ObjectiveIt remains unclear if intraoperative lung-protective strategies can reduce the rate of respiratory complications after heart surgery, partly because low-risk patients have been studied in the past. We established a screening model to easily identify a high-risk group for severe pulmonary complications (i.e., pneumonia or ARDS) that may be the ideal target population for the assessment of potential benefits of such measures. DesignRetrospective observational trial. SettingDepartments of cardiac surgery and cardiac anesthesia of university hospital. Participants: Consecutive patients undergoing heart surgery on cardiopulmonary bypass (CPB) and subsequent treatment at a dedicated cardiosurgical ICU between January 2019 and March 2021. InterventionsNone Measurements and main resultsOf 2572 patients undergoing surgery, 84 patients (3.3%) developed pneumonia/ARDS that significantly impacted outcome (i.e., longer ventilatory support (66 vs. 11%), higher reintubation rate (39 vs. 3%), prolonged length of ICU (33±36 vs. 4±10 days) and hospital stay (10±15 vs. 6±7 days), and higher in-hospital (43 vs. 9%) as well as 30-day (7 vs. 3%) mortality). Our screening model for severe pulmonary complications includes LVEF < 52%, EuroSCOREII > 5.9, CPB time > 123 minutes, left ventricular assist device or aortic repair surgery, and bronchodilatory therapy. A cut-off for the predicted risk of 2.5 % showed optimal sensivity and specificity with an AUC of 0.82. ConclusionWe suggest that future research on intraoperative lung protective measures should focus on this high-risk population and primarily aiming at mitigation of severe forms of postoperative pulmonary dysfunction associated with poor outcome and increased resource consumption.
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