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Effects of a Secondary Prevention Combination Therapy with beta-Blocker and Statin on Major Adverse Cardiovascular Events in Acute Coronary Syndrome Patients

BACKGROUND: The efficacy of a beta-blocker or statin alone versus combination therapy is uncertain. We compared the effects of a combination of beta-blocker and statin with those of one-drug therapies with regard to the occurrence of a major adverse cardiovascular event (MACE) in patients with acute...

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Autores principales: Zhu, Ling, Cui, Qianwei, Liu, Ying, Liu, Zhongwei, Zhang, Yong, Liu, Fuqiang, Wang, Junkui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453752/
https://www.ncbi.nlm.nih.gov/pubmed/32808600
http://dx.doi.org/10.12659/MSM.925114
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author Zhu, Ling
Cui, Qianwei
Liu, Ying
Liu, Zhongwei
Zhang, Yong
Liu, Fuqiang
Wang, Junkui
author_facet Zhu, Ling
Cui, Qianwei
Liu, Ying
Liu, Zhongwei
Zhang, Yong
Liu, Fuqiang
Wang, Junkui
author_sort Zhu, Ling
collection PubMed
description BACKGROUND: The efficacy of a beta-blocker or statin alone versus combination therapy is uncertain. We compared the effects of a combination of beta-blocker and statin with those of one-drug therapies with regard to the occurrence of a major adverse cardiovascular event (MACE) in patients with acute coronary syndrome (ACS). MATERIAL/METHODS: From 2011 to 2013, 636 ACS patients were included. Based on their risk category, enrolled subjects were assigned into 4 groups receiving consistent beta-blocker and/or statin treatment: no therapy group (n=139), with never use or inconsistent use beta-blocker and statin; beta-blocker monotherapy group (n=71); statin monotherapy group (n=149); and cotherapy group (n=277). RESULTS: Men composed 66.8% of the cohort, which had a mean age of 60.42±9.83 years. Compared with the no therapy group, the statin monotherapy group and cotherapy group had a lower risk of MACE (statin monotherapy group: adjusted hazard ratio [HR] 0.35, 95% confidence interval [CI] 0.20–0.60, P<.001; cotherapy group: adjusted HR 0.16, 95% CI 0.09–0.28, P<.001). Subgroup analysis indicated that, compared with beta-blocker monotherapy and statin monotherapy, cotherapy significantly reduced the risks of MACE occurrences in ACS patients (beta-blocker monotherapy group: adjusted HR 0.28, 95% CI 0.13–0.59, P=.001; statin monotherapy group: adjusted HR 0.54, 95% CI 0.29–0.98, P=.044). CONCLUSIONS: Beta-blocker and statin combination therapy lowered the risk of developing MACE in ACS patients.
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spelling pubmed-74537522020-09-03 Effects of a Secondary Prevention Combination Therapy with beta-Blocker and Statin on Major Adverse Cardiovascular Events in Acute Coronary Syndrome Patients Zhu, Ling Cui, Qianwei Liu, Ying Liu, Zhongwei Zhang, Yong Liu, Fuqiang Wang, Junkui Med Sci Monit Clinical Research BACKGROUND: The efficacy of a beta-blocker or statin alone versus combination therapy is uncertain. We compared the effects of a combination of beta-blocker and statin with those of one-drug therapies with regard to the occurrence of a major adverse cardiovascular event (MACE) in patients with acute coronary syndrome (ACS). MATERIAL/METHODS: From 2011 to 2013, 636 ACS patients were included. Based on their risk category, enrolled subjects were assigned into 4 groups receiving consistent beta-blocker and/or statin treatment: no therapy group (n=139), with never use or inconsistent use beta-blocker and statin; beta-blocker monotherapy group (n=71); statin monotherapy group (n=149); and cotherapy group (n=277). RESULTS: Men composed 66.8% of the cohort, which had a mean age of 60.42±9.83 years. Compared with the no therapy group, the statin monotherapy group and cotherapy group had a lower risk of MACE (statin monotherapy group: adjusted hazard ratio [HR] 0.35, 95% confidence interval [CI] 0.20–0.60, P<.001; cotherapy group: adjusted HR 0.16, 95% CI 0.09–0.28, P<.001). Subgroup analysis indicated that, compared with beta-blocker monotherapy and statin monotherapy, cotherapy significantly reduced the risks of MACE occurrences in ACS patients (beta-blocker monotherapy group: adjusted HR 0.28, 95% CI 0.13–0.59, P=.001; statin monotherapy group: adjusted HR 0.54, 95% CI 0.29–0.98, P=.044). CONCLUSIONS: Beta-blocker and statin combination therapy lowered the risk of developing MACE in ACS patients. International Scientific Literature, Inc. 2020-08-18 /pmc/articles/PMC7453752/ /pubmed/32808600 http://dx.doi.org/10.12659/MSM.925114 Text en © Med Sci Monit, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Clinical Research
Zhu, Ling
Cui, Qianwei
Liu, Ying
Liu, Zhongwei
Zhang, Yong
Liu, Fuqiang
Wang, Junkui
Effects of a Secondary Prevention Combination Therapy with beta-Blocker and Statin on Major Adverse Cardiovascular Events in Acute Coronary Syndrome Patients
title Effects of a Secondary Prevention Combination Therapy with beta-Blocker and Statin on Major Adverse Cardiovascular Events in Acute Coronary Syndrome Patients
title_full Effects of a Secondary Prevention Combination Therapy with beta-Blocker and Statin on Major Adverse Cardiovascular Events in Acute Coronary Syndrome Patients
title_fullStr Effects of a Secondary Prevention Combination Therapy with beta-Blocker and Statin on Major Adverse Cardiovascular Events in Acute Coronary Syndrome Patients
title_full_unstemmed Effects of a Secondary Prevention Combination Therapy with beta-Blocker and Statin on Major Adverse Cardiovascular Events in Acute Coronary Syndrome Patients
title_short Effects of a Secondary Prevention Combination Therapy with beta-Blocker and Statin on Major Adverse Cardiovascular Events in Acute Coronary Syndrome Patients
title_sort effects of a secondary prevention combination therapy with beta-blocker and statin on major adverse cardiovascular events in acute coronary syndrome patients
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453752/
https://www.ncbi.nlm.nih.gov/pubmed/32808600
http://dx.doi.org/10.12659/MSM.925114
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