Hope against hope: exploring the hopes and challenges of rural female caregivers of persons with advanced cancer
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Volume 12, issue 1, December 2013
44 articles in this issue
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Paediatric palliative care: development and pilot study of a ‘Directory’ of life-limiting conditions
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Place of death in haematological malignancy: variations by disease sub-type and time from diagnosis to death
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Cancer-related neuropathic pain in out-patient oncology clinics: a European survey
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Interventions to encourage discussion of end-of-life preferences between members of the general population and the people closest to them - a systematic literature review
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Do pilocarpine drops help dry mouth in palliative care patients: a protocol for an aggregated series of n-of-1 trials
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Preliminary estimation of the prevalence of chemotherapy-induced dysgeusia in Japanese patients with cancer
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A randomised, multicentre clinical trial of specialised palliative care plus standard treatment versus standard treatment alone for cancer patients with palliative care needs: the Danish palliative care trial (DanPaCT) protocol
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Evaluation of the living with hope program for rural women caregivers of persons with advanced cancer
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'My dreams are shuttered down and it hurts lots’–a qualitative study of palliative care needs and their management by HIV outpatient services in Kenya and Uganda
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Public awareness and attitudes toward palliative care in Northern Ireland
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Palliative care research on the island of Ireland over the last decade: a systematic review and thematic analysis of peer reviewed publications
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Novel open-source electronic medical records system for palliative care in low-resource settings
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Modelling the landscape of palliative care for people with dementia: a European mixed methods study
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Feedback on end-of-life care in dementia: the study protocol of the FOLlow-up project
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Musculoskeletal pain in older adults at the end-of-life: a systematic search and critical review of the literature with priorities for future research
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Improving palliative care outcomes for Aboriginal Australians: service providers’ perspectives
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Family members’ perceptions of end-of-life care across diverse locations of care
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Lung cancer diagnosed following emergency admission: a mixed methods study protocol to improve understanding of patients’ characteristics, needs, experiences and outcomes
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Is the effect of non-invasive ventilation on survival in amyotrophic lateral sclerosis age-dependent?
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Home-based functional walking program for advanced cancer patients receiving palliative care: a case series
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Dysphagia as a predictor of outcome and transition to palliative care among middle cerebral artery ischemic stroke patients
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The development of an instrument that can identify children with palliative care needs: the Paediatric Palliative Screening Scale (PaPaS Scale): a qualitative study approach
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Determinants of place of death: a population-based retrospective cohort study
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Evidence-based planning and costing palliative care services for children: novel multi-method epidemiological and economic exemplar
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Using aggregated single patient (N-of-1) trials to determine the effectiveness of psychostimulants to reduce fatigue in advanced cancer patients: a rationale and protocol
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Palliative care need and management in the acute hospital setting: a census of one New Zealand Hospital
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Early evaluation predicts pain relief of irradiated bone metastases: a single-center prospective study
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Symptom burden, palliative care need and predictors of physical and psychological discomfort in two UK hospitals
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International recommendations for outpatient palliative care and prehospital palliative emergencies – a prospective questionnaire-based investigation
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What is the extent of potentially avoidable admissions amongst hospital inpatients with palliative care needs?
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Developing children’s palliative care in Africa through beacon centres: lessons learnt
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Heterogeneity and changes in preferences for dying at home: a systematic review
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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
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Planning ahead with children with life-limiting conditions and their families: development, implementation and evaluation of ‘My Choices’
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The case for home based telehealth in pediatric palliative care: a systematic review
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Impact of a home-based social welfare program on care for palliative patients in the Basque Country (SAIATU Program)
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Evidence for the use of Levomepromazine for symptom control in the palliative care setting: a systematic review
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Decision-making capacity and communication about care of older people during their last three months of life
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