Nationwide monitoring of end-of-life care via the Sentinel Network of General Practitioners in Belgium: the research protocol of the SENTI-MELC study
Open Access
- 8 October 2007
- journal article
- Published by Springer Nature in BMC Palliative Care
- Vol. 6 (1) , 6
Abstract
Background: End-of-life care has become an issue of great clinical and public health concern. From analyses of official death certificates, we have societal knowledge on how many people die, at what age, where and from what causes. However, we know little about how people are dying. There is a lack of population-based and nationwide data that evaluate and monitor the circumstances of death and the care received in the final months of life. The present study was designed to describe the places of end-of-life care and care transitions, the caregivers involved in patient care and the actual treatments and care provided to dying patients in Belgium. The patient, residence and healthcare characteristics associated with these aspects of end-of-life care provision will also be studied. In this report, the protocol of the study is outlined. Methods/Design: We designed a nationwide mortality follow-back study with data collection in 2005 and 2006, via the nationwide Belgian Sentinel Network of General Practitioners (GPs) i.e. an existing epidemiological surveillance system representative of all GPs in Belgium, covering 1.75% of the total Belgian population. All GPs were asked to report weekly, on a standardized registration form, every patient (>1 year) in their practice who had died, and to identify patients who had died "non-suddenly." The last three months of these patients' lives were surveyed retrospectively. Several quality control measures were used to ensure data of high scientific quality. Discussion: In 2005 and 2006, respectively 1385 and 1305 deaths were identified of which 66% and 63% died non-suddenly. The first results are expected in 2007. Via this study, we will build a descriptive epidemiological database on end-of-life care provision in Belgium, which might serve as baseline measurement to monitor end-of-life care over time. The study will inform medical practice as well as healthcare authorities in setting up an end-of-life care policy. We publish the protocol here to inform others, in particular countries with analogue GP surveillance networks, on the possibilities of performing end-of-life care research. A preliminary analysis of the possible strengths, weaknesses and opportunities of our research is outlined.Keywords
This publication has 49 references indexed in Scilit:
- Hospitalisations at the end of life: using a sentinel surveillance network to study hospital use and associated patient, disease and healthcare factorsBMC Health Services Research, 2007
- Dying at home or in an institutionHealth Policy, 2006
- Measuring End-of-Life Care Outcomes RetrospectivelyJournal of Palliative Medicine, 2005
- Introduction: Papers from the National Institutes of Health State-of-the-Science Conference on Improving End-of-Life CareJournal of Palliative Medicine, 2005
- Resurrecting Treatment Histories of Dead PatientsJAMA, 2004
- Family Perspectives on End-of-Life Care at the Last Place of CareJAMA, 2004
- End-of-life decision-making in six European countries: descriptive studyThe Lancet, 2003
- Which terminally ill cancer patients in the United Kingdom receive care from community specialist palliative care nurses?Journal of Advanced Nursing, 2000
- Which terminally ill cancer patients in the United Kingdom receive care from community specialist palliative care nurses?Journal of Advanced Nursing, 2000
- Assistance from Family Members, Friends, Paid Care Givers, and Volunteers in the Care of Terminally Ill PatientsNew England Journal of Medicine, 1999