Literature DB >> 29808788

Researching children's perspectives in pediatric palliative care: A systematic review and meta-summary of qualitative research.

Luca Ghirotto1, Elena Busani2, Michela Salvati3, Valeria Di Marco4, Valeria Caldarelli5, Giovanna Artioli6.   

Abstract

OBJECTIVE: Qualitative research is pivotal in gaining understanding of individuals' experiences in pediatric palliative care. In the past few decades, the number of qualitative studies on pediatric palliative care has increased slightly, as has interest in qualitative research in this area. Nonetheless, a limited number of such studies have included the first-person perspective of children. The aim of this article is to understand the contribution of previous qualitative research on pediatric palliative care that included the voices of children.
METHOD: A systematic review of qualitative studies and a meta-summary were conducted. MEDLINE, CINAHL, PsycINFO, PsycARTICLES, and ERIC were searched without limitations on publication date or language. Eligible articles were qualitative research articles in which the participants were children ranging in age from 3 to 18 years.ResultWe retrieved 16 qualitative research articles reporting on 12 unique studies, and we selected two mixed-method articles. The meta-summary shows eight themes: the relationship with professional caregivers, pain and its management, "living beyond pain," the relationship between pediatric patients and their families, children's view on their treatment and service provision, meanings children give to their end-of-life situation, consequences of clinical decisions, and the relationships among children in pediatric palliative care and their peers.Significance of resultsThis meta-summary presents the "state of the art" of pediatric palliative care qualitative research on children and highlights additional research areas that warrant qualitative study.

Entities:  

Keywords:  Meta-summary; children's voice; neoplasm; pediatric palliative care; qualitative research

Mesh:

Year:  2018        PMID: 29808788     DOI: 10.1017/S1478951518000172

Source DB:  PubMed          Journal:  Palliat Support Care        ISSN: 1478-9515


  3 in total

1.  End of life care for infants, children and young people (ENHANCE): Protocol for a mixed methods evaluation of current practice in the United Kingdom [version 1; peer review: 2 approved].

Authors:  Andrew Papworth; Julia Hackett; Bryony Beresford; Fliss Murtagh; Helen Weatherly; Sebastian Hinde; Andre Bedendo; Gabriella Walker; Jane Noyes; Sam Oddie; Chakrapani Vasudevan; Richard Feltbower; Bob Phillips; Richard Hain; Gayathri Subramanian; Andrew Haynes; Lorna K Fraser
Journal:  NIHR Open Res       Date:  2022-05-13

2.  Congruence Gaps Between Adolescents With Cancer and Their Families Regarding Values, Goals, and Beliefs About End-of-Life Care.

Authors:  Sarah Friebert; Daniel H Grossoehme; Justin N Baker; Jennifer Needle; Jessica D Thompkins; Yao I Cheng; Jichuan Wang; Maureen E Lyon
Journal:  JAMA Netw Open       Date:  2020-05-01

3.  Identifying key elements for paediatric advance care planning with parents, healthcare providers and stakeholders: A qualitative study.

Authors:  Kerstin Hein; Kathrin Knochel; Vedrana Zaimovic; Daniel Reimann; Anna Monz; Nari Heitkamp; Gian Domenico Borasio; Monika Führer
Journal:  Palliat Med       Date:  2020-01-27       Impact factor: 4.762

  3 in total

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