Ausgabe 1/2023
Inhalt (205 Artikel)
Increasing palliative care capacity in primary care: study protocol of a cluster randomized controlled trial of the CAPACITI training program
Hsien Seow, Daryl Bainbridge, Samantha Winemaker, Kelli Stajduhar, Gregory Pond, Kathy Kortes-Miller, Denise Marshall, Frances Kilbertus, Jeff Myers, Leah Steinberg, Nadia Incardona, Oren Levine, Jose Pereira
Is aggressive care appropriate for patients with cancer complicated by pneumonia? A retrospective chart review in a tertiary hospital
Chanchanok Aramrat, Thawalrat Ratanasiri, Patama Gomutbutra
Lidocaine transdermal patches reduced pain intensity in neuropathic cancer patients already receiving opioid treatment
Jui-Hung Tsai, I-Ting Liu, Pei-Fang Su, Ying-Tzu Huang, Ge-Lin Chiu, Yu-Yeh Chen, Wei-Shu Lai, Peng-Chan Lin
Estimation of the demand for palliative care in non-oncologic patients in Chile
Nicolás Armijo, Tomás Abbot, Manuel Espinoza, Ximena Neculhueque, Carlos Balmaceda
Feasibility, use and benefits of patient-reported outcome measures in palliative care units: a multicentre observational study
Evelyn Müller, Regine Mayer-Steinacker, Deniz Gencer, Jens Keßler, Bernd Alt-Epping, Stefan Schönsteiner, Helga Jäger, Bettina Couné, Luise Elster, Muhammet Keser, Julia Rauser, Susanne Marquardt, Gerhild Becker
Correction: Assessing professional identity formation (PIF) amongst medical students in Oncology and Palliative Medicine postings: a SEBA guided scoping review
Kelly Jia Hui Teo, Mac Yu Kai Teo, Anushka Pisupati, Rui Song Ryan Ong, Chloe Keyi Goh, Claire Hui Xian Seah, You Ru Toh, Neha Burla, Natalie Song Yi Koh, Kuang Teck Tay, Yun Ting Ong, Min Chiam, Warren Fong, Limin Wijaya, Suzanne Pei Lin Goh, Lalit Kumar Radha Krishna
Monitoring the clinical practice of palliative sedation (PALSED) in patients with advanced cancer: an international, multicentre, non-experimental prospective observational study protocol
Maaike Rijpstra, Kris Vissers, Carlos Centeno, Johan Menten, Lukas Radbruch, Sebastiano Mercadante, Michael Van der Elst, Claudio Adile, Maria Arantzamendi, Evelien Kuip, Sheila Payne, Nancy Preston, Jeroen Hasselaar
Impact of a machine learning algorithm on time to palliative care in a primary care population: protocol for a stepped-wedge pragmatic randomized trial
Ethan P. Heinzen, Patrick M. Wilson, Curtis B. Storlie, Gabriel O. Demuth, Shusaku W. Asai, Gavin M. Schaeferle, Mairead M. Bartley, Rachel D. Havyer
How do cancer patients refuse treatment? A grounded theory study
Hamid Reza Khankeh, Reza Vojdani, Mahboobeh Saber, Mohamadhadi Imanieh
Enhancing end of life care on general internal medical wards: the 3 Wishes Project
Julie C. Reid, Brittany Dennis, Neala Hoad, France Clarke, Rajendar Hanmiah, Daniel Brandt Vegas, Anne Boyle, Feli Toledo, Jill C. Rudkowski, Mark Soth, Diane Heels-Ansdell, Andrew Cheung, Kathleen Willison, Thanh H. Neville, Jason Cheung, Anne Woods, Deborah Cook
Resilience in advanced cancer caregiving promoted by an intimate partner’s support network: insights through the lens of complexity science. A framework analysis
Sophie Opsomer, Sofie Joossens, Emelien Lauwerier, Jan De Lepeleire, Peter Pype
Correction: Specialised Paediatric PAlliativE CaRe: Assessing family, healthcare professionals and health system outcomes in a multi-site context of various care settings: SPhAERA study protocol
Karin Zimmermann, Michael Simon, Katrin Scheinemann, Eva Maria Tinner Oehler, Michèle Widler, Simone Keller, Günther Fink, Stefan Mitterer, Anne-Kathrin Gerber, Stefanie von Felten, Eva Bergstraesser
Dying, death and bereavement: developing a national survey of bereaved relatives
Diarmuid Ó Coimín, Daniela Rohde, Conor Foley, Tracy O’Carroll, Róisín Murphy
Bicentre, randomized, parallel-arm, sham-controlled trial of transcranial direct-current stimulation (tDCS) in the treatment of palliative care patients with refractory cancer pain
Jean-Paul Nguyen, Hélène Gaillard, Alcira Suarez, Élie Terzidis-Mallat, Diane Constant-David, Aurélien Van Langhenhove, Adrien Evin, Catherine Malineau, Son V. O. Tan, Alaa Mhalla, Jean-Pascal Lefaucheur, Julien Nizard
Preparedness, resilience and unmet needs of informal caregivers of advanced cancer patients in a Regional Mission Hospital in Kenya: Qualitative Study
Wesley Too, Faith Lelei, Mary Adam, Pete Halestrap
Reply to ‘Response to “The opinion of French pulmonologists and palliative care physicians on non-invasive ventilation during palliative sedation at end of life: a nationwide survey’’ ’
V. Guastella, A. Greil, C. Lambert, A. Lautrette
Response to “The opinion of French pulmonologists and palliative care physicians on non-invasive ventilation during palliative sedation at end of life: a nationwide survey’’
Robert Twycross, Christina Faull, David Wenzel, David Oliver
Impact of information and communication software on multiprofessional team collaboration in outpatient palliative care – a qualitative study on providers’ perspectives
Anastasia Suslow, Chantal Giehl, Jannis Hergesell, Horst Christian Vollmar, Ina Otte
Needs-based triggers for timely referral to palliative care for older adults severely affected by noncancer conditions: a systematic review and narrative synthesis
Arisa Kawashima, Catherine J. Evans
“I can’t make all this work.” End of life care provision in natural disasters: a qualitative study
Marguerite Kelly, Imogen Mitchell, Iain Walker, Jane Mears, Brett Scholz
Magnesium hydroxide versus macrogol/electrolytes in the prevention of opioid-induced constipation in incurable cancer patients: study protocol for an open-label, randomized controlled trial (the OMAMA study)
K.R.J. Kistemaker, A. de Graeff, M. Crul, G. de Klerk, P.M. van de Ven, M.P. van der Meulen, L. van Zuylen, M.A.H. Steegers
Health care providers’ perspectives on providing end-of-life psychiatric care in cardiology and oncology hospitals: a cross-sectional questionnaire survey
Kanako Ichikura, Shiho Matsuoka, Hiroki Chiba, Hina Ishida, Yuko Fukase, Hanako Murase, Hirokuni Tagaya, Takashi Takeuchi, Eisuke Matsushima
Barriers and facilitators for healthcare professionals to the implementation of Multidisciplinary Timely Undertaken Advance Care Planning conversations at the outpatient clinic (the MUTUAL intervention): a sequential exploratory mixed-methods study
Eline V. T. J. van Lummel, Yoeki Meijer, Dave H. T. Tjan, Johannes J. M. van Delden
Prevalence and associated factors of depressive symptoms among patients with cancer receiving radiotherapy in southern Thailand: a university hospital-based cross-sectional study
Jarurin Pitanupong, Wannapa Phirom, Rungarun Kittichet, Kanthee Anantapong
“My everyday life has returned to normal”- Experiences of patients and relatives with a palliative day care clinic: a qualitative evaluation study
Anne Müller, Alfred Paul, Johannes Best, Stephanie Kunkel, Raymond Voltz, Julia Strupp
Implementation, barriers, and recommendations for further development of advance care planning for the last phase of life in nursing homes in Germany (Gut-Leben): protocol for a mixed-methods study
Stephanie Stiel, Anna Levke Brütt, Jona T Stahmeyer, Anne W E Bockelmann, Tanja Schleef, Anna Völkel, Falk Hoffmann
Muslim patients in the U.S. confronting challenges regarding end-of-life and palliative care: the experiences and roles of hospital chaplains
Robert Klitzman, Gabrielle Di Sapia Natarelli, Elizaveta Garbuzova, Stephanie Sinnappan, Jay Al-Hashimi
The impacts of the scope of benefits expansion on hospice care among adult decedents: a nationwide longitudinal observational study
Tsung-Hsien Yu, Frank Leigh Lu, Chung-Jen Wei, Wei-Wen Wu
Simulation-based learning in palliative care in postgraduate nursing education: a scoping review
Karoline Skedsmo, Andréa Aparecida Gonçalves Nes, Hege Vistven Stenseth, Kristin Hofsø, Marie Hamilton Larsen, Deborah Hilderson, Dieter Smis, Carina Lundh Hagelin, Camilla Olaussen, Marianne Trygg Solberg, Hanne Maria Bingen, Mia Alexandra Ølnes, Simen A. Steindal
Palliative care in severe mental illnesses
Eva Katharina Masel, Bárbara Antunes, Christian Schulz-Quach
Perspectives across Canada about implementing a palliative approach in long-term care during COVID-19
Julia Kruizinga, Stephanie Lucchese, Shirin Vellani, Vanessa Maradiaga Rivas, Sandy Shamon, Karine Diedrich, Laurel Gillespie, Sharon Kaasalainen
Spiritual well-being correlates with quality of life of both cancer and non-cancer patients in palliative care - further validation of EORTC QLQ-SWB32 in Finnish
Raimo Goyarrola, Jari Lipsanen, Suvi-Maria Saarelainen, Raili Suviranta, Eeva Rahko, Annamarja Lamminmäki, Tuula Klaavuniemi, Satu Ahtiluoto, Antti Ohvanainen, Pekka Metso, Reino Pöyhiä
The clinical practice of palliative sedation in patients dying from COVID-19: a retrospective chart review
Maaike Rijpstra, Evelien Kuip, Jeroen Hasselaar, Kris Vissers
Assessing the implementation and effectiveness of early integrated palliative care in long-term care facilities in France: an interventional mixed-methods study protocol
Emmanuel Bagaragaza, Isabelle Colombet, Mireille Perineau, Philippe Aegerter, Frédéric Guirimand
The impact of the COVID-19 pandemic on processes, resource use and cost in palliative care
Farina Hodiamont, Caroline Schatz, Eva Schildmann, Zulfiya Syunyaeva, Katerina Hriskova, Constanze Rémi, Reiner Leidl, Susanne Tänzler, Claudia Bausewein
Mindfulness and compassion training on daily work with patients and within the multiprofessional palliative care team: a retrospective self-assessment study
Franziska Lautwein, Manuela Schallenburger, Alexandra Scherg, Daniel Schlieper, André Karger, Yesche Udo Regel, Jacqueline Schwartz, Martin Neukirchen
Views of people living with dementia and their carers on their present and future: a qualitative study
Danielle Nimmons, Jill Manthorpe, Emily West, Greta Rait, Elizabeth L Sampson, Steve Iliffe, Nathan Davies
Effect of palliative care decisions making on hospital service use at end-of-life in patients with malignant brain tumors: a retrospective study
Nelli-Sofia Nåhls, Riikka-Leena Leskelä, Tiina Saarto, Outi Hirvonen, Anu Anttonen
What do health care professionals want to know about assisted dying? Setting the research agenda in New Zealand
Jessica Young, Jeanne Snelling, Sophie Beaumont, Kate Diesfeld, Ben White, Lindy Willmott, Jacqualine Robinson, Annabel Ahuriri-Driscoll, Gary Cheung, Aida Dehkhoda, Richard Egan, James Jap, Te Hurinui Karaka-Clarke, Leanne Manson, Cam McLaren, Janine Winters
Physician-patient boundaries in palliative care
Chong Yao Ho, Nicole-Ann Lim, Nur Diana Abdul Rahman, Min Chiam, Jamie Xuelian Zhou, Gillian Li Gek Phua, Eng Koon Ong, Crystal Lim, Anupama Roy Chowdhury, Lalit Kumar Radha Krishna
Methadone rotation versus other opioid rotation for refractory cancer induced bone pain: protocol of an exploratory randomised controlled open-label study
Natasha Michael, Merlina Sulistio, Robert Wojnar, Alexandra Gorelik
How does ethnicity affect presence of advance care planning in care records for individuals with advanced disease? A mixed-methods systematic review
Jodie Crooks, Sophie Trotter, Ruby Bhatti OBE, Elizabeth Monaghan, Gemma Clarke
Death place and palliative outcome indicators in patients under palliative home care service: an observational study
Pei-Jung Chang, Cheng-Fu Lin, Ya-Huei Juang, Jui-Yu Chiu, Lung-Chun Lee, Shih-Yi Lin, Yu-Hui Huang
A pilot study on sports activities in pediatric palliative care: just do it
Irene Avagnina, Anna Santini, Irene Maghini, Eleonora Salamon, Simonetta Papa, Luca Giacomelli, Giorgio Perilongo, Caterina Agosto, Franca Benini
Palliative care stay room – designing, testing and evaluating a gamified social intervention to enhance palliative care awareness
Carla Reigada, Anna Sandgren, Sonia Rivas, Ana Carvajal, Santiago Hermida-Romero, Edgar Benítez, Guillem Ripoll, Inés Olza, Carlos Centeno, Beatriz Gómez
Death education for Palliative care: a european project for University students
Ines Testoni, Lucia Ronconi, Hod Orkibi, Gianmarco Biancalani, Melania Raccichini, Luca Franchini, Shoshi Keisari, Mihaela Bucuta, Krzysztof Cieplinski, Michael Wieser, Silvia Varani
Factors associated with suffering from dying in patients with cancer: a cross-sectional analytical study among bereaved caregivers
Angélica Arango-Gutiérrez, Socorro Moreno, Martín Rondón, Lucía I Arroyo, Liliana Ardila, Fabián Alexander Leal Arenas, José A Calvache, Esther de Vries
Attitudes and influencing factors of nursing assistants towards hospice and palliative care nursing in chinese nursing homes: a cross-sectional study
Zhuojun Ye, Limei Jing, Haoyu Zhang, Yongfa Qin, Hangqi Chen, Jiying Yang, Ruize Zhu, Jingrong Wang, Huiwen Zhang, Yifan Xu, Tianshu Chu
Palliative care and new technologies. The use of smart sensor technologies and its impact on the Total Care principle
Tabea Ott, Maria Heckel, Natalie Öhl, Tobias Steigleder, Nils C. Albrecht, Christoph Ostgathe, Peter Dabrock
Accuracy of clinical predictions of prognosis at the end-of-life: evidence from routinely collected data in urgent care records
M. Orlovic, J. Droney, V. Vickerstaff, J. Rosling, A. Bearne, M. Powell, J. Riley, P. McFarlane, J. Koffman, P. Stone
Giving and receiving thanks: a mixed methods pilot study of a gratitude intervention for palliative patients and their carers
Mathieu Bernard, Emmanuelle Poncin, Emilie Bovet, Emmanuel Tamches, Boris Cantin, Josiane Pralong, Gian Domenico Borasio
Uncertainty and probability in neonatal end-of-life decision-making: analysing real-time conversations between healthcare professionals and families of critically ill newborns
Regula Limacher, Jean-Claude Fauchère, Deborah Gubler, Manya Jerina Hendriks
Palliative care in advanced Huntington’s disease: a scoping review
Dorine J. Boersema-Wijma, Erik van Duijn, Anne-Wil Heemskerk, Jenny T. van der Steen, Wilco P. Achterberg
Experiences and perspectives of healthcare professionals implementing advance care planning for people suffering from life-limiting illness: a systematic review and meta-synthesis of qualitative studies
Nanxi Zhu, Liu Yang, Xianlin Wang, Jinmei Tuo, Liuliu Chen, Renli Deng, Rick Yiu Cho Kwan
Correction to: The impact of the COVID-19 pandemic on processes, resource use and cost in palliative care
Farina Hodiamont, Caroline Schatz, Eva Schildmann, Zulfiya Syunyaeva, Katerina Hriskova, Constanze Rémi, Reiner Leidl, Susanne Tänzler, Claudia Bausewein
Barrier analysis for continuity of palliative care from health facility to household among adult cancer patients in Addis Ababa, Ethiopia
Yonas Abate, Kalkidan Solomon, Yoseph Mamo Azmera, Marlieke de Fouw, Mirgissa Kaba
Context of a neonatal death affects parental perception of end-of-life care, anxiety and depression in the first year of bereavement
Gilles Cambonie, Chloé Desage, Pénélope Thaller, Anne Lemaitre, Karine Bertran de Balanda, Clémentine Combes, Arthur Gavotto
Structure and integration of specialty palliative care in three NCI-designated cancer centers: a mixed methods case study
Karen E. Schifferdecker, Rebecca L. Butcher, Genevra F. Murray, Kristin E. Knutzen, Nirav S. Kapadia, Gabriel A. Brooks, Garrett T. Wasp, Susan Eggly, Laura C. Hanson, Gabrielle B. Rocque, Amanda N. Perry, Amber E. Barnato
Protocol for the promoting resilience in stress management (PRISM) intervention: a multi-site randomized controlled trial for adolescents and young adults with advanced cancer
Alison O’Daffer, Liam Comiskey, Samantha R. Scott, Chuan Zhou, Miranda C. Bradford, Joyce P. Yi-Frazier, Abby R. Rosenberg
Comprehensive coordinated community based palliative care (C3PaC) model for cancer patients in North India: a mixed-method implementation research study protocol
Mayank Gupta, Ankita Kankaria, Soumya Swaroop Sahoo, Sushma Bhatnagar, Rakesh Kakkar, Anju Grewal, Gegal Pruthi, Lajya Devi Goyal
Liver-specific metastases as an independent prognostic factor in cancer patients receiving hospice care in hospital
Kun-Siang Huang, Yun-Hwa Huang, Chao-Tung Chen, Chia-Pei Chou, Bo-Lin Pan, Chih-Hung Lee
Correction to: palliative care in advanced Huntington’s disease: a scoping review
Dorine J. Boersema-Wijma, Erik van Duijn, Anne-Wil Heemskerk, Jenny T. van der Steen, Wilco P. Achterberg
Enhancing equity and diversity in palliative care clinical practice, research and education
Jonathan Koffman, Gilla K. Shapiro, Christian Schulz-Quach
A better interpretation of data regarding the opioid switching to methadone
Sebastiano Mercadante
Reply to “A better interpretation of data regarding the opioid switching to methadone”
Haiying Ding, Yu Song, Wenxiu Xin, Jiao Sun, Like Zhong, Qinfei Zhou, Chaoneng He, Liyan Gong, Luo Fang
Influencing factors of knowledge, attitude and behavior in children’s palliative care among pediatric healthcare workers: a cross-sectional survey in China
Lihui Zhu, Zhang Na, Yaojia Hu, Yi Xu, Tingwei Luo, Yuqiong Xiang, Sishan Jiang, Zhiqiang Zhang, Muhua Chen, Yuee Xiong
Children with palliative care needs in Papua New Guinea, and perspectives from their parents and health care workers: a qualitative study
Villa Watch, Gwenda Anga, Cornelia Kilalang, Francis Pulsan, John D Vince, Trevor Duke
The importance of developing palliative care quality indicators for the prison setting: why now, and next steps
Isabelle Schaefer, Nicole Heneka, Michelle DiGiacomo, Stacey Panozzo, Jane L. Phillips
The impact of COVID-19 on the experiences of patients and their family caregivers with medical assistance in dying in hospital
Eryn Tong, Rinat Nissim, Debbie Selby, Sally Bean, Elie Isenberg-Grzeda, Tharshika Thangarasa, Gary Rodin, Madeline Li, Sarah Hales
The clinical effect evaluation of multidisciplinary collaborative team combined with palliative care model in patients with terminal cancer: a randomised controlled study
Yu-Jing Liu, Li-Ping Wu, Hong Wang, Qing Han, Shu-Na Wang, Jing Zhang
Quality of life and depression in patients with amyotrophic lateral sclerosis – does the country of origin matter?
Katarzyna Ciećwierska, Dorothée Lulé, Maksymilian Bielecki, Olga Helczyk, Anna Maksymowicz-Śliwińska, Julia Finsel, Krzysztof Nieporęcki, Peter M. Andersen, Albert C. Ludolph, Magdalena Kuźma-Kozakiewicz
Palliative care in rural areas – collaboration between district nurses and doctors: an interview study
Ulla Näppä, Elin Nässén, Idun Winqvist
Applying terror management theory to patients with life-threatening illness: a systematic review
Mark Svet, Laura B. Portalupi, Tom Pyszczynski, Daniel D. Matlock, Larry A. Allen
Impact of an outpatient palliative care consultation and symptom clusters in terminal patients at a tertiary care center in Pakistan
Wardah Rafaqat, Abbas Raza Syed, Ibrahim Munaf Ahmed, Shiraz Hashmi, Ismat Jabeen, Samina Rajwani, Uqba Qamar, Muhammad Atif Waqar
Medical care costs at the end of life among older adults with cancer: a national health insurance data-based cohort study
Minjeong Jo, Yunji Lee, Taehwa Kim
Psychometrics of the Persian version of the program in palliative care education and practice questionnaire (German revised - PPCEP-GR)
Mohajer Abdoli, Katharina Fetz, Shahram Molavynejad, Hamid Sharif-Nia, Marziyeh Asadizaker
Death doula working practices and models of care: the views of death doula training organisations
Deb Rawlings, Lauren Miller-Lewis, Jennifer Tieman, Kate Swetenham
SPICT as a predictive tool for risk of 1-year health degradation and death in older patients admitted to the emergency department: a bicentric cohort study in Belgium
Delphine Bourmorck, Marie de Saint-Hubert, Marianne Desmedt, Ruth Piers, Julien Flament, Isabelle De Brauwer
Understanding pediatric palliative care within interdisciplinary palliative programs: a qualitative study
Patricia Rico-Mena, Javier Güeita-Rodríguez, Ricardo Martino-Alba, Lourdes Chocarro-Gonzalez, Ismael Sanz-Esteban, Domingo Palacios-Ceña
A comparison of palliative care and rapid emergency screening (P-CaRES) tool, broad and narrow criteria, and surprise questions to predict survival of older emergency department patients
Siripan Koyavatin, Shan Woo Liu, Jiraporn Sri-on
Exploring the telehealth readiness and its related factors among palliative care specialist nurses: a cross-sectional study in China
Junchen Guo, Yunyun Dai, Youwen Gong, Xianghua Xu, Yongyi Chen
Ambitions for palliative and end of life care: mapping examples of use of the framework across England
Erica Borgstrom, Joanne Jordan, Claire Henry
Advanced directives’ knowledge among Portuguese palliative patients and caregivers: do the sociodemographic factors influence it? A cross-sectional survey
Catarina Sampaio Martins, Rui Nunes
Trusting relationships between patients with non-curative cancer and healthcare professionals create ethical obstacles for informed consent in clinical trials: a grounded theory study
Mary Murphy, Eilís McCaughan, Gareth Thompson, Matthew A Carson, Jeffrey R Hanna, Monica Donovan, Richard H Wilson, Donna Fitzsimons
The dignity of terminally ill children in pediatric palliative care: perspectives of parents and healthcare providers
Siyu Cai, Qiaohong Guo, Junyi Lin, Chanjuan Deng, Huijun Li, Xuan Zhou
Russian nurses’ readiness for transcultural care of palliative patients
Nataliya Kasimovskaya, Natalia Geraskina, Elena Fomina, Svetlana Ivleva, Maria Krivetskaya, Nina Ulianova, Marina Zhosan
Non-pharmacological interventions to manage psychological distress in patients living with cancer: a systematic review
Carole A. Paley, Jason W. Boland, Martina Santarelli, Fliss E. M. Murtagh, Lucy Ziegler, Emma J. Chapman
Correction: The importance of developing palliative care quality indicators for the prison setting: why now, and next steps
Isabelle Schaefer, Nicole Heneka, Michelle DiGiacomo, Stacey Panozzo, Jane L. Phillips
Experiences of pain and pain management in advanced disease and serious illness for people from South Asian communities in Leeds and Bradford: a qualitative interview study
Gemma Clarke, Jodie Crooks, Michael I. Bennett, Zarina Mirza, Ruby Bhatti OBE, Wali Nazar, Rahila Mughal, Shenaz Ahmed
Associations of health literacy, personality traits, and pro-individualism with the willingness to complete advance directives in Taiwan
Duan-Rung Chen, Hui-Ching Weng
A qualitative exploration of allied health providers’ perspectives on cultural humility in palliative and end-of-life care
Hardeep Singh, Arta Taghavi Haghayegh, Riya Shah, Lovisa Cheung, Sachindri Wijekoon, Kevin Reel, Ruheena Sangrar
Interdisciplinary collaboration in serious illness conversations in patients with multiple myeloma and caregivers – a qualitative study
Cæcilie Borregaard Myrhøj, Dorte Toudal Viftrup, Mary Jarden, Stine Novrup Clemmensen
The outcomes of postgraduate palliative care education and training: assessment and comparison of nurses and physicians
Kevin Marciniak, Alexandra Scherg, Piret Paal, Stephen Mason, Frank Elsner
Translation and psychometric validation of the Persian version of palliative care attitudes scale in cancer patients
Sajjad Bagheri, Maasoumeh Barkhordari-Sharifabad
“Such an institution represents the circle of life” – bringing an inpatient hospice into an academic setting: a pre-implementation exploratory study
Kim Dillen, Thomas Montag, Birgit Weihrauch, Heidrun Golla, Raymond Voltz, Julia Strupp
Could palliative sedation be seen as unnamed euthanasia?: a survey among healthcare professionals in oncology
E. Lucchi, M. Milder, A. Dardenne, C. Bouleuc
Who cares for the carers? carerhelp: development and evaluation of an online resource to support the wellbeing of those caring for family members at the end of their life
Jennifer Tieman, Peter Hudson, Kristina Thomas, Di Saward, Deborah Parker
Physiotherapy applied to palliative care patients: a descriptive practice-based study
A Navarro-Meléndez, MJ Gimenez, Y Robledo-Donascimento, A Río-González, A Lendínez-Mesa
Key aspects of psychosocial needs in palliative care - a qualitative analysis within the setting of a palliative care unit in comparison with specialised palliative home care
Cathrin Michel, Hannah Seipp, Katrin Kuss, Michaela Hach, Andrea Kussin, Jorge Riera-Knorrenschild, Stefan Bösner
Health care providers’ early experiences of assisted dying in Aotearoa New Zealand: an evolving clinical service
Jeanne Snelling, Jessica Young, Sophie Beaumont, Kate Diesfeld, Ben White, Lindy Willmott, Jacqualine Robinson, Tess Moeke-Maxwell
Palliative care as a digital working world (PALLADiUM) - A mixed-method research protocol
Sandra Grimminger, Maria Heckel, Moritz Markgraf, Sarah Peuten, Moritz Wöhl, Henner Gimpel, Carsten Klein, Christoph Ostgathe, Tobias Steigleder, Werner Schneider
Improving palliative care for people with intellectual disability: a self-assessment of policies, practices and competencies in care services
Hille Voss, Anneke L. Francke, Anke J.E. de Veer
Improving serious illness communication: a qualitative study of clinical culture
Joanna Paladino, Justin J. Sanders, Erik K. Fromme, Susan Block, Juliet C. Jacobsen, Vicki A. Jackson, Christine S. Ritchie, Suzanne Mitchell
Using Palliative Leaders in Facilities to Transform Care for People with Alzheimer’s Disease (UPLIFT-AD): protocol of a palliative care clinical trial in nursing homes
Kathleen T. Unroe, Mary Ersek, Wanzhu Tu, Alexander Floyd, Todd Becker, Jessica Trimmer, Jodi Lamie, John Cagle
Palliative care needs of Jordanian women’s experience of living with stroke: a descriptive phenomenological study
Marwa Nayef Alhalabi, Inaam Abdulla Khalaf, Ruqayya Sayed Zeilani, Hala Ahmad Bawadi, Ahmad S. Musa, Abdulqadir J. Nashwan
Public perceptions of advance care planning (ACP) from an international perspective: a scoping review
Anne Canny, Bruce Mason, Kirsty Boyd
“Daring to deal with the difficult and unexpected” registered nurses’ confidential conversations with patients with palliative care needs: a qualitative interview study
Tove Stenman, Ulla Näppä, Ylva Rönngren, Christina Melin-Johansson
Encouraging outpatients in an acute hospital for the relief of cancer-related pain: a qualitative study
Miwa Hinata, Kikuko Miyazaki, Takeo Nakayama, Megumi Tokunaga, Toru Watanabe, Shuichi Nawata
More older adults died at their preferred place after implementation of a transmural care pathway for older adults at the end of life: a before-after study
Iris van Doorne, Marike A. de Meij, Juliette L. Parlevliet, Vera M. W. van Schie, Dick L. Willems, Bianca M. Buurman, Marjon van Rijn
Barriers and facilitators of electronic patient-reported outcome measures (e-PROMs) for patients in home palliative cancer care: a qualitative study of healthcare professionals’ perceptions
Letteria Consolo, Stella Colombo, Ilaria Basile, Daniele Rusconi, Tiziana Campa, Augusto Caraceni, Maura Lusignani
Designing and psychometric properties of the hospitalized patients’ spiritual needs questionnaire (HPSNQ) in the medical-surgical hospital setting
Fahimeh Alsadat Hosseini, Marzieh Momennasab, Joan Guàrdia-Olmos, Shahrzad Yektatalab, Maryam Shaygan, Armin Zareiyan
Exploring the influencing factors of unmet palliative care needs in Chinese patients with end-stage renal disease undergoing maintenance hemodialysis: a cross-sectional study
Xuefei Wang, Yongzhen Mo, Yingying Yuan, Yi Zhou, Yan Chen, Juan Sheng, Jing Liu
Socio-economic determinants for the place of last care: results from the acute palliative care unit of a large comprehensive cancer center in a high-income country in Europe
Sebastian M. Christ, Ellen Hünerwadel, Bigna Hut, Maiwand Ahmadsei, Oliver Matthes, Annina Seiler, Markus Schettle, David Blum, Caroline Hertler
The experiences of patients with advanced heart failure, family carers, and health professionals with palliative care services: a secondary reflexive thematic analysis of longitudinal interview data
Bader Nael Remawi, Amy Gadoud, Nancy Preston
Anxiety and depression disorders in oncological patients under palliative care at a hospital service: a cross-sectional study
Gustavo Souza Gontijo Garcia, Karina Cardoso Meira, Alessandra Hubner de Souza, Nathalia Sernizon Guimarães
Regional perspectives on the coordination and delivery of paediatric end-of-life care in the UK: a qualitative study
Andrew Papworth, Julia Hackett, Bryony Beresford, Fliss Murtagh, Helen Weatherly, Sebastian Hinde, Andre Bedendo, Gabriella Walker, Jane Noyes, Sam Oddie, Chakrapani Vasudevan, Richard G. Feltbower, Bob Phillips, Richard Hain, Gayathri Subramanian, Andrew Haynes, Lorna K. Fraser
Drug landscape in patients receiving general outpatient palliative care in Germany: results from a retrospective analysis of 10,464 patients
Sven H. Loosen, Jacqueline Schwartz, Steven Grewe, Sarah Krieg, Andreas Krieg, Tom Luedde, Yann-Nicolas Batzler, Karel Kostev, Martin Neukirchen, Christoph Roderburg
Effect of an educational intervention on nurses’ competence in activities of daily living support in end-of-life care using a pretest–posttest repeated measures design
Heidrun Gattinger, Stefan Ott, Carola Maurer, Brigitte Marty-Teuber, Virpi Hantikainen, André Fringer
Dry mouth in patients with a life-limiting condition or frailty: a study protocol for two intervention studies and a nested qualitative sub-study (the Dry mOuth Project, DROP)
Annelot I. van der Meulen, Evelien P. J. G. Neis, Ellen J. M. de Nijs, Bénédicte J. E. G. Coenegracht, Arianne Stoppelenburg, Marieke H. J. van den Beuken-van Everdingen, Yvette M. van der Linden
Exploring the challenges and roles of nurses in delivering palliative care for cancer patients and co-morbidities in Ghana
Evans Osei Appiah, Awube Menlah, Jiayun Xu, Awuku Adomaa Susana, Boateng Susana Agyekum, Isabella Garti, Pascal Kob, Joyce Kumah
Care challenges of home health patients living with dementia: a pathway forward with palliative care
Connie S. Cole, Ashley Dafoe, Caroline K. Tietbohl, Sarah R. Jordan, Amy G. Huebschmann, Hillary D. Lum, Christine D. Jones
Home-based care for people living with dementia at the end of life: the perspective of experts
Christiane Pinkert, Bernhard Holle
Preferences and end of life care for residents of aged care facilities: a mixed methods study
Moberley Sarah, Hewitt Jacqui, Attia John, Cole Janean, Bevington Joelle, Oldmeadow Christopher, Howard Zach, Hughes Rachel
Comparison of home-based palliative care delivered by community health workers versus usual care: research protocol for a pilot randomized controlled trial
Suparna Qanungo, Kathleen B. Cartmell, Martina Mueller, Melissa Butcher, Saswati Sarkar, Tyler-Gail Carlson, Mohan Madisetti, Gaurav Kumar
Expert-approved best practice recommendations on the use of sedative drugs and intentional sedation in specialist palliative care (SedPall)
Christoph Ostgathe, Claudia Bausewein, Eva Schildmann, Jeremias Bazata, Violet Handtke, Maria Heckel, Carsten Klein, Alexander Kremling, Sandra Kurkowski, Sophie Meesters, Andreas Seifert, Jorge Luis Torres Cavazos, Kerstin Ziegler, Christian Jäger, Jan Schildmann
Filling gaps in experiences religious understanding of people living with cancer in palliative care: a phenomenological qualitative study
Hellen Luiza Meireles Silva, Pedro Henrique Martins Valério, Cristiano Roque Antunes Barreira, Fernanda Maris Peria
Participatory development of a manual for the implementation of diversity-sensitive palliative and hospice care in Germany: a mixed-methods study protocol
Fabian Erdsiek, Yüce Yılmaz-Aslan, Patrick Brzoska
Healthcare professionals’ perspectives of the management of people with palliative care needs in the emergency department of a UK hospital
Jane Sausman, Azra Arif, Annie Young, John MacArtney, Cara Bailey, Jaimini Rajani, Rebecca Burt
Effects of a home-based palliative heart failure program on quality of life among the elderly: a clinical trial study
Mohammad Hossein Khajehpoor, Parvin Mangolian shahrbabaki, Esmat Nouhi
Evaluation of factors predicting the benefit from systemic oncological treatment for severely ill hospitalized patients: a retrospective study
Milena Brachmans Mascarenhas Neves, Yuri Costa Sarno Neves, Juliana Vieira Biason Bomonetto, Priscila Prais Carneiro Matos, Auro Del Giglio, Daniel de Iracema Gomes Cubero
“I didn’t know it was going to be like this.”: unprepared for end-of-Life care, the experiences of care aides care in long-term care
Laura Booi, Judith Sixsmith, Habib Chaudhury, Deborah O’connor, Claire Surr, Melanie Young, Andrew Sixsmith
Psychosocial-spiritual well-being is related to resilience and mindfulness in patients with severe and/or life-limiting medical illness
Polycarpe Bagereka, Rezvan Ameli, Ninet Sinaii, Marcelli Cristine Vocci, Ann Berger
Association between physicians’ characteristics and their knowledge, attitudes, and practices regarding advance care planning: a cross-sectional study
Ayaka Sakamoto, Ryota Inokuchi, Masao Iwagami, Kyoko Hanari, Nanako Tamiya
Kenyan palliative care providers’ and leaders’ perceptions of palliative care research needs and support to facilitate rigorous research
K. B. Cartmell, E. A. Doherty, N. Gikaara, Z. Ali, S. Qanungo, E. S. Melikam, R. A. Powell
A new scale assessing the stressors and rewards of children’s hospice work
Andrew Papworth, Andre Bedendo, Jo Taylor, Bryony Beresford, Suzanne Mukherjee, Lorna K Fraser, Lucy Ziegler
Dimensions of spiritual well-being in relation to physical and psychological symptoms: a cross-sectional study of advanced cancer patients admitted to a palliative care unit
Yilong Yang, Xinxin Zhao, Meng Cui, Yumei Wang
Patient and hospital characteristics associated with do-not-resuscitate/do-not-intubate orders: a cross-sectional study based on the Taiwan stroke registry
Hsu-Ling Yeh, Fang-I Hsieh, Li-Ming Lien, Wen-Hua Kuo, Jiann-Shing Jeng, Yu Sun, Cheng-Yu Wei, Po-Yen Yeh, Hei-Tung Yip, Cheng-Li Lin, Nicole Huang, Kai-Cheng Hsu
Dissemination and Implementation of a Community Health Worker Intervention for Disparities in Palliative Care (DeCIDE PC): a study protocol for a hybrid type 1 randomized controlled trial
Amn Siddiqi, Olivia Monton, Alison Woods, Taleaa Masroor, Shannon Fuller, Jill Owczarzak, Gayane Yenokyan, Lisa A. Cooper, Karen M. Freund, Thomas J. Smith, Jean S. Kutner, Kathryn L. Colborn, Robert Joyner, Ronit Elk, Fabian M. Johnston
Access to palliative care in patients with advanced cancer of the uterine cervix in the low- and middle-income countries: a systematic review
Francis Ooko, Tebogo Mothiba, Peter Van Bogaert, Johan Wens
A call to improve paediatric palliative care quality through research
Laure Dombrecht, Ana Lacerda, Joanne Wolfe, Jennifer Snaman
Interventions that may increase control at the end of life in persons with dementia: the cross-cultural CONT-END acceptability study protocol and pilot-testing
Hanneke J.A. Smaling, Xu Jingyuan, Miharu Nakanishi, Shiri Shinan-Altman, David R. Mehr, Lukas Radbruch, Jan Gaertner, Perla Werner, Wilco P. Achterberg, Jenny T. van der Steen
Implementing palliative care education into primary care practice: a qualitative case study of the CAPACITI pilot program
Midori Matthew, Daryl Bainbridge, Valerie Bishop, Christina Sinding, Samantha Winemaker, Frances Kilbertus, Katherine Kortes-Miller, Hsien Seow
National survey on the availability of oncology palliative care services at tertiary general and cancer hospitals in China
Xiaomei Li, Xin Shelley Wang, Haili Huang, Miao Liu, Yinan Wu, Jiaojiao Qiu, Boran Zhang, Linhong Cui, David Hui
Physicians’ attitudes and experiences about withholding/withdrawing life-sustaining treatments in pediatrics: a systematic review of quantitative evidence
Yajing Zhong, Alice Cavolo, Veerle Labarque, Chris Gastmans
Palliative care in Malawi: a scoping review
Natalie Palumbo, Alyssa Tilly, Eve Namisango, Christian Ntizimira, Lameck Thambo, Maria Chikasema, Gary Rodin
A survey of palliative care domains and the palliative care provision confidence of Thai family practitioners
Itthipon Wongprom, Arthit Chaithanasarn
Patient-reported outcome measures in children, adolescents, and young adults with palliative care needs—a scoping review
Heidi Holmen, Anette Winger, Simen A. Steindal, Kirsti Riiser, Charlotte Castor, Lisbeth Gravdal Kvarme, Kari L. Mariussen, Anja Lee
Barriers and facilitators to palliative care for patients with non-curable cancer in Colombia: perspectives of allied health and social care professionals
Cindy V. Mendieta, Esther de Vries, Maria Elizabeth Gomez-Neva, Angela Maria Muñoz-Escudero, Jose Andrés Calvache, Tracey McConnell
Swallowing disorders and mortality in adults with advanced cancer outside the head and neck and upper gastrointestinal tract: a systematic review
Danielle Nunes Moura Silva, Laélia Cristina Caseiro Vicente, Vanessa Laís Pontes Glória, Amélia Augusta de Lima Friche
The state of undergraduate palliative care education at Austrian medical schools – a mixed methods study
Véronique Toussaint, Piret Paal, Rainer Simader, Frank Elsner
Innovative communication approaches for initializing pediatric palliative care: perspectives of family caregivers and treating specialists
Lucie Hrdlickova, Kristyna Polakova, Martin Loucka
Specialist palliative care until the very end of life - reports of family caregivers and the multiprofessional team
Anneke Ullrich, Sven Goldbach, Wiebke Hollburg, Bettina Wagener, Annette Rommel, Marten Müller, Denise Kirsch, Katrin Kopplin-Foertsch, Holger Schulz, Carsten Bokemeyer, Karin Oechsle
Adaptation and validation of the Brazilian version of the Measure of Moral Distress for Healthcare Professionals (MMD-HP BR) in the context of palliative care
Julianna Rodrigues Beltrão, Marianna Rodrigues Beltrão, Rafaella Stradiotto Bernardelli, Renato Soleiman Franco, Elizabeth G. Epstein, Carla Corradi-Perini
Burnout and quality of life in Portuguese healthcare professionals working in oncology and palliative care—a preliminary study
Florbela Gonçalves, Margarida Gaudêncio
Palliative care in Ethiopia’s rural and regional health care settings: a qualitative study of enabling factors and implementation challenges
Atsede Aregay, Margaret O’Connor, Jill Stow, Nicola Ayers, Susan Lee
POMSNAME: an aide-mémoire to improve the assessment and documentation of palliative care – a longitudinal project
Ann Dadich, Martyna Gliniecka, Michelle Cull, Kerrie Womsley
Training nurses to facilitate and implement CURA in palliative care institutions: development and evaluation of a blended learning program
Malene van Schaik, Charlotte Kröger, Lisa Zuidema, Margreet Stolper, Guy Widdershoven, H. Roeline Pasman, Suzanne Metselaar
Appetite and its association with mortality in patients with advanced cancer – a Post-hoc Analysis from the Palliative D-study
Charlotte Goodrose-Flores, Stephanie E. Bonn, Caritha Klasson, Maria Helde Frankling, Ylva Trolle Lagerros, Linda Björkhem-Bergman
Continuous deep sedation at the end of life: a qualitative interview-study among health care providers on an evolving practice
Madelon T Heijltjes, Ghislaine JMW van Thiel, Judith AC Rietjens, Agnes van der Heide, Geeske Hendriksen, Johannes JM van Delden
Spiritual care from the perspective of family caregivers and nurses in palliative care: a qualitative study
Aslı Kurtgöz, Elif Keten Edis
Balancing pandemic public health restrictions and family support at the end of life: palliative care and bereavement experiences of parents whose child died during the COVID-19 pandemic
Adam Rapoport, David B. Nicholas, Rosslynn T. Zulla
Psychosocial burdens in palliative care – a longitudinal cohort study in nursing homes and impacts of the COVID-19 pandemic
Anna Bußmann, Natalie Pomorin
Psychosocial functioning in individuals with advanced oesophago-gastric cancer: a mixed methods systematic review
Cara Ghiglieri, Martin Dempster, Sam Wright, Lisa Graham-Wisener
Online modules to improve health professionals’ end-of-life law knowledge and confidence: a pre-post survey study
Rachel Feeney, Lindy Willmott, Penny Neller, Shih-Ning Then, Patsy Yates, Ben White
Structural characteristics and contractual terms of specialist palliative homecare in Germany
Maximiliane Jansky, Lia Heyl, Michaela Hach, Steven Kranz, Thomas Lehmann, Antje Freytag, Ulrich Wedding, Winfried Meißner, Sabine H. Krauss, Werner Schneider, Friedemann Nauck, Anna Bauer, Bianka Ditscheid, Cornelia Eichhorn, Elke Gaser, Ulrike Hammer, Aicko Helbig, Beata Hennig, Michelle Kaufmann, Markus Krause, Isabel Kruschel, Helmut L’hoest, Srikanth Maddela, Ursula Marschall, Martial Mboulla, Heiner Melching, Florian Mühler, Cornelia Nageler, Sara Parhizkari, Judith Rothaug, Joachim Saam, Sven Schulz, Kathleen Stichling, Horst C. Vollmar, Julia von Hayek
My virtual home: needs of patients in palliative cancer care and content effects of individualized virtual reality – a mixed methods study protocol
Christina Gerlach, Anja Greinacher, Bernd Alt-Epping, Cornelia Wrzus
Translation and cultural adaptation of the Greek integrated palliative care outcome scale (IPOS): challenges in a six-phase process
Despina Anagnostou, Stylianos Katsaragakis, Irene Panagiotou, Elisabeth Patiraki, Aliki Tserkezoglou
The expression of ultimate life goals in co-creative art processes with palliative cancer patients
Yvonne Weeseman, Michael Scherer-Rath, Nirav Christophe, Henny Dörr, Esther Helmich, Mirjam A. G. Sprangers, Niels van Poecke, Hanneke W. M. van Laarhoven
Patients’ preferences for delivering bad news in palliative care in Ethiopia: a qualitative study
Ephrem Abathun Ayalew, Ditaba David Mphuthi, Kholofelo Lorraine Matlhaba
Implementation of the Richmond Agitation-Sedation Scale (palliative version) on an inpatient palliative care unit
Shirley H. Bush, Katarzyna Bronicki, Michel Dionne, Natasha Lelievre, Peter G. Lawlor, Monisha Kabir
Caregiver strain among patients of palliative care in Sri Lanka: validation of modified caregiver strain index - Sinhala version
U. Ramadasa, S. Silva, U. Udumulla, S. Perera, S. Lekamwasam
Eye donation in hospice and hospital palliative care settings: perceptions, practice, and service development needs – findings from a national survey
Tracy Long-Sutehall, Anna Zatorska, Michelle Myall, Christina Faull, Adam Hurlow, Sarah Mollart, Clare Rayment, Jill Short, Jane Wale, Emma Winstanley, Mike Bracher
Measurement and documentation of quality indicators for the end-of-life care of hospital patients a nationwide retrospective record review study
F. M. Bijnsdorp, B. Schouten, A. K. L. Reyners, C. Wagner, A. L. Francke, S. M. van Schoten
Home care nurses facilitating planned home deaths. A focused ethnography
Anne Kristine Sørstrøm, Mette Spliid Ludvigsen, Ingjerd Gåre Kymre
Exploring the variations in death anxiety among oncology nurses in China: a latent class analysis
Xian Chen, Mengyu Su, Anne Arber, Chengping Qiao, Jinfeng Wu, Cuihua Sun, Dan Wang, Hui Zhou, Zhu Zhu
Specialist perinatal palliative care: a retrospective review of antenatal referrals to a children’s palliative care service over 14 years
Sophie Bertaud, Georgina Brightley, Nicola Crowley, Finella Craig, Dominic Wilkinson
Xerostomia in patients with advanced cancer: a scoping review of clinical features and complications
Maria Walsh, Norah Fagan, Andrew Davies
How do navigation programs address the needs of those living in the community with advanced, life-limiting Illness? A realist evaluation of programs in Canada
Robin Urquhart, Cynthia Kendell, Kathryn Pfaff, Kelli Stajduhar, Linda Patrick, Carren Dujela, Sarah Scruton, Faith Fauteux, Grace Warner
Nurses’ perceptions of the challenges involved in providing of end-of-life care to people with heart failure: a context-based study
Mostafa Akbarian-Rokni, Marjan Mardani-Hamooleh, Mohammad Abbasi, Naima Seyedfatemi, Sally Pezaro
Interrater agreement of multi-professional case review as reference standard for specialist palliative care need: a mixed-methods study
Evelyn Müller, Michael Josef Müller, Katharina Seibel, Christopher Boehlke, Henning Schäfer, Carsten Klein, Maria Heckel, Steffen T. Simon, Gerhild Becker
Healthcare practitioners’ perspectives of providing palliative care to patients from culturally diverse backgrounds: a qualitative systematic review
Colette Burke, Owen Doody, Barbara Lloyd
Symptom and problem clusters in German specialist palliative home care - a factor analysis of non-oncological and oncological patients’ symptom burden
Daniela Gesell, Farina Hodiamont, Julia Wikert, Eva Lehmann-Emele, Claudia Bausewein, Friedemann Nauck, Maximiliane Jansky
The responsibility to quench thirst by providing drinks when a relative is dying spouses’ experience in specialist palliative home care
Maria Friedrichsen, Nana Waldréus, Micha Milovanovic, Anne Söderlund Schaller, Pier Jaarsma, Tiny Jaarsma
Caring for patients during voluntarily stopping of eating and drinking (VSED): experiences of a palliative care team in Germany
Yann-Nicolas Batzler, Manuela Schallenburger, Pia Maletzki, Theresa Tenge, Daniel Schlieper, Jacqueline Schwartz, Martin Neukirchen
Communication strategies used by medical physicians when delivering bad news at the Maputo Central Hospital, Mozambique: a cross-sectional study
Natália Ubisse Schmauch, Emilia Pinto, Francisca Rego, Luísa Castro, Jahit Sacarlal, Guilhermina Rego
Correction: Translation and cultural adaptation of the Greek integrated palliative care outcome scale (IPOS): challenges in a six-phase process
Despina Anagnostou, Stylianos Katsaragakis, Irene Panagiotou, Elisabeth Patiraki, Aliki Tserkezoglou
Experiences of the older spousal caregivers of patients with cancer during palliative chemotherapy: a qualitative descriptive study
Kengo Hirayama, Tomoki Kuribara, Miho Oshikiri
Palliative care research utilising intersectionality: a scoping review
Helen Butler, Merryn Gott, Doctor Kate Prebble, Doctor Sarah Fortune, Doctor Jackie Robinson
A shared decision-making model in pediatric palliative care: a qualitative study of healthcare providers
Siyu Cai, Lei Cheng, Ruixin Wang, Xuan Zhou, Xiaoxia Peng
Discharge to home from a palliative care unit: impact on survival and factors associated with home death after the discharge: a cohort study
Nozomu Murakami, Shinya Kajiura, Kouichi Tanabe, Kenichiro Tsukada, Kazuhiko Shibata, Yoshio Minabe, Tatsuya Morita, Ryuji Hayashi
The meaning of dignity in care during the COVID-19 pandemic: a qualitative study in acute and intensive care
Loredana Buonaccorso, Ludovica De Panfilis, Harvey Max Chochinov, Gianfranco Martucci, Marco Massari, Monica Cocchi, Maria Chiara Bassi, Silvia Tanzi
Palliative care for children: methodology for the development of a national clinical practice guideline
Kim C. van Teunenbroek, Leontien C. M. Kremer, A. A. Eduard Verhagen, Johannes M. A. Verheijden, Hester Rippen, Brigitt C. M. Borggreve, Erna M. C. Michiels, Renée L. Mulder, Inge M. L. Ahout, Mattijs W. Alsem, Esther M. M. van den Bergh, Loes Berkhout, Karin G. C. B. Bindels-de Heus, Govert Brinkhorst, Arno Colenbrander, Linda Corel, Catharina M. Delsman-van Gelder, Jennifer van Dijk, Jurrianne C. Fahner, Jeannette L. Falkenburg, Laurent Favié, Annemie F. S. Galimont-Collen, Karin Geleijns, Rosa Geurtzen, Annelies Gijsbertsen-Kool, Saskia J. Gischler, Marinka A. R. de Groot, Anne Haag, Lisette ‘t Hart-Kerkhoffs, Hanneke Heinen, Katja M. J. Heitink-Polle, Petra Honig-Mazer, Carolien S. M. Huizinga, Cindy Joosen, Carla C. M. Juffermans, Marijke C. Kars, Karolien Kisman, Hennie Knoester, Eline M. Kochen, Barbara de Koning, Tom de Leeuw, Jeffry Looijestijn, Hilda Mekelenkamp, Maarten O. Mensink, Selma Mulder, Mariska P. Nieuweboer, Sebastianus B. J. Oude Ophuis, Suzanne G. M. A. Pasmans, Elise M. van de Putte, Emmy Räkers, Liesbeth Rietveld, Irma M. Rigter, Christel D. Rohrich, Tanja van Roosmalen, Elisabeth J. Ruijgrok, Jolanda H. Schieving, Kim van der Schoot, Antoinette Y. N. Schouten-van Meeteren, Ellen Siegers-Bennink, Henriette Sjouwke, Tanneke Snijders-Groenendijk, Mara van Stiphout, Suzanne van de Vathorst, Leo van Vlimmeren, Mirjam A. de Vos, Nellie van Wageningen, Anne Weenink, Willemien de Weerd, Ilse H. Zaal-Schuller
The meaning of dying and death for children, their carers, and families: a scoping review
Christina M. Lamb, Kianna Ramer, Oluwakemi Amodu, Kelsey Groenenboom
Investigation of grief and posttraumatic growth related to patient loss in pediatric intensive care nurses: a cross-sectional study
Meral Turgut, Hatice Yıldız
Exploring the needs and coping strategies of family caregivers taking care of dying patients at home: a field study
Xiaotian Zhang, Tianmeng Xu, Yuan Qin, Minghui Wang, Zhaoyu Li, Jingyu Song, Qianqian Tang, Zidan Wang, Lijie Xu, Lingling Wu, Peng Yue
Building bridges of excellence: a comprehensive competence framework for nurses in hospice and palliative care—a mixed method study
Wei-Ying Li, Ying Fang, Yi-qing Liang, Shu-qin Zhu, Ling Yuan, Qin Xu, Yue Li, Yin-long Chen, Chang-xian Sun, Xiao-xu Zhi, Xiao-yan Li, Rong Zhou, Mai Du
Exploring the adaptive leisure activities of classified nursing model in elderly colon cancer patients: a perspective on interactive care
Yun-Zhao Lin, Po Chen, Meng-Meng Lin, Jia-Li Chen, Min-Min Shi, Feng Guo
The role of patients’ stories in medicine: a systematic scoping review
Elaine Li Ying Quah, Keith Zi Yuan Chua, Casper Keegan Ronggui Lin, Andrew Vimal Vijayan, Nur Amira Binte Abdul Hamid, Jasmine Lerk Juan Owyong, Neeta Satku, Natalie Woong, Crystal Lim, Gillian Li Gek Phua, Eng Koon Ong, Warren Fong, Lalit Kumar Radha Krishna
Caring for persons with Dementia: a qualitative study of the needs of carers following care recipient discharge from hospital
Janice Du Preez, Antonio Celenza, Christopher Etherton-Beer, Paula Moffat, Elissa Campbell, Glenn Arendts
Exploring knowledge, attitude, and intention towards advance care planning, advance directive, and the patient self-determination act among hemodialysis patients
Shang-Feng Tsai, Ching-Yi Chang, Jia-Yi Yang, Yu-Ying Ho, Ching-Ching Hsiao, Shu-Chuan Hsu, Shih-Yun Chen, Huan-Yi Lin, Te-Feng Yeh, Cheng-Hsu Chen
Parents’ hope in perinatal and neonatal palliative care: a scoping review
Aline Oliveira Silveira, Monika Wernet, Larissa Fernandes Franco, Patrícia Luciana Moreira Dias, Zaida Charepe
The NeoPACE study: study protocol for the development of a core outcome set for neonatal palliative care
Katie Gallagher, Kathy Chant, Alex Mancini, Myra Bluebond-Langner, Neil Marlow
Increasing access to palliative care for patients with advanced cancer of African and Latin American descent: a patient-oriented community-based study protocol
Anna Santos Salas, Sharon M. Watanabe, Aynharan Sinnarajah, Nahyeni Bassah, Fleur Huang, Jill Turner, Jacqueline Alcalde Castro, Hannah M. O’Rourke, Pilar Camargo-Plazas, Bukola Salami, María Santana, Katy Campbell, Omar Abdel-Rahman, Tracy Wildeman, Lisa Vaughn, Harkeert Judge, Sadia Ahmed, Bisi Adewale, Iqmat Iyiola, Nazret Russon, Atobrhan Godlu, María Castrellon Pardo, German Mendez Mendez, Edna Ramirez, Tibebe Weldehanna, Foto Asfaha, Meron Seyoum, Brenda Cameron, Bayo Oladele, Yinka Oladele
Public awareness of advance care planning and hospice palliative care: a nationwide cross-sectional study in Korea
Boram Kim, Junyong Lee, Youn Seon Choi