M3C-Necker, Paediatric Cardiology, Université Paris Descartes, Paris, France.
J Am Soc Echocardiogr. 2012 May;25(5):511-7. doi: 10.1016/j.echo.2012.01.011. Epub 2012 Feb 16.
Several adult studies have shown that sickle cell disease is associated with cardiac abnormalities and premature death. The aim of this study was to use speckle-tracking strain, a relatively load independent parameter, to evaluate systolic left ventricular (LV) and right ventricular (RV) function in a pediatric sickle cell disease population.
Twenty-eight patients with sickle cell disease (mean age, 10.0 ± 3.6 years; mean body surface area, 1.14 ± 0.27 m(2)) and 29 controls matched for age and body surface area were compared. Cardiac output, LV dimension, wall thickness and circumferential strain, LV and RV longitudinal systolic strain, conventional and tissue Doppler parameters, and pulmonary pressure were assessed.
LV cardiac output was significantly higher in patients, as were indexed LV systolic diameter, indexed LV mass, and E/E' septal ratio. Indexed LV diastolic diameter, wall thickness, LV shortening fraction, and global LV longitudinal and circumferential strains were similar in patients and controls. However, their global RV longitudinal strain was significantly lower, although tricuspid annular plane systolic excursion and color-coded tricuspid S-wave velocity were similar. Among patients, 21% had tricuspid regurgitation velocities > 2.5 m/sec, but none had tricuspid regurgitation velocities > 3 m/sec. Indexed LV diastolic dimension and systolic pulmonary artery pressure were significantly higher in patients whose hemoglobin was <80 g/L, but parameters of systolic and diastolic LV function were similar.
In children with sickle cell disease, LV diastolic function is significantly altered, although LV systolic function, evaluated by global longitudinal strain, is normal. In addition, cardiac output is increased, and elevated tricuspid regurgitation velocity is common, whereas it is never found in controls. Most importantly, global RV longitudinal systolic strain is significantly altered.
几项成人研究表明镰状细胞病与心脏异常和过早死亡有关。本研究旨在使用斑点追踪应变,一种相对负荷独立的参数,来评估儿科镰状细胞病人群的左心室(LV)和右心室(RV)收缩功能。
将 28 例镰状细胞病患者(平均年龄 10.0 ± 3.6 岁;平均体表面积 1.14 ± 0.27 m²)与年龄和体表面积匹配的 29 例对照组进行比较。评估心输出量、LV 尺寸、壁厚度和周向应变、LV 和 RV 纵向收缩应变、常规和组织多普勒参数以及肺动脉压。
患者的 LV 心输出量明显较高,LV 收缩期直径、LV 质量指数和 E/E'间隔比也较高。LV 舒张直径、壁厚度、LV 缩短分数、LV 整体纵向和周向应变在患者和对照组之间相似。然而,他们的整体 RV 纵向应变明显较低,尽管三尖瓣环平面收缩期位移和彩色三尖瓣 S 波速度相似。在患者中,有 21%的人三尖瓣反流速度 > 2.5 m/sec,但没有人三尖瓣反流速度 > 3 m/sec。LV 舒张末期指数和收缩期肺动脉压在血红蛋白 <80 g/L 的患者中明显升高,但 LV 收缩和舒张功能的参数相似。
在镰状细胞病儿童中,LV 舒张功能明显改变,尽管通过整体纵向应变评估的 LV 收缩功能正常。此外,心输出量增加,三尖瓣反流速度升高很常见,但在对照组中从未发现。最重要的是,整体 RV 纵向收缩应变明显改变。