| Autor: |
János Sándor, Elisabeth Dupont, Inbar Zucker, Simon de Lusignan, Tamara Poljičanin, Massimo Massi Benedetti, Soffia Gudbjörnsdottir, Christa Scheidt-Nave, Christin Heidemann, Ilmo Keskimäki, Iztok Štotl, Vasos Scoutellas, Fabrizio Carinci, Stella de Sabata, Kris Doggen, Róza Ádány, Simion Pruna, George Olympios, Joanna Polanska, Martti Arffman, Niek S. Klazinga, Paolo Di Bartolo, Ivan Pristaš, Joseph G. Azzopardi, Vivie Traynor, Concetta Tania Di Iorio, Jana Lepiksone, Marcello Monesi, Peter Rossing, Anita Maurina, Scott Cunningham, Przemka Jarosz-Chobot, Karianne Fjeld Løvaas |
| Rok vydání: |
2021 |
| Předmět: |
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| Zdroj: |
Frontiers in Clinical Diabetes and Healthcare. 2 |
| ISSN: |
2673-6616 |
| Popis: |
BackgroundRegistries and data sources contain information that can be used on an ongoing basis to improve quality of care and outcomes of people with diabetes. As a specific task of the EU Bridge Health project, we carried out a survey of diabetes-related data sources in Europe.ObjectivesWe aimed to report on the organization of different sources of diabetes information, including their governance, information infrastructure and dissemination strategies for quality control, service planning, public health, policy and research.MethodsSurvey using a structured questionnaire to collect targeted data from a network of collaborating institutions managing registries and data sources in 17 countries in the year 2017.ResultsThe 18 data sources participating in the study were most frequently academic centres (44.4%), national (72.2%), targeting all types of diabetes (61.1%) covering no more than 10% of the target population (44.4%). Although population-based in over a quarter of cases (27.8%), sources relied predominantly on provider-based datasets (38.5%), fewer using administrative data (16.6%). Data collection was continuous in the majority of cases (61.1%), but 50% could not perform data linkage. Public reports were more frequent (72.2%) as well as quality reports (77.8%), but one third did not provide feedback to policy and only half published ten or more peer reviewed papers during the last 5 years.ConclusionsThe heterogeneous implementation of diabetes registries and data sources hampers the comparability of quality and outcomes across Europe. Best practices exist but need to be shared more effectively to accelerate progress and deliver equitable results for people with diabetes. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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