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首页> 外文期刊>Ultrasound in obstetrics & gynecology: the official journal of the International Society of Ultrasound in Obstetrics and Gynecology >Impact of biometric measurement error on identification of small‐ and large‐for‐gestational‐age fetuses
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Impact of biometric measurement error on identification of small‐ and large‐for‐gestational‐age fetuses

机译:生物统计测量误差的影响小》的识别大量检测妊娠年龄胎儿

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摘要

ABSTRACT Objectives First, to obtain measurement‐error models for biometric measurements of fetal abdominal circumference (AC), head circumference (HC) and femur length (FL), and, second, to examine the impact of biometric measurement error on sonographic estimated fetal weight (EFW) and its effect on the prediction of small‐ (SGA) and large‐ (LGA) for‐gestational‐age fetuses with EFW ?10 th and ?90 th percentile, respectively. Methods Measurement error standard deviations for fetal AC, HC and FL were obtained from a previous large study on fetal biometry utilizing a standardized measurement protocol and both qualitative and quantitative quality‐control monitoring. Typical combinations of AC, HC and FL that gave EFW on the 10 th and 90 th percentiles were determined. A Monte‐Carlo simulation study was carried out to examine the effect of measurement error on the classification of fetuses as having EFW above or below the 10 th and 90 th percentiles. Results Errors were assumed to follow a Gaussian distribution with a mean of 0?mm and SDs, obtained from a previous well‐conducted study, of 6.93?mm for AC, 5.15?mm for HC and 1.38?mm for FL. Assuming errors according to such distributions, when the 10 th and 90 th percentiles are used to screen for SGA and LGA fetuses, respectively, the detection rates would be 78.0% at false‐positive rates of 4.7%. If the cut‐offs were relaxed to the 30 th and 70 th percentiles, the detection rates would increase to 98.2%, but at false‐positive rates of 24.2%. Assuming half of the spread in the error distribution, using the 10 th and 90 th percentiles to screen for SGA and LGA fetuses, respectively, the detection rates would be 86.6% at false‐positive rates of 2.3%. If the cut‐offs were relaxed to the 15 th and 85 th percentiles, respectively, the detection rates would increase to 97.0% and the false‐positive rates would increase to 6.3%. Conclusions Measurement error in fetal biometry causes substantial error in EFW, resulting in misclassification of SGA and LGA fetuses. The extent to which improvement can be achieved through effective quality assurance remains to be seen but, as a first step, it is important for practitioners to understand how biometric measurement error impacts the prediction of SGA and LGA fetuses. ? 2019 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of the International Society of Ultrasound in Obstetrics and Gynecology.
机译:抽象的目标第一,获得为生物地理测量误差模型测量胎儿腹部周长(AC),头围(HC)和股骨长度(FL),其次,检查的影响在超声生物测量误差估计胎儿体重(EFW)及其影响小的(SGA)和大的预测量(LGA)为检测妊娠年龄胎儿与EFW & ?和在?为胎儿测量误差标准差交流、HC和FL得到从先前的大利用标准化研究胎儿生物统计学定性和测量协议定量的质量控制监测。交流的组合、HC和给EFW FL确定了10 th和第90百分位数。一个蒙地卡罗模拟进行了研究检查测量误差的影响胎儿有EFW分类或以上低于10 th和第90百分位数。错误是认为高斯分布的意思是0 ?从之前的量进行了研究,获得的6.93 ?FL。根据这种假设错误分布,当10 th, 90百分位数是用来屏幕SGA和达到胎儿分别检测率是78.0%错误的积极率4.7%。减少偏移放宽到30 th和第70位百分位数,检测率会增加至98.2%,但在假积极率24.2%。假设在误差传播的一半分布,使用10 th和第90位百分位数屏幕SGA和LGA胎儿,分别检测率是86.6%假还是积极的利率为2.3%。放松15 th和第85百分位数,分别检测率会增加97.0%,假正利率将增加到6.3%。胎儿生物统计学导致重大错误SGA和EFW,导致误分类LGA胎儿。是通过有效的质量保证还有待观察,但作为第一步,它是如何理解重要的实践者生物测量误差影响预测胎儿SGA和地方。作者。约翰威利出版的妇科,代表国际社会的超声在妇产科。

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