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38例先天性膈疝的产前诊断及围产期结局:巴西一家三级中心的8年经验

Prenatal diagnosis and perinatal outcome of 38 cases with congenital diaphragmatic hernia: 8-year experience of a tertiary Brazilian center.

作者信息

Ruano Rodrigo, Bunduki Victor, Silva Marcos Marques, Yoshizaki Carlos Tadashi, Tanuri Uenis, Macksoud João Gilberto, Zugaib Marcelo

机构信息

Department of Obstetrics and Gynecology, Hospital das Clínicas, São Paulo University Medical School, Brazil.

出版信息

Clinics (Sao Paulo). 2006 Jun;61(3):197-202. doi: 10.1590/s1807-59322006000300003. Epub 2006 Jun 30.

Abstract

PURPOSE

To evaluate the perinatal results for neonates with congenital diaphragmatic hernia diagnosed prenatally.

METHOD

We reviewed data from 38 cases of congenital diaphragmatic hernia diagnosed prenatally from January 1995 to December 2003 in the Fetal Medicine Unit of the Department of Obstetrics and Gynecology, São Paulo University Medical School. The main data analyzed were gestational age at diagnosis, fetal karyotyping, side of diaphragmatic defect, presence of associated structural malformations, hepatic herniation, and severe mediastinal shift. Perinatal outcomes were obtained by reviewing hospital documents or by directly calling the patients' immediate relatives.

RESULTS

Mean gestational age at diagnosis was 29 weeks (range, 16-37 weeks). Thirty (79%) cases had a left diaphragmatic defect and 8 (21%) had a right lesion. Associated structural malformations were observed in 21 (55%) cases, in which 12 fetuses had a normal karyotype and 9 had chromosomal abnormalities. Isolated congenital diaphragmatic hernia was confirmed in 17 (45%) cases. The overall perinatal mortality rate was 92%. Rates of fetal deaths, early neonatal deaths, late neonatal deaths, and survival were 42%, 50%, 0%, and 8%, respectively, in cases with associated structural malformations but normal karyotyping; 56%, 44%, 0%, and 0% for cases with chromosomal abnormalities; and, 0%, 76%, 12%, and 12% in cases with isolated congenital diaphragmatic hernia. The neonatal mortality rate was 89% in cases with isolated congenital diaphragmatic hernia.

CONCLUSION

Perinatal mortality was very high in prenatally diagnosed cases of congenital diaphragmatic hernia. Earlier perinatal deaths are associated with the presence of other structural defects or chromosomal abnormalities. In cases of isolated congenital diaphragmatic hernia, mortality is related to the presence of herniated liver, right-sided lesion, and major mediastinal shift.

摘要

目的

评估产前诊断为先天性膈疝的新生儿的围产期结局。

方法

我们回顾了1995年1月至2003年12月在圣保罗大学医学院妇产科胎儿医学科产前诊断为先天性膈疝的38例病例的数据。分析的主要数据包括诊断时的孕周、胎儿核型分析、膈缺损的部位、是否存在相关结构畸形、肝脏疝入以及严重纵隔移位。通过查阅医院病历或直接致电患者的直系亲属来获取围产期结局。

结果

诊断时的平均孕周为29周(范围16 - 37周)。30例(79%)为左侧膈缺损,8例(21%)为右侧病变。21例(55%)观察到相关结构畸形,其中12例胎儿核型正常,9例有染色体异常。17例(45%)确诊为孤立性先天性膈疝。总体围产期死亡率为92%。在伴有相关结构畸形但核型正常的病例中,胎儿死亡率、早期新生儿死亡率、晚期新生儿死亡率和存活率分别为42%、50%、0%和8%;染色体异常的病例分别为56%、44%、0%和0%;孤立性先天性膈疝的病例分别为0%、76%、12%和12%。孤立性先天性膈疝病例的新生儿死亡率为89%。

结论

产前诊断为先天性膈疝的病例围产期死亡率非常高。早期围产期死亡与其他结构缺陷或染色体异常的存在有关。在孤立性先天性膈疝病例中,死亡率与肝脏疝入、右侧病变和严重纵隔移位的存在有关。

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