Literature DB >> 30030620

Care-related quality of life in caregivers of children with drug-resistant epilepsy.

Puneet Jain1, Jhananiee Subendran2, Mary Lou Smith2,3, Elysa Widjaja4,5,6.   

Abstract

BACKGROUND: Epilepsy in children negatively impacts on caregiver quality of life (QOL). The study aimed to evaluate the relationships between patient factors [demographics, clinical factors, health-related quality of life (HRQL)], contextual factors (socio-economic factors), caregiver mood, and caregiver QOL, and whether family factors mediate the relationship between patient HRQL and caregiver QOL.
METHODS: Children aged 4-18 years with medically intractable epilepsy were enrolled. Patient demographics, clinical data, patient HRQL [measured using Quality of Life in Childhood Epilepsy Questionnaire (QOLCE)], socio-economic factors, caregiver anxiety and depression, and family factors (adaptation, resources and demands) were assessed. Caregiver QOL was measured using CarerQol, which evaluates care-related QOL, incorporating the negative and positive effects of caregiving.
RESULTS: One hundred and eighty-one children were studied. In bivariable regression analysis, higher patient HRQL (QOLCE) (β = 0.54, p < 0.001) and household income (β = 10.49, p = 0.019) were associated with higher caregiver QOL. Higher depression (β = - 2.48, p < 0.001) and anxiety (β = - 2.04, p < 0.001) were associated with lower caregiver QOL. Seizure severity and other socio-economic factors did not influence caregiver QOL (all p > 0.05). In multivariable regression analysis, higher QOLCE (β = 0.21, p = 0.001), lower depression (β = - 1.07, p < 0.001) and lower anxiety (β = - 1.19, p < 0.001) were associated with higher caregiver QOL. Family demands and resources moderated the relationship between patient HRQL and caregiver QOL.
CONCLUSIONS: Patient HRQL and caregiver mood were more important correlates of caregiver QOL than seizure severity in medically intractable epilepsy. The findings are significant in delineating variables (caregiver mood and family factors) that are potentially modifiable, and show promise for improving caregiver QOL.

Entities:  

Keywords:  Caregivers; Medically intractable epilepsy; Pediatric epilepsy; Quality of life

Mesh:

Year:  2018        PMID: 30030620     DOI: 10.1007/s00415-018-8979-4

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  40 in total

1.  Impact of pediatric epilepsy on Indian families: influence of psychopathology and seizure related variables.

Authors:  Soumitra Shankar Datta; Titus Samson Premkumar; Shona Fielding; Sujith Chandy; Sudhir Kumar; John Eagles; Alice Cherian
Journal:  Epilepsy Behav       Date:  2006-05-24       Impact factor: 2.937

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Authors:  Paul A Harris; Robert Taylor; Robert Thielke; Jonathon Payne; Nathaniel Gonzalez; Jose G Conde
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3.  Correlates of health-related quality of life in children with drug resistant epilepsy.

Authors:  Lauryn Conway; Mary Lou Smith; Mark A Ferro; Kathy N Speechley; Mary B Connoly; O Carter Snead; Elysa Widjaja
Journal:  Epilepsia       Date:  2016-06-28       Impact factor: 5.864

4.  Life impact of caregiving for severe childhood epilepsy: Results of expert panels and caregiver focus groups.

Authors:  Mark P Jensen; Kendra S Liljenquist; Fraser Bocell; Arnold R Gammaitoni; Carey R Aron; Bradley S Galer; Dagmar Amtmann
Journal:  Epilepsy Behav       Date:  2017-07-19       Impact factor: 2.937

5.  Health-related quality of life and emotional well-being in parents of children with epilepsy referred for presurgical evaluation in Sweden.

Authors:  Colin Reilly; Charles Taft; Maria Nelander; Kristina Malmgren; Ingrid Olsson
Journal:  Epilepsy Behav       Date:  2015-10-24       Impact factor: 2.937

6.  Validation and standardization of the Generalized Anxiety Disorder Screener (GAD-7) in the general population.

Authors:  Bernd Löwe; Oliver Decker; Stefanie Müller; Elmar Brähler; Dieter Schellberg; Wolfgang Herzog; Philipp Yorck Herzberg
Journal:  Med Care       Date:  2008-03       Impact factor: 2.983

7.  Health-related quality of life and emotional wellbeing improve in parents after their children have undergone epilepsy surgery - A prospective population-based study.

Authors:  Colin Reilly; Charles Taft; Anna Edelvik; Ingrid Olsson; Kristina Malmgren
Journal:  Epilepsy Behav       Date:  2017-09-04       Impact factor: 2.937

8.  Quality of life and burden in caregivers of patients with epilepsy.

Authors:  Ana Carolina Westphal-Guitti; Neide Barreira Alonso; Rosa Cristina Vaz Pedroso Migliorini; Tatiana Indelicato da Silva; Auro Mauro Azevedo; Luís Otávio Sales Ferreira Caboclo; Américo Ceiki Sakamoto; Elza Márcia Targas Yacubian
Journal:  J Neurosci Nurs       Date:  2007-12       Impact factor: 1.230

9.  Measuring Care-Related Quality of Life of Caregivers for Use in Economic Evaluations: CarerQol Tariffs for Australia, Germany, Sweden, UK, and US.

Authors:  Renske J Hoefman; Job van Exel; Werner B F Brouwer
Journal:  Pharmacoeconomics       Date:  2017-04       Impact factor: 4.981

Review 10.  Caregiving process and caregiver burden: conceptual models to guide research and practice.

Authors:  Parminder Raina; Maureen O'Donnell; Heidi Schwellnus; Peter Rosenbaum; Gillian King; Jamie Brehaut; Dianne Russell; Marilyn Swinton; Susanne King; Micheline Wong; Stephen D Walter; Ellen Wood
Journal:  BMC Pediatr       Date:  2004-01-14       Impact factor: 2.125

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  7 in total

1.  Seizure burden in severe early-life epilepsy: Perspectives from parents.

Authors:  Anne T Berg; Karen Kaiser; Tracy Dixon-Salazar; Andi Elliot; Nancy McNamara; Mary Anne Meskis; Emily Golbeck; Priya Tatachar; Linda Laux; Carrie Raia; Janice Stanley; April Luna; Christian Rozek
Journal:  Epilepsia Open       Date:  2019-04-14

2.  Cannabidiol improves survival and behavioural co-morbidities of Dravet syndrome in mice.

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Journal:  BMJ Open       Date:  2022-02-22       Impact factor: 2.692

4.  Factors associated with care- and health-related quality of life of caregivers of children with juvenile idiopathic arthritis.

Authors:  Luiza R Grazziotin; Gillian Currie; Marinka Twilt; Maarten J IJzerman; Michelle M A Kip; Hendrik Koffijberg; Gouke Bonsel; Susanne M Benseler; Joost F Swart; Sebastiaan J Vastert; Nico M Wulffraat; Rae S M Yeung; Wineke Armbrust; J Merlijn van den Berg; Deborah A Marshall
Journal:  Pediatr Rheumatol Online J       Date:  2022-07-23       Impact factor: 3.413

5.  Caring for Children with an Autism Spectrum Disorder: Factors Associating with Health- and Care-Related Quality of Life of the Caregivers.

Authors:  Leontine W Ten Hoopen; Pieter F A de Nijs; Jorieke Duvekot; Kirstin Greaves-Lord; Manon H J Hillegers; Werner B F Brouwer; Leona Hakkaart-van Roijen
Journal:  J Autism Dev Disord       Date:  2021-11-01

6.  The Role of Associations in Reducing the Emotional and Financial Impact on Parents Caring for Children with Duchenne Muscular Dystrophy: A Cross-Cultural Study.

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7.  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
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  7 in total

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