Validation of the HAR Score for Prioritization of Patients Calling the Emergency Medical Service for Chest Pain by Emergency Call Dispatcher
Reg-HAR
1 other identifier
observational
796
1 country
3
Brief Summary
The lifetime prevalence of chest pain in the general population is 20-40%. The etiologies to be evoked from the outset of management are those of cardiovascular origin, such as acute coronary syndrome (ACS) and pulmonary embolism. ACS is responsible for almost 20% of deaths. Delay in treatment is a major prognostic factor, given the importance of coronary reperfusion. In France, one of the first contacts with the healthcare system is the medical regulation assistant (MRA) at the Centre 15. His or her role is to prioritize the call according to the identification of immediate signs of seriousness, and if necessary, to decide autonomously to send a rescue team before medical regulation. Depending on the reason for the call and any signs of seriousness, it prioritizes the call according to the expected response time. In line with current recommendations, all calls for chest pain should be answered by an emergency medical dispatcher (EMR) within 5 minutes. However, 60-90% of chest pain calls are not of cardiovascular origin. Their prioritization could therefore be re-qualified for longer response times. Given the frequency of this type of call, a more efficient MRA referral strategy is needed. To achieve this, decision-support tools would be essential. The performance of the HAR (History, Age and Risk Factors) score has been recently explored, derived from the HEART score, in a previous single-center prospective study in 2019. It stratifies the risk of a major cardiovascular event (MCE) into low (0 or 1 point), intermediate (2 or 3 points) or high (4, 5 or 6 points). Investigator's hypothesis is that the HAR score could be entrusted to MRA, to enable them to optimize the prioritization of patients calling with non-traumatic chest pain, by qualifying low-risk chest pain calls on the one hand, which could be prioritized in P2 SNP, and high-risk calls on the other, making it possible to anticipate the dispatch of an emergency service.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2025
Shorter than P25 for all trials
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 28, 2025
CompletedFirst Posted
Study publicly available on registry
March 5, 2025
CompletedStudy Start
First participant enrolled
May 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2025
CompletedMarch 24, 2025
March 1, 2025
7 months
February 28, 2025
March 19, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of major cardiovascular events
Number of major cardiovascular events is measured by presence of Death from cardiological causes, Type 1 or 2 myocardial infarction, Percutaneous coronary intervention, Surgical coronary bypass surgery
30 days
Secondary Outcomes (4)
Performance of the HAR Score: Sensitivity, Specificity, and Comparison Between EMR and MRA
From Day 0 to Day 30
Comparaison between rescue resources decided and predicted by the HAR score
From Day 0 to Day 30
Time delta between the end of the MRA's score suggesting the dispatch of equipment (HAR score ≥ 4 points) and the actual decision to dispatch equipment in the current situation.
From Day 0 to Day 30
Area under the ROC curve and Delong-Delong test
From Day 0 to Day 30
Study Arms (1)
call for chest pain
patients who call for chest pain
Interventions
A follow-up call is made to the patient 30 days (+ 5 days) after inclusion to check for the occurrence of an Major Cardio Vascular Event.
Eligibility Criteria
Patients calling center 15 for chest pain
You may qualify if:
- Patient of legal age (≥ 18 years)
- Calling Center 15 from 49, 72 or 37
- Expressing non-traumatic chest pain, even if this is not the main reason for seeking help.
You may not qualify if:
- Treatment in departments other than 49, 72 and 37
- Taken in charge in an emergency department of a private facility in the 49, 72 and 37 départements
- Poor understanding of the French language
- Non-affiliated or non-beneficiary of a social security scheme
- Person deprived of liberty by judicial or administrative decision
- Person under forced psychiatric care
- Person subject to a legal protection measure
- Person unable to express his/her non-opposition.
- Follow-up at Day 30 impossible for any reason
- Person having expressed his/her opposition to the collection of his/her data.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
Centre Hospitalier Universitaire d'Angers
Angers, 49000, France
Centre Hospitalier Le Mans
Le Mans, 72000, France
CHRU de Tours
Tours, 37000, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 28, 2025
First Posted
March 5, 2025
Study Start
May 2, 2025
Primary Completion
December 1, 2025
Study Completion
December 1, 2025
Last Updated
March 24, 2025
Record last verified: 2025-03