Symptom burden in palliative care patients: perspectives of patients, their family caregivers, and their attending physicians.
about
What to Do, and What Not to Do, When Diagnosing and Treating Breakthrough Cancer Pain (BTcP): Expert OpinionClinical Usefulness of Hydromorphone-OROS in Improving Sleep Disturbances in Korean Cancer Patients: A Multicenter, Prospective, Open-Label StudyBurden for family carers at the end of life; a mixed-method study of the perspectives of family carers and GPs.Efficacy of a brief manualized intervention Managing Cancer and Living Meaningfully (CALM) adapted to German cancer care settings: study protocol for a randomized controlled trial.Individual difficulties and resources - a qualitative analysis in patients with advanced lung cancer and their relatives.Bereaved family members' perspectives on suffering among older rural cancer patients in palliative home nursing care: A qualitative study.Existential behavioral therapy for informal caregivers of palliative patients: barriers and promoters of support utilization.Type and course of symptoms demonstrated in the terminal and dying phases by people with dementia in nursing homes.Pain in cancer patients: pain assessment by patients and family caregivers and problems experienced by caregivers.Validity and Reliability Assessment of the Persian Version of Therapy-Related Symptom Checklist.Detecting lung cancer relapse using self-evaluation forms weekly filled at home: the sentinel follow-up.Psychological distress and quality of life of palliative cancer patients and their caring relatives during home care.Validation of the "Quality of Life in Life-Threatening Illness--Family Carer Version" (QOLLTI-F) in German-speaking carers of advanced cancer patients.The Stress of Sadness: The Most Stressful Symptoms for Hospice Family Caregivers.A longitudinal communication approach in advanced lung cancer: A qualitative study of patients', relatives' and staff's perspectives.Alleviation of Psychological Distress and the Improvement of Quality of Life in Patients With Amyotrophic Lateral Sclerosis: Adaptation of a Short-Term Psychotherapeutic Intervention.The Heidelberg Milestones Communication Approach (MCA) for patients with prognosis <12 months: protocol for a mixed-methods study including a randomized controlled trial
P2860
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P2860
Symptom burden in palliative care patients: perspectives of patients, their family caregivers, and their attending physicians.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
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2013年學術文章
@zh-hant
name
Symptom burden in palliative c ...... nd their attending physicians.
@en
Symptom burden in palliative c ...... nd their attending physicians.
@nl
type
label
Symptom burden in palliative c ...... nd their attending physicians.
@en
Symptom burden in palliative c ...... nd their attending physicians.
@nl
prefLabel
Symptom burden in palliative c ...... nd their attending physicians.
@en
Symptom burden in palliative c ...... nd their attending physicians.
@nl
P2093
P2860
P1476
Symptom burden in palliative c ...... nd their attending physicians.
@en
P2093
Anja Mehnert
Carsten Bokemeyer
Karin Oechsle
Kathrin Goerth
P2860
P2888
P304
P356
10.1007/S00520-013-1747-1
P577
2013-02-21T00:00:00Z