Prehospital study to the use of HEART-score in chest pain patients

Prehospital Observational study Rotterdam Troponin. observational comparative study to the use of HEART score in the prehospital phase

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON26498

Enrollment

600

Registered

2017-08-08

Start date

2017-10-01

Completion date

Unknown

Last updated

2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pijn op de borst klachten ACS Chest pain ACS

Interventions

blood sample (Troponin) earlier in the proces

Eligibility

Inclusion criteria

Inclusion criteria: All patients over the age of 18 who, after assessment of the ambulance nurse, need to be transported to the hospital with complaints appropriate to a suspicious ACS - older than 18 years - legally capable to give consent -thoracic pain or complaints appropriate to a suspicious ACS -Understand the Dutch language sufficiently -signed informed consent - transported to Maasstad or Ikazia hospital

Exclusion criteria

Exclusion criteria: -legally incapable to give consent or comatose - incapable to understand the dutch language - STEMI on EKG - Missing EKG - Clear other cause of thoracic pain/complaints (pneumonia, aorta dissection, trauma, pneumothorax etc.) - impossibility iv venflon

Design outcomes

Primary

Measure	Time frame
Mace after 30 days, 3 months and 1 year Mace is defined as acute myocardial infraction, CAG, PCI, CABG or death	—

Secondary

Measure	Time frame
feasibility of HEART-score use in prehospital phase	—

Contacts

Public ContactN.W.P.L. van der Waarden

Ambulancezorg Rotterdam-Rijnmond AZRR

nvanderwaarden@azrr.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)