ST-segment Elevation Myocardial Infarction (STEMI)
Conditions
Brief summary
The purpose of this study is to develop a risk score to predict the risks of in-hospital major adverse cardiac events in ST-segment elevation myocardial infarction patients treated by primary percutaneous coronary intervention.
Detailed description
The CSPR trial is an observational clinical trial to derive and validate a readily useable risk score to identify patients at high risk of in-hospital major adverse cardiac events in 5594 patients presenting with a ST-segment elevation myocardial infarction and treated by primary percutaneous coronary intervention.
Interventions
no intervention
Sponsors
Study design
Eligibility
Inclusion criteria
1. Age≥18 2. ST-segment elevation myocardial infarction was defined according to the universal definition of myocardial infarction 3. STEMI treated by pPCI
Exclusion criteria
1. Patient with heart failure in admission 2. STEMI with symptom-onset-to-balloon time\>24h 3. pPCI was not successful or only underwent coronary angiography 4. Killip class ≥II in admission
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| in-hospital acute de novo heart failure | in-hospital outcome, until discharge | Killip class ≥II |
| cardiogenic shock | in-hospital outcome, until discharge | according to the universal definition |
| death | in-hospital outcome, until discharge | according to the universal definition |
Countries
China