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Family conferences and shared prioritisation to improve patient safety in the frail elderly (COFRAIL): study protocol of a cluster randomised intervention trial in primary care

BACKGROUND: Frailty in elderly patients is associated with an increased risk of poor health outcomes, including falls, delirium, malnutrition, hospitalisation, and mortality. Because polypharmacy is recognised as a possible major contributor to the pathogenesis of geriatric frailty, reducing inappro...

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Autores principales: Mortsiefer, Achim, Wilm, Stefan, Santos, Sara, Löscher, Susanne, Wollny, Anja, Drewelow, Eva, Ritzke, Manuela, Thürmann, Petra, Mann, Nina-Kristin, Meyer, Gabriele, Abraham, Jens, Icks, Andrea, Montalbo, Joseph, Wiese, Birgitt, Altiner, Attila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082941/
https://www.ncbi.nlm.nih.gov/pubmed/32197631
http://dx.doi.org/10.1186/s13063-020-4182-x
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author Mortsiefer, Achim
Wilm, Stefan
Santos, Sara
Löscher, Susanne
Wollny, Anja
Drewelow, Eva
Ritzke, Manuela
Thürmann, Petra
Mann, Nina-Kristin
Meyer, Gabriele
Abraham, Jens
Icks, Andrea
Montalbo, Joseph
Wiese, Birgitt
Altiner, Attila
author_facet Mortsiefer, Achim
Wilm, Stefan
Santos, Sara
Löscher, Susanne
Wollny, Anja
Drewelow, Eva
Ritzke, Manuela
Thürmann, Petra
Mann, Nina-Kristin
Meyer, Gabriele
Abraham, Jens
Icks, Andrea
Montalbo, Joseph
Wiese, Birgitt
Altiner, Attila
author_sort Mortsiefer, Achim
collection PubMed
description BACKGROUND: Frailty in elderly patients is associated with an increased risk of poor health outcomes, including falls, delirium, malnutrition, hospitalisation, and mortality. Because polypharmacy is recognised as a possible major contributor to the pathogenesis of geriatric frailty, reducing inappropriate medication exposure is supposed to be a promising approach to improve health-related quality of life and prevent adverse outcomes. A major challenge for the process of deprescribing of inappropriate polypharmacy is to improve the communication between general practitioner (GPs), patient and family carer. This study investigates the effects of a complex intervention in frail elderly patients with polypharmacy living at home. METHODS: This is a cluster randomised controlled trial including 136 GPs and 676 patients. Patients with a positive clinical screening for frailty are eligible if they are aged 70 years or older, receiving family or professional nursing care at home, and taking in five or more drugs per day. Exclusion criteria are higher grade of dementia and life expectancy of 6 months or less. The GPs of the intervention group receive an educational training promoting a deprescribing guideline and providing information on how to conduct a family conference focussing on prioritisation of treatment goals concerning drug therapy. During the 1-year intervention, GPs are expected to perform a total of three family conferences, each including a structured medication review with patients and their family carers. GPs of the control group will receive no training and will deliver care as usual. Geriatric assessment of all patients will be performed by study nurses during home visits at baseline and after 6 and 12 months. The primary outcome is the hospitalisation rate during the observation period of 12 months. Secondary outcomes are number and appropriateness of medications, mobility, weakness, cognition, depressive disorder, health-related quality of life, activities of daily living, weight, and costs of health care use. DISCUSSION: This study will provide evidence for a pragmatic co-operative and patient-centred educational intervention using family conferences to improve patient safety in frail elderly patients with polypharmacy. TRIAL REGISTRATION: German Clinical Trials Register, DRKS00015055 (WHO International Clinical Trials Registry Platform [ICTRP]). Registered on 6 February 2019.
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spelling pubmed-70829412020-03-23 Family conferences and shared prioritisation to improve patient safety in the frail elderly (COFRAIL): study protocol of a cluster randomised intervention trial in primary care Mortsiefer, Achim Wilm, Stefan Santos, Sara Löscher, Susanne Wollny, Anja Drewelow, Eva Ritzke, Manuela Thürmann, Petra Mann, Nina-Kristin Meyer, Gabriele Abraham, Jens Icks, Andrea Montalbo, Joseph Wiese, Birgitt Altiner, Attila Trials Study Protocol BACKGROUND: Frailty in elderly patients is associated with an increased risk of poor health outcomes, including falls, delirium, malnutrition, hospitalisation, and mortality. Because polypharmacy is recognised as a possible major contributor to the pathogenesis of geriatric frailty, reducing inappropriate medication exposure is supposed to be a promising approach to improve health-related quality of life and prevent adverse outcomes. A major challenge for the process of deprescribing of inappropriate polypharmacy is to improve the communication between general practitioner (GPs), patient and family carer. This study investigates the effects of a complex intervention in frail elderly patients with polypharmacy living at home. METHODS: This is a cluster randomised controlled trial including 136 GPs and 676 patients. Patients with a positive clinical screening for frailty are eligible if they are aged 70 years or older, receiving family or professional nursing care at home, and taking in five or more drugs per day. Exclusion criteria are higher grade of dementia and life expectancy of 6 months or less. The GPs of the intervention group receive an educational training promoting a deprescribing guideline and providing information on how to conduct a family conference focussing on prioritisation of treatment goals concerning drug therapy. During the 1-year intervention, GPs are expected to perform a total of three family conferences, each including a structured medication review with patients and their family carers. GPs of the control group will receive no training and will deliver care as usual. Geriatric assessment of all patients will be performed by study nurses during home visits at baseline and after 6 and 12 months. The primary outcome is the hospitalisation rate during the observation period of 12 months. Secondary outcomes are number and appropriateness of medications, mobility, weakness, cognition, depressive disorder, health-related quality of life, activities of daily living, weight, and costs of health care use. DISCUSSION: This study will provide evidence for a pragmatic co-operative and patient-centred educational intervention using family conferences to improve patient safety in frail elderly patients with polypharmacy. TRIAL REGISTRATION: German Clinical Trials Register, DRKS00015055 (WHO International Clinical Trials Registry Platform [ICTRP]). Registered on 6 February 2019. BioMed Central 2020-03-20 /pmc/articles/PMC7082941/ /pubmed/32197631 http://dx.doi.org/10.1186/s13063-020-4182-x Text en © The Author(s). 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Study Protocol
Mortsiefer, Achim
Wilm, Stefan
Santos, Sara
Löscher, Susanne
Wollny, Anja
Drewelow, Eva
Ritzke, Manuela
Thürmann, Petra
Mann, Nina-Kristin
Meyer, Gabriele
Abraham, Jens
Icks, Andrea
Montalbo, Joseph
Wiese, Birgitt
Altiner, Attila
Family conferences and shared prioritisation to improve patient safety in the frail elderly (COFRAIL): study protocol of a cluster randomised intervention trial in primary care
title Family conferences and shared prioritisation to improve patient safety in the frail elderly (COFRAIL): study protocol of a cluster randomised intervention trial in primary care
title_full Family conferences and shared prioritisation to improve patient safety in the frail elderly (COFRAIL): study protocol of a cluster randomised intervention trial in primary care
title_fullStr Family conferences and shared prioritisation to improve patient safety in the frail elderly (COFRAIL): study protocol of a cluster randomised intervention trial in primary care
title_full_unstemmed Family conferences and shared prioritisation to improve patient safety in the frail elderly (COFRAIL): study protocol of a cluster randomised intervention trial in primary care
title_short Family conferences and shared prioritisation to improve patient safety in the frail elderly (COFRAIL): study protocol of a cluster randomised intervention trial in primary care
title_sort family conferences and shared prioritisation to improve patient safety in the frail elderly (cofrail): study protocol of a cluster randomised intervention trial in primary care
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082941/
https://www.ncbi.nlm.nih.gov/pubmed/32197631
http://dx.doi.org/10.1186/s13063-020-4182-x
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