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Patterns of statin initiation and continuation in patients with breast or colorectal cancer, towards end-of-life

PURPOSE: Cross-sectional studies show that statins, used in cardiovascular disease prevention, are often discontinued approaching death. Studies investigating associations between statin exposure and cancer outcomes, not accounting for these exposure changes, are prone to reverse causation bias. The...

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Detalles Bibliográficos
Autores principales: Smith, Amelia, Murphy, Laura, Bennett, Kathleen, Barron, Thomas I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378743/
https://www.ncbi.nlm.nih.gov/pubmed/28101676
http://dx.doi.org/10.1007/s00520-017-3576-0
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author Smith, Amelia
Murphy, Laura
Bennett, Kathleen
Barron, Thomas I
author_facet Smith, Amelia
Murphy, Laura
Bennett, Kathleen
Barron, Thomas I
author_sort Smith, Amelia
collection PubMed
description PURPOSE: Cross-sectional studies show that statins, used in cardiovascular disease prevention, are often discontinued approaching death. Studies investigating associations between statin exposure and cancer outcomes, not accounting for these exposure changes, are prone to reverse causation bias. The aim of this study was to describe longitudinally the changes in statin initiation and continuation prior to death in patients with breast or colorectal cancer, thus establishing an appropriate exposure lag time. METHODS: This study was carried out using linked cancer registry and prescribing data. We identified patients who died of their cancer (cases) and cancer survivors were used as controls. The probability of initiating or continuing statin use was estimated up to 5 years prior to death (or index date). Conditional binomial models were used to estimate relative risks and risk differences for associations between approaching cancer death and statin use. RESULTS: Compared to controls, the probability of continued statin use in breast cancer cases was significantly lower 3 months prior to death (RR 0.86 95% CI 0.79, 0.94). Similarly, in colorectal cancer cases, the probability of continued statin use was significantly lower 3 months prior to colorectal cancer death (RR 0.77 95% CI 0.68, 0.88). CONCLUSION: A significant proportion of patients will cease statin treatment in the months prior to a colorectal or breast cancer death. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00520-017-3576-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-53787432017-04-17 Patterns of statin initiation and continuation in patients with breast or colorectal cancer, towards end-of-life Smith, Amelia Murphy, Laura Bennett, Kathleen Barron, Thomas I Support Care Cancer Original Article PURPOSE: Cross-sectional studies show that statins, used in cardiovascular disease prevention, are often discontinued approaching death. Studies investigating associations between statin exposure and cancer outcomes, not accounting for these exposure changes, are prone to reverse causation bias. The aim of this study was to describe longitudinally the changes in statin initiation and continuation prior to death in patients with breast or colorectal cancer, thus establishing an appropriate exposure lag time. METHODS: This study was carried out using linked cancer registry and prescribing data. We identified patients who died of their cancer (cases) and cancer survivors were used as controls. The probability of initiating or continuing statin use was estimated up to 5 years prior to death (or index date). Conditional binomial models were used to estimate relative risks and risk differences for associations between approaching cancer death and statin use. RESULTS: Compared to controls, the probability of continued statin use in breast cancer cases was significantly lower 3 months prior to death (RR 0.86 95% CI 0.79, 0.94). Similarly, in colorectal cancer cases, the probability of continued statin use was significantly lower 3 months prior to colorectal cancer death (RR 0.77 95% CI 0.68, 0.88). CONCLUSION: A significant proportion of patients will cease statin treatment in the months prior to a colorectal or breast cancer death. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00520-017-3576-0) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-01-18 2017 /pmc/articles/PMC5378743/ /pubmed/28101676 http://dx.doi.org/10.1007/s00520-017-3576-0 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial 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.
spellingShingle Original Article
Smith, Amelia
Murphy, Laura
Bennett, Kathleen
Barron, Thomas I
Patterns of statin initiation and continuation in patients with breast or colorectal cancer, towards end-of-life
title Patterns of statin initiation and continuation in patients with breast or colorectal cancer, towards end-of-life
title_full Patterns of statin initiation and continuation in patients with breast or colorectal cancer, towards end-of-life
title_fullStr Patterns of statin initiation and continuation in patients with breast or colorectal cancer, towards end-of-life
title_full_unstemmed Patterns of statin initiation and continuation in patients with breast or colorectal cancer, towards end-of-life
title_short Patterns of statin initiation and continuation in patients with breast or colorectal cancer, towards end-of-life
title_sort patterns of statin initiation and continuation in patients with breast or colorectal cancer, towards end-of-life
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378743/
https://www.ncbi.nlm.nih.gov/pubmed/28101676
http://dx.doi.org/10.1007/s00520-017-3576-0
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