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Left ventricular function in persistent pulmonary hypertension of the newborn. Computer analysis of the echocardiogram.

机译:新生儿持续性肺动脉高压中的左心室功能。超声心动图的计算机分析。

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摘要

Regional and global left ventricular function was assessed in 23 neonates with persistent pulmonary hypertension using computer assisted analysis of their left ventricular echocardiograms and compared with that in 50 healthy neonates. End diastolic left ventricular dimension was normal and end systolic dimension increased while percentage left ventricular shortening and peak velocity of circumferential fibre shortening decreased indicating impaired systolic performance. The peak rate of increase in left ventricular diameter in early diastole was significantly decreased and the durations of the rapid filling and isovolumic relaxation periods were prolonged suggesting resistance to left ventricular filling due to changes in diastolic myocardial properties. This abnormal left ventricular cavity function may have been due to a combination of increased diastolic wall thickness, reduced percentage systolic wall thickening, increased relative wall thickness, and pronounced reduction in peak rates of systolic wall thickening and diastolic wall thinning Seven neonates with persistent pulmonary hypertension died, and of the three examined at necropsy all had left ventricular hypertrophy and two extensive subendocardial haemorrhage and infarction affecting the right and left ventricular papillary muscles. Thus left ventricular dysfunction appears to be a common feature in neonates with this disorder and may be readily detected using computer analysis of left ventricular echocardiograms. Unfortunately, no single echo measurement was useful prognostically. Left ventricular dysfunction in persistent pulmonary hypertension probably results from a combination of hypoxaemia, acidaemia, and pulmonary hypertension, and although it may contribute to the high mortality in this syndrome, a correlation between the severity of left ventricular dysfunction and clinical outcome could not be shown.
机译:使用计算机辅助分析方法对23例持续性肺动脉高压的新生儿评估左室局部和整体左室功能,并与50例健康新生儿进行比较。舒张末期的左心室尺寸正常,收缩末期的尺寸增加,而左心室缩短的百分比和圆周纤维缩短的峰值速度降低,表明收缩性能受损。舒张早期早期左心室直径增加的峰值速率显着降低,并且快速充盈和等容舒张期的持续时间延长,这表明由于舒张心肌特性的改变而导致的对左心室充盈的抵抗。这种异常的左心室功能可能是由于舒张壁厚度增加,收缩壁壁增厚百分比降低,相对壁厚度增加,以及收缩壁壁增厚和舒张壁壁变薄的峰值速率明显降低的综合原因所致。7例持续性肺动脉高压的新生儿死者,尸检中的三者均患有左心室肥大,其中两例广泛的心内膜下出血和梗塞影响了左右心室乳头肌。因此,左心功能不全似乎是患有这种疾病的新生儿的常见特征,可以通过对左心室超声心动图的计算机分析容易地检测到。不幸的是,没有任何回声测量在预测上有用。持续性肺动脉高压中的左心室功能障碍可能是低氧血症,酸血症和肺动脉高压的综合症,尽管可能导致该综合征的高死亡率,但尚不能证明左心室功能障碍的严重程度与临床结果之间的相关性。

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