Dalhousie University, Halifax, Nova Scotia, Canada.
J Pediatr. 2011 Aug;159(2):227-31. doi: 10.1016/j.jpeds.2011.01.008. Epub 2011 Mar 12.
To determine if dexamethasone given to premature infants with bronchopulmonary dysplasia would result in cardiac diastolic dysfunction in early childhood, a topic unstudied in humans.
We compared seven children ages 3 to 8 years born at 26 weeks' gestation and given dexamethasone for bronchopulmonary dysplasia with eight gestation-matched and age-matched control children using echocardiography to assess measures of systolic and diastolic function. All dexamethasone patients had resolved hypertrophic cardiomyopathy.
Dexamethasone patients had the same normal τ and isovolumic relaxation time (24.9 ± 2.8 and 54.6 ± 6.3 ms) as control patients (22.1 ± 3.0 and 48.8 ± 6.7 ms). Peak A velocities were the same in dexamethasone patients as in control patients (59.5 ± 15 versus 49.4 ± 5.8 cm/s, P = .10), resulting in unchanged E:A ratios (1.89 ± 0.57 versus 2.15 ± 0.43, P = .22). Peak E velocity and E-wave deceleration times were not different. We found no significant differences in measures of systolic function (heart rate-corrected velocity of circumferential fiber shortening, wall stress, and ejection fraction). Left ventricular mass was the same between the groups confirming resolution of hypertrophic cardiomyopathy.
These data are consistent with normal myocardial relaxation, suggesting that long-term diastolic function is reassuringly normal in children who received dexamethasone as premature infants with resolution of hypertrophic cardiomyopathy.
确定接受地塞米松治疗的支气管肺发育不良早产儿是否会导致儿童早期出现舒张功能障碍,这是一个尚未在人类中研究过的课题。
我们通过超声心动图比较了 7 名胎龄 26 周、接受地塞米松治疗支气管肺发育不良的儿童(3 至 8 岁)和 8 名胎龄匹配、年龄匹配的对照组儿童,以评估收缩和舒张功能的指标。所有地塞米松患儿均已治愈肥厚型心肌病。
地塞米松患儿的 τ 和等容舒张时间与对照组患儿相同(24.9±2.8 毫秒和 54.6±6.3 毫秒)(22.1±3.0 毫秒和 48.8±6.7 毫秒)。地塞米松患儿的峰值 A 速度与对照组患儿相同(59.5±15 厘米/秒与 49.4±5.8 厘米/秒,P=0.10),因此 E:A 比值不变(1.89±0.57 与 2.15±0.43,P=0.22)。峰值 E 速度和 E 波减速时间没有差异。我们没有发现收缩功能指标(周径纤维缩短率、壁应力和射血分数的心率校正速度)有显著差异。两组左心室质量无差异,证实肥厚型心肌病已治愈。
这些数据提示心肌舒张功能正常,表明接受地塞米松治疗的早产儿在肥厚型心肌病治愈后,其舒张功能长期保持正常。