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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).
The family origin questionnaire (FOQ) is mandatory for all antenatal…
The FOQ is mandatory for all antenatal booking blood requests submitted in…
Data reporting template for period 1 January to 31 March 2024, with guidance for NHS antenatal and newborn screening programmes in England.
Data collection template for the annual collection of data to measure performance against programme standards.
Forms for sickle cell and thalassaemia (SCT) screening laboratories to send antenatal data to the national programme.
Data reporting template for period 1 October to 31 December 2023, with guidance for child health information services (CHIS).
Data reporting template for period 1 January to 31 March 2024, with guidance for the NHS Fetal Anomaly Screening Programme (FASP) in England.
Independent midwives should complete this form to register with the online ordering system for newborn blood spot screening cards.
Letter templates to confirm a parent or carer has declined newborn blood spot screening.
Use these log sheets to record and review equipment use in local Newborn Hearing Screening Programmes (NHSP).
Use this letter to inform mothers about their carrier result, as well as invite the biological father for a blood test.
Template for child health records departments (CHRD) to collect and submit newborn blood spot screening data.
Submit data on women who are already known to the Sloane Project when they have been diagnosed with a further breast cancer, regional or distant event.
This template is used to notify GPs of a suspected positive newborn blood spot screening result of congenital hypothyroidism (CHT).
Use this form to submit research requests to the NHS abdominal aortic aneurysm (AAA) screening programme, for research involving patients or their data.
Invite expectant fathers for sickle cell and thalassaemia screening when the mother carries an unusual haemoglobin gene.
For the notification of diagnosis of cases not identified through screening, this form covers the 6 inherited metabolic diseases (IMDs).
Maternity unit data return form and laboratory data return form for data from 1 April 2016 to 31 March 2017.
Use this form to record and submit data to the Sloane Project.
Don’t include personal or financial information like your National Insurance number or credit card details.
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