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Patterns of paediatric end-of-life care: a chart review across different care settings in Switzerland
Karin Zimmermann1,2,3, Eva Cignacco4,5, Sandra Engberg6
1Department Public Health (DPH), Nursing Science, University of Basel, Bernoullistrasse 28, 4056, Basel, Switzerland. karin.zimmermann@unibas.ch.
Insights
Paediatric end-of-life care in Switzerland involves intensive interventions and high medication use, with symptom burden varying by diagnosis. Community care access was limited for children who died at home.
Area of Science:
- Medical Research
- Palliative Care
- Pediatrics
Background:
- Paediatric end-of-life care demands specialized knowledge of subspecialties and disease-specific aspects.
- Effective care requires a thorough understanding by healthcare teams.
Purpose of the Study:
- To comprehensively describe, explore, and compare current paediatric end-of-life care practices.
- To analyze practices across four distinct diagnostic groups and various healthcare settings in Switzerland.
Main Methods:
- Nationwide retrospective chart review of paediatric patients who died in 2011-2012.
- Data collected from 13 hospitals, 2 long-term institutions, and 10 community providers across Switzerland.
- Included patients with cardiac, neurological, oncological conditions, or neonatal deaths.
Main Results:
- Most deaths (62%) occurred in intensive care units, often after life-sustaining treatment withdrawal (84%).
- High reliance on invasive interventions and medication (median 12 drugs in last week).
- Patients experienced an average of 6.42 symptoms, varying by diagnostic group; limited community healthcare utilization.
Conclusions:
- The study offers a broad overview of real-world paediatric end-of-life care practices in Switzerland.
- Findings highlight the need to expand specialized palliative and end-of-life care services, including community-based support.
- Addressing the specific needs of seriously ill children and their families requires enhanced service provision.
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.
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