Lieve Van den Block1, Tinne Smets2, Nanja van Dop2, Eddy Adang3, Paula Andreasen4, Danni Collingridge Moore5, Yvonne Engels6, Harriet Finne-Soveri4, Katherine Froggatt5, Giovanni Gambassi7, Violetta Kijowska8, Bregje Onwuteaka-Philipsen9, H Roeline Pasman9, Sheila Payne5, Ruth Piers10, Katarzyna Szczerbińska8, Maud Ten Koppel9, Nele Van Den Noortgate10, Jenny T van der Steen9, Myrra Vernooij-Dassen11, Luc Deliens12. 1. Department of Family Medicine and Chronic Care, End-of-Life Care Research Group, Vrije Universiteit Brussel (VUB) and Ghent University, Brussels, Belgium. Electronic address: lvdblock@vub.ac.be. 2. Department of Family Medicine and Chronic Care, End-of-Life Care Research Group, Vrije Universiteit Brussel (VUB) and Ghent University, Brussels, Belgium. 3. Department of Health Evidence, Radboud University Medical Center, Nijmegen, the Netherlands. 4. National Institute for Health and Welfare, Helsinki, Finland. 5. International Observatory on End-of-Life Care, Lancaster University, Lancaster, United Kingdom. 6. Department of Anesthesiology, Pain, and Palliative Medicine, Radboud University Medical Center, Nijmegen, the Netherlands. 7. Università Cattolica del Sacro Cuoro, Rome, Italy. 8. Unit for Research on Aging Society, Department of Sociology of Medicine, Epidemiology and Preventive Medicine Chair, Faculty of Medicine, Jagiellonian University Medical College, Krakow, Poland. 9. EMGO Institute for Health and Care research, Expertise Center for Palliative Care, VU University Medical Center, Amsterdam, the Netherlands. 10. Department of Family Medicine and Chronic Care, End-of-Life Care Research Group, Vrije Universiteit Brussel (VUB) and Ghent University, Brussels, Belgium; Department of Geriatric Medicine, Ghent University Hospital, Ghent, Belgium. 11. Radboud University Medical Center, IQ healthcare, Nijmegen, the Netherlands. 12. Department of Family Medicine and Chronic Care, End-of-Life Care Research Group, Vrije Universiteit Brussel (VUB) and Ghent University, Brussels, Belgium; Department of Medical Oncology, Ghent University Hospital, Ghent, Belgium.
Abstract
OBJECTIVES: Although a growing number of older people are dying in care homes, palliative care has developed in these settings only recently. Cross-country representative comparative research hardly exists in this area. As part of a large EU-funded project, we aim to undertake representative comparative research in care homes in Europe, to describe and compare 6 countries in terms of (1) resident outcomes, quality and costs of palliative and end-of-life care; and (2) palliative care structures and staff knowledge and attitudes toward palliative care. We also aim to explore country, facility, staff, patient, and care characteristics related to better outcomes at resident level. DESIGN AND METHODS: To obtain a representative nationwide sample, we will conduct a large-scale cross-sectional study of deceased residents in care homes in Belgium, Finland, Italy, the Netherlands, Poland, and the United Kingdom, using proportional stratified random sampling (taking into account region, facility type and bed capacity). In each country, all participating care homes retrospectively report all deaths of residents in and outside the facilities over the previous 3-month period. For each case, structured questionnaires, including validated instruments, are sent to (1) the administrator/manager, (2) staff member most involved in care, (3) treating physician (general practitioner or elderly care physician), and (4) a closely involved relative. It is estimated that, per country, 50 care homes are needed on average to obtain a minimum of 200 deceased residents. Collected data include clinical and sociodemographic characteristics, quality of dying, quality and costs of palliative care and end-of-life care, and palliative care structures at the facility level and country level. To obtain a representative view of staff knowledge and attitudes regarding palliative care, PACE will conduct a cross-sectional study of staff working in the participating care homes. CONCLUSION: Considering the growing challenges associated with aging in all European countries, there is an urgent need to build a robust international comparative evidence base that can inform the development of policies to target improved palliative care in care homes. By describing this research protocol, we hope to inform international research in care homes on how to perform representative end-of-life care research in these settings and better understand which systems are associated with better outcomes.
OBJECTIVES: Although a growing number of older people are dying in care homes, palliative care has developed in these settings only recently. Cross-country representative comparative research hardly exists in this area. As part of a large EU-funded project, we aim to undertake representative comparative research in care homes in Europe, to describe and compare 6 countries in terms of (1) resident outcomes, quality and costs of palliative and end-of-life care; and (2) palliative care structures and staff knowledge and attitudes toward palliative care. We also aim to explore country, facility, staff, patient, and care characteristics related to better outcomes at resident level. DESIGN AND METHODS: To obtain a representative nationwide sample, we will conduct a large-scale cross-sectional study of deceased residents in care homes in Belgium, Finland, Italy, the Netherlands, Poland, and the United Kingdom, using proportional stratified random sampling (taking into account region, facility type and bed capacity). In each country, all participating care homes retrospectively report all deaths of residents in and outside the facilities over the previous 3-month period. For each case, structured questionnaires, including validated instruments, are sent to (1) the administrator/manager, (2) staff member most involved in care, (3) treating physician (general practitioner or elderly care physician), and (4) a closely involved relative. It is estimated that, per country, 50 care homes are needed on average to obtain a minimum of 200 deceased residents. Collected data include clinical and sociodemographic characteristics, quality of dying, quality and costs of palliative care and end-of-life care, and palliative care structures at the facility level and country level. To obtain a representative view of staff knowledge and attitudes regarding palliative care, PACE will conduct a cross-sectional study of staff working in the participating care homes. CONCLUSION: Considering the growing challenges associated with aging in all European countries, there is an urgent need to build a robust international comparative evidence base that can inform the development of policies to target improved palliative care in care homes. By describing this research protocol, we hope to inform international research in care homes on how to perform representative end-of-life care research in these settings and better understand which systems are associated with better outcomes.
Authors: Lara Pivodic; Tinne Smets; Nele Van den Noortgate; Bregje D Onwuteaka-Philipsen; Yvonne Engels; Katarzyna Szczerbińska; Harriet Finne-Soveri; Katherine Froggatt; Giovanni Gambassi; Luc Deliens; Lieve Van den Block Journal: Palliat Med Date: 2018-10-01 Impact factor: 4.762
Authors: Katherine Froggatt; Sheila Payne; Hazel Morbey; Michaela Edwards; Harriet Finne-Soveri; Giovanni Gambassi; H Roeline Pasman; Katarzyna Szczerbińska; Lieve Van den Block Journal: J Am Med Dir Assoc Date: 2017-04-12 Impact factor: 4.669
Authors: J Gilissen; L Pivodic; C Gastmans; R Vander Stichele; L Deliens; E Breuer; L Van den Block Journal: BMC Geriatr Date: 2018-02-14 Impact factor: 3.921
Authors: Danni Collingridge Moore; Sheila Payne; Thomas Keegan; Luc Deliens; Tinne Smets; Giovanni Gambassi; Marika Kylänen; Violetta Kijowska; Bregje Onwuteaka-Philipsen; Lieve Van den Block Journal: Int J Environ Res Public Health Date: 2020-04-16 Impact factor: 3.390
Authors: Tinne Smets; Lara Pivodic; Ruth Piers; H Roeline W Pasman; Yvonne Engels; Katarzyna Szczerbińska; Marika Kylänen; Giovanni Gambassi; Sheila Payne; Luc Deliens; Lieve Van den Block Journal: Palliat Med Date: 2018-07-04 Impact factor: 4.762
Authors: M Ten Koppel; H R W Pasman; J T van der Steen; H P J van Hout; M Kylänen; L Van den Block; T Smets; L Deliens; G Gambassi; K Froggatt; K Szczerbińska; B D Onwuteaka-Philipsen Journal: BMC Palliat Care Date: 2019-08-29 Impact factor: 3.234
Authors: Danni Collingridge Moore; Sheila Payne; Lieve Van den Block; Maud Ten Koppel; Katarzyna Szczerbińska; Katherine Froggatt Journal: BMC Res Notes Date: 2019-08-14
Authors: Anne B Wichmann; Eddy M M Adang; Kris C P Vissers; Katarzyna Szczerbińska; Marika Kylänen; Sheila Payne; Giovanni Gambassi; Bregje D Onwuteaka-Philipsen; Tinne Smets; Lieve Van den Block; Luc Deliens; Myrra J F J Vernooij-Dassen; Yvonne Engels Journal: PLoS One Date: 2018-09-25 Impact factor: 3.240
Authors: Marc Tanghe; Nele Van Den Noortgate; Lara Pivodic; Luc Deliens; Bregje Onwuteaka-Philipsen; Katarzyna Szczerbinska; Harriet Finne-Soveri; Danni Collingridge-Moore; Giovanni Gambassi; Lieve Van den Block; Ruth Piers Journal: Eur J Public Health Date: 2019-02-01 Impact factor: 3.367