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Open Lung Protective Ventilation in Cardiac Surgery (PROVECS)

Primary Purpose

Hypoxemia

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Open lung protective ventilation strategy
Sponsored by
Assistance Publique Hopitaux De Marseille
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypoxemia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Cardiac surgery planned with CPB and sternotomy.
  • Age > 18 years old.

Exclusion Criteria:

  • Urgent surgery : cardiac transplantation, aortic dissection, active endocarditis.
  • Aortic arch surgery with circulatory arrest.
  • LVAD surgery.
  • Acute or chronic preoperative hypoxemia (PaO2 < 65 mmHg in air).
  • Preoperative shock state requiring catecholamines.
  • LVEF < 40%.
  • Pulmonary hypertension with systolic pulmonary artery pressure > 50 mmHg.
  • Severe right ventricular dysfunction (TDI tricuspid annular systolic velocity < 10 cm.s-1).
  • Chronic kidney disease (Glomerular filtration rate < 30 mL/min).
  • Body Mass Index > 35kg/m2.
  • Patient's refusal.

Sites / Locations

  • CHU de Bordeaux
  • Hôpital Louis Pradel HCL
  • Assistance Publique Hopitaux de Marseille
  • CHU MontpellierHôpital Arnaud de VILLENEUVE
  • Hôpital Européen Georges Pompidou AP-HP
  • CHU Strasbourg

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Open lung protective ventilation

Conventional strategy

Arm Description

Recruitment maneuvers (30 cmH2O during 30 seconds) after intubation, after CPB initiation, before aortic declamping and at ICU arrival. PEEP at 8 cmH2O. Ultraprotective ventilation during CPB: PEEP 8 cmH2O, Tidal volume 3mL/kg, Respiratory rate 12 cycles per minute, FiO2 40%. Assigned intervention - Procedure: patients are randomized and ventilated with the open lung strategy from intubation to detubation.

No recruitment maneuvers. PEEP at 2 cmH2O. During CPB: continuous positive pressure at 2 cmH2O.

Outcomes

Primary Outcome Measures

Post-operative pulmonary complications defined as a composite endpoint
Mild hypoxemia Moderate hypoxemia Severe hypoxemia Severe bronchospam Radiological atelectasis Respiratory acidosis Pneumonia Pleural effusion Acute Respiratory Distress Syndrome Need for reintubation Need for reintubation

Secondary Outcome Measures

Postoperative extrapulmonary complication
Systemic inflammatory response syndrome Sepsis Septic chock Mediastinitis Pericardial tamponade Surgical bleeding Acute kidney failure (KDIGO stage 2 or 3) Postoperative atrial fibrillation Cardiogenic chock Delirium
ICU free Days
Days alive and free from the need of intensive care

Full Information

First Posted
July 7, 2016
Last Updated
March 17, 2023
Sponsor
Assistance Publique Hopitaux De Marseille
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1. Study Identification

Unique Protocol Identification Number
NCT02866578
Brief Title
Open Lung Protective Ventilation in Cardiac Surgery
Acronym
PROVECS
Official Title
Open Lung Protective Ventilation During Cardiac Surgery With Cardiopulmonary Bypass : a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
September 23, 2016 (Actual)
Primary Completion Date
May 7, 2018 (Actual)
Study Completion Date
May 7, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique Hopitaux De Marseille

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Cardiac surgery with cardiopulmonary bypass (CPB) frequently induces post-operative respiratory dysfunction. The post-operative pulmonary complications (PPCs) significantly increase the peri-operative morbidity and require invasive treatments during longer and more expensive ICU stays. A specific pathophysiology involving general anesthesia and CPB-related factors (inflammation, pulmonary ischemia) has been clearly demonstrated and pulmonary atelectasis seems to play a central role in the occurence of these PPCs. The open lung approach is a ventilation strategy that aims to "open the lung and keep it open" using different ventilatory settings. The efficacy of that strategy is not demonstrated in the global surgical population. However, its application in the perioperative care of cardiac surgery patients could be of great interest by counteracting the development of atelectasis. The purpose of this multicentre, double blinded, randomized controlled study is to evaluate the influence of a perioperative multimodal protective ventilation strategy based on the "open lung approach" on postoperative outcomes during the first 7 days following cardiac surgery. Participating centres will include 500 adult patients undergoing scheduled on-pump cardiac surgery. The open lung approach will combine recruitment maneuvers (RM), positive end expiratory pressure (PEEP) at 8 cmH2O from intubation to detubation and continuation of ultraprotective ventilation during CPB. It will be compared to a conventional approach without RM, with PEEP at 2 cmH2O and discontinuation of ventilation during CPB. The primary endpoint is any post-operative pulmonary complication. The secondary endpoints are any post-operative extra-pulmonary complications and the number of ICU-free days to day 7.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoxemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
494 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Open lung protective ventilation
Arm Type
Experimental
Arm Description
Recruitment maneuvers (30 cmH2O during 30 seconds) after intubation, after CPB initiation, before aortic declamping and at ICU arrival. PEEP at 8 cmH2O. Ultraprotective ventilation during CPB: PEEP 8 cmH2O, Tidal volume 3mL/kg, Respiratory rate 12 cycles per minute, FiO2 40%. Assigned intervention - Procedure: patients are randomized and ventilated with the open lung strategy from intubation to detubation.
Arm Title
Conventional strategy
Arm Type
No Intervention
Arm Description
No recruitment maneuvers. PEEP at 2 cmH2O. During CPB: continuous positive pressure at 2 cmH2O.
Intervention Type
Procedure
Intervention Name(s)
Open lung protective ventilation strategy
Primary Outcome Measure Information:
Title
Post-operative pulmonary complications defined as a composite endpoint
Description
Mild hypoxemia Moderate hypoxemia Severe hypoxemia Severe bronchospam Radiological atelectasis Respiratory acidosis Pneumonia Pleural effusion Acute Respiratory Distress Syndrome Need for reintubation Need for reintubation
Time Frame
first 7 days post-operatively.
Secondary Outcome Measure Information:
Title
Postoperative extrapulmonary complication
Description
Systemic inflammatory response syndrome Sepsis Septic chock Mediastinitis Pericardial tamponade Surgical bleeding Acute kidney failure (KDIGO stage 2 or 3) Postoperative atrial fibrillation Cardiogenic chock Delirium
Time Frame
First 7 days post operatively
Title
ICU free Days
Description
Days alive and free from the need of intensive care
Time Frame
First 7 days post operatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cardiac surgery planned with CPB and sternotomy. Age > 18 years old. Exclusion Criteria: Urgent surgery : cardiac transplantation, aortic dissection, active endocarditis. Aortic arch surgery with circulatory arrest. LVAD surgery. Acute or chronic preoperative hypoxemia (PaO2 < 65 mmHg in air). Preoperative shock state requiring catecholamines. LVEF < 40%. Pulmonary hypertension with systolic pulmonary artery pressure > 50 mmHg. Severe right ventricular dysfunction (TDI tricuspid annular systolic velocity < 10 cm.s-1). Chronic kidney disease (Glomerular filtration rate < 30 mL/min). Body Mass Index > 35kg/m2. Patient's refusal.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Urielle DESALBRES
Organizational Affiliation
AP-HM
Official's Role
Study Director
Facility Information:
Facility Name
CHU de Bordeaux
City
Bordeaux
Country
France
Facility Name
Hôpital Louis Pradel HCL
City
Lyon
Country
France
Facility Name
Assistance Publique Hopitaux de Marseille
City
Marseille
ZIP/Postal Code
13354
Country
France
Facility Name
CHU MontpellierHôpital Arnaud de VILLENEUVE
City
Montpellier
Country
France
Facility Name
Hôpital Européen Georges Pompidou AP-HP
City
Paris
Country
France
Facility Name
CHU Strasbourg
City
Strasbourg
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31576435
Citation
Lagier D, Fischer F, Fornier W, Huynh TM, Cholley B, Guinard B, Heger B, Quintana G, Villacorta J, Gaillat F, Gomert R, Degirmenci S, Colson P, Lalande M, Benkouiten S, Minh TH, Pozzi M, Collart F, Latremouille C, Vidal Melo MF, Velly LJ, Jaber S, Fellahi JL, Baumstarck K, Guidon C; PROVECS Study Group. Effect of open-lung vs conventional perioperative ventilation strategies on postoperative pulmonary complications after on-pump cardiac surgery: the PROVECS randomized clinical trial. Intensive Care Med. 2019 Oct;45(10):1401-1412. doi: 10.1007/s00134-019-05741-8. Epub 2019 Oct 1.
Results Reference
derived
PubMed Identifier
30424770
Citation
Lagier D, Fischer F, Fornier W, Fellahi JL, Colson P, Cholley B, Jaber S, Baumstarck K, Guidon C; PROVECS investigators and the ARCOTHOVA group. A perioperative surgeon-controlled open-lung approach versus conventional protective ventilation with low positive end-expiratory pressure in cardiac surgery with cardiopulmonary bypass (PROVECS): study protocol for a randomized controlled trial. Trials. 2018 Nov 13;19(1):624. doi: 10.1186/s13063-018-2967-y.
Results Reference
derived

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Open Lung Protective Ventilation in Cardiac Surgery

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