One in every 100 children dies before completing one year of life. Around 68 percent of infant mortality is attributed to deaths of children before completing 1 month. 15,000 children die every day – Child mortality is an everyday tragedy of enormous scale that rarely makes the headlines Child mortality rates have declined in all world regions, but the world is not on track to reach the Sustainable Development Goal for child mortality Before the Modern Revolution child mortality was very high in all societies that we have knowledge of – a quarter of all children died in the first year of life, almost half died before reaching the end of puberty Over the last two centuries all countries in the world have made very rapid progress against child mortality. From 1800 to 1950 global mortality has halved from around 43% to 22.5%. Since 1950 the mortality rate has declined five-fold to 4.5% in 2015. All countries in the world have benefitted from this progress In the past it was very common for parents to see children die, because both, child mortality rates and fertility rates were very high. In Europe in the mid 18th century parents lost on average between 3 and 4 of their children Based on this overview we are asking where the world is today – where are children dying and what are they dying from?

5.4 million children died in 2017 – Where did these children die? Pneumonia is the most common cause of death, preterm births and neonatal disorders is second, and diarrheal diseases are third – What are children today dying from? This is the basis for answering the question what can we do to make further progress against child mortality? We will extend this entry over the course of 2020.

@article{owidchildmortality, author = {Max Roser, Hannah Ritchie and Bernadeta Dadonaite}, title = {Child and Infant Mortality}, journal = {Our World in Data}, year = {2013}, note = {https://ourworldindata.org/child-mortality} }

Context

The world made remarkable progress in child survival in the past few decades, and millions of children have better survival chances than in 1990–5 1 in 26 children died before reaching age five in 2018, compared to 1 in 11 in 1990. Moreover, progress in reducing child mortality has been accelerated in the 2000–2018 period compared with the 1990s, with the annual rate of reduction in the global under-five mortality rate increasing from 2.0 percent in 1990–2000 to 3.8 percent in 2000–2018. Despite the global progress in reducing child mortality over the past few decades, an estimated 5.3 million children under age five died in 2018–roughly half of those deaths occurred in sub-Saharan Africa.

Content this dataset content the child mortality rate more than 200 countries.

Acknowledgments Thanks for UNICEF for sharing data.

Inspiration This dataset provides complete information about child mortality rate. There are many inferences that can be made from this dataset. There are a few things I would like to understand from this dataset.

1. Various factors affecting child mortality.
2. What are all the factors that make the difference between rich and poor countries?
3. What could be done to decrease the child mortality rate in poor countries?

The Mortality - Infant Deaths (from Linked Birth / Infant Death Records) online databases on CDC WONDER provide counts and rates for deaths of children under 1 year of age, occuring within the United States to U.S. residents. Information from death certificates has been linked to corresponding birth certificates. Data are available by county of mother's residence, child's age, underlying cause of death, sex, birth weight, birth plurality, birth order, gestational age at birth, period of prenatal care, maternal race and ethnicity, maternal age, maternal education and marital status. Data are available since 1995. The data are produced by the National Center for Health Statistics.

Effective June 28, 2023, this dataset will no longer be updated. Similar data are accessible from CDC WONDER (https://wonder.cdc.gov/mcd-icd10-provisional.html).

Deaths involving coronavirus disease 2019 (COVID-19) with a focus on ages 0-18 years in the United States.

Rank, number of deaths, percentage of deaths, and age-specific mortality rates for the leading causes of death, by age group and sex, 2000 to most recent year.

This dataset of U.S. mortality trends since 1900 highlights childhood mortality rates by age group for age at death. Age-adjusted death rates (deaths per 100,000) after 1998 are calculated based on the 2000 U.S. standard population. Populations used for computing death rates for 2011–2017 are postcensal estimates based on the 2010 census, estimated as of July 1, 2010. Rates for census years are based on populations enumerated in the corresponding censuses. Rates for noncensus years between 2000 and 2010 are revised using updated intercensal population estimates and may differ from rates previously published. Data on age-adjusted death rates prior to 1999 are taken from historical data (see References below). Age groups for childhood death rates are based on age at death. SOURCES CDC/NCHS, National Vital Statistics System, historical data, 1900-1998 (see https://www.cdc.gov/nchs/nvss/mortality_historical_data.htm); CDC/NCHS, National Vital Statistics System, mortality data (see http://www.cdc.gov/nchs/deaths.htm); and CDC WONDER (see http://wonder.cdc.gov). REFERENCES National Center for Health Statistics, Data Warehouse. Comparability of cause-of-death between ICD revisions. 2008. Available from: http://www.cdc.gov/nchs/nvss/mortality/comparability_icd.htm. National Center for Health Statistics. Vital statistics data available. Mortality multiple cause files. Hyattsville, MD: National Center for Health Statistics. Available from: https://www.cdc.gov/nchs/data_access/vitalstatsonline.htm. Kochanek KD, Murphy SL, Xu JQ, Arias E. Deaths: Final data for 2017. National Vital Statistics Reports; vol 68 no 9. Hyattsville, MD: National Center for Health Statistics. 2019. Available from: https://www.cdc.gov/nchs/data/nvsr/nvsr68/nvsr68_09-508.pdf. Arias E, Xu JQ. United States life tables, 2017. National Vital Statistics Reports; vol 68 no 7. Hyattsville, MD: National Center for Health Statistics. 2019. Available from: https://www.cdc.gov/nchs/data/nvsr/nvsr68/nvsr68_07-508.pdf. National Center for Health Statistics. Historical Data, 1900-1998. 2009. Available from: https://www.cdc.gov/nchs/nvss/mortality_historical_data.htm.

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 ten 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), the ninth sweep was conducted in 2013 when respondents were aged 55 (held under SN 7669), and the tenth sweep was conducted in 2020-24 when the respondents were aged 60-64 (held under SN 9412).

A Secure Access version of the NCDS is available under SN 9413, containing detailed sensitive variables not available under Safeguarded access (currently only sweep 10 data). Variables include uncommon health conditions (including age at diagnosis), full employment codes and income/finance details, and specific life circumstances (e.g. pregnancy details, year/age of emigration from GB).

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 Safeguarded Licence (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.

Multi-omics Data and Risk Scores Data (GN 33592)
Proteomics analyses were run on the blood samples collected from NCDS participants in 2002-2004 and are available under SL SN 9254. Metabolomics analyses were conducted on respondents of sweep 10 and are available under SL SN 9411. Polygenic indices are available under SL SN 9439. Derived summary scores have been created that combine the estimated effects of many different genes on a specific trait or characteristic, such as a person's risk of Alzheimer's disease, asthma, substance abuse, or mental health disorders, for example. These scores can be combined with existing survey data to offer a more nuanced understanding of how cohort members' outcomes may be shaped.

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 data tracks the deaths of children up to 18 years old and whether or not the child, youth or their family were involved with a children's aid society within 12 months of their death. This data is provided to the Office of the Chief Coroner by the Registrar General of Ontario and by children's aid societies and has not been independently verified by the Office of the Chief Coroner.

Live births, stillbirths and linked infant deaths occurring annually in England and Wales, and associated risk factors.

The map shows the latest available data for mortality up to the age of 15. In several countries, the rate has declined to about 0.3%, a mortality rate that is more than 100 times lower than in the past. This was achieved in just a few generations. Progress can be fast.

In the richest parts of the world, child deaths have become very rare, but differences across countries are high. Niger is the country with the highest rate, 15% of newborns die as children.

The fact that several countries show that it is possible for 99.7% of children to survive shows us what the world can aspire to. Global health has improved, and it is on us to make sure that this progress continues to bring the daily tragedy of child deaths to an end.

Our ancestors could have surely not imagined what is reality today. Let’s make it our goal to give children everywhere the chance to live a long and healthy life. The chart above also shows the dramatic progress that was recently achieved. Most children in the world still died at extremely high rates well into the 20th century. Even as recently as 1950 – a time that some readers might well remember – one in four children died globally.

More recently, during our lifetimes, the world has achieved an entirely unprecedented improvement. In a brief episode of human history, the global death rate of children declined from around 50% to 4%.

After millennia of suffering and failure, the progress against child mortality is, for me, one of the greatest achievements of humanity.

This is not an improvement that is only achieved by a few countries. The rate has declined in every single country in the world.

Effective September 27, 2023, this dataset will no longer be updated. Similar data are accessible from wonder.cdc.gov.

Deaths involving COVID-19, pneumonia, and influenza reported to NCHS by sex, age group, and jurisdiction of occurrence.

The injuries that led to the child's death may have been sustained prior to DFPS being granted to legal custody. For example, in Fiscal Year 2016 six children died while in DFPS Conservatorship (five while in Foster Care). However, four of these children sustained the injuries that led to their death prior to being placed in DFPS custody.

This chart includes child fatalities investigated and confirmed by Child Protective Investigations, Day Care Investigations, and Residential Child Care Investigations, and Adult Protective Services. Fatality information does not include corrections or updates, if any, that may subsequently be made to DFPS data after fiscal year end.

Only Children in DFPS Legal Responsibility (Conservatorship) are included. You can further filter to see how many were in Foster Care at the time of death.

The Adult Protective Provider Investigations division was tranferred to the Texas Health and Human Services Commission (HHSC) in Fiscal Year 2018.

This dashboard addresses Texas Family Code Section 264.017, Subsection (b) (4) and (5).

THIS DATASET WAS LAST UPDATED AT 7:11 AM EASTERN ON DEC. 1

OVERVIEW

2019 had the most mass killings since at least the 1970s, according to the Associated Press/USA TODAY/Northeastern University Mass Killings Database.

In all, there were 45 mass killings, defined as when four or more people are killed excluding the perpetrator. Of those, 33 were mass shootings . This summer was especially violent, with three high-profile public mass shootings occurring in the span of just four weeks, leaving 38 killed and 66 injured.

A total of 229 people died in mass killings in 2019.

The AP's analysis found that more than 50% of the incidents were family annihilations, which is similar to prior years. Although they are far less common, the 9 public mass shootings during the year were the most deadly type of mass murder, resulting in 73 people's deaths, not including the assailants.

One-third of the offenders died at the scene of the killing or soon after, half from suicides.

About this Dataset

The Associated Press/USA TODAY/Northeastern University Mass Killings database tracks all U.S. homicides since 2006 involving four or more people killed (not including the offender) over a short period of time (24 hours) regardless of weapon, location, victim-offender relationship or motive. The database includes information on these and other characteristics concerning the incidents, offenders, and victims.

The AP/USA TODAY/Northeastern database represents the most complete tracking of mass murders by the above definition currently available. Other efforts, such as the Gun Violence Archive or Everytown for Gun Safety may include events that do not meet our criteria, but a review of these sites and others indicates that this database contains every event that matches the definition, including some not tracked by other organizations.

This data will be updated periodically and can be used as an ongoing resource to help cover these events.

Using this Dataset

To get basic counts of incidents of mass killings and mass shootings by year nationwide, use these queries:

Mass killings by year

Mass shootings by year

To get these counts just for your state:

Filter killings by state

Definition of "mass murder"

Mass murder is defined as the intentional killing of four or more victims by any means within a 24-hour period, excluding the deaths of unborn children and the offender(s). The standard of four or more dead was initially set by the FBI.

This definition does not exclude cases based on method (e.g., shootings only), type or motivation (e.g., public only), victim-offender relationship (e.g., strangers only), or number of locations (e.g., one). The time frame of 24 hours was chosen to eliminate conflation with spree killers, who kill multiple victims in quick succession in different locations or incidents, and to satisfy the traditional requirement of occurring in a “single incident.”

Offenders who commit mass murder during a spree (before or after committing additional homicides) are included in the database, and all victims within seven days of the mass murder are included in the victim count. Negligent homicides related to driving under the influence or accidental fires are excluded due to the lack of offender intent. Only incidents occurring within the 50 states and Washington D.C. are considered.

Methodology

Project researchers first identified potential incidents using the Federal Bureau of Investigation’s Supplementary Homicide Reports (SHR). Homicide incidents in the SHR were flagged as potential mass murder cases if four or more victims were reported on the same record, and the type of death was murder or non-negligent manslaughter.

Cases were subsequently verified utilizing media accounts, court documents, academic journal articles, books, and local law enforcement records obtained through Freedom of Information Act (FOIA) requests. Each data point was corroborated by multiple sources, which were compiled into a single document to assess the quality of information.

In case(s) of contradiction among sources, official law enforcement or court records were used, when available, followed by the most recent media or academic source.

Case information was subsequently compared with every other known mass murder database to ensure reliability and validity. Incidents listed in the SHR that could not be independently verified were excluded from the database.

Project researchers also conducted extensive searches for incidents not reported in the SHR during the time period, utilizing internet search engines, Lexis-Nexis, and Newspapers.com. Search terms include: [number] dead, [number] killed, [number] slain, [number] murdered, [number] homicide, mass murder, mass shooting, massacre, rampage, family killing, familicide, and arson murder. Offender, victim, and location names were also directly searched when available.

This project started at USA TODAY in 2012.

Contacts

Contact AP Data Editor Justin Myers with questions, suggestions or comments about this dataset at jmyers@ap.org. The Northeastern University researcher working with AP and USA TODAY is Professor James Alan Fox, who can be reached at j.fox@northeastern.edu or 617-416-4400.

Background: Mortality rate rapidly decreases with age after birth, and, simultaneously, the spectrum of death causes show remarkable changes with age. This study analyzed age-associated decreases in mortality rate from diseases of all main chapters of the 10th revision of the International Classification of Diseases.Methods: The number of deaths was extracted from the mortality database of the World Health Organization. As zero cases could be ascertained for a specific age category, the Halley method was used to calculate the mortality rates in all possible calendar years and in all countries combined.Results: All causes mortality from the 1st day of life to the age of 10 years can be represented by an inverse proportion model with a single parameter. High coefficients of determination were observed for total mortality in all populations (arithmetic mean = 0.9942 and standard deviation = 0.0039).Slower or no mortality decrease with age was detected in the 1st year of life, while the inverse proportion method was valid for the age range [1, 10) years in most of all main chapters with three exceptions. The decrease was faster for the chapter “Certain conditions originating in the perinatal period” (XVI).The inverse proportion was valid already from the 1st day for the chapter “Congenital malformations, deformations and chromosomal abnormalities” (XVII).The shape of the mortality decrease was very different for the chapter “Neoplasms” (II) and the rates of mortality from neoplasms were age-independent in the age range [1, 10) years in all populations.Conclusion: The theory of congenital individual risks of death is presented and can explain the results. If it is valid, latent congenital impairments may be present among all cases of death that are not related to congenital impairments. All results are based on published data, and the data are presented as a supplement.

This report draws on data from the National Child Mortality Database (NCMD) to investigate infection related deaths in children and young people, and to draw out learning and recommendations for service providers and policymakers. This NCMD thematic report aims to identify common characteristics of children and young people who died with and because of an infection, investigate factors associated with these deaths and identify common themes, to help inform policymakers, commissioners, those providing services to children and young people, and those involved in reviewing deaths of children and young people.

The infant mortality rate is defined as the number of deaths of children under one year of age, expressed per 1 000 live births. Some of the international variation in infant mortality rates is due to variations among countries in registering practices for premature infants. The United States and Canada are two countries which register a much higher proportion of babies weighing less than 500g, with low odds of survival, resulting in higher reported infant mortality. In Europe, several countries apply a minimum gestational age of 22 weeks (or a birth weight threshold of 500g) for babies to be registered as live births. This indicator is measured in terms of deaths per 1 000 live births.

This indicator is a summary measure of premature mortality, providing an explicit way of weighting deaths occurring at younger ages, which may be preventable. The calculation of Potential Years of Life Lost (PYLL) involves summing up deaths occurring at each age and multiplying this with the number of remaining years to live up to a selected age limit (age 75 is used in OECD Health Statistics). In order to assure cross-country and trend comparison, the PYLL are standardised, for each country and each year. The total OECD population in 2010 is taken as the reference population for age standardisation. This indicator is presented as a total and per gender. It is measured in years lost per 100 000 inhabitants (total), per 100 000 men and per 100 000 women, aged 0-69.

Life expectancy at birth is defined as how long, on average, a newborn can expect to live, if current death rates do not change. However, the actual age-specific death rate of any particular birth cohort cannot be known in advance. If rates are falling, actual life spans will be higher than life expectancy calculated using current death rates. Life expectancy at birth is one of the most frequently used health status indicators. Gains in life expectancy at birth can be attributed to a number of factors, including rising living standards, improved lifestyle and better education, as well as greater access to quality health services. This indicator is presented as a total and per gender and is measured in years.

Commissioned by the Healthcare Quality Improvement Partnership (HQIP) on behalf of NHS England, this report includes analysis of 3,347 children who died in England between 1 April 2019 and 31 March 2020 and investigates the characteristics of their deaths to identify if socio-economic deprivation is associated with childhood mortality.

This is a source dataset for a Let's Get Healthy California indicator at https://letsgethealthy.ca.gov/. Infant Mortality is defined as the number of deaths in infants under one year of age per 1,000 live births. Infant mortality is often used as an indicator to measure the health and well-being of a community, because factors affecting the health of entire populations can also impact the mortality rate of infants. Although California’s infant mortality rate is better than the national average, there are significant disparities, with African American babies dying at more than twice the rate of other groups. Data are from the Birth Cohort Files. The infant mortality indicator computed from the birth cohort file comprises birth certificate information on all births that occur in a calendar year (denominator) plus death certificate information linked to the birth certificate for those infants who were born in that year but subsequently died within 12 months of birth (numerator). Studies of infant mortality that are based on information from death certificates alone have been found to underestimate infant death rates for infants of all race/ethnic groups and especially for certain race/ethnic groups, due to problems such as confusion about event registration requirements, incomplete data, and transfers of newborns from one facility to another for medical care. Note there is a separate data table "Infant Mortality by Race/Ethnicity" which is based on death records only, which is more timely but less accurate than the Birth Cohort File. Single year shown to provide state-level data and county totals for the most recent year. Numerator: Infants deaths (under age 1 year). Denominator: Live births occurring to California state residents. Multiple years aggregated to allow for stratification at the county level. For this indicator, race/ethnicity is based on the birth certificate information, which records the race/ethnicity of the mother. The mother can “decline to state”; this is considered to be a valid response. These responses are not displayed on the indicator visualization.

Analysis of child deaths, 2019-20. 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.

Rank, number of deaths, percentage of deaths, and mortality rates for the leading causes of infant death (under one year of age), by sex, 2000 to most recent year.