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Place of death of children with complex chronic conditions: cross-national study of 11 countries.

Artikel i vetenskaplig tidskrift
Författare Cecilia Håkanson
Joakim Öhlén
Ulrika Kreicbergs
Marylou Cardenas-Turanzas
Donna M Wilson
Martin Loucka
Sandra Frache
Lucia Giovannetti
Wayne Naylor
YongJoo Rhee
Miguel Ruiz Ramos
Joan Teno
Kim Beernaert
Luc Deliens
Dirk Houttekier
Joachim Cohen
Publicerad i European Journal of Pediatrics
Volym 176
Nummer/häfte 3
Sidor 327-335
ISSN 1432-1076
Publiceringsår 2017
Publicerad vid Centrum för personcentrerad vård vid Göteborgs universitet (GPCC)
Institutionen för vårdvetenskap och hälsa
Sidor 327-335
Språk en
Länkar dx.doi.org/10.1007/s00431-016-2837-...
www.ncbi.nlm.nih.gov/entrez/query.f...
Ämneskategorier Omvårdnad, Palliativ medicin

Sammanfattning

Cross-national understanding of place of death is crucial for health service systems for their provision of efficient and equal access to paediatric palliative care. The objectives of this population-level study were to examine where children with complex chronic conditions (CCC) die and to investigate associations between places of death and sex, cause of death and country. The study used death certificate data of all deceased 1- to 17-year-old children (n = 40,624) who died in 2008, in 11 European and non-European countries. Multivariable logistic regression was performed to determine associations between place of death and other factors. Between 24.4 and 75.3% of all children 1-17 years in the countries died of CCC. Of these, between 6.7 and 42.4% died at home. In Belgium and the USA, all deaths caused by CCC other than malignancies were less likely to occur at home, whereas in Mexico and South Korea, deaths caused by neuromuscular diseases were more likely to occur at home than malignancies. In Mexico (OR = 0.91, 95% CI: 0.83-1.00) and Sweden (OR = 0.35, 95% CI: 0.15-0.83), girls had a significantly lower chance of dying at home than boys.This study shows large cross-national variations in place of death. These variations may relate to health system-related infrastructures and policies, and differences in cultural values related to place of death, although this needs further investigation. The patterns found in this study can inform the development of paediatric palliative care programs internationally. What is known: • There is a scarcity of population-level studies investigating where children with CCC die in different countries. • Cross-national understanding of place of death provides information to health care systems for providing efficient and equal access to paediatric palliative care. What is new : • There are large cross-national variations in the place of death of children with CCC, with few deathsoccuring at home in some countries whereas hospital deaths are generally most common. • In general, deaths caused by neuromuscular diseases and malignancies occur at home more often thanother CCC.

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