Newborn Screening Expansion in the UK Newborn Screening Expansion in the UK
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SBUK

Newborn Screening Expansion in the UK

The number of diseases newborn babies to be tested for to increase from 5 to 9 following pilot, but still low compared to US and European countries

Save Babies UK, the charity that supports families in the UK and Ireland affected by Krabbe Disease, today welcomes the UK National Screening Committee’s decision to expand newborn screening to nine rare genetic disorders from five, but also calls for swift and concerted action to bring the UK closer in line with its international peers.

Newborn screening is a simple blood test, commonly called the heel prick test, where a spot of blood is taken from a baby’s heel within a few days of birth. From this blood sample, a baby can be screened for many diseases. Early diagnosis and immediate treatment can save a baby’s life or prevent a seriously limiting medical condition.

Following a 12 month pilot programme in Yorkshire and other parts of England between July 2012 and July 2013, the UK National Screening Committee has taken the decision to increase the number of diseases currently screened for from five to nine, although the pilot programme screened for an additional 5.

Although Save Babies UK welcomes the progress made by the UK National Screening Committee, it notes that the UK lags far behind other countries across the world. In the USA, there is a legal requirement to screen for a minimum of 30 diseases, with some US States already testing for between 40 and 60 conditions, while New Zealand screens for 28.

Equally, the UK is far behind many European nations; for example, Austria screens for 29 diseases, closely followed by Iceland, Spain, Portugal, the Netherlands and Germany, all of which screen for more than 20.

While not one of the diseases currently screened for, Krabbe Disease – a rare genetic disorder affecting the nervous system – affects approximately 2 to 3 children each year in the UK. Babies born with Krabbe Disease go undiagnosed at birth until they become unwell and generally die before the age of 2. Once a baby has presented symptoms, the child cannot be successfully treated. Early diagnosis therefore is critical.

Several US States screen for Krabbe Disease as part of their newborn screening programme.

Pat Roberts, Executive Director of Save Babies UK, comments: “While we welcome the fact that the National Screening Committee has decided to almost double the number of diseases that newborn babies will be tested for, getting this far has been very slow.

“At this rate, it will be decades before the UK’s newborn screening programme is in line with the US and many European countries, and in that time, too many children and their families will have to cope with life-limiting illnesses that could be treated or cured if diagnosed sooner.”

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Report of the Scientific Workshop on Krabbe Disease – 2014

 

Pat Roberts from Save Babies UK (SBUK) and who is a member of the UK LSD Collaborative is please to present the final report of the first Krabbe scientific workshop held in the UK in 2013.
The report has valuable content and information, and the board of trustees and the editorial board from SBUK hope you find what is contained of interest. They have accepted feedback from attendees that a further International conference in the UK would be of value and they will review the timing of a conference in light of developments on Krabbe Disease.  In the meantime if you require any further information at any time please do not hesitate to contact us.
To read the report please click here or the icon below to make it appear in a new page.

[gview file=”http://lsdcollaborative.org.uk/wp-content/uploads/2014/06/Report-of-the-Scientific-Workshop-on-Krabbe-Disease.pdf” width=”600px”]

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