Ausgabe 1/2012
Inhalt (26 Artikel)
Outcomes 'out of africa': the selection and implementation of outcome measures for palliative care in Africa
Julia Downing, Steffen T Simon, Faith N Mwangi-Powell, Hamid Benalia, Barbara A Daveson, Irene J Higginson, Richard Harding, Claudia Bausewein
Autonomic dysfunction in patients with advanced cancer; prevalence, clinical correlates and challenges in assessment
Carol A Stone, Rose Anne Kenny, Brid Nolan, Peter G Lawlor
A region-based palliative care intervention trial using the mixed-method approach: Japan OPTIM study
Tatsuya Morita, Mitsunori Miyashita, Akemi Yamagishi, Nobuya Akizuki, Yoshiyuki Kizawa, Yutaka Shirahige, Miki Akiyama, Kei Hirai, Motohiro Matoba, Masako Yamada, Taketoshi Matsumoto, Takuhiro Yamaguchi, Kenji Eguchi
Assessment of the face validity of two pain scales in Kenya: a validation study using cognitive interviewing
Kristin TL Huang, Claudio Owino, Rachel C Vreeman, Mildred Hagembe, Festus Njuguna, R Matthew Strother, Gregory P Gramelspacher
Developing and testing a strategy to enhance a palliative approach and care continuity for people who have dementia: study overview and protocol
Christine Toye, Andrew L Robinson, Moyez Jiwa, Sharon Andrews, Fran McInerney, Barbara Horner, Kristi Holloway, Brigit Stratton
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
An online survey of Australian physicians reported practice with the off-label use of nebulised frusemide
Phillip J Newton, Patricia M Davidson, Christine Sanderson
Under-diagnosis of pain by primary physicians and late referral to a palliative care team
Masako Akashi, Eiji Yano, Etsuko Aruga
Home and community based care program assessment for people living with HIV/AIDS in Arba Minch, Southern Ethiopia
Taddese Alemu Zerfu, Yaliso Yaya, Selamawit Dagne, Kebede Deribe, Horacio Ruiseñor-Escudero, Sibhatu Biadgilign
Evaluation of a hospice rapid response community service: a controlled evaluation
Claire Butler, Laura M Holdsworth, Simon Coulton, Heather Gage
The broad spectrum of unbearable suffering in end-of-life cancer studied in dutch primary care
Cees DM Ruijs, Ad JFM Kerkhof, Gerrit van der Wal, Bregje D Onwuteaka-Philipsen
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
The ACA training programme to improve communication between general practitioners and their palliative care patients: development and applicability
Willemjan Slort, Annette H Blankenstein, Bernardina S Wanrooij, Henriëtte E van der Horst, Luc Deliens
Factors associated with the severity and improvement of fatigue in patients with advanced cancer presenting to an outpatient palliative care clinic
Sriram Yennu, Diana L Urbauer, Eduardo Bruera
After you: conversations between patients and healthcare professionals in planning for end of life care
Kathryn Almack, Karen Cox, Nima Moghaddam, Kristian Pollock, Jane Seymour
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 Max Chochinov
Electronic monitoring of symptoms and syndromes associated with cancer: methods of a randomized controlled trial SAKK 95/06 E-MOSAIC
David Blum, Dieter Koeberle, Karin Ribi, Shu-Fang Hsu Schmitz, Urs Utiger, Dirk Klingbiel, Florian Strasser
Perspectives on care and communication involving incurably ill Turkish and Moroccan patients, relatives and professionals: a systematic literature review
Fuusje M de Graaff, Patriek Mistiaen, Walter LJM Devillé, Anneke L Francke
Clinical aspects of palliative care in advanced Parkinson’s disease
Johan Lokk, Ahmad Delbari
Parental palliative cancer: psychosocial adjustment and health-related quality of life in adolescents participating in a German family counselling service
Franziska Kühne, Thomas Krattenmacher, Corinna Bergelt, Johanna C Ernst, Hans-Henning Flechtner, Daniel Führer, Wolfgang Herzog, Kai v Klitzing, Georg Romer, Birgit Möller
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
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
End-of-life medical decisions in France: a death certificate follow-up survey 5 years after the 2005 act of parliament on patients’ rights and end of life
Sophie Pennec, Alain Monnier, Silvia Pontone, Régis Aubry
Using respiratory rate and thoracic movement to assess respiratory insufficiency in amyotrophic lateral sclerosis: a preliminary study
Waltteri Siirala, Tarja Saaresranta, Arno Vuori, Sanna Salanterä, Klaus T Olkkola, Riku Aantaa
Palliative patients cared for at home by PAMINO-trained and other GPs – health-related quality of life as measured by QLQ-C15-PAL and POS
Katja Hermann, Peter Engeser, Joachim Szecsenyi, Antje Miksch
Older patients’ attitudes towards and experiences of patient-physician end-of-life communication: a secondary analysis of interviews from British, Dutch and Belgian patients
Natalie Evans, H Roeline W Pasman, Sheila A Payne, Jane Seymour, Sabine Pleschberger, Reginald Deschepper, Bregje D Onwuteaka-Philipsen