Derivation and validation of predictive indices for 30-day mortality after coronary and valvular surgery in Ontario, Canada
- PMID: 34810162
- PMCID: PMC8608458
- DOI: 10.1503/cmaj.202901
Derivation and validation of predictive indices for 30-day mortality after coronary and valvular surgery in Ontario, Canada
Abstract
Background: Coronary artery bypass grafting (CABG) and surgical aortic valve replacement (AVR) are the 2 most common cardiac surgery procedures in North America. We derived and externally validated clinical models to estimate the likelihood of death within 30 days of CABG, AVR or combined CABG + AVR.
Methods: We obtained data from the CorHealth Ontario Cardiac Registry and several linked population health administrative databases from Ontario, Canada. We derived multiple logistic regression models from all adult patients who underwent CABG, AVR or combined CABG + AVR from April 2017 to March 2019, and validated them in 2 temporally distinct cohorts (April 2015 to March 2017 and April 2019 to March 2020).
Results: The derivation cohorts included 13 435 patients who underwent CABG (30-d mortality 1.73%), 1970 patients who underwent AVR (30-d mortality 1.68%) and 1510 patients who underwent combined CABG + AVR (30-d mortality 3.05%). The final models for predicting 30-day mortality included 15 variables for patients undergoing CABG, 5 variables for patients undergoing AVR and 5 variables for patients undergoing combined CABG + AVR. Model discrimination was excellent for the CABG (c-statistic 0.888, optimism-corrected 0.866) AVR (c-statistic 0.850, optimism-corrected 0.762) and CABG + AVR (c-statistic 0.844, optimism-corrected 0.776) models, with similar results in the validation cohorts.
Interpretation: Our models, leveraging readily available, multidimensional data sources, computed accurate risk-adjusted 30-day mortality rates for CABG, AVR and combined CABG + AVR, with discrimination comparable to more complex American and European models. The ability to accurately predict perioperative mortality rates for these procedures will be valuable for quality improvement initiatives across institutions.
© 2021 CMA Joule Inc. or its licensors.
Conflict of interest statement
Competing interests: Louise Sun received support from the Canadian Institutes of Health Research (CIHR) for article processing charges. Dr. Sun was named National New Investigator by the Heart and Stroke Foundation of Canada, and is supported by a Clinical Research Chair in Big Data and Cardiovascular Outcomes at the University of Ottawa. Douglas Lee is the Ted Rogers Chair in Heart Function Outcomes, University Health Network, University of Toronto. Dr. Lee also received a research grant from CorHealth Ontario and a foundation grant from the Canadian Institutes of Health Research (CIHR). Peter Austin is supported by a Mid-Career Investigator Award from the Heart and Stroke Foundation. Dr. Austin also reports receiving a CIHR Project Grant, paid to Sunnybrook Research Institute. No other competing interests were declared.
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