Phase of Illness (Palliative Care Phase) in Palliative Care: A Literature review

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Published inJournal of Japanese Society of Cancer Nursing Vol. 37; p. 37_156_ohinata
Main Authors Miyashita, Mitsunori, Ohinata, Hironori, Aoyama, Maho
Format Journal Article
LanguageJapanese
Published Japanese Society of Cancer Nursing 05.10.2023
一般社団法人 日本がん看護学会
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ISSN0914-6423
2189-7565
DOI10.18906/jjscn.37_156_ohinata

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Author Miyashita, Mitsunori
Ohinata, Hironori
Aoyama, Maho
Author_FL 青山 真帆
宮下 光令
Ohinata Hironori
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DocumentTitleAlternate 緩和ケアにおけるPhase of Illness(Palliative Care Phase)に関する文献レビュー
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References 15) 角允博. 【非がん疾患に対する緩和ケア】疾患別の特性 multimorbidityと緩和ケア. 内科. 127 (2), 255-257 (2021
8) Palliative Care Outcomes Collaboration (PCOC). History of phases of palliative care. Universty of Wollongong. 2013. https://documents.uow.edu.au/content/groups/public/@web/@chsd/@pcoc/documents/doc/uow191808.pdf, (参照2021-8-20
31) Ding J, Johnson CE, Lee YCO, et al. Characteristics of people with dementia vs other conditions on admission to inpatient palliative care. Journal of the American Geriatrics Society. 68 (8), 1825-1833 (2020
21) Currow DC, Eagar K, Aoun S, et al. Is it feasible and desirable to collect voluntarily quality and outcome data nationally in palliative oncology care? Journal of Clinical Oncology. 26 (23), 3853-3859 (2008
20) Lucey M, O’Reilly M, Currow D, et al. Is inpatient hospice care clinically effective? Using phase of illness to evaluate care outcomes for patients admitted to a specialist palliative care unit in Ireland. Journal of Palliative Medicine. 23 (4), 535-541 (2020
32) Sakurai H, Miyashita M, Imai K, et al. Validation of the Integrated Palliative care Outcome Scale (IPOS) - Japanese Version. Japanese Journal of Clinical Oncology. 49 (3), 257-262 (2019
2) Higginson IJ, Addington-Hall JM. Palliative care needs to be provided on basis of need rather than diagnosis. BMJ. 318 (7176), 123 (1999
1) World Health Organization. National cancer control programmes : policies and managerial guidelines. 2nd ed. World Health Organization. 2002. https://apps.who.int/iris/handle/10665/42494, (参照2022-9-2
36) Fernando G, Hughes S. Team approaches in palliative care: a review of the literature. International Journal of Palliative Nursing. 25 (9), 444-451 (2019
4) Wenham S, Cumming M, Saurman E. Improving palliative and end-of-life care for rural and remote Australians. Public Health Research & Plactice. 30 (1), 3012001 (2020
12) Murtagh F. C-CHANGE: Delivering high quality and cost-effective care across the range of complexity for those with advanced conditions in the last year of life. Dimensions. 2011. https://app.dimensions.ai/details/grant/grant.5147811, (参照 2023-8-22
14) Kamal AH, Bausewein C, Casarett DJ, et al. Standards, Guidelines, and Quality measures for successful specialty palliative care integration into oncology: current Approaches and Future Directions. Journal of Clinical Oncology. 38 (9), 987-994 (2020
24) Clayton J, Fardell B, Hutton-Potts J, et al. Parenteral antibiotics in a palliative care unit: prospective analysis of current practice. Palliative Medicine. 17 (1), 44-48 (2003
25) Mather H, Guo P, Firth A, et al. Phase of illness in palliative care: cross-sectional analysis of clinical data from community, hospital and hospice patients. Palliative Medicine. 32 (2), 404-412 (2018
17) Eagar K, Green J, Gordon R. An Australian casemix classification for palliative care: technical development and results. Palliative Medicine. 18 (3), 217-226 (2004
34) 森田達也. 2018年度調査研究報告 日本・韓国・台湾 第2期共同研究. ホスピス財団. 2018. https://www.hospat.org/assets/templates/hospat/pdf/report_2018/2018-4.pdf, (参照2021-8-26
3) Sepúlveda C, Marlin A, Yoshida T, et al. Palliative care: the World Health Organization’s global perspective. Journal of Pain and Symptom Management. 24 (2), 91-96 (2002
23) Masso M, Allingham SF, Banfield M, et al. Palliative care phase: inter-rater reliability and acceptability in a national study. Palliative Medicine. 29 (1), 22-30 (2015
9) Lee LA, Eagar KM, Smith MC. Subacute and non-acute casemix in Australia. The Medical Journal of Australia. 169 (S1), S22-25 (1998
13) 厚生労働省. がん対策推進基本計画 (第4期). 厚生労働省. 2023. https://www.mhlw.go.jp/content/10900000/001077564.pdf, (参照2023-4-1
16) Eagar K, Gordon R, Green J, et al. An Australian casemix classification for palliative care: lessons and policy implications of a national study. Palliative Medicine. 18 (3), 227-233 (2004
6) Murtagh F, Santarelli M, Bradshaw A, et al. Outcome Measures in Palliative Care. Hull York Medical School. 2019. https://www.hyms.ac.uk/assets/docs/research/outcome-measures-in-palliative-care.pdf, (参照 2023-8-22
10) Eagar K, Watters P, Currow DC, et al. The Australian Palliative Care Outcomes Collaboration (PCOC) --measuring the quality and outcomes of palliative care on a routine basis. Australian Health Review. 34 (2), 186-192 (2010
29) Becker C, Leidl R, Schildmann E, et al. A pilot study on patient-related costs and factors associated with the cost of specialist palliative care in the hospital: first steps towards a patient classification system in Germany. Cost Effectiveness and Resource Allocation. 16, 35 (2018
18) Currow DC, Allingham S, Yates P, et al. Improving national hospice/palliative care service symptom outcomes systematically through point-of-care data collection, structured feedback and benchmarking. Supportive Care in Cancer. 23 (2), 307-315 (2015
28) Ding J, Johnson CE, Qin X, et al. Palliative care needs and utilisation of different specialist services in the last days of life for people with lung cancer. European Journal of Cancer Care. 30 (1), e13331 (2021
30) Ekström M, Allingham SF, Eagar K, et al. Breathlessness During the Last Week of Life in Palliative Care: An Australian Prospective, Longitudinal Study. Journal of Pain and Symptom Management. 51 (5), 816-823 (2016
33) 宮下光令, 佐藤一樹, 清水恵. 緩和ケアの質の評価. 東北大学医学部保健学科紀要. 19 (2), 63-71 (2010
11) Department of Health and Social Care. Independent Palliative Care Funding Review. GOV-UK. 2011. https://www.gov.uk/government/publications/independent-palliative-care-funding-review, (参照2021-8-26
22) Ding J, Cook A, Qin X, et al. Palliative care needs and utilization of specialist services for people imminently dying with dementia: a national population-based study. International Journal of Nursing Studies. 109, 103655 (2020
35) 神津 三佳, 光多 恵子, 藤澤 陽子, 他. 終末期がん患者に関わる看護師の専門看護師・認定看護師の役割に対するニーズ. 日本がん看護学会誌. 24 (3), 45-51 (2010
19) Burke K, Coombes LH, Petruckevitch A, et al. Inter-rater reliability of the phase of illness tool in pediatric palliative care. The American Journal of Hospice & Palliative Care. 37 (10), 837-843 (2020
5) Palliative Care Outcomes Collaboration (PCOC). Palliative Care Outcomes Collaboration Clinical Manual. Universty of Wollongong. 2021. https://documents.uow.edu.au/content/groups/public/@web/@chsd/@pcoc/documents/doc/uow129133.pdf, (参照2021-8-26
26) Murtagh FE, Ramsenthaler C, Firth A, et al. A brief, patient- and proxy-reported outcome measure in advanced illness: Validity, reliability and responsiveness of the Integrated Palliative care Outcome Scale (IPOS). Palliative Medicine. 33 (8), 1045-1057 (2019
27) Woods JA, Katzenellenbogen JM, Murray K, et al. Occurrence and timely management of problems requiring prompt intervention among Indigenous compared with non-Indigenous Australian palliative care patients: a multijurisdictional cohort study. BMJ Open. 11 (3), e042268 (2021
7) de Wolf-Linder S, Dawkins M, Wicks F, et al. Which outcome domains are important in palliative care and when? An international expert consensus workshop, using the nominal group technique. Palliative Medicine. 33 (8), 1058-1068 (2019
References_xml – reference: 3) Sepúlveda C, Marlin A, Yoshida T, et al. Palliative care: the World Health Organization’s global perspective. Journal of Pain and Symptom Management. 24 (2), 91-96 (2002)
– reference: 8) Palliative Care Outcomes Collaboration (PCOC). History of phases of palliative care. Universty of Wollongong. 2013. https://documents.uow.edu.au/content/groups/public/@web/@chsd/@pcoc/documents/doc/uow191808.pdf, (参照2021-8-20)
– reference: 6) Murtagh F, Santarelli M, Bradshaw A, et al. Outcome Measures in Palliative Care. Hull York Medical School. 2019. https://www.hyms.ac.uk/assets/docs/research/outcome-measures-in-palliative-care.pdf, (参照 2023-8-22)
– reference: 2) Higginson IJ, Addington-Hall JM. Palliative care needs to be provided on basis of need rather than diagnosis. BMJ. 318 (7176), 123 (1999)
– reference: 20) Lucey M, O’Reilly M, Currow D, et al. Is inpatient hospice care clinically effective? Using phase of illness to evaluate care outcomes for patients admitted to a specialist palliative care unit in Ireland. Journal of Palliative Medicine. 23 (4), 535-541 (2020)
– reference: 25) Mather H, Guo P, Firth A, et al. Phase of illness in palliative care: cross-sectional analysis of clinical data from community, hospital and hospice patients. Palliative Medicine. 32 (2), 404-412 (2018)
– reference: 30) Ekström M, Allingham SF, Eagar K, et al. Breathlessness During the Last Week of Life in Palliative Care: An Australian Prospective, Longitudinal Study. Journal of Pain and Symptom Management. 51 (5), 816-823 (2016)
– reference: 1) World Health Organization. National cancer control programmes : policies and managerial guidelines. 2nd ed. World Health Organization. 2002. https://apps.who.int/iris/handle/10665/42494, (参照2022-9-2)
– reference: 32) Sakurai H, Miyashita M, Imai K, et al. Validation of the Integrated Palliative care Outcome Scale (IPOS) - Japanese Version. Japanese Journal of Clinical Oncology. 49 (3), 257-262 (2019)
– reference: 18) Currow DC, Allingham S, Yates P, et al. Improving national hospice/palliative care service symptom outcomes systematically through point-of-care data collection, structured feedback and benchmarking. Supportive Care in Cancer. 23 (2), 307-315 (2015)
– reference: 4) Wenham S, Cumming M, Saurman E. Improving palliative and end-of-life care for rural and remote Australians. Public Health Research & Plactice. 30 (1), 3012001 (2020)
– reference: 12) Murtagh F. C-CHANGE: Delivering high quality and cost-effective care across the range of complexity for those with advanced conditions in the last year of life. Dimensions. 2011. https://app.dimensions.ai/details/grant/grant.5147811, (参照 2023-8-22)
– reference: 26) Murtagh FE, Ramsenthaler C, Firth A, et al. A brief, patient- and proxy-reported outcome measure in advanced illness: Validity, reliability and responsiveness of the Integrated Palliative care Outcome Scale (IPOS). Palliative Medicine. 33 (8), 1045-1057 (2019)
– reference: 13) 厚生労働省. がん対策推進基本計画 (第4期). 厚生労働省. 2023. https://www.mhlw.go.jp/content/10900000/001077564.pdf, (参照2023-4-1)
– reference: 29) Becker C, Leidl R, Schildmann E, et al. A pilot study on patient-related costs and factors associated with the cost of specialist palliative care in the hospital: first steps towards a patient classification system in Germany. Cost Effectiveness and Resource Allocation. 16, 35 (2018)
– reference: 16) Eagar K, Gordon R, Green J, et al. An Australian casemix classification for palliative care: lessons and policy implications of a national study. Palliative Medicine. 18 (3), 227-233 (2004)
– reference: 28) Ding J, Johnson CE, Qin X, et al. Palliative care needs and utilisation of different specialist services in the last days of life for people with lung cancer. European Journal of Cancer Care. 30 (1), e13331 (2021)
– reference: 14) Kamal AH, Bausewein C, Casarett DJ, et al. Standards, Guidelines, and Quality measures for successful specialty palliative care integration into oncology: current Approaches and Future Directions. Journal of Clinical Oncology. 38 (9), 987-994 (2020)
– reference: 35) 神津 三佳, 光多 恵子, 藤澤 陽子, 他. 終末期がん患者に関わる看護師の専門看護師・認定看護師の役割に対するニーズ. 日本がん看護学会誌. 24 (3), 45-51 (2010)
– reference: 27) Woods JA, Katzenellenbogen JM, Murray K, et al. Occurrence and timely management of problems requiring prompt intervention among Indigenous compared with non-Indigenous Australian palliative care patients: a multijurisdictional cohort study. BMJ Open. 11 (3), e042268 (2021)
– reference: 7) de Wolf-Linder S, Dawkins M, Wicks F, et al. Which outcome domains are important in palliative care and when? An international expert consensus workshop, using the nominal group technique. Palliative Medicine. 33 (8), 1058-1068 (2019)
– reference: 31) Ding J, Johnson CE, Lee YCO, et al. Characteristics of people with dementia vs other conditions on admission to inpatient palliative care. Journal of the American Geriatrics Society. 68 (8), 1825-1833 (2020)
– reference: 33) 宮下光令, 佐藤一樹, 清水恵. 緩和ケアの質の評価. 東北大学医学部保健学科紀要. 19 (2), 63-71 (2010)
– reference: 34) 森田達也. 2018年度調査研究報告 日本・韓国・台湾 第2期共同研究. ホスピス財団. 2018. https://www.hospat.org/assets/templates/hospat/pdf/report_2018/2018-4.pdf, (参照2021-8-26)
– reference: 22) Ding J, Cook A, Qin X, et al. Palliative care needs and utilization of specialist services for people imminently dying with dementia: a national population-based study. International Journal of Nursing Studies. 109, 103655 (2020)
– reference: 11) Department of Health and Social Care. Independent Palliative Care Funding Review. GOV-UK. 2011. https://www.gov.uk/government/publications/independent-palliative-care-funding-review, (参照2021-8-26)
– reference: 10) Eagar K, Watters P, Currow DC, et al. The Australian Palliative Care Outcomes Collaboration (PCOC) --measuring the quality and outcomes of palliative care on a routine basis. Australian Health Review. 34 (2), 186-192 (2010)
– reference: 19) Burke K, Coombes LH, Petruckevitch A, et al. Inter-rater reliability of the phase of illness tool in pediatric palliative care. The American Journal of Hospice & Palliative Care. 37 (10), 837-843 (2020)
– reference: 36) Fernando G, Hughes S. Team approaches in palliative care: a review of the literature. International Journal of Palliative Nursing. 25 (9), 444-451 (2019)
– reference: 15) 角允博. 【非がん疾患に対する緩和ケア】疾患別の特性 multimorbidityと緩和ケア. 内科. 127 (2), 255-257 (2021)
– reference: 5) Palliative Care Outcomes Collaboration (PCOC). Palliative Care Outcomes Collaboration Clinical Manual. Universty of Wollongong. 2021. https://documents.uow.edu.au/content/groups/public/@web/@chsd/@pcoc/documents/doc/uow129133.pdf, (参照2021-8-26)
– reference: 17) Eagar K, Green J, Gordon R. An Australian casemix classification for palliative care: technical development and results. Palliative Medicine. 18 (3), 217-226 (2004)
– reference: 24) Clayton J, Fardell B, Hutton-Potts J, et al. Parenteral antibiotics in a palliative care unit: prospective analysis of current practice. Palliative Medicine. 17 (1), 44-48 (2003)
– reference: 9) Lee LA, Eagar KM, Smith MC. Subacute and non-acute casemix in Australia. The Medical Journal of Australia. 169 (S1), S22-25 (1998)
– reference: 21) Currow DC, Eagar K, Aoun S, et al. Is it feasible and desirable to collect voluntarily quality and outcome data nationally in palliative oncology care? Journal of Clinical Oncology. 26 (23), 3853-3859 (2008)
– reference: 23) Masso M, Allingham SF, Banfield M, et al. Palliative care phase: inter-rater reliability and acceptability in a national study. Palliative Medicine. 29 (1), 22-30 (2015)
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SubjectTerms care needs
palliative care
palliative care phase
phase of illness
ケアニーズ
緩和ケア
Title Phase of Illness (Palliative Care Phase) in Palliative Care: A Literature review
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