Statistics and Data
In performing a literature search, you can gather information for the narrative of your paper using Research Databases. However, many times you may need to use Statistics and Data to validate that narrative. Below are several sources for Healthcare Statistics and Data on the International, National, and State level.
Resources for Healthcare Statistics and Data
- Trends, Charts, and MapsGraph and chart data about clinical trials in the searchable collection from ClinicalTrials.gov.
- OECD Healthcare DataInternational Health Data from the Organization for Economic Cooperation and Development (OECD).
- StatistaAggregates statistical information on over 60,000 topics from more than 18,000 sources, including market research institutes, trade organizations, scientific journals, government databases, and many other private and public resources. Find more detailed information.
- Institute for Health Metrics and Evaluation (IHME)An independent population health research organization based at the University of Washington School of Medicine, the Institute for Health Metrics and Evaluation (IHME) works with collaborators around the world to develop timely, relevant, and scientifically valid evidence that illuminates the state of health everywhere.
- World Health Organization - World Health StatisticsWHO's annual World Health Statistics reports present the most recent health statistics for the WHO Member States and each edition supersedes the previous one. All reports are available for download in Adobe PDF and excel when applicable.
- CDC Data and StatisticsData, statistics, and other tools and resources from the Centers for Disease Control and Prevention (CDC).
- Agency for Healthcare Research and QualityResearch findings, data and statistical tools, reports and publications from Agency for Healthcare Research and Quality (AHRQ).
- CDC National Center for Health StatisticsDivision of the CDC that collects and reports accurate health statistics for better policy-making. Resource also provides information about publications, budget, and employment.
- Research at HHS Operating DivisionsTools and data from the Health and Human Services Operating Divisions for scientists, researchers, and the general public.
- All of US Researcher WorkbenchThe All of Us database provides clinical, environmental, and social lifestyle data to inform how these factors affect health conditions, to promote the advancement of biomedical research such as precision medicine. The "Data Browser" public data is aggregated data from participants’ physical measurements, surveys, wearables, and electronic health records. In the "Researcher Workbench" Registered Tier, UNCW researchers can view and analyze within the Workbench platform individual (not aggregated) human subjects' de-identified biomedical data. Responsible Conduct of Research training within the platform is required for registration.
- National Institute of Environmental Health SciencesPreventing disease by acknowledging and managing our environment continues to be a source of motivation and purpose for the NIEHS staff and our research partners.
- StatistaAggregates statistical information on over 60,000 topics from more than 18,000 sources, including market research institutes, trade organizations, scientific journals, government databases, and many other private and public resources. Find more detailed information.
- Sage DataProvides access to the extensive Data-Planet repository of standardized and structured statistical data. Through a single platform, users can search and browse 35 billion data points in over 4.9 billion datasets sourced from over 70 authoritative government and private sources, covering 16 subject areas. The platform's powerful functionality allows users to manipulate datasets, compare multiple indicators, chart trends over time and spatially represent data without requiring additional software programs. Multiple export options are provided. Find more information.
- State Health FactsHealth Data for states compiled by the Kaiser Family Foundation.
- CDC - Behavioral Risk Factor Surveillance SystemThe Behavioral Risk Factor Surveillance System (BRFSS) is the nation’s premier system of health-related telephone surveys that collect state data about U.S. residents regarding their health-related risk behaviors, chronic health conditions, and use of preventive services. BRFSS completes more than 400,000 adult interviews each year, making it the largest continuously conducted health survey system in the world.
- Census DataThe vision for data dissemination through data.census.gov is to improve the customer experience by making data available from one centralized place so that data users spend less time searching for data content and more time using it.
- United States Census BureauThe Census Bureau provides accurate, detailed, and up-to-date statistics—covering people and business—relating to health in America.
- County Health Rankings and RoadmapsThe CHR&R program provides data, evidence, guidance, and examples to build awareness of the multiple factors that influence health and support leaders in growing community power to improve health equity.
- City Health DashboardThe Department of Population Health at NYU Langone Health and the Robert F. Wagner School of Public Service at NYU created the Dashboard as a health improvement planning resource for U.S. cities. The Dashboard continues to grow, and is a one-stop resource for viewing and comparing data from multiple sources on health and the factors that shape health to guide local solutions.
- Rural Health Information HubThe Rural Health Information Hub, formerly the Rural Assistance Center, is funded by the Federal Office of Rural Health Policy to be a national clearinghouse on rural health issues.
Books
Data Quality Literacy by ISBN: 9798218417475Publication Date: 2024-10-24The book is an edited collection based on a seven-session national forum webinar series on data quality literacy. It covers topics including evaluating data quality: challenges & competencies, quality assurance in data creation, understanding & evaluating governmental data (U.S. & International), commercial data quality issues, data quality: reproducibility and preservation, data quality: evolving employer expectations, and librarians' role in cultivating data-literate citizens. This book is one of the deliverables of the Institute of Museum and Library Services funded project: Building Capacity of Academic Librarians in Understanding Quantitative Data, Data Quality Problems, and Evaluating Data Quality: A National Forum [RE-252357-OLS-22]. The project details and other deliverables including the national forum recordings and knowledge briefs are available on the project website: https://www.dataqualityliteracy.org.
- Know Your Chances: Understanding Health StatisticsThe goal of this book is to help you better understand health information by teaching you about the numbers behind the messages—the medical statistics on which the claims are based. The book will also familiarize you with risk charts, which are designed to help you put your health concerns in perspective. By learning to understand the numbers and knowing what questions to ask, you’ll be able to see through the hype and find the credible information—if any—that remains.