Caring for a person in advanced illness and suffering from breathlessness at home: threats and resources.
about
Psychosocial interventions for patients and caregivers in the age of new communication technologies: opportunities and challenges in cancer careDevelopment, effectiveness and cost-effectiveness of a new out-patient Breathlessness Support Service: study protocol of a phase III fast-track randomised controlled trial.Six key topics informal carers of patients with breathlessness in advanced disease want to learn about and why: MRC phase I study to inform an educational intervention.A day at a time: caregiving on the edge in advanced COPDCaregivers' perceived adequacy of support in end-stage lung disease: results of a population survey.Patients in 24-hour home care striving for control and safety.A qualitative study of informal caregivers' perspectives on the effects of idiopathic pulmonary fibrosis.A qualitative study of unmet healthcare needs in chronic obstructive pulmonary disease. A potential role for specialist palliative care?Dyadic coping, quality of life, and psychological distress among chronic obstructive pulmonary disease patients and their partners.Experiences of living and dying with COPD: a systematic review and synthesis of the qualitative empirical literature.Magnetoencephalography to investigate central perception of exercise-induced breathlessness in people with chronic lung disease: a feasibility pilot.A metasynthesis study of family caregivers' transition experiences caring for community-dwelling persons with advanced cancer at the end of life.From risky to safer home care: health care assistants striving to overcome a lack of training, supervision, and support.Time spent by people managing chronic obstructive pulmonary disease indicates biographical disruption.Recognition by family members that relatives with neurodegenerative disease are likely to die within a year: a meta-ethnography.A 10-year literature review of family caregiving for motor neurone disease: moving from caregiver burden studies to palliative care interventions.Conceptions of daily life in men living with a woman suffering from chronic obstructive pulmonary disease.An official American Thoracic Society workshop report: assessment and palliative management of dyspnea crisis.Experiences of patients undergoing pulmonary rehabilitation during an exacerbation of chronic respiratory disease.The experience of a multidisciplinary programme of pulmonary rehabilitation in primary health care from the next of kin's perspective: a qualitative study.Protection against perceptions of powerlessness and helplessness during palliative care: the family members' perspective.Assessing carer needs in chronic obstructive pulmonary disease.Individual experiences and impacts of a physiotherapist-led, non-pharmacological breathlessness programme for patients with intrathoracic malignancy: a qualitative study.Care challenges for informal caregivers of chronically ill lung patients: results from a questionnaire survey.Family Nursing Therapeutic Conversations in Heart Failure Outpatient Clinics in Denmark: Nurses' Experiences.Negotiating the care-giving role: family members' experience during critical exacerbation of COPD in Norway.Undefined and unpredictable responsibility: a focus group study of the experiences of informal caregiver spouses of patients with severe COPD.A Cross-Sectional Examination of the Association Between Dyspnea and Distress as Experienced by Palliative Home Care Clients and Their Informal Caregivers.Relatives of patients with amyotrophic lateral sclerosis: Their experience of care and support.Attitudes toward opioids for refractory dyspnea in COPD among Dutch chest physicians.Living with breathlessness: a survey of caregivers of breathless patients with lung cancer or heart failure.Conceptions of daily life in women living with a man suffering from chronic obstructive pulmonary disease.Family stories of end-of-life cancer care when unable to fulfill a loved one's wish to die at home.'Doubly deprived': a post-death qualitative study of primary carers of people who died in Western Australia.Struggling to retain living space: patients' stories about living with advanced chronic obstructive pulmonary disease.Treatment of dyspnoea in advanced cancer patients: ESMO Clinical Practice Guidelines.Breathlessness and crises in the context of advanced illness: A comparison between COPD and lung cancer patientsEvidence on home palliative care: Charting past, present, and future at the Cicely Saunders Institute – WHO Collaborating Centre for Palliative Care, Policy and RehabilitationDyadic Coping Among Couples with COPD: A Pilot Study
P2860
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P2860
Caring for a person in advanced illness and suffering from breathlessness at home: threats and resources.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Caring for a person in advance ...... t home: threats and resources.
@en
Caring for a person in advance ...... t home: threats and resources.
@nl
type
label
Caring for a person in advance ...... t home: threats and resources.
@en
Caring for a person in advance ...... t home: threats and resources.
@nl
prefLabel
Caring for a person in advance ...... t home: threats and resources.
@en
Caring for a person in advance ...... t home: threats and resources.
@nl
P2860
P1476
Caring for a person in advance ...... at home: threats and resources
@en
P2093
Marjolein H Gysels
P2860
P304
P356
10.1017/S1478951509000200
P577
2009-06-01T00:00:00Z