• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

胎儿肺动脉瓣狭窄轻至中度对双心室的影响。

Biventricular impact of mild to moderate fetal pulmonary valve stenosis.

机构信息

Fetal i+D Fetal Medicine Research Center, BCNatal - Barcelona Center for Maternal-Fetal and Neonatal Medicine (Hospital Clínic and Hospital Sant Joan de Déu), Institut Clínic de Ginecologia Obstetricia i Neonatologia, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Universitat de Barcelona and Centre for Biomedical Research on Rare Diseases (CIBER-ER), Barcelona, Spain.

Pediatric Cardiology, Hospital Sant Joan de Déu, Barcelona, Spain.

出版信息

Ultrasound Obstet Gynecol. 2018 Mar;51(3):349-356. doi: 10.1002/uog.17456.

DOI:10.1002/uog.17456
PMID:28295792
Abstract

OBJECTIVES

To define the pattern of fetal echocardiographic changes associated with isolated pulmonary valve stenosis (PS) and to correlate the echocardiographic findings with neonatal outcome and the need for postnatal pulmonary valvuloplasty within the first 12 months postpartum.

METHODS

This was a prospective cohort study between January 2009 and October 2015 of 16 fetuses with isolated PS and 48 controls matched by gestational age at ultrasound examination (± 2 weeks) evaluated at the Fetal Cardiology Unit at BCNatal (Barcelona). Standard fetal ultrasound and comprehensive echocardiography, which included cardiovascular morphometric parameters, and systolic and diastolic functional and timing measurements, were performed in all cases. Baseline characteristics and perinatal outcome were retrieved from clinical records. Cases were followed up until 12 months of age, and admission to intensive care unit, days of hospitalization, need for prostaglandins and requirement for postnatal surgery were reviewed. Fetal PS cases were analyzed according to the need for postnatal pulmonary valvuloplasty.

RESULTS

The study groups were similar in terms of baseline, fetal ultrasound and perinatal characteristics. Median gestational age at diagnosis of PS was 33.4 (range, 20.0-36.5) weeks. Most cases corresponded to mild or moderate PS; only three fetuses had reversed flow in the ductus arteriosus before delivery. Six (37.5%) newborns, including all three with reversed flow in the ductus arteriosus prenatally, required postnatal pulmonary valvuloplasty. Fetuses with PS presented with larger and more globular hearts, with increased myocardial wall thickness in the third trimester. Despite preserved right ventricular (RV) ejection fraction and systolic longitudinal motion, PS cases showed increased right cardiac output and signs of diastolic dysfunction, with higher ductus venosus pulsatility index (0.72 ± 0.32 vs 0.53 ± 0.16, P = 0.004) and tricuspid E/E' ratio (7.52 ± 3.07 vs 5.76 ± 1.79, P = 0.022). In addition, fetuses with PS displayed a compensatory increase in left ventricular (LV) radial and longitudinal motion, as shown by a higher ejection fraction (79.3 ± 8.23% vs 67.6 ± 11.3%, P = 0.003) and mitral annular-plane systolic excursion (5.94 ± 1.38 vs 5.0 ± 1.22 mm, P = 0.035). Finally, fetuses requiring postnatal pulmonary valvuloplasty showed a different pattern of echocardiographic findings from those not requiring valvuloplasty, with a significantly smaller RV and pulmonary valve diameter, reduced tricuspid annular-plane systolic excursion (5.08 ± 1.59 vs 8.07 ± 1.93 mm, P = 0.028), increased LV cardiac output (340 ± 16 vs 176 ± 44 mL/min/kg, P = 0.003) and more pronounced signs of LV diastolic dysfunction (mitral E' velocity, 5.78 ± 0.90 vs 8.16 ± 1.58 cm/s, P = 0.008).

CONCLUSIONS

Fetuses with PS present with more hypertrophic, larger and more globular hearts in the third trimester of pregnancy, associated with a higher right cardiac output and impaired biventricular relaxation. In addition, signs of increased LV contraction were observed. Our data suggest that RV and LV functional parameters could be useful for predicting the need for postnatal pulmonary valvuloplasty. Copyright © 2017 ISUOG. Published by John Wiley & Sons Ltd.

摘要

目的

确定单纯性肺动脉瓣狭窄(PS)胎儿心脏超声改变的模式,并将超声心动图结果与新生儿结局和出生后 12 个月内是否需要行肺动脉瓣成形术相关联。

方法

这是一项前瞻性队列研究,纳入了 2009 年 1 月至 2015 年 10 月期间在巴塞罗那 BCNatal 胎儿心脏病学中心接受检查的 16 例单纯 PS 胎儿和 48 例匹配胎龄(超声检查±2 周)的对照组。所有病例均行标准胎儿超声心动图和全面的超声心动图检查,包括心血管形态学参数、收缩和舒张功能及时相测量。从临床记录中检索基线特征和围产期结局。随访病例直至 12 个月龄,观察入重症监护病房、住院天数、是否需要前列腺素和是否需要行出生后手术。根据是否需要行出生后肺动脉瓣成形术对 PS 胎儿进行分析。

结果

两组在基线、胎儿超声和围产期特征方面相似。PS 的中位诊断孕周为 33.4 周(范围为 20.0-36.5 周)。大多数病例为轻度或中度 PS;仅 3 例胎儿在分娩前存在动脉导管内反流。6 例(37.5%)新生儿需要行出生后肺动脉瓣成形术,包括所有 3 例在产前存在动脉导管内反流的新生儿。PS 胎儿的心脏更大且呈球形,孕晚期心肌壁厚度增加。尽管右心室(RV)射血分数和收缩期纵向运动保留,但 PS 胎儿的右心输出量增加,舒张功能障碍的迹象更明显,表现为更高的静脉导管搏动指数(0.72±0.32 比 0.53±0.16,P=0.004)和三尖瓣 E/E'比值(7.52±3.07 比 5.76±1.79,P=0.022)。此外,PS 胎儿左心室(LV)径向和纵向运动代偿性增加,表现为射血分数更高(79.3±8.23%比 67.6±11.3%,P=0.003)和二尖瓣环平面收缩期位移更大(5.94±1.38 比 5.0±1.22 毫米,P=0.035)。最后,需要行出生后肺动脉瓣成形术的胎儿与不需要行瓣成形术的胎儿超声心动图表现不同,RV 和肺动脉瓣直径明显更小,三尖瓣环平面收缩期位移减少(5.08±1.59 比 8.07±1.93 毫米,P=0.028),LV 心输出量增加(340±16 比 176±44 毫升/分钟/千克,P=0.003),LV 舒张功能障碍的迹象更明显(二尖瓣 E'速度,5.78±0.90 比 8.16±1.58 厘米/秒,P=0.008)。

结论

PS 胎儿在妊娠晚期心脏更大、更呈球形,与右心输出量增加和双心室舒张功能障碍有关。此外,还观察到 LV 收缩功能增强的迹象。我们的数据表明,RV 和 LV 功能参数可能有助于预测出生后是否需要行肺动脉瓣成形术。版权所有©2017 ISUOG。约翰威利父子公司出版。

相似文献

1
Biventricular impact of mild to moderate fetal pulmonary valve stenosis.胎儿肺动脉瓣狭窄轻至中度对双心室的影响。
Ultrasound Obstet Gynecol. 2018 Mar;51(3):349-356. doi: 10.1002/uog.17456.
2
Immediate effects and outcome of in-utero pulmonary valvuloplasty in fetuses with pulmonary atresia with intact ventricular septum or critical pulmonary stenosis.胎儿肺动脉瓣成形术治疗伴完整室间隔的肺动脉闭锁或严重肺动脉瓣狭窄的即刻效果和结局。
Ultrasound Obstet Gynecol. 2018 Aug;52(2):230-237. doi: 10.1002/uog.19047.
3
Tissue Doppler imaging in fetuses with aortic stenosis and evolving hypoplastic left heart syndrome before and after fetal aortic valvuloplasty.胎儿主动脉瓣狭窄及左心发育不良综合征胎儿主动脉瓣成形术前、后组织多普勒成像。
Ultrasound Obstet Gynecol. 2016 May;47(5):608-15. doi: 10.1002/uog.14885. Epub 2016 Apr 17.
4
Urgent neonatal balloon atrial septostomy in simple transposition of the great arteries: predictive value of fetal cardiac parameters.大动脉转位单纯型的紧急新生儿球囊房间隔造口术:胎儿心脏参数的预测价值
Ultrasound Obstet Gynecol. 2021 May;57(5):756-768. doi: 10.1002/uog.22164.
5
Early cardiac remodeling in aortic coarctation: insights from fetal and neonatal functional and structural assessment.主动脉缩窄的早期心脏重构:来自胎儿和新生儿功能及结构评估的见解。
Ultrasound Obstet Gynecol. 2020 Dec;56(6):837-849. doi: 10.1002/uog.21970. Epub 2020 Nov 12.
6
Natural history of 107 cases of fetal aortic stenosis from a European multicenter retrospective study.一项欧洲多中心回顾性研究中107例胎儿主动脉狭窄的自然病史。
Ultrasound Obstet Gynecol. 2016 Sep;48(3):373-81. doi: 10.1002/uog.15876. Epub 2016 Aug 4.
7
Fetal cardiovascular remodeling persists at 6 months in infants with intrauterine growth restriction.宫内生长受限婴儿的胎儿心血管重塑在6个月时持续存在。
Ultrasound Obstet Gynecol. 2016 Sep;48(3):349-56. doi: 10.1002/uog.15767.
8
Cardiac output and blood flow redistribution in fetuses with D-loop transposition of the great arteries and intact ventricular septum: insights into pathophysiology.胎儿大动脉 D 型环转位伴室间隔完整时的心输出量和血流再分布:病理生理学见解。
Ultrasound Obstet Gynecol. 2017 Nov;50(5):612-617. doi: 10.1002/uog.17370.
9
Fetal Pulmonary Valvuloplasty in Fetuses with Right Ventricular Outflow Tract Obstructive Disease: Experience and Outcome of the First Five Cases in China.胎儿右心室流出道梗阻性疾病的胎儿肺动脉瓣成形术:中国前五例的经验和结果。
Pediatr Cardiol. 2021 Feb;42(2):340-348. doi: 10.1007/s00246-020-02488-8. Epub 2020 Oct 22.
10
[Prenatal interventional therapy in two cases with critical pulmonary stenosis or pulmonary atresia with intact ventricular septum].[两例重度肺动脉狭窄或室间隔完整型肺动脉闭锁的产前介入治疗]
Zhonghua Er Ke Za Zhi. 2018 Jun 2;56(6):445-450. doi: 10.3760/cma.j.issn.0578-1310.2018.06.008.

引用本文的文献

1
Fetal cardiac function in pregnancy affected by congenital heart disease: protocol for a multicentre prospective cohort study.先天性心脏病对孕期胎儿心脏功能的影响:一项多中心前瞻性队列研究方案
BMC Pregnancy Childbirth. 2025 Jan 30;25(1):99. doi: 10.1186/s12884-025-07145-7.
2
Assessment of right ventricular endocardial fibroelastosis in fetuses with critical pulmonary stenosis and pulmonary atresia with intact ventricular septum.评估患有严重肺动脉狭窄及室间隔完整的肺动脉闭锁胎儿的右心室心内膜弹力纤维增生症。
Front Pediatr. 2025 Jan 10;12:1518898. doi: 10.3389/fped.2024.1518898. eCollection 2024.
3
Clinical outcomes of the neonates with critical pulmonary stenosis: intrauterine versus postnatal transport.
重度肺动脉狭窄新生儿的临床结局:宫内转运与出生后转运
Transl Pediatr. 2024 Jul 31;13(7):1097-1105. doi: 10.21037/tp-24-42. Epub 2024 Jul 23.
4
Prenatal Predictors for Pulmonary Balloon Valvuloplasty in the Newborn.新生儿肺气球瓣膜成形术的产前预测因素。
Pediatr Cardiol. 2024 Apr;45(4):722-728. doi: 10.1007/s00246-024-03430-y. Epub 2024 Feb 27.
5
The Additional Role of the 3-Vessels and Trachea View in Screening for Congenital Heart Disease.三血管气管切面在先天性心脏病筛查中的额外作用。
Medicina (Kaunas). 2022 Feb 10;58(2):262. doi: 10.3390/medicina58020262.