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This observational study aimed to investigate the prognostic value of high-frequency QRS (HF-QRS) in patients with acute myocardial infarction (AMI) after percutaneous coronary intervention (PCI), as well as its potential role in diagnosing microvascular dysfunction. The main question it aims to answer is:
Participants underwent HF-QRS assessment and were prospectively followed for 1 year to record the incidence of major adverse cardiovascular events (MACE).
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| High-Frequency QRS | Device | All enrolled patients underwent HF-QRS assessment, with subsequent recording of MACE to evaluate the predictive value of HF-QRS parameters for clinical outcomes |
| Measure | Description | Time Frame |
|---|---|---|
| To evaluate the predictive value of high-frequency QRS (HF-QRS) parameters for major adverse cardiovascular events (MACE) within 1 year after PCI in AMI patients and to construct a prognostic risk prediction model. | 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| To evaluate the adjunctive diagnostic value of high-frequency QRS parameters for microvascular dysfunction in ACS patients following percutaneous coronary intervention | 12 months |
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Inclusion Criteria:
Diagnosed with acute myocardial infarction (AMI, including STEMI and NSTEMI) and underwent successful emergency PCI
Voluntarily participated and provided written informed consent
Exclusion Criteria:
QRS duration >120 ms (including paced rhythm, WPW syndrome, bundle branch block, or left ventricular hypertrophy with repolarization abnormalities)
Structural heart disease (congenital heart disease, cardiomyopathy, aortic dissection, etc.)
Persistent atrial fibrillation or malignant arrhythmias
History of cerebral hemorrhage or ischemic stroke within 1 month
Prolonged cardiopulmonary resuscitation or requiring advanced life support (IABP/ECMO, etc.)
Scheduled for imminent surgery with anticipated inability to complete HF-QRS assessment
Other life-threatening conditions including: Severe hepatic or renal dysfunction;Uncontrolled systemic diseases;Hematologic disorders;Active infections;Malignancy with life expectancy <1 year Other investigator-determined exclusionary conditions:Pregnancy;Concurrent participation in other clinical trials
Refusal to participate in the clinical study
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patients with acute myocardial infarction following percutaneous coronary intervention
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Yuan Lu, Ph.D | Contact | 13952110901 | 405983931@qq.com |
| Name | Affiliation | Role |
|---|---|---|
| Yong Huo, Ph.D | Department of Cardiology, Peking University First Hospital, Beijing, China | Study Chair |
| Yuan Lu, Ph.D | The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu 221002 | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The Affiliated Hospital of Xuzhou Medical University | Xuzhou | Jiangsu | 221000 | China |
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