Specialized pediatric palliative care services for children dying from cancer: A repeated cohort study on the developments of symptom management and quality of care over a 10-year period

Author:

Zernikow Boris12ORCID,Szybalski Katharina12,Hübner-Möhler Bettina12,Wager Julia12,Paulussen Michael3,Lassay Lisa4,Jorch Norbert5,Weber Carola6,Schneider Dominik T7,Janßen Gisela8,Oommen Prasad T8,Kuhlen Michaela8,Brune Thomas9,Wieland Regina10,Schündeln Michael10,Kremens Bernhard10,Längler Alfred11,Prokop Aram12,Kiener Rita13,Niehues Tim14,Rose Martina15,Baumann-Köhler Margit16,Pöppelmann Monika16,Thorer Heike16,Irnich Martin17,Sinha Kumar18,Wolfe Joanne19,Schmidt Pia12

Affiliation:

1. Paediatric Palliative Care Centre and German Paediatric Pain Centre, Children’s and Adolescents’ Hospital, Datteln, Germany

2. Department of Children’s Pain Therapy and Paediatric Palliative Care, School of Medicine, Faculty of Health, Witten/Herdecke University, Datteln, Germany

3. Children’s and Adolescents’ Hospital Datteln and Department of Pediatrics, School of Medicine, Faculty of Health, Witten/Herdecke University, Datteln, Germany

4. University Hospital Aachen, Division of Pediatric Hematology, Oncology and Stem Cell Transplantation, Department of Pediatrics, RWTH Aachen University, Aachen, Germany

5. Department of Pediatrics, Protestant Hospital Bielefeld, Bielefeld, Germany

6. Department of Pediatric Oncology, Hematology and Immunology, University Hospital Bonn, Bonn, Germany

7. Division of Pediatric Hematology and Oncology, Department of Pediatrics, Hospital Dortmund, Dortmund, Germany

8. Department of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, University Hospital Düsseldorf, Düsseldorf, Germany

9. Department of Pediatrics, Hospital Lippe-Detmold, Detmold, Germany

10. Hematology/Oncology, Pediatrics III, University Hospital Essen, Essen, Germany

11. Gemeinschaftskrankenhaus Herdecke and Integrative Pediatrics, School of Medicine, Faculty of Health, Witten/Herdecke University, Herdecke, Germany

12. Department of Pediatric Hematology/Oncology, Children’s Hospital Köln, Köln, Germany

13. Department of Paediatric Oncology and Hematology, Policlinic for Children and Adolescents, University Hospital Köln, Köln, Germany

14. Centre for Pediatrics and Adolescent Medicine, HELIOS Hospital Krefeld, Krefeld, Germany

15. Department for Children and Adolescents, Johannes Wesling Hospital Minden, Bochum University, Minden, Germany

16. Department of Paediatric Hematology and Oncology, Policlinic for Children and Adolescents, University Hospital Münster, Münster, Germany

17. Department of Paediatric Hematology and Oncology, Asklepios Hospital Sankt Augustin GmbH, Sankt Augustin, Germany

18. Department of Pediatrics, Helios Medical Centre, Witten-Herdecke University, Wuppertal, Germany

19. Department of Psychosocial Oncology and Palliative Care, Dana-Farber Cancer Institute, Boston Children’s Hospital, Harvard Medical School, Boston, MA, USA

Abstract

Background: About one quarter of children affected with cancer die. For children and their families, the end-of-life period is highly distressing. Aim: This study focused on how end-of-life care in pediatric cancer patients changed over a period of 10 years and if changes in pediatric palliative care structures were associated with quality of care. Design: Over a 10-year period, all pediatric oncology departments in one German federal state were invited to participate in a repeated cross-sectional cohort study at three time-points (2005, 2010, 2015). Departments invited parents whose children died due to cancer 5 years earlier to participate. Identical semi-structured interviews were conducted with each cohort by the Survey of Caring for Children with Cancer. In addition, departments provided information on their pediatric palliative care infrastructure. Participants: In total, 124 families participated; 73% of interviews were conducted with mothers, 18% with fathers, and 9% with both parents. Results: Parents’ perception of symptom occurrence, symptom burden, and effectiveness of symptom-related treatment remained stable over the 10-year period. Over time, the availability of pediatric palliative care ( p < 0.001) as well as quality and satisfaction ratings of care ( p < 0.001) increased significantly. A growing number of children received specialized pediatric palliative care at home during the end-of-life period ( p = 0.009). Along with this development, more families had the chance to plan the location of death ( p = 0.003), and more children died at the preferred location ( p = 0.001). Conclusion: Advances in the availability of pediatric palliative care were associated with improvement in some aspects of quality of care (e.g. location of death) while other aspects, such as effectiveness of symptom management, remained unchanged. Further research is required to determine whether additional improvement in structural quality may increase the effectiveness of symptom management.

Funder

Deutsche Kinderkrebsstiftung

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,General Medicine

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