Massera Daniele, Adlestein Elizabeth, Frejat Sumar, Wu Woon Y, Reuter Maria C, Xia Yuhe, Alvarez Isabel C, Sherrid Mark V
Hypertrophic Cardiomyopathy Program, Leon H. Charney Division of Cardiology NYU Langone Health New York NY USA.
Division of Biostatistics NYU Langone Health New York NY USA.
J Am Heart Assoc. 2025 Aug 5;14(15):e041565. doi: 10.1161/JAHA.125.041565. Epub 2025 Jul 17.
The clinical benefits of mavacamten in patients with obstructive hypertrophic cardiomyopathy previously treated with advanced therapies are not established.
Clinical and echocardiographic outcomes of patients treated with mavacamten for left ventricular outflow obstruction for at least 8 weeks were assessed based on prior treatment with one or more advanced therapies: disopyramide, septal myectomy, alcohol septal ablation, dual-chamber ventricular pacing with short atrioventricular delay; we also evaluated patients with left ventricular outflow obstruction that emerged as major driver of symptoms after aortic valve replacement.
We included 115 consecutive patients (mean age 66±12 years, 57% women, wall thickness 17±4 mm) on mavacamten for a median 45 (interquartile range, 22-61) weeks, of whom 53 (46%) patients were previously on disopyramide (n=45); underwent septal myectomy (n=8), alcohol septal ablation (n=6), or forced ventricular pacing (n=11); and 5 had previous aortic valve replacement. New York Heart Association class improved from 2.6±0.5 to 1.8±0.6 (<0.0001) in those with and without prior advanced therapy. Left ventricular systolic dysfunction (ejection fraction <50%) occurred in 12 (10%) patients, 8 (15%) in the advanced treatment group and 4 (7%) in those without (=0.13). Maximal provoked peak left ventricular outflow gradients decreased from 103 (77-130) mm Hg to 11 (8-21) mm Hg in patients with prior advanced therapy and from 101 (81-130) mm Hg to 13 (8-25) mm Hg in those without (=0.31).
Mavacamten is a safe and effective treatment for symptomatic left ventricular outflow obstruction in patients with obstructive hypertrophic cardiomyopathy resistant to previous advanced pharmacologic therapy, surgery, or alcohol septal ablation or who develop manifest left ventricular outflow obstruction after aortic valve replacement.
对于先前接受过先进治疗的梗阻性肥厚型心肌病患者,马伐卡坦的临床益处尚未明确。
基于先前接受过一种或多种先进治疗(丙吡胺、室间隔心肌切除术、酒精室间隔消融术、短房室延迟双腔心室起搏)对接受马伐卡坦治疗左心室流出道梗阻至少8周的患者的临床和超声心动图结果进行评估;我们还评估了主动脉瓣置换术后出现症状的主要驱动因素为左心室流出道梗阻的患者。
我们纳入了115例连续接受马伐卡坦治疗的患者(平均年龄66±12岁,57%为女性,室壁厚度17±4mm),中位治疗时间为45(四分位间距,22 - 61)周,其中53例(46%)患者先前服用丙吡胺(n = 45);接受室间隔心肌切除术(n = 8)、酒精室间隔消融术(n = 6)或强制心室起搏(n = 11);5例曾接受主动脉瓣置换术。无论有无先前的先进治疗,纽约心脏协会心功能分级均从2.6±0.5改善至1.8±0.6(<0.0001)。12例(10%)患者出现左心室收缩功能障碍(射血分数<50%),先进治疗组8例(15%),未接受先进治疗组4例(7%)(P = 0.13)。先前接受过先进治疗的患者,诱发的最大左心室流出道峰值梯度从103(77 - 130)mmHg降至11(8 - 21)mmHg,未接受先进治疗的患者从101(81 - 130)mmHg降至13(8 - 25)mmHg(P = 0.31)。
对于先前先进药物治疗、手术或酒精室间隔消融术耐药的梗阻性肥厚型心肌病患者,或主动脉瓣置换术后出现明显左心室流出道梗阻的患者,马伐卡坦是治疗有症状左心室流出道梗阻的一种安全有效的方法。