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Welcome to the NHS Newborn Blood Spot Screening Programme

  • Welcome

    The programme has responsibility for developing, implementing and maintaining a high quality, uniform screening programme for all newborn babies and their parents. Screening is offered for phenylketonuria (PKU), congenital hypothyroidism (CHT), sickle cell disease (SCD), cystic fibrosis (CF) and medium-chain acyl-CoA dehydrogenase deficiency (MCADD).
  • December 2013 Newsletter

    This issue of the programme newsletter includes the award-winning failsafe system, the new consultation to extend the number of conditions screened for, details of the new programme team and the publication of key performance indicators.
  • New CHT preterm repeat policy

    Find out more about the revised policy for CHT screening in preterm infants. The policy was implemented in all four UK countries on 1 April 2012.
  • Information for the public

    An introduction to newborn blood spot screening for parents and parents-to-be and the answers to some of your questions.
  • Resources for health professionals

    Browse our resources for health professionals. These include the screening pathway and condition specific materials.
  • New blood spot sampling guidelines

    These guidelines aim to support healthcare professionals in obtaining good quality samples and reducing the need for repeat samples.

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avoidable repeats  bar-coded label  blood spot card  blood spot sampling  CF  CHRD  CHT  consultation  data  expanded screening  failsafe  film  health professional handbook  laboratory  leaflets and booklets  MCADD  newsletter  NHS number  older babies  PKU  policies  preterm  public information  repeat samples  results  SCD  screening stories  serious incidents  standards  status codes 


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