Question to the Department of Health and Social Care:

To ask the Secretary of State for Health, what clinical outcomes data his Department holds for (a) sickle cell disease and (b) thalassaemia in each (i) clinical commissioning group area, (ii) trust area and (iii) national sickle cell and thalassaemia centre area.

NHS England requires commissioned providers to submit quality dashboard data on an annual basis. Key indicators include the percentage of patients on the National Haemoglobinopathy Register, those offered an annual review and the proportion of eligible patients offered and receiving neurological screening.