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先天性肺畸形胎儿的产后结局预测:2 年随访研究。

Prediction of postnatal outcome in fetuses with congenital lung malformation: 2-year follow-up study.

机构信息

Department of Obstetrics and Gynecology, Division of Obstetrics and Fetal Medicine, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Department of Pediatric Surgery and Intensive Care, Erasmus MC - Sophia Children's Hospital, Rotterdam, The Netherlands.

出版信息

Ultrasound Obstet Gynecol. 2021 Sep;58(3):428-438. doi: 10.1002/uog.23542.

Abstract

OBJECTIVES

To identify, in fetuses with a congenital lung malformation (CLM), prenatal predictors of the need for postnatal respiratory support and the need for surgery by calculating the CLM volume ratio (CVR), and to evaluate the concordance between the prenatal appearance and the postnatal type of CLM.

METHODS

This was an analysis of prenatal, perinatal and postnatal data from fetuses diagnosed with a CLM at the Erasmus University Medical Center - Sophia Children's Hospital in Rotterdam, The Netherlands, between January 2007 and December 2016. For all included fetuses, CVR was measured retrospectively on stored ultrasound images obtained at 18 + 1 to 24 + 6 weeks (US1), 25 + 0 to 29 + 6 weeks (US2) and/or 30 + 0 to 35 + 6 weeks' gestation (US3). Postnatal diagnosis of CLM was based on computed tomography or histology. Primary outcomes were the need for respiratory support within 24 h and surgery within 2 years after birth.

RESULTS

Of the 80 fetuses with a CLM included in this study, 14 (18%) required respiratory support on the first postnatal day, and 17 (21%) required surgery within 2 years. Only the CVR at US2 was predictive of the need for respiratory support, with a cut-off value of 0.39. Four of 16 (25%) fetuses which showed full regression of the CLM prenatally required respiratory support within 24 h after birth. The CVR at US1, US2 and US3 was predictive of surgery within 2 years. Overall, the prenatal appearance of the CLM showed low concordance with the postnatal type. Prenatally suspected microcystic congenital pulmonary airway malformation (CPAM) was shown on computed tomography after birth to be congenital lobar overinflation in 15/35 (43%) cases. Respiratory support within 24 h after birth and surgical resection within 28 days after birth were needed in all cases of macrocystic CPAM.

CONCLUSIONS

CVR can predict the need for respiratory support within 24 h after birth and for surgery within 2 years. Regression of a CLM prenatally does not rule out respiratory problems after birth. © 2020 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology. - Legal Statement: This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

摘要

目的

通过计算肺囊腺瘤体积比(CVR),确定胎儿先天性肺畸形(CLM)中需要出生后呼吸支持和手术的产前预测因子,并评估产前表现与出生后 CLM 类型之间的一致性。

方法

本研究对 2007 年 1 月至 2016 年 12 月期间在荷兰鹿特丹伊拉斯姆斯大学医学中心-索菲亚儿童医院诊断为 CLM 的胎儿的产前、围产期和产后数据进行了分析。对于所有纳入的胎儿,均通过回顾性测量存储的超声图像来计算 CVR,这些超声图像是在妊娠 18+1 至 24+6 周(US1)、25+0 至 29+6 周(US2)和/或 30+0 至 35+6 周时获得的。CLM 的产后诊断基于计算机断层扫描或组织学。主要结局是出生后 24 小时内需要呼吸支持和出生后 2 年内需要手术。

结果

本研究纳入 80 例 CLM 胎儿,14 例(18%)在出生后第 1 天需要呼吸支持,17 例(21%)在出生后 2 年内需要手术。只有 US2 时的 CVR 可预测呼吸支持的需要,其截断值为 0.39。4 例(25%)产前完全消退的 CLM 胎儿在出生后 24 小时内需要呼吸支持。US1、US2 和 US3 时的 CVR 可预测 2 年内的手术。总体而言,CLM 的产前表现与产后类型的一致性较低。出生后 CT 显示,15/35(43%)例疑似产前微囊型先天性肺气道畸形(CPAM)为先天性肺过度充气。所有大囊型 CPAM 均需在出生后 24 小时内进行呼吸支持和 28 天内进行手术切除。

结论

CVR 可预测出生后 24 小时内需要呼吸支持和 2 年内需要手术。CLM 产前消退并不能排除出生后的呼吸问题。© 2020 作者。超声在妇产科由约翰威立父子公司代表国际妇产科超声学会出版。-法律声明:这是一个开放获取的文章根据知识共享署名-非商业性-禁止演绎许可,允许在任何媒体中不受限制地使用、分发,前提是原始作品正确引用,使用是非商业性的,并且没有进行修改。

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