• It's Time for Heath Care

    The NHS Sickle Cell and Thalassaemia (SCT) screening programme is a genetic screening programme. This means that it also identifies people who are genetic carriers for sickle cell, thalassaemia and other haemoglobin disorders.

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    It's Time for Heath Care
  • Sickle cell and thalassaemia screening

    The NHS Sickle Cell and Thalassaemia (SCT) screening programme is a genetic screening programme. This means that it also identifies people who are genetic carriers for sickle cell, thalassaemia and other haemoglobin disorders.

    Read More
    Sickle cell and thalassaemia screening
  • Standards and Publications

    Access the latest clinical standards and guidelines

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    Standards and Publications

Sickle Cell Standards

Sickle Cell Disease in Childhood: Standards and Recommendations for Clinical Care 2019
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EVIP-Online Survey

Draft version of the European Vaccination Information Portal (EVIP) for your feedback
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UKTS Care Standards

Standards for the Clinical Care of Children and Adults with Thalassaemia in the UK.
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NHSBT Update

Washed RBC & the haemocrit of the product to use when programming for red cell Apheresis
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ASH Pocket Guides

A series of brief evidence-based pocket guides to help provide quality care to patients.
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New In Paperback

Genetics & Global Public Health: Sickle Call & Thalassaemia edited by S. Dyson and K.Atkin.
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UKFHD Meeting

Download the latest presentations from the 49th academic meeting
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Transcranial Scanning

Transcranial Doppler Scanning for Children with Sickle Cell Disease Standards and Guidance
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West Midlands Quality Review Service is a collaborative venture by NHS organisations in the West Midlands to improve the quality of health services by undertaking reviews of the quality of clinical services.
The National Haemoglobinopathy Registry is a database of patients with red cell disorders living in the UK. This new database collects data,which is required by the Department of Health from Haemoglobinopathy centres. The central aim of the registry is to improve patient care.
The National Institute for Health and Care Excellence (NICE) provides national guidance and advice to improve health and social care. Our guidance, advice, quality standards and information services for health, public health and social care. Also contains resources to help maximise use of evidence and guidance.
This Clinical Reference Group (CRG) covers Sickle Cell Disease (SCD), Thalassaemia and other very rare anaemias requiring lifelong transfusion and chelation. Haemoglobinopathies are complex disorders which although often grouped together and managed by the same specialist team, have distinct clinical manifestations and treatments.
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