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产前先天性膈疝的检测及其对预后的影响:法国奥弗涅地区12年经验

Antenatal detection and impact on outcome of congenital diaphragmatic hernia: a 12-year experience in Auvergne, France.

作者信息

Gallot Denis, Coste Karen, Francannet Christine, Laurichesse Hélène, Boda Carole, Ughetto Sylvie, Vanlieferinghen Philippe, Scheye Thierry, Vendittelli Françoise, Labbe Andre, Dechelotte Pierre J, Sapin Vincent, Lemery Didier

机构信息

CHU Clermont-Ferrand, Maternal Fetal Medecine Unit, Maternité Hôtel-Dieu, Boulevard Léon Malfreyt, 63003 Clermont-Ferrand Cedex, France.

出版信息

Eur J Obstet Gynecol Reprod Biol. 2006 Apr 1;125(2):202-5. doi: 10.1016/j.ejogrb.2005.06.030. Epub 2005 Aug 15.

Abstract

OBJECTIVE

To evaluate the detection rate of prenatal diagnosis and its impact on outcome in congenital diaphragmatic hernia (CDH).

STUDY DESIGN

We retrospectively studied 51 cases of CDH registered in the Auvergne area from January 1992 to December 2003 (Birth Defect Registry of Auvergne, Institut Européen des Génomutations). Our main outcome measurements were the detection rate of prenatal diagnosis, the incidence and types of associated anomalies and outcome (termination of pregnancy, in utero fetal demise, neonatal death, survival at the time of registration).

RESULTS

Twenty-nine cases of isolated CDH were identified of which 13 were detected prenatally (45%) at a mean gestational age of 26.1 weeks and 22 cases of CDH with associated anomalies with prenatal diagnosis of CDH or any associated anomaly in 16 (73%; p=0.03) at a mean gestational age of 23.9 weeks. In the prenatally detected group (29 cases), there was 1 (3%) in utero fetal death (IUFD), 17 (59%) terminations of pregnancy (TOP) and 11 (38%) live births with early neonatal death in 7 (24%) cases despite delivery in a tertiary care centre in 10/11 cases (four survivors=14%). Most of the undetected cases were isolated CDH (16/22=73%) of which 1 (5%) was a stillborn and 21 (95%) live births with 17 survivors (77%) although 15/21 (71%) were not born at the tertiary care centre (p=0.001). The overall survival rate was 41% with a large variability depending on associated anomalies and prenatal diagnosis (p<0.0001) (prenatally detected cases: 3/13 (23%) isolated CDH and 1/16 (6%) CDH with associated anomalies; undetected cases: 13/16 (81%) isolated CDH and 4/6 (67%) CDH with associated anomalies).

CONCLUSION

Prenatal diagnosis of CDH leads to the delivery of affected babies in tertiary care centres but it remains a challenge in particular for isolated CDH cases and it is associated with a lower survival rate. Associated anomalies contribute to prenatal detection, are related to a higher TOP rate but do not facilitate the detection of diaphragmatic defect per se.

摘要

目的

评估先天性膈疝(CDH)的产前诊断检出率及其对预后的影响。

研究设计

我们回顾性研究了1992年1月至2003年12月在奥弗涅地区登记的51例CDH病例(奥弗涅出生缺陷登记处,欧洲基因变异研究所)。我们的主要结局指标是产前诊断的检出率、相关畸形的发生率和类型以及结局(终止妊娠、宫内胎儿死亡、新生儿死亡、登记时存活)。

结果

确定了29例孤立性CDH,其中13例(45%)在平均孕周26.1周时产前检出,22例合并相关畸形的CDH中,16例(73%;p=0.03)在平均孕周23.9周时产前诊断出CDH或任何相关畸形。在产前检出组(29例)中,有1例(3%)宫内胎儿死亡(IUFD),17例(59%)终止妊娠(TOP),11例(38%)活产,其中7例(24%)早期新生儿死亡,尽管10/11例在三级医疗中心分娩(4名幸存者=14%)。大多数未检出病例为孤立性CDH(16/22=73%),其中1例(5%)为死产,21例(95%)活产,17例(77%)存活,尽管15/21例(71%)并非在三级医疗中心出生(p=0.001)。总体生存率为41%,根据相关畸形和产前诊断存在很大差异(p<0.0001)(产前检出病例:3/13例(23%)孤立性CDH和1/16例(6%)合并相关畸形的CDH;未检出病例:13/16例(81%)孤立性CDH和4/6例(67%)合并相关畸形的CDH)。

结论

CDH的产前诊断使患病婴儿在三级医疗中心分娩,但仍是一项挑战,特别是对于孤立性CDH病例,且与较低的生存率相关。相关畸形有助于产前检出,与较高的TOP率相关,但本身并不便于膈疝缺陷的检出。

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