Impact of Implementing a National Classification of Surgical Emergencies on Postoperative Morbidity and Mortality: a Prospective Multicenter Observational Study After Implementation.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSociété Française d'Anesthésie et de Réanimation

About this trial

The ACUTE committee of the French Society of Anesthesia and Intensive Care (SFAR), in consultation with surgical societies, has developed a national classification of surgical emergencies to define the ideal time to surgery for each indication.

The goal is to integrate this classification with a cognitive aid to improve patient triage and reduce waiting times for emergency surgery.

This classification will be presented at the 2026 SFAR Congress and as a practical decision-making tool.

A prospective, multicenter study will then evaluate its impact by measuring the rate of severe postoperative complications at 30 days using the Comprehensive Complication Index (CCI).

The study will include 2500 patients over two-week periods between February and June 2027.

Expected benefits include reduced patient morbidity and hospital stay, along with better emergency surgery planning and standardization across healthcare centers.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults (≥18 years) undergoing non-cardiac emergency surgery, defined as surgery with a preoperative anesthetic consultation performed less than 48 hours before the surgical procedure.

Disqualifiers

None

Trial population

Adults under legal protection (guardianship, curatorship, or judicial safeguard) Patients who object to the reuse of their personal data for research purposes

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Implementation of classification of surgical emergencies

    Other intervention

    Observation of practices prior and after implementation of classification of surgical emergencies

Treatment groups

2,500 Participants
are divided into 2 treatment groups
Group A: Before integration of classification of surgical emergencies0 interventions
Group B: After integration of classification of surgical emergencies1 intervention

Trial outcomes

Primary outcomes

1

Postoperative morbidity and mortality

Postoperative morbidity and mortality assessed using the Clavien-Dindo score and expressed on a continuous scale by the Comprehensive Complication Index (CCI) at 30 days (D30)Day 30

Time frame
At Day 30after surgery

Secondary outcomes

Other outcomes

Sponsors and contacts

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