Changes ahead for the national screening system
Changes ahead for the national screening system
Details of changes to the national screening system from 1 October, due to the closure of Public Health England.
Details of changes to the national screening system from 1 October, due to the closure of Public Health England.
Early access to sickle cell and thalassaemia screening and the early offer of prenatal diagnosis (PND) is important in giving women and couples time to consider their options.
We’re pleased to announce the publication of an updated version of the antenatal laboratory handbook for the NHS Sickle Cell and Thalassaemia (SCT) Screening Programme.
This study day is for non specialist nurses, midwives and health visitors working in SCT screening in England. Accredited by the Royal College of Midwives, I am pleased to say we are able to provide funding for eligible participants.
The NHS Newborn and Infant Physical Examination Programme (NIPE) held 5 regional events across the country to update health professionals involved in the the national programme.
Dr Anne Mackie, Director of PHE Screening, explains how inequalities affect screening and what actions we are taking to understand and address these differences.
Nurse endoscopists already undertake as much of 20% of the workload in an endoscopy unit. NHS Improving Quality initiatives have estimated clinical endoscopists could carry out up to 40% of low risk, high volume endoscopic procedures.
The annual call is your opportunity to make a proposal for a new topic to be considered by the UK NSC as part of its regular review process.
In this blog we recap the what blog articles we published during the summer month of August. The blogs were plentiful as we saw our subscription numbers pass the 4,000 mark.
We have recently updated and published a one page summary for healthcare professionals explaining which newborn screening tests can be offered at different ages if any of these were initially missed.
As part of a wider investigation into why women are tested late, we commissioned the UK Thalassaemia Society (UKTS) and Sickle Cell Society (SCS) to carry out face to face interviews with women and couples who had recent experience of the SCT programme.