The Patient-Reported Indicator Surveys (PaRIS) project is an OECD initiative that systematically collects Patient-Reported Outcome Measures (PROMs), Patient-Reported Experience Measures (PREMs), patient background factors (sociodemographic characteristics, health behaviours, and healthcare capabilities, including digital health literacy), and information on primary care practice characteristics.
PaRIS Cycle 1 focused on people aged 45 years and over who received primary care within the 6 months preceding the survey, 80% of which live with chronic conditions. Data collection of the first cycle took place in 2023-2024.
To support wider use of these data, the OECD has made the PaRIS public use files (PUF) available, enabling a broad range of applications, including academic research, policy analysis, and cross‑national comparisons, to contributing to public knowledge and policy learning.
The OECD PaRIS PUF for Cycle 1 (2023-2024) includes patient de-identified micro-data for 15 out of the 19 participating countries. The PUF can be used to cluster patients based on their primary care practice, but practice characteristics have been excluded for privacy reasons. The OECD is following very high standards for data protection and privacy. This means that some variables from the original dataset (the PaRIS International Dataset) have been removed, suppressed (e.g., ethnicity) or recoded (e.g., age) to avoid re-identification.
The files available online include : country-specific PUF, the codebook and data dictionary and the PaRIS patient questionnaire for Cycle 1 (2023-2024).
If you would like more information about the PaRIS international dataset, please contact paris_survey@oecd.org