Patterns of paediatric end-of-life care. a chart review across different care settings in Switzerland
Version
Published
Date Issued
2018
Author(s)
Zimmermann, Karin
Engberg, Sandra
Ramelet, Anne-Sylvie
von der Weid, Nicolas
Eskola, Katri
Bergsträsser, Eva
Ansari, Marc
Aebi, Christoph
Bär, Reta
Popovic, Maja Beck
Bernet, Vera
Brazzola, Pierluigi
Bucher, Hans Ulrich
Buder, Regula
Cagnazzo, Sandra
Dinten, Barbara
Dorsaz, Anouk
Elmer, Franz
Enriquez, Raquel
Fahrni-Nater, Patricia
Finkbeiner, Gabi
Frey, Bernhard
Frey, Urs
Greiner, Jeannette
Hassink, Ralph-Ingo
Keller, Simone
Kretschmar, Oliver
Kröll, Judith
Laubscher, Bernard
Leibundgut, Kurt
Malaer, Reta
Meyer, Andreas
Stüssi, Christoph
Nelle, Mathias
Neuhaus, Thomas
Niggli, Felix
Perrenoud, Geneviève
Pfammatter, Jean-Pierre
Plecko, Barbara
Rupf, Debora
Sennhauser, Felix
Stade, Caroline
Steinlin, Maja
Stoffel, Lilian
Vonarburg, Christian
von Vigier, Rodo
Wagner, Bendicht
Wieland, Judith
Wernz, Birgit
Type
Article
Language
English
Abstract
Background
Paediatric end-of-life care is challenging and requires a high level of professional expertise. It is important that healthcare teams have a thorough understanding of paediatric subspecialties and related knowledge of disease-specific aspects of paediatric end-of-life care. The aim of this study was to comprehensively describe, explore and compare current practices in paediatric end-of-life care in four distinct diagnostic groups across healthcare settings including all relevant levels of healthcare providers in Switzerland.
Methods
In this nationwide retrospective chart review study, data from paediatric patients who died in the years 2011 or 2012 due to a cardiac, neurological or oncological condition, or during the neonatal period were collected in 13 hospitals, two long-term institutions and 10 community-based healthcare service providers throughout Switzerland.
Results
Ninety-three (62%) of the 149 reviewed patients died in intensive care units, 78 (84%) of them following withdrawal of life-sustaining treatment. Reliance on invasive medical interventions was prevalent, and the use of medication was high, with a median count of 12 different drugs during the last week of life. Patients experienced an average number of 6.42 symptoms. The prevalence of various types of symptoms differed significantly among the four diagnostic groups. Overall, our study patients stayed in the hospital for a median of six days during their last four weeks of life. Seventy-two patients (48%) stayed at home for at least one day and only half of those received community-based healthcare.
Conclusions
The study provides a wide-ranging overview of current end-of-life care practices in a real-life setting of different healthcare providers. The inclusion of patients with all major diagnoses leading to disease- and prematurity-related childhood deaths, as well as comparisons across the diagnostic groups, provides additional insight and understanding for healthcare professionals. The provision of specialised palliative and end-of-life care services in Switzerland, including the capacity of community healthcare services, need to be expanded to meet the specific needs of seriously ill children and their families.
Paediatric end-of-life care is challenging and requires a high level of professional expertise. It is important that healthcare teams have a thorough understanding of paediatric subspecialties and related knowledge of disease-specific aspects of paediatric end-of-life care. The aim of this study was to comprehensively describe, explore and compare current practices in paediatric end-of-life care in four distinct diagnostic groups across healthcare settings including all relevant levels of healthcare providers in Switzerland.
Methods
In this nationwide retrospective chart review study, data from paediatric patients who died in the years 2011 or 2012 due to a cardiac, neurological or oncological condition, or during the neonatal period were collected in 13 hospitals, two long-term institutions and 10 community-based healthcare service providers throughout Switzerland.
Results
Ninety-three (62%) of the 149 reviewed patients died in intensive care units, 78 (84%) of them following withdrawal of life-sustaining treatment. Reliance on invasive medical interventions was prevalent, and the use of medication was high, with a median count of 12 different drugs during the last week of life. Patients experienced an average number of 6.42 symptoms. The prevalence of various types of symptoms differed significantly among the four diagnostic groups. Overall, our study patients stayed in the hospital for a median of six days during their last four weeks of life. Seventy-two patients (48%) stayed at home for at least one day and only half of those received community-based healthcare.
Conclusions
The study provides a wide-ranging overview of current end-of-life care practices in a real-life setting of different healthcare providers. The inclusion of patients with all major diagnoses leading to disease- and prematurity-related childhood deaths, as well as comparisons across the diagnostic groups, provides additional insight and understanding for healthcare professionals. The provision of specialised palliative and end-of-life care services in Switzerland, including the capacity of community healthcare services, need to be expanded to meet the specific needs of seriously ill children and their families.
Publisher DOI
Journal or Serie
BMC Pediatrics
ISSN
1471-2431
Organization
Volume
18
Issue
1
Publisher
BioMed Central
Submitter
ServiceAccount
Citation apa
Zimmermann, K., Cignacco Müller, E., Engberg, S., Ramelet, A.-S., von der Weid, N., Eskola, K., Bergsträsser, E., Ansari, M., Aebi, C., Bär, R., Popovic, M. B., Bernet, V., Brazzola, P., Bucher, H. U., Buder, R., Cagnazzo, S., Dinten, B., Dorsaz, A., Elmer, F., … Wernz, B. (2018). Patterns of paediatric end-of-life care. a chart review across different care settings in Switzerland. In BMC Pediatrics (Vol. 18, Issue 1). BioMed Central. https://doi.org/10.24451/arbor.6692
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