We found an increased incidence of new-onset BBB in patients undergoing transapical TAVR compared with transfemoral TAVR. Our findings correlate well with those of other TAVR studies [4,5,6]. The incidence of new-onset LBBB has been more exhaustively analyzed than new-onset RBBB, presumably due to more concerning clinical implications of new-onset LBBB. Published incidence rates of LBBB range from 4 to 65% with first-generation valves and 18–65% with balloon-expandable valves [1].
Other clinical risk factors that predict new-onset LBBB after TAVR include female gender, previous coronary artery bypass graft (CABG), pre-procedural QRS prolongation, diabetes mellitus, and prosthesis implantation depth within the LVOT, which is the most consistently reported predictor of intraventricular conduction delays [1]. We found an increased percentage of transapical TAVR patients in our study with low implantation depth, which may help to explain the increased risk of new-onset BBB in this group. Correspondingly, the transapical group was also at increased risk for needing TAV-in-TAV deployment to correct prosthesis malposition.
Our study also demonstrated a trend towards diabetes as an independent risk factor for new-onset LBBB in transapical TAVR patients. This is particularly concerning, as patients with LBBB and diabetes demonstrate more severe left ventricular systolic dysfunction than those with LBBB but without diabetes [7].
Overall, intra-procedural and post-procedural morbidity and mortality were also increased in the transapical group. This included increased risk for arrhythmias, peri-procedural MI, readmission, and all-cause mortality. We also witnessed a trend towards increased risk of acute kidney injury and significant post-procedural hemorrhage in the transapical group. These findings correspond with a recent publication by Stamou et al. who reported increased risk of blood transfusions, readmission, postoperative stroke, and atrial fibrillation in patients undergoing alternative access (non-femoral) TAVR [4]. Others have also noticed a trend towards improved 1-year survival rates in the transfemoral TAVR patients relative to the transapical approach [5].
Study limitations: this study was nonrandomized, with results that may be influenced by unmeasured confounders. The small number of certain outcomes, such as mortality, precludes a more detailed statistical analysis to evaluate for underlying confounding variables. This study was not designed to specifically evaluate mortality in transfemoral vs. transapical TAVR patients according to VARC-2 consensus guidelines [6] and we encourage future investigators to add to the body of literature in this regard. Data regarding specific valve type were not recorded. Also, data regarding the use of various atrioventricular node-blocking medications and electrocardiographic findings in our patients was not available.