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  4. Multicenter Randomized Controlled Crossover Trial Comparing Hemodynamic Optimization Against Echocardiographic Optimization of AV and VV Delay of Cardiac Resynchronization Therapy: The BRAVO Trial.
 
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Multicenter Randomized Controlled Crossover Trial Comparing Hemodynamic Optimization Against Echocardiographic Optimization of AV and VV Delay of Cardiac Resynchronization Therapy: The BRAVO Trial.
File(s)
1-s2.0-S1936878X18302110-main.pdf (867.83 KB)
Published version
Author(s)
Francis, DP
Type
Journal Article
Abstract
Objectives

BRAVO (British Randomized Controlled Trial of AV and VV Optimization) is a multicenter, randomized, crossover, noninferiority trial comparing echocardiographic optimization of atrioventricular (AV) and interventricular delay with a noninvasive blood pressure method.
Background

Cardiac resynchronization therapy including AV delay optimization confers clinical benefit, but the optimization requires time and expertise to perform.
Methods

This study randomized patients to echocardiographic optimization or hemodynamic optimization using multiple-replicate beat-by-beat noninvasive blood pressure at baseline; after 6 months, participants were crossed over to the other optimization arm of the trial. The primary outcome was exercise capacity, quantified as peak exercise oxygen uptake. Secondary outcome measures were echocardiographic left ventricular (LV) remodeling, quality-of-life scores, and N-terminal pro–B-type natriuretic peptide.
Results

A total of 401 patients were enrolled, the median age was 69 years, 78% of patients were men, and the New York Heart Association functional class was II in 84% and III in 16%. The primary endpoint, peak oxygen uptake, met the criterion for noninferiority (pnoninferiority = 0.0001), with no significant difference between the hemodynamically optimized arm and echocardiographically optimized arm of the trial (mean difference 0.1 ml/kg/min). Secondary endpoints for noninferiority were also met for symptoms (mean difference in Minnesota score 1; pnoninferiority = 0.002) and hormonal changes (mean change in N-terminal pro–B-type natriuretic peptide -10 pg/ml; pnoninferiority = 0.002). There was no significant difference in LV size (mean change in LV systolic dimension 1 mm; pnoninferiority < 0.001; LV diastolic dimension 0 mm; pnoninferiority <0.001). In 30% of patients the AV delay identified as optimal was more than 20 ms from the nominal setting of 120 ms.
Conclusions

Optimization of cardiac resynchronization therapy devices by using noninvasive blood pressure is noninferior to echocardiographic optimization. Therefore, noninvasive hemodynamic optimization is an acceptable alternative that has the potential to be automated and thus more easily implemented. (British Randomized Controlled Trial of AV and VV Optimization [BRAVO]; NCT01258829)
Date Issued
2019-08-01
Date Acceptance
2018-04-03
Citation
JACC: Cardiovascular Imaging
URI
http://hdl.handle.net/10044/1/58311
DOI
10.1016/j.jcmg.2018.02.014
ISSN
1936-878X
Publisher
Elsevier
Start Page
1407
End Page
1416
Journal / Book Title
JACC: Cardiovascular Imaging
Volume
12
Issue
8 (Part 1)
Copyright Statement
Crown Copyright © 2 018 Publish ed by Elsevier on behalf of the American College of Cardiology Foundation.
All rights reserved. This article is available open access under a CC-BY licence 4.0 (https://creativecommons.org/licenses/by/4.0/)
Sponsor
Wellcome Trust
British Heart Foundation
Grant Number
PS3162_WHCP
FS/13/44/30291
Subjects
Science & Technology
Life Sciences & Biomedicine
Cardiac & Cardiovascular Systems
Radiology, Nuclear Medicine & Medical Imaging
Cardiovascular System & Cardiology
biventricular pacing
cardiac resynchronization therapy
echocardiographic optimization
heart failure
hemodynamic optimization
optimization
CHRONIC HEART-FAILURE
ATRIOVENTRICULAR DELAY
SYSTOLIC FUNCTION
RESYNCHRONISATION
DESIGN
DEFIBRILLATOR
CONTRACTILITY
OUTCOMES
biventricular pacing
cardiac resynchronization therapy
echocardiographic optimization
heart failure
hemodynamic optimization
optimization
Cardiovascular System & Hematology
1102 Cardiorespiratory Medicine and Haematology
1103 Clinical Sciences
Publication Status
Published
Date Publish Online
2018-05-11
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