; acute peptic ulcer disease
Non-STEMI
Age
(yr)
Followed by INFUSION
Weight (kg)
Amount (mL)
3741 kg
4246 kg
4753 kg
5459 kg
6065 kg
6671 kg
7278 kg
7984 kg
8590 kg
9196 kg
97103 kg
104109 kg
110115 kg
116121 kg
>121 kg
3.4 mL
4.0 mL
4.5 mL
5.0 mL
5.6 mL
6.2 mL
6.8 mL
7.3 mL
7.9 mL
8.5 mL
9 mL
9.5 mL
10.2 mL
10.7 mL
11.3 mL
6 mL/hour
7 mL/hour
8 mL/hour
9 mL/hour
10 mL/hour
11 mL/hour
12 mL/hour
13 mL/hour
14 mL/hour
15 mL/hour
16 mL/hour
17 mL/hour
18 mL/hour
19 mL/hour
20 mL/hour
3 mL/hour
3.5 mL/hour
4 mL/hour
4.5 mL/hour
5 mL/hour
5.5 mL/hour
6 mL/hour
6.5 mL/hour
7 mL/hour
7.5 mL/hour
8 mL/hour
8.5 mL/hour
9 mL/hour
9.5 mL/hour
10 mL/hour
*Notes:
If patient presents to cath lab within 2 hours of first bolus, re-bolus with 180 mcg/kg over 12 minutes.
Do NOT re-bolus if >2 hours after first bolus (platelet inhibition should be therapeutic)
Start aspirin and unfractionated heparin (UFH) or enoxaparin, if not previously done and PCI has not been done:
UFH: Follow conventional ACS/Non-STEMI UFH dosage/admin at left.
Enoxaparin (Lovenox): Follow dosing/admin instructions above.
Obtain platelet count 3 hours after initial eptifibatide bolus.
Eptifibatide Contraindications: Active abnormal bleeding within previous 30 days or history of bleeding diathesis;
stroke within past 30 days or history of hemorrhagic stroke; severe hypertension (systolic >200 or diastolic >110) not
adequately controlled on antihypertensive therapy; major surgery within past 6 weeks; dependency on hemodialysis
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