英文摘要 |
In Taiwan, hospice palliative care was initiated by a private association in 1973. The first hospice ward was established at MacKay Memorial Hospital in 1990. The government officially took charge of the national hospice programs and administration of palliative care in 1995. In June of 2000, the Hospice Palliative Care Act was enacted by our government and further amended in 2002, 2011, and 2013. The aim of hospice palliative care is to respect the will of the terminally ill patients and to protect their right to decide on the treatment near end of the life. The Act clearly defines the meanings of cardio-pulmonary resuscitation (CPR), life-sustaining treatment (LST) and the designation of terminally ill patients, and also allows the terminally ill patients to express their willingness with regard to receiving these treatments. The will to receive non-applying LST was added into the Act in 2011. The requirements were the same as those for not receiving CPR. This article discusses the use of these applications from the perspective of ethics and law. Currently the Act consists of strict guidelines to help terminally ill patients decide when not to undergo CPR or receive LST, and at the same time provides standard protocol that clinical specialists should follow when helping terminally ill patients make the most suitable treatment or non-treatment decisions. However, conflicts and inconsistency remain in the application of the clinical practices outlined in this Act. Both physicians and the population as a whole need to explore the Act further and discuss it thoroughly in order to reach a better consensus on the meaning and application of palliative care practices. In this way, the aims set forth in Hospice Palliative Care Act can make more concrete and complete. (J Med Health. 2016;5(1):25-34) |