This dataset contains counts of live births for California as a whole based on information entered on birth certificates. Final counts are derived from static data and include out of state births to California residents, whereas provisional counts are derived from incomplete and dynamic data. Provisional counts are based on the records available when the data was retrieved and may not represent all births that occurred during the time period.

The final data tables include both births that occurred in California regardless of the place of residence (by occurrence) and births to California residents (by residence), whereas the provisional data table only includes births that occurred in California regardless of the place of residence (by occurrence). The data are reported as totals, as well as stratified by parent giving birth's age, parent giving birth's race-ethnicity, and birth place type. See temporal coverage for more information on which strata are available for which years.

Number and percentage of live births, by month of birth, 1991 to most recent year.

These statistics are derived from two data sources: the Maternity Indicators dataset where a mother’s intention to breastfeed prior to birth is recorded and the National Community Child Health Database (NCCHD) where data for breastfeeding at birth and for babies turning 10 days, 6 weeks and 6 months is recorded and refers to records where there was any breastfeeding. Both data sources are provided to the Welsh Government by Digital Health and Care Wales (DHCW). The Maternity Indicators dataset was established in 2016. It combines records from a mother’s initial assessment with a child’s birth record and enables Welsh Government to monitor its initial set of outcome indicators and performance measures (Maternity Indicators). These were established to measure the effectiveness and quality of Welsh maternity services. The Maternity Indicators dataset allows us to analyse characteristics of the mother’s pregnancy and birth process, of which ‘intention to breastfeed’ is one. The process for producing this data is complex largely because there can be multiple initial assessment data and records for both initial assessments and births are not always complete. The NCCHD was established in 2004 and consists of anonymised records for all children born, resident or treated in Wales and born after 1987. The database brings together data from local Community Child Health System databases which are held by local health boards (LHBs), and its main function is to provide an online record of a child’s health and care from birth to leaving school age. The statistics used in this release are based on the data recorded at birth and shortly after birth. Full details of every data item available on both the Maternity Indicators dataset and National Community Child Health Database are available through the NHS Wales Data Dictionary: http://www.datadictionary.wales.nhs.uk/#!WordDocuments/datasetstructure20.htm The data dictionary also defines how ethnic groups are classified, namely: • White (any white background) • Black (African, Caribbean, any other black background) • Asian (Pakistani, Bangladeshi, Chinese, Indian, any other Asian background) • Mixed/multiple (white and Asian, white and black African, white and black Caribbean, any other mixed background) • Other (any other ethnic group)

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.

The dataset is an open data from the Sistema de Informação de Nascidos Vivos (SINASC), which is a system implemented by the Brazilian federal government in the 1990s, with the purpose of collecting data on all live births in the national territory. The system makes it possible to provide information on birth rates for all levels of the Brazilian health system, as well as the development of relevant indicators in the strategic planning of management to support the planning of actions, activities, public policies and programs aimed at health.

The dataset is related to three years (2018, 2019 and 2020) of SINASC referring only to the state of Pernambuco, and it is composed of routine prenatal data, gestational history, sociodemographic data and data of newborns. born, including their weight. The pre-processed dataset has 10 attributes plus the target attribute ‘WEIGHT’, with 351,253 records, 29,625 low birth weight records and 321,628 adequate weight records. This dataset contains two CSV files: the first file “Dataset.csv” is the pre-processed dataset and the second “Attributes.csv” contains the description of each attribute.

This is a publication on maternity activity in English NHS hospitals. This report examines data relating to delivery and birth episodes in 2023-24, and the booking appointments for these deliveries. This annual publication covers the financial year ending March 2024. Data is included from both the Hospital Episodes Statistics (HES) data warehouse and the Maternity Services Data Set (MSDS). HES contains records of all admissions, appointments and attendances for patients admitted to NHS hospitals in England. The HES data used in this publication are called 'delivery episodes'. The MSDS collects records of each stage of the maternity service care pathway in NHS-funded maternity services, and includes information not recorded in HES. The MSDS is a maturing, national-level dataset. In April 2019, the MSDS transitioned to a new version of the dataset. This version, MSDS v2.0, is an update that introduced a new structure and content - including clinical terminology, in order to meet current clinical practice and incorporate new requirements. It is designed to meet requirements that resulted from the National Maternity Review, which led to the publication of the Better Births report in February 2016. This is the fifth publication of data from MSDS v2.0 and data from 2019-20 onwards is not directly comparable to data from previous years. This publication shows the number of HES delivery episodes during the period, with a number of breakdowns including by method of onset of labour, delivery method and place of delivery. It also shows the number of MSDS deliveries recorded during the period, with a breakdown for the mother's smoking status at the booking appointment by age group. It also provides counts of live born term babies with breakdowns for the general condition of newborns (via Apgar scores), skin-to-skin contact and baby's first feed type - all immediately after birth. There is also data available in a separate file on breastfeeding at 6 to 8 weeks. For the first time information on 'Smoking at Time of Delivery' has been presented using annual data from the MSDS. This includes national data broken down by maternal age, ethnicity and deprivation. From 2025/2026, MSDS will become the official source of 'Smoking at Time of Delivery' information and will replace the historic 'Smoking at Time of Delivery' data which is to become retired. We are currently undergoing dual collection and reporting on a quarterly basis for 2024/25 to help users compare information from the two sources. We are working with data submitters to help reconcile any discrepancies at a local level before any close down activities begin. A link to the dual reporting in the SATOD publication series can be found in the links below. Information on how all measures are constructed can be found in the HES Metadata and MSDS Metadata files provided below. In this publication we have also included an interactive Power BI dashboard to enable users to explore key NHS Maternity Statistics measures. The purpose of this publication is to inform and support strategic and policy-led processes for the benefit of patient care. This report will also be of interest to researchers, journalists and members of the public interested in NHS hospital activity in England. Any feedback on this publication or dashboard can be provided to enquiries@nhsdigital.nhs.uk, under the subject “NHS Maternity Statistics”.

We conducted an unmatched case-control study of 1,225,285 infants from a North Carolina Birth Cohort (2003-2015). Ozone and PM2.5 during critical exposure periods (gestational weeks 3-8) were estimated using residential address and a national spatiotemporal model at census tract centroid. Here we describe data sources for outcome (i.e., congenital heart defects) and exposure (i.e., ozone and PM2.5) data. This dataset is not publicly accessible because: EPA cannot release personally identifiable information regarding living individuals, according to the Privacy Act and the Freedom of Information Act (FOIA). This dataset contains information about human research subjects. Because there is potential to identify individual participants and disclose personal information, either alone or in combination with other datasets, individual level data are not appropriate to post for public access. Restricted access may be granted to authorized persons by contacting the party listed. It can be accessed through the following means: The North Carolina Birth Cohort data are not publicly available as it contains personal identifiable information. Data may be requested through the NCDHHS, Division of Public Health with proper approvals. Air pollutant concentrations for ozone and PM2.5 from the national spatiotemporal model are publicly available from EPA's website. Format: Birth certificate data from the State Center for Health Statistics of the NC Department of Health and Human Services linked with data from the Birth Defects Monitoring Program (NC BDMP) to create a birth cohort of all infants born in NC between 2003-2015. The NC BDMP is an active surveillance system that follows NC births to obtain birth defect diagnoses up to 1 year after the date of birth as well as identify infant deaths during the first year of life and include relevant information from the death certificate. A national spatiotemporal model provided data on predicted ozone PM2.5 concentrations over critical prenatal and time periods. The prediction model used data from research and regulatory monitors as well as a large (>200) array of geographic covariates to create fine scale spatial and temporal predictions. The model has a cross-validated R2 of 0.89 for PM2.5. Concentrations were predicted for daily throughout the study period at the centroid of each 2010 census tract in NC. This dataset is associated with the following publication: Arogbokun, O., T. Luben, J. Stingone, L. Engel, C. Martin, and A. Olshan. Racial disparities in maternal exposure to ambient air pollution during pregnancy and prevalence of congenital heart defects. AMERICAN JOURNAL OF EPIDEMIOLOGY. Johns Hopkins Bloomberg School of Public Health, 194(3): 709-721, (2025).

This dataset includes teen birth rates for females by age group, race, and Hispanic origin in the United States since 1960. Data availability varies by race and ethnicity groups. All birth data by race before 1980 are based on race of the child. Since 1980, birth data by race are based on race of the mother. For race, data are available for Black and White births since 1960, and for American Indians/Alaska Native and Asian/Pacific Islander births since 1980. Data on Hispanic origin are available since 1989. Teen birth rates for specific racial and ethnic categories are also available since 1989. From 2003 through 2015, the birth data by race were based on the “bridged” race categories (5). Starting in 2016, the race categories for reporting birth data changed; the new race and Hispanic origin categories are: Non-Hispanic, Single Race White; Non-Hispanic, Single Race Black; Non-Hispanic, Single Race American Indian/Alaska Native; Non-Hispanic, Single Race Asian; and, Non-Hispanic, Single Race Native Hawaiian/Pacific Islander (5,6). Birth data by the prior, “bridged” race (and Hispanic origin) categories are included through 2018 for comparison. National data on births by Hispanic origin exclude data for Louisiana, New Hampshire, and Oklahoma in 1989; New Hampshire and Oklahoma in 1990; and New Hampshire in 1991 and 1992. Birth and fertility rates for the Central and South American population includes other and unknown Hispanic. Information on reporting Hispanic origin is detailed in the Technical Appendix for the 1999 public-use natality data file (see ftp://ftp.cdc.gov/pub/Health_Statistics/NCHS/Dataset_Documentation/DVS/natality/Nat1999doc.pdf). SOURCES NCHS, National Vital Statistics System, birth data (see https://www.cdc.gov/nchs/births.htm); public-use data files (see https://www.cdc.gov/nchs/data_access/VitalStatsOnline.htm); and CDC WONDER (see http://wonder.cdc.gov/). REFERENCES National Office of Vital Statistics. Vital Statistics of the United States, 1950, Volume I. 1954. Available from: https://www.cdc.gov/nchs/data/vsus/vsus_1950_1.pdf. Hetzel AM. U.S. vital statistics system: major activities and developments, 1950-95. National Center for Health Statistics. 1997. Available from: https://www.cdc.gov/nchs/data/misc/usvss.pdf. National Center for Health Statistics. Vital Statistics of the United States, 1967, Volume I–Natality. 1969. Available from: https://www.cdc.gov/nchs/data/vsus/nat67_1.pdf. Martin JA, Hamilton BE, Osterman MJK, et al. Births: Final data for 2015. National vital statistics reports; vol 66 no 1. Hyattsville, MD: National Center for Health Statistics. 2017. Available from: https://www.cdc.gov/nchs/data/nvsr/nvsr66/nvsr66_01.pdf. Martin JA, Hamilton BE, Osterman MJK, Driscoll AK, Drake P. Births: Final data for 2016. National Vital Statistics Reports; vol 67 no 1. Hyattsville, MD: National Center for Health Statistics. 2018. Available from: https://www.cdc.gov/nvsr/nvsr67/nvsr67_01.pdf. Martin JA, Hamilton BE, Osterman MJK, Driscoll AK, Births: Final data for 2018. National vital statistics reports; vol 68 no 13. Hyattsville, MD: National Center for Health Statistics. 2019. Available from: https://www.cdc.gov/nchs/data/nvsr/nvsr68/nvsr68_13.pdf.

Annual live births in England and Wales by age of mother and father, type of registration, median interval between births, number of previous live-born children and National Statistics Socio-economic Classification (NS-SEC).

The WIC Infant and Toddler Feeding Practices Study–2 (WIC ITFPS-2) (also known as the “Feeding My Baby Study”) is a national, longitudinal study that captures data on caregivers and their children who participated in the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) around the time of the child’s birth. The study addresses a series of research questions regarding feeding practices, the effect of WIC services on those practices, and the health and nutrition outcomes of children on WIC. Additionally, the study assesses changes in behaviors and trends that may have occurred over the past 20 years by comparing findings to the WIC Infant Feeding Practices Study–1 (WIC IFPS-1), the last major study of the diets of infants on WIC. This longitudinal cohort study has generated a series of reports. These datasets include data from caregivers and their children during the prenatal period and during the children’s first five years of life (child ages 1 to 60 months). A full description of the study design and data collection methods can be found in Chapter 1 of the Second Year Report (https://www.fns.usda.gov/wic/wic-infant-and-toddler-feeding-practices-st...). A full description of the sampling and weighting procedures can be found in Appendix B-1 of the Fourth Year Report (https://fns-prod.azureedge.net/sites/default/files/resource-files/WIC-IT...). Processing methods and equipment used Data in this dataset were primarily collected via telephone interview with caregivers. Children’s length/height and weight data were objectively collected while at the WIC clinic or during visits with healthcare providers. The study team cleaned the raw data to ensure the data were as correct, complete, and consistent as possible. Study date(s) and duration Data collection occurred between 2013 and 2019. Study spatial scale (size of replicates and spatial scale of study area) Respondents were primarily the caregivers of children who received WIC services around the time of the child’s birth. Data were collected from 80 WIC sites across 27 State agencies. Level of true replication Unknown Sampling precision (within-replicate sampling or pseudoreplication) This dataset includes sampling weights that can be applied to produce national estimates. A full description of the sampling and weighting procedures can be found in Appendix B-1 of the Fourth Year Report (https://fns-prod.azureedge.net/sites/default/files/resource-files/WIC-IT...). Level of subsampling (number and repeat or within-replicate sampling) A full description of the sampling and weighting procedures can be found in Appendix B-1 of the Fourth Year Report (https://fns-prod.azureedge.net/sites/default/files/resource-files/WIC-IT...). Study design (before–after, control–impacts, time series, before–after-control–impacts) Longitudinal cohort study. Description of any data manipulation, modeling, or statistical analysis undertaken Each entry in the dataset contains caregiver-level responses to telephone interviews. Also available in the dataset are children’s length/height and weight data, which were objectively collected while at the WIC clinic or during visits with healthcare providers. In addition, the file contains derived variables used for analytic purposes. The file also includes weights created to produce national estimates. The dataset does not include any personally-identifiable information for the study children and/or for individuals who completed the telephone interviews. Description of any gaps in the data or other limiting factors Please refer to the series of annual WIC ITFPS-2 reports (https://www.fns.usda.gov/wic/infant-and-toddler-feeding-practices-study-2-fourth-year-report) for detailed explanations of the study’s limitations. Outcome measurement methods and equipment used The majority of outcomes were measured via telephone interviews with children’s caregivers. Dietary intake was assessed using the USDA Automated Multiple Pass Method (https://www.ars.usda.gov/northeast-area/beltsville-md-bhnrc/beltsville-h...). Children’s length/height and weight data were objectively collected while at the WIC clinic or during visits with healthcare providers. Resources in this dataset:Resource Title: ITFP2 Year 5 Enroll to 60 Months Public Use Data CSV. File Name: itfps2_enrollto60m_publicuse.csvResource Description: ITFP2 Year 5 Enroll to 60 Months Public Use Data CSVResource Title: ITFP2 Year 5 Enroll to 60 Months Public Use Data Codebook. File Name: ITFPS2_EnrollTo60m_PUF_Codebook.pdfResource Description: ITFP2 Year 5 Enroll to 60 Months Public Use Data CodebookResource Title: ITFP2 Year 5 Enroll to 60 Months Public Use Data SAS SPSS STATA R Data. File Name: ITFP@_Year5_Enroll60_SAS_SPSS_STATA_R.zipResource Description: ITFP2 Year 5 Enroll to 60 Months Public Use Data SAS SPSS STATA R DataResource Title: ITFP2 Year 5 Ana to 60 Months Public Use Data CSV. File Name: ampm_1to60_ana_publicuse.csvResource Description: ITFP2 Year 5 Ana to 60 Months Public Use Data CSVResource Title: ITFP2 Year 5 Tot to 60 Months Public Use Data Codebook. File Name: AMPM_1to60_Tot Codebook.pdfResource Description: ITFP2 Year 5 Tot to 60 Months Public Use Data CodebookResource Title: ITFP2 Year 5 Ana to 60 Months Public Use Data Codebook. File Name: AMPM_1to60_Ana Codebook.pdfResource Description: ITFP2 Year 5 Ana to 60 Months Public Use Data CodebookResource Title: ITFP2 Year 5 Ana to 60 Months Public Use Data SAS SPSS STATA R Data. File Name: ITFP@_Year5_Ana_60_SAS_SPSS_STATA_R.zipResource Description: ITFP2 Year 5 Ana to 60 Months Public Use Data SAS SPSS STATA R DataResource Title: ITFP2 Year 5 Tot to 60 Months Public Use Data CSV. File Name: ampm_1to60_tot_publicuse.csvResource Description: ITFP2 Year 5 Tot to 60 Months Public Use Data CSVResource Title: ITFP2 Year 5 Tot to 60 Months Public Use SAS SPSS STATA R Data. File Name: ITFP@_Year5_Tot_60_SAS_SPSS_STATA_R.zipResource Description: ITFP2 Year 5 Tot to 60 Months Public Use SAS SPSS STATA R DataResource Title: ITFP2 Year 5 Food Group to 60 Months Public Use Data CSV. File Name: ampm_foodgroup_1to60m_publicuse.csvResource Description: ITFP2 Year 5 Food Group to 60 Months Public Use Data CSVResource Title: ITFP2 Year 5 Food Group to 60 Months Public Use Data Codebook. File Name: AMPM_FoodGroup_1to60m_Codebook.pdfResource Description: ITFP2 Year 5 Food Group to 60 Months Public Use Data CodebookResource Title: ITFP2 Year 5 Food Group to 60 Months Public Use SAS SPSS STATA R Data. File Name: ITFP@_Year5_Foodgroup_60_SAS_SPSS_STATA_R.zipResource Title: WIC Infant and Toddler Feeding Practices Study-2 Data File Training Manual. File Name: WIC_ITFPS-2_DataFileTrainingManual.pdf

This report was released in September 2010. However, recent demographic data is available on the datastore - you may find other datasets on the Datastore useful such as: GLA Population Projections, National Insurance Number Registrations of Overseas Nationals, Births by Birthplace of Mother, Births and Fertility Rates, Office for National Statistics (ONS) Population Estimates

FOCUSONLONDON2010:POPULATIONANDMIGRATION

London is the United Kingdom’s only city region. Its population of 7.75 million is 12.5 per cent of the UK population living on just 0.6 per cent of the land area. London’s average population density is over 4,900 persons per square kilometre, this is ten times that of the second most densely populated region.

Between 2001 and 2009 London’s population grew by over 430 thousand, more than any other region, accounting for over 16 per cent of the UK increase.

This report discusses in detail the population of London including Population Age Structure, Fertility and Mortality, Internal Migration, International Migration, Population Turnover and Churn, and Demographic Projections.

Population and Migration report is the first release of the Focus on London 2010-12 series. Reports on themes such as Income, Poverty, Labour Market, Skills, Health, and Housing are also available.

PRESENTATION:

To access an interactive presentation about population changes in London click the link to see it on Prezi.com

FACTS:

• Top five boroughs for babies born per 10,000 population in 2008-09:
• 1. Newham – 244.4
• 2. Barking and Dagenham – 209.3
• 3. Hackney – 205.7
• 4. Waltham Forest – 202.7
• 5. Greenwich – 196.2
• ...
• 32. Havering – 116.8
• 33. City of London – 47.0
• In 2009, Barnet overtook Croydon as the most populous London borough. Prior to this Croydon had been the largest since 1966
• Population per hectare of land used for Domestic building and gardens is highest in Tower Hamlets
• In 2008-09, natural change (births minus deaths) led to 78,000 more Londoners compared with only 8,000 due to migration. read more about this or click play on the chart below to reveal how regional components of populations change have altered over time.

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 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.

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.

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.

Baltimore City Child Health

An Exploration of 2010 Birth, Prenatal Visit, Lead Exposure and Teen Birth Rates

By City of Baltimore [source]

About this dataset

This Baltimore City Child and Family Health Indicators dataset provides us with crucial information that can support the health and well-being of Baltimore City residents. It contains 13 indicators such as low birth weight, prenatal visits, teen births, and more. This data is sourced from the Maryland Department of Health & Mental Hygiene (DHMH), Baltimore Substance Abuse Systems (BSAS), theBaltimore City Health Department, and the US Census Bureau. Through this data set we can gain a better understanding of how Baltimore City citizens’ health compares to other areas and how it has changed over time. By investigating this dataset we are given an opportunity to create potential strategies for providing better care for our community. With discoveries from these indicators, together as a city we can bring about lasting change in protecting public health within Baltimore

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How to use the dataset

This dataset provides valuable information about the health and wellbeing of children and families in Baltimore City in 2010. The data is organized by CSA (Census Statistical Area) and includes stats on term births, low birth weight births, prenatal visits, teen births, and lead testing. This dataset can be used to analyze trends in children's health over time as well as identify potential areas that need more attention or resources.

To use this dataset: - Read through the data dictionary to understand what each column represents.
- Choose which columns you would like to explore further.
- Filter or subset the data as you see fit then visualize it with graphs or maps to better understand how conditions vary across neighborhoods in Baltimore City.
- Consider comparing the data from this year with prior years if available for deeper analysis of changes over time.
- Look for correlations among columns that could help explain disparities between neighborhoods and create strategies for improving outcomes through policy interventions or other programs designed specifically for those areas needs

Research Ideas

• Mapping health disparities in high-risk areas to target public health interventions.
• Identifying neighborhoods in need of additional resources for prenatal care, infant care, and lead testing and create specific programs to address these needs.
• Creating an online dashboard that displays real time data on Baltimore City’s population health indicators such as birth weight, teenage pregnancies, and lead poisoning for the public to access easily

Acknowledgements

If you use this dataset in your research, please credit the original authors. Data Source

License

License: CC0 1.0 Universal (CC0 1.0) - Public Domain Dedication No Copyright - You can copy, modify, distribute and perform the work, even for commercial purposes, all without asking permission. See Other Information.

Columns

File: BNIA_Child_Fam_Health_2010.csv | Column name | Description | |:---------------|:----------------------------------------------------------| | the_geom | Geometry of the Census Statistical Area (CSA) (Geometry) | | CSA2010 | Census Statistical Area (CSA) (String) | | termbir10 | Total number of term births in 2010 (Integer) | | birthwt10 | Total number of low birth weight births in 2010 (Integer) | | prenatal10 | Total number of prenatal visits in 2010 (Integer) | | teenbir10 | Total number of teen births in 2010 (Integer) | | leadtest10 | Total number of lead tests conducted in 2010 (Integer) |

Acknowledgements

If you use this dataset in your research, please credit the original authors. If you use this dataset in your research, please credit City of Baltimore.

Abstract copyright UK Data Service and data collection copyright owner.Background:The Millennium Cohort Study (MCS) is a large-scale, multi-purpose longitudinal dataset providing information about babies born at the beginning of the 21st century, their progress through life, and the families who are bringing them up, for the four countries of the United Kingdom. The original objectives of the first MCS survey, as laid down in the proposal to the Economic and Social Research Council (ESRC) in March 2000, were:to chart the initial conditions of social, economic and health advantages and disadvantages facing children born at the start of the 21st century, capturing information that the research community of the future will requireto provide a basis for comparing patterns of development with the preceding cohorts (the National Child Development Study, held at the UK Data Archive under GN 33004, and the 1970 Birth Cohort Study, held under GN 33229)to collect information on previously neglected topics, such as fathers' involvement in children's care and developmentto focus on parents as the most immediate elements of the children's 'background', charting their experience as mothers and fathers of newborn babies in the year 2000, recording how they (and any other children in the family) adapted to the newcomer, and what their aspirations for her/his future may beto emphasise intergenerational links including those back to the parents' own childhoodto investigate the wider social ecology of the family, including social networks, civic engagement and community facilities and services, splicing in geo-coded data when availableAdditional objectives subsequently included for MCS were:to provide control cases for the national evaluation of Sure Start (a government programme intended to alleviate child poverty and social exclusion)to provide samples of adequate size to analyse and compare the smaller countries of the United Kingdom, and include disadvantaged areas of EnglandFurther information about the MCS can be found on the Centre for Longitudinal Studies web pages.The content of MCS studies, including questions, topics and variables can be explored via the CLOSER Discovery website.The first sweep (MCS1) interviewed both mothers and (where resident) fathers (or father-figures) of infants included in the sample when the babies were nine months old, and the second sweep (MCS2) was carried out with the same respondents when the children were three years of age. The third sweep (MCS3) was conducted in 2006, when the children were aged five years old, the fourth sweep (MCS4) in 2008, when they were seven years old, the fifth sweep (MCS5) in 2012-2013, when they were eleven years old, the sixth sweep (MCS6) in 2015, when they were fourteen years old, and the seventh sweep (MCS7) in 2018, when they were seventeen years old.End User Licence versions of MCS studies:The End User Licence (EUL) versions of MCS1, MCS2, MCS3, MCS4, MCS5, MCS6 and MCS7 are held under UK Data Archive SNs 4683, 5350, 5795, 6411, 7464, 8156 and 8682 respectively. The longitudinal family file is held under SN 8172.Sub-sample studies:Some studies based on sub-samples of MCS have also been conducted, including a study of MCS respondent mothers who had received assisted fertility treatment, conducted in 2003 (see EUL SN 5559). Also, birth registration and maternity hospital episodes for the MCS respondents are held as a separate dataset (see EUL SN 5614).Release of Sweeps 1 to 4 to Long Format (Summer 2020)To support longitudinal research and make it easier to compare data from different time points, all data from across all sweeps is now in a consistent format. The update affects the data from sweeps 1 to 4 (from 9 months to 7 years), which are updated from the old/wide to a new/long format to match the format of data of sweeps 5 and 6 (age 11 and 14 sweeps). The old/wide formatted datasets contained one row per family with multiple variables for different respondents. The new/long formatted datasets contain one row per respondent (per parent or per cohort member) for each MCS family. Additional updates have been made to all sweeps to harmonise variable labels and enhance anonymisation. 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 MCS that are not held at the UKDS, see the CLS Genetic data and biological samples webpage.Secure Access datasets:Secure Access versions of the MCS have more restrictive access conditions than versions available under the standard End User Licence or Special Licence (see 'Access data' tab above).Secure Access versions of the MCS include:detailed sensitive variables not available under EUL. These have been grouped thematically and are held under SN 8753 (socio-economic, accommodation and occupational data), SN 8754 (self-reported health, behaviour and fertility), SN 8755 (demographics, language and religion) and SN 8756 (exact participation dates). These files replace previously available studies held under SNs 8456 and 8622-8627detailed geographical identifier files which are grouped by sweep held under SN 7758 (MCS1), SN 7759 (MCS2), SN 7760 (MCS3), SN 7761 (MCS4), SN 7762 (MCS5 2001 Census Boundaries), SN 7763 (MCS5 2011 Census Boundaries), SN 8231 (MCS6 2001 Census Boundaries), SN 8232 (MCS6 2011 Census Boundaries), SN 8757 (MCS7), SN 8758 (MCS7 2001 Census Boundaries) and SN 8759 (MCS7 2011 Census Boundaries). These files replace previously available files grouped by geography SN 7049 (Ward level), SN 7050 (Lower Super Output Area level), and SN 7051 (Output Area level)linked education administrative datasets for Key Stages 1, 2 and 4 held under SN 8481 (England). This replaces previously available datasets for Key Stage 1 (SN 6862) and Key Stage 2 (SN 7712)linked education administrative datasets for Key Stage 1 held under SN 7414 (Scotland)linked education administrative dataset for Key Stages 1, 2, 3 and 4 under SN 9085 (Wales)linked NHS Patient Episode Database for Wales (PEDW) for MCS1 – MCS5 held under SN 8302linked Scottish Medical Records data held under SNs 8709, 8710, 8711, 8712, 8713 and 8714;Banded Distances to English Grammar Schools for MCS5 held under SN 8394linked Health Administrative Datasets (Hospital Episode Statistics) for England for years 2000-2019 held under SN 9030linked Hospital of Birth data held under SN 5724.The linked education administrative datasets held under SNs 8481,7414 and 9085 may be ordered alongside the MCS detailed geographical identifier files only if sufficient justification is provided in the application. Users are also only allowed access to either 2001 or 2011 of Geographical Identifiers Census Boundaries studies. So for MCS5 either SN 7762 (2001 Census Boundaries) or SN 7763 (2011 Census Boundaries), for the MCS6 users are only allowed either SN 8231 (2001 Census Boundaries) or SN 8232 (2011 Census Boundaries); and the same applies for MCS7 so either SN 8758 (2001 Census Boundaries) or SN 8759 (2011 Census Boundaries).Researchers applying for access to the Secure Access MCS datasets should indicate on their ESRC Accredited Researcher application form the EUL dataset(s) that they also wish to access (selected from the MCS Series Access web page). The Millennium Cohort Study: Sweep 3 Banded Distances to Current, First, Second, and Third Choice Schools study provides banded distances to the current, first, second, and third choice school of MCS cohort members at sweep 3 (2006). The cohort members would therefore be aged between four and six years old, and have entered the primary school education system.

This is a publication on maternity activity in English NHS hospitals. This report examines data relating to delivery and birth episodes in 2022-23, and the booking appointments for these deliveries. This annual publication covers the financial year ending March 2023. Data is included from both the Hospital Episodes Statistics (HES) data warehouse and the Maternity Services Data Set (MSDS). HES contains records of all admissions, appointments and attendances for patients admitted to NHS hospitals in England. The HES data used in this publication are called 'delivery episodes'. The MSDS collects records of each stage of the maternity service care pathway in NHS-funded maternity services, and includes information not recorded in HES. The MSDS is a maturing, national-level dataset. In April 2019 the MSDS transitioned to a new version of the dataset. This version, MSDS v2.0, is an update that introduced a new structure and content - including clinical terminology, in order to meet current clinical practice and incorporate new requirements. It is designed to meet requirements that resulted from the National Maternity Review, which led to the publication of the Better Births report in February 2016. This is the fourth publication of data from MSDS v2.0 and data from 2019-20 onwards is not directly comparable to data from previous years. This publication shows the number of HES delivery episodes during the period, with a number of breakdowns including by method of onset of labour, delivery method and place of delivery. It also shows the number of MSDS deliveries recorded during the period, with breakdowns including the baby's first feed type, birthweight, place of birth, and breastfeeding activity; and the mothers' ethnicity and age at booking. There is also data available in a separate file on breastfeeding at 6 to 8 weeks. The count of Total Babies includes both live and still births, and previous changes to how Total Babies and Total Deliveries were calculated means that comparisons between 2019-20 MSDS data and later years should be made with care. Information on how all measures are constructed can be found in the HES Metadata and MSDS Metadata files provided below. In this publication we have also included an interactive Power BI dashboard to enable users to explore key NHS Maternity Statistics measures. The purpose of this publication is to inform and support strategic and policy-led processes for the benefit of patient care. This report will also be of interest to researchers, journalists and members of the public interested in NHS hospital activity in England. Any feedback on this publication or dashboard can be provided to enquiries@nhsdigital.nhs.uk, under the subject “NHS Maternity Statistics”.

United States US: Fertility Rate: Total: Births per Woman data was reported at 1.800 Ratio in 2016. This records a decrease from the previous number of 1.843 Ratio for 2015. United States US: Fertility Rate: Total: Births per Woman data is updated yearly, averaging 2.002 Ratio from Dec 1960 (Median) to 2016, with 57 observations. The data reached an all-time high of 3.654 Ratio in 1960 and a record low of 1.738 Ratio in 1976. United States US: Fertility Rate: Total: Births per Woman data remains active status in CEIC and is reported by World Bank. The data is categorized under Global Database’s USA – Table US.World Bank: Health Statistics. Total fertility rate represents the number of children that would be born to a woman if she were to live to the end of her childbearing years and bear children in accordance with age-specific fertility rates of the specified year.; ; (1) United Nations Population Division. World Population Prospects: 2017 Revision. (2) Census reports and other statistical publications from national statistical offices, (3) Eurostat: Demographic Statistics, (4) United Nations Statistical Division. Population and Vital Statistics Reprot (various years), (5) U.S. Census Bureau: International Database, and (6) Secretariat of the Pacific Community: Statistics and Demography Programme.; Weighted average; Relevance to gender indicator: it can indicate the status of women within households and a woman’s decision about the number and spacing of children.

Background:
The Millennium Cohort Study (MCS) is a large-scale, multi-purpose longitudinal dataset providing information about babies born at the beginning of the 21st century, their progress through life, and the families who are bringing them up, for the four countries of the United Kingdom. The original objectives of the first MCS survey, as laid down in the proposal to the Economic and Social Research Council (ESRC) in March 2000, were:

• to chart the initial conditions of social, economic and health advantages and disadvantages facing children born at the start of the 21st century, capturing information that the research community of the future will require
• to provide a basis for comparing patterns of development with the preceding cohorts (the National Child Development Study, held at the UK Data Archive under GN 33004, and the 1970 Birth Cohort Study, held under GN 33229)
• to collect information on previously neglected topics, such as fathers' involvement in children's care and development
• to focus on parents as the most immediate elements of the children's 'background', charting their experience as mothers and fathers of newborn babies in the year 2000, recording how they (and any other children in the family) adapted to the newcomer, and what their aspirations for her/his future may be
• to emphasise intergenerational links including those back to the parents' own childhood
• to investigate the wider social ecology of the family, including social networks, civic engagement and community facilities and services, splicing in geo-coded data when available

Additional objectives subsequently included for MCS were:

• to provide control cases for the national evaluation of Sure Start (a government programme intended to alleviate child poverty and social exclusion)
• to provide samples of adequate size to analyse and compare the smaller countries of the United Kingdom, and include disadvantaged areas of England

Further information about the MCS can be found on the Centre for Longitudinal Studies web pages.

The content of MCS studies, including questions, topics and variables can be explored via the CLOSER Discovery website.

The first sweep (MCS1) interviewed both mothers and (where resident) fathers (or father-figures) of infants included in the sample when the babies were nine months old, and the second sweep (MCS2) was carried out with the same respondents when the children were three years of age. The third sweep (MCS3) was conducted in 2006, when the children were aged five years old, the fourth sweep (MCS4) in 2008, when they were seven years old, the fifth sweep (MCS5) in 2012-2013, when they were eleven years old, the sixth sweep (MCS6) in 2015, when they were fourteen years old, and the seventh sweep (MCS7) in 2018, when they were seventeen years old.

End User Licence versions of MCS studies:
The End User Licence (EUL) versions of MCS1, MCS2, MCS3, MCS4, MCS5, MCS6 and MCS7 are held under UK Data Archive SNs 4683, 5350, 5795, 6411, 7464, 8156 and 8682 respectively. The longitudinal family file is held under SN 8172.

Sub-sample studies:
Some studies based on sub-samples of MCS have also been conducted, including a study of MCS respondent mothers who had received assisted fertility treatment, conducted in 2003 (see EUL SN 5559). Also, birth registration and maternity hospital episodes for the MCS respondents are held as a separate dataset (see EUL SN 5614).


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 MCS that are not held at the UKDS, see the CLS Genetic data and biological samples webpage.

Secure Access datasets:
Secure Access versions of the MCS have more restrictive access conditions than versions available under the standard End User Licence or Special Licence (see 'Access data' tab above).

Secure Access versions of the MCS include:

• detailed sensitive variables not available under EUL. These have been grouped thematically and are held under SN 8753 (socio-economic, accommodation and occupational data), SN 8754 (self-reported health, behaviour and fertility), SN 8755 (demographics, language and religion) and SN 8756 (exact participation dates). These files replace previously available studies held under SNs 8456 and 8622-8627
  
• detailed geographical identifier files which are grouped by sweep held under SN 7758 (MCS1), SN 7759 (MCS2), SN 7760 (MCS3), SN 7761 (MCS4), SN 7762 (MCS5 2001 Census Boundaries), SN 7763 (MCS5 2011 Census Boundaries), SN 8231 (MCS6 2001 Census Boundaries), SN 8232 (MCS6 2011 Census Boundaries), SN 8757 (MCS7), SN 8758 (MCS7 2001 Census Boundaries) and SN 8759 (MCS7 2011 Census Boundaries). These files replace previously available files grouped by geography SN 7049 (Ward level), SN 7050 (Lower Super Output Area level), and SN 7051 (Output Area level)
• linked education administrative datasets for Key Stages 1, 2, 4 and 5 held under SN 8481 (England). This replaces previously available datasets for Key Stage 1 (SN 6862) and Key Stage 2 (SN 7712)
  
• linked education administrative datasets for Key Stage 1 held under SN 7414 (Scotland)
• linked education administrative dataset for Key Stages 1, 2, 3 and 4 under SN 9085 (Wales)
  
• linked NHS Patient Episode Database for Wales (PEDW) for MCS1 – MCS5 held under SN 8302
• linked Scottish Medical Records data held under SNs 8709, 8710, 8711, 8712, 8713 and 8714;
• Banded Distances to English Grammar Schools for MCS5 held under SN 8394
• linked Health Administrative Datasets (Hospital Episode Statistics) for England for years 2000-2019 held under SN 9030
• linked Hospital of Birth data held under SN 5724.

The linked education administrative datasets held under SNs 8481,7414 and 9085 may be ordered alongside the MCS detailed geographical identifier files only if sufficient justification is provided in the application.

Researchers applying for access to the Secure Access MCS datasets should indicate on their ESRC Accredited Researcher application form the EUL dataset(s) that they also wish to access (selected from the MCS Series Access web page).

Participants for the Millennium Cohort Study: Age 9 months, Sweep 1, 2003: Survey of Mothers who Received Assisted Fertility Treatment were drawn from existing MCS respondents. Consenting parents who had reported having any medical infertility treatment for the pregnancy covered by MCS were sent a postal questionnaire which asked more detail about their experiences of infertility treatment. Much of the resulting statistical analysis involved comparing the women who had received different types of infertility treatment, either with each other or with women who had received no such treatment. All analyses allowed for the clustered, stratified sample design, with re-weighting included where necessary to allow for the different sampling proportions.

For the second edition (March 2008), a new version of the data file was deposited, with the family serial number variable (famsrno) replaced by a new serial number variable, mcsid (MCS Research Serial Number). The documentation remains unchanged.

This dataset contains percent preterm and very preterm live births by race/ethnic group of mother. Preterm births are all live births less than 37 weeks of gestation. Very preterm births are all live births less than 32 weeks of gestation. Important growth and development occur throughout pregnancy, especially in the final months and weeks. There is a higher risk of serious disability or death the earlier a baby is born. Gestational age is based on obstetric estimate at delivery (OE). Data includes births with gestational age of 17-47 weeks. Note: The race and ethnic groups in this table utilize eight mutually exclusive race and ethnicity categories. These categories are Hispanic and the following Non-Hispanic categories of Multi-Race, African-American, American Indian (includes Eskimo and Aleut), Asian, Pacific Islander (includes Hawaiian), White (includes Other race) and Unknown (includes refused to state and missing). Data should not be compared to other data where gestational age is based on the date of last normal menses (LMP) and not OE. The National Center for Health Statistics recently transitioned to using an OE-based gestational age measure due to increasing evidence of its greater validity compared with the LMP-based measure. (http://www.cdc.gov/nchs/data/nvsr/nvsr64/nvsr64_05.pdf)

A computerized data set of demographic, economic and social data for 227 countries of the world. Information presented includes population, health, nutrition, mortality, fertility, family planning and contraceptive use, literacy, housing, and economic activity data. Tabular data are broken down by such variables as age, sex, and urban/rural residence. Data are organized as a series of statistical tables identified by country and table number. Each record consists of the data values associated with a single row of a given table. There are 105 tables with data for 208 countries. The second file is a note file, containing text of notes associated with various tables. These notes provide information such as definitions of categories (i.e. urban/rural) and how various values were calculated. The IDB was created in the U.S. Census Bureau''s International Programs Center (IPC) to help IPC staff meet the needs of organizations that sponsor IPC research. The IDB provides quick access to specialized information, with emphasis on demographic measures, for individual countries or groups of countries. The IDB combines data from country sources (typically censuses and surveys) with IPC estimates and projections to provide information dating back as far as 1950 and as far ahead as 2050. Because the IDB is maintained as a research tool for IPC sponsor requirements, the amount of information available may vary by country. As funding and research activity permit, the IPC updates and expands the data base content. Types of data include: * Population by age and sex * Vital rates, infant mortality, and life tables * Fertility and child survivorship * Migration * Marital status * Family planning Data characteristics: * Temporal: Selected years, 1950present, projected demographic data to 2050. * Spatial: 227 countries and areas. * Resolution: National population, selected data by urban/rural * residence, selected data by age and sex. Sources of data include: * U.S. Census Bureau * International projects (e.g., the Demographic and Health Survey) * United Nations agencies Links: * ICPSR: http://www.icpsr.umich.edu/icpsrweb/ICPSR/studies/08490

This dataset presents the estimated percentage of babies born alive before 37 weeks of pregnancy are completed, by country. Preterm birth is a leading cause of neonatal morbidity and mortality. Understanding national rates supports efforts to improve antenatal care, timely interventions, and newborn outcomes. These estimates are adapted from Liang et al. (2024), based on the Global Burden of Disease Study 2021, and provide a globally comparable measure of preterm birth burden.Data Source:The Lancet: https://www.thelancet.com/journals/eclinm/article/PIIS2589-5370(24)00419-X/fulltext Data Dictionary: The data is collated with the following columns:Column headingContent of this columnPossible valuesRefNumerical counter for each row of data, for ease of identification1+CountryShort name for the country195 countries in total – all 194 WHO member states plus PalestineISO3Three-digit alphabetical codes International Standard ISO 3166-1 assigned by the International Organization for Standardization (ISO). e.g. AFG (Afghanistan)ISO22 letter identifier code for the countrye.g. AF (Afghanistan)ICM_regionICM Region for countryAFR (Africa), AMR (Americas), EMR (Eastern Mediterranean), EUR (Europe), SEAR (South east Asia) or WPR (Western Pacific)CodeUnique project code for each indicator:GGTXXnnnGG=data group e.g. OU for outcomeT = N for novice or E for ExpertXX = identifier number 00 to 30nnn = identifier name eg mmre.g. OUN01sbafor Outcome Novice Indicator 01 skilled birth attendance Short_nameIndicator namee.g. maternal mortality ratioDescriptionText description of the indicator to be used on websitee.g. Maternal mortality ratio (maternal deaths per 100,000 live births)Value_typeDescribes the indicator typeNumeric: decimal numberPercentage: value between 0 & 100Text: value from list of text optionsY/N: yes or noValue_categoryExpect this to be ‘total’ for all indicators for Phase 1, but this could allow future disaggregation, e.g. male/female; urban/ruraltotalYearThe year that the indicator value was reported. For most indicators, we will only report if 2014 or more recente.g. 2020Latest_Value‘LATEST’ if this is the most recent reported value for the indicator since 2014, otherwise ‘No’. Useful for indicators with time trend data.LATEST or NOValueIndicator valuee.g. 99.8. NB Some indicators are calculated to several decimal places. We present the value to the number of decimal places that should be displayed on the Hub.SourceFor Caesarean birth rate [OUN13cbr] ONLY, this column indicates the source of the data, either OECD when reported, or UNICEF otherwise.OECD or UNICEFTargetHow does the latest value compare with Global guidelines / targets?meets targetdoes not meet targetmeets global standarddoes not meet global standardRankGlobal rank for indicator, i.e. the country with the best global score for this indicator will have rank = 1, next = 2, etc. This ranking is only appropriate for a few indicators, others will show ‘na’1-195Rank out ofThe total number of countries who have reported a value for this indicator. Ranking scores will only go as high as this number.Up to 195TrendIf historic data is available, an indication of the change over time. If there is a global target, then the trend is either getting better, static or getting worse. For mmr [OUN04mmr] and nmr [OUN05nmr] the average annual rate of reduction (arr) between 2016 and latest value is used to determine the trend:arr <-1.0 = getting worsearr >=-1.0 AND <=1.0 = staticarr >1.0 = getting betterFor other indicators, the trend is estimated by comparing the average of the last three years with the average ten years ago:decreasing if now < 95% 10 yrs agoincreasing if now > 105% 10 yrs agostatic otherwiseincreasingdecreasing Or, if there is a global target: getting better,static,getting worseNotesClarification comments, when necessary LongitudeFor use with mapping LatitudeFor use with mapping DateDate data uploaded to the Hub the following codes are also possible values: not reported does not apply don’t know This is one of many datasets featured on the Midwives’ Data Hub, a digital platform designed to strengthen midwifery and advocate for better maternal and newborn health services.