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26.
233 Accesses
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Impact of a home-based social welfare program on care for palliative patients in the Basque Country (SAIATU Program)
Emilio Herrera Molina, Roberto Nuño-Solinis, Gorka Espiau Idioaga, Silvia Librada Flores, Naomi Hasson, Juan F Orueta Medía BMC Palliative Care 2013, 12:3 (30 January 2013)
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27.
230 Accesses
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The experience of palliative patients and their families of a family meeting utilised as an instrument for spiritual and psychosocial care: A qualitative study
Heather M Tan, Anne Wilson, Ian Olver, Christopher Barton BMC Palliative Care 2011, 10:7 (24 March 2011)
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28.
228 Accesses
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International recommendations for outpatient palliative care and prehospital palliative emergencies – a prospective questionnaire-based investigation
Christoph HR Wiese, Christoph L Lassen, Utz E Bartels, Mahmoud Taghavi, Saleem Elhabash, Bernhard M Graf, Gerd G Hanekop BMC Palliative Care 2013, 12:10 (21 February 2013)
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29.
228 Accesses
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Towards a standardized method of developing quality indicators for palliative care: protocol of the Quality indicators for Palliative Care (Q-PAC) study
Kathleen Leemans, Joachim Cohen, Anneke L Francke, Robert Vander Stichele, Susanne JJ Claessen, Lieve Van den Block, Luc Deliens BMC Palliative Care 2013, 12:6 (8 February 2013)
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30.
213 Accesses
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Piloting the role of a pharmacist in a community palliative care multidisciplinary team: an Australian experience
Safeera Y Hussainy, Margaret Box, Sandy Scholes BMC Palliative Care 2011, 10:16 (31 October 2011)
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31.
208 Accesses
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A national study of chaplaincy services and end-of-life outcomes
Kevin J Flannelly, Linda L Emanuel, George F Handzo, Kathleen Galek, Nava R Silton, Melissa Carlson BMC Palliative Care 2012, 11:10 (2 July 2012)
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Editor’s summary
Chaplaincy services may contribute to a lower number of hospital deaths and increased hospice admissions, which might be attributable to chaplains' assistance to patients and families in making end-of-life decisions.
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32.
206 Accesses
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Palliative care in advanced dementia; A mixed methods approach for the development of a complex intervention
Elizabeth L Sampson, Ingela Thuné-Boyle, Riitta Kukkastenvehmas, Louise Jones, Adrian Tookman, Michael King, Martin R Blanchard BMC Palliative Care 2008, 7:8 (11 July 2008)
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33.
201 Accesses
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The lived experience of breathlessness and its implications for care: a qualitative comparison in cancer, COPD, heart failure and MND
Marjolein H Gysels, Irene J Higginson BMC Palliative Care 2011, 10:15 (17 October 2011)
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34.
190 Accesses
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Identifying bereaved subjects at risk of complicated grief: Predictive value of questionnaire items in a cohort study
Mai-Britt Guldin, Maja O'Connor, Ineta Sokolowski, Anders B Jensen, Peter Vedsted BMC Palliative Care 2011, 10:9 (16 May 2011)
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35.
182 Accesses
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A proposed systems approach to the evaluation of integrated palliative care
Daryl Bainbridge, Kevin Brazil, Paul Krueger, Jenny Ploeg, Alan Taniguchi BMC Palliative Care 2010, 9:8 (10 May 2010)
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Editor’s summary
Palliative care patients require complex packages of treatment and social support in a seamless, cost-effective manner, and collaboration within the palliative care network that accounts for each contributing factor may provide optimal care that meets patients' needs.
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36.
177 Accesses
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European Association for Palliative Care (EAPC) framework for palliative sedation: an ethical discussion
Niklas Juth, Anna Lindblad, Niels Lynöe, Manne Sjöstrand, Gert Helgesson BMC Palliative Care 2010, 9:20 (13 September 2010)
Abstract | Full text | PDF
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Editor’s summary
Frameworks should convey that the best interest and autonomous decisions of the patients are the primary concerns when considering palliative sedation and a patient's judgement on when suffering is intolerable should guide decision-making at the end of life.
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37.
175 Accesses
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Integrating palliative care within acute stroke services: developing a programme theory of patient and family needs, preferences and staff perspectives
Christopher R Burton, Sheila Payne BMC Palliative Care 2012, 11:22 (9 November 2012)
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38.
169 Accesses
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Ensuring competency in end-of-life care: controlling symptoms
Frank D Ferris, Charles F von Gunten, Linda L Emanuel BMC Palliative Care 2002, 1:5 (30 July 2002)
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39.
168 Accesses
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The case for home based telehealth in pediatric palliative care: a systematic review
Natalie Bradford, Nigel R Armfield, Jeanine Young, Anthony C Smith BMC Palliative Care 2013, 12:4 (1 February 2013)
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40.
166 Accesses
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Factors associated with place of death in Addis Ababa, Ethiopia
Aderaw Anteneh, Tekebash Araya, Awoke Misganaw BMC Palliative Care 2013, 12:14 (26 March 2013)
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41.
159 Accesses
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The attitudes of brain cancer patients and their caregivers towards death and dying: a qualitative study
Nir Lipsman, Abby Skanda, Jonathan Kimmelman, Mark Bernstein BMC Palliative Care 2007, 6:7 (8 November 2007)
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42.
156 Accesses
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Decision-making capacity and communication about care of older people during their last three months of life
Pam J Kaspers, Bregje D Onwuteaka-Philipsen, Dorly JH Deeg, H Roeline W Pasman BMC Palliative Care 2013, 12:1 (10 January 2013)
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43.
153 Accesses
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Effectiveness of a hand-held fan for breathlessness: a randomised phase II trial
Claudia Bausewein, Sara Booth, Marjolein Gysels, Robert Kühnbach, Irene J Higginson BMC Palliative Care 2010, 9:22 (19 October 2010)
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44.
149 Accesses
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The perspectives of clinical staff and bereaved informal care-givers on the use of continuous sedation until death for cancer patients: The study protocol of the UNBIASED study
Jane Seymour, Judith Rietjens, Jayne Brown, Agnes van der Heide, Sigrid Sterckx, Luc Deliens, the UNBIASED study team BMC Palliative Care 2011, 10:5 (4 March 2011)
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45.
147 Accesses
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The perspectives of bereaved family carers on dying at home: the study protocol of ‘unpacking the home: family carers’ reflections on dying at home
Sheila Payne, Sarah Brearley, Christine Milligan, David Seamark, Carol Thomas, Xu Wang, Susan Blake, Mary Turner BMC Palliative Care 2012, 11:23 (22 November 2012)
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46.
144 Accesses
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What "best practice" could be in Palliative Care: an analysis of statements on practice and ethics expressed by the main Health Organizations
Gaia Barazzetti, Claudia Borreani, Guido Miccinesi, Franco Toscani BMC Palliative Care 2010, 9:1 (7 January 2010)
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Editor’s summary
Policies and position statements from international health organizations generally lack a consistent model of palliative care, perhaps due to cultural variation and the need to adapt care to each patient's needs and values.
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47.
137 Accesses
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End-of-life care in a COPD patient awaiting lung transplantation: a case report
Daisy JA Janssen, Martijn A Spruit, Joan D Does, Jos MGA Schols, Emiel FM Wouters BMC Palliative Care 2010, 9:6 (28 April 2010)
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48.
135 Accesses
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Is dignity therapy feasible to enhance the end of life experience for people with motor neurone disease and their family carers?
Brenda Bentley, Samar M Aoun, Moira O’Connor, Lauren J Breen, Harvey Chochinov BMC Palliative Care 2012, 11:18 (20 September 2012)
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49.
130 Accesses
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Early evaluation predicts pain relief of irradiated bone metastases: a single-center prospective study
Pierre Truntzer, David Atlani, Marius Pop, Jean-Baptiste Clavier, Sébastien Guihard, Catherine Schumacher, Georges Noel BMC Palliative Care 2013, 12:12 (13 March 2013)
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50.
128 Accesses
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Recommendations for improving the end-of-life care system for homeless populations: A qualitative study of the views of Canadian health and social services professionals
Ryan McNeil, Manal Guirguis-Younger, Laura B Dilley BMC Palliative Care 2012, 11:14 (15 September 2012)
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