The National Death Index (NDI) is a centralized database of death record information on file in state vital statistics offices. Working with these state offices, the National Center for Health Statistics (NCHS) established the NDI as a resource to aid epidemiologists and other health and medical investigators with their mortality ascertainment activities. Assists investigators in determining whether persons in their studies have died and, if so, provide the names of the states in which those deaths occurred, the dates of death, and the corresponding death certificate numbers. Investigators can then make arrangements with the appropriate state offices to obtain copies of death certificates or specific statistical information such as manner of death or educational level. Cause of death codes may also be obtained using the NDI Plus service. Records from 1979 through 2011 are currently available and contain a standard set of identifying information on each death. Death records are added to the NDI file annually, approximately 12 months after the end of a particular calendar year. 2012 should be available summer 2014. Early Release Program for 2013 is now available. The NDI service is available to investigators solely for statistical purposes in medical and health research. The service is not accessible to organizations or the general public for legal, administrative, or genealogy purposes.
This dataset examines the number of unidentified persons reported to the Centers for Disease Control and Preventions (CDC) National Death Index (NDI), by State, from 1980 to 2004. This report also looks at the number of unidentified human remains reported to the Federal Bureau of Investigations (FBI) National Crime Information Center (NCIC) Unidentified Person File. It describes the characteristics by race and gender and the manner of death. Highlights include the following: Between 1980 and 2004, about 10,300 unidentified human remains were reported to the National Death Index (NDI). Almost three-quarters of unidentified persons were reported by 5 states; Arizona, California, Florida, New York, and Texas. Of the 2,900 National Crime Information Center records that contained data on the manner of death, 27% were ruled homicides; 12%, accidental deaths; 7%, natural causes; and 5%, suicides. The majority of unidentified persons were white (70%); blacks made up 15% of unidentified persons; and race could not be determined in 13% of the cases. For more information about this data go to: http://www.ojp.usdoj.gov/bjs/abstract/uhrus04.htm
https://www.icpsr.umich.edu/web/ICPSR/studies/2183/termshttps://www.icpsr.umich.edu/web/ICPSR/studies/2183/terms
This data collection supplies date and cause of death data for sample persons included in the National Health Interview Surveys (NHIS) for the years 1986 through 1994. Beginning with survey year 1986, linkage information was collected on NHIS respondents aged 18 and older to allow for matching with other data systems such as the National Death Index (NDI). The Multiple Cause of Death (MCD) data files contain information on those persons with scores high enough to be considered deceased or scores high enough that they may be included in an analysis as deceased. The Ineligible Cases data files contain person IDs of those NHIS participants under the age of 18 as well as those with insufficient information to permit linkage with the NDI. These cases should be excluded from the NHIS survey data files prior to analysis. Linkage of the NHIS respondents with the NDI provides a longitudinal component to the NHIS that allows for the ascertainment of vital status. The addition of vital status permits the use of NHIS data to estimate survival, mortality, and life expectancy while using the richness of the NHIS questionnaires, both core and supplements, as covariates. These data files must be used in conjunction with the basic NHIS data files (1986 [ICPSR 8976], 1987 [ICPSR 9195], 1988 [ICPSR 9412], 1989 [ICPSR 9583], 1990 [ICPSR 9839], 1991 [ICPSR 6049], 1992 [ICPSR 6343], 1993 [ICPSR 6534], 1994 [ICPSR 6724]). Variables included in the MCD files cover year of interview, quarter, household number, person number, month and year of death, vital status, and causes of death. The Ineligible Cases files contain a person ID that matches columns 3-16 on the NHIS public use data files.
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Annual data on deaths registered by age, sex and selected underlying cause of death. Tables also provide both mortality rates and numbers of deaths over time.
The Registry of Vital Records and Statistics collects and produces statistical data about births, deaths and other vital events in the Commonwealth.
This data collection presents information about the causes of all recorded deaths occurring in the United States, Puerto Rico, the Virgin Islands, and Guam during 1994. Data are provided concerning underlying causes of death, multiple conditions that caused the death, place of death, residence of the deceased (e.g., region, division, state, county), whether an autopsy was performed, and the month and day of the week of the death. In addition, data are supplied on the sex, race, age, marital status, education, usual occupation, and origin or descent of the deceased. Mortality detail data for 1994 also can be extracted from this file. The mortality detail records are contained in the first 159 positions of these multiple cause records. The multiple cause of death fields were coded from the MANUAL OF THE INTERNATIONAL STATISTICAL CLASSIFICATION OF DISEASES, INJURIES, AND CAUSE-OF-DEATH, NINTH REVISION (ICD-9), VOLUMES 1 AND 2. (Source: downloaded from ICPSR 7/13/10)
Please Note: This dataset is part of the historical CISER Data Archive Collection and is also available at ICPSR -- https://doi.org/10.3886/ICPSR02201.v2. We highly recommend using the ICPSR version as they made this dataset available in multiple data formats.
Description:This data deposit contains the Numerical Identification Death Files (National Archives Identifier 23845618), the NUMIDENT SS-5 Application Files (National Archives Identifier 23845613), the NUMIDENT Claims Files (National Archives Identifier 23852747), and the associated technical documentation. Data Acquisition:These files were e-delivered to Anthony Wray via secure link by the Electronic Records Division of the National Archives and Records Administration (NARA) on 17 October 2019, as per a digitized reproduction order (Quote QO1-525370500 and Quote QO1-528389077). The packing slip is included in the data deposit (docs/Packing Slip.PDF).Rights to Publish:The data are in the public domain, as confirmed by emails received from NARA on 28 December 2023 and 3 January 2024 (see docs/permission_to_publish_email.pdf).How to Cite: Please adhere to the citation and data usage guidelines when using this dataset. See the included LICENSE.txt and README.md files for details. Details:The Numerical Identification Files (NUMIDENT), 1936–2007, series contains records for every Social Security number (SSN) assigned to individuals with a verified death or who would have been over 110 years old by December 31, 2007. There are three types of entries in NUMIDENT: application (SS-5), claim, and death records. A NUMIDENT record may contain more than one entry. Information contained in NUMIDENT records includes: each applicant's full name, SSN, date of birth, place of birth, citizenship, sex, father's name, mother's maiden name, and race/ethnic description (optional). NUMIDENT includes information regarding any subsequent changes made to the applicant's record, including name changes and life or death claims. The death records in NUMIDENT do not include any State reported deaths in accordance with the Social Security Act section 205(r). There are 72,182,729 SS-5 records entries; 25,230,486 claim record entries; and 49,459,293 death record entries.See https://catalog.archives.gov/id/12004494 for more information.Related Data:Visit the CenSoc Project for public micro datasets linked to NUMIDENT: https://censoc.berkeley.edu/.
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Users can access data about mortality statistics related to occupation exposures. Background The National Occupational Mortality Survey (NOMS) is maintained by the National Institute for Occupational Safety and Health (NIOSH). The data base offers age-adjusted proportionate mortality ratios and summary statistics for roughly 500 occupational groups and 300 industry groups. User Functionality Users can search proportionate mortality ratio (PMR) data by sex, race, cause of death, industry (using census industry codes) or occupation, and age catego ries (15-54, 15-64, 65+). Additionally users can access over 3,000 premade charts and tables for quick access to selected chronic disease data. Twenty-two site-specific cancers and 17 cardiovascular, neurodegenerative, diabetes, and renal disease multiple cause PMRs are presented for the largest fifteen industries in each of eight sectors: agriculture, forestry, fishing; mining; construction; manufacturing, wholesale and retail trade; transportation, warehousing and utilities; healthcare and social assistance; and services. Data Notes The NOMS database presents the results of a multiple cause death analysis of death by industry based on data from more than 11,000,000 death records for adults, race and gender combined, age 18 and above that died during the years 1984-1998 in twenty-seven U.S. states. The states are Alaska, Colorado, Georgia, Hawaii, Idaho, Indiana, Kansas, Kentucky, Maine, Missouri, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Penn sylvania, Rhode Island, South Carolina, Tennessee, Utah, Vermont, Washington, West Virginia, and Wisconsin. Data acquired from data searches is available for download in HTML or Comma-Separated Value (CSV) format. Premade charts are available for download in excel.
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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.
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Users can search this database pertaining to respiratory conditions such as asthma, pneumonia, bronchitis, and tuberculosis. BackgroundThe National Occupational Respiratory Mortality System (NORMS) is developed and maintained by National Institute of Occupational Safety and Health (NIOSH) of the Centers for Disease Control and Prevention (CDC). This surveillance system includes respiratory conditions such as: asthma, pneumonia, bronchitis, tuberculosis, lung cancer, and silicosis, among others. User FunctionalityUsers can generate national- or occupation-specific queries. Users can gener ate tables, charts and maps containing the summary statistics such as number of deaths, crude death rates, age-adjusted death rates, and years of potential life lost (YPLL ). Users can also download the dataset and/or data queries into Microsoft Excel. Data NotesThis website provides data history regarding revisions to the dataset. Data from additional sources (i.e., population estimates, comparative standard population, and life-table values) are also available. National mortality data is derived from the National Center for Health Statistics (NCHS) multiple cause of death records. These data are updated annually since 1968, unless otherwise indicated. Data are available on national, state, and county levels. The most recent d ata available is from 2007.
Data on death rates for suicide in the United States, by age, sex, race, and Hispanic origin. Data are from Health, United States. SOURCE: National Center for Health Statistics, National Vital Statistics System, Mortality File. Search, visualize, and download these and other estimates from over 150 health topics with the NCHS Data Query System (DQS), available from: https://www.cdc.gov/nchs/dataquery/index.htm.
The Charleston Heart Study (CHS) is a prospective cohort study of 2,283 subjects (1,394 whites, 889 blacks) in which risk factors of coronary disease have been examined for the past 43 years. The CHS began enrolling a random selection of community residents who in 1960 were 35 years of age and older ����?? including men and women, black and white. A unique feature of this cohort is the fact that 102 high socio-economic status (SES) black men were purposefully included. The primary hypothesis of the original study was to investigate racial differences in the manifestation and risk factors for coronary disease. Over the ensuing 40+ years, a variety of outcome measurements were incorporated into the re-examination of the participants, including psychosocial, behavioral, aging and functional measures. Subjects were initially interviewed and examined in 1960 and 1963. Subsequent interviews and examinations took place during the following time periods: 1974-1975, 1984-1985, 1987-1989, and 1990-1991. During the most recent questionnaire (1990-1991), the following topics were examined: general health, smoking, functional disability, physical disability, cardiovascular health, sexual dysfunction, cognitive disability, depression, coffee consumption, medication history, medical history, nutrition, and body image. In addition, serum samples and blood pressure measurements were taken, and a physical exam was performed by a physician. A search of the National Death Index was completed through the year 2000, matching individuals with date and cause of death. Vital status of the CHS study participants through 12-31-2000 is presented below. Dead * White Men 539 (82.5%) * White Women 500 (67.5%) * Black Men 281 (84.4%) * High SES Black Men 59 (57.8%) * Black Women 343 (75.6%) Data Availability: Datasets are stored in the National Archive of Computerized Data on Aging (NACDA) in the ICPSR as Study No. 4050. Data are also available from the Medical University of South Carolina Library; contact a PI, Paul J. Nietert, nieterpj (at) musc.edu for further information. * Dates of Study: 1960-2000 * Study Features: Longitudinal, Minority Oversamples, Anthropometric Measures * Sample Size: 1960: 2,283 (baseline) Link ICPSR, http://www.icpsr.umich.edu/icpsrweb/ICPSR/studies/04050
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Abstract (en): The National Violent Death Reporting System (NVDRS) collects data on violent deaths, i.e., suicides, homicides, and legal intervention, including terrorism-related incidents. The system also includes some other types of deaths, namely deaths due to undetermined intent and unintentional deaths due to firearms. One of the main reasons for including these types of deaths is that there is overlap in how these deaths are coded. For example, a particular poisoning case may be classified as an undetermined death in one state, but in a neighboring state, the same case may be coded as a suicide or an unintentional poisoning. NVDRS is an incident-based system that collects data from different data sources, including death certificates, coroner and medical examiner records, police reports, crime lab data, and child fatality review records. The system collects data on a violent incident, the deaths belonging to that incident, the injury mechanisms leading to death, and the alleged perpetrators (suspects) involved in the violent incident. The relationship of the victim to the suspect is also recorded, as are the relationships of each person to the injury mechanisms included. State health departments participating in NVDRS typically identify relevant violent deaths as their death certificates are filed and then establish the details of the cases from medical examiner, coroner, and law enforcement records. Data collection is ongoing as the source documents from the different data providers become available at different times and intervals. The data represent the violent incidents that occurred between January and December of that data year as submitted by the participating states. ICPSR data undergo a confidentiality review and are altered when necessary to limit the risk of disclosure. ICPSR also routinely creates ready-to-go data files along with setups in the major statistical software formats as well as standard codebooks to accompany the data. In addition to these procedures, ICPSR performed the following processing steps for this data collection: Created online analysis version with question text.; Checked for undocumented or out-of-range codes.. The 2004 data year includes information from 13 states (Alaska, Colorado, Georgia, Maryland, Massachusetts, North Carolina, New Jersey, Oklahoma, Oregon, Rhode Island, South Carolina, Virginia, and Wisconsin). These states combined accounted for 23.4 percent of the 2003 United States population, but 22.7 percent of the suicides and 21.9 percent of the homicides in the United States in 2002. Smallest Geographic Unit: state
Data on death rates for neoplasms in the United States, by age, sex, race, and Hispanic origin. Data are from Health, United States. SOURCE: National Center for Health Statistics, National Vital Statistics System, Mortality File. Search, visualize, and download these and other estimates from over 120 health topics with the NCHS Data Query System (DQS), available from: https://www.cdc.gov/nchs/dataquery/index.htm.
Objective:Â Â To evaluate the prognosis of ischemic stroke patients according to the timing of an atrial fibrillation (AF) diagnosis, we created an inception cohort of incident stroke events and compared the risk of death between stroke patients with a)Â sinus rhythm; b)Â known atrial fibrillation (KAF); and c) AF diagnosed after stroke (AFDAS).Â
Methods:  We utilized the Penn AF Free study to create an inception cohort of patients with incident stroke.  Mortality events were identified after linkage with the National Death Index through June 30, 2017.  We also evaluated initiation of anticoagulants and antiplatelets across the study duration.  Cox proportional hazards models evaluated associations between stroke subtypes and death.
Results:  We identified 1,489 individuals who developed an incident ischemic stroke event:  985 did not develop AF at any point during the study period, 215 had KAF before stroke, 160 had AF detected ≤6 months after stroke and 129 had AF detected >6 mon...
Data on death rates for diseases of heart in the United States, by age, sex, race, and Hispanic origin. Data are from Health, United States. SOURCE: National Center for Health Statistics, National Vital Statistics System, Mortality File. Search, visualize, and download these and other estimates from over 120 health topics with the NCHS Data Query System (DQS), available from: https://www.cdc.gov/nchs/dataquery/index.htm.
https://search.gesis.org/research_data/datasearch-httpwww-da-ra-deoaip--oaioai-da-ra-de519141https://search.gesis.org/research_data/datasearch-httpwww-da-ra-deoaip--oaioai-da-ra-de519141
Abstract (en): The Deaths in Custody Reporting Program (DCRP) is an annual data collection conducted by the Bureau of Justice Statistics (BJS). The DCRP began in 2000 under the Death in Custody Reporting Act of 2000 (P.L. 106-297). It is the only national statistical collection that obtains detailed information about deaths in adult correctional facilities. The DCRP collects data on persons dying in state prisons, local jails and in the process of arrest. Each collection is a separate subcollection, but each is under the umbrella of the DCRP collection. The DCRP collects inmate death records from each of the nation's 50 state prison systems and approximately 2,800 local jail jurisdictions. In addition, this program collects records of all deaths occurring during the process of arrest. Data are collected directly from state and local law enforcement agencies. Death records include information on decedent personal characteristics (age, race or Hispanic origin, and sex), decedent criminal background (legal status, offense type, and time served), and the death itself (date, time, location, and cause of death, as well as information on the autopsy and medical treatment provided for any illness or disease). This data collection represents a single year of DCRP Jails data. The variable names and coding, while similar to other years, have not been standardized across years. The concatenated multi-year versions of the DCRP Jails population data have been edited to correct outliers and other data anomalies. Researchers are encouraged to use the concatenated multi-year data for final jail population data. Deaths of individuals in jails. Smallest Geographic Unit: county paper and pencil interview (PAPI)
Objective
To investigate the hypothesis that patients diagnosed with PNES on video-EEG monitoring (VEM) have increased mortality by comparison to the general population.
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Methods
This retrospective cohort study included patients evaluated in VEM units of three tertiary hospitals in Melbourne, Australia, between January 1st, 1995 and December 31st, 2015. Diagnosis was based on consensus opinion of experienced epileptologists and neuropsychiatrists at each hospital. Mortality was determined in patients diagnosed with PNES, epilepsy or both conditions, by linkage to the Australian National Death Index (NDI). Lifetime history of psychiatric disorders in PNES was determined from formal neuropsychiatric reports.Â
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Results
5,508 patients underwent VEM. 674 (12.2%) were diagnosed with PNES, 3064 (55.6%) with epilepsy, 175 (3.2%) with both conditions, and 1,595 (29.0%) received other diagnoses or had no diagnosis made. The standardised mortality ratio (SMR) of patients d...
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Abstract (en): These data are a collection of demographic statistics for the populations of 125 countries or areas throughout the world, prepared by the Statistical Office of the United Nations. The units of analysis are both country and data year. The primary source of data is a set of questionnaires sent monthly and annually to national statistical services and other appropriate government offices. Data include statistics on approximately 50 types of causes of death for the years 1966 through 1974 for males, females, and total populations. Causes of death in 125 countries or areas throughout the world between the years 1966 and 1974. 2005-11-04 On 2005-03-14 new files were added to one or more datasets. These files included additional setup files as well as one or more of the following: SAS program, SAS transport, SPSS portable, and Stata system files. The metadata record was revised 2005-11-04 to reflect these additions. The causes of death are classified according to the 6th, 7th, and 8th versions of an abbreviated list of the World Health Organization's INTERNATIONAL STATISTICAL CLASSIFICATION OF DISEASES, INJURIES, AND CAUSES OF DEATH. Therefore, data for causes of death are not necessarily comparable across countries or data years. Users should refer to Variable 5 in the Variable List for full discussion of this problem. Users interested in comparing deaths for countries or years that use different versions of the Abbreviated list should consult two publications: A. Joan Klebba, and Alice B. Dolman. COMPARABILITY OF MORTALITY STATISTICS FOR THE SEVENTH AND EIGHTH REVISIONS OF THE INTERNATIONAL CLASSIFICATION OF DISEASES, UNITED STATES. Rockville, MD: United States Department of Health, Education, and Welfare. Public Health Service. Health Services and Mental Health Administration. National Center for Health Statistics, 1975, and World Health Organization. MANUAL OF THE INTERNATIONAL STATISTICAL CLASSIFICATION OF DISEASES, INJURIES, AND CAUSES OF DEATH. Geneva, Switzerland: World Health Organization, 1967.The user should note that countries have data covering a variety of time spans (the maximum span being 1965-1973), and the data have not been padded to supply missing data codes for those years for which a country does not have data. Thus, Egypt has data for years 1965 through 1972, while Kenya has data for only 1970. (See Appendix D in the codebook to determine the years for which a country has data.)It is important that any user of these data consult the United Nations' DEMOGRAPHIC YEARBOOK, 1976, for further explanation of the data's limitations. Certain countries have modified reporting procedures which are presented in both the footnotes and the technical notes accompanying the tables in the Yearbook. There is no way to identify these problems using only the machine-readable data.In order to eliminate unnecessary repetition of identifying information, data were merged so that each record now contains all the data for a country for one particular year. In this process, breakdowns of deaths by ethnic group and/or urban/rural classification were omitted since only a few countries provided such information. Each record now contains the data for the number of deaths from each cause of death for male, female, and total.While the data appear to be in a rectangular matrix, such is not the case. This occurs because different versions of the abbreviated list are referenced in different data years. The lack of a rectangular data matrix does little to restrict the manageability of the dataset. See codebook for examples.While the data have been reformatted and documented by ICPSR staff, there has been no attempt to verify the accuracy and consistency of the data received from the U.N. Statistical Office.
The Death Registrations in England and Wales, 1993-2023: 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:
The National Death Index (NDI) is a centralized database of death record information on file in state vital statistics offices. Working with these state offices, the National Center for Health Statistics (NCHS) established the NDI as a resource to aid epidemiologists and other health and medical investigators with their mortality ascertainment activities. Assists investigators in determining whether persons in their studies have died and, if so, provide the names of the states in which those deaths occurred, the dates of death, and the corresponding death certificate numbers. Investigators can then make arrangements with the appropriate state offices to obtain copies of death certificates or specific statistical information such as manner of death or educational level. Cause of death codes may also be obtained using the NDI Plus service. Records from 1979 through 2011 are currently available and contain a standard set of identifying information on each death. Death records are added to the NDI file annually, approximately 12 months after the end of a particular calendar year. 2012 should be available summer 2014. Early Release Program for 2013 is now available. The NDI service is available to investigators solely for statistical purposes in medical and health research. The service is not accessible to organizations or the general public for legal, administrative, or genealogy purposes.