OOIR: Observatory of International Research

Papers

(The H4-Index of Palliative Medicine is 24. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-08-01 to 2026-08-01.)

Article	Citations
Neuropalliative care for progressive neurological diseases: A scoping review on models of care and priorities for future research	767
What are we planning, exactly? The perspectives of people with intellectual disabilities, their carers and professionals on end-of-life care planning: A focus group study	94
Assessing the suitability of the Carer Support Needs Assessment Tool (CSNAT-Paediatric) for use with parents of children with a life-limiting condition: A qualitative secondary analysis	55
Posttraumatic growth in palliative care settings: A scoping review of prevalence, characteristics and interventions	54
Complexity and function of family involvement in advance care planning: A qualitative study of perspectives from people living with advanced cancer, family members and healthcare professionals	45
Living experiences of people with advance cancer with low socioeconomic status: A systematic review of qualitative evidence	44
“Walk me through the final day”: A thematic analysis study on the family caregiver experience of the Medical Assistance in Dying procedure day	44
REstoring Sleep and Energy using a mulTimodal non-pharmacological intervention in advanced Cancer: A feasibility study (RESET-C)	43
‘Saying goodbye’. . . A systematic integrative review of palliative caregiving in intergenerational living contexts	43
Maybe for unbearable suffering: Diverse racial, ethnic and cultural perspectives of assisted dying. A scoping review	36
Mistletoe extract in patients with advanced pancreatic cancer: Health-related quality of life in a double-blind, randomized, placebo-controlled trial (MISTRAL)	33
Preserving the integrity of personhood in people with advanced cancer: An in-depth qualitative study among patients, relatives, and care professionals	33
Views of patients with progressive illness and carers about the role of digital advance care planning systems to record and share information: A qualitative study	33
Mixed methods process evaluation of an advance care planning intervention among nursing home staff	32
Propofol for palliative sedation: A systematic review of clinical outcomes, safety, and ethical implications	30
Parents’ experiences of being involved in medical decision-making for their child with a life-limiting condition: A systematic review with narrative synthesis	29
Utilizing intricate care networks : An ethnography of patients and families navigating palliative care in a resource-limited setting	29
Differences in palliative care needs between cancer patients and non-cancer patients at the start of specialized palliative care: A nationwide register-based study	28
End-of-life experience patterns among older adults and their association with pain near death: A population-based study	28
The 13th World Research Congress of the European Association for Palliative Care	26
Corrigendum to Updating international consensus on best practice in care of the dying: A Delphi study	26
Identifying, exploring and integrating the spiritual dimension in proactive care planning: A mixed methods evaluation of a communication training intervention for multidisciplinary palliative care tea	26
The experience of nurses when providing care across acts that may be perceived as death hastening: A qualitative evidence synthesis	25
Facilitating equitable access to hospice care in socially deprived areas: A mixed methods multiple case study	25
‘Sadly I think we are sort of still quite white, middle-class really’ – Inequities in access to bereavement support: Findings from a mixed methods study	24