Literature DB >> 29762072

Healthcare Users' Experiences of Communicating with Healthcare Professionals About Children Who Have Life-Limiting Conditions: A Qualitative Systematic Review.

Stuart Ekberg1,2, Natalie K Bradford3, Anthony Herbert3,4, Susan Danby5, Patsy Yates1,6.   

Abstract

BACKGROUND: Globally, an estimated eight million children could benefit from palliative care each year. Effective communication about children with life-limiting conditions is well recognized as a critical component of high-quality pediatric palliative care.
OBJECTIVE: To synthesize existing qualitative research exploring healthcare users' experiences of communicating with healthcare professionals about children with life-limiting conditions.
DESIGN: The results of a systematic literature search were screened independently by two reviewers. Raw data and analytic claims were extracted from included studies and were synthesized using thematic analysis methods for systematic reviews. DATA SOURCES: MEDLINE, PubMed, CINAHL, Embase, PsycINFO, Scopus, Web of Science, ProQuest, and ScienceDirect were searched for articles published in English between 1990 and May 2017.
RESULTS: This review included 29 studies conducted across 11 countries and involving at least 979 healthcare users (adults [n = 914], patients [n = 25], and siblings [n = 40]). The four domains of communication experience identified through thematic synthesis are: Information, Emotion, Collaboration, and Relationship. Although included studies were from a range of settings and diverse populations, further research is needed to explore whether and how domains of communication experience differ across settings and populations. In particular, further research about children's palliative care experiences is needed.
CONCLUSIONS: Healthcare users typically value communication with healthcare professionals: that (1) is open and honest, (2) acknowledges emotion, (3) actively involves healthcare users, and (4) occurs within established and trusting relationships.

Entities:  

Keywords:  children; communication; interpersonal relations; palliative care; pediatrics; qualitative research

Mesh:

Year:  2018        PMID: 29762072     DOI: 10.1089/jpm.2017.0422

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  5 in total

1.  An Observational Study on the Effects of Delayed Initiation of End-of-Life Care in Terminally ill Young Adults in the Intensive Care Unit.

Authors:  Anirban Hom Choudhuri; Sakshi Duggal; Bhuvna Ahuja; Rajeev Uppal
Journal:  Indian J Palliat Care       Date:  2021-02-17

2.  Metaphors that shape parents' perceptions of effective communication with healthcare practitioners following child death: a qualitative UK study.

Authors:  Sarah Turner; Jeannette Littlemore; Julie Taylor; Eloise Parr; A E Topping
Journal:  BMJ Open       Date:  2022-01-25       Impact factor: 2.692

3.  Making room for life and death at the same time - a qualitative study of health and social care professionals' understanding and use of the concept of paediatric palliative care.

Authors:  Anette Winger; Elena Albertini Früh; Heidi Holmen; Lisbeth Gravdal Kvarme; Anja Lee; Vibeke Bruun Lorentsen; Nina Misvær; Kirsti Riiser; Simen A Steindal
Journal:  BMC Palliat Care       Date:  2022-04-11       Impact factor: 3.234

4.  Attending to child agency in paediatric palliative care consultations: Adults' use of tag questions directed to the child.

Authors:  Katie Ekberg; Stuart Ekberg; Lara Weinglass; Anthony Herbert; Johanna Rendle-Short; Myra Bluebond-Langner; Patsy Yates; Natalie Bradford; Susan Danby
Journal:  Sociol Health Illn       Date:  2022-01-28

5.  What hinders and helps in the end-of-life decision-making process for children: Parents' and physicians' views.

Authors:  Ilse H Zaal-Schuller; Rosa Geurtzen; Dick L Willems; Mirjam A de Vos; Marije Hogeveen
Journal:  Acta Paediatr       Date:  2022-01-31       Impact factor: 4.056

  5 in total

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