Measuring Up Before Birth: The New Normal.
Measuring Up Before Birth: The New Normal.
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出生前测量:新常态。
DOI:
10.1161/circimaging.118.008008
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发表时间:
2018
期刊:
影响因子:
--
通讯作者:
Peyvandi,Shabnam
中科院分区:
文献类型:
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作者:
Moon-Grady,AnitaJ;Peyvandi,Shabnam
Fetal echocardiography for disease detection is challenging. Not only are there technical obstacles—maternal body habitus, variable and often unfavorable fetal position, to name a few—but in most obstetric and many cardiology practices, the vast majority of fetuses will be normal. Large numbers are referred for cardiac imaging either as part of routine screening because of risk factors or after an abnormal screen, such as nuchal translucency above 95th percentile; only a small subset will be abnormal. Add to this that nearly all fetal cardiac abnormalities are asymptomatic in fetal life because of the presence of the fetal shunts and the ability of the fetoplacental circulation to redirect flow while maintaining oxygen delivery in a normal range. Hence, a subtle abnormality becomes easy to overlook, a valve or vessel that is just barely subjectively abnormal may incorrectly pass muster in a busy clinic or be passed off as a poor image blamed on the operator or even the fetus. But as imaging platforms and operator expertise have been improving over the decades, so too has our understanding that even apparently minor deviations from normal in early to mid-gestation may have dire consequences for the newborn and the need to accurately and precisely assign a value of normal versus abnormal even for seemingly minor lesions is moving into mainstream. 1 Here, though, the fetal echocardiographer encounters another issue, that of the constantly changing ruler by which to judge the fetal cardiac structure dimensions throughout gestation. Luckily, this issue is familiar to pediatric cardiologists: cardiac structures vary with patient size, and patient size varies with patient age in predictable, model-able ways. The most common method for expressing a given patient’s valve and vessel dimensions is to transform a measurement to a Z score or the number of SDs above or below the expected mean value for a population of similar size. In practice, once a best-fit relationship is defined for a set of measurements from the normal population, an SD and mean can be derived at each body size point. Although seemingly simple in concept, the behavior of cardiac anthropometric measurements is such that the normal distribution may vary at different patient sizes, especially at extremes; a property termed heteroscedasticity. Therefore, to have confidence in a normal range, a fairly large number of patients at each body size is necessary when generating normal value equations. In the fetus, weight is not directly measurable but rather estimated from linear measurements. If gestational age is known, it can be used to extrapolate the fetal weight; however, it is important to note that fetal size varies with gestational age and that there is a range of normal body sizes in the fetus, a measure with its own innate heteroscedasticity. 2