| 1 | Guidance on Conducting and REporting DElphi Studies (CREDES) in palliative care: Recommendations based on a methodological systematic review | Palliative Medicine | 2017 | 1,539 |
| 2 | The effects of advance care planning on end-of-life care: A systematic review | Palliative Medicine | 2014 | 1,230 |
| 3 | White paper defining optimal palliative care in older people with dementia: A Delphi study and recommendations from the European Association for Palliative Care | Palliative Medicine | 2014 | 848 |
| 4 | The McGill Quality of Life Questionnaire: a measure of quality of life appropriate for people with advanced disease. A preliminary study of validity and acceptability | Palliative Medicine | 1995 | 642 |
| 5 | Truth may hurt but deceit hurts more: communication in palliative care | Palliative Medicine | 2002 | 437 |
| 6 | Evidence on the cost and cost-effectiveness of palliative care: A literature review | Palliative Medicine | 2014 | 434 |
| 7 | Where people die (1974—2030): past trends, future projections and implications for care | Palliative Medicine | 2008 | 413 |
| 8 | Supporting best practice in reflexive thematic analysis reporting in Palliative Medicine: A review of published research and introduction to the Reflexive Thematic Analysis Reporting Guidelines (RTARG) | Palliative Medicine | 2024 | 409 |
| 9 | How many people need palliative care? A study developing and comparing methods for population-based estimates | Palliative Medicine | 2014 | 396 |
| 10 | Exploring the spiritual needs of people dying of lung cancer or heart failure: a prospective qualitative interview study of patients and their carers | Palliative Medicine | 2004 | 394 |
| 11 | Sympathy, empathy, and compassion: A grounded theory study of palliative care patients’ understandings, experiences, and preferences | Palliative Medicine | 2017 | 394 |
| 12 | Truth-telling in discussing prognosis in advanced life-limiting illnesses: a systematic review | Palliative Medicine | 2007 | 385 |
| 13 | Validity of the McGill Quality of Life Questionnaire in the palliative care setting: a multi-centre Canadian study demonstrating the importance of the existential domain | Palliative Medicine | 1997 | 375 |
| 14 | Do specialist palliative care teams improve outcomes for cancer patients? A systematic literature review | Palliative Medicine | 1998 | 368 |
| 15 | What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness | Palliative Medicine | 2003 | 351 |
| 16 | Review: The understanding of spirituality and the potential role of spiritual care in end-of-life and palliative care: a meta-study of qualitative research | Palliative Medicine | 2010 | 340 |
| 17 | Depression in advanced disease: a systematic review Part 1. Prevalence and case finding | Palliative Medicine | 2002 | 334 |
| 18 | Systematic review of the problems and issues of accessing specialist palliative care by patients, carers and health and social care professionals | Palliative Medicine | 2004 | 327 |
| 19 | Implementing patient-reported outcome measures in palliative care clinical practice: A systematic review of facilitators and barriers | Palliative Medicine | 2014 | 322 |
| 20 | A comparison of the palliative care needs of patients dying from chronic respiratory diseases and lung cancer | Palliative Medicine | 2001 | 317 |
| 21 | What is the impact of population ageing on the future provision of end-of-life care? Population-based projections of place of death | Palliative Medicine | 2018 | 314 |
| 22 | 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 | 2019 | 313 |
| 23 | Management guidelines for motor neurone disease patients on non-invasive ventilation at home | Palliative Medicine | 2006 | 297 |
| 24 | Breakthrough pain characteristics and syndromes in patients with cancer pain. An international survey | Palliative Medicine | 2004 | 293 |
| 25 | Older people's views about home as a place of care at the end of life | Palliative Medicine | 2004 | 292 |
| 26 | Education, implementation, and policy barriers to greater integration of palliative care: A literature review | Palliative Medicine | 2016 | 286 |
| 27 | A randomized controlled trial of aromatherapy massage in a hospice setting | Palliative Medicine | 2004 | 285 |
| 28 | Fatigue in palliative care patients — an EAPC approach | Palliative Medicine | 2008 | 274 |
| 29 | Challenges in palliative care research; recruitment, attrition and compliance: experience from a randomized controlled trial | Palliative Medicine | 1999 | 272 |
| 30 | Advanced cancer patients’ prognostic information preferences: a review | Palliative Medicine | 2009 | 272 |
| 31 | Delirium prevalence, incidence, and implications for screening in specialist palliative care inpatient settings: A systematic review | Palliative Medicine | 2013 | 271 |
| 32 | The meaning of the lived experience of hope in patients with cancer in palliative home care | Palliative Medicine | 2001 | 270 |
| 33 | Dying from cancer: results of a national population-based investigation | Palliative Medicine | 1995 | 269 |
| 34 | Survival prediction in terminal cancer patients: a systematic review of the medical literature | Palliative Medicine | 2000 | 261 |
| 35 | Dying in the hospital setting: A systematic review of quantitative studies identifying the elements of end-of-life care that patients and their families rank as being most important | Palliative Medicine | 2015 | 249 |
| 36 | Can home care maintain an acceptable quality of life for patients with terminal cancer and their relatives? | Palliative Medicine | 1994 | 243 |
| 37 | Symptoms in 400 patients referred to palliative care services: prevalence and patterns | Palliative Medicine | 2003 | 242 |
| 38 | The healthcare needs of chronic obstructive pulmonary disease patients in the last year of life | Palliative Medicine | 2005 | 242 |
| 39 | The Edmonton Symptom Assessment System: a 15-year retrospective review of validation studies (1991–2006) | Palliative Medicine | 2008 | 239 |
| 40 | Symptom burden and quality of life in end-stage renal disease: a study of 179 patients on dialysis and palliative care | Palliative Medicine | 2009 | 237 |
| 41 | Symptom prevalence and quality of life of patients with end-stage liver disease: A systematic review and meta-analysis | Palliative Medicine | 2019 | 234 |
| 42 | Patients’ and caregivers’ needs, experiences, preferences and research priorities in spiritual care: A focus group study across nine countries | Palliative Medicine | 2018 | 230 |
| 43 | Opioids and the immune system | Palliative Medicine | 2006 | 229 |
| 44 | A matter of definition – key elements identified in a discourse analysis of definitions of palliative care | Palliative Medicine | 2008 | 222 |
| 45 | Haematological malignancy: are patients appropriately referred for specialist palliative and hospice care? A systematic review and meta-analysis of published data | Palliative Medicine | 2011 | 221 |
| 46 | Understanding Compassion Satisfaction, Compassion Fatigue and Burnout: A survey of the hospice palliative care workforce | Palliative Medicine | 2013 | 220 |
| 47 | Where do cancer patients die? Ten-year trends in the place of death of cancer patients in England | Palliative Medicine | 1998 | 219 |
| 48 | Preference for place of care and place of death in palliative care: are these different questions? | Palliative Medicine | 2008 | 219 |
| 49 | Advance Care Planning in palliative care: A systematic literature review of the contextual factors influencing its uptake 2008–2012 | Palliative Medicine | 2014 | 219 |
| 50 | A multicentre international study of sedation for uncontrolled symptoms in terminally ill patients | Palliative Medicine | 2000 | 218 |
