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Statin intensity and risk for cardiovascular events after heart transplantation

AIMS: Statins improve survival and reduce rejection and cardiac allograft vasculopathy after heart transplantation (HT). The impact of different statin intensities on clinical outcomes has never been assessed. We set out to determine the impact of statin exposure on cardiovascular outcomes after HT....

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Autores principales: Golbus, Jessica R., Adie, Sarah, Yosef, Matheos, Murthy, Venkatesh L., Aaronson, Keith D., Konerman, Matthew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524051/
https://www.ncbi.nlm.nih.gov/pubmed/32578953
http://dx.doi.org/10.1002/ehf2.12784
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author Golbus, Jessica R.
Adie, Sarah
Yosef, Matheos
Murthy, Venkatesh L.
Aaronson, Keith D.
Konerman, Matthew C.
author_facet Golbus, Jessica R.
Adie, Sarah
Yosef, Matheos
Murthy, Venkatesh L.
Aaronson, Keith D.
Konerman, Matthew C.
author_sort Golbus, Jessica R.
collection PubMed
description AIMS: Statins improve survival and reduce rejection and cardiac allograft vasculopathy after heart transplantation (HT). The impact of different statin intensities on clinical outcomes has never been assessed. We set out to determine the impact of statin exposure on cardiovascular outcomes after HT. METHODS AND RESULTS: We performed a retrospective study of 346 adult patients who underwent HT from 2006 to 2018. Statin intensity was determined longitudinally after HT based on American College of Cardiology/American Heart Association (ACC/AHA) guidelines. The primary outcome was the time to the first primary event defined as the composite of heart failure hospitalization, myocardial infarction, revascularization, and all‐cause mortality. Secondary outcomes included time to significant rejection and time to moderate–severe cardiac allograft vasculopathy. Adverse events were evaluated for subjects on high‐intensity statin therapy. A Cox proportional hazards model was used to evaluate the relationship between clinical variables, statin intensity, and outcomes. Most subjects were treated with low‐intensity statin therapy although this declined from 89.9% of the population at 1month after HT to 42.8% at 5years after HT. History of ischaemic cardiomyopathy, significant acute rejection, older donor age, and lesser statin intensity (p ≤ 0.001) were associated with reduced time to the primary outcome in a multivariable Cox model. Greater intensity of statin therapy was most beneficial early after HT. There were no statin‐related adverse events for the 14 subjects on high‐intensity statin therapy. CONCLUSIONS: Greater statin intensity was associated with a reduction in adverse cardiovascular outcomes after HT.
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spelling pubmed-75240512020-10-02 Statin intensity and risk for cardiovascular events after heart transplantation Golbus, Jessica R. Adie, Sarah Yosef, Matheos Murthy, Venkatesh L. Aaronson, Keith D. Konerman, Matthew C. ESC Heart Fail Original Research Articles AIMS: Statins improve survival and reduce rejection and cardiac allograft vasculopathy after heart transplantation (HT). The impact of different statin intensities on clinical outcomes has never been assessed. We set out to determine the impact of statin exposure on cardiovascular outcomes after HT. METHODS AND RESULTS: We performed a retrospective study of 346 adult patients who underwent HT from 2006 to 2018. Statin intensity was determined longitudinally after HT based on American College of Cardiology/American Heart Association (ACC/AHA) guidelines. The primary outcome was the time to the first primary event defined as the composite of heart failure hospitalization, myocardial infarction, revascularization, and all‐cause mortality. Secondary outcomes included time to significant rejection and time to moderate–severe cardiac allograft vasculopathy. Adverse events were evaluated for subjects on high‐intensity statin therapy. A Cox proportional hazards model was used to evaluate the relationship between clinical variables, statin intensity, and outcomes. Most subjects were treated with low‐intensity statin therapy although this declined from 89.9% of the population at 1month after HT to 42.8% at 5years after HT. History of ischaemic cardiomyopathy, significant acute rejection, older donor age, and lesser statin intensity (p ≤ 0.001) were associated with reduced time to the primary outcome in a multivariable Cox model. Greater intensity of statin therapy was most beneficial early after HT. There were no statin‐related adverse events for the 14 subjects on high‐intensity statin therapy. CONCLUSIONS: Greater statin intensity was associated with a reduction in adverse cardiovascular outcomes after HT. John Wiley and Sons Inc. 2020-06-24 /pmc/articles/PMC7524051/ /pubmed/32578953 http://dx.doi.org/10.1002/ehf2.12784 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research Articles
Golbus, Jessica R.
Adie, Sarah
Yosef, Matheos
Murthy, Venkatesh L.
Aaronson, Keith D.
Konerman, Matthew C.
Statin intensity and risk for cardiovascular events after heart transplantation
title Statin intensity and risk for cardiovascular events after heart transplantation
title_full Statin intensity and risk for cardiovascular events after heart transplantation
title_fullStr Statin intensity and risk for cardiovascular events after heart transplantation
title_full_unstemmed Statin intensity and risk for cardiovascular events after heart transplantation
title_short Statin intensity and risk for cardiovascular events after heart transplantation
title_sort statin intensity and risk for cardiovascular events after heart transplantation
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524051/
https://www.ncbi.nlm.nih.gov/pubmed/32578953
http://dx.doi.org/10.1002/ehf2.12784
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