Literature DB >> 27247087

Health-related quality-of-life outcome measures in paediatric palliative care: A systematic review of psychometric properties and feasibility of use.

Lucy H Coombes1, Theresa Wiseman2,3, Grace Lucas2, Amrit Sangha2, Fliss Em Murtagh4.   

Abstract

BACKGROUND: The number of children worldwide requiring palliative care services is increasing due to advances in medical care and technology. The use of outcome measures is important to improve the quality and effectiveness of care. AIM: To systematically identify health-related quality-of-life outcome measures that could be used in paediatric palliative care and examine their feasibility of use and psychometric properties.
DESIGN: A systematic literature review and analysis of psychometric properties. DATA SOURCES: PsychInfo, Medline and EMBASE were searched from 1 January 1990 to 10 December 2014. Hand searches of the reference list of included studies and relevant reviews were also performed.
RESULTS: From 3460 articles, 125 papers were selected for full-text assessment. A total of 41 articles met the eligibility criteria and examined the psychometric properties of 22 health-related quality-of-life measures. Evidence was limited as at least half of the information on psychometric properties per instrument was missing. Measurement error was not analysed in any of the included articles and responsiveness was only analysed in one study. The methodological quality of included studies varied greatly.
CONCLUSION: There is currently no 'ideal' outcome assessment measure for use in paediatric palliative care. The domains of generic health-related quality-of-life measures are not relevant to all children receiving palliative care and some domains within disease-specific measures are only relevant for that specific population. Potential solutions include adapting an existing measure or developing more individualized patient-centred outcome and experience measures. Either way, it is important to continue work on outcome measurement in this field.
© The Author(s) 2016.

Entities:  

Keywords:  Outcome assessment (healthcare); child; paediatrics; palliative care; psychometrics; quality of life

Mesh:

Year:  2016        PMID: 27247087      PMCID: PMC5117129          DOI: 10.1177/0269216316649155

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  58 in total

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2.  Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.

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3.  Rising national prevalence of life-limiting conditions in children in England.

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4.  The measurement of symptoms in young children with cancer: the validation of the Memorial Symptom Assessment Scale in children aged 7-12.

Authors:  John J Collins; Tom D Devine; Gina S Dick; Elizabeth A Johnson; Henry A Kilham; C Ross Pinkerton; M M Stevens; Howard T Thaler; Russell K Portenoy
Journal:  J Pain Symptom Manage       Date:  2002-01       Impact factor: 3.612

5.  Development and validation of a measure of the impact of epilepsy on a young person's quality of life: Glasgow epilepsy outcome scale for young persons (GEOS-YP).

Authors:  Kathryn H Townshend; Liam Dorris; Margaret J McEwan; Sarah E Aylett; Martin J Brodie; Mary O'Regan; Colin A Espie
Journal:  Epilepsy Behav       Date:  2007-11-05       Impact factor: 2.937

6.  Description and psychometric properties of the CP QOL-Teen: a quality of life questionnaire for adolescents with cerebral palsy.

Authors:  Elise Davis; Andrew Mackinnon; Melanie Davern; Roslyn Boyd; India Bohanna; Elizabeth Waters; H Kerr Graham; Susan Reid; Dinah Reddihough
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7.  The development of a new measure of quality of life for children with congenital cardiac disease.

Authors:  Susan Macran; Yvonne Birks; Jonathan Parsons; Patricia Sloper; Geoff Hardman; Paul Kind; Carin van Doorn; David Thompson; Robert Lewin
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8.  The PedsQL 4.0 as a pediatric population health measure: feasibility, reliability, and validity.

Authors:  James W Varni; Tasha M Burwinkle; Michael Seid; Douglas Skarr
Journal:  Ambul Pediatr       Date:  2003 Nov-Dec

Review 9.  Measurement properties of disease-specific questionnaires in patients with neck pain: a systematic review.

Authors:  Jasper M Schellingerhout; Arianne P Verhagen; Martijn W Heymans; Bart W Koes; Henrica C de Vet; Caroline B Terwee
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10.  Paediatric palliative care: development and pilot study of a 'Directory' of life-limiting conditions.

Authors:  Richard Hain; Mary Devins; Richard Hastings; Jayne Noyes
Journal:  BMC Palliat Care       Date:  2013-12-11       Impact factor: 3.234

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2.  Enhancing validity, reliability and participation in self-reported health outcome measurement for children and young people: a systematic review of recall period, response scale format, and administration modality.

Authors:  L Coombes; K Bristowe; C Ellis-Smith; J Aworinde; L K Fraser; J Downing; M Bluebond-Langner; L Chambers; F E M Murtagh; R Harding
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3.  Approaching the third decade of paediatric palliative oncology investigation: historical progress and future directions.

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4.  Symptoms and Concerns Among Children and Young People with Life-Limiting and Life-Threatening Conditions: A Systematic Review Highlighting Meaningful Health Outcomes.

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5.  Specialist paediatric palliative care for children and young people with cancer: A mixed-methods systematic review.

Authors:  Johanna Taylor; Alison Booth; Bryony Beresford; Bob Phillips; Kath Wright; Lorna Fraser
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Review 6.  Emerging Methodologies in Pediatric Palliative Care Research: Six Case Studies.

Authors:  Katherine E Nelson; James A Feinstein; Cynthia A Gerhardt; Abby R Rosenberg; Kimberley Widger; Jennifer A Faerber; Chris Feudtner
Journal:  Children (Basel)       Date:  2018-02-26

7.  How do professionals assess the quality of life of children with advanced cancer receiving palliative care, and what are their recommendations for improvement?

Authors:  Josianne Avoine-Blondin; Véronique Parent; Léonor Fasse; Clémentine Lopez; Nago Humbert; Michel Duval; Serge Sultan
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8.  Development and psychometric validation of the family-centered multidimensional outcome measure for pediatric palliative care targeted to children with severe neurological impairmentis-A multicenter prospective study.

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9.  Pain assessment tools in paediatric palliative care: A systematic review of psychometric properties and recommendations for clinical practice.

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Review 10.  Quality Indicators in Pediatric Palliative Care: Considerations for Latin America.

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