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Family Caregiver Heart Failure

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Introduction Heart failure is a difficult disease to manage; and every patient’s family experiences the disease uniquely. Caring for a sick family member is never an easy task. For years, families have relied on hospitals to care for sick loved ones; however some families need to care for their loved more than what just a hospital can facilitate. In the article “Family Caregivers’ Experiences of Caring for Patients with Heart Failure” by (Etemadifar et al., 2015, p.153-160) the level of evidence in this research article is a level IV. This type of level includes consensus panels and opinion of respected authorities.

Research Problem and Hypothesis
The research problem is the poor heath condition of the caregivers and patients with heart …show more content…
This is a qualitative research article without variables. The research design used here is descriptive in regards to the definition given; “the research is designed to describe in detail some process, event, or outcome. Such a design is used when very little is known about the research question or topic.” (Houser, 2015, p.474) This study does so by using twenty-one family caregivers from three educational hospitals composed of three heart wards and two-outpatient clinics. I believe this method was chosen due to the fact that there are not a lot of people out there to compare this study to. There is not a accurate was to have a control because anything can happen to the patient at any give time and it might not be able to be duplicated in a controlled environment. Also, it is hard to be able duplicate the process again because not all patients are the same and not all caregivers are …show more content…
In addition, they were caregivers to one family member only. “Caregivers with physical or psychological disorders or with communication difficulties were excluded from the study” (Etemadifar et al., 2015, p.153). All potential participants were selected by Shahram Etemadifar before study to affirm they were within the previously stated criteria and that they were cognitively competent to give informed consent. Subjects who were invited to participate portray a variation in their experiences with regard to age, gender, employment status, relationship to the patient, education, marital status, income and duration of caring. After consent was obtained, researchers using semi-structured, face-to-face interviews and field notes gathered additional information from each subject. All interviews took place in secluded settings in a secure site chosen by the participants. There were three interviews conducted at the participants’ place of work. There where also sixteen interviews conducted in the hospitals where the patients were seen. Then the last two interviews took place at the patient’s home. The participants were asked a serious of thought provoking questions, which lead to different questions based on answers provided. These interviews lasted over a period of six months. The steps in this study are not easily reproducible. There are memos to develop an audit trail

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