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Quality of care for people with multimorbidity: a focus group study with patients and their relatives
BACKGROUND: Prevalence of people with multimorbidity rises. Multimorbidity constitutes a challenge to the healthcare system, and treatment of patients with multimorbidity is prone to high-quality variations. Currently, no set of quality indicators (QIs) exists to assess quality of care, let alone in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208013/ https://www.ncbi.nlm.nih.gov/pubmed/34130962 http://dx.doi.org/10.1136/bmjopen-2020-047025 |
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author | Pohontsch, Nadine Janis Schulze, Josefine Hoeflich, Charlotte Glassen, Katharina Breckner, Amanda Szecsenyi, Joachim Lühmann, Dagmar Scherer, Martin |
author_facet | Pohontsch, Nadine Janis Schulze, Josefine Hoeflich, Charlotte Glassen, Katharina Breckner, Amanda Szecsenyi, Joachim Lühmann, Dagmar Scherer, Martin |
author_sort | Pohontsch, Nadine Janis |
collection | PubMed |
description | BACKGROUND: Prevalence of people with multimorbidity rises. Multimorbidity constitutes a challenge to the healthcare system, and treatment of patients with multimorbidity is prone to high-quality variations. Currently, no set of quality indicators (QIs) exists to assess quality of care, let alone incorporating the patient perspective. We therefore aim to identify aspects of quality of care relevant to the patients’ perspective and match them to a literature-based set of QIs. METHODS: We conducted eight focus groups with patients with multimorbidity and three focus groups with patients’ relatives using a semistructured guide. Data were analysed using Kuckartz’s qualitative content analysis. We derived deductive categories from the literature, added inductive categories (new quality aspects) and translated them into QI. RESULTS: We created four new QIs based on the quality aspects relevant to patients/relatives. Two QIs (patient education/self-management, regular updates of medication plans) were consented by an expert panel, while two others were not (periodical check-ups, general practitioner-coordinated care). Half of the literature-based QIs, for example, assessment of biopsychosocial support needs, were supported by participants’ accounts, while more technical domains regarding assessment and treatment regimens were not addressed in the focus groups. CONCLUSION: We show that focus groups with patients and relatives adding relevant aspects in QI development should be incorporated by default in QI development processes and constitute a reasonable addition to traditional QI development. Our QI set constitutes a framework for assessing the quality of care in the German healthcare system. It will facilitate implementation of treatment standards and increase the use of existing guidelines, hereby helping to reduce overuse, underuse and misuse of healthcare resources in the treatment of patients with multimorbidity. TRIAL REGISTRATION NUMBER: German clinical trials registry (DRKS00015718), Pre-Results. |
format | Online Article Text |
id | pubmed-8208013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-82080132021-06-30 Quality of care for people with multimorbidity: a focus group study with patients and their relatives Pohontsch, Nadine Janis Schulze, Josefine Hoeflich, Charlotte Glassen, Katharina Breckner, Amanda Szecsenyi, Joachim Lühmann, Dagmar Scherer, Martin BMJ Open General practice / Family practice BACKGROUND: Prevalence of people with multimorbidity rises. Multimorbidity constitutes a challenge to the healthcare system, and treatment of patients with multimorbidity is prone to high-quality variations. Currently, no set of quality indicators (QIs) exists to assess quality of care, let alone incorporating the patient perspective. We therefore aim to identify aspects of quality of care relevant to the patients’ perspective and match them to a literature-based set of QIs. METHODS: We conducted eight focus groups with patients with multimorbidity and three focus groups with patients’ relatives using a semistructured guide. Data were analysed using Kuckartz’s qualitative content analysis. We derived deductive categories from the literature, added inductive categories (new quality aspects) and translated them into QI. RESULTS: We created four new QIs based on the quality aspects relevant to patients/relatives. Two QIs (patient education/self-management, regular updates of medication plans) were consented by an expert panel, while two others were not (periodical check-ups, general practitioner-coordinated care). Half of the literature-based QIs, for example, assessment of biopsychosocial support needs, were supported by participants’ accounts, while more technical domains regarding assessment and treatment regimens were not addressed in the focus groups. CONCLUSION: We show that focus groups with patients and relatives adding relevant aspects in QI development should be incorporated by default in QI development processes and constitute a reasonable addition to traditional QI development. Our QI set constitutes a framework for assessing the quality of care in the German healthcare system. It will facilitate implementation of treatment standards and increase the use of existing guidelines, hereby helping to reduce overuse, underuse and misuse of healthcare resources in the treatment of patients with multimorbidity. TRIAL REGISTRATION NUMBER: German clinical trials registry (DRKS00015718), Pre-Results. BMJ Publishing Group 2021-06-15 /pmc/articles/PMC8208013/ /pubmed/34130962 http://dx.doi.org/10.1136/bmjopen-2020-047025 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | General practice / Family practice Pohontsch, Nadine Janis Schulze, Josefine Hoeflich, Charlotte Glassen, Katharina Breckner, Amanda Szecsenyi, Joachim Lühmann, Dagmar Scherer, Martin Quality of care for people with multimorbidity: a focus group study with patients and their relatives |
title | Quality of care for people with multimorbidity: a focus group study with patients and their relatives |
title_full | Quality of care for people with multimorbidity: a focus group study with patients and their relatives |
title_fullStr | Quality of care for people with multimorbidity: a focus group study with patients and their relatives |
title_full_unstemmed | Quality of care for people with multimorbidity: a focus group study with patients and their relatives |
title_short | Quality of care for people with multimorbidity: a focus group study with patients and their relatives |
title_sort | quality of care for people with multimorbidity: a focus group study with patients and their relatives |
topic | General practice / Family practice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208013/ https://www.ncbi.nlm.nih.gov/pubmed/34130962 http://dx.doi.org/10.1136/bmjopen-2020-047025 |
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