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Assessment of Quality of Life of Family Members of Inpatients with End-Stage Disease
R Buzgova, R Kozakova, L Sikorova
Jazyk angličtina Země Spojené státy americké
Grantová podpora
NT13417
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
Nursing & Allied Health Database (ProQuest) od 1998-04-01 do 2015-12-31
Health & Medicine (ProQuest) od 1998-04-01 do 2015-12-31
Psychology Database (ProQuest) od 1998-04-01 do 2015-12-31
Odkazy
PubMed
26856126
DOI
10.1177/082585971503100407
Knihovny.cz E-zdroje
- MeSH
- dospělí MeSH
- Karnofského skóre MeSH
- kvalita života * MeSH
- lidé středního věku MeSH
- lidé MeSH
- pacienti hospitalizovaní MeSH
- paliativní péče * psychologie MeSH
- psychiatrické posuzovací škály MeSH
- rodina * psychologie MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- socioekonomické faktory MeSH
- umírající * MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Geografické názvy
- Česká republika MeSH
BACKGROUND: An important aim of palliative care is to ensure the highest possible quality of life (QoL) for the family members of patients. AIM: We aimed to determine the QoL of family members of hospitalized patients with end-stage disease, as well as differences in QoL based on socio-demographic characteristics and the patient's functional status, psychological distress, and QoL. METHODS: Study participants were 292 family members of terminally ill patients at University Hospital, Ostrava, Czech Republic. To evaluate family members' QoL, we used the Quality of Life in Life-Threatening Illness--Family Carer Version (QOLLTI-F). We used the Hospital Anxiety and Depression Scale (HADS) and the Karnofsky Performance Status (KPS) Scale to assess patients' functional status and psychological distress. RESULTS: A statistically significant difference was found in QoL evaluation based on family members' socio-demographic characteristics in education, employment, and age. A significantly lower QoL score was observed for patients' life partners in six domains. A correlation was found between patients' poorer functional status and family members' lower QoL. We found lower global QoL in family members of patients with depression. CONCLUSION: Family support is a cornerstone of palliative care. Palliative care professionals should focus on at-risk family members--the life partners of patients, the unemployed, younger people, and those whose ill loved one has a poor functional status.
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