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Using death certificate data to study place of death in 9 European countries: opportunities and weaknesses
- Source :
- BMC Public Health, Vol 7, Iss 1, p 283 (2007), BMC Public Health, BMC PUBLIC HEALTH
- Publication Year :
- 2007
- Publisher :
- Springer Science and Business Media LLC, 2007.
-
Abstract
- Background: Systematic and reliable epidemiological information at population level, preferably cross-national, is needed for an adequate planning of (end-of-life) health care policies, e.g. concerning place of death, but is currently lacking. This study illustrates opportunities and weaknesses of death certificate data to provide such information on place of death and associated factors in nine European countries (seven entire countries and five regions). Methods: We investigated the possibility and modality of all partners in this international comparative study (BE, DK, IT, NL, NO, SE, UK) to negotiate a dataset containing all deaths of one year with their national/regional administration of mortality statistics, and analysed the availability of information about place of death as well as a number of clinical, socio-demographic, residential and healthcare system factors. Results: All countries negotiated a dataset, but rules, procedures, and cost price to get the data varied strongly between countries. In total, about 1.1 million deaths were included. For four of the nine countries not all desired categories for place of death were available. Most desired clinical and socio-demographic information was available, be it sometimes via linkages with other population databases. Healthcare system factors could be made available by linking existing healthcare statistics to the residence of the deceased. Conclusion: Death certificate data provide information on place of death and on possibly associated factors and confounders in all studied countries. Hence, death certificate data provide a unique opportunity for cross-national studying and monitoring of place of death. However, modifications of certain aspects of death certificate registration and rules of data-protection are perhaps required to make international monitoring of place of death more feasible and accurate. © 2007 Cohen et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
- Subjects :
- Male
Palliative care
LIFE CARE
Databases, Factual
PEOPLE DIE
PALLIATIVE CARE
Cost of Illness
Risk Factors
Health care
Medicine and Health Sciences
Medicine
Child
HOSPITAL DEATH
Terminal Care
education.field_of_study
Health Policy
lcsh:Public aspects of medicine
Middle Aged
ILL CANCER-PATIENTS
Europe
Child, Preschool
END
Female
HEALTH
Quality-Adjusted Life Years
PREDICTING PLACE
Research Article
Adult
Cross-Cultural Comparison
Adolescent
PATIENTS DIE
Population
Death Certificates
HOME-CARE
Place of death
Environmental health
Humans
Mortality
education
Health policy
Aged
Public Health Informatics
Actuarial science
business.industry
Infant, Newborn
Public Health, Environmental and Occupational Health
Infant
lcsh:RA1-1270
Public health informatics
Residence
Death certificate
Biostatistics
business
Subjects
Details
- ISSN :
- 14712458
- Volume :
- 7
- Database :
- OpenAIRE
- Journal :
- BMC Public Health
- Accession number :
- edsair.doi.dedup.....1ffdafd77bcc4e8f026a64214cebbde5
- Full Text :
- https://doi.org/10.1186/1471-2458-7-283