Conducting national burden of disease studies in small countries in Europe- a feasible challenge?

Burden of disease Cyprus DALY European Burden of Disease Network Iceland Luxembourg Malta Montenegro Morbidity Mortality YLD YLL

Journal

Archives of public health = Archives belges de sante publique
ISSN: 0778-7367
Titre abrégé: Arch Public Health
Pays: England
ID NLM: 9208826

Informations de publication

Date de publication:
11 May 2021
Historique:
received: 21 04 2020
accepted: 03 05 2021
entrez: 11 5 2021
pubmed: 12 5 2021
medline: 12 5 2021
Statut: epublish

Résumé

Burden of Disease (BoD) studies use disability-adjusted life years (DALYs) as a population health metric to quantify the years of life lost due to morbidity and premature mortality for diseases, injuries and risk factors occurring in a region or a country. Small countries usually face a number of challenges to conduct epidemiological studies, such as national BoD studies, due to the lack of specific expertise and resources or absence of adequate data. Considering Europe's small countries of Cyprus, Iceland, Luxembourg, Malta and Montenegro, the aim was to assess whether the various national data sources identified are appropriate to perform national BoD studies. The five small countries have a well-established mortality registers following the ICD10 classification, which makes calculation of years of life lost (YLL) feasible. A number of health information data sources were identified in each country, which can provide prevalence data for the calculation of years lived with disability (YLD) for various conditions. These sources include disease-specific registers, hospital discharge data, primary health care data and epidemiological studies, provided by different organisations such as health directorates, institutes of public health, statistical offices and other bodies. Hence, DALYs can be estimated at a national level through the combination of the YLL and YLD information. On the other hand, small countries face unique challenges such as difficulty to ensure sample representativeness, variations in prevalence estimates especially for rarer diseases, existence of a substantial proportion of non-residents affiliated to healthcare systems and potential exclusion from some European or international initiatives. Recently established BoD networks may provide a platform for small countries to share experiences, expertise, and engage with countries and institutions that have long-standing experience with BoD assessment. Apart from mortality registries, adequate health data sources, notably for cancer, are potentially available at the small states to perform national BoD studies. Investing in sharing expert knowledge through engagement of researchers in BoD networks can enable the conduct of country specific BoD studies and the establishment of more accurate DALYs estimates. Such estimates can enable local policymakers to reflect on the relative burden of the different conditions that are contributing to morbidity and mortality at a country level.

Sections du résumé

BACKGROUND BACKGROUND
Burden of Disease (BoD) studies use disability-adjusted life years (DALYs) as a population health metric to quantify the years of life lost due to morbidity and premature mortality for diseases, injuries and risk factors occurring in a region or a country. Small countries usually face a number of challenges to conduct epidemiological studies, such as national BoD studies, due to the lack of specific expertise and resources or absence of adequate data. Considering Europe's small countries of Cyprus, Iceland, Luxembourg, Malta and Montenegro, the aim was to assess whether the various national data sources identified are appropriate to perform national BoD studies.
MAIN BODY METHODS
The five small countries have a well-established mortality registers following the ICD10 classification, which makes calculation of years of life lost (YLL) feasible. A number of health information data sources were identified in each country, which can provide prevalence data for the calculation of years lived with disability (YLD) for various conditions. These sources include disease-specific registers, hospital discharge data, primary health care data and epidemiological studies, provided by different organisations such as health directorates, institutes of public health, statistical offices and other bodies. Hence, DALYs can be estimated at a national level through the combination of the YLL and YLD information. On the other hand, small countries face unique challenges such as difficulty to ensure sample representativeness, variations in prevalence estimates especially for rarer diseases, existence of a substantial proportion of non-residents affiliated to healthcare systems and potential exclusion from some European or international initiatives. Recently established BoD networks may provide a platform for small countries to share experiences, expertise, and engage with countries and institutions that have long-standing experience with BoD assessment.
CONCLUSION CONCLUSIONS
Apart from mortality registries, adequate health data sources, notably for cancer, are potentially available at the small states to perform national BoD studies. Investing in sharing expert knowledge through engagement of researchers in BoD networks can enable the conduct of country specific BoD studies and the establishment of more accurate DALYs estimates. Such estimates can enable local policymakers to reflect on the relative burden of the different conditions that are contributing to morbidity and mortality at a country level.

Identifiants

pubmed: 33971960
doi: 10.1186/s13690-021-00599-z
pii: 10.1186/s13690-021-00599-z
pmc: PMC8112005
doi:

Types de publication

Letter

Langues

eng

Pagination

73

Références

Eur J Public Health. 2018 Aug 1;28(4):773-778
pubmed: 29697771
Arch Public Health. 2020 Jan 9;78:3
pubmed: 31921418
Lancet. 2015 Jan 10;385(9963):117-71
pubmed: 25530442
Eur J Public Health. 2020 Feb 1;30(1):2-3
pubmed: 31978226
BMC Health Serv Res. 2020 Apr 7;20(1):293
pubmed: 32264910
Lancet. 2013 Jul 6;382(9886):9-11
pubmed: 23684252
Lancet. 2020 Oct 17;396(10258):1204-1222
pubmed: 33069326
Biomed Res Int. 2018 Apr 23;2018:7236194
pubmed: 29850556

Auteurs

Sarah Cuschieri (S)

Department of Anatomy, Faculty of Medicine and Surgery, University of Malta, Msida, Malta. sarah.cuschieri@um.edu.mt.

Elena Pallari (E)

MRC Clinical Trials and Methodology Unit, University College London, 90 High Holborn, London, WC1V 6LJ, England.

Natasa Terzic (N)

Center for Health System Development, Institute of Public Health of Montenegro, Podgorica, Montenegro.

Ala'a Alkerwi (A)

Directorate of Health, Service Epidemiologiy and Statistics, Luxembourg, Luxembourg.

Rannveig Sigurvinsdottir (R)

Department of Psychology, Reykjavik University, Reykjavik, Iceland.

Inga Dora Sigfusdottir (ID)

Department of Psychology, Reykjavik University, Reykjavik, Iceland.
Teacher's College, Columbia University, New York, NY, USA.

Brecht Devleesschauwer (B)

Department of Epidemiology and Public Health, Sciensano, Brussels, Belgium.
Department of Veterinary Public Health and Food Safety, Ghent University, Merelbeke, Belgium.

Classifications MeSH