The research we do today inspires the procedures you will perform tomorrow. That’s why we’re committed to continued scientific advancement, and studies that investigate the safety and performance of new technologies.
Our trials aim to build upon one another by adding new variables which further challenge valve safety and efficacy. Our COMMENCE trial increased the patient population from the EU Feasibility trial, and the RESILIENCE trial is designed to look at different outcome measures to help further establish long-term valve durability.
Learn more about the current methodologies, promising results and conclusions of the various RESILIA tissue studies in the tabs below.
RESILIA tissue is building a track record of study data.
|2010||Juvenile sheep study|
|2011||EU human feasibility study in Poland|
|2012||US aortic/mitral COMMENCE IDE study|
|2017||INSPIRIS RESILIA valve approved by FDA|
|2018||RESILIENCE study begins|
Juvenile Sheep Study
A randomized assessment of an advanced tissue preservation technology in the juvenile sheep model4
The aim of the study was to assess the effects of RESILIA tissue technology on valve function and durability in a chronic sheep model. The model was designed to mirror the accelerated calcification seen in younger humans.
- 45 juvenile sheep were randomized and either a PERIMOUNT mitral valve (6900P, control group) or the same valve design incorporating the RESILIA tissue preservation technology (test group) was implanted in the mitral position
- All valves were 25 mm
- A transthoracic echocardiography was performed at 1 week and at 8 months postoperatively
- Necropsy was performed at 8 months, and the valves were examined radiographically (soft tissue radiograph), histologically (hematoxylin and eosin and Von Kossa staining), and chemically (calcium content)
- 31 animals (14 controls and 17 test animals) remained in perfect condition during the 8-month follow-up period
- Echocardiography at 1 week showed normal valve function in both groups
- At 8 months, cardiac output increased significantly to the same extent in both groups (vs baseline; P < .01). The mean transvalvular pressure gradient also increased, but significantly more in the control group compared with the test group (P = .03)
- Flow turbulence across the prosthesis was increased in the control valves compared with the test valves. The test valves had significantly less calcium content than the controls (1.9 ± 0.3 vs 6.8 ± 1.6 μg/mg; P = .002). This was confirmed by radiographic analysis and histology (see images below)
No clinical data are available that evaluate the long-term impact of RESILIA tissue in patients.
This study demonstrates that the novel tissue preservation technology, when applied to the PERIMOUNT mitral valve, significantly improves hemodynamic and anti-calcification properties compared with the standard PERIMOUNT valve.
EU Feasibility Study
5-year outcomes after aortic valve replacement with a novel RESILIA tissue bioprosthesis1
The EU Feasibility study investigated the safety and performance in AVR patients of a bioprosthesis with RESILIA tissue. Absence of structural valve deterioration (SVD) and stable transvalvular gradients were observed through 5 years.
- Prospective, multicenter, single-arm, trial conducted at two sites
- 133 patients underwent surgical AVR with an Edwards Pericardial Aortic Bioprosthesis with RESILIA tissue (model 11000A)
- Mean age 65.3 ± 13.5 years, with (26%) ≤ 60 years
- 19 or 21 mm valve implanted in 43.6% of patients
- Median follow up = 5 years; Total late follow-up time of 565.2 patient years (LPY)
- Safety events
- No cases of SVD 0%/LPY
- Late all-cause mortality 3.2%/LPY
- Late valve thrombosis 0.2%/LPY
- Late endocarditis 0.2%/LPY
- Late major paravalvular leak 0.0%/LPY
- Stable hemodynamic performance observed at 5 years
- Mean gradient was 14.8 ± 7.6 mmHg
- Average EOA was 1.4 ± 0.5 cm2
The RESILIA tissue valve demonstrated excellent hemodynamic performance and safety outcomes over 5 years of follow-up.
Five-year outcomes of the COMMENCE Trial investigating aortic valve replacement with a novel tissue bioprosthesis2
The COMMENCE trial is an FDA pivotal trial designed to evaluate the safety and effectiveness of a bioprosthetic valve with the novel RESILIA tissue.
- Prospective, multinational, multicenter (n = 27), single-arm, FDA Investigational Device Exemption trial
- 689 patients underwent surgical AVR with the Edwards Pericardial Aortic Bioprosthesis with RESILIA tissue (model 11000A)
- Mean age 66.9 ± 11.6 years, with 140 patients (21%) under 60 years
- 71.8% male
- 26% NYHA Class III/IV
- Mean STS PROM 2.0 ± 1.8%
- 59% isolated AVR
- 2898 aggregate patient-years of follow up
- Follow up: 4.3 ± 1.4 yrs (n = 471)
- Safety endpoints, probability event-free at 5 years:
- All-cause mortality, 89.2%
- Major paravalvular leak, 99.5%
- Endocarditis, 97.8%
- Improved hemodynamic performance compared to baseline was observed through 5 years:
- Mean gradient was 10.2 ± 4.6 at 1 year, 10.2 ± 4.5 at 2 years, and 10.8 ± 5.7 at 3 years, 11.1 ± 5.7 mmHg at 4 years, and 11.5 ± 6.0 at 5 years
- Favorable safety profile and stable hemodynamics of RESILIA tissue in a bovine aortic valve
- No SVD through 5 yrs, stable gradients, and freedom from regurgitation all support durability over the observational period.
- Follow-up continues on the long-term safety and effectiveness of this new tissue
RESILIENCE Study Design
Study Design of the Prospective Non-Randomized Single Arm Multicenter Evaluation of the Durability of Aortic Bioprosthetic Valves with RESILIA Tissue in Subjects under 65 Years Old (RESILIENCE Trial)3
The objective of the RESILIENCE trial is to determine the time to valve failure due to valve deterioration requiring re-intervention, as well as to collect/investigate early potential predictors of valve durability (e.g. calcification and hemodynamic deterioration) in RESILIA tissue. The RESILIENCE trial is the first prospective study to associate both clinical and imaging definitions of SVD with long-term (11 years) bioprosthetic valve durability.
- Multicenter, prospective, non-randomized, single-arm, observational trial
- Up to 250 patients who previously underwent SAVR with a RESILIA tissue valve will be enrolled at up to 15 investigational centers across the United States and Europe
- Includes patients <65 years old; at time of implant this is a population that is at higher risk to develop SVD
- First patient enrolled on November 21, 2018
- Anticipated 3 year enrollment period
- Patients undergo a TTE and non-contrast CT at 5, 7, 9, and 11 years post-valve implant (Figure 1).
View Figure 1
- The definition of SVD used in this study, is the one proposed by Dvir et al. includes four stages: Stage o: no SVD; Stage 1: Morphological SVD; Stage 2: Moderate hemodynamic SVD; and Stage 3: Severe hemodynamic SVD
Echocardiography and CT Core Laboratories will be responsible for independently evaluating TTEs and CTs submitted by trial sites and will report upon the primary and secondary outcomes of the trial.
- The morphology and mobility of the bioprosthetic valve leaflets will be visually assessed in multiple views by 2D echocardiography
- Non-contrast CT images will be acquired using a 64 slice or dual-source scanner
- Valve leaflet calcification will be measured by the volumetric method that identifies calcium within the valve leaflets
- The total volume of calcification over the 3 valve leaflets will be calculated and expressed in mm3
The RESILIENCE trial is the first prospective study that uses both clinical and imaging definitions of SVD to provide a comprehensive description of all stages of SVD and determine the long-term (11 years) durability of the RESILIA tissue in a aortic valve.
Explore our current RESILIA tissue products
INSPIRIS RESILIA aortic valveLearn more
- Bartus K et al., Eur J Cardiothorac Surg. 2020; doi:10.1093/ejcts/ezaa311
- Bavaria J, Griffith B, Heimansohn DA, et al. Presented at the Society of Thoracic Surgeons Annual Meeting, January 2021.
- Pibarot P, et al. Structural Heart. 2020;4(1):46-52.
- Flameng W, et al. J Thorac Cardiovasc Surg. 2015;149:340–5.
For professional use
For a listing of indications, contraindications, precautions, warnings, and potential adverse events, please refer to the Instructions for Use (consult eifu.edwards.com where applicable).
Edwards devices placed on the European market meeting the essential requirements referred to in Article 3 of the Medical Device Directive 93/42/EEC bear the CE marking of conformity.
Edwards, Edwards Lifesciences, the stylized E logo, Carpentier-Edwards, COMMENCE, INSPIRIS, INSPIRIS RESILIA, Magna, Magna Ease, PERI, PERIMOUNT, RESILIA, and VFit are trademarks or service marks of Edwards Lifesciences Corporation or its affiliates. All other trademarks are the property of their respective owners.
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