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The Effectiveness of Polypill for the Prevention of Cardiovascular Disease: A Meta-Analysis of Randomized Controlled Trials

A significant global health concern, cardiovascular disease (CVD) is characterized by a rising prevalence and accompanying mortality rates. It is crucial to implement primary and secondary prevention strategies, particularly in resource-scarce settings. Polypills, which combine blood pressure, chole...

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Autores principales: Virk, Ghazala S, Sharma, Ashutosh, Khan, Momin R, Shah, Krushi, Mengar, Jaina, Chaudhari, Sandipkumar S, Batool, Saima, Saleem, Faraz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645397/
https://www.ncbi.nlm.nih.gov/pubmed/38022292
http://dx.doi.org/10.7759/cureus.47032
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author Virk, Ghazala S
Sharma, Ashutosh
Khan, Momin R
Shah, Krushi
Mengar, Jaina
Chaudhari, Sandipkumar S
Batool, Saima
Saleem, Faraz
author_facet Virk, Ghazala S
Sharma, Ashutosh
Khan, Momin R
Shah, Krushi
Mengar, Jaina
Chaudhari, Sandipkumar S
Batool, Saima
Saleem, Faraz
author_sort Virk, Ghazala S
collection PubMed
description A significant global health concern, cardiovascular disease (CVD) is characterized by a rising prevalence and accompanying mortality rates. It is crucial to implement primary and secondary prevention strategies, particularly in resource-scarce settings. Polypills, which combine blood pressure, cholesterol, and homocysteine drugs, hold significant potential for lowering the risk of CVD. This study follows PRISMA meta-analysis guidelines. Two researchers conducted an extensive literature search. Inclusion criteria encompassed RCT design, polypill use, a four-week duration, and one meta-analysis outcome. Primary outcomes included MACE and CV mortality, while secondary outcomes encompassed SBP and LDL-C changes. Data extraction was performed independently, and conflicts were resolved. Review Manager 5.4 with random effects was employed for statistical analysis, and ROB 2.0 bias evaluation was conducted. The study reported CVD mortality and MACE risk ratios (RRs) with 95% CIs, as well as SBP and LDL-C weighted mean differences (MD). A total of 24 trials were included in this meta-analysis. The results revealed that the polypill was associated with a decreased risk of CVD mortality and major adverse cardiovascular events (MACE). Additionally, a significant reduction in systolic blood pressure (SBP) and low-density lipoprotein cholesterol (LDL-C) was observed. This meta-analysis showed that polypill is a viable medication for reducing the risk of CVD mortality and MACE. It is also a beneficial medication for lowering LDL-C levels and SBP.
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spelling pubmed-106453972023-10-14 The Effectiveness of Polypill for the Prevention of Cardiovascular Disease: A Meta-Analysis of Randomized Controlled Trials Virk, Ghazala S Sharma, Ashutosh Khan, Momin R Shah, Krushi Mengar, Jaina Chaudhari, Sandipkumar S Batool, Saima Saleem, Faraz Cureus Internal Medicine A significant global health concern, cardiovascular disease (CVD) is characterized by a rising prevalence and accompanying mortality rates. It is crucial to implement primary and secondary prevention strategies, particularly in resource-scarce settings. Polypills, which combine blood pressure, cholesterol, and homocysteine drugs, hold significant potential for lowering the risk of CVD. This study follows PRISMA meta-analysis guidelines. Two researchers conducted an extensive literature search. Inclusion criteria encompassed RCT design, polypill use, a four-week duration, and one meta-analysis outcome. Primary outcomes included MACE and CV mortality, while secondary outcomes encompassed SBP and LDL-C changes. Data extraction was performed independently, and conflicts were resolved. Review Manager 5.4 with random effects was employed for statistical analysis, and ROB 2.0 bias evaluation was conducted. The study reported CVD mortality and MACE risk ratios (RRs) with 95% CIs, as well as SBP and LDL-C weighted mean differences (MD). A total of 24 trials were included in this meta-analysis. The results revealed that the polypill was associated with a decreased risk of CVD mortality and major adverse cardiovascular events (MACE). Additionally, a significant reduction in systolic blood pressure (SBP) and low-density lipoprotein cholesterol (LDL-C) was observed. This meta-analysis showed that polypill is a viable medication for reducing the risk of CVD mortality and MACE. It is also a beneficial medication for lowering LDL-C levels and SBP. Cureus 2023-10-14 /pmc/articles/PMC10645397/ /pubmed/38022292 http://dx.doi.org/10.7759/cureus.47032 Text en Copyright © 2023, Virk et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Virk, Ghazala S
Sharma, Ashutosh
Khan, Momin R
Shah, Krushi
Mengar, Jaina
Chaudhari, Sandipkumar S
Batool, Saima
Saleem, Faraz
The Effectiveness of Polypill for the Prevention of Cardiovascular Disease: A Meta-Analysis of Randomized Controlled Trials
title The Effectiveness of Polypill for the Prevention of Cardiovascular Disease: A Meta-Analysis of Randomized Controlled Trials
title_full The Effectiveness of Polypill for the Prevention of Cardiovascular Disease: A Meta-Analysis of Randomized Controlled Trials
title_fullStr The Effectiveness of Polypill for the Prevention of Cardiovascular Disease: A Meta-Analysis of Randomized Controlled Trials
title_full_unstemmed The Effectiveness of Polypill for the Prevention of Cardiovascular Disease: A Meta-Analysis of Randomized Controlled Trials
title_short The Effectiveness of Polypill for the Prevention of Cardiovascular Disease: A Meta-Analysis of Randomized Controlled Trials
title_sort effectiveness of polypill for the prevention of cardiovascular disease: a meta-analysis of randomized controlled trials
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645397/
https://www.ncbi.nlm.nih.gov/pubmed/38022292
http://dx.doi.org/10.7759/cureus.47032
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