Caring for family members with chronic physical illness: a critical review of caregiver literature
about
A proposed systems approach to the evaluation of integrated palliative care.Depressive symptoms in lung cancer patients and their family caregivers and the influence of family environment.Family members of people with alcohol or drug dependence: health problems and medical cost compared to family members of people with diabetes and asthma.Comparison of health care needs of child family members of adults with alcohol or drug dependence versus adults with asthma or diabetes.Becoming a caregiver: new family carers' experience during the transition from hospital to home.Perceived mental health status of drug users with HIV: concordance between caregivers and care recipient reports and associations with caregiving burden and reciprocity.Quality of life of caregiver spouses of veterans with bilateral lower extremity amputations.A randomized trial of mobile health support for heart failure patients and their informal caregivers: impacts on caregiver-reported outcomes.Social capital and mental health among mothers in Vietnam who have children with disabilitiesAnterior Urethral Stricture Disease Negatively Impacts the Quality of Life of Family MembersQuality of life and the related factors in spouses of veterans with chronic spinal cord injury.Long-term health-related quality of life of stroke survivors and their spousal caregiversLay information mediary behavior uncovered: exploring how nonprofessionals seek health information for themselves and others online.Factors influencing changes in health related quality of life of caregivers of persons with multiple chronic conditions.Determinants of Quality of Life in the Caregivers of Iranian War Survivors with Bilateral Lower-Limb Amputation after More than Two DecadesA European consensus on outcome measures for psychosocial intervention research in dementia care.Caregiver Burden among Adults Caring for People Living with HIV/AIDS (PLWHA) in Southern India.Effects of caregiver burden on quality of life and coping strategies utilized by caregivers of adult patients with inflammatory bowel disease.Instruments measuring the disease-specific quality of life of family carers of people with neurodegenerative diseases: a systematic review.Self-management in epilepsy: Why and how you should incorporate self-management in your practiceSupport interventions for caregivers of physically disabled adults: a systematic review.Needs and Concerns of Family Caregivers of Persons With Type 2 Diabetes: An Integrated Review of Cross-cultural Literature With Implications for the American Indian Population.Impacts of COPD on family carers and supportive interventions: a narrative review.Needs of caregivers of cancer patients: validation of the Mexican version of the Support Person Unmet Needs Survey (SPUNS-SFM).Preventive Services Use Among African American and Latino Adult Caregivers in South Los Angeles.Sleep problems, anxıety, depressıon and fatıgue on famıly members of adult intensıve care unıt patıents.Managing multiple chronic conditions in Singapore - Exploring the perspectives and experiences of family caregivers of patients with diabetes and end stage renal disease on haemodialysis.THE ASSESSMENT OF CAREGIVER BURDEN IN CAREGIVERS OF HEMODIALYSIS PATIENTS.Family caregivers' views on coordination of care in Huntington's disease: a qualitative study.Factors predicting distress among parents/caregivers of children with neurological disease and home enteral nutrition.What are the harms of refusing to allow living kidney donation? An expanded view of risks and benefits.Evaluation of an educational programme for family members of patients living with heart failure: a randomised controlled trial.The evaluation of family impact of recessive dystrophic epidermolysis bullosa using the Italian version of the Family Dermatology Life Quality Index.Caregivers burden of older adults with chronic illnesses in the community: a cross-sectional study.Quality of life at 6 years after occupational injury.Caregiver Burden in Medical versus Psychiatric Patients: A Cross-sectional Comparative Study.Depression Among Caregivers of Patients With Dementia.Relatives' quality of life and psychological disturbance: a new concern of SLE management.Do informal caregivers in mental illness feel more burdened? A comparative study of mental versus somatic illnesses.Burden of caregivers of children and adolescents with Down Syndrome.
P2860
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P2860
Caring for family members with chronic physical illness: a critical review of caregiver literature
description
2004 nî lūn-bûn
@nan
2004 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Caring for family members with ...... review of caregiver literature
@ast
Caring for family members with ...... review of caregiver literature
@en
Caring for family members with ...... review of caregiver literature
@nl
type
label
Caring for family members with ...... review of caregiver literature
@ast
Caring for family members with ...... review of caregiver literature
@en
Caring for family members with ...... review of caregiver literature
@nl
prefLabel
Caring for family members with ...... review of caregiver literature
@ast
Caring for family members with ...... review of caregiver literature
@en
Caring for family members with ...... review of caregiver literature
@nl
P2860
P3181
P356
P1476
Caring for family members with ...... review of caregiver literature
@en
P2093
Brad Zebrack
Jung-won Lim
P2860
P2888
P3181
P356
10.1186/1477-7525-2-50
P407
P577
2004-09-17T00:00:00Z
P5875
P6179
1001491020