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Evaluation of the risk of cardiovascular events with clarithromycin using both propensity score and self‐controlled study designs
AIM: Some previous studies suggest a long term association between clarithromycin use and cardiovascular events. This study investigates this association for clarithromycin given as part of Helicobacter pylori treatment (HPT). METHODS: Our source population was the Clinical Practice Research Datalin...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972168/ https://www.ncbi.nlm.nih.gov/pubmed/27090996 http://dx.doi.org/10.1111/bcp.12983 |
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author | Root, Adrian A. Wong, Angel Y. S. Ghebremichael‐Weldeselassie, Yonas Smeeth, Liam Bhaskaran, Krishnan Evans, Stephen J. W. Brauer, Ruth Wong, Ian Chi Kei Navaratnam, Vidya Douglas, Ian |
author_facet | Root, Adrian A. Wong, Angel Y. S. Ghebremichael‐Weldeselassie, Yonas Smeeth, Liam Bhaskaran, Krishnan Evans, Stephen J. W. Brauer, Ruth Wong, Ian Chi Kei Navaratnam, Vidya Douglas, Ian |
author_sort | Root, Adrian A. |
collection | PubMed |
description | AIM: Some previous studies suggest a long term association between clarithromycin use and cardiovascular events. This study investigates this association for clarithromycin given as part of Helicobacter pylori treatment (HPT). METHODS: Our source population was the Clinical Practice Research Datalink (CPRD), a UK primary care database. We conducted a self‐controlled case series (SCCS), a case–time–control study (CTC) and a propensity score adjusted cohort study comparing the rate of cardiovascular events in the 3 years after exposure to HPT containing clarithromycin with exposure to clarithromycin free HPT. Outcomes were first incident diagnosis of myocardial infarction (MI), arrhythmia and stroke. For the cohort analysis we included secondary outcomes all cause and cardiovascular mortality. RESULTS: Twenty‐eight thousand five hundred and fifty‐two patients were included in the cohort. The incidence rate ratio of first MI within 1 year of exposure to HPT containing clarithromycin was 1.07 (95% CI 0.85, 1.34, P = 0.58) and within 90 days was 1.43 (95% CI 0.99, 2.09 P = 0.057) in the SCCS analysis. CTC and cohort results were consistent with these findings. CONCLUSIONS: There was some evidence for a short term association for first MI but none for a long term association for any outcome. |
format | Online Article Text |
id | pubmed-4972168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49721682016-08-17 Evaluation of the risk of cardiovascular events with clarithromycin using both propensity score and self‐controlled study designs Root, Adrian A. Wong, Angel Y. S. Ghebremichael‐Weldeselassie, Yonas Smeeth, Liam Bhaskaran, Krishnan Evans, Stephen J. W. Brauer, Ruth Wong, Ian Chi Kei Navaratnam, Vidya Douglas, Ian Br J Clin Pharmacol Pharmacoepidemiology AIM: Some previous studies suggest a long term association between clarithromycin use and cardiovascular events. This study investigates this association for clarithromycin given as part of Helicobacter pylori treatment (HPT). METHODS: Our source population was the Clinical Practice Research Datalink (CPRD), a UK primary care database. We conducted a self‐controlled case series (SCCS), a case–time–control study (CTC) and a propensity score adjusted cohort study comparing the rate of cardiovascular events in the 3 years after exposure to HPT containing clarithromycin with exposure to clarithromycin free HPT. Outcomes were first incident diagnosis of myocardial infarction (MI), arrhythmia and stroke. For the cohort analysis we included secondary outcomes all cause and cardiovascular mortality. RESULTS: Twenty‐eight thousand five hundred and fifty‐two patients were included in the cohort. The incidence rate ratio of first MI within 1 year of exposure to HPT containing clarithromycin was 1.07 (95% CI 0.85, 1.34, P = 0.58) and within 90 days was 1.43 (95% CI 0.99, 2.09 P = 0.057) in the SCCS analysis. CTC and cohort results were consistent with these findings. CONCLUSIONS: There was some evidence for a short term association for first MI but none for a long term association for any outcome. John Wiley and Sons Inc. 2016-06-08 2016-08 /pmc/articles/PMC4972168/ /pubmed/27090996 http://dx.doi.org/10.1111/bcp.12983 Text en © 2016 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of The British Pharmacological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Pharmacoepidemiology Root, Adrian A. Wong, Angel Y. S. Ghebremichael‐Weldeselassie, Yonas Smeeth, Liam Bhaskaran, Krishnan Evans, Stephen J. W. Brauer, Ruth Wong, Ian Chi Kei Navaratnam, Vidya Douglas, Ian Evaluation of the risk of cardiovascular events with clarithromycin using both propensity score and self‐controlled study designs |
title | Evaluation of the risk of cardiovascular events with clarithromycin using both propensity score and self‐controlled study designs |
title_full | Evaluation of the risk of cardiovascular events with clarithromycin using both propensity score and self‐controlled study designs |
title_fullStr | Evaluation of the risk of cardiovascular events with clarithromycin using both propensity score and self‐controlled study designs |
title_full_unstemmed | Evaluation of the risk of cardiovascular events with clarithromycin using both propensity score and self‐controlled study designs |
title_short | Evaluation of the risk of cardiovascular events with clarithromycin using both propensity score and self‐controlled study designs |
title_sort | evaluation of the risk of cardiovascular events with clarithromycin using both propensity score and self‐controlled study designs |
topic | Pharmacoepidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972168/ https://www.ncbi.nlm.nih.gov/pubmed/27090996 http://dx.doi.org/10.1111/bcp.12983 |
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