Clinical Investigation
Family Caregiving for Patients With Heart Failure: Types of Care Provided and Gender Differences

https://doi.org/10.1016/j.cardfail.2009.12.019Get rights and content

Abstract

Background

Knowledge about the potential burden for family caregivers related to the care of patients with heart failure (HF) is limited. The aims of the study were to compare the kind and amount of care provided by partners of HF patients and partners of healthy individuals and to examine the associations between gender and the performance of caregiving tasks.

Methods and Results

Caregiving tasks performed by 338 partners of HF patients were compared with those performed by 1202 partners of healthy individuals. Partners (age 70 ± 9, 76% female) of HF patients were more likely to provide personal care compared with partners (age 65 ± 7, 66% female) of healthy individuals after controlling for their age. However, the magnitude of the odds ratios (OR) differed by gender of partners (OR for male 6.7; 95% confidence interval [CI] 3.9–11.4; OR for female 3.7; 95% CI 2.7–5.1). Partners of HF patients were more likely to provide emotional care than partners of healthy individuals, controlling for age and gender (OR 2.4; 95% CI 1.5–3.6). Male partners of HF patients were more likely to provide personal care compared to female partners of HF patients (OR 1.9; 95% CI 1.1–3.2).

Conclusions

The care performed by partners of HF patients is above and beyond normal spousal assistance. The study underscores the crucial role of family caregivers in the care of HF patients and encourages health care providers to address the needs of both HF patients and their caregivers.

Section snippets

Participants and Procedure

A cross-sectional, comparative design was used to answer the research questions. Caregiving data obtained from a sample of partners of HF patients were compared with those from a reference group of individuals living with a healthy partner drawn from the general population in the Netherlands. The study was approved by the Central Ethics Committee and the investigation conformed to the principles outlined in the Declaration of Helsinki.

Response Rate

Among 1023 HF patients enrolled in the Coordinating study evaluating Outcomes of Advising and Counselling in Heart failure trial, 605 patients (59%) were married or living with a partner. At 12 months after the initial hospitalization, 441 questionnaires were sent out because 112 patients had died before 12 months and 52 partners were unable or refused to complete the questionnaires. Four hundred and seven partners (92%) returned the questionnaire. To make a comparison to the reference group,

Discussion

This is the first study conducted to compare the kind and amount of caregiving tasks performed by partners of HF patients with those of healthy individuals from the general population. Compared with partners of healthy individuals, partners of HF patients were significantly more likely to perform caregiving tasks to help their partner physically and emotionally. Partners of HF patients were more likely to provide personal care and emotional care compared with partners of healthy individuals

References (29)

  • M.L. Luttik et al.

    Marital status, quality of life, and clinical outcome in patients with heart failure

    Heart Lung

    (2006)
  • J.A. Bennett et al.

    Validity and reliability of the NYHA classes for measuring research outcomes in patients with cardiac disease

    Heart Lung

    (2002)
  • V. Konstam et al.

    Depression and anxiety in heart failure

    J Card Fail

    (2005)
  • American Heart Association. Heart disease and stroke statistics-2009 update. Dallas, TX;...
  • K. Dickstein et al.

    ESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2008: the task force for the diagnosis and treatment of acute and chronic heart failure 2008 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association of the ESC (HFA) and endorsed by the European Society of Intensive Care Medicine (ESICM)

    Eur J Heart Fail

    (2008)
  • T.R. Gure et al.

    Degree of disability and patterns of caregiving among older Americans with congestive heart failure

    J Gen Intern Med

    (2008)
  • M.L. Luttik et al.

    The importance and impact of social support on outcomes in patients with heart failure: an overview of the literature

    J Cardiovasc Nurs

    (2005)
  • G.J. Molloy et al.

    Family caregiving and congestive heart failure. Review and analysis

    Eur J Heart Fail

    (2005)
  • S.E. Karmilovich

    Burden and stress associated with spousal caregiving for individuals with heart failure

    Prog Cardiovasc Nurs

    (1994)
  • M.L. Luttik et al.

    Caregiver burden in partners of heart failure patients: limited influence of disease severity

    Eur J Heart Fail

    (2007)
  • T. Bakas et al.

    Family caregiving in heart failure

    Nurs Res

    (2006)
  • A.J. Walker et al.

    Informal caregiving to aging family members: a critical review

    Fam Relat

    (1995)
  • M. Hagedoorn et al.

    Failing in spousal caregiving: the ‘identity-relevant stress’ hypothesis to explain sex differences in caregiver distress

    Br J Health Psychol

    (2002)
  • M. Pinquart et al.

    Gender differences in caregiver stressors, social resources, and health: An updated meta-analysis

    J Gerontol B Psychol Sci Soc Sci

    (2006)
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    Supported by the Netherlands Heart Foundation (grant number NHF-2000Z003)

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