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Study of Ventilator Associated Event During Intensive Care After Resuscitated Cardiac Arrest.

Study of Ventilator Associated Event During Intensive Care After Resuscitated Cardiac Arrest.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06466980
Acronym
VAE-ACR
Enrollment
150
Registered
2024-06-20
Start date
2024-06-27
Completion date
2025-12-31
Last updated
2025-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest With Successful Resuscitation, Mechanical Ventilation

Keywords

Ventilator associated event, cardiac arrest, ventilator-acquired pneumonia, ventilator associated pneumonia

Brief summary

The aim is to describe the incidence, characteristics, risk factors and outcome of complications acquired under mechanical ventilation (called ventilator-associated events) according to the new CDC criteria, in a population of patients admitted in intensive care unit after cardiac arrest.

Detailed description

Cardiac arrest (CA) survivors are frequently admitted to intensive care units. Despite improvements in management techniques, the prognosis of these patients remains poor, with mortality exceeding 90% for out-of-hospital CA and around 80% for in-hospital CA, along with a high risk of severe neurological issue. The management of these patients in intensive care requires the use of invasive mechanical ventilation. Complications occurring under mechanical ventilation have been the subject of many researches. Early bacterial pneumonia or ventilator-acquired pneumonia appears as the primary cause of respiratory worsening, and several studies have already focused on their incidence and prevention. However, studies on the benefits of antibiotic therapy or antibiotic prophylaxis for early pulmonary infections are of tricky analysis, particularly when they do not consider respiratory condition or mortality for their primary outcome measure. A new definition of complications associated with mechanical ventilation (VAEs) has been established by the Centers for Disease Control and Prevention (CDC) since 2013. It offers a more relevant tool for monitoring the impact of preventive measures on morbidity and mortality, with a more objective definition that goes beyond just tracking ventilator-associated pneumonia. Several studies have since analyzed the incidence and impact of VAEs on cohorts of intensive care patients, confirming the association between VAEs and morbidity and mortality. However, to our knowledge, none have targeted a population of cardiac arrest survivors.

Interventions

OTHERVentilator associated event

Measure of incidence of Ventilator associated event

Sponsors

Centre Hospitalier Sud Francilien
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult male or female * Non-pregnant female * Successfully resuscitated from cardiac arrest during primary care * Invasive mechanical ventilation initiated during resuscitation and continued for at least 4 days * No decision to limit life-sustaining therapies within 24 hours following admission to intensive care * No requirement of arteriovenous circulatory support during intensive care management

Exclusion criteria

\- patients who opposed to the use of their data

Design outcomes

Primary

MeasureTime frameDescription
numberat day 28Incidence of ventilator associated event

Secondary

MeasureTime frameDescription
Associated factorsat day 28Associated factors of ventilator associated event
number of pneumoniasat day 28Ventilator associated pneumonia according to the American Thoracic Society definition
timeat day 28Mechanical ventilation duration
number of deathsat day 28In-hospital mortality

Countries

France

Contacts

Primary ContactFabrice COOK, MD
fabrice.cook@chsf.fr01 61 69 52 28
Backup ContactCaroline TOURTE
caroline.tourte@chsf.fr01 61 69 31 50

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026