Healthcare implications Physicians, nurses, unlicensed assistive personal and other members of the interdisciplinary care team within the acute and long term care settings are faced with an epidemic. The prevalence of congestive heart failure and detriment to the health care system that CHF patients pose to the formal caregiver is different than the psychosocial effects the patient places on the familial or non-formal caregiver after discharge. Heart failure is a chronic condition marked by the hearts inability to pump blood to the tissues for adequate oxygenation (Bare, Cheever,Hinkle, Smeltzer 2005, p. 825). Complications of CHF provide for difficulty completing activities of daily living due to shortness of breath, loss of stamina and overall decreased ability to function independently. Johnston, Molloy, and Witham (2005), suggest in their systemic review article titled, Family caregiving and congestive heart failure. Review and analysis; that CHF patients and their familial care givers do not receive enough support to keep up with the demands of the disease. The article implies that patients need more education at the time of discharge from the hospital and that caregivers need continued social support to stave off depression and burn out that comes with the demands of caring for a relative with CHF. The study tries to find strengths and weaknesses within healthcare that can prevent exacerbations for both patient and caregiver. Study Conduction The research article by Johnston, et al. (2005) is a meta synthesis of three qualitative studies and a review of 13 quantitative studies. The literature review consisted of three databases: PsychINFO, Medline and Web of Science. The search criterion was reviewed over the course of ten years (1993-2003). Key words the researchers used were: heart failure, cardiac failure, carer, caregiver, partner, spouse and family. To substantiate their hypothesis that there is EVIDENCE BASED CHF FAMILY CARE 3
a disservice to patients and their families with CHF the researchers compare and contrast the volume of studies conducted on patients with other chronic illnesses, such as cancer and stroke and the outcomes it placed on caregivers for those types of patients. The qualitative studies suggest that the higher acuity of care required by the CHF patient the higher stress and demand on the caregiver, but mentions further research (randomized control trial at the time of discharge) with these patients is needed. The downfalls of the quantitative studies are the small sample sizes that are not representative of all the populations that experience increased stress when caring for CHF family members. Results/Limitations/Comparison The comprehensive analysis of the outcomes for CHF patients is summed up in the fact that two thirds of hospitalizations are preventable with proper tertiary prevention and education (Johnston et al, 2005). Patients families that were involved in discharge planning and education felt better prepared to care for their family member. The strengths in this analysis is that it offers solutions, such as conducting more studies to ascertain outcomes of patients and family members and suggests education and community responsibility in caring for chronic CHF patients and results of clinical trials to determine caregiver strain. The article suggests that less severe cases of CHF affect caregiver stress more than the severe cases due to noncompliance. This article shares an opinion of the authors that caregivers face more stress than those people that face Alzheimers disease, which is a disease that affects cognition and has physical manifestations. The comparison of these two distinct diseases and lobbying that one is more of a hardship on a family, as opposed to another is unfounded by research because , as the article suggests there is little evidence to support the effects of caregiver strain. Rather than comparing two separate EVIDENCE BASED CHF FAMILY CARE 4
disease processes it may beneficial to form an individualized plan of care for each family and how they cope with illness and stress. Plan of Care To provide individuals and their families with holistic care and support that prevents unnecessary hospitalizations nurses need to be at the forefront of discharge planning. To accommodate the care of a CHF patient education is necessary. Medication and activity compliance is essential to achieve optimal outcomes. One of the most important things that nurses can do is empower their patients. Patients need to recognize that they are not helpless and that they can influence the direction of their lives and the outcomes of treatment, (Bare, et al, 2010, p. 837). Patients are shown to respond to treatment and comply with medication regimes if they are given choices and autonomy. Caregivers will feel less pressure to give total care if a patient is encouraged to perform self-care. The Joint Commission has standards of care for patients with heart failure that are basic. These standards should be implemented into nursing practice for all patients and family members. (Bare et al , 2005, p.836) Some topics for nurses to discuss are: nutrition, especially low sodium diet, reducing anxiety and using stress relieving mechanisms such as guided imagery, monitoring weight daily and keeping scheduled appointments with cardiologist and general practitioner. Relevance of study to nursing practice Heart failure is the most common reason for hospitalization of people older than 65 years of age. There are 5 million people in the United States with chronic heart failure (Bare et al, 2005, p.825). As nurses there is the capacity to be advocates for patients and family members in times of stress and improve quality of life for those with chronic disease and the people that support them. The authors of this study have brought about valid points, that, in healthcare the EVIDENCE BASED CHF FAMILY CARE 5
focus in current research appears to be on acute onset of conditions such as Alzheimers disease and stroke and the psychosocial implications it places on caregivers, but there is little evidence supporting those with chronic conditions, such as congestive heart failure and those that are a part of their care.
EVIDENCE BASED CHF FAMILY CARE 6
References Bare,B.G., Cheever,K.H., Hinkle, J.L., & Smeltzer,S.C. (2010). Brunner & Suddarths Textbook of Medical Surgical Nursing.Philedelphia:Wolters-Kluwer, Lippincott,Williams & Wilkins. Johnston, D.W., Molloy, G.J., & Witham, M.D. (2005). Family caregiving and congestive heart failure. Review and analysis. The European Journal of Heart Failure, 7, 592-603. doi: 10.1016/j.ejheart.2004.07.008