Comparar métodos
Examine os métodos selecionados lado a lado; as linhas que diferem ficam destacadas.
| Inventário de Dignidade do Paciente× | Agendamento de Avaliação da Equipe de Suporte× | |
|---|---|---|
| Área | Cuidados paliativos | Cuidados paliativos |
| Família | Process / pipeline | Process / pipeline |
| Ano de origem≠ | 2008 | 1997 |
| Autor original≠ | Chochinov, Hassard, McClement, and colleagues (University of Manitoba) | Baker, Speck, and Cohen |
| Tipo≠ | Self-report | Clinician-rated observational scale |
| Fonte seminal≠ | Chochinov, H. M., Hassard, T., McClement, S., Hack, T., Kristjanson, L. J., Harlos, M., Speca, M., & Tool, T. (2008). The Patient Dignity Inventory: a novel way of measuring dignity-related distress in palliative care. Journal of Pain and Symptom Management, 36(6), 559–571. DOI ↗ | Baker, A., Speck, P., & Cohen, D. (1997). Support Team Assessment Schedule (STAS): Development of a new instrument for the evaluation of support to patients and families in palliative care. Journal of Palliative Care, 13(2), 39–45. link ↗ |
| Outros nomes | PDI, Dignity Inventory | STAS, STAS-A |
| Relacionados | 5 | 5 |
| Resumo≠ | The Patient Dignity Inventory (PDI) is a 25-item self-report measure assessing dignity-related distress in patients with advanced cancer and life-limiting illness. Developed by Chochinov and colleagues at the University of Manitoba in 2008, the PDI operationalizes 'dignity' as a multidimensional construct encompassing illness-related functional decline, psychosocial concerns (fear, hopelessness, suicidality), body image distress, existential meaning, and social connection—dimensions often overlooked by symptom-focused assessment. The PDI enables clinicians to identify and address dignity threats systematically, preventing the existential despair that can accompany terminal illness even when physical symptoms are well-controlled. | The Support Team Assessment Schedule (STAS) is a clinician-rated observational instrument assessing the impact of palliative care support on patients with advanced illness and their families across seven key domains: pain, symptoms, anxiety, family well-being, communication, and support adequacy. Developed by Baker, Speck, and Cohen in 1997, the STAS has become a standard quality-of-life outcome measure in community palliative care, hospice, and research, enabling teams to systematically monitor the effectiveness of their interventions and identify patients and families in crisis. |
| ScholarGateConjunto de dados ↗ |
|
|