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    The content on this page is not current guidance and is only for the purposes of the consultation process.

    1 Draft recommendations

    When SAVR is not suitable or is high risk

    1.2

    Clinicians wanting to do TAVI when SAVR is not suitable or is high risk should:

    • Inform the clinical governance leads in their healthcare organisation.

    • Ensure that people (and their families and carers as appropriate) understand the procedure's safety and efficacy, and any uncertainties about these.

    • Take account of NICE's advice on shared decision making, including NICE's information for the public.

    • Audit and review clinical outcomes of everyone having the procedure. The main efficacy and safety outcomes identified in this guidance can be entered into NICE's interventional procedure outcomes audit tool (for use at local discretion).

    • Discuss the outcomes of the procedure during their annual appraisal to reflect, learn and improve.

    1.3

    Healthcare organisations should:

    • Ensure systems are in place that support clinicians to collect and report data on outcomes and safety for everyone having this procedure.

    • Regularly review data on outcomes and safety for this procedure.

    When SAVR is suitable and is not high risk

    1.4

    More research is needed on TAVI for native aortic valve regurgitation when SAVR is suitable and is not high risk before it can be used in the NHS.

    1.5

    This procedure should only be done as part of a formal research study and a research ethics committee needs to have approved its use.

    For everyone having TAVI for native aortic valve regurgitation

    1.6

    Patient selection should be done by an experienced multidisciplinary team, which must include:

    • interventional cardiologists experienced in the procedure

    • cardiac surgeons

    • an expert in cardiac imaging, and

    • when appropriate, a cardiac anaesthetist and a specialist in medicine for older people.

      The multidisciplinary team should determine the risk level for each patient and the TAVI valve most suitable for them.

    1.7

    TAVI is a technically challenging procedure that should only be done in specialised centres and only by teams with specific training and experience in complex endovascular interventions. Units doing this procedure should have both cardiac and vascular surgical support for the emergency treatment of complications and subsequent care.

    1.8

    Enter details about everyone having TAVI for native aortic valve regurgitation into the UK TAVI registry, managed by the National Institute for Cardiovascular Outcomes Research. Contact nicor.auditenquiries@nhs.net for details.

    What evidence generation and research is needed

    1.9

    Further evidence generation and research should be in the form of suitably powered randomised controlled trials and patient registries across all risk categories. The trials should report details of:

    • patient selection

    • comparisons between TAVI and SAVR or medical treatment

    • comparisons between different TAVI prosthetic aortic valves

    • long-term outcomes, including:

      • valve durability and reintervention rates

      • the need for a second TAVI valve-in-valve implantation

    • safety outcomes, including embolisation, stroke and myocardial infarction.

    Why the committee made these recommendations

    Evidence on TAVI for native aortic regurgitation when SAVR is not suitable or is high risk shows well-recognised safety concerns. Evidence on short-term efficacy is limited and comes mainly from small observational studies or registries. So, when SAVR is not suitable or the person has a high risk of complications from surgery, the procedure can be used with special arrangements for clinical governance, consent, and audit or research.

    There is not enough evidence on efficacy and safety when SAVR is suitable and is not high risk. So, for these people, the procedure should only be used in research.

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