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Dissecting a qualitative study essay

The hospice, Dementia, Caregivers, Hospice Attention

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Excerpt from Essay:

United States, an estimated 5. a couple of million persons suffer from Alzheimer’s disease plus the number is definitely expected to increase dramatically above the next 3 decades (reviewed simply by Lewis, 2014). Dementia attention has as a result become a significant burden within the healthcare program and will only worsen as time passes. The costs of dementia treatment would be higher if not for the efforts made by family members caregivers, contributions which reduce the cost of care by nearly half, nevertheless the psychological and physical fee on caregivers has ended in additional medical expenses, getting an estimated $9. 1 billion for 2012. Care-giver support is definitely therefore necessary to lowering the overall cost of dementia care, nevertheless a number of obstacles exist which prevent maximum health final results for both patients and caregivers, including those interfering with timely referrals to the hospice care. Among the different limitations, those linked to physicians needs to be among the least complicated to change.

Even though a significant physique of study exists that has examined physician-associated barriers to hospice testimonials and end-of-life (EOL) care in general, zero qualitative studies have been performed which evaluated barriers in the perspective of informal caregivers. In other words, it was unclear whether these boundaries mattered to informal caregivers and dementia patients.

Study Purpose and Research Issue

The purpose of the analysis can be inferred from the initially question Lewis (2014) asked the study individuals: “Please identify for me your experiences searching for formal end-of-life care, and in particular hospice proper care, for your loved one. Please reveal any thoughts, feelings, and specific experiences” (p. 1224). As the author of this examine states, apart from this problem, all other questions were created to elaborate on this kind of main topic. Lewis (2014) was therefore interested in understanding the experiences of informal caregivers as they looked after a loved one experiencing end-stage dementia, and who tried to get hold of needed providers from their physicians.

Explicit research questions, apart from the one mentioned above, were not formulated simply by Lewis (2014) because the analyze design was phenomenological; nevertheless , five main themes appeared which concentrated and identified the issues the writer felt had been important. These types of themes were: “(a) a period of loss and frustration building up to the end of life; (b) a change in mentality when the caregiver becomes away from a curative way of thinking and begins to opt out of life-prolonging treatment options; (c) the impression that no one is there if the caregiver starts to seek palliative care options; (d) the feeling that hospice, when offered, is too small, too late; and

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