Surgical Emergencies Gradation and Postoperative Outcome

NCT05888948 | Unknown

• 1 other identifier: PI2022_843_0056
• Study Type: observational
• Target: 700
• Locations: 1 country
• Sites: 1

Brief Summary

Reducing surgical waiting time has been shown to be associated with a reduction in postoperative morbidity and mortality in this type of surgery. The use of a gradation of surgical emergencies makes it possible to prioritise them in an objective, consensual manner and to carry them out within a theoretical expected waiting time relative to the degree of urgency. The investigators hypothesise that exceeding the theoretical expected waiting time relative to the degree of urgency defined by the gradation of surgical emergencies is associated with an increase in postoperative morbidity and mortality in emergency surgery. The objective is to assess the impact on post-operative morbidity and mortality of waiting times exceeding the theoretical expected time by grading the surgical emergencies of patients undergoing emergency surgery.

Conditions

Emergency Surgery; Mortality

Keywords

emergency surgery; gradation; Complication; mortality

Outcome Measures

Primary Outcomes (3)

• Number Post-operative complications

  1 year

• Mortality at 1 year

  1 year

• Length of stay in intensive care unit

  1 year

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients requiring non-cardiac emergency surgery at the Amiens-Picardie University Hospital will be included. A posteriori grading will be performed according to an institutionally recognised gradation. Each grade is subject to a theoretical maximum time for surgical management. The surgical waiting time and the waiting time exceeding the theoretical expected time of the gradation will be analysed.

You may qualify if:

• age \> 18 years old.
• Non-cardiac emergency surgery.

You may not qualify if:

• Minor patients
• Emergency cardiac surgery
• Patients under guardianship or curators
• Pregnant women
• Patients who object to their personal data being used in research

Sponsors & Collaborators

• Centre Hospitalier Universitaire, Amiens: lead

Study Sites (1)

CHU Amiens-Picardie

Amiens, 80054, France

RECRUITING

Central Study Contacts

Stéphane BAR, MD

CONTACT

03 22 08 79 06; bar.stephane@chu-amiens.fr

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 25, 2023
• First Posted: June 5, 2023
• Study Start: April 25, 2022
• Primary Completion: April 1, 2024
• Study Completion: April 1, 2024
• Last Updated: June 7, 2023

Record last verified: 2023-05

Data Sharing

• IPD Sharing: Will not share

Locations

FR (1)