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临床试验/NCT05059093
NCT05059093已完成不适用

Developing and Testing Deep Learning Models for Fetal Biometry and Amniotic Volume Assessment in Routine Fetal Ultrasound Scans

Deepecho6 个研究点 分布在 1 个国家目标入组 122 人开始时间: 2021年10月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Deepecho
入组人数
122
试验地点
6
主要终点
Overall accuracy for the biometric parameters measurement and amniotic fluid volume assessment

研究概览

简要总结

Routine fetal ultrasound scan during the second trimester of the pregnancy is a low-cost, noninvasive screening modality that has been proven to lower fetal mortality by up to 20%. One of the critical elements of this exam is the measurement of fetal biometric parameters, which are the head circumference (HC), biparietal diameter (BPD), abdominal circumference (AC), and femur length (FL) measured on biometry standard planes. Those standard planes are taken according to quality standards first described by Salomon et al. and used as the guidelines of the International Society of Ultrasound in Obstetrics and Gynecology (ISUOG). The biometric parameters extracted from them are essential to diagnose fetal growth restriction (FGR), the world's first cause of perinatal fetal mortality.

Such measurements and image quality assessment are time-consuming tasks that are prone to inter and intraobserver variability depending on the level of skill of the sonographer or the physician performing the exam.

Amniotic fluid (AF) volume assessment is also an essential step in routine screening scans allowing the diagnosis of oligo or hydramnios, both associated with increased fetal mortality rates.

The AF is measured by two main "semi-quantitative" techniques: Amniotic Fluid Index (AFI) and the single deepest pocket (SDP). The latter is more specific as it lowers the overdiagnosis of oligo-amnios without any impact on mortality or morbidity and is easier to perform for the sonographer (only one measurement versus four in the case of the AFI technique). However, AF assessment remains a time-consuming and poorly reproducible task.

Attempts to automate such biometric measurements and AF volume assessment have been made using Artificial Intelligence (AI) and deep learning (DL) tools. Studies showed excellent results "in silico," reaching up to 98 %, 95%, 93 % dice score coefficients for HC, AC, and FL measurements and 89 % DSC for AFI measurements. However, they were all conducted retrospectively without validation on prospectively acquired images.

Reviews and experts have stressed the need for quality peer-reviewed prospective studies to assess AI tools' performance with real-world data. Their performance is expected to be worse and to reflect better their use in the clinical workflow.

This study aims to develop DL models to automate HC, BPD, AC, and FL measurements and AF volume assessment from retrospectively acquired data and test their performances to those of clinicians and experts on prospective real-world fetal US scans.

详细描述

The DL models will be trained, validated, and tested on the retrospectively acquired data first. This data will consist of fetal US images gathered in the participating medical centers after patient-level anonymization. The ground truth for the models will consist of annotations made by radiologists and obstetricians for classification and segmentation purposes. The DL models will be trained to perform the following tasks:

  • Detection of the following standard planes as described in the ISUOG guidelines: transthalamic, transventricular, transcerebellar, abdominal, and femoral planes on video loops.
  • Image quality scoring according to the ISUOG guidelines of the transthalamic, abdominal and femoral planes.
  • Fetal cranium, abdomen, and femur segmentation to measure HC, BPD AC, and FL.
  • Detection of AF pockets.
  • Segmentation of AF pockets and extraction of pockets depth in order to evaluate the SDP measurement

Physicians will be asked to save additional images and video loops additional to their routine screening in the prospective examinations:

  • Eight images: transthalamic, abdominal, and femoral standard planes with and without calipers, SDP with and without calipers.

  • Four video loops up to five seconds each:

  • A cephalic loop encompassing the transcerebellar, transthalamic, and transventricular planes.

  • An abdominal loop going from the four-chamber view of the heart to a cross-section of the kidneys and back.

  • A femoral loop with the probe parallel to the sagittal axis of the femur sweeping from side to side.

  • A whole amniotic cavity loop, with the probe perpendicular to the ground applying as little pressure as possible on the patient's abdomen, sweeping from the uterine fundus to the cervix, once or twice depending on the volume of the amniotic cavity.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Single or multiple viable pregnancies with a gestational age of 14 weeks or more as dated on a first trimester US scan with the crown-rump length (CRL) measurement or grossly estimated from the last menstrual period (LMP).
  • Routine programmed US scan.
  • Patient's consent is obtained.
  • Patient over 18 years old.

排除标准

  • Emergency indication for the fetal ultrasound
  • Major morphological malformations that do not allow proper measurement of the cranium, abdominal or lower limb, for example, anencephaly, omphalocele, lower limb phocomelia.
  • Fetal death.

结局指标

主要结局

Overall accuracy for the biometric parameters measurement and amniotic fluid volume assessment

时间窗: up to 20 weeks

Mean Absolute Error between the model's HC, BPD, AC, FL, and SDP measurements (in mm), the RT clinician's, and the panel's

次要结局

  • Image quality(Up to 20 weeks)
  • Small-for-Gestational-Age fetus detection accuracy, sensitivity and specificity(Up to 20 weeks)
  • Oligohydramnios and polyhydramnios detection accuracy, sensitivity, and specificity(Up to 20 weeks)

研究者

发起方
Deepecho
申办方类型
Industry
责任方
Sponsor

研究点 (6)

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