Relevant bibliographies by topics / Standards of hospice care

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

Academic literature on the topic 'Standards of hospice care'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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Journal articles on the topic "Standards of hospice care"

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Connor, Stephen R., Chris Cody, and Stephen G. Arter. "Pharmaceutical Care Standards for Hospice Providers." Journal of Pharmaceutical Care in Pain & Symptom Control 2, no. 4 (January 1994): 5–14. http://dx.doi.org/10.1300/j088v02n04_02.

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Olson, Sharon L. "Hospice day care standards development in Michigan." American Journal of Hospice Care 6, no. 2 (March 1989): 35–39. http://dx.doi.org/10.1177/104990918900600217.

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Lum, Hillary D., Carolyn Horney, David Koets, Jean S. Kutner, and Daniel D. Matlock. "Availability of Heart Failure Medications in Hospice Care." American Journal of Hospice and Palliative Medicine® 33, no. 10 (July 10, 2016): 924–28. http://dx.doi.org/10.1177/1049909115603689.

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Background: Availability of cardiac medications in hospice for acute symptom management of heart failure is unknown. This study explored hospice approaches to cardiac medications for patients with heart failure. Methods: Descriptive study using a quantitative survey of 46 US hospice agencies and clinician interviews. Results: Of 31 hospices that provided standard home medication kits for acute symptom management, only 1 provided medication with cardiac indications (oral furosemide). Only 22% of the hospice agencies had a specific cardiac medication kit. Just over half (57%) of the agencies could provide intravenous inotropic therapy, often in multiple hospice settings. Clinicians described an individualized approach to cardiac medications for patients with heart failure. Conclusion: This study highlights opportunities for practice guidelines that inform medical therapy for hospice patients with heart failure.
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EISENBERGER, ANDREW, and JOMARIE ZELEZNIK. "Care planning for pressure ulcers in hospice: The team effect." Palliative and Supportive Care 2, no. 3 (September 2004): 283–89. http://dx.doi.org/10.1017/s1478951504040374.

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Objective: The standards of care for patients at risk for or with a pressure ulcer in hospitals and nursing homes focus on prevention and ulcer healing using an interdisciplinary approach. Although not a primary hospice condition, pressure ulcers are not uncommon in dying patients. Their management in hospices, particularly the involvement of family caregivers, has not been studied. The objective of this study is to identify the factors that influence care planning for the prevention and treatment of pressure ulcers in hospice patients and develop a taxonomy to use for further study.Methods: A telephone survey was conducted with 18 hospice directors of clinical services and 10 direct-care nurses. Descriptive qualitative data analysis using grounded theory was utilized.Results: The following three themes were identified: (1) the primary role of the hospice nurse is an educator rather than a wound care provider; (2) hospice providers perceive the barriers and burdens of family caregiver involvement in pressure ulcer care to be bodily location of the pressure ulcer, unpleasant wound characteristics, fear of causing pain, guilt, and having to acknowledge the dying process when a new pressure ulcer develops; and (3) the “team effect” describes the collaboration between family caregivers and the health care providers to establish individualized achievable goals of care ranging from pressure ulcer prevention to acceptance of a pressure ulcer and symptom palliation.Significance of results: Pressure ulcer care planning is a model of collaborative decision making between family caregivers and hospice providers for a condition that occurs as a secondary condition in hospice. A pressure ulcer places significant burdens on family caregivers distinct from common end-of-life symptoms whose treatment is directed at the patient. Because the goals of pressure ulcer care appear to be individualized for a dying patient and their caregivers, the basis of quality-of-care evaluations should be the process of care rather than the outcome of an incident pressure ulcer.
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Walker, Andreas, and Christof Breitsameter. "Ethical decision-making in hospice care." Nursing Ethics 22, no. 3 (June 29, 2014): 321–30. http://dx.doi.org/10.1177/0969733014534873.

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Background: Hospices are based on a holistic approach which places the physical, psychological, social and spiritual welfare of their patients at the forefront of their work. Furthermore, they draw up their own mission statements which they are at pains to follow and seek to conduct their work in accordance with codes of ethics and standards of care. Research question and design: Our study researched what form the processes and degrees of latitude in decision-making take in practice when questions of an ethical and ethically relevant nature arise. We used a qualitative approach. Data collection and evaluation was based on the methods of grounded theory. Ethical considerations: The study was reported to the relevant Ethics Commission who had raised no objections following the submission of the study protocol. The study at the hospices was approved by the directors of the hospices and the nursing teams. The rights of the participants were protected by obtaining informed consent. Results: Medication in the prefinal phase and questions affecting the provision of solids and liquids in the end-of-life phase have an ethical dimension. In the context of these two fields, decisions are taken collectively. A nurse’s individual (and ethically relevant) leeway in decision-making processes is restricted to the nurse’s own style of administering care. The nurse’s decision-making often depends to a far greater degree on her ability to adapt her concept of ideal care to fit the practical realities of her work than to any conceptual framework. Discussion: An adaptive process is necessary for the nurse because she is required to incorporate the four pillars of hospice care – namely, physical, psychological, social and spiritual care – into the practice of her daily work. Conclusion: Ethically relevant decisions are often characterised by nurses adjusting their aspiration levels to the practical conditions with which they are confronted.
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TANG, SIEW TZUH, RUTH MCCORKLE, and ELIZABETH H. BRADLEY ph.d. "Determinants of death in an inpatient hospice for terminally ill cancer patients." Palliative and Supportive Care 2, no. 4 (December 2004): 361–70. http://dx.doi.org/10.1017/s1478951504040489.

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Objective:Despite the strong emphasis on home-based end-of-life care in the United States and the recognition of dying at home as a gold standard of quality of care, hospice home care is not a panacea and death at home may not be feasible for every terminally ill cancer patient. Admission to an inpatient hospice and dying there may become a necessary and appropriate solution to distressing patients or exhausted families. However, the factors associated with death in an inpatient hospice have not been examined in previous studies.Methods:A prospective cohort study was conducted to investigate the determinants of death in an inpatient hospice for terminally ill cancer patients. Approximately two-fifths (40.8%) of the 180 terminally ill cancer patients in this study died in inpatient hospices over the 3-year study period.Results:Results from Cox proportional hazards model with adjustment for covariates revealed several factors that were significantly associated with dying in inpatient hospice, as opposed to home, in a nursing home, or in the hospital. Patients were more likely to die in an inpatient hospice if they received hospice care before death (hazard ratio [HR] = 7.32, 95% confidence interval [CI]: 3.21–16.67), if they had a prestated preference to die in an inpatient hospice (HR = 4.86, 95% CI: 2.24–10.51), if they resided in New Haven County (HR = 1.70, 95% CI: 1.00–2.93), or if they experienced higher levels of functional dependency (HR = 1.05, 95% CI: 1.02–1.08).Significance of results:The high prevalence of inpatient hospice deaths for terminally ill cancer patients in this study was related to the local health care system characteristics, health care needs at the end of life, and personal preference of place of death. Findings from this study may shed light on future directions for developing end-of-life care tailored to the needs of cancer patients who are admitted to hospices and eventually die there.
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Bainbridge, Daryl, Mohanna Giruparajah, Hanyan Zou, and Hsien Seow. "The care experiences of patients who die in residential hospice: A qualitative analysis of the last three months of life from the views of bereaved caregivers." Palliative and Supportive Care 16, no. 4 (June 29, 2017): 421–31. http://dx.doi.org/10.1017/s147895151700058x.

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AbstractObjective:Despite the increasing prominence of residential hospices as a place of death and that, in many regards, this specialized care represents a gold standard, little is known about the care experience in this setting. Using qualitative survey data, we examined the positive and negative perceptions of care in hospices and in other prior settings.Method:Qualitative comments were extracted from the CaregiverVoice survey completed by bereaved caregivers of decedents who had died in 16 residential hospices in Ontario, Canada. On this survey, caregivers reported what was good and bad about the services provided during the last three months of life as separate open-text questions. A constant-comparison method was employed to derive themes from the responses.Results:A total of 550 caregivers completed the survey, 94% (517) of whom commented on either something good (84%) and/or bad (49%) about the care experience. In addition to residential hospice, the majority of patients represented also received palliative care in the home (69%) or hospital (59%). Overall, most positive statements were about care in hospice (71%), whereas the negative statements tended to refer to other settings (81%). The hospice experience was found to exemplify care that was compassionate and holistic, in a comforting environment, offered by providers who were personable, dedicated, and informative. These humanistic qualities of care and the extent of support were generally seen to be lacking from the other settings.Significance of results:Our examination of the good and bad aspects of palliative care received is unique in qualitatively exploring palliative care experiences across multiple settings, and specifically that in hospices. Investigation of these perspectives affirmed the elements of care that dying patients and their family caregivers most value and that the hospices were largely effective at addressing. These findings highlight the need for reinforcing these qualities in other end-of-life settings to create comforting and supportive environments.
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McMAHON, ROBIN L. "An ethical dilemma in a hospice setting." Palliative and Supportive Care 1, no. 1 (March 2003): 79–87. http://dx.doi.org/10.1017/s1478951503030013.

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The codes of ethics of the National Hospice and Palliative Care Organization and the National Association of Social Workers support ethical standards of client self-determination and confidentiality. Lack of societal consensus on the parameters of a terminally ill person's right to die continues to confound at times the health care field, including hospice programs. This article explores an actual case where a hospice social worker faced an ethical dilemma related to the sanctity of life versus patient autonomy. While a more seasoned social worker might have chosen a different alternative to the dilemma, this case illustrates the importance of creating an interdisciplinary rather than multidisciplinary hospice team and the need for ongoing dialogue on how to support patient choice.
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Naysmith, A. "Quality, Standards, Organisational and Clinical Audit for Hospice and Palliative Care Services." Quality and Safety in Health Care 2, no. 1 (March 1, 1993): 70. http://dx.doi.org/10.1136/qshc.2.1.70-a.

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HEAD, BARBARA. "Who Sets the Standard for Hospice Care?" Home Healthcare Nurse 19, no. 3 (March 2001): 175. http://dx.doi.org/10.1097/00004045-200103000-00016.

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Dissertations / Theses on the topic "Standards of hospice care"

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Sharifi, Nahal Alsadat. "Children's Hospice Care." Thesis, Virginia Tech, 2016. http://hdl.handle.net/10919/71772.

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With advancements in medical technology, the mechanics of dying and death has changed significantly. Centuries ago, people mostly died of infectious diseases. From the time they were diagnosed, to the time of their death did not take long. Today, public health has improved remarkably. We have a better control over infectious diseases, but we have to deal with cancer and other chronic illnesses. The long period of treatment for such illnesses makes us spend a lot of our time in healthcare facilities such as hospitals, hospices, and care homes. Unfortunately, in many cases, these facilities do not pay much attention to emotional and spiritual needs of their patients and are mostly designed around their own institutional and technological needs. In that regard, these buildings become pretty awful places with no natural light and long corridors. Today, due to the nature of chronic diseases that we mostly deal with, hospice care facilities are becoming more popular. The idea of a hospice is to focus on quality of the place for families and patients who have already spent a lot of their time in a hospital setting. The goal is provide humane care for patients who do not have much time left, to make sure that they live the remainder of their lives as comfortably and as fully as possible. It is important to remember that when such facilities are designed for children, we need to pay extra attention to their unique needs. It is important to provide opportunities for children with terminal illnesses to continue to learn and grow. This thesis is exploration of an architectural setting in which children with a terminal prognosis would spend the last few weeks of their lives. Located in Old Town Alexandria, Virginia, this project takes advantage of the existing nature of the site to create an oasis for families who have gone through an exhausting battle with an untreatable disease. The goal is to shift the focus from curing to healing and to create a nurturing place that helps to bring normalcy back to the lives of patients and their families.
Master of Architecture
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Cho, Yuen-yee Christine. "Hospice." Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B2595099x.

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Cho, Yuen-yee Christine, and 曹婉怡. "Hospice." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1999. http://hub.hku.hk/bib/B3198454X.

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Ho, Man-chuen Anthony. "A hospice in Sandy Bay." Hong Kong : University of Hong Kong, 1995. http://sunzi.lib.hku.hk/hkuto/record.jsp?B25946043.

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Mak, Kiu-yan Wayne. "Towards nirvanna : a Buddhist hospice /." Hong Kong : University of Hong Kong, 1996. http://sunzi.lib.hku.hk/hkuto/record.jsp?B25955585.

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Moran, Karen Ann. "The experiences of hospice patients and the music therapy clinician in hospice care." Scholarly Commons, 2011. https://scholarlycommons.pacific.edu/uop_etds/765.

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This thesis reports on a phenomenological inquiry into the experiences of hospice patients and music therapy clinician in end of life care. Three total participants were included in this study, two hospice patients and the music therapy clinician. Interventions included singing familiar songs, music for relaxation and Music and Imagery, an adaptation of the Bonny Method of Guided Imagery and Music. Each hospice patient participated in two music therapy sessions, plus an interview. Data included audio recorded sessions and interview, a process journal kept by music therapist, clinical observations, and one of the participant's mandala. Data was analyzed according to Moustakas' modification of the Stevick - Colaizzi - Keen method of Transcendental Phenomenology. Experiences for the hospice patients include themes of Positive Experience with Music, Positive Experience with Music and Pain, Negative Experience with Music, Music and Imagery, The Artist, Coping, The Mandala, Processing Music and Imagery and Transcendence. Experiences for the therapist include Feelings, Clinical Awareness, Meeting my Own Needs, Desire to Help, Ebb and Flow, and the Guide Following. Implications for further research are given.
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Ferrel, Cynthia Lynn. "The experience of critical care nurses in initiating hospice care." abstract and full text PDF (free order & download UNR users only), 2008. http://0-gateway.proquest.com.innopac.library.unr.edu/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:1453534.

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Taylor, Sarah Fese. "Understanding Quality of Care in a Hospice Setting." ScholarWorks, 2018. https://scholarworks.waldenu.edu/dissertations/5272.

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Assuring quality of care for patients who face the end of life has been a major concern for those in hospice settings. Limited research is available that has a focus on understanding what quality of care in a hospice setting looks like. This research is important to provide insight into hospice health care providers' perceptions of the quality of care in the hospice setting and on the indicators that influence care quality. A qualitative phenomenological approach was used to answer the research questions on the perspectives of the health care providers in the hospice care setting regarding the quality of care and the factors that health care providers perceive as important to the quality of care in the hospice setting. Kolcaba's comfort theory served as the theoretical framework that guided the preparation of the questions used for the interviews and for interpreting the findings. Data collection was conducted through structured interviews with a sample of 15 hospice health care providers. Interviews were held in a private office of the hospice setting. After Walden Institutional Review Board approval, participants consented and interviews commenced. Data were transcribed and Nvivo software was used to assist with identifying major themes. Recommendations from the study reflect Kolcaba's comfort theory providing patient-centered care and enhanced quality of care for patients in a hospice setting. The research findings and recommendations will help promote a positive social change by raising awareness for effective provider communication, staffing, education and adequacy of resources in the hospice setting.
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Gore, Maria. "LGBT affirming environments in hospice care settings." Honors in the Major Thesis, University of Central Florida, 2013. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/848.

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The documented experiences and perceptions of lesbian, gay, bisexual, and transgender (LGBT) patients receiving hospice or palliative care gives merit to the need for the implementation of LGBT affirming environments in hospice care settings. The guidelines for creating these affirming environments are described in this paper. Applying the Donabedian (1988) model of structure, process, and outcome this thesis project analyzes identified interventions relevant to the implementation of LGBT affirming environments in hospice care settings. Utilizing a formal PICO questioning method, a search strategy was devised and studies were identified based on established criteria. The results suggest that there is a paucity of data in relation to the implementation of LGBT affirming environments in hospice care settings. In an effort to assist in identifying existing interventions that have not been studied this project also includes a recommended survey tool to measure the active efforts of hospice organizations to implement LGBT affirming environments.
B.S.W.
Bachelors
Health and Public Affairs
Social Work
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Parker-Oliver, Debra. "The diffusion of hospice care in Missouri /." free to MU campus, to others for purchase, 2000. http://wwwlib.umi.com/cr/mo/fullcit?p9988689.

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Books on the topic "Standards of hospice care"

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Hospice standards manual. Chicago, Ill: Joint Commission on Accreditation of Hospitals, 1986.

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Association, American Nurses'. Standards and scope of hospice nursing practice. Kansas City, Mo. (2420 Pershing Rd., Kansas City 64108): The Association, 1987.

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Executive, Scotland Scottish. Draft national care standards for hospice care: A consultation paper. [Edinburgh]: Scottish Executive, 2001.

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Association, Hospice and Palliative Nurses. Hospice and palliative nursing: Scope and standards of practice. 4th ed. Silver Spring, Md: American Nurses Association, 2007.

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Smith, Curtis E. A hospice guide book: Hospice care : a wise choice providing quality comfort care through the end of life's journey. Bloomington, IN: Inspiring Voices, 2012.

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Hospice and palliative care handbook: Quality, compliance, and reimbursement. St. Louis: Mosby-Year Book, 1999.

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Medicine, Univeristy of Sheffield Department of Community. Good practise in terminal care: Some standards and guidelines for hospice inpatient units and day hospices. Sheffield: University of Sheffield Medical School, 1988.

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Higginson, Irene. Quality, standards, organisational and clinical audit for hospice and palliative care services. London: National Council for Hospice and Specialist Palliative Care Services, 1992.

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Hospice and palliative care handbook: Quality, compliance, and reimbursement. 2nd ed. St. Louis: Mosby, 2005.

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Joint Commission on Accreditation of Healthcare Organizations. Using performance measurement to improve outcomes in home care and hospice settings. Oakbrook Terrace, Ill: Joint Commission on Accreditation of Healthcare Organizations, 1999.

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Book chapters on the topic "Standards of hospice care"

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Cundiff, David. "Hospice Care and Standard Oncology." In Euthanasia is Not the Answer, 133–47. Totowa, NJ: Humana Press, 1992. http://dx.doi.org/10.1007/978-1-4612-0415-2_9.

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Klein, Sandra Jacoby. "Hospice care." In Cancer Treatment and Research, 173–88. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2325-9_11.

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Orbell, Sheina, Havah Schneider, Sabrina Esbitt, Jeffrey S. Gonzalez, Jeffrey S. Gonzalez, Erica Shreck, Abigail Batchelder, et al. "Hospice Care." In Encyclopedia of Behavioral Medicine, 985. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-1005-9_100818.

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Oberoi-Jassal, Ritika, Jason Pope, and Navdeep Jassal. "Hospice Care." In Pain, 937–39. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-99124-5_199.

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Yun, Young Ho. "Hospice." In Encyclopedia of Trauma Care, 769–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29613-0_219.

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Breakwell, Susan. "Hospice." In Clinical Case Studies in Home Health Care, 447–57. West Sussex UK: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118785744.ch42.

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Powers, Richard E., and Heather L. Herrington. "Hospice Dementia Care." In Dementia Care, 261–98. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-18377-0_16.

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Ogden, Danna. "Hospice Medicine." In Pain Management and Palliative Care, 205–10. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2462-2_29.

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Wuestenberg, Kimm. "Harmonizing Hospice Needs." In Clinical Small Animal Care, 89–93. Ames, Iowa, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119264927.ch9.

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Greer, David. "Hospice as Advocacy." In Advocacy in Health Care, 19–26. Totowa, NJ: Humana Press, 1986. http://dx.doi.org/10.1007/978-1-4612-5004-3_3.

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Conference papers on the topic "Standards of hospice care"

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Allan, Gail. "O-7 The implementation of palliative and end of life care standards in scottish prisons." In Leading, Learning and Innovating, Hospice UK 2017 National Conference, 22–24 November 2017, Liverpool. British Medical Journal Publishing Group, 2017. http://dx.doi.org/10.1136/bmjspcare-2017-hospice.7.

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Gay, Hannah, Kate Hall, and Joanne Bowen. "59 Improving identification and recording of the gold standards framework (GSF) within russells hall hospital, dudley." In Accepted Oral and Poster Abstract Submissions, The Palliative Care Congress 1 Specialty: 3 Settings – home, hospice, hospital 19–20 March 2020 | Telford International Centre. British Medical Journal Publishing Group, 2020. http://dx.doi.org/10.1136/spcare-2020-pcc.80.

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Bowen, Joanne, Kate Hall, and Karen Lewis. "67 Gold standards framework implementation dudley group NHS foundation trust." In Accepted Oral and Poster Abstract Submissions, The Palliative Care Congress 1 Specialty: 3 Settings – home, hospice, hospital 25 – 26 March 2021 | A virtual event, hosted by Make it Edinburgh Live, the Edinburgh International Conference Centre’s hybrid event platform. British Medical Journal Publishing Group, 2021. http://dx.doi.org/10.1136/spcare-2021-pcc.85.

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Treterova, Silvie. "MULTIDISCIPLINARY TEAM IN HOME HOSPICE CARE." In 6th SWS International Scientific Conference on Social Sciences ISCSS 2019. STEF92 Technology, 2019. http://dx.doi.org/10.5593/sws.iscss.2019.3/s12.074.

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Wolkowski, Anna, and Emma Wolverson. "P-87 Hospice-enabled dementia care: joint working between a hospice and an acute dementia care unit." In Transforming Palliative Care, Hospice UK 2018 National Conference, 27–28 November 2018, Telford. British Medical Journal Publishing Group, 2018. http://dx.doi.org/10.1136/bmjspcare-2018-hospiceabs.112.

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Ward, Brenda, Sarah Bache, and Philippa Olliver. "9 In house teaching of communication skills using experiential training for hospice staff at a hospice in birmingham." In The APM’s Annual Supportive and Palliative Care Conference, In association with the Palliative Care Congress, “Towards evidence based compassionate care”, Bournemouth International Centre, 15–16 March 2018. British Medical Journal Publishing Group, 2018. http://dx.doi.org/10.1136/bmjspcare-2018-aspabstracts.36.

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Miller, Gemma, and Agnes Rupango. "P-214 The twining relationship between LOROS hospice and Ndi Moyo hospice." In Transforming Palliative Care, Hospice UK 2018 National Conference, 27–28 November 2018, Telford. British Medical Journal Publishing Group, 2018. http://dx.doi.org/10.1136/bmjspcare-2018-hospiceabs.239.

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Birch, Helen, Debbie Lawson, and Rachel Kennedy. "P-40 Guide to opening up hospice care." In Dying for change: evolution and revolution in palliative care, Hospice UK 2019 National Conference, 20–22 November 2019, Liverpool. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjspcare-2019-huknc.64.

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Clarke, Jo. "P-282 Rennie grove hospice care preceptorship programme." In Leading, Learning and Innovating, Hospice UK 2017 National Conference, 22–24 November 2017, Liverpool. British Medical Journal Publishing Group, 2017. http://dx.doi.org/10.1136/bmjspcare-2017-hospice.307.

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Henderson, Donall, Aine Abbott, Paul McIvor, and Damien McMullan. "P-193 Enhanced day hospice – collaborative self care." In People, Partnerships and Potential, 16 – 18 November 2016, Liverpool. British Medical Journal Publishing Group, 2016. http://dx.doi.org/10.1136/bmjspcare-2016-001245.215.

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Reports on the topic "Standards of hospice care"

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Gao, Tingting, Yang Wang, and Hong Jiang. A Meta analysis of Hospice care in Chinese intensive care unit. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, December 2020. http://dx.doi.org/10.37766/inplasy2020.12.0007.

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Bongiovanni, Annette, and Mary Greenan. Hospice Africa Uganda: End-of-project evaluation of palliative care services. Population Council, 2009. http://dx.doi.org/10.31899/hiv11.1019.

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Cohen, Lewis, Mark Unruh, Michael Germain, Naihua Duan, and John Griffith. Effect of End-of-Life Care Planning Discussions on Hospice Use Among Patients Receiving Dialysis for Kidney Failure. Patient-Centered Outcomes Research Institute® (PCORI), May 2020. http://dx.doi.org/10.25302/05.2020.cd.13047360.

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Sriram, Ram D., and Steven J. Fenves. Manufacturing metrology and standards for the health care enterprise program summary. Gaithersburg, MD: National Institute of Standards and Technology, 2008. http://dx.doi.org/10.6028/nist.ir.7487.

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NAPICU. National minimum standards for psychiatric intensive care in general adult services. NAPICU, 2014. http://dx.doi.org/10.20299/napicu.2017.001.

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Phillips, David, and Polly Simpson. National standards, local risks: the geography of local authority funded social care, 2009–10 to 2015–16. The IFS, April 2017. http://dx.doi.org/10.1920/re.ifs.2017.0128.

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Giroux, Virginia A. A Comparison of Diabetes Management in a Federal Prison With the National Standards of Care Published by the ADA in 1998. Fort Belvoir, VA: Defense Technical Information Center, April 2000. http://dx.doi.org/10.21236/ad1012311.

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Millican, Sharon M. HIPAA Privacy and Security Standards: A Gap Analysis for the Compliance Challenge at the Northern Arizona VA Health Care System (NAVAHCS). Fort Belvoir, VA: Defense Technical Information Center, June 2002. http://dx.doi.org/10.21236/ada421231.

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Ajema, Carol, Emily Rogena, Hadley Muchela, Buluma Bwire, and Nduku Kilonzo. Standards required in maintaining the chain of evidence in the context of post rape care services: Findings of a study conducted in Kenya. Population Council, 2009. http://dx.doi.org/10.31899/rh13.1007.

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EUROPEAN STANDARDS OF CARE FOR NEWBORN HEALTH. Chernivtsi, Ukraine: Higher State Educational Establishment of Ukraine Bukovinian State Medical University, 2019. http://dx.doi.org/10.24061/2413-4260.ix.3.33.2019.1.

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Abstract:
Medical treatment and care for preterm and sick newborn babies in European countries varies greatly. Significant differences are not only limited to the survival rates of such infants. In some European countries, preterm birth is also more commonly associated with chronic physical and mental disability than in others. This effect is exacerbated by the fact that in some parts of Europe, further assistance to these vulnerable children after discharge from the hospital (follow-up and early intervention) is not structured or even does not exist at all. Given the high level of inequality in health care delivery, agreed definitions and clear recommendations for infrastructure, medical processes, care procedures, and staffing capabilities are needed to compare and adjust the conditions of care in Europe. Therefore, there is an absolute need to ensure that high-level care is equally available throughout and for everyone. European standards of care for newborn health, developed on the initiative and under the project of the European Foundation for the Care of Newborn Infants (EFCNI), will help to overcome differences in clinical practice, structure and organization of care, as well as training of healthcare professionals. This publication presents the part of the standards regarding health care for preterm and sick infants.
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