Reperfusion strategies in the emergency treatment of ST-segment elevation myocardial infarction☆
Affiliations
- Department of Emergency Medicine, The Cleveland Clinic, Cleveland, OH 44195, USA
Correspondence
- Corresponding author. Tel.: +1 216 445 4546.

Affiliations
- Department of Emergency Medicine, The Cleveland Clinic, Cleveland, OH 44195, USA
Correspondence
- Corresponding author. Tel.: +1 216 445 4546.

Affiliations
- Department of Emergency Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA
Affiliations
- Division of Cardiovascular Medicine, The University of Texas Medical School at Houston and The Memorial Hermann Heart and Vascular Institute, Houston, TX 77225, USA
Affiliations
- Department of Surgery, Division of Emergency Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA
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Fig. 1
Change in mortality associated with time to fibrinolytic treatment [7] . All patients in the ASSET and Late Assessment of Thrombolytic Efficacy (LATE) studies were included because the tabular information available from these trials subdivided by delay was not subdivided by electrocardiogram results. BBB indicates bundle branch block. Adapted with permission from Lancet 1994;343:311-22.
Fig. 2
Change in mortality associated with medical contact-to-balloon time [10] . OR indicates odds ratio; CI, confidence interval. Adapted with permission from JAMA 2000;283:2941-47.
Fig. 3
“Lytic decision zones” for the emergency physician. The shaded boxes indicate the periods of unknown time delays during which a decision must be made about whether or not to administer a fibrinolytic. *ACC/AHA guidelines state that an invasive strategy is generally preferred for patients presenting more than 3 hours after symptom onset [1] .
Fig. 4
Absolute risk reduction in 4- to 6-week mortality with primary PCI as a function of PCI-related time delay [28] . Circle sizes reflect the sample sizes of individual studies included in the analysis. Values greater than 0 represent benefit and values less than 0 represent harm (indicating that fibrinolysis is favored). The solid line represents the weighted meta-regression analysis. Reprinted with permission from Am J Cardiol 2003;92:824-6 [28] .
Fig. 5
Hypothetical construct of the relationship among the time from onset of symptoms of acute MI to reperfusion therapy, mortality reduction, and extent of myocardial salvage [35] . The benefit of reperfusion therapy with regard to mortality is greatest in the first 2 to 3 hours after symptom onset, most likely a consequence of myocardial salvage. After this critical early period, the magnitude of the mortality benefit is much reduced, and as the mortality reduction curve flattens, time to reperfusion therapy is less critical. If a treatment strategy is able to move patients back up the curve, a benefit would be expected. The benefit of a shift from point A or B to point C would be substantial, but the benefit of a shift from point A to point B would be small. A treatment strategy that delays therapy during the early critical period, such as patient transfer for PCI, would be harmful (shift from point D to point C or point B). Reprinted with permission from JAMA 2005;293:979-86.
Abstract
Prompt restoration of blood flow is the primary treatment goal in ST-segment elevation myocardial infarction to optimize clinical outcomes. The ED plays a critical role in rapid triage, diagnosis, and management of ST-elevation myocardial infarction, and in the decision about which of the 2 recommended reperfusion options, that is, pharmacologic and mechanical (catheter-based) strategies, to undertake. Guidelines recommend percutaneous coronary intervention (PCI) if the medical contact-to-balloon time can be kept under 90 minutes, and timely administration of fibrinolytics if greater than 90 minutes. Most US hospitals do not have PCI facilities, which means the decision becomes whether to treat with a fibrinolytic agent, transfer, or both, followed by PCI if needed. Whichever reperfusion approach is used, successful treatment depends on the ED having an integrated and efficient protocol that is followed with haste. Protocols should be regularly reviewed to accommodate changes in clinical practice arising from ongoing clinical trials.
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☆Source of support: preparation of this manuscript was supported by PDL BioPharma Inc.
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