A STUDY BEFORE/AFTER THE IMPLEMENTATION OF AN ANTI-INFECTIOUS PRESCRIPTION AID

University Hospital Center (CHU)

Status: Completed

Conditions: Septic Shock; Sepsis

Treatments: Device: Anti-infectious prescription support tool

Study type: Observational

Funder types: Other

Identifiers

NCT05140213

RECHMPL21_0685

Details and patient eligibility

About

Anti-infective strategy is a major public health problem. This is a before-and-after study of an anti-infectious prescription tool with a comparison of mortality at 30 days (then 3 and 6 months) between the two inclusion phases of 6 months each.

Enrollment: 371 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Major patients
• Sepsis or septic shock
• Oral consent

Exclusion criteria

• minor patients
• death before antibiotherapy
• care limitations
• pre-hospital antibiotherapy

Trial design

371 participants in 2 patient groups

Group 1 : Before

Description:

"Before" phase including 186 patients patients included before the implementation of the prescription support tool

Treatment:

Device: Anti-infectious prescription support tool

Group 2 : After

Description:

"After" phase including 185 patients patients included after the implementation of the prescription support tool

Treatment:

Device: Anti-infectious prescription support tool