Department of Cardiology, International Centre for Circulatory Health, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Department of Cardiology, Royal Brompton & Harefield NHS Trust, Middlesex, United Kingdom.
JACC Cardiovasc Imaging. 2019 Aug;12(8 Pt 1):1407-1416. doi: 10.1016/j.jcmg.2018.02.014. Epub 2018 May 16.
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 (p = 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; p = 0.002) and hormonal changes (mean change in N-terminal pro-B-type natriuretic peptide -10 pg/ml; p = 0.002). There was no significant difference in LV size (mean change in LV systolic dimension 1 mm; p < 0.001; LV diastolic dimension 0 mm; p <0.001). In 30% of patients the AV delay identified as optimal was more than 20 ms from the nominal setting of 120 ms.
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).
BRAVO(英国房室和室间隔优化的随机对照试验)是一项多中心、随机、交叉、非劣效性试验,比较了超声心动图优化房室(AV)和室间隔延迟与非侵入性血压方法。
心脏再同步治疗包括 AV 延迟优化可带来临床获益,但优化需要时间和专业知识来进行。
该研究将患者随机分配至超声心动图优化组或使用多次重复逐搏非侵入性血压的血流动力学优化组,在基线时进行;6 个月后,参与者交叉至试验的另一个优化臂。主要结局是运动能力,用峰值运动摄氧量来量化。次要结局测量是超声心动图左心室(LV)重构、生活质量评分和 N 末端 pro-B 型利钠肽。
共纳入 401 例患者,中位年龄 69 岁,78%为男性,84%为纽约心脏协会心功能 II 级,16%为 III 级。主要终点,峰值摄氧量符合非劣效性标准(p=0.0001),试验中血流动力学优化组和超声心动图优化组之间无显著差异(平均差异 0.1ml/kg/min)。次要终点也符合非劣效性标准,用于症状(明尼苏达评分平均差异 1;p=0.002)和激素变化(N 末端 pro-B 型利钠肽平均变化 -10pg/ml;p=0.002)。LV 大小无显著差异(LV 收缩期内径平均变化 1mm;p<0.001;LV 舒张期内径 0mm;p<0.001)。在 30%的患者中,确定为最佳的 AV 延迟大于 120ms 的标称设置 20ms。
使用非侵入性血压对心脏再同步治疗设备进行优化不劣于超声心动图优化。因此,非侵入性血流动力学优化是一种可接受的替代方法,具有自动化的潜力,因此更容易实施。(英国房室和室间隔优化的随机对照试验 [BRAVO];NCT01258829)。