Literature DB >> 21411148

Descriptive study of partners' experiences of living with severe heart failure.

Christopher C Imes1, Cynthia M Dougherty, Gail Pyper, Mark D Sullivan.   

Abstract

PURPOSE: This qualitative study sought to describe the experiences of living with severe heart failure (HF) from the perspective of the partner.
METHODS: In-depth, semistructured interviews were conducted with 14 partners of individuals diagnosed with severe HF. Content analysis was performed to derive the main themes and subthemes of responses.
RESULTS: Three main themes were derived from the data: (1) My Experience of HF in My Loved One, (2) Experience With Healthcare Providers, and the (3) Patient's Experience of HF as Perceived by the Partner.
CONCLUSION: The severity of the patient's disease limited the partner's lifestyle, resulting in social isolation and difficulties in planning for the future for both the patient and the partner. The partners were unprepared to manage the disease burden at home without consistent information and assistance by healthcare providers. Moreover, end-of-life planning was neither encouraged by healthcare providers nor embraced by patients or partners.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21411148      PMCID: PMC3089716          DOI: 10.1016/j.hrtlng.2010.12.007

Source DB:  PubMed          Journal:  Heart Lung        ISSN: 0147-9563            Impact factor:   2.210


  28 in total

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4.  Living with heart failure: depression and quality of life in patients and spouses.

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5.  Family caregiving in heart failure.

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Review 7.  Cognitive deficits in patients with heart failure: a review of the literature.

Authors:  Susan J Bennett; Mary Jane Sauvé
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8.  Burden and stress associated with spousal caregiving for individuals with heart failure.

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9.  Family caregiver outcomes in heart failure.

Authors:  Susan J Pressler; Irmina Gradus-Pizlo; Suzanne D Chubinski; George Smith; Susanne Wheeler; Jingwei Wu; Rebecca Sloan
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10.  For better and for worse: Quality of life impaired in HF patients as well as in their partners.

Authors:  Marie Louise Luttik; Tiny Jaarsma; Nic J G M Veeger; Dirk J van Veldhuisen
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  8 in total

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Review 2.  The situation of caregivers in heart failure and their role in improving patient outcomes.

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Review 3.  Family caregiving for persons with heart failure at the intersection of heart failure and palliative care: a state-of-the-science review.

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4.  Competence, Compassion, and Care of the Self: Family Caregiving Needs and Concerns in Heart Failure.

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5.  Comparison of patient and partner quality of life and health outcomes in the first year after an implantable cardioverter defibrillator (ICD).

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6.  The Motivations of Iranian Patients With Cardiovascular Disease to Seek Health Information: A Qualitative Study.

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7.  Palliative care for patients with heart failure: facilitators and barriers - a cross sectional survey of German health care professionals.

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8.  'Who Cares?' The experiences of caregivers of adults living with heart failure, chronic obstructive pulmonary disease and coronary artery disease: a mixed methods systematic review.

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  8 in total

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