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Psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care
BACKGROUND: This study prospectively evaluated distress, depressive and anxiety symptoms as well as associated factors in family caregivers (FC) of advanced cancer patients at initiation of specialist inpatient palliative care. METHODS: Within 72 h after the patient’s first admission, FCs were asked...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6862724/ https://www.ncbi.nlm.nih.gov/pubmed/31739802 http://dx.doi.org/10.1186/s12904-019-0469-7 |
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author | Oechsle, Karin Ullrich, Anneke Marx, Gabriella Benze, Gesine Heine, Julia Dickel, Lisa-Marie Zhang, Youyou Wowretzko, Feline Wendt, Kim Nikola Nauck, Friedemann Bokemeyer, Carsten Bergelt, Corinna |
author_facet | Oechsle, Karin Ullrich, Anneke Marx, Gabriella Benze, Gesine Heine, Julia Dickel, Lisa-Marie Zhang, Youyou Wowretzko, Feline Wendt, Kim Nikola Nauck, Friedemann Bokemeyer, Carsten Bergelt, Corinna |
author_sort | Oechsle, Karin |
collection | PubMed |
description | BACKGROUND: This study prospectively evaluated distress, depressive and anxiety symptoms as well as associated factors in family caregivers (FC) of advanced cancer patients at initiation of specialist inpatient palliative care. METHODS: Within 72 h after the patient’s first admission, FCs were asked to complete German versions of the Distress Thermometer, Generalized Anxiety Disorder 7-item scale (GAD-7), Patient Health Questionnaire depression module 9-item scale (PHQ-9) for outcome measure. Multivariate logistic regression analyses were used to identify associated factors. RESULTS: In 232 FCs (62% spouses/partners), mean level of distress was 7.9 (SD 1.8; range, 2–10) with 95% presenting clinically relevant distress levels. Most frequent problems were sadness (91%), sorrows (90%), anxiety (78%), exhaustion (77%) and sleep disturbances (73%). Prevalence rates of moderate to severe anxiety and depressive symptoms were 47 and 39%, respectively. Only 25% of FCs had used at least one source of support previously. In multivariate regression analysis, being female (OR 2.525), spouse/partner (OR 2.714), exhaustion (OR 10.267), and worse palliative care outcome ratings (OR 1.084) increased the likelihood for moderate to severe anxiety symptom levels. Being female (OR 3.302), low socio-economic status (OR 6.772), prior patient care other than home-based care (OR 0.399), exhaustion (OR 3.068), sleep disturbances (OR 4.183), and worse palliative care outcome ratings (OR 1.100) were associated with moderate to severe depressive symptom levels. CONCLUSIONS: FCs of patients presenting with indication for specialist palliative care suffer from high distress and relevant depressive and anxiety symptoms, indicating the high need of psychological support not only for patients, but also their FCs. Several socio-demographic and care-related risk-factors influence mental burden of FCs and should be in professional caregivers’ focus in daily clinical practice. |
format | Online Article Text |
id | pubmed-6862724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68627242019-12-11 Psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care Oechsle, Karin Ullrich, Anneke Marx, Gabriella Benze, Gesine Heine, Julia Dickel, Lisa-Marie Zhang, Youyou Wowretzko, Feline Wendt, Kim Nikola Nauck, Friedemann Bokemeyer, Carsten Bergelt, Corinna BMC Palliat Care Research Article BACKGROUND: This study prospectively evaluated distress, depressive and anxiety symptoms as well as associated factors in family caregivers (FC) of advanced cancer patients at initiation of specialist inpatient palliative care. METHODS: Within 72 h after the patient’s first admission, FCs were asked to complete German versions of the Distress Thermometer, Generalized Anxiety Disorder 7-item scale (GAD-7), Patient Health Questionnaire depression module 9-item scale (PHQ-9) for outcome measure. Multivariate logistic regression analyses were used to identify associated factors. RESULTS: In 232 FCs (62% spouses/partners), mean level of distress was 7.9 (SD 1.8; range, 2–10) with 95% presenting clinically relevant distress levels. Most frequent problems were sadness (91%), sorrows (90%), anxiety (78%), exhaustion (77%) and sleep disturbances (73%). Prevalence rates of moderate to severe anxiety and depressive symptoms were 47 and 39%, respectively. Only 25% of FCs had used at least one source of support previously. In multivariate regression analysis, being female (OR 2.525), spouse/partner (OR 2.714), exhaustion (OR 10.267), and worse palliative care outcome ratings (OR 1.084) increased the likelihood for moderate to severe anxiety symptom levels. Being female (OR 3.302), low socio-economic status (OR 6.772), prior patient care other than home-based care (OR 0.399), exhaustion (OR 3.068), sleep disturbances (OR 4.183), and worse palliative care outcome ratings (OR 1.100) were associated with moderate to severe depressive symptom levels. CONCLUSIONS: FCs of patients presenting with indication for specialist palliative care suffer from high distress and relevant depressive and anxiety symptoms, indicating the high need of psychological support not only for patients, but also their FCs. Several socio-demographic and care-related risk-factors influence mental burden of FCs and should be in professional caregivers’ focus in daily clinical practice. BioMed Central 2019-11-18 /pmc/articles/PMC6862724/ /pubmed/31739802 http://dx.doi.org/10.1186/s12904-019-0469-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Oechsle, Karin Ullrich, Anneke Marx, Gabriella Benze, Gesine Heine, Julia Dickel, Lisa-Marie Zhang, Youyou Wowretzko, Feline Wendt, Kim Nikola Nauck, Friedemann Bokemeyer, Carsten Bergelt, Corinna Psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care |
title | Psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care |
title_full | Psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care |
title_fullStr | Psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care |
title_full_unstemmed | Psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care |
title_short | Psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care |
title_sort | psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6862724/ https://www.ncbi.nlm.nih.gov/pubmed/31739802 http://dx.doi.org/10.1186/s12904-019-0469-7 |
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