Our national data sets collect information from care records, systems and organisations on specific areas of health and care. This is used to inform policy and monitor and improve care.
The Department of Health and NHS England tell us to collect data so they can learn about specific areas of policy interest and measure the progress of policy initiatives. We work with these partners and groups of health and social care professionals, patients, and IT systems suppliers to design and develop these collections.
The Standardisation Committee for Care Information (SCCI) provides assurance for all national data sets.
The Children and Young People's Health Services Data Set (CYPHS) provides information on children and young people in contact with health services.
The Critical Care Minimum Data Set is collected from all hospitals and other locations which provide all elements of critical care, to support payment, commissioning and national policy analysis.
The Mental Health Services Data Set (MHSDS) collects data on the care of children, young people and adults who use mental health, learning disabilities and autism spectrum disorder services.
This national data set provides data about the performance of NHS care providers in complying with the government standards set for how long patients should wait for cancer treatment.
The Neonatal Critical Care Minimum Data Set (NCCMDS) provides a record of what happens to a patient when they receive neonatal critical care in a Neonatal Intensive Care Unit (NICU), Maternity Ward or Neonatal Transitional Care Ward.
The Paediatric Critical Care Minimum Data Set (PCCMDS) records what happens to a patient when they receive paediatric critical care in a Paediatric Intensive Care Unit (PICU) or other critical care setting suitable for children.