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Prehospital Translation of Chest Pain Tools

Translating Evidence-Based Chest Pain Decision Aids to the Prehospital Environment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03494556
Acronym
RESCUE
Enrollment
365
Registered
2018-04-11
Start date
2018-04-18
Completion date
2020-09-09
Last updated
2023-07-25

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

Conditions

Acute Coronary Syndrome, Pulmonary Embolism

Brief summary

Decision aids such as the HEART Pathway, Emergency Department Assessment of Chest Pain Score (EDACS), Revised Geneva Score and PERC Score have similar ability to accurately risk stratify Emergency Department (ED) patients with possible Acute Coronary Syndrome (ACS) and Pulmonary Embolism (PE) and have become standard practice in the ED setting. This study seeks to determine whether prehospital use of these decision aids is feasible and determine which are the most sensitive and specific for prediction of ACS and PE, respectively.

Detailed description

To accomplish our Specific Aims the study team proposes a prospective, observational pilot study of four rapid risk stratification tools, the HEART Pathway Score, EDACS score, revised Geneva score, and PERC score, among 250 chest pain patients within two large EMS systems. The proposed pilot study has broad-based support from local and state EMS agencies, including Cumberland and New Hanover County EMS agencies. Each tool will be pilot tested and compared in the prehospital setting for feasibility and accuracy. Paramedics will be trained in risk stratification tool use and then will prospectively collect the clinical data needed to calculate each risk stratification score when caring for adults with chest pain. Completed paramedic risk assessments will be used to determine feasibility. Patients will be followed for 30 days to determine occurrence of ACS and PE events and the sensitivity of each risk stratification decision aid will be determined.

Interventions

OTHERData Collection

Paramedic will use data collected during routine care to complete four risk stratification tools.

Sponsors

Cape Fear Valley Mobile Integrated Healthcare Cumberland County EMS
CollaboratorUNKNOWN
New Hanover Regional Medical Center EMS
CollaboratorUNKNOWN
Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age greater than or equal to 21 * Acute non-traumatic chest pain * Transported by Cumberland or New Hanover County EMS to a local Emergency Department

Exclusion criteria

* Patients with evidence of ST elevation myocardial infarction (STEMI) on ECG * Inter-facility transports (transfers) * Patients with unstable vital signs * Prisoners * Non-english speakers

Design outcomes

Primary

MeasureTime frameDescription
Determine whether prehospital chest pain decision aid use is feasible.24 hoursParamedics and blinded Emergency Department providers will be complete four risk stratification tools on a convenience sample of patients with acute chest pain. Inter-rater reliability (kappa) will be determined for each tool.

Secondary

MeasureTime frameDescription
Compare decision aids to determine which are the most sensitive and specific30 daysDestination hospitals have well established linkages between the prehospital and hospital Electronic Medical Record (EMR) facilitating patient outcome ascertainment. Data will be abstracted from the EMR to determine occurrence of 30 day study outcomes.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026