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General practice performance in referral for suspected cancer: influence of number of cases and case-mix on publicly reported data
BACKGROUND: Publicly available data show variation in GPs' use of urgent suspected cancer (USC) referral pathways. We investigated whether this could be due to small numbers of cancer cases and random case-mix, rather than due to true variation in performance. METHODS: We analysed individual GP...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647257/ https://www.ncbi.nlm.nih.gov/pubmed/25880009 http://dx.doi.org/10.1038/bjc.2015.110 |
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author | Murchie, P Chowdhury, A Smith, S Campbell, N C Lee, A J Linden, D Burton, C D |
author_facet | Murchie, P Chowdhury, A Smith, S Campbell, N C Lee, A J Linden, D Burton, C D |
author_sort | Murchie, P |
collection | PubMed |
description | BACKGROUND: Publicly available data show variation in GPs' use of urgent suspected cancer (USC) referral pathways. We investigated whether this could be due to small numbers of cancer cases and random case-mix, rather than due to true variation in performance. METHODS: We analysed individual GP practice USC referral detection rates (proportion of the practice's cancer cases that are detected via USC) and conversion rates (proportion of the practice's USC referrals that prove to be cancer) in routinely collected data from GP practices in all of England (over 4 years) and northeast Scotland (over 7 years). We explored the effect of pooling data. We then modelled the effects of adding random case-mix to practice variation. RESULTS: Correlations between practice detection rate and conversion rate became less positive when data were aggregated over several years. Adding random case-mix to between-practice variation indicated that the median proportion of poorly performing practices correctly identified after 25 cancer cases were examined was 20% (IQR 17 to 24) and after 100 cases was 44% (IQR 40 to 47). CONCLUSIONS: Much apparent variation in GPs' use of suspected cancer referral pathways can be attributed to random case-mix. The methods currently used to assess the quality of GP-suspected cancer referral performance, and to compare individual practices, are misleading. These should no longer be used, and more appropriate and robust methods should be developed. |
format | Online Article Text |
id | pubmed-4647257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46472572016-05-26 General practice performance in referral for suspected cancer: influence of number of cases and case-mix on publicly reported data Murchie, P Chowdhury, A Smith, S Campbell, N C Lee, A J Linden, D Burton, C D Br J Cancer Epidemiology BACKGROUND: Publicly available data show variation in GPs' use of urgent suspected cancer (USC) referral pathways. We investigated whether this could be due to small numbers of cancer cases and random case-mix, rather than due to true variation in performance. METHODS: We analysed individual GP practice USC referral detection rates (proportion of the practice's cancer cases that are detected via USC) and conversion rates (proportion of the practice's USC referrals that prove to be cancer) in routinely collected data from GP practices in all of England (over 4 years) and northeast Scotland (over 7 years). We explored the effect of pooling data. We then modelled the effects of adding random case-mix to practice variation. RESULTS: Correlations between practice detection rate and conversion rate became less positive when data were aggregated over several years. Adding random case-mix to between-practice variation indicated that the median proportion of poorly performing practices correctly identified after 25 cancer cases were examined was 20% (IQR 17 to 24) and after 100 cases was 44% (IQR 40 to 47). CONCLUSIONS: Much apparent variation in GPs' use of suspected cancer referral pathways can be attributed to random case-mix. The methods currently used to assess the quality of GP-suspected cancer referral performance, and to compare individual practices, are misleading. These should no longer be used, and more appropriate and robust methods should be developed. Nature Publishing Group 2015-05-26 2015-04-16 /pmc/articles/PMC4647257/ /pubmed/25880009 http://dx.doi.org/10.1038/bjc.2015.110 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Epidemiology Murchie, P Chowdhury, A Smith, S Campbell, N C Lee, A J Linden, D Burton, C D General practice performance in referral for suspected cancer: influence of number of cases and case-mix on publicly reported data |
title | General practice performance in referral for suspected cancer: influence of number of cases and case-mix on publicly reported data |
title_full | General practice performance in referral for suspected cancer: influence of number of cases and case-mix on publicly reported data |
title_fullStr | General practice performance in referral for suspected cancer: influence of number of cases and case-mix on publicly reported data |
title_full_unstemmed | General practice performance in referral for suspected cancer: influence of number of cases and case-mix on publicly reported data |
title_short | General practice performance in referral for suspected cancer: influence of number of cases and case-mix on publicly reported data |
title_sort | general practice performance in referral for suspected cancer: influence of number of cases and case-mix on publicly reported data |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647257/ https://www.ncbi.nlm.nih.gov/pubmed/25880009 http://dx.doi.org/10.1038/bjc.2015.110 |
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