Prenatal Diagnosis of Fetal Aqueductal Stenosis: A Multicenter Prospective Observational Study through the North American Fetal Therapy Network.

IF 1.6 3区 医学 Q3 OBSTETRICS & GYNECOLOGY Fetal Diagnosis and Therapy Pub Date : 2024-01-01 Epub Date: 2024-02-06 DOI:10.1159/000536037
Stephen P Emery, Samia Lopa, Erika Peterson, Angie C Jelin, Marjorie C Treadwell, Juliana Gebb, Henry L Galan, Eric Bergh, Amanda Criebaum, Amelia McLennan, Joseph Lillegard, Yair J Blumenfeld
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Abstract

Introduction: A critical component of an evidence-based reassessment of in-utero intervention for fetal aqueductal stenosis (fetal AS) is determining if the prenatal diagnosis can be accurately made at a gestational age amenable to in-utero intervention.

Methods: A multicenter, prospective, observational study was conducted through the North American Fetal Therapy Network (NAFTNet). Pregnancies complicated by severe central nervous system (CNS) ventriculomegaly (lateral ventricle diameter >15 mm) not secondary to a primary diagnosis (myelomeningocele, encephalocele, etc.) were recruited at diagnosis. Imaging and laboratory findings were recorded in an online REDCap database. After evaluation, investigators were asked to render their degree of confidence in the diagnosis of fetal AS. The prenatal diagnosis was compared to the postnatal diagnosis obtained through neonatal neuroimaging. Performance characteristics of ultrasound and magnetic resonance imaging (MRI) were calculated, as was the mean gestational age at diagnosis.

Results: Between April 2015 and October 2022, eleven NAFTNet centers contributed 64 subjects with severe fetal CNS ventriculomegaly. Of these, 56 had both prenatal and postnatal diagnoses recorded. Ultrasound revealed 32 fetal AS true positives, 4 false positives, 7 false negatives, and 13 true negatives, rendering a sensitivity of 0.82, a specificity of 0.76, a positive predictive value of 0.89, and a negative predictive value of 0.65. The mean gestational age at diagnosis by ultrasound was 25.5 weeks (std +/- 4.7 weeks). The proportion of agreement (true positive + true negative/n) was highest at 24 weeks gestation. For fetal MRI (n = 35), the sensitivity for fetal AS was 0.95, specificity was 0.69, positive predictive value was 0.84, and negative predictive value was 0.90. MRI was performed at 25 weeks on average.

Conclusion: The prenatal diagnosis of fetal AS can be made with accuracy at a gestational age potentially amenable to in-utero intervention. Only 7% of subjects were incorrectly diagnosed prenatally with fetal AS by ultrasound and 11% by MRI. Diagnostic accuracy of fetal AS will likely improve with increased experience.

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胎儿导水管狭窄的产前诊断:通过北美胎儿治疗网络(NAFTNet)进行的多中心前瞻性观察研究。
导言:以证据为基础重新评估胎儿导水管狭窄(胎儿 AS)的宫内干预的一个重要组成部分是确定产前诊断是否能在适合宫内干预的胎龄准确做出:通过北美胎儿治疗网络(NAFTNet)开展了一项多中心、前瞻性观察研究。在确诊时,对合并严重中枢神经系统脑室肥大(侧脑室直径大于 15 毫米)且非继发于原发性诊断(骨髓脑、颅脑等)的孕妇进行招募。成像和实验室检查结果记录在在线 REDCap 数据库中。评估结束后,调查人员被要求对胎儿AS的诊断给出其可信度。产前诊断结果与通过新生儿神经影像学检查获得的产后诊断结果进行了比较。计算了超声和核磁共振成像的性能特征,以及诊断时的平均胎龄:2015年4月至2022年10月期间,11个NAFTNet中心共提供了64例严重胎儿中枢神经室肥大患者。其中,56人的产前和产后诊断均有记录。超声检查显示 32 例胎儿 AS 真阳性、4 例假阳性、7 例假阴性和 13 例真阴性,灵敏度为 0.82,特异性为 0.76,阳性预测值为 0.89,阴性预测值为 0.65。超声诊断的平均胎龄为 25.5 周(std +/-4.7w)。妊娠24周时的一致性比例(真阳性+真阴性/n)最高。对于胎儿核磁共振成像(n=35),胎儿 AS 的敏感性为 0.95,特异性为 0.69,阳性预测值为 0.84,阴性预测值为 0.90。核磁共振成像平均在 25 周进行:结论:胎儿导水管狭窄的产前诊断可以在胎龄时准确做出,并有可能进行宫内干预。只有7%的受试者在产前被超声错误诊断为胎儿AS,11%的受试者被核磁共振错误诊断为胎儿AS。随着经验的增加,胎儿 AS 的诊断准确率可能会提高。
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来源期刊
Fetal Diagnosis and Therapy
Fetal Diagnosis and Therapy 医学-妇产科学
CiteScore
4.70
自引率
9.10%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The first journal to focus on the fetus as a patient, ''Fetal Diagnosis and Therapy'' provides a wide range of biomedical specialists with a single source of reports encompassing the common discipline of fetal medicine.
期刊最新文献
Transplacental sirolimus for reversal of fetal heart failure due to fetal cardiac rhabdomyoma: fetal and maternal considerations. A rare case of dichorionic twins concordant for arterial tortuosity syndrome: case report and review of the literature. Reflections on the 40th IFMSS meeting Visby-Stockholm 2023. Fetal Extrahepatic Porto systemic Venous Shunts: prenatal diagnosis management and therapy: 21 years of evolving insights. Medical and early developmental outcomes for patients with congenital ventriculomegaly.
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