Page 143 - Read Online
P. 143

Novotny et al. Vessel Plus 2022;6:51  https://dx.doi.org/10.20517/2574-1209.2021.139  Page 13 of 15

               echocardiographic information (e.g., aortic valve area, gradient across the valve, velocity across the valve,
               and dimensionless index), this clinical information was not available for endpoint risk-adjustment. Based on
               billing codes alone, continuous arrhythmias could not be distinguished from intermittent arrhythmias to
               analyze for a differential effect on outcomes. Additionally, SPARCS does not include medication details (i.e.,
               national drug codes); thus, the impact of different medical management approaches using specific drug
               therapies either pre-procedure or perioperatively could not be further investigated.

               In conclusion, Pre-operative AF/AFL was not associated with 30-day readmission or the composite
               endpoint, consisting of major complications and/or operative mortality, following r-SAVR and viv-TAVR.
               However, this study identified other predictors of these adverse outcomes, including black race, Elixhauser
               mortality score, and cerebrovascular disease, which may allow clinicians to identify patients at elevated
               r-AVR risk.


               DECLARATIONS
               Acknowledgements
               Special thanks are provided to the Biostatistical Consulting Core Lab (Dr. Jie Yang, Director) and to the
               Scholarly Concentration Program Research Track (Dr. Howard Fleit, Dr. A. Laurie Shroyer, and Ms.
               Rhonda Kearns) at the Renaissance School of Medicine, Stony Brook University for their support of this
               medical student research project. Additionally, special thanks are provided to the Office of Quality and
               Patient Safety in the New York State Department of Health in Albany, New York for their support for Dr.
               Pryor’s SPARCS database records extraction.

               Authors’ contributions
               Study conception and design: Novotny S, Dokko J, Shroyer AL, Bilfinger T
               Data acquisition: Novotny S, Agha S, Yaligar A, Kolba N, Tummala V, Shroyer AL, Bilfinger T
               Data analysis: Zhang X, Shroyer AL, Bilfinger T
               Administrative, technical, and material support: Parikh PB, Pryor AD, Tannous HJ, Shroyer AL, Bilfinger T
               Manuscript writing: Novotny S, Dokko J, Zhang X, Agha S, Yaligar A, Shroyer AL, Bilfinger T
               Manuscript editing: Novotny S, Dokko J, Zhang X, Agha S, Yaligar A, Kolba N, Tummala V, Parikh PB,
               Pryor AD, Tannous HJ, Shroyer AL, Bilfinger T


               Availability of data and materials
               Data was obtained from the 2005-2018 New York State Statewide Planning and Research Cooperative
               System database.


               Financial support and sponsorship
               The Stony Brook Renaissance School of Medicine small grant (Dr. Parikh -Principal Investigator; Dr.
               Shroyer, co-Principal Investigator) and the Division of Cardiothoracic Surgery General T. F. Cheng
               endowment (Dr. Tannous-Principal Investigator) provided partial support for this project.

               Conflicts of interest
               The authors declared that there are no conflicts of interest.

               Ethical approval and consent to participate
               This study (IRB2021-00563: Pre-AF r-AVR SPARCS Study) relies on deidentified data reports; thus, this
               study was determined to be “not human subjects research” by the institutional review board of the Stony
               Brook University Committee on Research in Human Subjects on November 2, 2021.
   138   139   140   141   142   143   144   145   146   147   148