Relevant bibliographies by topics / Terminally ill – Home care – Botswana

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Terminally ill – Home care – Botswana'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Terminally ill – Home care – Botswana"

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Ndaba-Mbata, R. D., and E. S. Seloilwe. "Home-based care of the terminally ill in Botswana: knowledge and perceptions." International Nursing Review 47, no. 4 (2000): 218–23. http://dx.doi.org/10.1046/j.1466-7657.2000.00023.x.

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Norwood, Michael. "Home care of the terminally ill." American Journal of Health-System Pharmacy 47, no. 8_suppl (1990): S23—S26. http://dx.doi.org/10.1093/ajhp/47.8_suppl_1.s23.

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Kawagoe, Shohei. "Home care medicine for terminally ill patients." Rinsho Shinkeigaku 53, no. 11 (2013): 1295. http://dx.doi.org/10.5692/clinicalneurol.53.1295.

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Phillips, Kay. "Pediatric hospice: Home care for the terminally ill child." Journal of Home Health Care Practice 1, no. 3 (1988): 37–50. http://dx.doi.org/10.1177/108482238800100308.

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Peruselli, Carlo, Elena Camporesi, A. Maria Colombo, et al. "Nursing Care Planning for Terminally Ill Cancer Patients Receiving Home Care." Journal of Palliative Care 8, no. 4 (1992): 4–7. http://dx.doi.org/10.1177/082585979200800402.

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Nursing home care for terminally ill cancer patients was organized according to nursing care plans that were based on diagnoses as recommended by the North American Nursing Diagnosis Association (NANDA). This study was carried out among a sample of 40 patients receiving home health care for a period of 1 to 19 weeks. More than 697 nursing diagnoses were identified in the study. The most frequently recorded nursing diagnoses were anxiety, constipation, and diminished food intake. Fifteen of the 40 patients in the study were able to complete a weekly self-report of their symptoms. The patients’
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Saleh, Fatima, and Catherine S. O’Neill. "The experiences of caregivers providing home care for terminally ill family members at the end of life: A phenomenological study in Bahrain." Clinical Nursing Studies 6, no. 3 (2018): 57. http://dx.doi.org/10.5430/cns.v6n3p57.

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Objective: The aim of the study was to explore the lived experience of caregivers providing home care for terminally ill family members, with the objectives of describing their experiences of caring for relatives who are terminally ill with cancer and the needs of home caregiving in Bahrain.Methods: The study adopted a Heideggerian, hermeneutic phenomenological design, with a purposive sample of eight family caregivers. Data was generated through one to one, in-depth interviews and analyzed using Interpretative Phenomenological Analysis.Results: Three main themes emerged from the data: (1) the
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Bendiane, PhDc, Marc Karim, Anne-Deborah Bouhnik, PhDc, Roger Favre, PhD, et al. "Morphine prescription in end-of-life care and euthanasia: French home nurses’ opinions." Journal of Opioid Management 3, no. 1 (2007): 21. http://dx.doi.org/10.5055/jom.2007.0035.

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Objective: This study aimed to investigate factors that might lead French homecare nurses to consider the pre-scription of high-dose morphine to terminally ill patients to be euthanasia.Methods: The researchers conducted an anonymous telephone survey among a random sample of602 French homecare nurses (response rate = 75percent) in 2005.Results: Overall, 27percent of responding home nurses considered prescribing high-dose morphine to terminally ill patients to be euthanasia. Such an opinion was more frequently held by older nurses, those who had not followed terminally ill patients during the p
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Boycheva, Tsvetka, and Mariya Dimitrova. "PROBLEMS OF FAMILIES WITH TERMINALLY ILL." Knowledge International Journal 28, no. 2 (2018): 603–11. http://dx.doi.org/10.35120/kij2802603b.

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In recent decades, there has been a growing public interest in palliative care. This is dictated by the ever increasing number of people who need it. With advances in medical science and the development of new technologies, life expectancy has increased, but at the same time, the number of years spent in illness and suffering has increased. Still, death is not defeated, but pain and suffering can be relieved, and the quality of life of the terminally ill and their families can be improved. Palliative care is overwhelming. They target the patient and his family. They meet the psychic, social, s
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Owens, Darrell A. "Hydration in the Terminally Ill." Journal of Hospice & Palliative Nursing 9, no. 3 (2007): 122–23. http://dx.doi.org/10.1097/01.njh.0000270001.36496.bd.

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HIRABAYASHI, YUKA, MITSUNORI MIYASHITA, MASAKO KAWA, KEIKO KAZUMA, KOHSUKE YAMASHITA, and NAOYUKI OKAMOTO. "Factors relating to terminally ill cancer patients' willingness to continue living at home during the early phase of home care after discharge from clinical cancer centers in Japan." Palliative and Supportive Care 5, no. 1 (2007): 19–30. http://dx.doi.org/10.1017/s1478951507070046.

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Objective: To assess the willingness of Japanese terminally ill cancer patients to continue living at home during the early phase of home care after discharge from a Clinical Cancer Center (CCC) in Japan, and to identify factors relating to their willingness to continue living at home.Methods: A cross-sectional questionnaire survey of a convenient sample of both Japanese terminally ill cancer patients and their caregivers (PFCs) was conducted (n = 294, effective response rate 25.0%). Questionnaires were mailed and medical records were accessed for 73 pairs of respondents, comprising one termin
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Dissertations / Theses on the topic "Terminally ill – Home care – Botswana"

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Webb, Nicole Marie. "Factors affecting young adults' opinions about hospice and home death." Birmingham, Ala. : University of Alabama at Birmingham, 2009. https://www.mhsl.uab.edu/dt/2009p/webb.pdf.

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Thesis (Ph. D.)--University of Alabama at Birmingham, 2009.<br>Title from PDF title page (viewed Sept. 2, 2009). Additional advisors: Virginia G. (Wadley) Bradley, Elizabeth A. Kvale, Kathryn L. Burgio, Edwin W. Cook III. Includes bibliographical references.
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Choy, Yin-san Catherine, and 蔡妍珊. "An exploratory study on anticipatory grieving: case studies of spouses of terminally ill patients." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1987. http://hub.hku.hk/bib/B31247799.

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Chapman, Kimberly J. (Kimberly Jane). "The relationships among general coping style, hope, and anticipatory grief in family members of terminally ill individuals with cancer receiving home care." Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=22724.

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Family members have been observed to cope with the losses inherent in terminal illness by grieving. Little is known, however, about the factors which influence their grieving before the death of a significant other. This paper describes an exploratory, cross-sectional, correlational study designed to examine the relationships among general coping style, hope, and anticipatory grief in a convenience sample of 61 family members of individuals with terminal cancer. The organizing framework for this study was based on grief theory, Lazarus and Folkman's (1984) theory of stress and coping, and Davi
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Ng, Lai-nga, and 吳麗雅. "An exploratory study on an interventive approach to work with the spouse of patients with terminal illness." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1987. http://hub.hku.hk/bib/B31247957.

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Iverson, P. Dianne. "Spiritual care of the dying : a community nursing perspective /." View thesis, 2003. http://library.uws.edu.au/adt-NUWS/public/adt-NUWS20031009.093517/index.html.

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Thesis (M. N.) (Hons.) -- University of Western Sydney, 2003.<br>A thesis submitted in total fulfillment of the requirements for the degree of Master of Nursing (Honours), Faculty of Nursing and Community Health, Department of Nursing, University of Western Sydney, February, 2003. Bibliography : leaves 190-205.
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Monteiro, Fernanda Silva. "Manejo familiar da alimentação de pacientes oncológicos gravemente enfermos." Universidade Federal de Alagoas, 2014. http://www.repositorio.ufal.br/handle/riufal/1752.

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This is a dissertation Programme Postgraduate Sensu Strictu Nursing, School of Nursing and Pharmacy, Federal University of Alagoas. Given that cancer at some point in evolution of the disease patients need to solve food problems, nursing adopts guidance to patients and their families as part of their care process, thus seeking a comprehensive and humane care. Based on this finding , this paper focuses the response of family members of cancer patients to dietary changes presented by the patient seriously ill. Aims to identify the experience of handling the family regarding the power of family s
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Cameron, Barbara. "Palliative Care Services Utilization and Location of Death." Thèse, Université d'Ottawa / University of Ottawa, 2012. http://hdl.handle.net/10393/22907.

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In this study, the utilization of palliative care services, acute care services, and location of death for clients who were palliative and receiving services from Champlain Community Care Access Centre (CCAC) in Ontario during their last month of life were investigated. An adaptation of Andersen?s Behavioral Model of Health Services Utilization provided context and structure to this study. This is an historical, quantitative descriptive study using chart audits for data collection. The data on CCAC clients who were palliative and who died during the month of July 2009 were tracked during their
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Mooka, Dorethy. "Examining home-based care of chronically/terminally ill persons by family care givers and their interaction with professional health care providers." Thesis, 2004. http://hdl.handle.net/10500/10330.

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According to the Ministry of Health (1996:26), the most common chronic/terminal illnesses were cardiovascular disorders, diabetes, cancer, mental disorders, HIV/AIDS, tuberculosis and asthma. Long term treatment and care and the growing incidence of these conditions necessitated the introduction of home-based care (HBC). Consequently, family care givers play a major role in the provision of care to chronically/terminally ill patients and professional health care providers adopt a supervisory role. This study examined the quality of home care services provided in Botswana. The availabil
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CHEN, YUEH-JUNG, and 陳月蓉. "The use of action research to improve the hospice home care for the terminally ill peace process." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/w7a64b.

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碩士<br>輔英科技大學<br>護理系碩士班<br>105<br>Background: In the Chinese culture, "home" is the result of a person's life, and getting home is the attribution of the value of life. However, medical technology advanced greatly, family try to extend the lives of patients. In the end of patient's life, family and physicians do their best to provide excessive medical intervention. They tend to keep patients in hospital for advanced medical care. In view of excessive use of unnecessary medical measures in terminal care, we should stress the importance of the lack of psychosocial care, family support, and indivi
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Grifka, Karen B. "The perceived needs of family members of the terminally ill in the home setting a research report submitted in partial fulfillment ... /." 1986. http://catalog.hathitrust.org/api/volumes/oclc/68787830.html.

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Books on the topic "Terminally ill – Home care – Botswana"

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Appleton, Michael. At home with terminal illness: A family guide to hospice in the home. Prentice Hall Career & Technology, 1995.

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Appleton, Michael. At home with terminal illness: Afamily guide to hospice in the home. Prentice Hall Career & Technology, 1995.

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Caring for the dying at home: A practical guide. Free Association, 2004.

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1929-, Mooney Margaret L., ed. The lonely pain of cancer: Home care for the terminally ill. SHARP Pub., 1991.

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Lunt, Barry. Home care teams and hospital support teams for the terminally ill. Macmillan Fund for Cancer Research, 1989.

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Ba-bayit ṿe-lo be-mosad: ʻal ha-zekhut la-mut ba-bayit. Eshel, ha-Agudah le-tikhnun ule-fituaḥ sherutim le-maʻan ha-zaḳen be-Yiśraʼel, 2006.

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Ward, Audrey. Home care services for the terminally ill: A report for the Nuffield Foundation. (Medical Care Research Unit, Department of Community Medicine, University of Sheffield Medical School), 1985.

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Haneda, Sumiko. Owari yokereba subete yoshi. Iwanami Shoten, 2009.

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Elizabeth, Williams. Help me-- I'm dying: A handbook for those caring for the terminally ill at home. Longman Paul, 1989.

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(Organization), Age Concern England, ed. Caring for someone who is dying. 2nd ed. Age Concern England, 2003.

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Book chapters on the topic "Terminally ill – Home care – Botswana"

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Alban-Jones, Cathy, and Lorraine Moth. "Home care for terminally ill haematology patients." In Palliative Care Consultations in Haemato-oncology. Oxford University Press, 2003. http://dx.doi.org/10.1093/acprof:oso/9780198528081.003.0014.

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Woo, Raymond Kam-wing, Annie Oi Ling Kwok, and Doris Man Wah Tse. "Preferred Place of Care and Death Among the Terminally Ill." In Sustainable Health and Long-Term Care Solutions for an Aging Population. IGI Global, 2018. http://dx.doi.org/10.4018/978-1-5225-2633-9.ch015.

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The research on patients' preferred place of care and death has received increasing attention in recent decades. In palliative care, one of the main goals is to facilitate patients to stay in their preferred place of care, and to die in the place of their choice. Although ‘home' is often quoted as the most preferred place of care and death among the terminally-ill in other places, local studies suggested otherwise. In Hong Kong, death is highly institutionalized with the vast majority of deaths occurring in public hospitals. Local culture, health care system and its provision and accessibility, presence of public health care policy on palliative care and care for the terminally-ill are among the factors affecting patients' preferred and actual place of care and death. This chapter is going to provide an overview of the recent studies and to discuss the topic from the Asian perspectives, and to highlight on the debates on the related policies.
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Emmanuel Ndiok, Akon, Emilia Oyira, and Busisiwe Ncama. "Holistic/Palliative Management of Patient’s Health Care and Home Situation in a Depressed Economy." In Palliative Care [Working Title]. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.92736.

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In most middle and low economic nations, problem in the active management of health complaints is patients defaulting on follow-up appointments, attributable to financial constraints and cost of health services due to economic recession. This increases the danger of aggravation and deterioration of the condition and leads to re-hospitalisation. Most terminally ill patients and elderly prefer to be cared for at home by family caregivers or paid health professionals towards the end of their life. Holistic/palliative care is a key component of home health care. Current structure of health and social care services shows that the home is gradually becoming a significant location of long-term care. Holistic care as advocated by Florence Nightingale and others takes cognizance of the care of total human being looking at the spiritual, physical, social and psychosocial care of individual. Quality care for patients and their families can be achieved by establishing principles of holistic/palliative care as an integral part of daily practice both in the hospital and home care, as advocated by the WHO. Challenges in seeking to do this can be overcome if adequate funding is allocated for palliative care activities and setting up machineries for training of families on home care.
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Conference papers on the topic "Terminally ill – Home care – Botswana"

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Truhlarova, Zuzana. "HOME CARE FOR TERMINALLY ILL." In 2nd International Multidisciplinary Scientific Conference on Social Sciences and Arts SGEM2015. Stef92 Technology, 2015. http://dx.doi.org/10.5593/sgemsocial2015/b11/s2.072.

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