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Implementing a QCancer risk tool into general practice consultations: an exploratory study using simulated consultations with Australian general practitioners

BACKGROUND: Reducing diagnostic delays in primary care by improving the assessment of symptoms associated with cancer could have significant impacts on cancer outcomes. Symptom risk assessment tools could improve the diagnostic assessment of patients with symptoms suggestive of cancer in primary car...

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Autores principales: Chiang, P P-C, Glance, D, Walker, J, Walter, F M, Emery, J D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385980/
https://www.ncbi.nlm.nih.gov/pubmed/25734392
http://dx.doi.org/10.1038/bjc.2015.46
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author Chiang, P P-C
Glance, D
Walker, J
Walter, F M
Emery, J D
author_facet Chiang, P P-C
Glance, D
Walker, J
Walter, F M
Emery, J D
author_sort Chiang, P P-C
collection PubMed
description BACKGROUND: Reducing diagnostic delays in primary care by improving the assessment of symptoms associated with cancer could have significant impacts on cancer outcomes. Symptom risk assessment tools could improve the diagnostic assessment of patients with symptoms suggestive of cancer in primary care. We aimed to explore the use of a cancer risk tool, which implements the QCancer model, in consultations and its potential impact on clinical decision making. METHODS: We implemented an exploratory ‘action design' method with 15 general practitioners (GPs) from Victoria, Australia. General practitioners applied the risk tool in simulated consultations, conducted semi-structured interviews based on the normalisation process theory and explored issues relating to implementation of the tool. RESULTS: The risk tool was perceived as being potentially useful for patients with complex histories. More experienced GPs were distrustful of the risk output, especially when it conflicted with their clinical judgement. Variable interpretation of symptoms meant that there was significant variation in risk assessment. When a risk output was high, GPs were confronted with numerical risk outputs creating challenges in consultation. CONCLUSIONS: Significant barriers to implementing electronic cancer risk assessment tools in consultation could limit their uptake. These relate not only to the design and integration of the tool but also to variation in interpretation of clinical histories, and therefore variable risk outputs and strong beliefs in personal clinical intuition.
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spelling pubmed-43859802015-04-07 Implementing a QCancer risk tool into general practice consultations: an exploratory study using simulated consultations with Australian general practitioners Chiang, P P-C Glance, D Walker, J Walter, F M Emery, J D Br J Cancer Full Paper BACKGROUND: Reducing diagnostic delays in primary care by improving the assessment of symptoms associated with cancer could have significant impacts on cancer outcomes. Symptom risk assessment tools could improve the diagnostic assessment of patients with symptoms suggestive of cancer in primary care. We aimed to explore the use of a cancer risk tool, which implements the QCancer model, in consultations and its potential impact on clinical decision making. METHODS: We implemented an exploratory ‘action design' method with 15 general practitioners (GPs) from Victoria, Australia. General practitioners applied the risk tool in simulated consultations, conducted semi-structured interviews based on the normalisation process theory and explored issues relating to implementation of the tool. RESULTS: The risk tool was perceived as being potentially useful for patients with complex histories. More experienced GPs were distrustful of the risk output, especially when it conflicted with their clinical judgement. Variable interpretation of symptoms meant that there was significant variation in risk assessment. When a risk output was high, GPs were confronted with numerical risk outputs creating challenges in consultation. CONCLUSIONS: Significant barriers to implementing electronic cancer risk assessment tools in consultation could limit their uptake. These relate not only to the design and integration of the tool but also to variation in interpretation of clinical histories, and therefore variable risk outputs and strong beliefs in personal clinical intuition. Nature Publishing Group 2015-03-31 2015-03-03 /pmc/articles/PMC4385980/ /pubmed/25734392 http://dx.doi.org/10.1038/bjc.2015.46 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Full Paper
Chiang, P P-C
Glance, D
Walker, J
Walter, F M
Emery, J D
Implementing a QCancer risk tool into general practice consultations: an exploratory study using simulated consultations with Australian general practitioners
title Implementing a QCancer risk tool into general practice consultations: an exploratory study using simulated consultations with Australian general practitioners
title_full Implementing a QCancer risk tool into general practice consultations: an exploratory study using simulated consultations with Australian general practitioners
title_fullStr Implementing a QCancer risk tool into general practice consultations: an exploratory study using simulated consultations with Australian general practitioners
title_full_unstemmed Implementing a QCancer risk tool into general practice consultations: an exploratory study using simulated consultations with Australian general practitioners
title_short Implementing a QCancer risk tool into general practice consultations: an exploratory study using simulated consultations with Australian general practitioners
title_sort implementing a qcancer risk tool into general practice consultations: an exploratory study using simulated consultations with australian general practitioners
topic Full Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385980/
https://www.ncbi.nlm.nih.gov/pubmed/25734392
http://dx.doi.org/10.1038/bjc.2015.46
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