Literature DB >> 21465330

Quality of life and emotional burden of primary caregivers: a case-control study of multiple sclerosis patients in Greece.

Andreas A Argyriou1, Panagiotis Karanasios, Amalia A Ifanti, Gregoris Iconomou, Konstantinos Assimakopoulos, Alexandra Makridou, Fotini Giannakopoulou, Nicolaos Makris.   

Abstract

PURPOSE: Our aim was to assess the perceived emotional burden and quality of life (QOL) in a sample of Greek primary caregivers of patients with multiple sclerosis (MS).
METHODS: Twenty-two male and 13 female primary caregivers (mean age 47.3 ± 12.4 years), and an equal number of patients with MS, completed the Greek validated version of the hospital anxiety and depression scale (HADS) and the Greek validated version of EuroQOL (EQ-5D). Thirty-five age-, gender-, and education-matched healthy controls were used for comparison.
RESULTS: Caregivers experienced higher degree of anxiety than depression. The mean score of the HADS-A subscale was 9.5 ± 4 (range 3-15), and the mean score of the HADS-D subscale was 7.1 ± 3.1 (range 2-14). The mean scores of caregivers on both HADS-A and HADS-D were significantly higher than the controls' (P < 0.0001). Twenty-two caregivers were diagnosed with manifesting anxiety, whereas 12 of them also presented depression. Highly educated caregivers were more prone to manifest increased levels of anxiety and depression. The increased psychological distress was further supported by the responses in the anxiety/depression dimension on the EQ-5D: 27 reported a moderate level of anxiety/depression and three indicated an extreme degree. The caregivers reported a mean EQ-VAS value of 61.9 ± 13.8 (range 40-100), with 10 caregivers rating their health status a score of 50 or lower; the controls scored significantly higher (90.3 ± 7.1; P < 0.0001).
CONCLUSION: The sample of caregivers we studied was psychologically burdened to a significant degree, a fact that obviously deteriorates their QOL. Appropriate psychopharmacological interventions are warranted to reduce caregivers' burden.

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Year:  2011        PMID: 21465330     DOI: 10.1007/s11136-011-9899-2

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


  29 in total

Review 1.  EQ-5D: a measure of health status from the EuroQol Group.

Authors:  R Rabin; F de Charro
Journal:  Ann Med       Date:  2001-07       Impact factor: 4.709

2.  Basic and escalating immunomodulatory treatments in multiple sclerosis: current therapeutic recommendations.

Authors:  H Wiendl; K V Toyka; P Rieckmann; R Gold; H-P Hartung; R Hohlfeld
Journal:  J Neurol       Date:  2008-10-29       Impact factor: 4.849

3.  Validity of the EuroQoL (EQ-5D) instrument in a Greek general population.

Authors:  Nick Kontodimopoulos; Evelina Pappa; Dimitris Niakas; John Yfantopoulos; Christina Dimitrakaki; Yannis Tountas
Journal:  Value Health       Date:  2008-05-16       Impact factor: 5.725

Review 4.  International comparisons in valuing EQ-5D health states: a review and analysis.

Authors:  Richard Norman; Paula Cronin; Rosalie Viney; Madeleine King; Deborah Street; Julie Ratcliffe
Journal:  Value Health       Date:  2009-08-20       Impact factor: 5.725

5.  Quality of life of primary caregivers of hospice patients with cancer.

Authors:  S C McMillan
Journal:  Cancer Pract       Date:  1996 Jul-Aug

6.  Caregiver quality of life in multiple sclerosis: a multicentre Italian study.

Authors:  F Patti; M P Amato; M A Battaglia; M Pitaro; P Russo; C Solaro; M Trojano
Journal:  Mult Scler       Date:  2007-01-29       Impact factor: 6.312

7.  Identifying the concerns of informal carers in palliative care.

Authors:  S Payne; P Smith; S Dean
Journal:  Palliat Med       Date:  1999-01       Impact factor: 4.762

8.  Quality of life among persons with multiple sclerosis and their caregivers.

Authors:  K J Aronson
Journal:  Neurology       Date:  1997-01       Impact factor: 9.910

9.  Informal caregiving in multiple sclerosis patients: data from the Madrid Demyelinating Disease Group study.

Authors:  Jesús Rivera-Navarro; José Manuel Morales-González; Julián Benito-León
Journal:  Disabil Rehabil       Date:  2003-09-16       Impact factor: 3.033

Review 10.  Assessment of caregiver burden in families of persons with multiple sclerosis.

Authors:  Marijean Buhse
Journal:  J Neurosci Nurs       Date:  2008-02       Impact factor: 1.230

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  9 in total

1.  Mental Health and Health-Related Quality of Life in Multiple Sclerosis Caregivers in Mexico.

Authors:  Gillian G Leibach; Marilyn Stern; Adriana Aguayo Arelis; Miguel Angel Macias Islas; Brenda Viridiana Rábago Barajas
Journal:  Int J MS Care       Date:  2016 Jan-Feb

2.  Moving beyond family: unequal burden across mental health patients' social networks.

Authors:  Lambert Zixin Li; Jason Yucheng Bian; Senhu Wang
Journal:  Qual Life Res       Date:  2021-02-10       Impact factor: 4.147

3.  Caregiver Burden in Primary Congenital Glaucoma.

Authors:  Aditi Kantipuly; Manju R Pillai; Sujani Shroff; Rakhee Khatiwala; Ganesh V Raman; S R Krishnadas; Alan Lee Robin; Joshua R Ehrlich
Journal:  Am J Ophthalmol       Date:  2019-05-10       Impact factor: 5.258

4.  Variation in the spillover effects of illness on parents, spouses, and children of the chronically ill.

Authors:  Tara A Lavelle; Eve Wittenberg; Kara Lamarand; Lisa A Prosser
Journal:  Appl Health Econ Health Policy       Date:  2014-04       Impact factor: 2.561

5.  How illness affects family members: a qualitative interview survey.

Authors:  Eve Wittenberg; Adrianna Saada; Lisa A Prosser
Journal:  Patient       Date:  2013       Impact factor: 3.883

6.  Care Partners and Multiple Sclerosis: Differential Effect on Men and Women.

Authors:  Tamara McKenzie; Mary Elizabeth Quig; Tuula Tyry; Ruth Ann Marrie; Gary Cutter; Edward Shearin; Kamau Johnson; James Simsarian
Journal:  Int J MS Care       Date:  2015 Nov-Dec

Review 7.  Disutility of illness for caregivers and families: a systematic review of the literature.

Authors:  Eve Wittenberg; Lisa A Prosser
Journal:  Pharmacoeconomics       Date:  2013-06       Impact factor: 4.981

8.  Mediational Model of Multiple Sclerosis Impairments, Family Needs, and Caregiver Mental Health in Guadalajara, Mexico.

Authors:  Melody N Mickens; Paul B Perrin; Adriana Aguayo; Brenda Rabago; Miguel A Macías-Islas; Juan Carlos Arango-Lasprilla
Journal:  Behav Neurol       Date:  2018-01-17       Impact factor: 3.342

9.  Assessment of the Burden of Multiple Sclerosis Patients' Caregivers in Saudi Arabia.

Authors:  Hussein Algahtani; Bader Shirah; Abdulrahman Bayazeed; Abdullah Alghamdi; Malik Almailabi; Mohammed Algharib; Faisal Alkahtani
Journal:  Cureus       Date:  2020-01-14
  9 in total

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