Retrospective Assessment of Referral of a Major Trauma Patient

ConditionTrauma Injury
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorHôpital NOVO

About this trial

The aim of this study is to find out whether major trauma patients from the Val d'Oise are referred to the appropriate trauma centre for their care and to assess the quality of triage within the Val d'Oise department.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Between the 1st January 2023 and the 31th December 2023

Regulated by SAMU 95 with suspected major trauma

Sending an MCIU

At least 1 Vittel criterion*

Disqualifiers

Death on site

Care by an MICU team outside the 95

Minor patients and legal protection

Transport refusals

Trial population

Patients regulated by SAMU 95 with suspected major trauma between the 1st January 2023 and the 31th December 2023.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Data Collection

    Other intervention

    Collection of medical data from MICU intervention file and the medical records of patients at the destination hospital

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Triage assessment of a major trauma patient

The criterion is the evaluation of the referral of the major trauma patient after post-Medics injury assessment into over, normo and under-triage The over-triage patient is referred to a level I trauma centre with an Injury Severity Score (ISS) \<16 The normo-triage patients are either referred to: * a level 1 trauma centre with an ISS \>15 * the local scanner and then to an intensive care unit at the scanner site * in the emergency department and then to a surgical unit * emergency with a return home afterwards The under-triage patient is either referred to: * the local scanner and then to a level 1 trauma centre * initially emergency with hospitalisation in an intensive care or continuing care unit afterwards

Time frame
At the end of the study, an average of 9 month

Secondary outcomes

1

Assess if the intervention time is correlated with an under-triage

The correlation will be assessed by the proportion of patients under-triaged during the following hours: * 7am to 9am * From 6pm to 9pm * From 9pm to 7am i.e. the ratio between the number of under-triaged patients and the number of major trauma patients treated during the defined time slots.

Time frame
At the end of the study, an average of 9 month
2

Assess if presumed alcohol intoxication is correlated with a higher rate of under-triage

The correlation will be assessed by the proportion of patients under-triaged in patients with suspected alcohol intoxication. Presence of suspected alcohol intoxication assessed clinically i.e. the ratio between the number of under-triaged patients with suspected alcohol intoxication and the total number of major trauma patients

Time frame
At the end of the study, an average of 9 month
3

Assess if deliberate toxic poisoning is correlated with a higher rate of under-triage

The correlation will be assessed by the proportion of patients under-triaged in patients with suspected deliberate toxic poisoning. Presence of deliberate toxic poisoning assessed clinically i.e. the ratio between the number of under-triaged patients with suspected deliberate toxic poisoning and the total number of major trauma patients

Time frame
At the end of the study, an average of 9 month
4

Assess if the TRENAU grade is predictive in pre-hospital of an appropriate referral following an intra-hospital trauma assessment

The criterion will be assessed by the correlation between TRENAU grade and level of trauma centre for final admission : TRENAU A in a level 1 trauma centre TRENAU B in a level 2 trauma centre TRENAU C in a level 3 trauma centre The TRENAU grade (Trauma System du Réseau Nord Alpin des Urgences) is used to classify major trauma patients into 3 categories (A, B and C) in the pre-hospital phase, so that they can be referred to the appropriate level of hospital

Time frame
At the end of the study, an average of 9 month

Other outcomes

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