In the following maps, the U.S. states are divided into groups based on the rates at which people developed or died from cancer in 2013, the most recent year for which incidence data are available.

The rates are the numbers out of 100,000 people who developed or died from cancer each year.

Incidence Rates by State The number of people who get cancer is called cancer incidence. In the United States, the rate of getting cancer varies from state to state.

*Rates are per 100,000 and are age-adjusted to the 2000 U.S. standard population.

‡Rates are not shown if the state did not meet USCS publication criteria or if the state did not submit data to CDC.

†Source: U.S. Cancer Statistics Working Group. United States Cancer Statistics: 1999–2013 Incidence and Mortality Web-based Report. Atlanta (GA): Department of Health and Human Services, Centers for Disease Control and Prevention, and National Cancer Institute; 2016. Available at: http://www.cdc.gov/uscs.

Death Rates by State Rates of dying from cancer also vary from state to state.

*Rates are per 100,000 and are age-adjusted to the 2000 U.S. standard population.

†Source: U.S. Cancer Statistics Working Group. United States Cancer Statistics: 1999–2013 Incidence and Mortality Web-based Report. Atlanta (GA): Department of Health and Human Services, Centers for Disease Control and Prevention, and National Cancer Institute; 2016. Available at: http://www.cdc.gov/uscs.

Source: https://www.cdc.gov/cancer/dcpc/data/state.htm

Cancer Mortality & Incidence Rates: (Country LVL)

Investigating Cancer Trends over time

By Data Exercises [source]

About this dataset

This dataset is a comprehensive collection of data from county-level cancer mortality and incidence rates in the United States between 2000-2014. This data provides an unprecedented level of detail into cancer cases, deaths, and trends at a local level. The included columns include County, FIPS, age-adjusted death rate, average death rate per year, recent trend (2) in death rates, recent 5-year trend (2) in death rates and average annual count for each county. This dataset can be used to provide deep insight into the patterns and effects of cancer on communities as well as help inform policy decisions related to mitigating risk factors or increasing preventive measures such as screenings. With this comprehensive set of records from across the United States over 15 years, you will be able to make informed decisions regarding individual patient care or policy development within your own community!

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How to use the dataset

This dataset provides comprehensive US county-level cancer mortality and incidence rates from 2000 to 2014. It includes the mortality and incidence rate for each county, as well as whether the county met the objective of 45.5 deaths per 100,000 people. It also provides information on recent trends in death rates and average annual counts of cases over the five year period studied.

This dataset can be extremely useful to researchers looking to study trends in cancer death rates across counties. By using this data, researchers will be able to gain valuable insight into how different counties are performing in terms of providing treatment and prevention services for cancer patients and whether preventative measures and healthcare access are having an effect on reducing cancer mortality rates over time. This data can also be used to inform policy makers about counties needing more target prevention efforts or additional resources for providing better healthcare access within at risk communities.

When using this dataset, it is important to pay close attention to any qualitative columns such as “Recent Trend” or “Recent 5-Year Trend (2)” that may provide insights into long term changes that may not be readily apparent when using quantitative variables such as age-adjusted death rate or average deaths per year over shorter periods of time like one year or five years respectively. Additionally, when studying differences between different counties it is important to take note of any standard FIPS code differences that may indicate that data was collected by a different source with a difference methodology than what was used in other areas studied

Research Ideas

• Using this dataset, we can identify patterns in cancer mortality and incidence rates that are statistically significant to create treatment regimens or preventive measures specifically targeting those areas.
• This data can be useful for policymakers to target areas with elevated cancer mortality and incidence rates so they can allocate financial resources to these areas more efficiently.
• This dataset can be used to investigate which factors (such as pollution levels, access to medical care, genetic make up) may have an influence on the cancer mortality and incidence rates in different US counties

Acknowledgements

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

License

License: Dataset copyright by authors - You are free to: - Share - copy and redistribute the material in any medium or format for any purpose, even commercially. - Adapt - remix, transform, and build upon the material for any purpose, even commercially. - You must: - Give appropriate credit - Provide a link to the license, and indicate if changes were made. - ShareAlike - You must distribute your contributions under the same license as the original. - Keep intact - all notices that refer to this license, including copyright notices.

Columns

File: death .csv | Column name | Description | |:-------------------------------------------|:-------------------------------------------------------------------...

** Description**

This dataset contains data about lung cancer Mortality and is a comprehensive collection of patient information, specifically focused on individuals diagnosed with cancer. This dataset contains comprehensive information on 800,000 individuals related to lung cancer diagnosis, treatment, and outcomes. With 16 well-structured columns. This large-scale dataset is designed to aid researchers, data scientists, and healthcare professionals in studying patterns, building predictive models, and enhancing early detection and treatment strategies.

🌍 The Societal Impact of Lung Cancer

Lung cancer is not just a disease — it's a global crisis that steals time, health, and hope from millions of people every year. As the #1 cause of cancer deaths worldwide, it takes more lives annually than breast, colon, and prostate cancer combined.

But behind every statistic is a story:

A parent who never saw their child graduate.

A worker who had to leave their job too soon.

A community that lost a leader, a friend, a neighbor.

Why does this matter? Lung cancer often goes undetected until it's too late. It’s aggressive, silent, and devastating — especially in underserved areas where early detection is rare and treatment options are limited. It doesn’t just affect patients. It affects families, economies, and healthcare systems on a massive scale.

This dataset represents more than numbers. It represents 800,000 real-world stories — people who can help us unlock patterns, train models, and advance life-saving research.

By working with this data, you're not just analyzing a dataset — you're stepping into the fight against one of humanity’s deadliest diseases.

Let’s turn insight into impact. (😊The above descriptions is generated with the help of AI, Just wanted to share this dataset That all. Thank you)

This is historical data. The update frequency has been set to "Static Data" and is here for historic value. Updated on 8/14/2024 Cancer Mortality Rate - This indicator shows the age-adjusted mortality rate from cancer (per 100,000 population). Maryland’s age adjusted cancer mortality rate is higher than the US cancer mortality rate. Cancer impacts people across all population groups, however wide racial disparities exist. Link to Data Details

Dataset Card for Lung Cancer

  Dataset Summary

The effectiveness of cancer prediction system helps the people to know their cancer risk with low cost and it also helps the people to take the appropriate decision based on their cancer risk status. The data is collected from the website online lung cancer prediction system .

  Supported Tasks and Leaderboards

[More Information Needed]

  Languages

[More Information Needed]

  Dataset Structure… See the full description on the dataset page: https://huggingface.co/datasets/nateraw/lung-cancer.

Death rate has been age-adjusted by the 2000 U.S. standard population. Single-year data are only available for Los Angeles County overall, Service Planning Areas, Supervisorial Districts, City of Los Angeles overall, and City of Los Angeles Council Districts.Lung cancer is a leading cause of cancer-related death in the US. People who smoke have the greatest risk of lung cancer, though lung cancer can also occur in people who have never smoked. Most cases are due to long-term tobacco smoking or exposure to secondhand tobacco smoke. Cities and communities can take an active role in curbing tobacco use and reducing lung cancer by adopting policies to regulate tobacco retail; reducing exposure to secondhand smoke in outdoor public spaces, such as parks, restaurants, or in multi-unit housing; and improving access to tobacco cessation programs and other preventive services.For more information about the Community Health Profiles Data Initiative, please see the initiative homepage.

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Demographic Summary of Available Imaging

Characteristic	Value (N = 26254)
Age (years)	Mean ± SD: 61.4± 5 Median (IQR): 60 (57-65) Range: 43-75
Sex	Male: 15512 (59%) Female: 10742 (41%)
Race	White: 23969 (91.3%) Black: 1135 (4.3%) Asian: 547 (2.1%) American Indian/Alaska Native: 88 (0.3%) Native Hawaiian/Other Pacific Islander: 87 (0.3%) Unknown: 428 (1.6%)
Ethnicity	Not Available

Background: The aggressive and heterogeneous nature of lung cancer has thwarted efforts to reduce mortality from this cancer through the use of screening. The advent of low-dose helical computed tomography (CT) altered the landscape of lung-cancer screening, with studies indicating that low-dose CT detects many tumors at early stages. The National Lung Screening Trial (NLST) was conducted to determine whether screening with low-dose CT could reduce mortality from lung cancer.

Methods: From August 2002 through April 2004, we enrolled 53,454 persons at high risk for lung cancer at 33 U.S. medical centers. Participants were randomly assigned to undergo three annual screenings with either low-dose CT (26,722 participants) or single-view posteroanterior chest radiography (26,732). Data were collected on cases of lung cancer and deaths from lung cancer that occurred through December 31, 2009. This dataset includes the low-dose CT scans from 26,254 of these subjects, as well as digitized histopathology images from 451 subjects.

Results: The rate of adherence to screening was more than 90%. The rate of positive screening tests was 24.2% with low-dose CT and 6.9% with radiography over all three rounds. A total of 96.4% of the positive screening results in the low-dose CT group and 94.5% in the radiography group were false positive results. The incidence of lung cancer was 645 cases per 100,000 person-years (1060 cancers) in the low-dose CT group, as compared with 572 cases per 100,000 person-years (941 cancers) in the radiography group (rate ratio, 1.13; 95% confidence interval [CI], 1.03 to 1.23). There were 247 deaths from lung cancer per 100,000 person-years in the low-dose CT group and 309 deaths per 100,000 person-years in the radiography group, representing a relative reduction in mortality from lung cancer with low-dose CT screening of 20.0% (95% CI, 6.8 to 26.7; P=0.004). The rate of death from any cause was reduced in the low-dose CT group, as compared with the radiography group, by 6.7% (95% CI, 1.2 to 13.6; P=0.02).

Conclusions: Screening with the use of low-dose CT reduces mortality from lung cancer. (Funded by the National Cancer Institute; National Lung Screening Trial ClinicalTrials.gov number, NCT00047385).

Data Availability: A summary of the National Lung Screening Trial and its available datasets are provided on the Cancer Data Access System (CDAS). CDAS is maintained by Information Management System (IMS), contracted by the National Cancer Institute (NCI) as keepers and statistical analyzers of the NLST trial data. The full clinical data set from NLST is available through CDAS. Users of TCIA can download without restriction a publicly distributable subset of that clinical data, along with the CT and Histopathology images collected during the trial. (These previously were restricted.)

I was interested in investigating cancer incidence levels in the US by looking at how they vary by race or state. All the data is collected online from Centers for Disease Control and Prevention, State Cancer Profiles, and United States Census Bureau. This dataset can be used to answer questions on the correlation between poverty levels, insurance levels and cancer incidence levels. Further, one can find which cancers affect a certain race more or a certain state.

Note: DPH is updating and streamlining the COVID-19 cases, deaths, and testing data. As of 6/27/2022, the data will be published in four tables instead of twelve.

The COVID-19 Cases, Deaths, and Tests by Day dataset contains cases and test data by date of sample submission. The death data are by date of death. This dataset is updated daily and contains information back to the beginning of the pandemic. The data can be found at https://data.ct.gov/Health-and-Human-Services/COVID-19-Cases-Deaths-and-Tests-by-Day/g9vi-2ahj.

The COVID-19 State Metrics dataset contains over 93 columns of data. This dataset is updated daily and currently contains information starting June 21, 2022 to the present. The data can be found at https://data.ct.gov/Health-and-Human-Services/COVID-19-State-Level-Data/qmgw-5kp6 .

The COVID-19 County Metrics dataset contains 25 columns of data. This dataset is updated daily and currently contains information starting June 16, 2022 to the present. The data can be found at https://data.ct.gov/Health-and-Human-Services/COVID-19-County-Level-Data/ujiq-dy22 .

The COVID-19 Town Metrics dataset contains 16 columns of data. This dataset is updated daily and currently contains information starting June 16, 2022 to the present. The data can be found at https://data.ct.gov/Health-and-Human-Services/COVID-19-Town-Level-Data/icxw-cada . To protect confidentiality, if a town has fewer than 5 cases or positive NAAT tests over the past 7 days, those data will be suppressed.

COVID-19 cases and associated deaths that have been reported among Connecticut residents, broken down by race and ethnicity. All data in this report are preliminary; data for previous dates will be updated as new reports are received and data errors are corrected. Deaths reported to the either the Office of the Chief Medical Examiner (OCME) or Department of Public Health (DPH) are included in the COVID-19 update.

The following data show the number of COVID-19 cases and associated deaths per 100,000 population by race and ethnicity. Crude rates represent the total cases or deaths per 100,000 people. Age-adjusted rates consider the age of the person at diagnosis or death when estimating the rate and use a standardized population to provide a fair comparison between population groups with different age distributions. Age-adjustment is important in Connecticut as the median age of among the non-Hispanic white population is 47 years, whereas it is 34 years among non-Hispanic blacks, and 29 years among Hispanics. Because most non-Hispanic white residents who died were over 75 years of age, the age-adjusted rates are lower than the unadjusted rates. In contrast, Hispanic residents who died tend to be younger than 75 years of age which results in higher age-adjusted rates.

The population data used to calculate rates is based on the CT DPH population statistics for 2019, which is available online here: https://portal.ct.gov/DPH/Health-Information-Systems--Reporting/Population/Population-Statistics. Prior to 5/10/2021, the population estimates from 2018 were used.

Rates are standardized to the 2000 US Millions Standard population (data available here: https://seer.cancer.gov/stdpopulations/). Standardization was done using 19 age groups (0, 1-4, 5-9, 10-14, ..., 80-84, 85 years and older). More information about direct standardization for age adjustment is available here: https://www.cdc.gov/nchs/data/statnt/statnt06rv.pdf

Categories are mutually exclusive. The category “multiracial” includes people who answered ‘yes’ to more than one race category. Counts may not add up to total case counts as data on race and ethnicity may be missing. Age adjusted rates calculated only for groups with more than 20 deaths. Abbreviation: NH=Non-Hispanic.

Data on Connecticut deaths were obtained from the Connecticut Deaths Registry maintained by the DPH Office of Vital Records. Cause of death was determined by a death certifier (e.g., physician, APRN, medical examiner) using their best clinical judgment. Additionally, all COVID-19 deaths, including suspected or related, are required to be reported to OCME. On April 4, 2020, CT DPH and OCME released a joint memo to providers and facilities within Connecticut providing guidelines for certifying deaths due to COVID-19 that were consistent with the CDC’s guidelines and a reminder of the required reporting to OCME.25,26 As of July 1, 2021, OCME had reviewed every case reported and performed additional investigation on about one-third of reported deaths to better ascertain if COVID-19 did or did not cause or contribute to the death. Some of these investigations resulted in the OCME performing postmortem swabs for PCR testing on individuals whose deaths were suspected to be due to COVID-19, but antemortem diagnosis was unable to be made.31 The OCME issued or re-issued about 10% of COVID-19 death certificates and, when appropriate, removed COVID-19 from the death certificate. For standardization and tabulation of mortality statistics, written cause of death statements made by the certifiers on death certificates are sent to the National Center for Health Statistics (NCHS) at the CDC which assigns cause of death codes according to the International Causes of Disease 10th Revision (ICD-10) classification system.25,26 COVID-19 deaths in this report are defined as those for which the death certificate has an ICD-10 code of U07.1 as either a primary (underlying) or a contributing cause of death. More information on COVID-19 mortality can be found at the following link: https://portal.ct.gov/DPH/Health-Information-Systems--Reporting/Mortality/Mortality-Statistics

Data are subject to future revision as reporting changes.

Starting in July 2020, this dataset will be updated every weekday.

Additional notes: A delay in the data pull schedule occurred on 06/23/2020. Data from 06/22/2020 was processed on 06/23/2020 at 3:30 PM. The normal data cycle resumed with the data for 06/23/2020.

A network outage on 05/19/2020 resulted in a change in the data pull schedule. Data from 5/19/2020 was processed on 05/20/2020 at 12:00 PM. Data from 5/20/2020 was processed on 5/20/2020 8:30 PM. The normal data cycle resumed on 05/20/2020 with the 8:30 PM data pull. As a result of the network outage, the timestamp on the datasets on the Open Data Portal differ from the timestamp in DPH's daily PDF reports.

Starting 5/10/2021, the date field will represent the date this data was updated on data.ct.gov. Previously the date the data was pulled by DPH was listed, which typically coincided with the date before the data was published on data.ct.gov. This change was made to standardize the COVID-19 data sets on data.ct.gov.

This study aimed to identify the trends in the incidence of thymic cancer, i.e., thymoma, thymic carcinoma, and thymic neuroendocrine tumor, in the United States. Data from the United States Cancer Statistics (USCS) database (2001–2015) and those from the Surveillance, Epidemiology, and End Results (SEER) database (SEER 9 [1973–2015], SEER 13 [1992–2015], and SEER 18 [2000–2015]) were used in this study. All incidences were per 100,000 population at risk. The trends in incidence were described as annual percent change (APC) using the Joinpoint regression program. Data from the USCS (2001–2015) database showed an increase in thymic cancer diagnosis with an APC of 4.89% from 2001 to 2006, which is mainly attributed to the significant increase in the incidence of thymoma and thymic carcinoma particularly in women. The incidence of thymic cancer did not increase from 2006 to 2015, which may be attributed to the increase in the diagnosis of thymic carcinoma from 2004 to 2015, with a concomitant decrease in thymoma from 2008 to 2015. Before declining, the age-specific incidence of thymic cancer peaked at ages 70–74 years, with a peak incidence at 1.06 per 100,000 population, and decreased in older age groups. The incidence of thymic cancer was higher in men than in women. Asian/Pacific Islanders had the highest incidence of thymoma, followed by black and then white people. The incidence of thymic carcinoma increased from 2004 to 2015, with a concomitant decrease in thymoma from 2008 to 2015. Asian/Pacific Islanders had the highest incidence of thymoma than other races.

WONDER online databases include county-level Compressed Mortality (death certificates) since 1979; county-level Multiple Cause of Death (death certificates) since 1999; county-level Natality (birth certificates) since 1995; county-level Linked Birth / Death records (linked birth-death certificates) since 1995; state & large metro-level United States Cancer Statistics mortality (death certificates) since 1999; state & large metro-level United States Cancer Statistics incidence (cancer registry cases) since 1999; state and metro-level Online Tuberculosis Information System (TB case reports) since 1993; state-level Sexually Transmitted Disease Morbidity (case reports) since 1984; state-level Vaccine Adverse Event Reporting system (adverse reaction case reports) since 1990; county-level population estimates since 1970. The WONDER web server also hosts the Data2010 system with state-level data for compliance with Healthy People 2010 goals since 1998; the National Notifiable Disease Surveillance System weekly provisional case reports since 1996; the 122 Cities Mortality Reporting System weekly death reports since 1996; the Prevention Guidelines database (book in electronic format) published 1998; the Scientific Data Archives (public use data sets and documentation); and links to other online data sources on the "Topics" page.

The Cancer Prevention Studies (CPS) aim to understand why and how certain people develop cancer while others remain cancer-free. In 1982, the CPS-II cohort was established and includes approximately 1.2 million men and women, aged at least 30 years, recruited by American Cancer Society (ACS) volunteers in all 50 states of the United States of America and Puerto Rico. Participants have been followed biannually for mortality. The CPS-II Nutrition Cohort was established as a subgroup of the larger CPS-II cohort, in which approximately 185,000 individuals have been followed biennially for cancer incidence, diet, and other exposures, since 1992. The CPS-II Lifelink Cohort/Biorepository was initiated in 1998, and collected blood samples from 40,000 participants and cheek cell samples from 70,000 participants in the CPS-II Nutrition Survey cohort.

Context

Millions of people around the world suffer from cancer without any hope of treatment due to the extravagant treatment costs.

Content

In this dataset you'll find the total money spent on treating different cancers.

Acknowledgements

This data comes from https://data.world/xprizeai-health/expenditures-for-cancer-care.

BackgroundThe usefulness of aspirin to defend against cardiovascular disease in both primary and secondary settings is well recognized by the medical profession. Multiple studies also have found that daily aspirin significantly reduces cancer incidence and mortality. Despite these proven health benefits, aspirin use remains low among populations targeted by cardiovascular prevention guidelines. This article seeks to determine the long-term economic and population-health impact of broader use of aspirin by older Americans at higher risk for cardiovascular disease.Methods and FindingsWe employ the Future Elderly Model, a dynamic microsimulation that follows Americans aged 50 and older, to project their lifetime health and spending under the status quo and in various scenarios of expanded aspirin use. The model is based primarily on data from the Health and Retirement Study, a large, representative, national survey that has been ongoing for more than two decades. Outcomes are chosen to provide a broad perspective of the individual and societal impacts of the interventions and include: heart disease, stroke, cancer, life expectancy, quality-adjusted life expectancy, disability-free life expectancy, and medical costs. Eligibility for increased aspirin use in simulations is based on the 2011–2012 questionnaire on preventive aspirin use of the National Health and Nutrition Examination Survey. These data reveal a large unmet need for daily aspirin, with over 40% of men and 10% of women aged 50 to 79 presenting high cardiovascular risk but not taking aspirin. We estimate that increased use by high-risk older Americans would improve national life expectancy at age 50 by 0.28 years (95% CI 0.08–0.50) and would add 900,000 people (95% CI 300,000–1,400,000) to the American population by 2036. After valuing the quality-adjusted life-years appropriately, Americans could expect $692 billion (95% CI 345–975) in net health benefits over that period.ConclusionsExpanded use of aspirin by older Americans with elevated risk of cardiovascular disease could generate substantial population health benefits over the next twenty years and do so very cost-effectively.

The National Health Interview Surveys (NHIS) continuously monitor illness and injury, disability and chronic impairments, and health services used by people in the United States. In 1987, additional interviews were conducted with two subsamples of NHIS respondents to gather data on cancer control and epidemiology. Like the Cancer Control supplement, this Cancer Epidemiology supplement included questions on acculturation (in terms of language, ethnicity, and place of birth), dietary knowledge, smoking and tobacco use, and occupational history. The Cancer Epidemiology supplement also included questions on frequency and portion sizes of food and drink items, vitamin and mineral intake, reproduction, hormone use, family's and respondent's history of cancer, height and weight, and participation in social activities. Approximately 90 demographic, health status, and health care variables from the core data files are included on the supplement file. (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 at https://doi.org/10.3886/ICPSR09341.v1. We highly recommend using the ICPSR version as they may make this dataset available in multiple data formats in the future.

Demographic Trends and Health Outcomes in the U.S

Inequalities,Risk Factors and Access to Care

By Data Society [source]

About this dataset

This dataset contains key demographic, health status indicators and leading cause of death data to help us understand the current trends and health outcomes in communities across the United States. By looking at this data, it can be seen how different states, counties and populations have changed over time. With this data we can analyze levels of national health services use such as vaccination rates or mammography rates; review leading causes of death to create public policy initiatives; as well as identify risk factors for specific conditions that may be associated with certain populations or regions. The information from these files includes State FIPS Code, County FIPS Code, CHSI County Name, CHSI State Name, CHSI State Abbreviation, Influenza B (FluB) report count & expected cases rate per 100K population , Hepatitis A (HepA) Report Count & expected cases rate per 100K population , Hepatitis B (HepB) Report Count & expected cases rate per 100K population , Measles (Meas) Report Count & expected cases rate per 100K population , Pertussis(Pert) Report Count & expected case rate per 100K population , CRS report count & expected case rate per 100K population , Syphilis report count and expected case rate per 100k popuation. We also look at measures related to preventive care services such as Pap smear screen among women aged 18-64 years old check lower/upper confidence intervals seperately ; Mammogram checks among women aged 40-64 years old specified lower/upper conifence intervals separetly ; Colonosopy/ Proctoscpushy among men aged 50+ measured in lower/upper limits ; Pneumonia Vaccination amongst 65+ with loewr/upper confidence level detail Additionally we have some interesting trend indicating variables like measures of birth adn death which includes general fertility ratye ; Teen Birth Rate by Mother's age group etc Summary Measures covers mortality trend following life expectancy by sex&age categories Vressionable populations access info gives us insight into disablilty ratio + access to envtiromental issues due to poor quality housing facilities Finally Risk Factors cover speicfic hoslitic condtiions suchs asthma diagnosis prevelance cancer diabetes alcholic abuse smoking trends All these information give a good understanding on Healthy People 2020 target setings demograpihcally speaking hence will aid is generating more evience backed policies

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What the Dataset Contains

This dataset contains valuable information about public health relevant to each county in the United States, broken down into 9 indicator domains: Demographics, Leading Causes of Death, Summary Measures of Health, Measures of Birth and Death Rates, Relative Health Importance, Vulnerable Populations and Environmental Health Conditions, Preventive Services Use Data from BRFSS Survey System Data , Risk Factors and Access to Care/Health Insurance Coverage & State Developed Types of Measurements such as CRS with Multiple Categories Identified for Each Type . The data includes indicators such as percentages or rates for influenza (FLU), hepatitis (HepA/B), measles(MEAS) pertussis(PERT), syphilis(Syphilis) , cervical cancer (CI_Min_Pap_Smear - CI_Max\Pap \Smear), breast cancer (CI\Min Mammogram - CI \Max \Mammogram ) proctoscopy (CI Min Proctoscopy - CI Max Proctoscopy ), pneumococcal vaccinations (Ci min Pneumo Vax - Ci max Pneumo Vax )and flu vaccinations (Ci min Flu Vac - Ci Max Flu Vac). Additionally , it provides information on leading causes of death at both county levels & national level including age-adjusted mortality rates due to suicide among teens aged between 15-19 yrs per 100000 population etc.. Furthermore , summary measures such as age adjusted percentage who consider their physical health fair or poor are provided; vulnerable populations related indicators like relative importance score for disabled adults ; preventive service use related ones ranging from self reported vaccination coverage among men40-64 yrs old against hepatitis B virus etc...

Getting Started With The Dataset

To get started with exploring this dataset first your need to understand what each column in the table represents: State FIPS Code identifies a unique identifier used by various US government agencies which denote states . County FIPS code denotes counties wi...

IntroductionThe purpose of this study is to culturally adapt the Awareness and Beliefs about Cancer (ABC) measure for use in the Hispanic/Latino population living in the United States (US).MethodsIn accordance with Patient Reported Outcomes (PRO) Consortium guidelines for cross-cultural adaptation of measures for content and linguistic validity, we conducted: two forward-translations, reconciliation, two back-translations, revision and harmonization, six cognitive interviews, revision, external expert review, and finalization of the version. We used a mixed methods approach, conducting cognitive interviews with Hispanic/Latino community members while also convening an expert panel of six clinicians, health professionals, and community representatives and including the in the entire process. After cross-culturally adapting the ABC measure, we assessed the psychometric properties of the instrument using item response theory analysis. Item parameters, discrimination and category thresholds, and standard errors were calculated. For each of the adapted subdomains, we used item information curves to report the graphical profile of item effectiveness.ResultsTwenty-two Hispanic/Latino community members were enrolled in cognitive interviews, and Hispanics/Latinos fluent in Spanish completed the measure to assess its psychometric properties. Cognitive interviews revealed opportunities to improve items. Key changes from the original measure include the inclusion of gender inclusive language and an inquiry into e-cigarette use on items related to smoking habits. Psychometric property analyses revealed that the anticipated delay in seeking medical help, general cancer beliefs, and cancer screening beliefs and behaviors subdomains had some slope parameters that were < 1; this implies that those items were not able to adequately discriminate the latent trait and had poor performance.DiscussionThe adapted ABC measure for US Hispanics/Latinos meets content and linguistic validity standards, with construct validity confirmed for cancer symptom recognition and barriers to symptomatic presentation subdomains, but revisions are necessary for others, highlighting the need for ongoing refinement to ensure the cultural appropriateness of instruments.

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.

IntroductionSepsis-related mortality in middle-aged and older pancreatic cancer patients constitutes a significant public health issue. This study seeks to analyze trends in the age-adjusted mortality rate (AAMR) for sepsis-related fatalities among these patients in the United States from 1999 to 2023, employing data from the most recent CDC WONDER database. The temporal patterns revealed from this analysis are anticipated to guide subsequent research and public health initiatives.MethodsThe CDC WONDER database was used to look at how many middle-aged and older pancreatic cancer patients in the U.S. died from sepsis between 1999 and 2023. The study utilized AAMR to evaluate temporal mortality patterns among adults aged 45 and older, categorized by race, census region, urban/rural residency, and state, using the Joinpoint regression tool. We calculated the annual percent change (APC) and the average annual percent change (AAPC), and we supplied 95% confidence intervals.ResultsDuring the study period, the sepsis-related death rate among middle-aged and elderly pancreatic cancer patients exhibited a notable increase, with an AAPC of 2.89. Male patients consistently demonstrated a greater AAMR compared to females, with a notable increase recorded [AAPC = 2.73 (95% CI 1.61 to 3.87)]. Black or African American patients had the greatest AAMR, which also went up a lot [AAPC = 2.62 (95% CI 1.76 to 3.48)]. The mortality burden increased significantly with age, reaching its highest point in the 75–84 age range. A regional study found that the Midwest had the highest rise in AAMR [AAPC = 3.74 (95% CI 2.50 to 5.00)]. Urban people consistently exhibited a higher AAMR compared to rural communities, despite the most significant increase in AAMR occurring among rural populations [AAPC = 3.51 (95% CI 2.09 to 4.94)].ConclusionThis study’s findings reveal substantial inequalities among gender, ethnicity, age, and geographic regions. These differences show how important it is to quickly implement targeted measures to lower mortality, especially among individuals at high risk.

Leading Causes of Death US

1980–2009 by Sex, Race, and Hispanic Origin

By Health [source]

About this dataset

This fascinating dataset takes a look at the leading causes of death in the United States from 1980-2009, broken down by sex, race, and Hispanic origin. This data sheds light on how mortality in the US has changed over time among these categories. Accounting for everything from heart disease to cancer to suicide, this insight can be used by health researchers and policy makers to gain a better understanding of disparities in healthcare and deaths across different groups. Whether studying questions related to public health or more targeted population issues such as gender biases in death rates, this dataset provides an important resource for anyone interested in examining mortality across demographic lines

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How to use the dataset

This dataset can be used to explore some of the leading causes of death in the United States from 1980 to 2009, broken down by sex, race, and Hispanic origin. This data can be used to better understand mortality trends and risk factors associated with different populations in America.

By using this dataset you can compare and contrast mortality rates across different gender, racial, and ethnic groups during this time period. You can also compare different causes of death within these demographic categories to see if there are any patterns over time or notable differences between groups.

You could even use this data to track changes across population groups as a whole or look at details for specific years or types of causes of death in particular groups. With this information one may gain insight into health disparities across population segments in America— aiding advocates for social change & public policy shifts toward improved health outcomes for all Americans!

Research Ideas

• Analyzing regional or state-level differences in mortality rates over time.
• Examining the beahvioral factors or risk factors associated with each cause of death for different genders and populations.
• Examining the prevalence of each cause of death as a proportion to an overall population trend in different socio-economic categories such as race or income level

Acknowledgements

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

License

License: Dataset copyright by authors - You are free to: - Share - copy and redistribute the material in any medium or format for any purpose, even commercially. - Adapt - remix, transform, and build upon the material for any purpose, even commercially. - You must: - Give appropriate credit - Provide a link to the license, and indicate if changes were made. - ShareAlike - You must distribute your contributions under the same license as the original. - Keep intact - all notices that refer to this license, including copyright notices.

Columns

File: Selected_Trend_Table_from_Health_United_States_2011._Leading_causes_of_death_and_numbers_of_deaths_by_sex_race_and_Hispanic_origin_United_States_1980_and_2009.csv | Column name | Description | |:-------------------|:---------------------------------------------------------------------------------------------------------| | Group | The group of people the cause of death applies to (e.g. men, women, whites, blacks, hispanics). (String) | | Year | The year the cause of death was recorded. (Integer) | | Cause of death | The cause of death. (String) | | Flag | A flag indicating whether the cause of death is considered a leading cause. (Boolean) | | Deaths | The number of deaths attributed to the cause of death. (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 Health.