Novosti – izkušnje – pobude: potovanje od klinične medicinske sestre do raziskovalke v zdravstveni negi* by Birgit H. Rasmussen, prevod/transl.: Majda Pahor

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Existential aspects documented in older people’s patient records in the context of specialized palliative care: a retrospective review by Marina Sjöberg, Birgit H. Rasmussen, Anna-Karin Edberg, Ingela Beck

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Symptoms, problems and quality of life in patients newly diagnosed with oesophageal and gastric cancer – a comparative study of treatment strategy by Karin Dalhammar, Jimmie Kristensson, Dan Falkenback, Birgit H. Rasmussen, Marlene Malmström

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Nurses' experiences of using the Integrated Palliative care Outcome Scale with patients in specialized palliative care—A qualitative focus group study by Ingela Beck, Kicki Törnquist, Anders Gruvebäck, Birgit. H. Rasmussen, Ulrika Olsson Möller

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Increased patient satisfaction by integration of palliative care into geriatrics—A prospective cohort study by Maria E. C. Schelin, Carl Johan Fürst, Birgit H. Rasmussen, Christel Hedman

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Increased patient satisfaction by integration of palliative care into geriatrics-A prospective cohort study. by Maria E C Schelin, Carl Johan Fürst, Birgit H Rasmussen, Christel Hedman

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A novel care guide for personalised palliative care – a national initiative for improved quality of care by Dröfn Birgisdóttir, Anette Duarte, Anna Dahlman, Bengt Sallerfors, Birgit H. Rasmussen, Carl Johan Fürst

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Sensations, symptoms, and then what? Early bodily experiences prior to diagnosis of lung cancer. by Britt-Marie Bernhardson, Carol Tishelman, Birgit H Rasmussen, Senada Hajdarevic, Marlene Malmström, Trine Laura Overgaard Hasle, Louise Locock, Lars E Eriksson

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Similarities and differences between China and Sweden regarding the core features of palliative care for people aged 60 or older: a systematic scoping review by Gerd Ahlström, Hongli Huang, Yu Luo, Christina Bökberg, Birgit H. Rasmussen, Eva I. Persson, Lian Xue, Le Cai, Pingfen Tang, Magnus Persson, Jingjing Huang

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Complexity in non-pharmacological caregiving activities at the end of life: an international qualitative study. by Olav Lindqvist, Carol Tishelman, Carina Lundh Hagelin, Jean B Clark, Maria L Daud, Andrew Dickman, Franzisca Domeisen Benedetti, Maren Galushko, Urska Lunder, Gunilla Lundquist, Guido Miccinesi, Sylvia B Sauter, Carl Johan Fürst, Birgit H Rasmussen, OPCARE9 Group

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Development of an international Core Outcome Set (COS) for best care for the dying person: study protocol by Sofia C. Zambrano, Dagny Faksvåg Haugen, Agnes van der Heide, Vilma A. Tripodoro, John Ellershaw, Carl Johan Fürst, Raymond Voltz, Stephen Mason, María L. Daud, Gustavo De Simone, Kerstin Kremeike, Svandis Iris Halfdanardottir, Valgerdur Sigurdardottir, Jeremy Johnson, Simon Allan, Haroon Hafeez, Catarina Simões, Katrin Ruth Sigurdardottir, Birgit H. Rasmussen, Paula Williamson, Steffen Eychmüller, in collaboration with the iLIVE consortium

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Live well, die well – an international cohort study on experiences, concerns and preferences of patients in the last phase of life: the research protocol of the iLIVE study by Birgit H Rasmussen, Vilma Tripodoro, Gabriel Goldraij, John Ellershaw, Stephen Mason, Agnes van der Heide, Carin C D van der Rijt, Lia van Zuylen, Judit Simon, Michael Berger, Raymond Voltz, Melanie Joshi, Claudia Fischer, Katrin Ruth Sigurdardottir, Julia Strupp, Berivan Yildiz, Valgerdur Sigurdardottir, Hugo M van der Kuy, Steffen Eychmüller, Simon Allan, Rosemary Hughes, Tamsin Mcglinchey, Ida J Korfage, Carl Johan Fürst, Anne Goossensen, Mark Boughey, Dagny Faksvåg Haugen, Urska Lunder, Pilar Barnestein-Fonseca, Misa Bakan, Andri Christen, Gustavo G De Simone, Martina Egloff, Eline E C M Elsten, Eric C T Geijteman, Svandis Iris Halfdanardottir, Christel Hedman, Tanja Hoppe, Grethe Skorpen Iversen, Hana Kodba-Ceh, Nora Lüthi, Maria Luisa Martín-Roselló, Silvi Montilla, Inmaculada Ruiz-Torreras, Maria E C Schelin, Ruthmarijke Smeding, Kjersti Solvåg, Verónica I Veloso, Eva Vibora-Martin, Sofia C Zambrano

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