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Place of death of people living with Parkinson's disease: a population-level study in 11 countries

K. Moens, D. Houttekier, L. Van den Block, R. Harding, L. Morin, S. Marchetti, A. Csikos, M. Loucka, WA. Naylor, DM. Wilson, J. Teno, M. Cardenas-Turanzas, Y. Rhee, FJ. Garcia-Leon, L. Deliens, J. Cohen,

. 2015 ; 14 (-) : 28. [pub] 20150520

Jazyk angličtina Země Anglie, Velká Británie

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc16010173

BACKGROUND: Most people prefer to receive end-of-life care in familiar surroundings rather than in hospital. This study examines variation in place of death for people dying from Parkinson's disease (PD) across 11 European and non-European countries. METHODS: Using death certificate data of 2008 for Belgium, France, Italy, Hungary, Czech Republic, New Zealand, USA, Canada, Mexico, South Korea and Spain for all deaths with PD as an underlying cause (ICD-10 code: G20) cross-national differences in place of death were examined. Associations between place of death and patient socio-demographic and regional characteristics were evaluated using multivariable binary logistic regression analyses. RESULTS: The proportion of deaths in hospital ranged from 17% in the USA to 75% in South Korea. Hospital was the most prevalent place of death in France (40%), Hungary (60%) and South Korea; nursing home in New Zealand (71%), Belgium (52%), USA (50%), Canada (48%) and Czech Republic (44%); home in Mexico (73%), Italy (51%) and Spain (46%). The chances of dying in hospital were consistently higher for men (Belgium, France, Italy, USA, Canada), those younger than 80 years (Belgium, France, Italy, USA, Mexico), and those living in areas with a higher provision of hospital beds (Italy, USA). CONCLUSIONS: In several countries a substantial proportion of deaths from PD occurs in hospitals, although this may not be the most optimal place of terminal care and death. The wide variation between countries in the proportion of deaths from PD occurring in hospital indicates a potential for many countries to reduce these proportions.

Citace poskytuje Crossref.org

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$a BACKGROUND: Most people prefer to receive end-of-life care in familiar surroundings rather than in hospital. This study examines variation in place of death for people dying from Parkinson's disease (PD) across 11 European and non-European countries. METHODS: Using death certificate data of 2008 for Belgium, France, Italy, Hungary, Czech Republic, New Zealand, USA, Canada, Mexico, South Korea and Spain for all deaths with PD as an underlying cause (ICD-10 code: G20) cross-national differences in place of death were examined. Associations between place of death and patient socio-demographic and regional characteristics were evaluated using multivariable binary logistic regression analyses. RESULTS: The proportion of deaths in hospital ranged from 17% in the USA to 75% in South Korea. Hospital was the most prevalent place of death in France (40%), Hungary (60%) and South Korea; nursing home in New Zealand (71%), Belgium (52%), USA (50%), Canada (48%) and Czech Republic (44%); home in Mexico (73%), Italy (51%) and Spain (46%). The chances of dying in hospital were consistently higher for men (Belgium, France, Italy, USA, Canada), those younger than 80 years (Belgium, France, Italy, USA, Mexico), and those living in areas with a higher provision of hospital beds (Italy, USA). CONCLUSIONS: In several countries a substantial proportion of deaths from PD occurs in hospitals, although this may not be the most optimal place of terminal care and death. The wide variation between countries in the proportion of deaths from PD occurring in hospital indicates a potential for many countries to reduce these proportions.
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$a Houttekier, Dirk $u Vrije Universiteit Brussel (VUB) & Ghent University, End-of-Life Care Research Group, Brussels, Belgium. Dirk.Houttekier@vub.ac.be.
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$a Van den Block, Lieve $u Vrije Universiteit Brussel (VUB) & Ghent University, End-of-Life Care Research Group, Brussels, Belgium. lvdblock@vub.ac.be.
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$a Harding, Richard $u Department of Palliative Care, King's College London, Cicely Saunders Institute, Policy & Rehabilitation, Bessemer Road, Denmark Hill, London, SE5 9PJ, UK. Richard.Harding@kcl.ac.uk.
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$a Morin, Lucas $u French National Observatory on End-of-Life Care, Paris, France. lucas.morin.observatoire@gmail.com.
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$a Marchetti, Stefano $u Italian National Institute of Statistics, Rome, Italy. stmarche@istat.it.
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$a Csikos, Agnes $u University of Pécs Medical School, Pécs, Hungary. agnes.csikoska@gmail.com.
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$a Loucka, Martin $u Center for Palliative Care, Prague, Czech Republic. martin.loucka@gmail.com.
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$a Naylor, Wayne A $u Hospice Waikato, Hamilton, New Zealand. wayne.naylor@hospicewaikato.org.nz.
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$a Wilson, Donna M $u University of Alberta, Edmonton, Alberta, Canada. donna.wilson@ualberta.ca.
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$a Teno, Joan $u Brown University, Department of Community Health, Rhode Island, USA. joan_teno@brown.edu.
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$a Cardenas-Turanzas, Marylou $u The University of Texas, MD Anderson Cancer Center, Houston, TX, USA. mcardena@mdanderson.org.
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$a Rhee, YongJoo $u Dongduk Women's University, Seoul, Korea. yrh759@dongduk.ac.kr.
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$a Garcia-Leon, Francisco Javier $u Consejería de Igualdad, Salud y Bienestar Social. Agencia de Evaluación de Tecnologías Sanitarias de Andalucía (AETSA), Sevilla, Spain. fjavier.garcia.leon@juntadeandalucia.es.
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$a Deliens, Luc $u Vrije Universiteit Brussel (VUB) & Ghent University, End-of-Life Care Research Group, Brussels, Belgium. Luc.Deliens@vub.ac.be.
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$a Cohen, Joachim $u Vrije Universiteit Brussel (VUB) & Ghent University, End-of-Life Care Research Group, Brussels, Belgium. Joachim.Cohen@vub.ac.be.
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