Open Spinal Dysraphism Without Hindbrain Herniation-Natural History and Postnatal Outcome.

IF 2.7 2区 医学 Q2 GENETICS & HEREDITY
Prenatal Diagnosis Pub Date : 2025-08-01 Epub Date: 2025-07-08 DOI:10.1002/pd.6855
I Bedei, C C Kik, R Axt-Fliedner, P L J DeKoninck, W Ventura, S Köhler, M Schulze, T Struffert, M Kolodziej, D Diehl, B Sass, J K H Spoor, C Keil
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引用次数: 0

Abstract

Objective: To report the natural history of fetuses with open spinal dysraphism (OSD) without hindbrain herniation (HBH) during second-trimester evaluation.

Methods: A multicenter retrospective cohort study was conducted across three prenatal centers to evaluate fetuses with OSD. We reviewed cases with postnatally confirmed OSD without prenatal HBH at 19-27 weeks. Standardized prenatal evaluation consisted of repetitive ultrasound and magnetic resonance imaging. Postnatal outcome measures involved imaging, intraoperative findings and neurological function tests.

Results: Among 280 fetuses with OSD, evaluated at a median gestational age of 21 weeks, a total of 12 (4%) lacked HBH. Moderate ventriculomegaly was observed in 33% of cases without HBH. Corpus callosum anomalies were not detected. Postnatally, HBH was present in 50%, while the shunt rate remained low (20%). In 80%, postnatal motor function (MF) was equal to or better based on the anatomical level. In 33%, MF after birth declined in comparison to the first fetal functional assessment in the second trimester.

Conclusion: Fetuses with OSD and absent HBH in the second trimester demonstrate a low postnatal shunt rate. MF was frequently impaired at the initial second-trimester assessment, and in about a third of cases, postnatal MF seemed to have worsened. These findings may inform counseling and question the place of fetal surgery for this subgroup.

Abstract Image

Abstract Image

无后脑疝的开放性脊柱发育异常-自然史和产后结局。
目的:报道无后脑疝(HBH)的开放式脊柱发育异常(OSD)胎儿在妊娠中期评估中的自然病史。方法:在三个产前中心进行了多中心回顾性队列研究,以评估患有OSD的胎儿。我们回顾了19-27周出生后确诊的无产前HBH的OSD病例。标准化的产前评估包括重复超声和磁共振成像。产后结果测量包括影像学、术中发现和神经功能测试。结果:在280例OSD胎儿中,在中位胎龄为21周时评估,共有12例(4%)缺乏HBH。无HBH的病例中有33%出现中度脑室增大。未发现胼胝体异常。出生后,50%的人出现HBH,而分流率仍然很低(20%)。在80%的患者中,产后运动功能(MF)在解剖学水平上等于或更好。与妊娠中期首次胎儿功能评估相比,33%的孕妇出生后MF下降。结论:妊娠中期伴有OSD和HBH缺失的胎儿具有较低的产后分流率。在最初的妊娠中期评估中,MF经常受损,在大约三分之一的病例中,产后MF似乎恶化了。这些发现可能会为咨询提供信息,并对该亚群的胎儿手术地点提出质疑。
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来源期刊
Prenatal Diagnosis
Prenatal Diagnosis 医学-妇产科学
CiteScore
5.80
自引率
13.30%
发文量
204
审稿时长
2 months
期刊介绍: Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling
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