Gender-based analysis of patient outcomes and safety of surgical aortic valve replacement

December 15, 2023

Andreas Zierer

Prof. Günter Laufer

Dr. Forcillo

Aortic Highlights course, 2023

Prof. Treede

Aortic Highlights course, 2023

Dr. Vitanova

Aortic Highlights course, 2023

Dr. Winkler

Aortic Highlights course, 2023

Prof. Von Bardeleben

Aortic Highlights Course, 2023

Prof. Sabine Bleiziffer

MVT Aortic course 2022, vol.2

Live Case filmed at Hezrklinik Hirslanden, with:

Prof. Augusto D’Onofrio

MVT Aortic 2022, vol.2

– What’s less invasive than minimally-invasive surgery? Micro-invasive.

– The initial pros and cons of each approach are clear, but what about the outcomes?

– Don’t forget to implement Enhanced Recovery After cardiac Surgery (ERAS) protocols.

Prof. Michael Borger

MVT Aortic 2022, vol.2

Alexey Dashkevich

MVT Aortic 2022, Vol.2

– Is the patient 50-65 years old? Be sure to think about re-intervention, keep the guidelines in mind, and fully inform the patient.

– Which type of anticoagulation therapy should be used?

– Don’t forget, a Ross procedure may be an option.

Prof. Ruggero De Paulis

MVT Aortic 2022, vol.1

– Many surgical options, very comprehensive, and very unbiased

– A redo-SAVR is not as simple as just “redoing” the procedure: beware of higher risk and more complex procedures

– Very clear 7-step removal process of the original valve prosthesis

-Pros and cons of different pledgets, suture techniques, valve positioning, valve sizing, and more

Insights from INDURE registry

Prof. Ruggero De Paulis

Virtual Industry Symposium

Prosthetic valve choice and mode of intervention for aortic valve replacement in younger patients have been controversial because of concerns about long-term durability. The 2021 update to the ESC/EACTS guidelines for the management of valvular heart disease makes recommendations for patients with severe aortic stenosis, based on available evidence and
valve replacement innovation.1

In patients with severe aortic stenosis, age is now a key determining factor in the initial
choice between SAVR or TAVI. This change simplifies the initial patient treatment pathway
and preferred mode of intervention for patients with severe aortic stenosis.

The guidelines emphasise that while the durability of surgical bioprosthetic valves
beyond 10 years is well established, evidence supporting the durability of TAVI valves is
more limited.

As valve durability is a key consideration in younger patients (<75 years) at low surgical risk, SAVR (if feasible) is the preferred treatment option. SAVR is also recommended for patients who are unsuitable for transfemoral TAVI and operable.

The guidelines recommend TAVI for older patients (≥75 years) and those who are inoperable or high risk for surgery (particularly if feasible via the transfemoral approach).

SAVR or TAVI are recommended for remaining patients according to individual
clinical, anatomical and procedural characteristics.

Prosthesis selection: Tissue or mechanical valve?

If the Heart Team and patient agree that SAVR is the way forward, the choice between mechanical and biological valves comes to the fore. Key factors for the Heart Team to consider are:

  • The patient’s life expectancy
  • Lifestyle and environmental factors
  • Bleeding and thromboembolic risk related to anticoagulation
  • Potential for surgical or transcatheter reintervention
  • Informed patient choice


The evidence continues to support the use of aortic bioprostheses for patients over 65 years of age, but just how durable are bioprostheses?

Latest recommendations are supported by real-world evidence and consistent clinical outcomes

Several large, long-term studies have demonstrated the excellent long-term durability of the Carpentier-Edwards PERIMOUNT aortic valve.2–9

Carpentier-Edwards PERIMOUNT valve

Overall expected valve durability of the PERIMOUNT aortic valve is 19.7 years.2-4

  • Broken down by age, durability was
    • 17.6 years for patients aged ≤60 years
    • 19 years for patients aged 50–65 years
    • 22.1 years for patients aged 60–70 years
  • Twenty-year probability of explant due to SVD across all age groups is 5.4%7
  • Younger age at implantation is associated with a higher risk of structural valve deterioration,2,6-9 but durability is good even in these younger patients2,6-9

Recommended resources

References

1. Vahanian A, Beyersdorf F, Praz F et al. 2021 ESC/EACTS Guidelines for the management of valvular heart disease. Eur Heart J. 2021:

2. Bourguignon T, Bouquiaux-Stablo A-L, Candolfi P et al. Very long-term outcomes of the Carpentier-Edwards Perimount valve in aortic position. Ann Thorac Surg. 2015; 99: 831–7.

3. Bourguignon T, El Khoury R, Candolfi P et al. Very long-term outcomes of the Carpentier-Edwards Perimount aortic valve in patients aged 60 or younger. Ann Thorac Surg. 2015; 100: 853–9.

4. Bourguignon T, Lhommet P, El Khoury R et al. Very long-term outcomes of the Carpentier-Edwards Perimount aortic valve in patients aged 50–65 years. Eur J Cardio-Thorac Surg. 2016; 49: 1462–8.

5. Forcillo J, El Hamamsy I, Stevens LM et al. The Perimount valve in the aortic position: Twenty-year experience with patients under 60 years old. Ann Thorac Surg. 2014; 97: 1526–32.

6. Forcillo J, Pellerin M, Perrault LP et al. Carpentier-Edwards pericardial valve in the aortic position: 25-years experience. Ann Thorac Surg. 2013; 96: 486–93.

7. Johnston DR, Soltesz EG, Vakil N et al. Long-term durability of bioprosthetic aortic valves: Implications from 12,569 implants. Ann Thorac Surg. 2015; 99: 1239–47.

8. McClure RS, Narayanasamy N, Wiegerinck E et al. Late outcomes for aortic valve replacement with the Carpentier-Edwards pericardial bioprosthesis: up to 17-year follow-up in 1,000 patients. Ann Thorac Surg. 2010; 89: 1410–6.

9. Minakata K, Tanaka S, Okawa Y et al. Long-term outcome of the Carpentier-Edwards Pericardial valve in the aortic position in Japanese Patients. Circ J. 2014; 78: 882–9.

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, Carpentier-Edwards PERIMOUNT, INSPIRIS, INSPIRIS RESILIA, Magna, Magna Ease, PERI, PERIMOUNT, RESILIA and SAPIEN are trademarks of Edwards Lifesciences Corporation. All other trademarks are the property of their respective owners.

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Dr. Mark Hall

MVT Aortic 2021