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Progression of dementia in elderly patients nursing assignment help
How the progression of dementia in elderly patients affect the family relationships of
informal carers in the UKAbstractThe purpose of this research is to analyze the effects of
dementia on informal carersā€™ relationships with their loved ones. Understanding the
demands placed on both the person with dementia and the person providing informal care
is essential for meeting the needs of both parties. Many studies and institutions focus only
on the needs of patients, rather than the needs of the informal carers. This study highlights
the need and requirement of providing supplementary assistance to informal carers. The
research analyzed and compared data from several sources in a systematic literature
review to provide an answer to the question.The findings indicated that in order to prevent
strained relationships with their loved ones, carers need additional knowledge on how to
manage the sickness and the stress brought on by the weight of the illness. We hypothesize
that Assistive Technology might be useful for lowering healthcare costs by improving access
to specialists in areas such as diagnosis, medication, and mental health treatment, as well as
easing the burden on primary care physicians. Case managers may also keep track of
patients and help family members all along the care pathway: they do this by collecting and
sharing information with the different health professionals involved, in this specific
instance the informal caregivers. In order to meet the needs of families dealing with
dementia, further study is needed to determine whether certain teaching strategies for
informal care providers could be optimal. Get your nursing assignment help today.Table of
ContentsChapter 1: Introduction 4References 5Chapter 1:
IntroductionBackgroundDementia, as described by Duong et al. (2017), is a clinical illness
characterized by gradual deterioration in cognitive abilities that eventually compromises an
individualā€™s capacity to carry out daily tasks without assistance. Dementia makes people
more reliant on others, both emotionally and physically, as pointed out by Cunningham et
al. (2015). According to Gale et al. (2018), primary neurologic, medical, and
neuropsychiatric disorders all contribute to the development of dementia.
Neurodegenerative dementias like Alzheimer disease and Lewy body dementia are very
frequent among the elderly. According to the latest data, there were around 850,000
persons living with dementia in the UK in 2019. It was 1 in every 14 adults over the age of
65 (Alzheimer society, 2020).Introduction Alzheimerā€™s disease and dementia are similar in
that they both cause a slow but steady decline in mental capacity. Dementia patientsā€™
reliance on others for care grows as the disease progresses. As the frequency and intensity
of symptoms rise, it becomes more difficult to go about everyday life and take part in social
activities. Because of this, there may be instances when a person needs constant attention.
Care may be required for a long time since the sickness itself might last for years (on
average, seven) (Molsa et al., 1986).Dementia rates are set to rise following the ageing of the
world population (Zwaanswijk et al., 2013). However, the supply of medical experts is not
likely to increase to cater for the needs of an ageing population. Dementia patients will,
therefore, rely more and more on their informal carers which include relatives and friends.
While a person with dementia is admitted to a long-term care facility, they will continue to
get the same kind of care they had when they were living at home (Turcotte, 2013). When
care is given regularly or for an extended length of time, the emotional and physical health
of the carer may suffer (Turcotte, 2013). In particular, the length of time spent providing
care before to a loved oneā€™s admittance into a nursing home was the most significant
predictor of how much less of a burden a loved one would feel thereafter. Caregiver sadness
and patient behavioral change ratings were the most important factors in determining
when and whether a person with dementia will be institutionalized (Yeh et al., 2002).
Caregiving may seem more burdensome since it takes longer and there are more people
who need it.The stress of caring for someone with dementia is compounded by the fact that
informal caregivers must adjust to the personā€™s condition and behavioral changes. Dementia
is a degenerative disease with an uncertain course, which presents significant difficulties for
informal carers. Caregivers reported a variety of losses at various levels of the family and
utilized a wide range of strategies to deal with grief and keep the family unit functioning
(Coelho et al., 2007). The majority of carers report receiving little to no informal assistance,
are unfamiliar with official services, and struggle to anticipate their loved oneā€™s care
requirements. Caregiver reports of inadequate preparation to offer care. Therefore, it is
crucial to provide assistance to informal carers so as to improve their quality of life and
forestall severe caregiver stress. ā€˜Alzheimer meeting locations for patients and familiesā€™ are
only one example of the many professional support services offered in the Netherlands and
elsewhere in Western Europe for those affected by Alzheimerā€™s disease (Bos, 2008). Despite
this, many informal carersā€™ support requirements go unfulfilled because they either cannot
access the resources they need or believe that the professional care they get is not
adequately tailored to their specific situation (Parveen, Peltier & Oyebode, 2017).Role of
informal carers in the care of older people: https://writinghelpsite.com/tag/nursing-
assignment-help/ Negative outcomes are often linked to informal caring. Caregiving has no
harmful consequences at first [Metzelthin et al., 2017]. However, the burden on caregivers
grows as a result of a number of factors [Metzelthin et al., 2017]. These include the care
recipientā€™s increased morbidities and disability levels, the length of time the caregiver
spends providing care, the number of tasks the caregiver must perform, the type of care
provided (in-home versus institutional), and the caregiverā€™s gender and age. Organizational
factors (e.g., received assistance), caregiver autonomy, and caregiving needs all have a role
in the quality of life of informal carers [Farina et al., 2017]. In British, the average period
spent caring for an older relative is considered to be somewhere between two and eight
years [Emrich et al., 2012]. It might be a very lengthy period with plenty of unexpected
difficulties. It is possible that organizational and structural factors, rather than emotional
motivations like a feeling of obligation, play a role in the choice to offer informal care. For
this reason, it is important for decision-makers to have insight into the preferences, wants,
and desires of informal carers in order to design care structures that are conducive to the
lifestyles of all parties and that seamlessly integrate care into the homes of (possible)
caregivers. If you need criminology assignment help, visit the top writing
service.individuals may be more likely to care for a care-dependent person informally if
there are organizational and structural changes that make day-to-day caregiving easier and
if there are incentives. Outpatient care structures could be improved by making care
arrangements fit the wants and needs of unpaid caregivers about how care for the elderly is
set up. Due to population shifts, there are now more people in need of nursing care due to
their advanced age and weak condition. This deterioration in health is followed by an all-
encompassing process of adjusting to new circumstances on the part of the elderly and their
loved ones. A preventative strategy to care planning is required to satisfy the demand for
the altered service use and the load limit or breaking point for carers [Klinidtworth et al.,
2017]. However, understanding the motivations of informal carers is crucial for taking their
load limit and prospective capabilities into consideration. As a result, we conducted a
literature review to learn more about the wants and needs of informal caregivers. This
study explores in depth how the British people feels about caring for the elderly and their
expected willingness to do so. [De Jong et al., 2020].Being a caretaker in an informal setting
may be quite taxing. Many people become caregivers without adequately preparing for the
responsibilities involved, and they may not have many other options. This might be due to a
moral or legal need to give care, a lack of formal alternatives, or a lack of knowledge about
available options. Caregivers also incur substantial additional expenses due to the
intangible nature of informal caregiving. These include the health effects of the physical and
psychological load endured and the potential costs of missed wages, jobs, and pension
benefits. Caregivers who do not get sufficient assistance may experience financial hardship,
health problems, and feelings of loneliness as a result of providing unpaid care. More than a
thousand family caregivers from around Europe were surveyed by COFACE Families Europe
in 2017. The degree to which informal caregivers are impacted by these difficulties varies
according to factors such as the kind of care regime in which they participate, the
caregiverā€™s life stage when they take on this role, and the caregiverā€™s access to resources and
decision-making power.Research question as shown at
https://epicessayhelp.com/tag/education-assignment-help/Aimsobjectives,Caregiver
perspectives on the benefits and drawbacks of their work, as well as the factors that
contribute to a favourable or bad experience in their interactions with patientsā€™ families,
will be included in a comprehensive study.Role conflict theory in care givingStephens and
Franksā€™s (1999) conflicting demands hypothesis and Goodeā€™s (1960) scarcity model of role
theory is both based on the idea that individuals have scarce time and energy to do all of
their duties. Role conflict occurs when distinct positions have conflicting demands, while
role strain occurs when people feel burdened, exhausted, or tense as a consequence of
juggling all of their responsibilities. Role conflict arises, according to scarcity theory, when
the responsibilities of one role (such as job) interfere with those of another (such as caring
for an elderly loved one). A woman who is both a full-time employee and a caregiver for an
elderly family member has a lot on her plate. As a result, she may experience role conflict, in
which she must choose between her numerous duties, and role overload, in which she is
unable to fulfill all of her tasks. The focus of this work is on the relationship between CIW
and WIC and role strain, in this instance, caregiving burden and job stress, even though both
role overload and role conflict contribute to role strain (Cooper et al., 2001).. Role tension,
or role strain, was identified by MacEwen and Barling (1991) as a result of juggling paid
employment outside the house with the responsibility of caring for young children. Because
of the unpredictable nature of having to care for an elderly loved one, the fact that these
responsibilities often arise out of the blue and without warning, that they often grow in
complexity and scope over time, and that they are often triggered by unexpected events like
a health crisis, working with and caring for the elderly can be a very demanding experience.
Consistent with the hypothesis that role conflict causes role strain This research adds
significantly to the existing body of knowledge in three key ways as suggested at nursing
expert writers.The findings of the study by Gordon et al. (2012) indicate evidence for two
separate variables, WIC and CIW, each with its own set of antecedents and outcomes,
lending credence to a bidirectional perspective of workā€“caregiving conflict. Overall, the
findings indicate that older working women face stress due to the dual obligations of caring
and employment. The demands of the workplace are a significant factor in determining
whether or not caring interferes with work (CIW) or the caregiving burden (WIC) or the
work load (WB). However, the effects of caring obligations are confined to the domestic
sphere (Gordon et al., 2012). Together, these pressures cause older working women a great
deal of stress and tension between their careers and their caring responsibilities. These
findings contribute to the research on the challenges that older women face in caregiving
and the workforce.Workplace pressures have far-reaching impacts (Glasgow & Zoucha,
2011) that affect not just job role strain but also caregiving role strain. When caring
obligations expand, older women may see their work as more fundamental to their identity,
which may have a negative effect on other areas of their lives and lead to difficult mental
and behavioral shifts. Findings from a 2012 study by Gordon et al. demonstrate the value of
social support in alleviating stress for older women who are also caregivers in and out of
the workplace. Given the negative correlations between instrumental support for caregivers
and load, and between emotional support at work and stress, it is clear that social support is
essential for mitigating these undesirable results. There may be some overlap between the
degree of help employees receive at work and how much work they really have to complete,
as shown by Gordon et al. (2012)ā€™s concept of work-interfering-with-caregiving (WIC). For
caregivers, it is tremendously beneficial to have aid in both the professional and family
realms. See https://nursingexpertwriters.com/tag/my-nursing-assignment-help/ for
more.Caregiver stress is strongly correlated with the length of caring and the degree of
patient dependence. Care load is also based on the patientā€™s reliance degree, which is
influenced by their cognitive and behavioral impairments. The trajectory of a particular
diseaseā€™s treatment and the social support requirements of both the patient and the
caregiver ought to be taken into account when designing interventions to alleviate burden.
Changing gender norms so that males take on more responsibility around the home might
ease the heavy load women carry.

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Progression of dementia in elderly patients nursing assignment help.docx

  • 1. Progression of dementia in elderly patients nursing assignment help How the progression of dementia in elderly patients affect the family relationships of informal carers in the UKAbstractThe purpose of this research is to analyze the effects of dementia on informal carersā€™ relationships with their loved ones. Understanding the demands placed on both the person with dementia and the person providing informal care is essential for meeting the needs of both parties. Many studies and institutions focus only on the needs of patients, rather than the needs of the informal carers. This study highlights the need and requirement of providing supplementary assistance to informal carers. The research analyzed and compared data from several sources in a systematic literature review to provide an answer to the question.The findings indicated that in order to prevent strained relationships with their loved ones, carers need additional knowledge on how to manage the sickness and the stress brought on by the weight of the illness. We hypothesize that Assistive Technology might be useful for lowering healthcare costs by improving access to specialists in areas such as diagnosis, medication, and mental health treatment, as well as easing the burden on primary care physicians. Case managers may also keep track of patients and help family members all along the care pathway: they do this by collecting and sharing information with the different health professionals involved, in this specific instance the informal caregivers. In order to meet the needs of families dealing with dementia, further study is needed to determine whether certain teaching strategies for informal care providers could be optimal. Get your nursing assignment help today.Table of ContentsChapter 1: Introduction 4References 5Chapter 1: IntroductionBackgroundDementia, as described by Duong et al. (2017), is a clinical illness characterized by gradual deterioration in cognitive abilities that eventually compromises an individualā€™s capacity to carry out daily tasks without assistance. Dementia makes people more reliant on others, both emotionally and physically, as pointed out by Cunningham et al. (2015). According to Gale et al. (2018), primary neurologic, medical, and neuropsychiatric disorders all contribute to the development of dementia. Neurodegenerative dementias like Alzheimer disease and Lewy body dementia are very frequent among the elderly. According to the latest data, there were around 850,000 persons living with dementia in the UK in 2019. It was 1 in every 14 adults over the age of 65 (Alzheimer society, 2020).Introduction Alzheimerā€™s disease and dementia are similar in that they both cause a slow but steady decline in mental capacity. Dementia patientsā€™ reliance on others for care grows as the disease progresses. As the frequency and intensity of symptoms rise, it becomes more difficult to go about everyday life and take part in social
  • 2. activities. Because of this, there may be instances when a person needs constant attention. Care may be required for a long time since the sickness itself might last for years (on average, seven) (Molsa et al., 1986).Dementia rates are set to rise following the ageing of the world population (Zwaanswijk et al., 2013). However, the supply of medical experts is not likely to increase to cater for the needs of an ageing population. Dementia patients will, therefore, rely more and more on their informal carers which include relatives and friends. While a person with dementia is admitted to a long-term care facility, they will continue to get the same kind of care they had when they were living at home (Turcotte, 2013). When care is given regularly or for an extended length of time, the emotional and physical health of the carer may suffer (Turcotte, 2013). In particular, the length of time spent providing care before to a loved oneā€™s admittance into a nursing home was the most significant predictor of how much less of a burden a loved one would feel thereafter. Caregiver sadness and patient behavioral change ratings were the most important factors in determining when and whether a person with dementia will be institutionalized (Yeh et al., 2002). Caregiving may seem more burdensome since it takes longer and there are more people who need it.The stress of caring for someone with dementia is compounded by the fact that informal caregivers must adjust to the personā€™s condition and behavioral changes. Dementia is a degenerative disease with an uncertain course, which presents significant difficulties for informal carers. Caregivers reported a variety of losses at various levels of the family and utilized a wide range of strategies to deal with grief and keep the family unit functioning (Coelho et al., 2007). The majority of carers report receiving little to no informal assistance, are unfamiliar with official services, and struggle to anticipate their loved oneā€™s care requirements. Caregiver reports of inadequate preparation to offer care. Therefore, it is crucial to provide assistance to informal carers so as to improve their quality of life and forestall severe caregiver stress. ā€˜Alzheimer meeting locations for patients and familiesā€™ are only one example of the many professional support services offered in the Netherlands and elsewhere in Western Europe for those affected by Alzheimerā€™s disease (Bos, 2008). Despite this, many informal carersā€™ support requirements go unfulfilled because they either cannot access the resources they need or believe that the professional care they get is not adequately tailored to their specific situation (Parveen, Peltier & Oyebode, 2017).Role of informal carers in the care of older people: https://writinghelpsite.com/tag/nursing- assignment-help/ Negative outcomes are often linked to informal caring. Caregiving has no harmful consequences at first [Metzelthin et al., 2017]. However, the burden on caregivers grows as a result of a number of factors [Metzelthin et al., 2017]. These include the care recipientā€™s increased morbidities and disability levels, the length of time the caregiver spends providing care, the number of tasks the caregiver must perform, the type of care provided (in-home versus institutional), and the caregiverā€™s gender and age. Organizational factors (e.g., received assistance), caregiver autonomy, and caregiving needs all have a role in the quality of life of informal carers [Farina et al., 2017]. In British, the average period spent caring for an older relative is considered to be somewhere between two and eight years [Emrich et al., 2012]. It might be a very lengthy period with plenty of unexpected difficulties. It is possible that organizational and structural factors, rather than emotional motivations like a feeling of obligation, play a role in the choice to offer informal care. For
  • 3. this reason, it is important for decision-makers to have insight into the preferences, wants, and desires of informal carers in order to design care structures that are conducive to the lifestyles of all parties and that seamlessly integrate care into the homes of (possible) caregivers. If you need criminology assignment help, visit the top writing service.individuals may be more likely to care for a care-dependent person informally if there are organizational and structural changes that make day-to-day caregiving easier and if there are incentives. Outpatient care structures could be improved by making care arrangements fit the wants and needs of unpaid caregivers about how care for the elderly is set up. Due to population shifts, there are now more people in need of nursing care due to their advanced age and weak condition. This deterioration in health is followed by an all- encompassing process of adjusting to new circumstances on the part of the elderly and their loved ones. A preventative strategy to care planning is required to satisfy the demand for the altered service use and the load limit or breaking point for carers [Klinidtworth et al., 2017]. However, understanding the motivations of informal carers is crucial for taking their load limit and prospective capabilities into consideration. As a result, we conducted a literature review to learn more about the wants and needs of informal caregivers. This study explores in depth how the British people feels about caring for the elderly and their expected willingness to do so. [De Jong et al., 2020].Being a caretaker in an informal setting may be quite taxing. Many people become caregivers without adequately preparing for the responsibilities involved, and they may not have many other options. This might be due to a moral or legal need to give care, a lack of formal alternatives, or a lack of knowledge about available options. Caregivers also incur substantial additional expenses due to the intangible nature of informal caregiving. These include the health effects of the physical and psychological load endured and the potential costs of missed wages, jobs, and pension benefits. Caregivers who do not get sufficient assistance may experience financial hardship, health problems, and feelings of loneliness as a result of providing unpaid care. More than a thousand family caregivers from around Europe were surveyed by COFACE Families Europe in 2017. The degree to which informal caregivers are impacted by these difficulties varies according to factors such as the kind of care regime in which they participate, the caregiverā€™s life stage when they take on this role, and the caregiverā€™s access to resources and decision-making power.Research question as shown at https://epicessayhelp.com/tag/education-assignment-help/Aimsobjectives,Caregiver perspectives on the benefits and drawbacks of their work, as well as the factors that contribute to a favourable or bad experience in their interactions with patientsā€™ families, will be included in a comprehensive study.Role conflict theory in care givingStephens and Franksā€™s (1999) conflicting demands hypothesis and Goodeā€™s (1960) scarcity model of role theory is both based on the idea that individuals have scarce time and energy to do all of their duties. Role conflict occurs when distinct positions have conflicting demands, while role strain occurs when people feel burdened, exhausted, or tense as a consequence of juggling all of their responsibilities. Role conflict arises, according to scarcity theory, when the responsibilities of one role (such as job) interfere with those of another (such as caring for an elderly loved one). A woman who is both a full-time employee and a caregiver for an elderly family member has a lot on her plate. As a result, she may experience role conflict, in
  • 4. which she must choose between her numerous duties, and role overload, in which she is unable to fulfill all of her tasks. The focus of this work is on the relationship between CIW and WIC and role strain, in this instance, caregiving burden and job stress, even though both role overload and role conflict contribute to role strain (Cooper et al., 2001).. Role tension, or role strain, was identified by MacEwen and Barling (1991) as a result of juggling paid employment outside the house with the responsibility of caring for young children. Because of the unpredictable nature of having to care for an elderly loved one, the fact that these responsibilities often arise out of the blue and without warning, that they often grow in complexity and scope over time, and that they are often triggered by unexpected events like a health crisis, working with and caring for the elderly can be a very demanding experience. Consistent with the hypothesis that role conflict causes role strain This research adds significantly to the existing body of knowledge in three key ways as suggested at nursing expert writers.The findings of the study by Gordon et al. (2012) indicate evidence for two separate variables, WIC and CIW, each with its own set of antecedents and outcomes, lending credence to a bidirectional perspective of workā€“caregiving conflict. Overall, the findings indicate that older working women face stress due to the dual obligations of caring and employment. The demands of the workplace are a significant factor in determining whether or not caring interferes with work (CIW) or the caregiving burden (WIC) or the work load (WB). However, the effects of caring obligations are confined to the domestic sphere (Gordon et al., 2012). Together, these pressures cause older working women a great deal of stress and tension between their careers and their caring responsibilities. These findings contribute to the research on the challenges that older women face in caregiving and the workforce.Workplace pressures have far-reaching impacts (Glasgow & Zoucha, 2011) that affect not just job role strain but also caregiving role strain. When caring obligations expand, older women may see their work as more fundamental to their identity, which may have a negative effect on other areas of their lives and lead to difficult mental and behavioral shifts. Findings from a 2012 study by Gordon et al. demonstrate the value of social support in alleviating stress for older women who are also caregivers in and out of the workplace. Given the negative correlations between instrumental support for caregivers and load, and between emotional support at work and stress, it is clear that social support is essential for mitigating these undesirable results. There may be some overlap between the degree of help employees receive at work and how much work they really have to complete, as shown by Gordon et al. (2012)ā€™s concept of work-interfering-with-caregiving (WIC). For caregivers, it is tremendously beneficial to have aid in both the professional and family realms. See https://nursingexpertwriters.com/tag/my-nursing-assignment-help/ for more.Caregiver stress is strongly correlated with the length of caring and the degree of patient dependence. Care load is also based on the patientā€™s reliance degree, which is influenced by their cognitive and behavioral impairments. The trajectory of a particular diseaseā€™s treatment and the social support requirements of both the patient and the caregiver ought to be taken into account when designing interventions to alleviate burden. Changing gender norms so that males take on more responsibility around the home might ease the heavy load women carry.