The AHA Guidelines and Scientific Statements Handbook

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Chapter 3 ST-Elevation Myocardial Infarction

angina, MI, CABG, or PCI. Evaluation of the patient’s
complaints should focus on chest discomfort, associ-
ated symptoms, sex- and age-related differences in
presentation, hypertension, diabetes mellitus, possibil-
ity of aortic dissection, risk of bleeding, and clinical
cerebrovascular disease (amaurosis fugax, face/limb
weakness or clumsiness, face/limb numbness or sensory
loss, ataxia, or vertigo). (Level of Evidence: C)



  1. Physical examination (Table 3.1)
    Class I
    1 A physical examination should be performed to
    aid in the diagnosis and assessment of the extent,
    location, and presence of complications of STEMI.
    (Level of Evidence: C)
    2 A brief, focused, and limited neurological exami-
    nation to look for evidence of prior stroke or cogni-
    tive defi cits should be performed on STEMI patients
    before administration of fi brinolytic therapy. (Level
    of Evidence: C)

  2. Electrocardiogram
    Class I
    1 A 12-lead ECG should be performed and shown
    to an experienced emergency physician within 10
    minutes of ED arrival for all patients with chest dis-
    comfort (or anginal equivalent) or other symptoms
    suggestive of STEMI. (Level of Evidence: C)
    2 If the initial ECG is not diagnostic of STEMI but
    the patient remains symptomatic, and there is a high
    clinical suspicion for STEMI, serial ECGs at 5- to
    10-minute intervals or continuous 12-lead ST-
    segment monitoring should be performed to detect
    the potential development of ST elevation. (Level of
    Evidence: C)


3 In patients with inferior STEMI, right-sided ECG
leads should be obtained to screen for ST elevation
suggestive of right ventricular (RV) infarction. (See
Section 7.6.6 of the full-text guidelines and the ACC/
AHA/ASE 2003 Guideline Update for the Clinical
Application of Echocardiography.) (Level of Evi-
dence: B)


  1. Laboratory examinations
    Class I
    Laboratory examinations should be performed as
    part of the management of STEMI patients but
    should not delay the implementation of reperfusion
    therapy. (Level of Evidence: C)

  2. Biomarkers of cardiac damage
    Class I
    1 Cardiac-specifi c troponins should be used as the
    optimum biomarkers for the evaluation of patients
    with STEMI who have coexistent skeletal muscle
    injury. (Level of Evidence: C)
    2 For patients with ST elevation on the 12-lead ECG
    and symptoms of STEMI, reperfusion therapy should
    be initiated as soon as possible and is not contingent
    on a biomarker assay. (Level of Evidence: C)


Class IIa
Serial biomarker measurements can be useful to
provide supportive noninvasive evidence of reperfu-
sion of the infarct artery after fi brinolytic therapy in
patients not undergoing angiography within the fi rst
24 hours after fi brinolytic therapy. (Level of Evi-
dence: B)

Class III
Serial biomarker measurements should not be relied
on to diagnose reinfarction within the fi rst 18 hours
after the onset of STEMI. (Level of Evidence: C)

a. Bedside testing for serum cardiac biomarkers
Class I
1 Although handheld bedside (point-of-care) assays
may be used for a qualitative assessment of the pres-
ence of an elevated level of a serum cardiac bio-
marker, subsequent measurements of cardiac
biomarker levels should be performed with a quan-
titative test. (Level of Evidence: B)
2 For patients with ST elevation on the 12-lead ECG
and symptoms of STEMI, reperfusion therapy

Table 3.1 Brief physical examination in the Émergency
Department



  1. Airway, Breathing, Circulation (ABC)

  2. Vital signs, general observation

  3. Presence or absence of jugular venous distension

  4. Pulmonary auscultation for rales

  5. Cardiac auscultation for murmurs and gallops

  6. Presence or absence of stroke

  7. Presence or absence of pulses

  8. Presence or absence of systemic hypoperfusion (cool, clammy,
    pale, ashen)

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