Key result
Bioprosthetic SAVR with INSPIRIS RESILIA in patients under 60 shows ~98% one-year survival.
Why the study?
Safety and clinical outcomes at 1 year needed assessment in patients under 60 years of age undergoing bioprosthetic surgical aortic valve replacement.
Does bioprosthetic surgical aortic valve replacement provide good safety, haemodynamic performance, and quality of life at 1 year in patients under 60 years?
Observational (n=421)
Yes
Does bioprosthetic surgical aortic valve replacement provide good safety, haemodynamic performance, and quality of life at 1 year in patients under 60 years?
In patients under 60 years, the INSPIRIS RESILIA bioprosthetic aortic valve demonstrated excellent 1-year safety, haemodynamic performance, and quality of life improvements.
Supports short-term use of INSPIRIS RESILIA in select patients <60; leaves open durability and randomized comparisons.
OBJECTIVES: We report 1-year safety and clinical outcomes in patients <60 years undergoing bioprosthetic surgical aortic valve intervention. METHODS: The INSPIRIS RESILIA Durability Registry is a prospective, multicentre registry to assess clinical outcomes of patients <60 years. Patients with planned SAVR with or without concomitant replacement of the ascending aorta and/or coronary bypass surgery were included. Time-related valve safety, haemodynamic performance and quality of life (QoL) at 1 year were assessed. RESULTS: A total of 421 patients were documented with a mean age of 53.5 years, 76.5% being male and 27.2% in NYHA class III/IV. Outcomes within 30 days included cardiovascular-related mortality (0.7%), time-related valve safety (VARC-2; 5.8%), thromboembolic events (1.7%), valve-related life-threatening bleeding (VARC-2; 4.3%) and permanent pacemaker implantation (3.8%). QoL was significantly increased at 6 months and sustained at 1 year. Freedom from all-cause mortality at 1 year was 98.3% (95% confidence interval 97.1; 99.6) and 81.8% were NYHA I versus 21.9% at baseline. No patient developed structural valve deterioration stage 3 (VARC-3). The mean aortic pressure gradient was 12.6 mmHg at 1 year and the effective orifice area was 1.9 cm2. CONCLUSIONS: The 1-year data from the INSPIRIS RESILIA valve demonstrate good safety and excellent haemodynamic performance as well as an early QoL improvement. CLINICAL TRIAL REGISTRATION: clinicaltrials.gov: NCT03666741.
No takes yet. Share an insight, caveat, or question.
Meuris et al. (2023) conducted an observational in Planned surgical aortic valve replacement (n=421). INSPIRIS RESILIA bioprosthetic surgical aortic valve was evaluated on Freedom from all-cause mortality at 1 year (95% CI 97.1-99.6). Bioprosthetic surgical aortic valve replacement using the INSPIRIS RESILIA valve in patients <60 years demonstrated 98.3% freedom from all-cause mortality at 1 year (95% CI 97.1-99.6).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: