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| 완화 의료 요구 평가 도구× | 맥길 삶의 질 척도× | |
|---|---|---|
| 분야 | 완화의료 | 완화의료 |
| 계열 | Process / pipeline | Process / pipeline |
| 기원 연도≠ | 2004 | 1995 |
| 창시자≠ | Developed by palliative care researchers and clinicians to address systematic gap assessment | Cohen, Mount, Strobel, and Bui |
| 유형≠ | Clinician-rated interview or patient self-report | Self-report |
| 원전≠ | Gardiner, C., Brereton, L., Frey, R., Wilkinson, J., & Ingleton, C. (2011). Exploring the financial impact of palliative care on patients and families. Current Opinion in Supportive and Palliative Care, 5(1), 58–65. link ↗ | Cohen, S. R., Mount, B. M., Strobel, M. G., & Bui, F. (1995). The McGill Quality of Life Questionnaire: a measure of quality of life appropriate for people facing advanced cancer. Journal of Palliative Care, 11(3), 6–15. link ↗ |
| 별칭≠ | NAPC, Needs Assessment Palliative Care | MQOL |
| 관련 | 5 | 5 |
| 요약≠ | The Needs Assessment Tool for Palliative Care (NAPC) is a comprehensive, multidomain assessment framework designed to systematically identify unmet palliative and supportive care needs in patients with advanced illness and their families. Rather than a numerical scale, the NAPC functions as a structured clinical interview and resource allocation guide, helping palliative care teams deliver holistic, person-centered care by addressing physical, psychological, social, spiritual, and practical dimensions simultaneously. | The McGill Quality of Life Questionnaire (MQOL) is a 17-item, multidimensional self-report measure specifically developed for people with advanced cancer and other life-limiting illnesses. Created by Cohen, Mount, and colleagues at McGill University in 1995, the MQOL captures physical, functional, emotional, spiritual, and social dimensions of quality of life in a concise, patient-centered format. It has become a standard outcome measure in palliative care research, hospice quality improvement, and cancer centers internationally. |
| ScholarGate데이터셋 ↗ |
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