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Mapping European research networks providing health data: results from the InfAct Joint Action on health information
BACKGROUND: Research networks offer multidisciplinary expertise and promote information exchange between researchers across Europe. They are essential for the European Union’s (EU) health information system as providers of health information and data. The aim of this mapping exercise was to identify...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744039/ https://www.ncbi.nlm.nih.gov/pubmed/35012667 http://dx.doi.org/10.1186/s13690-021-00766-2 |
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author | Unim, Brigid Haverinen, Elsi Mattei, Eugenio Carle, Flavia Faragalli, Andrea Gesuita, Rosaria Thissen, Martin Abboud, Linda Grisetti, Tiziana Bogaert, Petronille Palmieri, Luigi |
author_facet | Unim, Brigid Haverinen, Elsi Mattei, Eugenio Carle, Flavia Faragalli, Andrea Gesuita, Rosaria Thissen, Martin Abboud, Linda Grisetti, Tiziana Bogaert, Petronille Palmieri, Luigi |
author_sort | Unim, Brigid |
collection | PubMed |
description | BACKGROUND: Research networks offer multidisciplinary expertise and promote information exchange between researchers across Europe. They are essential for the European Union’s (EU) health information system as providers of health information and data. The aim of this mapping exercise was to identify and analyze EU research networks in terms of health data collection methods, quality assessment, availability and accessibility procedures. METHODS: A web-based search was performed to identify EU research networks that are not part of international organizations (e.g., WHO-Europe, OECD) and are involved in collection of data for health monitoring or health system performance assessment. General characteristics of the research networks (e.g., data sources, representativeness), quality assessment procedures, availability and accessibility of health data were collected through an ad hoc extraction form. RESULTS: Fifty-seven research networks, representative at national, international or regional level, were identified. In these networks, data are mainly collected through administrative sources, health surveys and cohort studies. Over 70% of networks provide information on quality assessment of their data collection procedures. Most networks share macrodata through articles and reports, while microdata are available from ten networks. A request for data access is required by 14 networks, of which three apply a financial charge. Few networks share data with other research networks (8/49) or specify the metadata-reporting standards used for data description (9/49). CONCLUSIONS: Improving health information and availability of high quality data is a priority in Europe. Research networks could play a major role in tackling health data and information inequalities by enhancing quality, availability, and accessibility of health data and data sharing across European networks. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13690-021-00766-2. |
format | Online Article Text |
id | pubmed-8744039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87440392022-01-10 Mapping European research networks providing health data: results from the InfAct Joint Action on health information Unim, Brigid Haverinen, Elsi Mattei, Eugenio Carle, Flavia Faragalli, Andrea Gesuita, Rosaria Thissen, Martin Abboud, Linda Grisetti, Tiziana Bogaert, Petronille Palmieri, Luigi Arch Public Health Research BACKGROUND: Research networks offer multidisciplinary expertise and promote information exchange between researchers across Europe. They are essential for the European Union’s (EU) health information system as providers of health information and data. The aim of this mapping exercise was to identify and analyze EU research networks in terms of health data collection methods, quality assessment, availability and accessibility procedures. METHODS: A web-based search was performed to identify EU research networks that are not part of international organizations (e.g., WHO-Europe, OECD) and are involved in collection of data for health monitoring or health system performance assessment. General characteristics of the research networks (e.g., data sources, representativeness), quality assessment procedures, availability and accessibility of health data were collected through an ad hoc extraction form. RESULTS: Fifty-seven research networks, representative at national, international or regional level, were identified. In these networks, data are mainly collected through administrative sources, health surveys and cohort studies. Over 70% of networks provide information on quality assessment of their data collection procedures. Most networks share macrodata through articles and reports, while microdata are available from ten networks. A request for data access is required by 14 networks, of which three apply a financial charge. Few networks share data with other research networks (8/49) or specify the metadata-reporting standards used for data description (9/49). CONCLUSIONS: Improving health information and availability of high quality data is a priority in Europe. Research networks could play a major role in tackling health data and information inequalities by enhancing quality, availability, and accessibility of health data and data sharing across European networks. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13690-021-00766-2. BioMed Central 2022-01-10 /pmc/articles/PMC8744039/ /pubmed/35012667 http://dx.doi.org/10.1186/s13690-021-00766-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Unim, Brigid Haverinen, Elsi Mattei, Eugenio Carle, Flavia Faragalli, Andrea Gesuita, Rosaria Thissen, Martin Abboud, Linda Grisetti, Tiziana Bogaert, Petronille Palmieri, Luigi Mapping European research networks providing health data: results from the InfAct Joint Action on health information |
title | Mapping European research networks providing health data: results from the InfAct Joint Action on health information |
title_full | Mapping European research networks providing health data: results from the InfAct Joint Action on health information |
title_fullStr | Mapping European research networks providing health data: results from the InfAct Joint Action on health information |
title_full_unstemmed | Mapping European research networks providing health data: results from the InfAct Joint Action on health information |
title_short | Mapping European research networks providing health data: results from the InfAct Joint Action on health information |
title_sort | mapping european research networks providing health data: results from the infact joint action on health information |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744039/ https://www.ncbi.nlm.nih.gov/pubmed/35012667 http://dx.doi.org/10.1186/s13690-021-00766-2 |
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