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Towards person-centred quality care for children with life-limiting and life-threatening illness: Self-reported symptoms, concerns and priority outcomes from a multi-country qualitative study.

Authors :
Wolfe, Joanne
Bluebond-Langner, Myra
Namisango, Eve
Bristowe, Katherine
Murtagh, Fliss EM
Downing, Julia
Powell, Richard A
Abas, Melanie
Lohfeld, Lynne
Ali, Zipporah
Atieno, Mackuline
Haufiku, Desiderius
Guma, Samuel
Luyirika, Emmanuel BK
Mwangi-Powell, Faith N
Higginson, Irene J
Harding, Richard
Source :
Palliative Medicine. Mar2020, Vol. 34 Issue 3, p319-335. 17p. 4 Charts.
Publication Year :
2020

Abstract

Background: Paediatric life-limiting and life-threatening conditions (life-limiting conditions) place significant strain on children, families and health systems. Given high service use among this population, it is essential that care addresses their main symptoms and concerns. Aim: This study aimed to identify the symptoms, concerns and other outcomes that matter to children with life-limiting conditions and their families in sub-Saharan Africa. Setting and participants: Cross-sectional qualitative study in Kenya, Namibia, South Africa and Uganda. Children/caregivers of children aged 0–17 years with life-limiting conditions were purposively sampled by age, sex and diagnosis. Children aged 7 and above self-reported; caregiver proxies reported for children below 7 and those aged 7 and above unable to self-report. Results: A total of 120 interviews were conducted with children with life-limiting conditions (n = 61; age range: 7–17 years), and where self-report was not possible, caregivers (n = 59) of children (age range: 0–17) were included. Conditions included advanced HIV (22%), cancer (19%), heart disease (16%) endocrine, blood and immune disorders (13%), neurological conditions (12%), sickle cell anaemia (10%) and renal disease (8%). Outcomes identified included physical concerns – pain and s ymptom distress; psycho-social concerns – family and social relationships, ability to engage with age-appropriate activities (e.g. play, school attendance); existential concerns – worry about death, and loss of ambitions; health care quality – child- and adolescent-friendly services. Priority psycho-social concerns and health service factors varied by age. Conclusion: This study bridges an important knowledge gap regarding symptoms, concerns and outcomes that matter to children living with life-limiting conditions and their families and informs service development and evaluation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02692163
Volume :
34
Issue :
3
Database :
Academic Search Index
Journal :
Palliative Medicine
Publication Type :
Academic Journal
Accession number :
142247553
Full Text :
https://doi.org/10.1177/0269216319900137