| 英文摘要 |
The primary objective of advancing medical technology is to preserve patients' lives and alleviate their suffering rather than prolonging their existence and increasing distress. Currently, non-hospice wards exhibit a 72.5% coverage rate for end-stage cancer patients receiving hospice palliative care, with a 72.7% signing rate for Do Not Resuscitate (DNR) directives. A critical analysis revealed that the ''End-stage Cancer Patients Problem Assessment Form'' lacks coverage of hematological symptoms, contributing to a consultation and care team ratio of only 43.5%. The rapid progression of diseases, coupled with delayed communication of decisions to patients, results in a lack of awareness about the first aid process and the subsequent painful situations among patients and their families. The root cause analysis identified that the omission of hematological symptoms in the ''Patients with Terminal Cancer Appraisal Forms'' led to inconsistent disease assessments by physicians, causing concerns and hindering effective hospice consultations. To address these challenges, initiatives were implemented, including the development of ''Shared Decision-Making Tools,'' ''First-Aid Equipment Icon Cards,'' and ''Life Choices'' health education materials. Additionally, programs such as ''Healing Five Communication'' and ''Patient Autonomy Rights Law cum Tranquility and Donation'' health lectures were organized. These interventions significantly improved the rates of end-stage cancer patients signing DNR directives, increasing from 72.7% to 89.7%. The consultation rate for hospice team care also rose from 43.5% to 88.2%. Patient satisfaction with the explanation process increased from 73.1% to 90.4%. These improvements demonstrate the effectiveness of the initiatives, reducing end-stage cancer patients' pain during the dying process, improving their quality of life, and fostering holistic care for their families. |