About this trial
People who call emergency medical services (EMS) with chest pain or other possible heart-related symptoms are often taken to hospital for further testing. However, only a small proportion of these patients are ultimately diagnosed with a serious heart condition such as a heart attack. This means that many patients undergo hospital transport and evaluation even though their risk is low.
In hospitals, a blood test called high-sensitivity cardiac troponin is commonly used to help diagnose or rule out heart attacks. It is not yet well established whether this type of test can be used safely and effectively earlier, in the prehospital setting.
This study will investigate whether it is feasible to measure high-sensitivity troponin in the ambulance and how well the test can identify patients at low risk of serious heart conditions. A small blood sample will be taken as part of routine care and analyzed using a portable device. The test result will not be used to guide treatment or decisions during the study.
The study will assess how well the test predicts heart-related events within 30 days and how practical it is to perform the test in real-life emergency settings. The results may help guide future research on how to improve early assessment and decision-making for patients with suspected heart disease.
Eligibility criteria
Qualifiers
Age 18 years or older
Assessed by one of the participating EMS units equipped for POCT sampling
Presentation with symptoms suggestive of acute coronary syndrome
Planned transport to hospital for further evaluation
Disqualifiers
ST-segment elevation on prehospital electrocardiogram
Clinical condition requiring immediate life-saving intervention precluding study procedures
Interhospital transport
Prior inclusion in the study within 30 days
Trial design
Treatments tested in this trial
- Prehospital high-sensitivity cardiac troponin I measurement