Skip to content

Symptoms of Acute Coronary Syndrome in Medical Regulation

Symptoms of Acute Coronary Syndrome in Medical Regulation: a Retrospective Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05902130
Acronym
SCAST+
Enrollment
208
Registered
2023-06-13
Start date
2023-01-01
Completion date
2023-10-01
Last updated
2023-12-26

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

Conditions

Acute Coronary Syndrome

Keywords

acute coronary syndrome, out-hospital care, medical regulation

Brief summary

The main objective was to analyze the impact of the gender of the attending physician in the differences in the management of ST+ ACS between men and women. This study will be conducted in partnership with the interventional cardiology team of the CHR Metz-Thionville and SAMU (emergency call center) of Moselle, which has a detailed registry of coronary angiographies at the center. A retrospective observational study will be carried out over a typical period outside of covid at the CHR Metz Mercy (2021-2022) based on coronary angiographies performed in the context of ST+ ACS at the CHR of patients referred by the center 15. The patient's medical record will be analyzed, going back to his call to the 15 via tape listening. The number of subjects required being calculated at 104 men and 104 women, these patients will be selected from the database of our cardiologist colleagues and we will match one man to one woman by comparing the delays of several items (1st medical contact, time of 1st ECG, medicalization or not, delay of call to the cardiologist, delay of coronary angiography...) according to the sex of the regulator. The consequences of a difference in management will be also evaluated by analyzing in-hospital mortality, mortality at 30 days of management, and functional sequelae at discharge (grades of dyspnea, disturbance of myocardial contractility, LVEF at discharge). This study based on the differences in questioning according to the gender of the regulating physician would allow better identification of the factors that increase the delay in the management of ST+ ACS in women, and to find avenues of correction in order to limit the loss of opportunity for patients. The patients included who are still alive will receive a notification of non-objection by mail.

Interventions

OTHERsymptoms of a myocardial infarction

Analysis of the differences in symptoms of a myocardial infarction between a man and a woman

Sponsors

Centre Hospitalier Régional Metz-Thionville
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* patient with emergency coronary angiography for ST+ ACS * having made a call to the Emergency Center for the same reason

Exclusion criteria

* non-real ST+ ACS

Design outcomes

Primary

MeasureTime frameDescription
Delay between the call to the emergency center and the first contact with a physicianEnd of the call to the emergency center, less than 10 minDelay (minutes:seconds)

Secondary

MeasureTime frameDescription
Dispatch of a medical ambulance (Y/N)End of the call to the emergency center, an average of 20 minNumber (%)
Delay between the call to the emergency center and the first coronary angiographyAt hospital discharge, an average of 2 hoursDelay (minutes)
Delay between the call to the emergency center and the first electrocardiogramAt hospital discharge, an average of 2 hoursDelay (hours:minutes)
Day 30 mortality30 days after the call to emergency centerNumber (%)
Left Ventricular Ejection FractionAt hospital discharge, less than 30 daysPercentage
In-hospital mortality30 days after the call to emergency centerNumber (%)

Countries

France

Outcome results

None listed

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