Literature DB >> 24453750

Self-reported burden among caregivers of patients with multiple sclerosis.

Shaloo Gupta1, Amir Goren1, Amy L Phillips1, Michelle Stewart1.   

Abstract

Multiple sclerosis (MS) and Alzheimer's disease (AD) are chronic and progressive diseases that may impose a significant burden on caregivers and patients' immediate families. Extensive research shows MS and AD caregiver burden on physical and mental health, but no direct comparisons between MS and AD caregivers have been reported in the literature. The objective of this study was to examine the extent of MS caregiver burden compared with that of noncaregivers and AD caregivers. Data were obtained from the 2009 National Health and Wellness Survey administered online to a US representative adult sample (N = 75,000). Respondents reported health status, quality of life, work productivity, health-care utilization, and caregiver status. Multivariable regressions, adjusting for key characteristics (eg, age, gender, marital status, depression), were conducted to explore differences between MS caregivers (n = 215) and noncaregivers (n = 69,224) and between MS caregivers and AD caregivers (n = 1341). The results indicated that MS caregivers had significantly greater activity impairment (P = .01), poorer mental (P = .015) and physical (P = .002) health status, lower health utility scores (P = .002), and more traditional health-care provider visits (P < .001), emergency room (ER) visits (P < .001), and hospitalizations (P = .001) than noncaregivers, adjusting for covariates. After adjustments, MS caregivers had greater activity impairment (P = .044), more ER visits (P = .017), and more hospitalizations (P = .008) than AD caregivers. Significant work productivity differences were not observed across groups, possibly owing to fewer employed respondents. Thus, in this study, MS caregivers had significantly more burden than noncaregivers, and for some measures, even AD caregivers. The results reveal the hidden toll on those providing care for MS patients and highlight the need for health-care providers to recognize their burden so that appropriate measures can be implemented.

Entities:  

Year:  2012        PMID: 24453750      PMCID: PMC3882984          DOI: 10.7224/1537-2073-14.4.179

Source DB:  PubMed          Journal:  Int J MS Care        ISSN: 1537-2073


  34 in total

1.  The validity and reproducibility of a work productivity and activity impairment instrument.

Authors:  M C Reilly; A S Zbrozek; E M Dukes
Journal:  Pharmacoeconomics       Date:  1993-11       Impact factor: 4.981

2.  Daily negative interactions and mood among patients and partners dealing with multiple sclerosis (MS): the moderating effects of emotional support.

Authors:  Annet M Kleiboer; Roeline G Kuijer; Joop J Hox; Peter J H Jongen; Stephan T F M Frequin; Jozien M Bensing
Journal:  Soc Sci Med       Date:  2006-09-29       Impact factor: 4.634

3.  Caregiver burden among informal caregivers assisting people with multiple sclerosis.

Authors:  Robert J Buchanan; Dagmar Radin; Chunfeng Huang
Journal:  Int J MS Care       Date:  2011

4.  National estimates of the quantity and cost of informal caregiving for the elderly with dementia.

Authors:  K M Langa; M E Chernew; M U Kabeto; A R Herzog; M B Ofstedal; R J Willis; R B Wallace; L M Mucha; W L Straus; A M Fendrick
Journal:  J Gen Intern Med       Date:  2001-11       Impact factor: 5.128

5.  Loneliness and depression in caregivers of persons with Alzheimer's disease or related disorders.

Authors:  R Beeson; S Horton-Deutsch; C Farran; M Neundorfer
Journal:  Issues Ment Health Nurs       Date:  2000-12       Impact factor: 1.835

6.  Caregiving as a risk factor for mortality: the Caregiver Health Effects Study.

Authors:  R Schulz; S R Beach
Journal:  JAMA       Date:  1999-12-15       Impact factor: 56.272

7.  Assessing mood in patients with multiple sclerosis.

Authors:  Madeleine J Groom; Nadina B Lincoln; Valerie M Francis; Talal F Stephan
Journal:  Clin Rehabil       Date:  2003-12       Impact factor: 3.477

8.  Multiple sclerosis.

Authors:  Alastair Compston; Alasdair Coles
Journal:  Lancet       Date:  2008-10-25       Impact factor: 79.321

9.  Impact of recently diagnosed multiple sclerosis on quality of life, anxiety, depression and distress of patients and partners.

Authors:  A C J W Janssens; P A van Doorn; J B de Boer; F G A van der Meché; J Passchier; R Q Hintzen
Journal:  Acta Neurol Scand       Date:  2003-12       Impact factor: 3.209

10.  Huntington's disease from the patient, caregiver and physician's perspectives: three sides of the same coin?

Authors:  Krzysztof Banaszkiewicz; Emilia J Sitek; Monika Rudzińska; Witold Sołtan; Jarosław Sławek; Andrzej Szczudlik
Journal:  J Neural Transm (Vienna)       Date:  2012-03-08       Impact factor: 3.575

View more
  14 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.  Quantifying the burden of informal caregiving for patients with cancer in Europe.

Authors:  Amir Goren; Isabelle Gilloteau; Michael Lees; Marco DaCosta Dibonaventura
Journal:  Support Care Cancer       Date:  2014-02-05       Impact factor: 3.603

3.  The Experiences of Multiple Sclerosis Patients' Family Caregivers at the First Hospitalization of Their Patients: A Qualitative Study.

Authors:  Banafsheh Tehranineshat; Shahrzad Yektatalab; Marzieh Momennasab; Mostafa Bijani; Fateme Mohammadi
Journal:  Patient Prefer Adherence       Date:  2020-07-13       Impact factor: 2.711

4.  Association of Unemployment and Informal Care with Stigma in Multiple Sclerosis: Evidence from the Survey on Living with Neurological Conditions in Canada.

Authors:  Celestin Hategeka; Anthony L Traboulsee; Katrina McMullen; Larry D Lynd
Journal:  Int J MS Care       Date:  2019 Sep-Oct

5.  Daily activity level improvement with antidepressant medications predicts long-term clinical outcomes in outpatients with major depressive disorder.

Authors:  Manish K Jha; Raymond B Teer; Abu Minhajuddin; Tracy L Greer; A John Rush; Madhukar H Trivedi
Journal:  Neuropsychiatr Dis Treat       Date:  2017-03-15       Impact factor: 2.570

6.  Under-Treatment of Patients with Moderate to Severe Psoriasis in the United States: Analysis of Medication Usage with Health Plan Data.

Authors:  April W Armstrong; J Will Koning; Simon Rowse; Huaming Tan; Carla Mamolo; Mandeep Kaur
Journal:  Dermatol Ther (Heidelb)       Date:  2016-11-30

7.  Self-reported burden of caregiver of adults with depression: a cross-sectional study in five Western European countries.

Authors:  B L Balkaran; D H Jaffe; D Umuhire; B Rive; R U Milz
Journal:  BMC Psychiatry       Date:  2021-06-21       Impact factor: 3.630

8.  Costs of formal and informal home care and quality of life for patients with multiple sclerosis in sweden.

Authors:  Marianne Svensson; Liberty Fajutrao
Journal:  Mult Scler Int       Date:  2014-03-04

9.  Impact of caring for persons with Alzheimer's disease or dementia on caregivers' health outcomes: findings from a community based survey in Japan.

Authors:  Amir Goren; William Montgomery; Kristin Kahle-Wrobleski; Tomomi Nakamura; Kaname Ueda
Journal:  BMC Geriatr       Date:  2016-06-10       Impact factor: 3.921

10.  Improving communication with multiple sclerosis patients.

Authors:  Raed A Alroughani
Journal:  Neurosciences (Riyadh)       Date:  2015-04       Impact factor: 0.735

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.