Specialised Paediatric PAlliativE CaRe: Assessing family, healthcare professionals and health system outcomes in a multi-site context of various care settings: SPhAERA study protocol

Karin Zimmermann, Michael Simon, Katrin Scheinemann, Eva Maria Tinner Oehler, Michèle Widler, Simone Keller, Günther Fink, Stefan Mitterer, Anne-Kathrin Gerber, Stefanie von Felten, Eva Bergstraesser, Karin Zimmermann, Michael Simon, Katrin Scheinemann, Eva Maria Tinner Oehler, Michèle Widler, Simone Keller, Günther Fink, Stefan Mitterer, Anne-Kathrin Gerber, Stefanie von Felten, Eva Bergstraesser

Abstract

Background: The number of children and adolescents living with life-limiting conditions and potentially in need for specialised paediatric palliative care (SPPC) is rising. Ideally, a specialised multiprofessional team responds to the complex healthcare needs of children and their families. The questions of, how SPPC is beneficial, for whom, and under what circumstances, remain largely unanswered in the current literature. This study's overall target is to evaluate the effectiveness of a SPPC programme in Switzerland with respect to its potential to improve patient-, family-, health professional-, and healthcare-related outcomes.

Methods: This comparative effectiveness study applies a quasi-experimental design exploring the effectiveness of SPPC as a complex intervention at one treatment site in comparison with routine care provided in a generalised PPC environment at three comparison sites. As the key goal of palliative care, quality of life - assessed at the level of the patient-, the family- and the healthcare professional - will be the main outcome of this comparative effectiveness research. Other clinical, service, and economic outcomes will include patient symptom severity and distress, parental grief processes, healthcare resource utilisation and costs, direct and indirect health-related expenditure, place of death, and introduction of SPPC. Data will be mainly collected through questionnaire surveys and chart analysis.

Discussion: The need for SPPC has been demonstrated through numerous epidemiological and observational studies. However, in a healthcare environment focused on curative treatment and struggling with limited resources, the lack of evidence contributes to a lack of acceptance and financing of SPPC which is a major barrier against its sustainability. This study will contribute to current knowledge by reporting individual and child level outcomes at the family level and by collecting detailed contextual information on healthcare provision. We hope that the results of this study can help guiding the expansion and sustainability of SPPC and improve the quality of care for children with life-limiting conditions and their families internationally.

Trial registration: Registered prospectively on ClinicalTrials.gov on January 22, 2020. NCT04236180 PROTOCOL VERSION: Amendment 2, March 01, 2021.

Keywords: Clinical trials; Complex intervention; Effectiveness research; Palliative care; Pediatrics; Study protocol.

Conflict of interest statement

The authors declare that they have no competing interests.

© 2022. The Author(s).

Figures

Fig. 1
Fig. 1
Overview of the study’s setup, timeline and outcomes

References

    1. Fraser LK, Gibson-Smith D, Jarvis S, Norman P, Parslow RC. Estimating the current and future prevalence of life-limiting conditions in children in England. Palliat Med. 2021;35(9):1641–1651. doi: 10.1177/0269216320975308.
    1. Radbruch L, De Lima L, Knaul F, Wenk R, Ali Z, Bhatnaghar S, Blanchard C, Bruera E, Buitrago R, Burla C, et al. Redefining palliative care-a new consensus-based definition. J Pain Symptom Manag. 2020;60(4):754–764. doi: 10.1016/j.jpainsymman.2020.04.027.
    1. Benini F, Papadatou D, Bernada M, Craig F, De Zen L, Downing J, Drake R, Friedrichsdorf S, Garros D, Giacomelli L, et al. International standards for pediatric palliative care: from IMPaCCT to GO-PPaCS. J Pain Symptom Manag. 2022;63(5):e529–e543. doi: 10.1016/j.jpainsymman.2021.12.031.
    1. Feudtner C, Womer J, Augustin R, Remke S, Wolfe J, Friebert S, Weissman D. Pediatric palliative care programs in children's hospitals: a cross-sectional national survey. Pediatrics. 2013;132(6):1063–1070. doi: 10.1542/peds.2013-1286.
    1. Damschroder LJ, Aron DC, Keith RE, Kirsh SR, Alexander JA, Lowery JC. Fostering implementation of health services research findings into practice: a consolidated framework for advancing implementation science. Implement Sci. 2009;4:50. doi: 10.1186/1748-5908-4-50.
    1. Downing J, Knapp C, Muckaden MA, Fowler-Kerry S, Marston J, Committee IS. Priorities for global research into children's palliative care: results of an international Delphi study. BMC Palliat Care. 2015;14:36. doi: 10.1186/s12904-015-0031-1.
    1. Thienprayoon R, Jones E, Humphrey L, Ragsdale L, Williams C, Klick JC. The pediatric palliative improvement network: a national healthcare learning collaborative. J Pain Symptom Manag. 2022;63(1):131–139. doi: 10.1016/j.jpainsymman.2021.06.020.
    1. Feudtner C, Rosenberg AR, Boss RD, Wiener L, Lyon ME, Hinds PS, Bluebond-Langner M, Wolfe J. Challenges and priorities for pediatric palliative care research in the U.S. and similar practice settings: report from a pediatric palliative care research network workshop. J Pain Symptom Manag. 2019;58(5):909–917.e903. doi: 10.1016/j.jpainsymman.2019.08.011.
    1. Kavalieratos D, Corbelli J, Zhang D, Dionne-Odom JN, Ernecoff NC, Hanmer J, Hoydich ZP, Ikejiani DZ, Klein-Fedyshin M, Zimmermann C, et al. Association between palliative care and patient and caregiver outcomes: a systematic review and meta-analysis. JAMA. 2016;316(20):2104–2114. doi: 10.1001/jama.2016.16840.
    1. Huang IC, Shenkman EA, Madden VL, Vadaparampil S, Quinn G, Knapp CA. Measuring quality of life in pediatric palliative care: challenges and potential solutions. Palliat Med. 2010;24(2):175–182. doi: 10.1177/0269216309352418.
    1. Mitchell S, Morris A, Bennett K, Sajid L, Dale J. Specialist paediatric palliative care services: what are the benefits? Arch Dis Child. 2017;102(10):923–929. doi: 10.1136/archdischild-2016-312026.
    1. Vermaes IP, van Susante AM, van Bakel HJ. Psychological functioning of siblings in families of children with chronic health conditions: a meta-analysis. J Pediatr Psychol. 2012;37(2):166–184. doi: 10.1093/jpepsy/jsr081.
    1. Tay J, Widger K, Stremler R. Self-reported experiences of siblings of children with life-threatening conditions: a scoping review. J Child Health Care. 2021:13674935211026113. 10.1177/13674935211026113.
    1. Sinclair S, Raffin-Bouchal S, Venturato L, Mijovic-Kondejewski J, Smith-MacDonald L. Compassion fatigue: a meta-narrative review of the healthcare literature. Int J Nurs Stud. 2017;69:9–24. doi: 10.1016/j.ijnurstu.2017.01.003.
    1. Robins PM, Meltzer L, Zelikovsky N. The experience of secondary traumatic stress upon care providers working within a children's hospital. J Pediatr Nurs. 2009;24(4):270–279. doi: 10.1016/j.pedn.2008.03.007.
    1. Lin SC, Huang MC, Yasmara D, Wuu HL. Impact of palliative care on end-of-life care and place of death in children, adolescents, and young adults with life-limiting conditions: a systematic review. Palliat Support Care. 2021;19(4):488–500. doi: 10.1017/S1478951520001455.
    1. Conte T, Mitton C, Trenaman LM, Chavoshi N, Siden H. Effect of pediatric palliative care programs on health care resource utilization and costs among children with life-threatening conditions: a systematic review of comparative studies. CMAJ Open. 2015;3(1):E68–E75. doi: 10.9778/cmajo.20140044.
    1. Chong PH, De Castro Molina JA, Teo K, Tan WS. Paediatric palliative care improves patient outcomes and reduces healthcare costs: evaluation of a home-based program. BMC Palliat Care. 2018;17(1):11. doi: 10.1186/s12904-017-0267-z.
    1. Lysecki DL, Gupta S, Rapoport A, Rhodes E, Spruin S, Vadeboncoeur C, Widger K, Tanuseputro P. Children’s health care utilization and cost in the last year of life: a cohort comparison with and without regional specialist pediatric palliative care. J Palliat Med. 2022;25(7):1031–1040. doi: 10.1089/jpm.2021.0175.
    1. McCubbin MA, McCubbin HI. Families coping with illness: the resiliency model of family stress, adjustment and adaptation. In: Danielson CB, Hamel-Bissel B, Winstead-Fry P, editors. Families, health & illness: perspectives on coping and intervention. St. Louis: Mosby; 1989.
    1. Antonovsky A, Sourani T. Family sense of coherence and family adaptation. J Marriage Fam. 1988;50(1):79–92. doi: 10.2307/352429.
    1. Persson C, Benzein E, Arestedt K. Assessing family resources: validation of the Swedish version of the family hardiness index. Scand J Caring Sci. 2016;30(4):845–855. doi: 10.1111/scs.12313.
    1. Osenga K, Postier A, Dreyfus J, Foster L, Teeple W, Friedrichsdorf SJ. A comparison of circumstances at the end of life in a hospital setting for children with palliative care involvement versus those without. J Pain Symptom Manag. 2016;52(5):673–680. doi: 10.1016/j.jpainsymman.2016.05.024.
    1. Baker JN, Levine DR, Hinds PS, Weaver MS, Cunningham MJ, Johnson L, Anghelescu D, Mandrell B, Gibson DV, Jones B, et al. Research priorities in pediatric palliative care. J Pediatr. 2015;167(2):467–470.e463. doi: 10.1016/j.jpeds.2015.05.002.
    1. Bergstraesser E, Hain RD, Pereira JL. The development of an instrument that can identify children with palliative care needs: the Paediatric Palliative Screening Scale (PaPaS Scale): a qualitative study approach. BMC Palliat Care. 2013;12(1):20. doi: 10.1186/1472-684X-12-20.
    1. Zurich UCsH. Konzept Pädiatrische Palliative Care. Zurich: University Children's Hospital Zurich; 2016. p. 22.
    1. Cohen R, Leis AM, Kuhl D, Charbonneau C, Ritvo P, Ashbury FD. QOLLTI-F: measuring family carer quality of life. Palliat Med. 2006;20(8):755–767. doi: 10.1177/0269216306072764.
    1. Baars RM, Atherton CI, Koopman HM, Bullinger M, Power M, group D. The European DISABKIDS project: development of seven condition-specific modules to measure health related quality of life in children and adolescents. Health Qual Life Outcomes. 2005;3:70.
    1. Collins JJ, Byrnes ME, Dunkel IJ, Lapin J, Nadel T, Thaler HT, Polyak T, Rapkin B, Portenoy RK. The measurement of symptoms in children with cancer. J Pain Symptom Manag. 2000;19(5):363–377. doi: 10.1016/S0885-3924(00)00127-5.
    1. Collins JJ, Devine TD, Dick GS, Johnson EA, Kilham HA, Pinkerton CR, Stevens MM, Thaler HT, Portenoy RK. The measurement of symptoms in young children with cancer: the validation of the memorial symptom assessment scale in children aged 7-12. J Pain Symptom Manag. 2002;23(1):10–16. doi: 10.1016/S0885-3924(01)00375-X.
    1. KIDSCREEN - health related quality of life questionnaire for children and young people and their parents. 2011. . Accessed 30 May 2017.
    1. ProQOL, Professional Quality of Life. 2021. . Accessed 22 Sept 2022.
    1. Wittkowski J. Würzburger Trauerinventar: Mehrdimensionale Erfassung des Verlusterlebens. Göttingen: Hogrefe Verlag GmbH; 2013. p. 66.
    1. Angermeyer MC, Kilian R, Matschinger H. WHOQOL-100 und WHOQOL-BREF: Handbuch für die deutschsprachige Version der WHO Instrumente zur Erfassung von Lebensqualität. Göttingen: Hogrefe-Verlag; 2000.
    1. Stamm BH. The concise ProQOL manual. 2nd ed. Pocatello: ; 2010.
    1. Groh G, Borasio GD, Nickolay C, Bender HU, von Luttichau I, Fuhrer M. Specialized pediatric palliative home care: a prospective evaluation. J Palliat Med. 2013;16(12):1588–1594. doi: 10.1089/jpm.2013.0129.
    1. R Core Team . R: a language and environment for statistical computing. Vienna: R Foundation for Statistical Computing; 2018.
    1. Pinheiro J, Bates D, Team RC . nlme: linear and nonlinear mixed effects models. R package version 3.1–137 edn. 2018.
    1. Fabbro T. sse: sample size estimation. R package version 0.6–4 edn. 2018.
    1. Portney LG. Foundations of clinical research: applications to evidence-based practice. 4. Philadelphia: F.A. Davis Company; 2020.
    1. Widger K, Medeiros C, Trenholm M, Zuniga-Villanueva G, Streuli JC. Indicators used to assess the impact of specialized pediatric palliative care: a scoping review. J Palliat Med. 2019;22(2):199–219. doi: 10.1089/jpm.2018.0420.

Source: PubMed

3
Prenumerera