Provisional counts of the number of deaths registered in England and Wales, by age, sex, region and Index of Multiple Deprivation (IMD), in the latest weeks for which data are available.

The number of deaths registered in England and Wales due to and involving coronavirus (COVID-19). Breakdowns include age, sex, region, local authority, Middle-layer Super Output Area (MSOA), indices of deprivation and place of death. Includes age-specific and age-standardised mortality rates.

Annual data on death registrations by single year of age for the UK (1974 onwards) and England and Wales (1963 onwards).

Provisional counts of the number of deaths registered in England and Wales, including deaths involving coronavirus (COVID-19), by local authority, health board and place of death in the latest weeks for which data are available. The occurrence tabs in the 2021 edition of this dataset were updated for the last time on 25 October 2022.

Live births by usual residence of mother, and General Fertility Rates (GFR), and Deaths and Standardised Mortality Ratio (SMR) by ward and local authority.

The births and deaths data comes from ONS Vital Statistics Table 4.
Small area data is only available directly from ONS under licence.

The general fertility rate (GFR) is the number of live births per 1,000 women aged 15-44.

SMR measures whether the population of an area has a higher or lower number of deaths than expected based on the age profile of the population (more deaths are expected in older populations). The SMR is defined as follows: SMR = (Observed no. of deaths per year)/(Expected no. of deaths per year).

Rates are provisional, they are based on the GLA 2011 based SHLAA ward projections (standard) released in January 2012. At national level, however, they are based on the mid-year population estimates.

More information is on the ONS website.

The National Child Development Study (NCDS) is a continuing longitudinal study that seeks to follow the lives of all those living in Great Britain who were born in one particular week in 1958. The aim of the study is to improve understanding of the factors affecting human development over the whole lifespan.

The NCDS has its origins in the Perinatal Mortality Survey (PMS) (the original PMS study is held at the UK Data Archive under SN 2137). This study was sponsored by the National Birthday Trust Fund and designed to examine the social and obstetric factors associated with stillbirth and death in early infancy among the 17,000 children born in England, Scotland and Wales in that one week. Selected data from the PMS form NCDS sweep 0, held alongside NCDS sweeps 1-3, under SN 5565.

Survey and Biomeasures Data (GN 33004):
To date there have been nine attempts to trace all members of the birth cohort in order to monitor their physical, educational and social development. The first three sweeps were carried out by the National Children's Bureau, in 1965, when respondents were aged 7, in 1969, aged 11, and in 1974, aged 16 (these sweeps form NCDS1-3, held together with NCDS0 under SN 5565). The fourth sweep, also carried out by the National Children's Bureau, was conducted in 1981, when respondents were aged 23 (held under SN 5566). In 1985 the NCDS moved to the Social Statistics Research Unit (SSRU) - now known as the Centre for Longitudinal Studies (CLS). The fifth sweep was carried out in 1991, when respondents were aged 33 (held under SN 5567). For the sixth sweep, conducted in 1999-2000, when respondents were aged 42 (NCDS6, held under SN 5578), fieldwork was combined with the 1999-2000 wave of the 1970 Birth Cohort Study (BCS70), which was also conducted by CLS (and held under GN 33229). The seventh sweep was conducted in 2004-2005 when the respondents were aged 46 (held under SN 5579), the eighth sweep was conducted in 2008-2009 when respondents were aged 50 (held under SN 6137) and the ninth sweep was conducted in 2013 when respondents were aged 55 (held under SN 7669).

Four separate datasets covering responses to NCDS over all sweeps are available. National Child Development Deaths Dataset: Special Licence Access (SN 7717) covers deaths; National Child Development Study Response and Outcomes Dataset (SN 5560) covers all other responses and outcomes; National Child Development Study: Partnership Histories (SN 6940) includes data on live-in relationships; and National Child Development Study: Activity Histories (SN 6942) covers work and non-work activities. Users are advised to order these studies alongside the other waves of NCDS.

From 2002-2004, a Biomedical Survey was completed and is available under End User Licence (EUL) (SN 8731) and Special Licence (SL) (SN 5594). Proteomics analyses of blood samples are available under SL SN 9254.

Linked Geographical Data (GN 33497):
A number of geographical variables are available, under more restrictive access conditions, which can be linked to the NCDS EUL and SL access studies.

Linked Administrative Data (GN 33396):
A number of linked administrative datasets are available, under more restrictive access conditions, which can be linked to the NCDS EUL and SL access studies. These include a Deaths dataset (SN 7717) available under SL and the Linked Health Administrative Datasets (SN 8697) available under Secure Access.

Additional Sub-Studies (GN 33562):
In addition to the main NCDS sweeps, further studies have also been conducted on a range of subjects such as parent migration, unemployment, behavioural studies and respondent essays. The full list of NCDS studies available from the UK Data Service can be found on the NCDS series access data webpage.

How to access genetic and/or bio-medical sample data from a range of longitudinal surveys:
For information on how to access biomedical data from NCDS that are not held at the UKDS, see the CLS Genetic data and biological samples webpage.

Further information about the full NCDS series can be found on the Centre for Longitudinal Studies website.
The National Child Development Deaths Dataset, 1958-2014: Special Licence Access contains data on known deaths among members of the NCDS birth cohort from 1958 to 2013. Information on deaths has been taken from the records maintained by the organisations responsible for the study over the life time of the study: the National Birthday Trust Fund, the National Children’s Bureau (NCB), the Social Statistics Research Unit (SSRU) and the CLS. The information has been gleaned from a variety of sources, including death certificates and other information from the National Health Service Central Register (NHSCR), and from relatives and friends during survey activities and cohort maintenance work by telephone, letter and e-mail. It includes all deaths up to 31st December 2013. In only 6 cases are the date of death unknown. By the end of December 8.7 per cent of the cohort were known to have died.

The National Child Development Study Response and Outcomes Dataset, 1958-2013 (SN 5560) covers other responses and outcomes of the cohort members and should be used alongside this dataset.

For the 3rd edition (July 2018) an updated version of the data was deposited. The new edition includes data on known deaths among members of the National Child Development Study (NCDS) birth cohort up to 2016. The user guide has also been updated.

This table contains provisional data on the number of deaths among the population of the Netherlands.

The data can be broken down by gender and age group.

Data available from: 1971

Status of the figures: The figures for the years 1971 to 2023 inclusive are final. The figures as of 2024 are provisional. These figures may change with each renewal of the publication due to the fact that death registrations received later are still included. As this method is different from the method used for monthly mortality figures, minor discrepancies may occur.

Changes as of 7 March 2025: The provisional figures of week 7 and 8 of 2025 have been added.

When will new figures be published? From May 2024, the table will be updated once every two weeks with provisional figures of the two weeks before the current week number minus one. Publication is usually delayed around public holidays (e.g. Ascension Day and Boxing Day).

These datasets include all deaths registered in England and Wales for the time periods specified.

Data are supplied to ONS by the Local Registration Service, in partnership with the General Register Office (GRO). Coding for cause of death is carried out according to the World Health Organization (WHO) International Classification of Diseases (ICD-10) and internationally agreed rules, allowing for international comparisons. Deaths registered in England and Wales to those usually resident outside of England and Wales are included. Deaths registered outside of England and Wales to those usually resident in England and Wales are excluded.

This data comprises the finalised annual Death Registration data which covers the period 1993-2019. For the latest Death Registration data (2020-2021), please see 'Death registration data - Provisional.'

Abstract copyright UK Data Service and data collection copyright owner.

The Death Registrations in England and Wales, 1993-2022: Secure Access study includes annual data files for all deaths registered in England and Wales from 1993 to 2022. Death registration is a legal requirement under the Births and Deaths Registration Act 1836. The registration of deaths occurring in England and Wales is a service carried out by the Local Registration Service in partnership with the General Register Office (GRO). Information collected at death registration is recorded on the Registration Online (RON) system by registrars. The information supplied at the time of registration is from 1 of 4 sources:

1. details supplied by the doctor when certifying a death
2. details supplied by the informant to the registrar
3. details supplied by a coroner to the registrar following an investigation
4. details derived from the information supplied above

Death registration data are passed to the Office for National Statistics electronically from GRO for statistical purposes. Each annual dataset is a static file of death registration records available at the time the annual subset was closed. Revisions to records can still be made after the subset has been finalised but these will not be reflected in the annual dataset or used to compile statistics. The annual datasets include deaths that have been registered in that calendar year, a small percentage of these deaths may have occurred in previous years (2.9% in 2001 and 4.8% in 2015). Deaths to those usually resident in England or Wales who die abroad are not included in the dataset. Deaths registered in England and Wales to those whose usual residence is outside England and Wales are included.

Further information about mortality statistics is available from the Office for National Statistics deaths web page.

Prospective users will need to apply for access to this controlled access data via the UK Data Service Secure Lab. Further information is available on the Apply to Access Controlled Data in SecureLab web pages.

Latest edition information:
For the ninth edition (May 2024), the 2022 data file has been added to the study, along with the latest Mortality statistics in England and Wales QMI documentation file.

Main Topics:

Full details of the variables included are in the 'Deaths Variable Catalogue' and in 'Deaths Metadata' available from the Documentation section. Not all variables are available every year but the main areas covered include:

• registration details (date of registration)
• characteristics of the death (age, date of birth and gender of deceased, date of death, death certificate information, date last seen alive, manner of death, post-mortem information)
• cause of death variables for aged 28 days and over and for aged under 28 days (cause of death coded using International Classification of Diseases (ICD) using ICD9 for deaths from 1993-2000 and ICD10 for deaths from 2001-2020)
• marital status / spouse details (spouse age and date of birth)
• occupation, employment status and socio-economic classification
• place of death (communal establishment information, ICD place of accident and workplace codes)
• geography variables (country of residence, country of birth, country and postcode of usual residence, postcode of place of death)

This dataset as reported to the Rural Payments Agency contains a list of cattle born in Wales since 1 August 1996 and 31 December 2009 and slaughtered in England and Scotland in 2009 Attribution statement:

The survey of medical end-of-life decisions presents information on medical end-of-life decisions by attending physicians. For this survey, a random sample is taken from death certificates at Statistics Netherlands on persons listed in the Dutch population register who died in the months August to November inclusive of the survey year. The sample is raised to an annual figure.

This table concerns deaths by medical end-of-life decisions, cause of death and age.

Data available from: 2010, 2015 and 2021

Status of the figures: All data are definite.

Changes as of 26 May 2023: - Figures for 2021 have been added. - In 2021, there were 96 deceased persons with unknown 'medical end-of-life'. These were only added to the total. The underlying numbers therefore do not add up to the total.

When will new figures be published? The survey takes place every five years. In 2020, the survey was postponed by one year due to the high workload in the healthcare sector on account of COVID-19. As a result, there is a one-off six-year interval between 2015 and 2021.

This publication of the SHMI relates to discharges in the reporting period March 2023 - February 2024. The SHMI is the ratio between the actual number of patients who die following hospitalisation at the trust and the number that would be expected to die on the basis of average England figures, given the characteristics of the patients treated there. The SHMI covers patients admitted to hospitals in England who died either while in hospital or within 30 days of being discharged. To help users of the data understand the SHMI, trusts have been categorised into bandings indicating whether a trust's SHMI is 'higher than expected', 'as expected' or 'lower than expected'. For any given number of expected deaths, a range of observed deaths is considered to be 'as expected'. If the observed number of deaths falls outside of this range, the trust in question is considered to have a higher or lower SHMI than expected. The expected number of deaths is a statistical construct and is not a count of patients. The difference between the number of observed deaths and the number of expected deaths cannot be interpreted as the number of avoidable deaths or excess deaths for the trust. The SHMI is not a measure of quality of care. A higher than expected number of deaths should not immediately be interpreted as indicating poor performance and instead should be viewed as a 'smoke alarm' which requires further investigation. Similarly, an 'as expected' or 'lower than expected' SHMI should not immediately be interpreted as indicating satisfactory or good performance. Trusts may be located at multiple sites and may be responsible for 1 or more hospitals. A breakdown of the data by site of treatment is also provided, as well as a breakdown of the data by diagnosis group. Further background information and supporting documents, including information on how to interpret the SHMI, are available on the SHMI homepage (see Related Links).

The Public Health Research Database (PHRD) is a linked asset which currently includes Census 2011 data; Mortality Data; Hospital Episode Statistics (HES); GP Extraction Service (GPES) Data for Pandemic Planning and Research data. Researchers may apply for these datasets individually or any combination of the current 4 datasets.

The purpose of this dataset is to enable analysis of deaths involving COVID-19 by multiple factors such as ethnicity, religion, disability and known comorbidities as well as age, sex, socioeconomic and marital status at subnational levels. 2011 Census data for usual residents of England and Wales, who were not known to have died by 1 January 2020, linked to death registrations for deaths registered between 1 January 2020 and 8 March 2021 on NHS number. The data exclude individuals who entered the UK in the year before the Census took place (due to their high propensity to have left the UK prior to the study period), and those over 100 years of age at the time of the Census, even if their death was not linked. The dataset contains all individuals who died (any cause) during the study period, and a 5% simple random sample of those still alive at the end of the study period. For usual residents of England, the dataset also contains comorbidity flags derived from linked Hospital Episode Statistics data from April 2017 to December 2019 and GP Extraction Service Data from 2015-2019.

Excess Winter Deaths (EWD) by age and conditions (underlying cause of death) expressed as average per year based on 7 years pooled data, 2004-2011. EWD trend expressed as average per year based on 3 years data.

The Excess Winter Mortality Index (EWM Index was calculated based on the 'ONS Method' which defines the winter period as December to March, and the non-winter period as August to November of that same year and April to July of the following year.

This winter period was selected as they are the months which over the last 50 years have displayed above average monthly mortality. However, if mortality starts to increase prior to this, for example in November, the number of deaths in the non-winter period will increase, which in turn will decrease the estimate of excess winter mortality.

The EWM Index will be partly dependent on the proportion of older people in the population as most excess winter deaths effect older people (there is no standardisation in this calculation by age or any other factor).

Excess winter mortality is calculated as winter deaths (deaths occurring in December to March) minus the average of non-winter deaths (April to July of the current year and August to November of the previous year). The Excess winter mortality index is calculated as excess winter deaths divided by the average non-winter deaths, expressed as a percentage.

Relevant link: http://www.wmpho.org.uk/excesswinterdeathsinEnglandatlas/

Notes:

This indicator is designed to accompany the SHMI publication. The SHMI includes all deaths reported of patients who were admitted to non-specialist acute trusts in England and either died while in hospital or within 30 days of discharge. Deaths related to COVID-19 are excluded from the SHMI. A contextual indicator on the percentage of deaths reported in the SHMI which occurred in hospital and the percentage which occurred outside of hospital is produced to support the interpretation of the SHMI. Notes: 1. For discharges in the reporting period April 2024 - May 2024, almost all of the records for Wirral University Teaching Hospital NHS Foundation Trust (trust code RBL) have been submitted without an NHS number. This will have affected the linkage of the HES data to the ONS death registrations data and may have resulted in a smaller number of deaths occurring outside hospital within 30 days of discharge being identified for this trust than would have otherwise been the case. The results for this trust should therefore be interpreted with caution. 2. There is a shortfall in the number of records for North Middlesex University Hospital NHS Trust (trust code RAP), Northumbria Healthcare NHS Foundation Trust (trust code RTF), The Rotherham NHS Foundation Trust (trust code RFR), and The Shrewsbury and Telford Hospital NHS Trust (trust code RXW). Values for these trusts are based on incomplete data and should therefore be interpreted with caution. 3. A number of trusts are now submitting Same Day Emergency Care (SDEC) data to the Emergency Care Data Set (ECDS) rather than the Admitted Patient Care (APC) dataset. The SHMI is calculated using APC data. Removal of SDEC activity from the APC data may impact a trust’s SHMI value and may increase it. More information about this is available in the Background Quality Report. 4. Further information on data quality can be found in the SHMI background quality report, which can be downloaded from the 'Resources' section of this page.

This table contains the number of persons died as a result of murder or manslaughter, where the crime scene is located in the Netherlands. The victims can be residents or non-residents of the Netherlands. The data can be split by location of the crime, method, age and sex. The criterion is the date of death, the date of the criminal act can be in the previous year. Since 2013 Statistics Netherlands is using Iris for automatic coding for causes of death. This improved the international comparison of the data. The change in coding did cause a considerable shift in the statistics. Since 2013 the (yearly) ICD-10 updates are applied. However for murder and manslaughter no changes in coding have taken place. The ICD-10 codes that belong to murder and manslaughter are X85-Y09.

Data available from: 1996

Status of the figures: The figures up to and including 2023 are final.

Changes as of January 23rd 2025: The figures for 2023 are made final.

When will new figures be published: In the third quarter of 2025 the provisional figures for 2024 will be published.

The National Child Development Study (NCDS) is a continuing longitudinal study that seeks to follow the lives of all those living in Great Britain who were born in one particular week in 1958. The aim of the study is to improve understanding of the factors affecting human development over the whole lifespan.

The NCDS has its origins in the Perinatal Mortality Survey (PMS) (the original PMS study is held at the UK Data Archive under SN 2137). This study was sponsored by the National Birthday Trust Fund and designed to examine the social and obstetric factors associated with stillbirth and death in early infancy among the 17,000 children born in England, Scotland and Wales in that one week. Selected data from the PMS form NCDS sweep 0, held alongside NCDS sweeps 1-3, under SN 5565.

Survey and Biomeasures Data (GN 33004):
To date there have been nine attempts to trace all members of the birth cohort in order to monitor their physical, educational and social development. The first three sweeps were carried out by the National Children's Bureau, in 1965, when respondents were aged 7, in 1969, aged 11, and in 1974, aged 16 (these sweeps form NCDS1-3, held together with NCDS0 under SN 5565). The fourth sweep, also carried out by the National Children's Bureau, was conducted in 1981, when respondents were aged 23 (held under SN 5566). In 1985 the NCDS moved to the Social Statistics Research Unit (SSRU) - now known as the Centre for Longitudinal Studies (CLS). The fifth sweep was carried out in 1991, when respondents were aged 33 (held under SN 5567). For the sixth sweep, conducted in 1999-2000, when respondents were aged 42 (NCDS6, held under SN 5578), fieldwork was combined with the 1999-2000 wave of the 1970 Birth Cohort Study (BCS70), which was also conducted by CLS (and held under GN 33229). The seventh sweep was conducted in 2004-2005 when the respondents were aged 46 (held under SN 5579), the eighth sweep was conducted in 2008-2009 when respondents were aged 50 (held under SN 6137) and the ninth sweep was conducted in 2013 when respondents were aged 55 (held under SN 7669).

Four separate datasets covering responses to NCDS over all sweeps are available. National Child Development Deaths Dataset: Special Licence Access (SN 7717) covers deaths; National Child Development Study Response and Outcomes Dataset (SN 5560) covers all other responses and outcomes; National Child Development Study: Partnership Histories (SN 6940) includes data on live-in relationships; and National Child Development Study: Activity Histories (SN 6942) covers work and non-work activities. Users are advised to order these studies alongside the other waves of NCDS.

From 2002-2004, a Biomedical Survey was completed and is available under End User Licence (EUL) (SN 8731) and Special Licence (SL) (SN 5594). Proteomics analyses of blood samples are available under SL SN 9254.

Linked Geographical Data (GN 33497):
A number of geographical variables are available, under more restrictive access conditions, which can be linked to the NCDS EUL and SL access studies.

Linked Administrative Data (GN 33396):
A number of linked administrative datasets are available, under more restrictive access conditions, which can be linked to the NCDS EUL and SL access studies. These include a Deaths dataset (SN 7717) available under SL and the Linked Health Administrative Datasets (SN 8697) available under Secure Access.

Additional Sub-Studies (GN 33562):
In addition to the main NCDS sweeps, further studies have also been conducted on a range of subjects such as parent migration, unemployment, behavioural studies and respondent essays. The full list of NCDS studies available from the UK Data Service can be found on the NCDS series access data webpage.

How to access genetic and/or bio-medical sample data from a range of longitudinal surveys:
For information on how to access biomedical data from NCDS that are not held at the UKDS, see the CLS Genetic data and biological samples webpage.

Further information about the full NCDS series can be found on the Centre for Longitudinal Studies website.

The National Child Development Study: Linked Health Administrative Datasets (Hospital Episode Statistics), England, 1997-2017: Secure Access includes data files from the NHS Digital HES database for those cohort members who provided consent to health data linkage in the Age 50 sweep. The HES database contains information about all hospital admissions in England. The following linked HES data are available:

1) Accident and Emergency (A&E)
The A&E dataset details each attendance to an Accident and Emergency care facility in England, between 01-04-2007 and 31-03-2017 (inclusive). It includes major A&E departments, single speciality A&E departments, minor injury units and walk-in centres in England.

2) Admitted Patient Care (APC)
The APC data summarises episodes of care for admitted patients, where the episode occurred between 01-04-1997 and 31-03-2017 (inclusive).

3) Critical Care (CC)
The CC dataset covers records of critical care activity between 01-04-2009 and 31-03-2017 (inclusive).

4) Out Patient (OP)
The OP dataset lists the outpatient appointments between 01-04-2003 and 31-03-2017 (inclusive).

CLS/ NHS Digital Sub-licence agreement
NHS Digital has given CLS permission for onward sharing of the Next Steps/HES dataset via the UKDS Secure Lab. In order to ensure data minimisation, NHS Digital requires that researchers only access the HES variables needed for their approved research project. Therefore, the HES linked data provided by the UKDS to approved researchers will be subject to sub-setting of variables. The researcher will need to request a specific sub-set of variables from the Next Steps HES data dictionary, which will subsequently make available within their UKDS Secure Account. Once the researcher has finished their research, the UKDS will delete the tailored dataset for that specific project. Any party wishing to access the data deposited at the UK Data Service will be required to enter into a Licence agreement with CLS (UCL), in addition to the agreements signed with the UKDS, provided in the application pack.

Latest edition information
For the second edition (September 2022), 7 previously unavailable variables have been added to the A&E, APC and OP data files. The User Guide has also been updated, along with the variable list, to reflect the changes.

NISRA publish timely but provisional counts of deaths registered by the General Register Office for Northern Ireland (GRO). Weekly totals are presented alongside a 5-year weekly average number of deaths for the same week over the last five years.