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Introduction Aortic stenosis (AS) is the most common valvular heart disease, affecting 12,4% of elderly patients over 75 years old. For those needing SAVR but who are ineligible to undergo such a demanding procedure, TAVI is a less invasive approach. Methods This study used data from patients undergoing SU-AVR at U.Z. Gasthuisberg, Leuven and data reported in the literature concerning TAVI to compare short- and long-term outcomes in both groups for moderate risk patients. The patients from the SU-AVR were a subgroup from a multi-center study, the Cavalier trial. A literature search was performed to attain data from patients, with a EUROSCORE II or STS risk score similar to the SU-AVR group, undergoing TAVI. Results The rate of permanent pacemaker implantation at hospital discharge after SU-AVR was 7.9%. At 1,2 and 3 years, the Kaplan-Meier survival rate was 90.2, 85.1 and 78.1, respectively. Median in-hospital length of stay after SU-AVR was 13.9±9.1. Occurrence of any paravalvular or mild to moderate central aortic valve leakage was 8.6% and 5.3%, respectively. Median transaortic peak gradient and mean gradient after SU-AVR were 27.8±10.3 and 15.3±6.1. The median effective orifice area at discharge was 1.53±0.5. Discussion We found that SU-AVR had a better survival, less need for pacemaker implantation and lower rates of paravalvular leakage, whereas TAVI had lower aortic-valve gradients, larger aortic valve areas and a shorter hospital stay. The overall better survival of patients treated with SU-AVR can partially be contributed to their slightly younger age. It is not known if the better hemodynamics in the TAVI group have a clinical effect, as aortic-valve hemodynamics are substantially improved in both the TAVI and SU-AVR group. Conclusion TAVI and SU-AVR are both safe alternatives to SAVR with proven efficacies. TAVI remains most beneficial in high risk patients while SU-AVR has found its place filling the gap between SAVR and TAVI. Studying Perceval valve (SU-AVR) data from U.Z. Gasthuisberg corroborates many findings described in the literature such as the higher incidence of paravalvular leakage and favorable valvular gradients in the TAVI group. However, lower mortality and need for pacemaker implantation in our Perceval cohort offer a slight discrepancy as these were not shown to be significantly different in previous publications. Future studies should focus on randomized trials and long term follow-up, as life expectancies for TAVI and SU-AVR candidates continue to increase.
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Introduction: Lung transplantation offers hope to patients with end-stage lung disease, but chronic lung allograft dysfunction (CLAD) affects 50% of recipients within five years post-transplant. Alloimmunity and infections play significant roles in CLAD's development. Previous studies have shown that polymorphisms (single nucleotide polymorphisms = SNP) in the pentraxin-3 (PTX3) gene can influence the risk of invasive Aspergillus infection in hematopoietic stem-cell transplantation. This study investigates the impact of PTX3 polymorphisms in lung transplant recipients and donors on the incidence of Aspergillus infection, Pseudomonas aeruginosa infection, CMV infection, acute cellular rejection and (CLAD-free) survival. Methods: We selected a cohort of lung transplant recipients and their donors. Clinical and demographic data were collected for our various endpoints. DNA was extracted from blood samples and sequenced to become the genotype of PTX3-gen for each donor and recipient. Kaplan-Meier survival curves were used to assess the relationship between genetics and clinical data. Results: Aspergillus infection and colonization were not significantly linked to PTX3 SNPs. However Pseudomonas aeruginosa colonization was significantly correlated with donor SNP rs2120243 (P = 0.0442). No significant associations were found between CMV infection and PTX3 polymorphisms. A significant correlation was seen between acute cellular rejection and recipient SNP rs2305619 (P = 0.0500) and SNP rs3816527 (P = 0.0434). No significant impact on (CLAD-free) survival was observed. Conclusion: PTX3 polymorphisms appear to significantly impact Pseudomonas aeruginosa colonization and acute cellular rejection in lung transplant recipients. Although these polymorphisms seem to have a potential impact on CMV infection and survival, this relationship was not statistically significant. Contrary to expectations, PTX3 polymorphisms did not significantly correlate with Aspergillus fumigatus isolation. Further research is going on to understand the mechanisms behind these associations and their potential implications for post-transplant care.
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