Triage in Acute Chest Pain Evaluation in primary care

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON20102

Enrollment

2500

Registered

2019-03-05

Start date

2018-11-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Any etiology that underlies undifferentiated chest pain

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients who telephone the out-of-office-hours primary care with symptoms of chest pain

Exclusion criteria

Exclusion criteria: Age <18; Declined study participation (opt-out); traumatic chest pain

Design outcomes

Primary

Measure	Time frame
The outcomes of interest are the safety and efficiency of the proposed triage strategies (NTS and/or Marburg) for "urgent diagnosis and/or fatal outcome". The definition of “urgent diagnosis and/or fatal outcome” is defined as: death from any cause, acute coronary syndrome and/or urgent coronary revascularization, acute thoracic aortic dissection, pulmonary embolism, acute heart failure, peri(myo)carditis, (tension)pneumothorax.	—

Measure

Time frame

The outcomes of interest are the safety and efficiency of the proposed triage strategies (NTS and/or Marburg) for "urgent diagnosis and/or fatal outcome". The definition of “urgent diagnosis and/or fatal outcome” is defined as: death from any cause, acute coronary syndrome and/or urgent coronary revascularization, acute thoracic aortic dissection, pulmonary embolism, acute heart failure, peri(myo)carditis, (tension)pneumothorax.

—

Secondary

Measure	Time frame
The secondary outcome measure will be "major adverse cardiac events", defined as cardiovascular death, acute coronary syndrome, and/or urgent coronary revascularization.	—

Contacts

Public ContactRalf Harskamp

Amsterdam UMC - AMC

r.e.harskamp@amc.nl0205667683

Outcome results