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To ask the Scottish Government what action it is taking to raise awareness of, and improve access to, screening for young sudden cardiac death. (S7O-00419)
Official Report · Chamber
General Question Time
This is the draft Official Report. The final version may differ.
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To ask the Scottish Government what action it is taking to raise awareness of, and improve access to, screening for young sudden cardiac death. (S7O-00419)
The Scottish Government, like all United Kingdom nations, follows the UK National Screening Committee’s recommendations. I recognise the important work being done by organisations such as Cardiac Risk in the Young and the DH9 Foundation to raise awareness of cardiac risk in young people.
Although the National Screening Committee has said that it recognises the devastating impact of sudden cardiac death, its most recent review found that evidence did not support the introduction of population screening. My predecessor wrote to the committee to ask whether it planned to review that recommendation; it is now doing so and its conclusions will be published.
Although there is no formal national screening programme, guidance from the network for inherited cardiac conditions Scotland supports the assessment of families after a sudden cardiac death, including, where appropriate, genetic screening of first-degree relatives. We will continue to work with the network to ensure fair and timely access to testing across Scotland, including through the national sudden cardiac death project.
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Every week, there are at least 12 young sudden cardiac deaths in the United Kingdom. My constituent Ebony Morrice was just two days away from her 18th birthday when she died suddenly from an undiagnosed heart condition while at a concert with her mum. A milestone that should have brought her family together in celebration instead became a birthday that they would have to face without her. Her parents, Melanie and Ally, are in the public gallery, watching, hoping and fighting for their daughter’s memory. Through the Ebs memorial fund, they are campaigning to prevent other young people from going undiagnosed, as Ebony was. Will the minister, along with the Cabinet Secretary for Health and Care, commit to meeting them to hear Ebony’s story and explain what more can be done on cardiac screening and awareness to prevent young lives like Ebony’s from being lost?
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First, I give my heartfelt condolences to Ally and Melanie on the loss of their daughter Ebony. I can only imagine how devastating the impact of her loss has been. I am more than happy to commit to meeting them, and I am keen to implement throughout the country any learning that NHS Highland can share in relation to Ebony’s care.
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The standard test for assessing the risk of a young person experiencing a sudden cardiac death is a basic questionnaire and a non-invasive electrocardiogram. In a sense, it is all about data and, as such, it is probably the perfect place for NHS Scotland to utilise artificial intelligence. What investment has the Scottish Government made in AI-enabled scanning so that diagnostic tests can become more routine and potentially more accurate?
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I will write to Jackie Baillie on her question about AI.
It is important that we remember that we are talking about population-level screening. Although I absolutely understand the desire for a screening programme and I guarantee that, if evidence is found to support one, Scotland will waste no time in implementing it, we must recognise that all population-level screening has the potential to do harm as well as good.
It is vital that our interventions in Scotland continue to be evidence led. That is why we follow the guidance of the UK National Screening Committee, which plays a vital role in ensuring that screening programmes genuinely improve outcomes. We must let its review progress independently.
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