Harmath Agnes, Hajdú Júlia, Pete Barbara, Papp Zoltán
Semmelweis Egyetem, Altalános Orvostudományi Kar, I Szülészeti és Nogyógyászati Klinika, Budapest.
Orv Hetil. 2006 Jul 9;147(27):1259-65.
Review of perinatally diagnosed congenital diaphragmatic hernia cases with regard to time of diagnosis, side of hernia, mode of delivery, organs herniated into the thorax, main group of associated malformations and the outcome.
The authors analysed the data of 104 cases from records of I. Department of Obstetrics and Gynecology Semmelweis University Budapest between July 1, 1990 and June 30, 2005. The observed period was analysed in two parts.
Prenatal ultrasound was performed in 93 cases. In 6 cases (6.5%) the prenatally diagnosed congenital diaphragmatic hernia postnatally proved to be a different non-cardiac thoracic malformation. 50.4% of the pre- and postnatally verified 87 congenital diaphragmatic hernia cases were diagnosed before the 24th week of gestation. 11 hernias were identified postnatally. From the diagnosed 98 cases 69 (70.4%) occurred as a part of multiple anomalies. The hernia was left-sided in 86.7%, and both-sided in 4 cases. In 1990-1997, the percentage of right-sided hernia was 4% while in the second period it was 13%. Delivery was performed in 51 cases, with prenatal diagnosis in 40 cases. From the 51 newborns 14 were alive, thus the survival rate was 27.5%. The survival rate of the newborns delivered by cesarean section was three times higher than that of the vaginally delivered ones. There was termination in 38 cases, 6 of which were isolated malformation. Intrauterine or subpartu death occurred in 5 cases. We have no data about the outcome of the pregnancy in four cases. The liver, spleen and stomach thoracic herniation was twice as high in the second period as it was in the first period, but their correlation did not change.
According to the analysis of the 15 years' data the herniated organs, the multiplex malformations as well as the mode of delivery influence the survival in a large number of cases. Early diagnosis portends a large hernia, a higher malformation rate, and the worse prognosis.
回顾围产期诊断的先天性膈疝病例,涉及诊断时间、疝的部位、分娩方式、疝入胸腔的器官、主要相关畸形组及结局。
作者分析了布达佩斯塞梅尔维斯大学第一妇产科1990年7月1日至2005年6月30日记录中的104例病例数据。观察期分为两部分进行分析。
93例进行了产前超声检查。6例(6.5%)产前诊断为先天性膈疝的病例,产后证实为不同的非心脏性胸部畸形。在87例经产前和产后证实的先天性膈疝病例中,50.4%在妊娠24周前被诊断。11例疝在产后被发现。在诊断出的98例病例中,69例(70.4%)是多发畸形的一部分。疝位于左侧的占86.7%,双侧的有4例。1990 - 1997年,右侧疝的比例为4%,而在第二个时期为13%。51例进行了分娩,其中40例有产前诊断。51例新生儿中14例存活,因此存活率为27.5%。剖宫产分娩的新生儿存活率比阴道分娩的高两倍。38例终止妊娠,其中6例为孤立畸形。5例发生宫内或产时死亡。4例无妊娠结局数据。第二时期肝脏、脾脏和胃疝入胸腔的发生率是第一时期的两倍,但它们之间的相关性未改变。
根据15年的数据分析,疝入器官、多发畸形以及分娩方式在大量病例中影响存活率。早期诊断预示着疝较大、畸形率较高且预后较差。