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The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.

Redefining Palliative Care—A New Consensus-Based Definition

Open access
Radbruch, Lukas, De Lima, Liliana, Knaul, Felicia, Wenk, Roberto, Ali, Zipporah, Bhatnaghar, Sushma, Blanchard, Charmaine, Bruera, Eduardo, Buitrago, Rosa, Burla, Claudia, Callaway, Mary, Munyoro, Esther Cege, Centeno, Carlos, Cleary, Jim, Connor, Stephen, Davaasuren, Odontuya, Downing, Julia, Foley, Kathleen, Goh, Cynthia, Gomez-Garcia, Wendy, Harding, Richard, Khan, Quach T., Larkin, Phillippe, Leng, Mhoira, Luyirika, Emmanuel, Marston, Joan, Moine, Sebastien, Osman, Hibah, Pettus, Katherine, Puchalski, Christina, Rajagopal, M.R., Spence, Dingle, Spruijt, Odette, Venkateswaran, Chitra, Wee, Bee, Woodruff, Roger, Yong, Jinsun, Pastrana, Tania·2020·Journal of Pain and Symptom Management

Abstract

CONTEXT: The International Association for Hospice and Palliative Care developed a consensus-based definition of palliative care (PC) that focuses on the relief of serious health-related suffering, a concept put forward by the Lancet Commission Global Access to Palliative Care and Pain Relief. OBJECTIVE: The main objective of this article is to present the research behind the new definition. METHODS: The three-phased consensus process involved health care workers from countries in all income levels. In Phase 1, 38 PC experts evaluated the components of the World Health Organization definition and suggested new/revised ones. In Phase 2, 412 International Association for Hospice and Palliative Care members in 88 countries expressed their level of agreement with the suggested components. In Phase 3, using results from Phase 2, the expert panel developed the definition. RESULTS: The consensus-based definition is as follows: Palliative care is the active holistic care of individuals across all ages with serious health-related suffering due to severe illness and especially of those near the end of life. It aims to improve the quality of life of patients, their families and their caregivers. The definition includes a number of bullet points with additional details as well as recommendations for governments to reduce barriers to PC. CONCLUSION: Participants had significantly different perceptions and interpretations of PC. The greatest challenge faced by the core group was trying to find a middle ground between those who think that PC is the relief of all suffering and those who believe that PC describes the care of those with a very limited remaining life span.

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Metadata

Authors
Radbruch, L., De Lima, L., Knaul, F., Wenk, R., Ali, Z., Bhatnaghar, S., Blanchard, C., Bruera, E., Buitrago, R., Burla, C., Callaway, M., Munyoro, E. C., Centeno, C., Cleary, J., Connor, S., Davaasuren, O., Downing, J., Foley, K., Goh, C., Gomez-Garcia, W., Harding, R., Khan, Q. T., Larkin, P., Leng, M., Luyirika, E., Marston, J., Moine, S., Osman, H., Pettus, K., Puchalski, C., Rajagopal, M. R., Spence, D., Spruijt, O., Venkateswaran, C., Wee, B., Woodruff, R., Yong, J., & Pastrana, T.
Venue
Journal of Pain and Symptom Management
Publisher
Elsevier BV
Published
2020-10
Volume
60
Issue
4
Pages
754-764
ISSN
0885-3924 (ISSN-L)
OpenAlex
W3023463185
Cited by
1,249
References
18
FWCI
87.25
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Redefining Palliative Care—A New Consensus-Based Definition. https://app.cochat.ai/papers/10.1016/j.jpainsymman.2020.04.027
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Radbruch, L., De Lima, L., Knaul, F., Wenk, R., Ali, Z., Bhatnaghar, S., Blanchard, C., Bruera, E., Buitrago, R., Burla, C., Callaway, M., Munyoro, E. C., Centeno, C., Cleary, J., Connor, S., Davaasuren, O., Downing, J., Foley, K., Goh, C., . . . Pastrana, T. (2020). Redefining Palliative Care—A New Consensus-Based Definition. Journal of Pain and Symptom Management. https://doi.org/10.1016/j.jpainsymman.2020.04.027

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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