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Individual patient data meta-analysis of beta-blockers in heart failure: rationale and design

ABSTRACT: The Beta-Blockers in Heart Failure Collaborative Group (BB-HF) was formed to obtain and analyze individual patient data from the major randomized controlled trials of beta-blockers in heart failure. Even though beta-blockers are an established treatment for heart failure, uptake is still s...

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Autores principales: Kotecha, Dipak, Manzano, Luis, Altman, Douglas G, Krum, Henry, Erdem, Guliz, Williams, Nicola, Flather, Marcus D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564787/
https://www.ncbi.nlm.nih.gov/pubmed/23327629
http://dx.doi.org/10.1186/2046-4053-2-7
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author Kotecha, Dipak
Manzano, Luis
Altman, Douglas G
Krum, Henry
Erdem, Guliz
Williams, Nicola
Flather, Marcus D
author_facet Kotecha, Dipak
Manzano, Luis
Altman, Douglas G
Krum, Henry
Erdem, Guliz
Williams, Nicola
Flather, Marcus D
author_sort Kotecha, Dipak
collection PubMed
description ABSTRACT: The Beta-Blockers in Heart Failure Collaborative Group (BB-HF) was formed to obtain and analyze individual patient data from the major randomized controlled trials of beta-blockers in heart failure. Even though beta-blockers are an established treatment for heart failure, uptake is still sub-optimal. Further, the balance of efficacy and safety remains uncertain for common groups including older persons, women, those with impaired renal function and diabetes. Our aim is to provide clinicians with a thorough and definitive evidence-based assessment of these agents. We have identified 11 large randomized trials of beta-blockers versus placebo in heart failure and plan to meta-analyze the data on an individual patient level. In total, these trials have enrolled 18,630 patients. Uniquely, the BB-HF group has secured access to the individual data for all of these trials, with the participation of key investigators and pharmaceutical companies. Our principal objectives include deriving an overall estimate of efficacy for all-cause mortality and cardiovascular hospitalization. Importantly, we propose a statistically-robust sub-group assessment according to age, gender, diabetes and other key factors; analyses which are only achievable using an individual patient data meta-analysis. Further, we aim to provide an assessment of economic benefit and develop a risk model for the prognosis of patients with chronic heart failure. This paper outlines inclusion criteria, search strategies, outcome measures and planned statistical analyses. TRIAL REGISTRATION: Clinical trial registration information: http://clinicaltrials.gov/ct2/show/NCT00832442
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spelling pubmed-35647872013-02-08 Individual patient data meta-analysis of beta-blockers in heart failure: rationale and design Kotecha, Dipak Manzano, Luis Altman, Douglas G Krum, Henry Erdem, Guliz Williams, Nicola Flather, Marcus D Syst Rev Methodology ABSTRACT: The Beta-Blockers in Heart Failure Collaborative Group (BB-HF) was formed to obtain and analyze individual patient data from the major randomized controlled trials of beta-blockers in heart failure. Even though beta-blockers are an established treatment for heart failure, uptake is still sub-optimal. Further, the balance of efficacy and safety remains uncertain for common groups including older persons, women, those with impaired renal function and diabetes. Our aim is to provide clinicians with a thorough and definitive evidence-based assessment of these agents. We have identified 11 large randomized trials of beta-blockers versus placebo in heart failure and plan to meta-analyze the data on an individual patient level. In total, these trials have enrolled 18,630 patients. Uniquely, the BB-HF group has secured access to the individual data for all of these trials, with the participation of key investigators and pharmaceutical companies. Our principal objectives include deriving an overall estimate of efficacy for all-cause mortality and cardiovascular hospitalization. Importantly, we propose a statistically-robust sub-group assessment according to age, gender, diabetes and other key factors; analyses which are only achievable using an individual patient data meta-analysis. Further, we aim to provide an assessment of economic benefit and develop a risk model for the prognosis of patients with chronic heart failure. This paper outlines inclusion criteria, search strategies, outcome measures and planned statistical analyses. TRIAL REGISTRATION: Clinical trial registration information: http://clinicaltrials.gov/ct2/show/NCT00832442 BioMed Central 2013-01-18 /pmc/articles/PMC3564787/ /pubmed/23327629 http://dx.doi.org/10.1186/2046-4053-2-7 Text en Copyright ©2013 Kotecha et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Kotecha, Dipak
Manzano, Luis
Altman, Douglas G
Krum, Henry
Erdem, Guliz
Williams, Nicola
Flather, Marcus D
Individual patient data meta-analysis of beta-blockers in heart failure: rationale and design
title Individual patient data meta-analysis of beta-blockers in heart failure: rationale and design
title_full Individual patient data meta-analysis of beta-blockers in heart failure: rationale and design
title_fullStr Individual patient data meta-analysis of beta-blockers in heart failure: rationale and design
title_full_unstemmed Individual patient data meta-analysis of beta-blockers in heart failure: rationale and design
title_short Individual patient data meta-analysis of beta-blockers in heart failure: rationale and design
title_sort individual patient data meta-analysis of beta-blockers in heart failure: rationale and design
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564787/
https://www.ncbi.nlm.nih.gov/pubmed/23327629
http://dx.doi.org/10.1186/2046-4053-2-7
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