Please note that the URL for this site has changed to a 'phe.org.uk' address from 'nhs.uk'. This reflects changes we have made to hosting for this site.
E-learning for all NHS Screening Programmes has moved to the Health Education England's e-learning for Healthcare (e-LfH) website.
Read more about the move to e-LfH and how to sign-up to e-learning for Healthcare (e-LfH).
You are here: Programme Specific > Newborn Blood Spot
 

Newborn Blood Spot

 

Education and Training for the Newborn Blood Spot Programme

The newborn blood spot screening programme's overall objective is the assurance of high quality screening services for babies and their parents. All babies in England are offered screening for:

  • sickle cell disease (SCD)
  • cystic fibrosis (CF)
  • congenital hypothyroidism (CHT)
  • six inherited metabolic diseases (IMDs) - phenylketonuria (PKU), medium-chain acyl-CoA dehydrogenase deficiency (MCADD), maple syrup urine disease (MSUD), isovaleric acidaemia (IVA), glutaric aciduria type 1 (GA1) and homocystinuria (pyridoxine unresponsive) (HCU)

Resources include:

In addition, there are some key message slides which highlight key facts and figures about all the screening programmes and can be used to facilitate a short update session or used for individual learning.

 

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E-learning for the NHS Screening Programmes moved to Health Education England's e-learning for Healthcare (e-LfH) website on 3 April 2017.

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