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Information on the programme, including the screening tests, commissioning, quality assurance, education and training.
Data reports, data collection templates and research application guidance for the NHS sickle cell and thalassaemia (SCT) screening programme.
Population screening programmes: NHS sickle cell and thalassaemia (SCT) screening programme. The latest pages tagged as SCT will appear here.
Training and continuing professional development for people working in the sickle cell and thalassaemia screening programme in England.
Guidance for commissioning and offering sickle cell and thalassaemia screening.
Advice for people who commission, fund, deliver and evaluate health outreach programmes.
Guidance for healthcare professionals covering the pathway for sickle cell and thalassaemia screening.
Essential elements for implementation of the family origin questionnaire (FOQ) to help assess if a person is a likely carrier for sickle cell and thalassaemia (SCT).
These documents list sickle cell and thalassaemia high and low prevalence NHS Trusts in England and explain how prevalence is determined.
Forms for sickle cell and thalassaemia (SCT) screening laboratories to send antenatal data to the national programme.
Screening standards for the sickle cell and thalassaemia (SCT) antenatal and newborn screening programme.
Information and resources for health professionals who provide counselling for people at risk of having a baby with sickle cell disease or thalassaemia.
A collection of the annual reports for Sickle cell and thalassaemia screening (SCT) standards from 2021/22 inclusive.
Invite expectant fathers for sickle cell and thalassaemia screening when the mother carries an unusual haemoglobin gene.
Leaflet for expectant fathers explaining antenatal screening for sickle cell and thalassaemia.
This document sets out guidance for commissioning care services for people with sickle cell disease, thalassaemia and other haemoglobin conditions.
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