Literature DB >> 25381122

Measuring caregiver outcomes in palliative care: a construct validation study of two instruments for use in economic evaluations.

Renske Hoefman1, Hareth Al-Janabi, Nikki McCaffrey, David Currow, Julie Ratcliffe.   

Abstract

PURPOSE: Providing care to patients nearing the end of life can place a considerable burden on caregivers. Hence, policy decisions on interventions in palliative care should be guided by information on this burden. This study investigates construct validation of two preference-based caregiver outcome instruments suitable for economic evaluations: the Carer Experience Scale (CES) and the Care-related Quality of Life (CarerQol) instrument. Moreover, this study reports caregiver experiences in end-of-life care.
METHODS: Data were collected with written questionnaires among caregivers of patients receiving palliative care services in the Southern metropolitan area of Adelaide, South Australia (n = 97). The effect of caregiving on caregivers was measured with the CES, CarerQol, Process Utility (PU) and Caregiver Strain Index (CSI). Convergent, discriminative and clinical validity were studied.
RESULTS: As hypothesized, higher negative effect of caregiving measured on the CES was associated with higher negative effect on the CarerQol. Both the CES and CarerQol were associated in the expected positive direction with less strain from caregiving (CSI), more positive care experiences and more PU from caring. Caregivers' and care recipients' health status and duration of caregiving were negatively associated with caring experiences.
CONCLUSIONS: Our findings suggest that the CES and CarerQol validly assess the effect of caregiving on caregivers in end-of-life care. Economic evaluations in end-of-life care should attempt to incorporate such instruments to provide a more holistic assessment of the true impact of interventions, especially where family and friends are heavily involved in caregiving.

Entities:  

Mesh:

Year:  2014        PMID: 25381122     DOI: 10.1007/s11136-014-0848-8

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  57 in total

Review 1.  Measures used to assess burden among caregivers of stroke patients: a review.

Authors:  J M Anne Visser-Meily; Marcel W M Post; Ingrid I Riphagen; Eline Lindeman
Journal:  Clin Rehabil       Date:  2004-09       Impact factor: 3.477

2.  Reproducibility of the Caregiver Strain Index and the Caregiver Reaction Assessment in partners of stroke patients living in the Dutch community.

Authors:  Marcel W M Post; Helma Festen; Ingrid G van de Port; Johanna M A Visser-Meily
Journal:  Clin Rehabil       Date:  2007-11       Impact factor: 3.477

3.  How to include informal care in economic evaluations.

Authors:  Renske J Hoefman; Job van Exel; Werner Brouwer
Journal:  Pharmacoeconomics       Date:  2013-12       Impact factor: 4.981

4.  Give me a break! Informal caregiver attitudes towards respite care.

Authors:  Job van Exel; Gjalt de Graaf; Werner Brouwer
Journal:  Health Policy       Date:  2008-04-15       Impact factor: 2.980

5.  Palliative caregivers who would not take on the caring role again.

Authors:  David C Currow; Catherine Burns; Meera Agar; Jane Phillips; Nikki McCaffrey; Amy P Abernethy
Journal:  J Pain Symptom Manage       Date:  2011-01-12       Impact factor: 3.612

6.  Uncovering an invisible network of direct caregivers at the end of life: a population study.

Authors:  Catherine M Burns; Amy P Abernethy; Eleanora Dal Grande; David C Currow
Journal:  Palliat Med       Date:  2013-04-15       Impact factor: 4.762

7.  What really matters: an inquiry into the relative importance of dimensions of informal caregiver burden.

Authors:  N J A van Exel; W B F Brouwer; B van den Berg; M A Koopmanschap; G A M van den Bos
Journal:  Clin Rehabil       Date:  2004-09       Impact factor: 3.477

8.  Evidence of spillover of illness among household members: EQ-5D scores from a US sample.

Authors:  Eve Wittenberg; Grant A Ritter; Lisa A Prosser
Journal:  Med Decis Making       Date:  2012-10-25       Impact factor: 2.583

9.  Family caregiver burden: results of a longitudinal study of breast cancer patients and their principal caregivers.

Authors:  Eva Grunfeld; Doug Coyle; Timothy Whelan; Jennifer Clinch; Leonard Reyno; Craig C Earle; Andrew Willan; Raymond Viola; Marjorie Coristine; Teresa Janz; Robert Glossop
Journal:  CMAJ       Date:  2004-06-08       Impact factor: 8.262

10.  A new test of the construct validity of the CarerQol instrument: measuring the impact of informal care giving.

Authors:  Renske J Hoefman; N Job A van Exel; Sandra Looren de Jong; W Ken Redekop; Werner B F Brouwer
Journal:  Qual Life Res       Date:  2011-01-01       Impact factor: 4.147

View more
  9 in total

1.  Spillover Effects on Caregivers' and Family Members' Utility: A Systematic Review of the Literature.

Authors:  Eve Wittenberg; Lyndon P James; Lisa A Prosser
Journal:  Pharmacoeconomics       Date:  2019-04       Impact factor: 4.981

2.  Carer administration of as-needed subcutaneous medication for breakthrough symptoms in people dying at home: the CARiAD feasibility RCT.

Authors:  Marlise Poolman; Jessica Roberts; Stella Wright; Annie Hendry; Nia Goulden; Emily Af Holmes; Anthony Byrne; Paul Perkins; Zoe Hoare; Annmarie Nelson; Julia Hiscock; Dyfrig Hughes; Julie O'Connor; Betty Foster; Liz Reymond; Sue Healy; Penney Lewis; Bee Wee; Rosalynde Johnstone; Rossela Roberts; Anne Parkinson; Sian Roberts; Clare Wilkinson
Journal:  Health Technol Assess       Date:  2020-05       Impact factor: 4.014

3.  Informal care: choice or constraint?

Authors:  Hareth Al-Janabi; Fiona Carmichael; Jan Oyebode
Journal:  Scand J Caring Sci       Date:  2017-04-12

4.  CARer-ADministration of as-needed subcutaneous medication for breakthrough symptoms in homebased dying patients (CARiAD): study protocol for a UK-based open randomised pilot trial.

Authors:  Marlise Poolman; Jessica Roberts; Anthony Byrne; Paul Perkins; Zoe Hoare; Annmarie Nelson; Julia Hiscock; Dyfrig Hughes; Betty Foster; Julie O'Connor; Liz Reymond; Sue Healy; Rossela Roberts; Bee Wee; Penney Lewis; Rosalynde Johnstone; Sian Roberts; Emily Holmes; Stella Wright; Annie Hendry; Clare Wilkinson
Journal:  Trials       Date:  2019-02-07       Impact factor: 2.279

5.  Developing a new quality of life instrument with older people for economic evaluation in aged care: study protocol.

Authors:  Julie Ratcliffe; Ian Cameron; Emily Lancsar; Ruth Walker; Rachel Milte; Claire Louise Hutchinson; Kate Swaffer; Stuart Parker
Journal:  BMJ Open       Date:  2019-05-24       Impact factor: 2.692

6.  Quality of life among caregivers of people with end-stage kidney disease managed with dialysis or comprehensive conservative care.

Authors:  Karan K Shah; Fliss E M Murtagh; Kevin McGeechan; Susan M Crail; Aine Burns; Rachael L Morton
Journal:  BMC Nephrol       Date:  2020-05-04       Impact factor: 2.388

7.  Quality of Life Among Informal Caregivers of Patients With Degenerative Cervical Myelopathy: Cross-Sectional Questionnaire Study.

Authors:  Oliver Daniel Mowforth; Benjamin Marshall Davies; Mark Reinhard Kotter
Journal:  Interact J Med Res       Date:  2019-11-07

8.  Measuring the effectiveness of digital nursing technologies: development of a comprehensive digital nursing technology outcome framework based on a scoping review.

Authors:  Tobias Krick; Kai Huter; Kathrin Seibert; Dominik Domhoff; Karin Wolf-Ostermann
Journal:  BMC Health Serv Res       Date:  2020-03-24       Impact factor: 2.655

9.  Diseases Costs and Impact of the Caring Role on Informal Carers of Children with Neuromuscular Disease.

Authors:  Alicia Aurora Rodríguez; Óscar Martínez; Imanol Amayra; Juan Francisco López-Paz; Mohammad Al-Rashaida; Esther Lázaro; Patricia Caballero; Manuel Pérez; Sarah Berrocoso; Maitane García; Paula María Luna; Paula Pérez-Núñez; Nicole Passi
Journal:  Int J Environ Res Public Health       Date:  2021-03-15       Impact factor: 3.390

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.