Chapter 3 ST-Elevation Myocardial Infarctionangina, 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)
- 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)
- 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)- 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)
- 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 therapyTable 3.1 Brief physical examination in the Émergency
Department
- Airway, Breathing, Circulation (ABC)
- Vital signs, general observation
- Presence or absence of jugular venous distension
- Pulmonary auscultation for rales
- Cardiac auscultation for murmurs and gallops
- Presence or absence of stroke
- Presence or absence of pulses
- Presence or absence of systemic hypoperfusion (cool, clammy,
 pale, ashen)
