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Prioritizing health information for national health reporting - a Delphi study of the Joint Action on Health Information (InfAct)
Archives of Public Health, Volume: 80, Issue: 1, Start page: 25
Swansea University Author: Ronan Lyons
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DOI (Published version): 10.1186/s13690-021-00760-8
Abstract
Background: Health information (HI) strategies exist in several EU Member States, however, they mainly focus on technical issues and improving governance rather than on content-related priority setting. There is also little research available about national prioritization processes underlying HI dev...
| Published in: | Archives of Public Health |
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| ISSN: | 2049-3258 |
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Springer Science and Business Media LLC
2022
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| URI: | https://cronfa.swan.ac.uk/Record/cronfa59164 |
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<?xml version="1.0"?><rfc1807><datestamp>2022-01-12T15:28:58.3138218</datestamp><bib-version>v2</bib-version><id>59164</id><entry>2022-01-12</entry><title>Prioritizing health information for national health reporting - a Delphi study of the Joint Action on Health Information (InfAct)</title><swanseaauthors><author><sid>83efcf2a9dfcf8b55586999d3d152ac6</sid><firstname>Ronan</firstname><surname>Lyons</surname><name>Ronan Lyons</name><active>true</active><ethesisStudent>false</ethesisStudent></author></swanseaauthors><date>2022-01-12</date><abstract>Background: Health information (HI) strategies exist in several EU Member States, however, they mainly focus on technical issues and improving governance rather than on content-related priority setting. There is also little research available about national prioritization processes underlying HI development for policy support in the EU. The aim of this study was to broaden the knowledge base on HI prioritization strategies and to encourage expert exchange towards good practice models. A specific focus was put on HI produced for national health reporting, this being a crucial tool for policy advice. Methods: We conducted a literature search to identify published and grey literature on national HI prioritization. This was followed by a two-round Policy Delphi study, where we explored which processes and methods exist in EU Member States and associated countries for the prioritization of HI collection. In the first round, information about these processes was gathered in semi-structured questions; in the second round, participants were asked to rank the identified approaches for desirability and feasibility. The survey was conducted online; participants were recruited from the membership of the Joint Action on Health Information (InfAct – Information for Action). Results: 119 experts were contacted, representing 40 InfAct partner institutions in 28 EU Member States and associated countries. Of these, 28 experts responded fully or partially to the first round, and six to the second round. In the first round, more than half of the respondents reported the existence of structured HI prioritization processes in their countries. To prioritize HI, a clear preference was given in the second round for a formal, horizontal process which includes different experts and stakeholders. National public health institutes were named desirable key stakeholders in this process, and also desirable and feasible coordinators for stakeholder coordination. Conclusion: Health information prioritization methods and procedures reflect the heterogeneity of national public health systems in European countries. Mapping, sharing and ranking prioritization methods and procedures for “good practices” provides a meaningful basis for expert knowledge exchange on HI development. We recommend to make this process part of a future sustainable EU health information system and to use the information gathered in this project to initiate the development of a guidance “Good Practice HI Prioritization” among EU Member States and associated countries.</abstract><type>Journal Article</type><journal>Archives of Public Health</journal><volume>80</volume><journalNumber>1</journalNumber><paginationStart>25</paginationStart><paginationEnd/><publisher>Springer Science and Business Media LLC</publisher><placeOfPublication/><isbnPrint/><isbnElectronic/><issnPrint/><issnElectronic>2049-3258</issnElectronic><keywords>Health information; Health information inequalities; Health information systems; Strategy; Prioritization; Delphi</keywords><publishedDay>11</publishedDay><publishedMonth>1</publishedMonth><publishedYear>2022</publishedYear><publishedDate>2022-01-11</publishedDate><doi>10.1186/s13690-021-00760-8</doi><url/><notes/><college>COLLEGE NANME</college><CollegeCode>COLLEGE CODE</CollegeCode><institution>Swansea University</institution><apcterm/><funders>This publication was funded by the European Union’s Health Programme (2014–2020).</funders><lastEdited>2022-01-12T15:28:58.3138218</lastEdited><Created>2022-01-12T15:22:41.6405125</Created><path><level id="1">Faculty of Medicine, Health and Life Sciences</level><level id="2">Swansea University Medical School - Medicine</level></path><authors><author><firstname>Angela</firstname><surname>Fehr</surname><order>1</order></author><author><firstname>Stefanie</firstname><surname>Seeling</surname><order>2</order></author><author><firstname>Anselm</firstname><surname>Hornbacher</surname><order>3</order></author><author><firstname>Martin</firstname><surname>Thißen</surname><order>4</order></author><author><firstname>Petronille</firstname><surname>Bogaert</surname><order>5</order></author><author><firstname>Marie</firstname><surname>Delnord</surname><order>6</order></author><author><firstname>Ronan</firstname><surname>Lyons</surname><order>7</order></author><author><firstname>Mariken J.</firstname><surname>Tijhuis</surname><order>8</order></author><author><firstname>Peter</firstname><surname>Achterberg</surname><order>9</order></author><author><firstname>Thomas</firstname><surname>Ziese</surname><order>10</order></author></authors><documents><document><filename>59164__22131__0cd7ab9ded084af9a86f47e6a20179ec.pdf</filename><originalFilename>59164.pdf</originalFilename><uploaded>2022-01-12T15:25:30.5187279</uploaded><type>Output</type><contentLength>2353076</contentLength><contentType>application/pdf</contentType><version>Version of Record</version><cronfaStatus>true</cronfaStatus><documentNotes>© The Author(s). 2022 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License</documentNotes><copyrightCorrect>true</copyrightCorrect><language>eng</language><licence>http://creativecommons.org/licenses/by/4.0/</licence></document></documents><OutputDurs/></rfc1807> |
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2022-01-12T15:28:58.3138218 v2 59164 2022-01-12 Prioritizing health information for national health reporting - a Delphi study of the Joint Action on Health Information (InfAct) 83efcf2a9dfcf8b55586999d3d152ac6 Ronan Lyons Ronan Lyons true false 2022-01-12 Background: Health information (HI) strategies exist in several EU Member States, however, they mainly focus on technical issues and improving governance rather than on content-related priority setting. There is also little research available about national prioritization processes underlying HI development for policy support in the EU. The aim of this study was to broaden the knowledge base on HI prioritization strategies and to encourage expert exchange towards good practice models. A specific focus was put on HI produced for national health reporting, this being a crucial tool for policy advice. Methods: We conducted a literature search to identify published and grey literature on national HI prioritization. This was followed by a two-round Policy Delphi study, where we explored which processes and methods exist in EU Member States and associated countries for the prioritization of HI collection. In the first round, information about these processes was gathered in semi-structured questions; in the second round, participants were asked to rank the identified approaches for desirability and feasibility. The survey was conducted online; participants were recruited from the membership of the Joint Action on Health Information (InfAct – Information for Action). Results: 119 experts were contacted, representing 40 InfAct partner institutions in 28 EU Member States and associated countries. Of these, 28 experts responded fully or partially to the first round, and six to the second round. In the first round, more than half of the respondents reported the existence of structured HI prioritization processes in their countries. To prioritize HI, a clear preference was given in the second round for a formal, horizontal process which includes different experts and stakeholders. National public health institutes were named desirable key stakeholders in this process, and also desirable and feasible coordinators for stakeholder coordination. Conclusion: Health information prioritization methods and procedures reflect the heterogeneity of national public health systems in European countries. Mapping, sharing and ranking prioritization methods and procedures for “good practices” provides a meaningful basis for expert knowledge exchange on HI development. We recommend to make this process part of a future sustainable EU health information system and to use the information gathered in this project to initiate the development of a guidance “Good Practice HI Prioritization” among EU Member States and associated countries. Journal Article Archives of Public Health 80 1 25 Springer Science and Business Media LLC 2049-3258 Health information; Health information inequalities; Health information systems; Strategy; Prioritization; Delphi 11 1 2022 2022-01-11 10.1186/s13690-021-00760-8 COLLEGE NANME COLLEGE CODE Swansea University This publication was funded by the European Union’s Health Programme (2014–2020). 2022-01-12T15:28:58.3138218 2022-01-12T15:22:41.6405125 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Angela Fehr 1 Stefanie Seeling 2 Anselm Hornbacher 3 Martin Thißen 4 Petronille Bogaert 5 Marie Delnord 6 Ronan Lyons 7 Mariken J. Tijhuis 8 Peter Achterberg 9 Thomas Ziese 10 59164__22131__0cd7ab9ded084af9a86f47e6a20179ec.pdf 59164.pdf 2022-01-12T15:25:30.5187279 Output 2353076 application/pdf Version of Record true © The Author(s). 2022 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License true eng http://creativecommons.org/licenses/by/4.0/ |
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Prioritizing health information for national health reporting - a Delphi study of the Joint Action on Health Information (InfAct) |
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Prioritizing health information for national health reporting - a Delphi study of the Joint Action on Health Information (InfAct) Ronan Lyons |
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Prioritizing health information for national health reporting - a Delphi study of the Joint Action on Health Information (InfAct) |
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Prioritizing health information for national health reporting - a Delphi study of the Joint Action on Health Information (InfAct) |
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Prioritizing health information for national health reporting - a Delphi study of the Joint Action on Health Information (InfAct) |
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Prioritizing health information for national health reporting - a Delphi study of the Joint Action on Health Information (InfAct) |
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Prioritizing health information for national health reporting - a Delphi study of the Joint Action on Health Information (InfAct) |
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83efcf2a9dfcf8b55586999d3d152ac6_***_Ronan Lyons |
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Ronan Lyons |
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Angela Fehr Stefanie Seeling Anselm Hornbacher Martin Thißen Petronille Bogaert Marie Delnord Ronan Lyons Mariken J. Tijhuis Peter Achterberg Thomas Ziese |
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Background: Health information (HI) strategies exist in several EU Member States, however, they mainly focus on technical issues and improving governance rather than on content-related priority setting. There is also little research available about national prioritization processes underlying HI development for policy support in the EU. The aim of this study was to broaden the knowledge base on HI prioritization strategies and to encourage expert exchange towards good practice models. A specific focus was put on HI produced for national health reporting, this being a crucial tool for policy advice. Methods: We conducted a literature search to identify published and grey literature on national HI prioritization. This was followed by a two-round Policy Delphi study, where we explored which processes and methods exist in EU Member States and associated countries for the prioritization of HI collection. In the first round, information about these processes was gathered in semi-structured questions; in the second round, participants were asked to rank the identified approaches for desirability and feasibility. The survey was conducted online; participants were recruited from the membership of the Joint Action on Health Information (InfAct – Information for Action). Results: 119 experts were contacted, representing 40 InfAct partner institutions in 28 EU Member States and associated countries. Of these, 28 experts responded fully or partially to the first round, and six to the second round. In the first round, more than half of the respondents reported the existence of structured HI prioritization processes in their countries. To prioritize HI, a clear preference was given in the second round for a formal, horizontal process which includes different experts and stakeholders. National public health institutes were named desirable key stakeholders in this process, and also desirable and feasible coordinators for stakeholder coordination. Conclusion: Health information prioritization methods and procedures reflect the heterogeneity of national public health systems in European countries. Mapping, sharing and ranking prioritization methods and procedures for “good practices” provides a meaningful basis for expert knowledge exchange on HI development. We recommend to make this process part of a future sustainable EU health information system and to use the information gathered in this project to initiate the development of a guidance “Good Practice HI Prioritization” among EU Member States and associated countries. |
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