Abstract

BackgroundPostoperative pulmonary complications are a leading cause of morbidity and mortality after cardiac surgery. There are no recommendations on mechanical ventilation associated with cardiopulmonary bypass (CPB) during surgery and anesthesiologists perform either no ventilation (noV) at all during CPB or maintain low tidal volume (LTV) ventilation. Indirect evidence points towards better pulmonary outcomes when LTV is performed but no large-scale prospective trial has yet been published in cardiac surgery.DesignThe MECANO trial is a single-center, double-blind, randomized, controlled trial comparing two mechanical ventilation strategies, noV and LTV, during cardiac surgery with CPB. In total, 1500 patients are expected to be included, without any restrictions. They will be randomized between noV and LTV on a 1:1 ratio. The noV group will receive no ventilation during CPB. The LTV group will receive 5 breaths/minute with a tidal volume of 3 mL/kg and positive end-expiratory pressure of 5 cmH2O. The primary endpoint will be a composite of all-cause mortality, early respiratory failure defined as a ratio of partial pressure of oxygen/fraction of inspired oxygen <200 mmHg at 1 hour after arrival in the ICU, heavy oxygenation support (defined as a patient requiring either non-invasive ventilation, mechanical ventilation or high-flow oxygen) at 2 days after arrival in the ICU or ventilator-acquired pneumonia defined by the Center of Disease Control. Lung recruitment maneuvers will be performed in the noV and LTV groups at the end of surgery and at arrival in ICU with an insufflation at +30 cmH20 for 5 seconds. Secondary endpoints are those composing the primary endpoint with the addition of pneumothorax, CPB duration, quantity of postoperative bleeding, red blood cell transfusions, revision surgery requirements, length of stay in the ICU and in the hospital and total hospitalization costs. Patients will be followed until hospital discharge.DiscussionThe MECANO trial is the first of its kind to compare in a double-blind design, a no-ventilation to a low-tidal volume strategy for mechanical ventilation during cardiac surgery with CPB, with a primary composite outcome including death, respiratory failure and postoperative pneumonia.Trial registrationClinicalTrials.gov, NCT03098524. Registered on 27 February 2017.

Highlights

  • Postoperative pulmonary complications are a leading cause of morbidity and mortality after cardiac surgery

  • The MECANO trial is the first of its kind to compare in a double-blind design, a no-ventilation to a lowtidal volume strategy for mechanical ventilation during cardiac surgery with cardiopulmonary bypass (CPB), with a primary composite outcome including death, respiratory failure and postoperative pneumonia

  • Endpoints The primary endpoint is a composite of overall death, early respiratory failure defined as partial pressure of oxygen (PaO2)/fraction of inspired oxygen (FiO2) ratio

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Summary

Discussion

Postoperative pulmonary complications (PPCs) are common and serious complications after cardiac surgery [15], despite continuing improvements in CPB techniques and postoperative intensive care. It is a single-blind study and focuses on indirect outcomes (PaO2/FiO2 ratio only) instead of harder clinical endpoints such as hospitalacquired pneumonia or death This explains why the number of patients to be included in CPBVENT is smaller (n = 720 vs n = 1500 in our study). The surgeon has the final say in the type of mechanical ventilation, i.e. he can stop any type of ventilation strategy during CPB as he sees fit This bias is addressed by systematically collecting the reason for and number of times that this may happen. The MECANO trial should help determine whether low-tidal ventilation is superior to no-ventilation, during cardiac surgery with CPB It is the first doubleblind trial of this kind, with a large population and focusing on hard clinical endpoints (Table 2, Additional file 1).

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