Pre-hospitale risicostratificatie bij patiënten met verdenking op een hartinfarct
- Conditions
- non-STEMImyocardial infarctionhartinfarctmyocardial infarctionHEART-scoreparamedicsambulance nursespre-hospital
- Registration Number
- NL-OMON26459
- Lead Sponsor
- Sponsor: Isala, Zwolle. Principal investigator: J.P. Ottervanger
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 1090
Inclusion Criteria
All out-of-hospital patients visited by an ambulance with a pre-hospital suspicion of non-STEMI ACS at first medical contact
Age ≥ 18 years
Exclusion Criteria
-Comatose state
-Cognitive impairment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint is the occurrence of MACE within 6 weeks of inclusion. MACE includes: myocardial infarction, PCI, CABG, death by all causes.
- Secondary Outcome Measures
Name Time Method Secondary outcomes are the occurrence of MACE within 6 months of inclusion, the number of patients that are secondarily referred to the hospital for cardiac reasons with a HEART score of ≤3 within 6 months after inclusion, discharge diagnosis of all patient primarily or secondarily referred to the hospital within 6 months after inclusion, health care costs, the number of inter-hospital transfers between PCI and non-PCI centres, length of hospital stay, performed diagnostics, cause of death, differences in patient characteristics between the low, intermediate and high risk groups, quality of life.