NCMD’s second annual report is based on data for children who died from 1 April 2019 to 31 March 2020 in England, providing analysis of the 3,347 children who died in that period – which equates to approximately 28 child deaths for every 100,000 children living in England.
Commissioned by the Healthcare Quality Improvement Partnership (HQIP) on behalf of NHS England, this report offers insights based on the characteristics of the deaths analysed in order to improve outcomes for children in the future. Notably, most deaths occurred before the age of one (63%) and, of these – where gestational age at birth was known – 69% were born preterm (before 37 weeks). In fact, 42% of all children who died were under 28 days old, prompting a recommendation to reduce the number of preterm births and improve outcomes after preterm delivery. In summary, the infant mortality rate (children under one year old) in England over this period was 3.4 deaths per 1,000 live births.
For the first time since the start of the child death review process in 2008, factors that are considered to be modifiable in children’s deaths have been analysed on a national scale and included in this report. These factors enable us to identify key areas for improvement. Across all categories of death, the most frequent modifiable factor identified was smoking by a parent or carer. The next most frequently identified factor was gaps in service delivery, while challenges with access to services and poor communication both also feature in the most frequently identified modifiable factors.
A number of other key findings relating to ethnicity, deprivation and location of death (where this data was recorded) are as follows:
- 62% of children who died were from a White ethnic group, while 19% were from an Asian or Asian British background, 9% were from a Black or Black British background, and 7% were from a Mixed ethnic background.
- There were approximately three times as many deaths of children who were resident in the most deprived neighbourhoods, compared to those from the least deprived neighbourhoods.
- 78% of child deaths occurred within a hospital setting, while 22% occurred elsewhere.
This report states a clear call to action for all professionals involved in planning or providing services to children to play an active part in reducing the number of children who die, encouraging them to use the data in this report to implement changes to address the issues highlighted by the report.
NCMD also recommends further improvements in the completeness and quality of child death data collected to allow for enhanced future analyses. It is further recommended that actions be put in place at local, regional and national levels to address the modifiable factors identified in this report.
“As a society it is incumbent upon us to learn from these tragedies and to identify ways in which we can change things to reduce the number of children who die in the future,” Professor Karen Luyt, NCMD Programme Lead
Finally, we would like to acknowledge that the data presented in this report represent babies, children and young people who have died; and each and every death is a devastating loss. We also wish to express our gratitude to the report’s authors and contributors, and to all Child Death Review (CDR) professionals for the data submitted to NCMD as part of the national CDR process.
To read the report in full, use the link below:
Further resources: To support understanding and sharing of this report, find below a number of infographics which highlight key findings:
Date for your diary: An online dissemination event to share key findings from this report will be held on 22 June 2021 from 1-2pm – to find out more (with details of how to register), click here.
Media enquiries: If you are a member of the public or a journalist requiring further information about this report, please contact the NHS England media team:
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