4.7 Article

Intramyocardial Hemorrhage and the Wave Front of Reperfusion Injury Compromising Myocardial Salvage

Journal

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
Volume 79, Issue 1, Pages 35-48

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2021.10.034

Keywords

hemorrhage; infarct expansion; myocardial infarction; reperfusion injury

Funding

  1. National Institutes of Health/NHLBI [HL133407, HL136578, HL147133]

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Reperfusion therapy for acute myocardial infarction can lead to myocardial hemorrhage, which increases the size of the infarction. Myocardial hemorrhage drives the expansion of myocardial infarction after reperfusion and compromises myocardial salvage. This has implications for acute care management, risk assessment, and future therapeutics.
BACKGROUND Reperfusion therapy for acute myocardial infarction (MI) is lifesaving. However, the benefit of reperfusion therapy can be paradoxically diminished by reperfusion injury, which can increase MI size. OBJECTIVES Hemorrhage is known to occur in reperfused MIs, but whether hemorrhage plays a role in reperfusion-mediated MI expansion is not known. METHODS We studied cardiac troponin kinetics (cTn) of ST-segment elevation MI patients (n = 70) classified by cardiovascular magnetic resonance to be hemorrhagic (70%) or nonhemorrhagic following primary percutaneous coronary intervention. To isolate the effects of hemorrhage from ischemic burden, we performed controlled canine studies (n = 25), and serially followed both cTn and MI size with time-lapse imaging. RESULTS CTn was not different before reperfusion; however, an increase in cTn following primary percutaneous coronary intervention peaked earlier (12 hours vs 24 hours; P < 0.05) and was significantly higher in patients with hemorrhage (P < 0.01). In hemorrhagic animals, reperfusion led to rapid expansion of myocardial necrosis culminating in epicardial involvement, which was not present in nonhemorrhagic cases (P < 0.001). MI size and salvage were not different at 1 hour postreperfusion in animals with and without hemorrhage (P = 0.65). However, within 72 hours of reperfusion, a 4-fold greater loss in salvageable myocardium was evident in hemorrhagic MIs (P < 0.001). This paralleled observations in patients with larger MIs occurring in hemorrhagic cases (P < 0.01). CONCLUSIONS Myocardial hemorrhage is a determinant of MI size. It drives MI expansion after reperfusion and compromises myocardial salvage. This introduces a clinical role of hemorrhage in acute care management, risk assessment, and future therapeutics. (C) 2022 by the American College of Cardiology Foundation.

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