全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用：99美元
投递稿件

为什么选择我们？ >>
- 开源期刊
- 同行审议
- 快速出刊
- 终身存储
- 免费检索
- 免费推广
- 更多...
- 搜索引擎

BMC Palliative Care

ISSN Print: 1472-684X

ISSN Online:

主页: http://www.biomedcentral.com/bmcpalliatcare

分享:




Go

Developing children's palliative care in Africa through beacon centres: lessons learnt

Julia D Downing, Joan Marston, Casey Selwyn, Laura Ross-Gakava

Heterogeneity and changes in preferences for dying at home: a systematic review

Barbara Gomes, Natalia Calanzani, Marjolein Gysels, Sue Hall, Irene J Higginson

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

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

The case for home based telehealth in pediatric palliative care: a systematic review

Natalie Bradford, Nigel R Armfield, Jeanine Young, Anthony C Smith

Planning ahead with children with life-limiting conditions and their families: development, implementation and evaluation of ‘My Choices’

Jane Noyes, Richard P Hastings, Mary Lewis, Richard Hain, Virginia Bennett, Lucie Hobson, Llinos Spencer

Impact of a home-based social welfare program on care for palliative patients in the Basque Country (SAIATU Program)

Emilio Herrera Molina, Roberto Nu？o-Solinis, Gorka Espiau Idioaga, Silvia Librada Flores, Naomi Hasson, Juan F Orueta Medía

Evidence for the use of Levomepromazine for symptom control in the palliative care setting: a systematic review

Isabel Dietz, Andrea Schmitz, Ingrid Lampey, Christian Schulz

What is the extent of potentially avoidable admissions amongst hospital inpatients with palliative care needs?

Merryn Gott, Clare Gardiner, Christine Ingleton, Mark Cobb, Bill Noble, Michael I Bennett, Jane Seymour

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 Block, Luc Deliens

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

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

Evaluation of a hospice rapid response community service: a controlled evaluation

Claire Butler, Laura M Holdsworth, Simon Coulton, Heather Gage

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, Onwuteaka-Philipsen D Bregje

Clinical aspects of palliative care in advanced Parkinson’s disease

Johan Lokk, Ahmad Delbari

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

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

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

Under-diagnosis of pain by primary physicians and late referral to a palliative care team

Masako Akashi, Eiji Yano, Etsuko Aruga

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

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

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

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, Henri？tte 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

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 Strother, Gregory P Gramelspacher

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

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

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 Schmitz, Urs Utiger, Dirk Klingbiel, Florian Strasser

Using respiratory rate and thoracic movement to assess respiratory insufficiency in amyotrophic lateral sclerosis: a preliminary study

Waltteri Siirala, Tarja Saaresranta, Arno Vuori, Sanna Salanter？, Klaus T Olkkola, Riku Aantaa

Home and community based care program assessment for people living with HIV/AIDS in Arba Minch, Southern Ethiopia

Taddese Zerfu, Yaliso Yaya, Selamawit Dagne, Kebede Deribe, Horacio Ruise？or-Escudero, Sibhatu Biadgilign

An online survey of Australian physicians reported practice with the off-label use of nebulised frusemide

Phillip J Newton, Patricia M Davidson, Christine Sanderson, on behalf of the Improving Palliative Care through Clinical Trials (ImPaCCT) group

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

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

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

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 M？ller

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, Project PRISMA

Hospital based palliative care in sub-Saharan Africa; a six month review from Malawi

Julia B Tapsfield, M Jane Bates

Palliative inpatients in general hospitals: a one day observational study in Belgium

Marianne S Desmedt, Yolande L de la Kethulle, Myriam I Deveugele, Emmanuel A Keirse, Dominique J Paulus, Johan J Menten, Steven R Simoens, Paul J vanden Berghe, Claire M Beguin

Intervention for depression among palliative care patients and their families: A study protocol for evaluation of a training program for professional care staff

David J Hallford, Marita P McCabe, David Mellor, Tanya E Davison, Denisa L Goldhammer, Kuruvilla George, Shane Storer

"Card sorting": a tool for research in ethics on treatment decision-making at the end of life in Alzheimer patients with a life threatening complication

Lionel Pazart, Chrystelle Vidal, Didier Chalon, Sophie Gauthier, Florent Schepens, Elodie Cretin, Jean-Louis Beal, Pierre Pfitzenmeyer, Régis Aubry

Knowledge and attitude of final - year medical students in Germany towards palliative care - an interinstitutional questionnaire-based study

Martin Weber, Sven Schmiedel, Friedemann Nauck, Bernd Alt-Epping

The effect on survival of continuing chemotherapy to near death

Akiko M Saito, Mary Landrum, Bridget A Neville, John Z Ayanian, Craig C Earle

Palliative care making a difference in rural Uganda, Kenya and Malawi: three rapid evaluation field studies

Liz Grant, Judith Brown, Mhoira Leng, Nadia Bettega, Scott A Murray

Age, gender, will, and use of home-visit nursing care are critical factors in home care for malignant diseases; a retrospective study involving 346 patients in Japan

Yuko Kodama, Tomoko Matsumura, Takuhiro Yamaguchi, Morihito Takita, Shohei Kawagoe, Yukihiro Kimura, Satoshi Hirahara, Hiroshi Suzuki, Hideki Ohta, Shigeru Onozawa, Tadashi Wada, Yukiyasu Nakamura, Kazushi Nakano, Masahiro Kami, Koichiro Yuji

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

Predictors of dying at home for patients receiving nursing services in Japan: A retrospective study comparing cancer and non-cancer deaths

Sumie Ikezaki, Naoki Ikegami

Mapping hospice patients' perception and verbal communication of end-of-life needs: an exploratory mixed methods inquiry

Bruce L Arnold

Cancer Carepartners: Improving patients' symptom management by engaging informal caregivers

Maria J Silveira, Charles W Given, Kemp B Cease, Alla Sikorskii, Barbara Given, Laurel L Northouse, John D Piette

Study protocol: optimization of complex palliative care at home via telemedicine. A cluster randomized controlled trial

Froukje Duursma, Henk J Schers, Kris CP Vissers, Jeroen Hasselaar

End of life care in sub-Saharan Africa: a systematic review of the qualitative literature

Marjolein Gysels, Christopher Pell, Lianne Straus, Robert Pool

Go




©2008-2020 OALib, Inc | Public user content licensed CC-BY 4.0 unless otherwise specified. OALib ISSN Online: 2333-9721 OALib ISSN Print: 2333-9705