[韩国国家临终关怀服务的发展]。

Taehan kanho. The Korean nurse Pub Date : 1997-07-01
S W Lee, E O Lee, H S Ahn, D S Heo, D S Kim, H S Kim, H J Lee
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引用次数: 0

摘要

韩国迫切需要建立临终关怀制度的原因如下:(1)随着老年人口的增加,慢性病患者急剧增加;(2)传统居住环境的迅速变化(例如,许多韩国人住在公寓大楼,这是近年来最流行的现代居住形式,更喜欢在医院里死去);晚期癌症患者的总体增加;(4)由于医院设施有限,晚期病人提前出院以容纳其他医疗保险受益人的最新趋势;(5)轻视生命尊严的社会氛围使安乐死容易被接受;(6)晚期艾滋病患者的医疗护理;(7)非人道的医疗制度、过度治疗和对麻醉品的无端恐惧等问题。过去,绝症患者常在这家医院接受治疗。然而,在这些日子里,由于医院设施不足,他们被迫在家接受护理,几乎得不到合格医务人员的帮助,医院甚至无法满足急诊病人的需要,也无法为有其他严重问题的医疗保险受益人提供优先护理。然而,在韩国,既没有任何行政机构也没有系统的医学研究来处理临终病人的需求水平,他们的家庭问题和临终关怀系统的资源。因此,大多数病人在生命的最后阶段无法得到适当的医疗照顾。本研究的目的是为目前营运的各类安宁疗护机构建立完整的资料库,并透过医疗资讯系统连结它们,进而发展出符合大多数韩国人需求的简易安宁疗护模式。我们的调查结果可以总结如下:全国有40个组织提供部分或全部安宁疗护。然而,这些组织与任何正式的医疗服务网络都没有联系。此外,与国际安宁疗护标准相比,我国安宁疗护的目标、疗护原则、受过适当训练的人员、教育计划、疗护标准、费用、对病人家属的咨询服务、专业人员的医疗照护程度、安宁疗护设施的状况、以及机构的管理,都没有明确的定义和组织。通过对临终病人的调查,分为安宁疗护病人和非安宁疗护病人,揭示了临终病人希望通过访护来帮助他们控制疼痛的需求、心理需求、社会需求和精神需求。超过90%的安宁疗护病人希望减轻他们的痛苦,而非安宁疗护病人除了希望控制疼痛外,还要求更多的心理、社会和精神上的帮助。本研究结果可用于(1)订定安宁疗护标准、(2)提供安宁疗护费用指导、(3)建立安宁疗护系统资料库、(4)开发软体、(5)透过mediinet建立沟通网络、(6)提供有组织的访家照护系统。这些信息对于从事癌症治疗、护理和社会福利项目的医务人员来说是宝贵的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Development in the National Hospice Care Service in Korea].

The urgent needs to establish hospice care systems in Korea arise from the following reasons: (1) a drastic increase in chronically ill patients with the increase of aged population: (2) rapid changes in living environment from the traditional habitation (e.g., Many Koreans living in apartment complexes, which is the most popular form of modern residence in recent years, prefer to die in the hospital.): the overall increase in patients with advanced cancer: (4) recent trends in early discharge of terminally ill patients from the limited hospital facilities to accommodate other medical insurance beneficiaries: (5) easy acceptance of euthanasia owing to the recent social atmosphere that belittles the dignity of human life: (6) medical and nursing care of AIDS patient in terminal stage: (7) and the problem associated with inhumane medical care system, overtreatment, and groundless fears against narcotics. Terminally ill patients were used to be treated in the hospital in the past. In these days, however, they are forced to have home cares with little assistance from the qualified medical personnel because of insufficient hospital facilities, which are even short for the need of emergency patients and provide priority cares to medical insurance beneficiaries with other acute problems. And yet, neither are there any administrative organizations nor systematic medical studies that deal with the level of terminally ill patient's need, their family's problems and resources of hospice care systems in Korea. Thus, most patients are not able to get appropriate medical care at the terminal stage of their lives. The objective of this study is to make comprehensive database for various hospice care organization currently in operation, link them through medical information system, and develop an easily accessible hospice care model that meets the need of most Korean people. Our survey results may be summarized as follows: Nationally there are 40 organizations that provide partial or full hospice care. However, these organizations are not linked to any formal medical service network. Furthermore, the objective of hospice care, care principles, personnel with appropriate training, educational programs, standard for care, costs, consulting service to patients' family members, the extent of medical care from professional staff members, status of hospice facility, and management of those institutions are neither clearly defined nor organized compared to the international hospice care standards. The surveys on patients of terminal stage, grouped in hospice and non-hospice care patients, reveal what they want visiting nursing care to help their pain control, psychological, social and spiritual demands. While the more than 90% of hospice care patients want to reduce their pains, the non-hospice care patients, in addition to their desire for pain control, demanded more psychological, social and spiritual helps as well. The results of this research could be utilized to (1) define the standard of hospice care, (2) provide the guidance for hospice medical care costs, (3) establish the database of hospice care systems, (4) develop softwares, (5) build communication network through Medinet, and (6) provide an organized visiting home nursing care system. These information should be a valuable resource to many medical staffs who are involved in cancer therapy, nursing care, and social welfare programs.

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