Multicenter Randomized Controlled Crossover Trial Comparing Hemodynamic Optimization Against Echocardiographic Optimization of AV and VV Delay of Cardiac Resynchronization Therapy

• Published in: JACC. Cardiovascular imaging 2019-08, Vol.12 (8), p.1407-1416
• Main Authors: Whinnett, Zachary I., Sohaib, S.M. Afzal, Mason, Mark, Duncan, Edward, Tanner, Mark, Lefroy, David, Al-Obaidi, Mohamed, Ellery, Sue, Leyva-Leon, Francisco, Betts, Tim, Dayer, Mark, Foley, Paul, Swinburn, Jon, Thomas, Martin, Khiani, Raj, Wong, Tom, Yousef, Zaheer, Rogers, Dominic, Kalra, Paul R., Dhileepan, Vignesh, March, Katherine, Howard, James, Kyriacou, Andreas, Mayet, Jamil, Kanagaratnam, Prapa, Frenneaux, Michael, Hughes, Alun D., Francis, Darrel P.
• Format: Article
• Language: English
• Subjects: biventricular pacing; cardiac resynchronization therapy; echocardiographic optimization; heart failure; hemodynamic optimization; optimization
• ISSN: 1936-878X; 1876-7591
• DOI: 10.1016/j.jcmg.2018.02.014

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