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孕期疑似患有主动脉缩窄胎儿的病程及结局

Course and outcome of fetuses suspected of having coarctation of the aorta during gestation.

作者信息

Axt-Fliedner R, Hartge D, Krapp M, Berg C, Geipel A, Koester S, Noack F, Germer U, Gembruch U

机构信息

OB & GYN, Helios-Klinikum Krefeld, Division of Prenatal Medicine, Lutherplatz 40, 47805 Krefeld.

出版信息

Ultraschall Med. 2009 Jun;30(3):269-76. doi: 10.1055/s-2008-1027556. Epub 2008 Sep 4.

Abstract

PURPOSE

To report the course and outcome of a group of fetuses with prenatal suspicion of coarctation of the aorta.

MATERIALS AND METHODS

Retrospective observational study in two tertiary fetal cardiology centers between 1993 - 2005.

RESULTS

96 fetuses of whom 52 infants were born alive were studied. Of the 52 liveborn infants, 34 had coarctation of the aorta (65.4 %), thirteen had prenatally diagnosed additional cardiac anomalies (VSD, ASD, aortic and pulmonary stenosis, persistent left superior vena cava) and three were managed as having hypoplastic left heart syndrome. Three neonates had additional extracardiac malformations diagnosed prenatally. 22 neonates underwent surgery, nineteen within the first ten days of life. One neonate only developed clinical signs of coarctation on the fourteenth day of life. The early surgical mortality was three of 22 (13.6 %). The mortality was influenced by prematurity. The survival rate on the basis of intention-to-treat was twenty-nine of 34 neonates with confirmed coarctation (85.3 %).

CONCLUSION

Coarctation of aorta during fetal life continues to be a difficult diagnosis. The potential of progressive hypoplasia of left heart structures during gestation in the case of fetal aortic isthmus stenosis with the development of a hypoplastic left heart should be kept in mind and therefore sequential echo-cardiography is recommended during gestation.

摘要

目的

报告一组产前疑似主动脉缩窄胎儿的病程及结局。

材料与方法

对1993年至2005年期间两个三级胎儿心脏病中心进行回顾性观察研究。

结果

共研究了96例胎儿,其中52例婴儿存活。在这52例存活婴儿中,34例患有主动脉缩窄(65.4%),13例产前诊断出合并其他心脏异常(室间隔缺损、房间隔缺损、主动脉和肺动脉狭窄、永存左上腔静脉),3例被诊断为左心发育不良综合征。3例新生儿产前诊断出合并心外畸形。22例新生儿接受了手术,其中19例在出生后十天内进行。1例新生儿在出生后第十四天才出现主动脉缩窄的临床症状。早期手术死亡率为22例中的3例(13.6%)。死亡率受早产影响。基于意向性治疗,34例确诊主动脉缩窄的新生儿中,29例存活(85.3%)。

结论

胎儿期主动脉缩窄仍然是一个难以诊断的疾病。对于胎儿主动脉峡部狭窄且可能发展为左心发育不良的情况,应考虑到孕期左心结构进行性发育不全的可能性,因此建议孕期进行系列超声心动图检查。

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