Public perception of palliative care: a survey of the general population di Monica C. Fliedner, Sofia C. Zambrano, Steffen Eychmueller

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Unmet Needs in Patients With Heart Failure: The Importance of Palliative Care in a Heart Failure Clinic di Valentina Gonzalez-Jaramillo, Maud Maessen, Maud Maessen, Nora Luethi, Jelena Guyer, Lukas Hunziker, Steffen Eychmüller, Sofia C. Zambrano, Sofia C. Zambrano

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Physicians’ emotion awareness and emotion regulation training during medical education: a systematic scoping review protocol di Sofia C Zambrano, Raphaël Bonvin, Anna Lange, Sissel Guttormsen Schär

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How to talk about dying? The development of an evidence-based model for communication with patients in their last days of life and their family caregivers di Sibylle J. Felber, Sofia C. Zambrano, Tommaso Guffi, Felix M. Schmitz, Beate G. Brem, Kai P. Schnabel, Sissel Guttormsen, Steffen Eychmüller

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Compassionate communities: How to assess their benefit? A protocol of a collaborative study between different countries di Valentina González-Jaramillo, Alicia Krikorian, Vilma Tripodoro, Margarita Jorge, Sofia C. Zambrano, Francy López, Maria Clara Vélez, Tatiana Noguera, Sebastián Orellana, Silvina Montilla, Andri Christen-Cevallos Rosero, Steffen Eychmüller

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‘Someone must do it’: multiple views on family’s role in end-of-life care – an international qualitative study di Vilma A. Tripodoro, Verónica I. Veloso, Eva Víbora Martín, Hana Kodba-Čeh, Miša Bakan, Birgit H. Rasmussen, Sofía C. Zambrano, Melanie Joshi, Svandis Íris Hálfdánardóttir, Guðlaug Helga Ásgeirsdóttir, Elisabeth Romarheim, Dagny Faksvåg Haugen, Tamsin McGlinchey, Berivan Yildiz, Pilar Barnestein-Fonseca, Anne Goossensen, Urška Lunder, Agnes van der Heide

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Development of an international Core Outcome Set (COS) for best care for the dying person: study protocol di 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 di 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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