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Updated: Feb 11, 2026

Objective Nociceptive Assessment in Ventilated ICU Patients: A Feasibility Study Using Pupillometry and the Nociceptive Flexion Reflex
Published on: July 4, 2018
Infection-related ventilator-associated complications in ICU patients colonised with extended-spectrum
François Barbier1, Sébastien Bailly2, Carole Schwebel3
1Medical ICU, La Source Hospital, CHR Orléans, Orléans, France.
Purpose:
To investigate the clinical significance of infection-related ventilator-associated complications (IVAC) and their impact on carbapenem consumption in mechanically ventilated (MV) patients colonised with extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBLE).
Methods:
Inception cohort study from the French prospective multicenter OUTCOMEREA database (17 ICUs, 1997-2015) including all ESBLE carriers (systematic rectal swabbing at admission then weekly and/or urinary or superficial surgical site colonisation) with MV duration > 48 h and ≥ 1 episode of IVAC after carriage documentation. All ICU-acquired infections were microbiologically documented.
Results:
The 318 enrolled ESBLE carriers (median age 68 years; males 67%; medical admission 68%; imported carriage 53%) experienced a total of 576 IVAC comprising 361 episodes (63%) without documented infection, 124 (21%) related to infections other than ventilator-associated pneumonia (VAP), 73 (13%) related to non-ESBLE VAP and 18 (3%) related to ESBLE VAP. Overall, ESBLE infections accounted for only 43 episodes (7%). Carbapenem exposure within the preceding 3 days was the sole independent predictor of ESBLE infection as the causative event of IVAC, with a protective effect (adjusted odds ratio 0.2, 95% confidence interval 0.05-0.6; P < 0.01). Carbapenems were initiated in 9% of IVAC without infection, 15% of IVAC related to non-VAP infections, 42% of IVAC related to non-ESBLE VAP, and 56% of IVAC related to ESBLE VAP (ESBLE VAP versus non-ESBLE VAP: P = 0.43).
Conclusions:
IVAC in ESBLE carriers mostly reflect noninfectious events but act as a strong driver of empirical carbapenem consumption. ESBLE infections are scarce yet hard to predict, strengthening the need for novel diagnostic approaches and carbapenem-sparing alternatives.
Insights
Infection-related ventilator-associated complications (IVAC) in extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBLE) carriers often stem from non-infectious causes, yet significantly increase carbapenem use. Predicting rare ESBLE infections requires better diagnostics and carbapenem-sparing strategies.
Area of Science:
- Infectious Diseases
- Critical Care Medicine
- Antimicrobial Stewardship
Background:
- Extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBLE) colonization is a concern in intensive care units.
- Mechanically ventilated (MV) patients are at risk for ventilator-associated complications (VAC).
- Understanding the drivers of antimicrobial consumption is crucial for stewardship.
Purpose of the Study:
- To determine the clinical significance of infection-related ventilator-associated complications (IVAC).
- To assess the impact of IVAC on carbapenem consumption in ESBLE-colonized, MV patients.
- To differentiate between infectious and non-infectious causes of IVAC in this population.
Main Methods:
- Prospective inception cohort study (OUTCOMEREA database, 1997-2015).
- Inclusion of ESBLE carriers with MV > 48h and at least one IVAC episode.
- Microbiological documentation of all ICU-acquired infections.
Main Results:
- 318 ESBLE carriers experienced 576 IVAC episodes; 63% were without documented infection.
- ESBLE infections accounted for only 7% of IVAC episodes.
- Prior carbapenem exposure was the sole predictor of ESBLE infection (protective effect).
- Carbapenem initiation increased with IVAC severity, from 9% (no infection) to 56% (ESBLE VAP).
Conclusions:
- IVAC in ESBLE carriers are frequently non-infectious but drive empirical carbapenem use.
- ESBLE infections are uncommon but difficult to predict.
- Novel diagnostic tools and carbapenem-sparing strategies are needed for ESBLE carriers.
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