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)
- 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 therapy
Table 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)