The safety and efficacy of using moxibustion and or acupuncture for cancer-related insomnia: a systematic review and meta-analysis of randomised controlled trials by Carol Chunfeng Wang, Ellen Yichun Han, Mark Jenkins, Xuepei Hong, Shuqin Pang, Lisa Whitehead, Deborah L. Kirk, Anne Williams

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The impact of poverty and deprivation at the end of life: a critical review by Jane Rowley, Naomi Richards, Emma Carduff, Merryn Gott

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Palliative care needs, concerns, and affirmative strategies for the LGBTQ population by Noelle Marie Javier

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Reflecting on choices and responsibility in palliative care in the context of social disadvantage by Maddy French, Lorraine Hansford, Tess Moeke-Maxwell

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Dividual identity in grief theories, palliative and bereavement care by Douglas J. Davies

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The impacts of partnering with cancer patients in palliative care research: a systematic review and meta-synthesis by Alessandra Paolucci, Ingrid Nielssen, Karen L. Tang, Aynharan Sinnarajah, Jessica E. Simon, Maria J. Santana

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Perceived policy-related barriers to palliative care implementation: a qualitative descriptive study by Atsede Aregay, Margaret O’Connor, Jill Stow, Nicola Ayers, Susan Lee

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Building an action plan to tackle palliative care inequality through multi-stakeholder platforms by Miguel Antonio Sánchez-Cárdenas, Marta Ximena León-Delgado, Luisa Fernanda Rodríguez-Campos, Juan Esteban Correa-Morales, Laura Vannesa González-Salazar, Ángela María Cañón Piñeros, Genny Paola Fuentes-Bermúdez, Lina María Vargas-Escobar

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Programme Abstracts of the 3rd International Seminar - A Human Rights based approach to Palliative Care: Towards Solutions for Public Health Palliative Care

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An agenda to develop Pediatric Palliative care programs to serve children with life-threatening and life-limiting conditions in the Gulf Cooperation Council countries by Qutaibah Alotaibi, Harold Siden

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Corrigendum to “How does Medical Assistance in Dying affect end-of-life care planning discussions? Experiences of Canadian multidisciplinary palliative care providers”

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Healthcare professionals’ perceived barriers in providing palliative care in primary care and nursing homes: a survey study by Katrin Kochems, Everlien de Graaf, Ginette M. Hesselmann, Marieke J. E. Ausems, Saskia C. C. M. Teunissen

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Corrigendum to “Supporting the dying is a community responsibility”

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Building capability in paediatric palliative care and enhancing education through the voice of parents: the Quality of Care Collaborative Australia by Leigh A. Donovan, Penelope J. Slater, Angela M. Delaney, Sarah J. Baggio, Anthony R. Herbert

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Changes in care managers’ positive attitudes toward dying patients compared to that of nurses by one-day online advance care planning communication training by Kyoko Oshiro, Shozo Okochi, Junko Nakashima, Tomoko Hirano, Shuichi Ohe, Hideki Kojima, Mitsunori Nishikawa

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The influence of context on the implementation of integrated palliative care in an academic teaching hospital in South Africa by Rene Krause, Liz Gwyther, Jill Olivier

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Benefits of integrating palliative care: a qualitative exploration of the perspectives of palliative care providers in a tertiary health facility in Ghana by Joshua Okyere, Kwaku Kissah-Korsah

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Place of death from dementia as an underlying cause during the COVID-19 pandemic in Japan: a cross-sectional study from national death certificates by Miharu Nakanishi, Syudo Yamasaki, Mai Sakai, Hatsumi Yoshii, Asao Ogawa, Atsushi Nishida

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‘It was brutal. It still is’: a qualitative analysis of the challenges of bereavement during the COVID-19 pandemic reported in two national surveys by Anna Torrens-Burton, Silvia Goss, Eileen Sutton, Kali Barawi, Mirella Longo, Kathy Seddon, Emma Carduff, Damian J.J. Farnell, Annmarie Nelson, Anthony Byrne, Rhiannon Phillips, Lucy E. Selman, Emily Harrop

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How does housing affect end-of-life care and bereavement in low-income communities? A qualitative study of the experiences of bereaved individuals and service providers in the Unit... by Lorraine Hansford, Felicity Thomas, Katrina Wyatt

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