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Advice for people who commission, fund, deliver and evaluate health outreach programmes.
Examples of NHS Sickle Cell and Thalassaemia screening programme resources used in outreach.
These research documents contributed to the community outreach approach used by the NHS Sickle Cell and Thalassaemia Screening Programme.
Training and continuing professional development for people working in the sickle cell and thalassaemia screening programme in England.
Information on the programme, including the screening tests, commissioning, quality assurance, education and training.
Population screening programmes: NHS sickle cell and thalassaemia (SCT) screening programme. The latest pages tagged as SCT will appear here.
Data reports, data collection templates and research application guidance for the NHS sickle cell and thalassaemia (SCT) screening programme.
Forms for sickle cell and thalassaemia (SCT) screening laboratories to send antenatal data to the national programme.
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).
Invite expectant fathers for sickle cell and thalassaemia screening when the mother carries an unusual haemoglobin gene.
Information to help healthcare professionals speak with parents at risk of having a child with sickle cell disease.
A collection of the annual reports for Sickle cell and thalassaemia screening (SCT) standards from 2021/22 inclusive.
Use this letter to inform mothers about their carrier result, as well as invite the biological father for a blood test.
This document sets out guidance for commissioning care services for people with sickle cell disease, thalassaemia and other haemoglobin conditions.
Outlines the community outreach work delivered by the screening programme since 2005, and how it was researched, planned, implemented and evaluated.
Information for parents of babies who carry the sickle cell gene.
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