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Page 12 of 15                  Dokko et al. Vessel Plus 2022;6:53  https://dx.doi.org/10.20517/2574-1209.2022.11

               reflecting comorbidity burden in patients undergoing r-AVR procedures was also shown to a predictor of
                                                                                            [36]
               MM and was similarly shown in a study by Nagaraja et al examining 40,604 TAVR patients .
               CONCLUSION
               Affecting 41% of the New York State r-AVR population, the r-AVR POAF/AFL rates are comparable to that
               of first-time AVR. Due to the increased risk of READMIT for these patients undergoing r-AVR, the “at
               risk” (i.e., older and cerebrovascular patients undergoing r-SAVR) may now be identified for possible
               prophylactic treatments such as antiarrhythmic medications post r-AVR procedure. With the increasing
               volume of SAVR and TAVR procedures being performed, there is also an increasing trend toward
               bioprosthetic valves and performing ViV-TAVR procedures.

               Over time, the r-AVR patients’ profiles have changed. In the latter time periods, there were higher
               proportions of patients who were older and patients with higher rates of cerebrovascular disease; these
               patients were “at risk” of readmission within 30 days. Importantly, black patients and/or patients with high
               Elixhauser comorbidity scores should be proactively identified by clinicians as “at risk” populations. With a
               focus on targeting these higher-risk r-AVR populations, future clinical trials should investigate innovative
               prophylaxis and treatment regimens that might improve the clinical outcomes and reduce the differential
               burden of health care costs incurred. Most importantly, post-r-AVR discharge continuity of care and
               specialty consultations should be investigated to assure successful convalescence of the POAF/AFL patients.


               Limitations
               This New York State observational study was limited by its retrospective, cohort study design due to
               possible unmeasured patient risk factors that may have been confounders impacting this study’s findings.
               As one potential source of bias, TAVR was initially restricted by the FDA to high-risk patients. Based on
               revisions in the TAVR eligibility criteria, TAVR was later made available to moderate-risk patients.


               With mandatory submissions for all billed encounters enforced by Department of Health audits, this New
               York statewide database is anticipated to be complete. Given these same billing codes were used in financial
               transactions by these healthcare facilities with insurance agencies, this database’s findings are most likely
               highly accurate. Although there is high confidence in the POAF/AFL propensity model, there was data
               sparsity identified for the MM and READMIT multivariate logistic regression models; using appropriate
               analytic techniques, however, these models also had relatively high c-indices with no calibration concerns
               identified; hence, the POAF/AFL association reported with the READMIT endpoint appears to be robust
               for this New York State-based r-AVR patient population.  Although this study’s r-AVR population was
               smaller in size, the SPARCS database represents the entire New York State population’s experience. Given
               that r-AVR procedures occur infrequently, future investigations should use regional or national databases to
               verify the generalizability of these New York State findings.


               DECLARATIONS
               Acknowledgements
               Thanks are sent to the Stony Brook University Renaissance School of Medicine’s Department of Surgery
               Division of Cardiothoracic Surgery staff (Ms. Kathleen O’Brien) and Scholarly Concentrations Programs
               Research Track staff (Dr. Howard Fleit and Ms. Rhonda Kearns) for their administrative oversight and
               support. Thanks are also sent to the Office of Quality and Patient Safety in the New York State Department
               of Health for their SPARCS database access, support and guidance with this project. Finally, our team
               acknowledges the biostatistical consultation and analytical support provided by the Biostatistical Consulting
               Core (Dr. Jie Yang and Ms. Xiaoyue Zhang) at the Renaissance School of Medicine, Stony Brook University.
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