acute ST segment elevation myocardial infarction
Conditions
Interventions
the observation group:Establishment of chest pain center mode
Control group:The chest pain center was not established
Sponsors
the First Affiliated Hospital of Guangxi Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1) aged 18~75 years old male and female; 2) STEMI patients receiving primary percutaneous coronary intervention treatment within 12 hours; 3) Patients and / or family members are willing to take part in the trial, and all patients gave written informed consent.
Exclusion criteria
Exclusion criteria: 1) patients with major surgical, traumatic, and bleeding history withi 6 months; 2) patients with contraindications to anticoagulation and antiplatelet therapy; 3) patients with hemorrhagic cerebrovascular accident or ischemic cerebrovascular accident within half a year; 4) patient with hemorrhagic disease or thrombocytopenia; 5) patient allergic to aspirin or contrast agents; 6) patient with severe hepatic or renal impairment; 7) patients with malignant tumor, or patients with incomplete clinical data or coronary angiography; 8) patients who refused to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| door to balloon;first medical contact;first medical contact to balloon;MACE incident within 30 days;MACE incident within 1 years;All-cause mortality in 30 days;All-cause mortality within 1 years; | — |
Secondary
| Measure | Time frame |
|---|---|
| hospital stay;cost of hospitalization; | — |
Countries
China
Contacts
Public ContactLang Li
Department of Cardiology, the First Affiliated Hospital of Guangxi Medical University
Outcome results
None listed