Ventilation in Cardiac Surgery

University Hospital, Caen1,000 enrolled

Overview

The purpose of this study is to evaluate prospectively ventilatory practices in the perioperative cardiac surgery period.

This is a International Multicentre Observational Trial on all adult cardiac surgery patients with cardiopulmonary bypass (CPB).

Study Type

OBSERVATIONAL

Enrollment

1,000

Conditions

Respiratory Complication Respiration, Artificial Anesthesia, General Bypass, Cardiopulmonary

Interventions

SurveyOTHER

An anonymised questionnaire will be answered for each includable consecutive patient after verifying the absence of exclusion criteria.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * All consecutive cardiac surgery patients with CPB during one predefined period, * Elective or urgent surgery as defined by EuroSCORE2. Exclusion Criteria: * Refusal of consent, * Pregnant women, * Age \< 18 years, * Heart transplant, ECLS, ventricular assist * Emergency or salvage surgery as defined by EuroSCORE2

Locations (10)

CUB Erasm, Université libre de Bruxelles

Brussels, Belgium

Universidade Federal de São Paulo (UNIFESP)

Brasil, Brazil

General University Hospital

Prague, Czechia

Caen University Hospital

Caen, France

Outcomes

Primary Outcomes

incidence of use prophylactic protective mechanical ventilation defined with with low tidal volume (6 to 8 ml / kg based on the ideal body weight)

percent

Time frame: 1 day

Secondary Outcomes

incidence of using positive end-expiratory pressure

(PEEP)\> 5 cmH2O

Time frame: 1 day

incidence of using at least 2 alveolar lung recruitment manoeuvres

percent

Time frame: 1 day

incidence of using a protective ventilation bundle combining prophylactic protective mechanical ventilation and at least 2 alveolar recruitment manoeuvres

percent

Time frame: 1 day

incidence of postoperative pulmonary complications

percent

Time frame: 1 month postoperatively

Central Contacts

Marc-Olivier Fischer, MD, PhD

CONTACT

+33 2 31 06 31 06 fischer-mo@chu-caen.fr

Jennifer Brunet, MD

CONTACT

33 2 31 06 31 06 brunet-j@chu-caen.fr

Data from ClinicalTrials.gov

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