Dalton city IL adult personals

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Dalton city IL adult personals

Hughes RG, editor. Susan C. Authors Susan C. Most patients have families that are providing some level of care and support. Family caregiving raises safety issues in two ways that should concern nurses in all settings. Second, family caregivers are unpaid providers who often need help to learn how to become competent, safe volunteer workers who can better protect their family members i. This chapter summarizes patient safetyand quality evidence from both of these perspectives.

The focus is on the adult caregiver who provides care and support primarily for adults with chronic illnesses and chronic health problems. The focus is not on those with developmental disabilities. In the first section, we discuss the evidence for protecting the caregiver from harm. The second section addresses research aimed at protecting the care recipient from an ill-prepared family caregiver.

For centuries, family members have provided care and support to each other during times of illness.

Dalton city IL adult personals

Who are these family caregivers, what do they do, and what harm do they face? What does the research tell us about ways to assess the needs of these hidden patients and evidence-based interventions to prevent or reduce potential injury and harm? This section answers these questions and highlights the need for nurses to proactively approach family caregivers as clients who need their support in their own right. The terms family caregiver and informal caregiver refer to an unpaid family member, friend, or neighbor who provides care to an individual who has an acute or chronic condition and needs assistance to manage a variety of tasks, from bathing, dressing, and taking medications to tube feeding and ventilator care.

Recent surveys estimate there are 44 million caregivers over the age of 18 years approximately one in every five adults. Those caring for someone 50 years or older are 47 years old—on average—and working at least part-time. About two out of three older care recipients get help from only one unpaid caregiver. Caregivers spend a substantial amount of time interacting with their care recipients, while providing care in a wide range of activities.

Nurses have a limited view of this interaction. Caregiving can last for a short period of postacute care, especially after a hospitalization, to more than 40 years of ongoing care for a person with chronic care needs. On average, informal caregivers devote 4. More than half of family caregivers provide 8 hours of care or more every week, and one in five provides more than 40 hours per week.

Dalton city IL adult personals

Most researchers in the caregiving field conceptualize the care that family members give as assistance with activities of daily living ADLs and instrumental activities of daily living IADLs. But those concepts do not adequately capture the complexity and stressfulness of caregiving. Supervising people with dementia and observing for early s of problems, such as medication side effects, are serious responsibilities as family members are often unable to interpret the meaning or the urgency.

Family caregivers often feel unprepared to provide care, have inadequate knowledge to deliver proper care, and receive little guidance from the formal health care providers. Due to inadequate knowledge and skill, family caregivers may be unfamiliar with the type of care they must provide or the amount of care needed.

Family caregivers may not know when they need community resources, and then may not know how to access and best utilize available resources. Caregivers get very little help from health careprofessionals in managi ng their tasks and the emotional demands of caregiving.

Health professionals in emergency departments and inpatient hospital settings do not adequately determine the after-care needs of older patients when they are being discharged. Effective discharge planning is impeded by gaps in communication between the hospital and community interface, such as illegible discharge summaries and delays in sending information to the physician. Many caregivers felt abandoned at a critical time, and none of the focus group participants had been referred by any health care professional in the hospital to community-based organizations for emotional support—or any other kind of support.

Caregivers are hidden patients themselves, with serious adverse physical and mental health consequences from their physically and emotionally demanding work as caregivers and reduced attention to their own health and health care. Declines in physical health and premature death among caregivers in general have been reported. Elderly spouses who experience stressful caregiving demands have a 63 percent higher mortality rate than their noncaregiver age-peers.

Declines in caregiver health have been particularly associated with caregivers who perceive themselves as burdened. Burton and colleagues 38 examined the relationships between provision of care by family members and their health behaviors and health maintenance. These researchers found that, with a high level of caregiving activities, the odds of the caregiver not getting rest, not having time to exercise, and actually not recuperating from illness were also high.

In addition, caregivers were more likely to forget to take their prescriptions for their own chronic illnesses. Providing care poses a threat to the overall health of caregivers, which can compromise their ability to continue to be caregivers. If caregivers are to continue to be able to provide care, relief from the distress and demands of maintaining the required care must be considered. Both highly negative and highly positive consequences of providing care may exist simultaneously. Picot and colleagues 4142 worked primarily with African American caregivers and found that the rewards perceived by caregivers were more important than coping.

A specific Picot Caregiver Reward Scale of 25 items exists and has been widely used to show that both rewards and costs can exist in the same care situation.

Dalton city IL adult personals

Caregivers who attempt to balance caregiving with their other activities, such as work, family, and leisure, may find it difficult to focus on the positive aspects of caregiving and often experience more negative reactions, such as an increased sense of burden. They have difficulty maintaining work roles while assisting family members. Low personal and household incomes and limited financial resources can result in increased caregiver risk for negative outcomes, particularly if there are substantial out-of-pocket costs for care recipient needs. Overall, financial concerns cause particular distress for caregivers during long treatment periods, 5253 as resources become depleted.

Higher-income families, with greater financial resources to purchase needed care, might not become as distressed or burdened as those with limited resources. Caregiver burden and depressive symptoms are the most common negative outcomes of providing care for the elderly and chronically ill.

The constant concern for managing disruptive behaviors such as turning on stoves, walking into the street, taking too many pills, yelling, screaming, or cursing also affects the caregivers negatively.

Dalton city IL adult personals

Caregivers may suffer severe fluctuations in sleep patterns over time, which may affect depression 65 and exacerbate symptoms of chronic illnesses. Pain management is an intractable problem for caregivers that in substantial caregiver distress, as caregivers assist with both nonpharmacologic and pharmacologic pain-management strategies.

The literature provides substantial evidence that caregivers are hidden patients in need of protection from physical and emotional harm. Interventions directed to the family caregiver should serve two purposes see Evidence Table. First, interventions can support the caregiver as client, directly reducing caregiver distress and the overall impact on their health and well-being. In this intervention approach, the caregiver is the recipient of the direct benefit and the patient benefits only secondarily.

Second, interventions can be aimed to help make the caregiver become more competent and confident, providing safe and effective care to the patient, which can indirectly reduce caregiver distress by reducing their load or increasing their sense of certainty and control.

Dalton city IL adult personals

In this section, we focus on the research evidence supporting caregivers as clients. Despite the importance of information and support to help family caregivers, studies on interventions to increase support for family caregivers have lagged far behind those provided for patients. Few randomized clinical trials of educational interventions directed toward family caregivers have been conducted or published, and there is limited research to inform us about skills training for caregivers to prevent back injuries, infection, and other potential risks inherent in the caregiver situation.

Recent meta-analyses of caregiver interventions found mixedwhich are important to note. Multicomponent interventions, rather than single interventions like support groups or education, ificantly reduced burden. Reasons for this are unclear.

The effectiveness of caregiver interventions lasts approximately 7 months. Few studies are funded for long-term followup. Comprehensive counseling sessions for spouses caring for a person with dementia help reduce depression.

Dalton city IL adult personals

An automated, interactive voice-response telephone support system for caregivers reduced burden for those caregivers with a lower sense of control over their situation. Home visits and enhanced social support also can help reduce caregiver depression. Zarit and colleagues 79 used a quasi-experimental de to demonstrate that caregivers who used adult day care services for their relatives with dementia had ificantly lower levels of caregiver stress, anger, and depression after 3 months of this respite care than a control group of similar caregivers who did not obtain this intervention.

Smeenk and colleagues 80 investigated the quality of life of family caregivers who received a home care intervention that consisted of a specialist nurse coordinator, a hour nurse telephone service with access to a home care team, a collaborative home care dossier and case file, and care protocols.

The care dossier was used to assist with communication and coordination between caregivers and health professionals. From these reports, specific patient intervention approaches were developed. The intervention ificantly improved caregiver quality of life at 1 week and 4 weeks after discharge from the hospital.

Houts and colleagues 81 describe a prescriptive program that is based on research on problem-solving training and therapy. COPE teaches caregivers how to de and carry out plans that focus on medical and psychosocial problems that are coordinated with care plans of health professionals. Although proponents of this program assert it has positive outcomes for caregivers, a formal evaluation of COPE was not found.

Twenty-five years of research have documented that the work of family caregiving can be stressful. That stress can adversely harm both the caregiver and the care recipient. This section addresses research aimed at protecting the care recipient from an ill-prepared or emotionally stressed family caregiver. It describes the link between the work of caregiving and patient harm, and examines interventions that aim to make the caregiver a better worker and less likely to harm the patient.

Dalton city IL adult personals

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