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Impact of comorbidity on risk of venous thromboembolism in patients with breast cancer: a Danish population-based cohort study

OBJECTIVES: To assess the interaction between comorbidity and breast cancer (BC) on the rate of venous thromboembolism (VTE) beyond what can be explained by the independent effects of BC and comorbidity. DESIGN: Population-based matched cohort study. SETTING: Denmark. PARTICIPANTS: Danish patients w...

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Autores principales: Ording, Anne Gulbech, Horváth-Puhó, Erzsébet, Garne, Jens Peter, Nyström, Petra Witt, Vyberg, Mogens, Sørensen, Henrik Toft, Lash, Timothy L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054647/
https://www.ncbi.nlm.nih.gov/pubmed/24902734
http://dx.doi.org/10.1136/bmjopen-2014-005082
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author Ording, Anne Gulbech
Horváth-Puhó, Erzsébet
Garne, Jens Peter
Nyström, Petra Witt
Vyberg, Mogens
Sørensen, Henrik Toft
Lash, Timothy L
author_facet Ording, Anne Gulbech
Horváth-Puhó, Erzsébet
Garne, Jens Peter
Nyström, Petra Witt
Vyberg, Mogens
Sørensen, Henrik Toft
Lash, Timothy L
author_sort Ording, Anne Gulbech
collection PubMed
description OBJECTIVES: To assess the interaction between comorbidity and breast cancer (BC) on the rate of venous thromboembolism (VTE) beyond what can be explained by the independent effects of BC and comorbidity. DESIGN: Population-based matched cohort study. SETTING: Denmark. PARTICIPANTS: Danish patients with BC (n=62 376) diagnosed in 1995–2010 and a comparison cohort of women without BC (n=304 803) from the general population were matched to the patients with BC on year of birth in 5-year intervals and on the specific diseases included in the Charlson Comorbidity Index (CCI) and atrial fibrillation and obesity. MEASURES: The rate ratios of VTE per 1000 person-years (PY) were computed by comorbidity levels using the CCI, and interaction contrasts (IC) were calculated as a measure of the excess or deficit VTE rate not explained by the independent effects of BC and comorbidity. RESULTS: Among patients with BC with a CCI score of 1, the 0–1 year VTE rate was 12/1000 PY, and interaction accounted for 10% of the rate (IC=3.2, 95% CI 0.5 to 5.9). Among patients with BC with CCI ≥4, the VTE rate was 17, and interaction accounted for 8% of the rate (IC=1.2, 95% CI −1.8 to 4.2). There was no interaction during 2–5 years of follow-up. CONCLUSIONS: There was only little interaction between BC and the CCI score on the rate of VTE.
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spelling pubmed-40546472014-06-13 Impact of comorbidity on risk of venous thromboembolism in patients with breast cancer: a Danish population-based cohort study Ording, Anne Gulbech Horváth-Puhó, Erzsébet Garne, Jens Peter Nyström, Petra Witt Vyberg, Mogens Sørensen, Henrik Toft Lash, Timothy L BMJ Open Oncology OBJECTIVES: To assess the interaction between comorbidity and breast cancer (BC) on the rate of venous thromboembolism (VTE) beyond what can be explained by the independent effects of BC and comorbidity. DESIGN: Population-based matched cohort study. SETTING: Denmark. PARTICIPANTS: Danish patients with BC (n=62 376) diagnosed in 1995–2010 and a comparison cohort of women without BC (n=304 803) from the general population were matched to the patients with BC on year of birth in 5-year intervals and on the specific diseases included in the Charlson Comorbidity Index (CCI) and atrial fibrillation and obesity. MEASURES: The rate ratios of VTE per 1000 person-years (PY) were computed by comorbidity levels using the CCI, and interaction contrasts (IC) were calculated as a measure of the excess or deficit VTE rate not explained by the independent effects of BC and comorbidity. RESULTS: Among patients with BC with a CCI score of 1, the 0–1 year VTE rate was 12/1000 PY, and interaction accounted for 10% of the rate (IC=3.2, 95% CI 0.5 to 5.9). Among patients with BC with CCI ≥4, the VTE rate was 17, and interaction accounted for 8% of the rate (IC=1.2, 95% CI −1.8 to 4.2). There was no interaction during 2–5 years of follow-up. CONCLUSIONS: There was only little interaction between BC and the CCI score on the rate of VTE. BMJ Publishing Group 2014-06-05 /pmc/articles/PMC4054647/ /pubmed/24902734 http://dx.doi.org/10.1136/bmjopen-2014-005082 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Oncology
Ording, Anne Gulbech
Horváth-Puhó, Erzsébet
Garne, Jens Peter
Nyström, Petra Witt
Vyberg, Mogens
Sørensen, Henrik Toft
Lash, Timothy L
Impact of comorbidity on risk of venous thromboembolism in patients with breast cancer: a Danish population-based cohort study
title Impact of comorbidity on risk of venous thromboembolism in patients with breast cancer: a Danish population-based cohort study
title_full Impact of comorbidity on risk of venous thromboembolism in patients with breast cancer: a Danish population-based cohort study
title_fullStr Impact of comorbidity on risk of venous thromboembolism in patients with breast cancer: a Danish population-based cohort study
title_full_unstemmed Impact of comorbidity on risk of venous thromboembolism in patients with breast cancer: a Danish population-based cohort study
title_short Impact of comorbidity on risk of venous thromboembolism in patients with breast cancer: a Danish population-based cohort study
title_sort impact of comorbidity on risk of venous thromboembolism in patients with breast cancer: a danish population-based cohort study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054647/
https://www.ncbi.nlm.nih.gov/pubmed/24902734
http://dx.doi.org/10.1136/bmjopen-2014-005082
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