SPECIALTY-SPECIFIC RESEARCH

How to Use Publicly Available Healthcare Datasets for Research

Guide · 1 min read · Last updated 2026-10-31

Publicly available healthcare datasets let you do research without collecting new patient data, but they have rules and limits. Check the licence, access conditions, ethics requirements and documentation, and plan an analysis that fits how the data were collected.

Examples of sources (access conditions differ)

  • National health surveys: NHANES and BRFSS in the United States (open to the public for analysis).
  • Hospital and critical-care data: MIMIC-IV (credentialed access after training and agreement).
  • Hospital administrative data: HCUP databases (purchase and data-use agreements).
  • Cancer registry data: SEER (data-use agreement for some files).
  • Global statistics: WHO Global Health Observatory and Global Burden of Disease results.
  • Biobanks: UK Biobank (approved applications and fees).

Steps

  1. Define the question and check that the dataset contains the variables you need with suitable definitions.
  2. Read the documentation: sampling design, weights, variable definitions, data dictionary, known limitations.
  3. Check access and licence: some need registration, training or fees; follow the terms, including limits on re-identification and sharing.
  4. Ask about ethics: secondary analysis of de-identified public data may be exempt or not human-subjects research under some rules, but your institution decides.
  5. Plan the analysis: many surveys need weights and design variables; seek statistical help.
  6. Report the data source, version, access date and variable definitions.

Illustrative example

Invented for teaching. A student wants to estimate hypertension prevalence by education level. She downloads a public survey, reads the guidance on weights and analytic notes, defines hypertension as stated in the survey documentation, asks her ethics office for a determination and analyses with a statistician's help.

Common pitfalls

  • Ignoring weights and clustering in survey data.
  • Attempting to link datasets in ways that could re-identify people.
  • Assuming that the data are error-free.

Key takeaways

  • Check access, licence, ethics and documentation before analysing.
  • Use appropriate methods and report the data source transparently.

References and further reading

  1. CDC National Center for Health Statistics. National Health and Nutrition Examination Survey (NHANES). Link
  2. CDC. Behavioral Risk Factor Surveillance System (BRFSS). Link
  3. PhysioNet. MIMIC-IV clinical database. Link
  4. Agency for Healthcare Research and Quality. Healthcare Cost and Utilization Project (HCUP). Link
  5. National Cancer Institute. Surveillance, Epidemiology, and End Results (SEER) Program. Link
  6. World Health Organization. Global Health Observatory data repository. Link
  7. Institute for Health Metrics and Evaluation. Global Burden of Disease (GBD) study. Link
  8. UK Biobank. Link

Related reading

This page is general educational information about research methods. It is not medical, legal or regulatory advice; follow your institution's ethics board and your target journal's instructions.