Question to the Department of Health and Social Care:

To ask His Majesty's Government which national body has formal responsibility for monitoring outcomes for placenta accreta spectrum, including missed antenatal diagnoses and maternal morbidity.

There are currently no plans to introduce mandatory national reporting of placenta accreta spectrum cases and outcomes. Neither Mothers and Babies: Reducing Risk through Audits and Confidential Enquiries across the UK (MBRRACE-UK) nor the National Maternity and Perinatal Audit record placenta accreta routinely in regular surveillance. However, MBRRACE-UK captures this data as part of their confidential enquiries relating to haemorrhage.

In 2020, NHS England commissioned placenta accreta networks in the United Kingdom which support local and regional screening, shared protocols, and co-ordinated referral pathways to specialist pregnancy accreta centres. Placenta accreta centres consist of highly experienced multidisciplinary teams with the expertise to manage this condition and improve the safety outcomes for women and babies.