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基于多机构回顾的日本产前诊断先天性膈疝经验。

The Japanese experience with prenatally diagnosed congenital diaphragmatic hernia based on a multi-institutional review.

作者信息

Okuyama Hiroomi, Kitano Yoshihiro, Saito Mari, Usui Noriaki, Morikawa Nobuyuki, Masumoto Kouji, Takayasu Hajime, Nakamura Tomoo, Ishikawa Hiroshi, Kawataki Motoyoshi, Hayashi Satoshi, Inamura Noboru, Nose Keisuke, Sago Haruhiko

机构信息

Department of Pediatric Surgery, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.

出版信息

Pediatr Surg Int. 2011 Apr;27(4):373-8. doi: 10.1007/s00383-010-2805-0. Epub 2010 Nov 28.

DOI:10.1007/s00383-010-2805-0
PMID:21113786
Abstract

PURPOSE

To review the recent Japanese experience with prenatally diagnosed congenital diaphragmatic hernia (CDH) based on a multi-institutional survey.

METHODS

A multicenter, retrospective cohort study was conducted on 117 patients born between 2002 and 2007 with isolated prenatally diagnosed CDH. All patients were managed by maternal transport, planned delivery, immediate resuscitation and gentle ventilation. The primary outcome measurements were the 90-day survival and intact discharge. The examined prenatal factors included gestational age (GA) at diagnosis, lung-to-head ratio (LHR), lung-to-thorax transverse area ratio (L/T) and liver position. Physical growth and motor/speech development were evaluated at 1.5 and 3 years of age. Data were expressed as the median (range).

RESULTS

The mean GA at diagnosis was 29 (17-40) weeks. The LHR and L/T were 1.56 (0.37-4.23) and 0.11 (0.04-0.25), respectively. There were 48 patients with liver up. The mean GA at birth was 38 (28-42) weeks. The 90-day survival rate and intact discharge rate were 79 and 63%, respectively. Twelve patients had major morbidity at discharge, and 71% of these patients had physical growth or developmental retardation at 3 years of age.

CONCLUSION

This multicenter study demonstrated that the 90-day survival rate of isolated prenatally diagnosed CDH was 79%, and that subsequent morbidity remained high. A new treatment strategy is needed to reduce the mortality and morbidity of severe CDH.

摘要

目的

基于一项多机构调查,回顾日本近期产前诊断先天性膈疝(CDH)的经验。

方法

对2002年至2007年间出生的117例产前诊断为孤立性CDH的患者进行了一项多中心回顾性队列研究。所有患者均通过母体转运、计划分娩、立即复苏和轻柔通气进行管理。主要结局指标为90天生存率和完整出院率。检查的产前因素包括诊断时的孕周(GA)、肺头比(LHR)、肺胸横截面积比(L/T)和肝脏位置。在1.5岁和3岁时评估身体生长和运动/语言发育情况。数据以中位数(范围)表示。

结果

诊断时的平均孕周为29(17 - 40)周。LHR和L/T分别为1.56(0.37 - 4.23)和0.11(0.04 - 0.25)。有48例肝脏上移。出生时的平均孕周为38(28 - 42)周。90天生存率和完整出院率分别为79%和63%。12例患者出院时有严重并发症,其中71%的患者在3岁时存在身体生长或发育迟缓。

结论

这项多中心研究表明,产前诊断为孤立性CDH的90天生存率为79%,且随后的并发症发生率仍然很高。需要一种新的治疗策略来降低严重CDH的死亡率和发病率。

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本文引用的文献

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Improvement in the outcome of patients with antenatally diagnosed congenital diaphragmatic hernia using gentle ventilation and circulatory stabilization.
Pediatr Surg Int. 2009 Jun;25(6):487-92. doi: 10.1007/s00383-009-2370-6. Epub 2009 May 7.
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Timing of delivery and survival rates for infants with prenatal diagnoses of congenital diaphragmatic hernia.产前诊断为先天性膈疝的婴儿的分娩时机和存活率
Pediatrics. 2009 Feb;123(2):494-502. doi: 10.1542/peds.2008-0528.
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Fetal magnetic resonance imaging in isolated diaphragmatic hernia: volume of herniated liver and neonatal outcome.孤立性膈疝的胎儿磁共振成像:肝脏疝出体积与新生儿结局
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Risk stratification for congenital diaphragmatic hernia by factors within 24 h after birth.出生后24小时内依据相关因素对先天性膈疝进行风险分层。
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Outcome of right-sided diaphragmatic hernia repair: a multicentre study.右侧膈疝修补术的结果:一项多中心研究。
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Value of prenatal magnetic resonance imaging in the prediction of postnatal outcome in fetuses with diaphragmatic hernia.产前磁共振成像在预测先天性膈疝胎儿产后结局中的价值。
Ultrasound Obstet Gynecol. 2008 Nov;32(6):793-9. doi: 10.1002/uog.6234.
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Ultrasound Obstet Gynecol. 2007 Nov;30(6):897-906. doi: 10.1002/uog.5164.
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