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胎儿颈部透明带的产前超声诊断及质量控制

Prenatal ultrasound diagnosis and quality control of fetal nuchal translucency.

作者信息

Yuan Xiaohua, Fu Yimei

机构信息

Department of Obstetrics Ultrasonography Room, Xiangya Hospital, Central South University, Changsha 410008, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2024 Apr 28;49(4):603-610. doi: 10.11817/j.issn.1672-7347.2024.240005.

Abstract

OBJECTIVES

In clinical ultrasound examinations, it is challenging to perform quality control on the images of each fetal nuchal translucency (NT) and crown-rump length (CRL). However, small measurement differences can increase the probability of false-positive or false-negative diagnosis. Therefore, it is necessary to establish a quality control system for fetal NT examination. This study aims to control the quality of fetal NT and CRL measurements, evaluate the accuracy of ultrasound physicians in early pregnancy NT measurements, and analyze the impact of increased fetal structure screening on the detection rate of chromosomal abnormalities.

METHODS

Data were collected from cases before and after 12 months of NT examination quality control, with 2 214 before quality control and 2 538 cases after quality control. Three quality control data metrics were analyzed: NT multiple of median (NT-MoM), standard deviation (SD) of logMoM [(SD) logMoM], and the slope of NT on CRL (SNC). The performance of NT measurements was monitored through the individual CRL NT-MoM within the 0.9-1.1 MoM range of the normal median curve, while grouped based on different years of experience (<3 years, 3-6 years, >6 years), and NT-MoM values among these groups were compared. Data on NT thickening, structural anomalies, and chromosomal abnormalities were retrospectively analyzed during the quality control period.

RESULTS

According to the curve equation of the American NTQR project group, the NT-MoM value before quality control was 0.921 7 MoM, the (SD) logMoM value was 0.091 92, and the SNC value was 12.20%. After quality control, the NT-MoM value was 0.948 3 MoM, the (SD) logMoM value was 0.094 81, and the SNC value was 11.43%. The comparison of NT-MoM values before and after quality control showed a statistically significant difference (<0.000 1). The comparison of NT-MoM values measured by ultrasound physicians with different years of experience before and after quality control also showed statistically significant differences (<0.000 1). The NT-MoM values for the 3-6 years and >6 years groups were higher after quality control (<0.05), while the <3 years group showed no significant difference before and after quality control (>0.05). After quality control, cases of NT thickening without significant structural abnormalities accounted for 19.05%, NT thickening with structural abnormalities accounted for 47.62%, and NT normal with structural abnormalities accounted for 33.33%. There were 36 cases of fetal heart abnormalities, accounting for 20.34% of the total abnormality rate, with a positive rate of 36% in chromosome tests.

CONCLUSIONS

After quality control, ultrasound physicians measure NT more accurately, but differences among measurements remain. Measurements by experienced ultrasound physicians are closer to expected values, usually lower than expected. Monitoring fetal NT and CRL measurements helps improve measurement accuracy. Increasing structural screening during NT examinations, especially for the fetal heart, enhances the detection rate of chromosomal abnormalities.

摘要

目的

在临床超声检查中,对每例胎儿颈部透明带(NT)和头臀长(CRL)图像进行质量控制具有挑战性。然而,微小的测量差异会增加假阳性或假阴性诊断的概率。因此,有必要建立胎儿NT检查的质量控制体系。本研究旨在控制胎儿NT和CRL测量的质量,评估超声医师在孕早期NT测量中的准确性,并分析增加胎儿结构筛查对染色体异常检出率的影响。

方法

收集NT检查质量控制前后12个月的病例数据,质量控制前2214例,质量控制后2538例。分析三个质量控制数据指标:NT中位数倍数(NT-MoM)、对数MoM的标准差(SD)logMoM]以及NT与CRL的斜率(SNC)。通过个体CRL NT-MoM在正常中位数曲线的0.9-1.1 MoM范围内监测NT测量的性能,同时根据不同年资(<3年、3-6年、>6年)进行分组,并比较这些组之间的NT-MoM值。在质量控制期间,对NT增厚、结构异常和染色体异常的数据进行回顾性分析。

结果

根据美国NTQR项目组的曲线方程,质量控制前NT-MoM值为0.9217 MoM,(SD)logMoM值为0.09192,SNC值为12.20%。质量控制后,NT-MoM值为0.9483 MoM,(SD)logMoM值为0.09481,SNC值为11.43%。质量控制前后NT-MoM值的比较显示差异有统计学意义(<0.0001)。质量控制前后不同年资超声医师测量的NT-MoM值比较也显示差异有统计学意义(<0.0001)。质量控制后,3-6年组和>6年组的NT-MoM值较高(<0.05),而<3年组质量控制前后差异无统计学意义(>0.05)。质量控制后,无明显结构异常的NT增厚病例占19.05%,有结构异常的NT增厚病例占47.62%,NT正常但有结构异常的病例占33.33%。胎儿心脏异常36例,占总异常率的20.34%,染色体检查阳性率为36%。

结论

质量控制后,超声医师测量NT更准确,但测量之间仍存在差异。经验丰富的超声医师的测量值更接近预期值,通常低于预期。监测胎儿NT和CRL测量有助于提高测量准确性。在NT检查期间增加结构筛查,尤其是对胎儿心脏的筛查,可提高染色体异常的检出率。

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