Coronary microvascular dysfunction (CMD) is increasingly recognized as an important indicator for long-term prognosis in patients with acute myocardial infarction (AMI). The angiography-derived index of microcirculatory resistance (angio-IMR) is a novel guidewire-free measure for CMD in patients with AMI. Ticagrelor has recently been suggested to have additional benefits on coronary microcirculation beyond its antiplatelet effect. This study was designed to compare the protective effects of ticagrelor and clopidogrel on CMD and prognostic impact in patients with AMI, using the angio-IMR as a novel assessment tool.
Study Type
OBSERVATIONAL
Enrollment
325
Patients with acute myocardial infarction randomly received dual antiplatelet therapy with with aspirin 100mg daily and either ticagrelor 90mg twice daily or clopidogrel 75mg once daily for at least 9 months after PCI as needed.
Second affiliated Hospital Zhejiang University School of Medicine
Hangzhou, Zhejiang, China
The improvement of angio-IMR
Difference between Angio-IMR at follow-up coronary angiography and Angio-IMR after PCI
Time frame: within 24 months post-PCI
Readmission for heart failure
Readmission for an acute exacerbation of chronic heart failure or acute heart failure
Time frame: Within 24 months post-PCI
Myocardial reinfarction
Another myocardial infarction with elevated myocardial enzymes and abnormal electrocardiograms
Time frame: Within 24 months post-PCI
Target vessel revascularization
Repeat revascularization was performed because of ischemia in the target-vessel territory
Time frame: Within 24 months post-PCI
Non-target vessel revascularization
Repeat revascularization was performed because of ischemia in the non-target vessel territory
Time frame: Within 24 months post-PCI
Cerebral hemorrhage
The occurrence of cerebral hemorrhage during the follow-up period was based on imaging CT and MRI
Time frame: Within 24 months post-PCI
Other bleeding events
Bleeding events such as gingival bleeding, skin bleeding, and gastrointestinal bleeding and so on, occurred during the follow-up period
Time frame: Within 24 months post-PCI
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