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使用超声对先天性肾畸形进行产前诊断。

Antenatal diagnosis of congenital renal malformations using ultrasound.

作者信息

Sanghvi K P, Merchant R H, Gondhalekar A, Lulla C P, Mehta A A, Mehta K P

机构信息

N. Wadia Maternity Hospital, Parel, Mumbai, India.

出版信息

J Trop Pediatr. 1998 Aug;44(4):235-40. doi: 10.1093/tropej/44.4.235.

Abstract

Our objectives were to determine the accuracy of antenatal sonography for the detection of congenital renal malformations and to characterize the type of malformations, seen in a 3-year prospective study at a university-affiliated maternity hospital. Participants were 31,217 pregnant women, during the study period, and subjects were 65 fetuses in whom renal malformations were detected on antenatal ultrasound. Pelvic ultrasound scans were performed at least once between 20 and 37 weeks' gestation on all pregnant women attending the antenatal clinic of the hospital for the detection of renal malformations. Fetal urinary sampling, diversion procedures, or termination of pregnancy were carried out as required in those detected to have renal anomalies. Postnatal diagnosis was confirmed by sonography or autopsy. Diagnostic procedures and renal surgery were performed postnatally if indicated. Sixty-five fetuses (0.2 per cent) were diagnosed to have congenital renal malformation antenatally at a mean gestational age of 28.4 weeks. A dilated urinary system was seen in 39, cystic renal disease in 15, agenesis/hypoplasia in six, combined lesions in four, and a horseshoe kidney in one. Oligohydramnios was noted in 20 (31 per cent) pregnancies. Multiple congenital malformations associated with renal anomalies were detected in 12 pregnancies. Termination was carried out at 20 weeks in two pregnancies for lethal malformations; fetal urinary sampling was done in two fetuses with obstructed uropathy, and a vesicoamniotic shunt inserted in one. Postnatal ultrasound confirmed a dilated urinary system in 32, cystic renal dysplasia in 15, renal aplasia/hypoplasia in five, combined lesions in six, and a horseshoe and an ectopic kidney in one each. Five infants were found to be normal. There were seven stillbirths and seven neonatal deaths. Radionuclide scans showed obstruction in nine, decreased renal function in six, and absent renal functions in 10 infants. Micturating cystourethrography demonstrated reflux in 11 and a non-refluxing non-obstructive dilated renal system in five babies. Renal surgery was performed in nine infants. The conclusions drawn from this study were that antenatal detection of renal disease is fairly accurate, even in an extremely busy hospital and certain types of malformations reported in other studies were not observed, despite a large cohort.

摘要

我们的目标是在一所大学附属妇产医院进行的为期3年的前瞻性研究中,确定产前超声检查对先天性肾畸形的检测准确性,并对所发现的畸形类型进行特征描述。研究对象为研究期间的31217名孕妇,其中65例胎儿在产前超声检查中被检测出患有肾畸形。对所有到该医院产前门诊就诊的孕妇,在妊娠20至37周期间至少进行一次盆腔超声扫描,以检测肾畸形。对那些被检测出有肾异常的孕妇,根据需要进行胎儿尿液采样、引流手术或终止妊娠。产后诊断通过超声检查或尸检得以证实。如有必要,产后进行诊断性检查和肾脏手术。65例胎儿(0.2%)在平均孕周28.4周时被产前诊断为先天性肾畸形。其中39例可见泌尿系统扩张,15例为肾囊性疾病,6例为肾缺如/发育不全,4例为合并病变,1例为马蹄肾。20例(31%)妊娠出现羊水过少。12例妊娠检测出与肾异常相关的多发先天性畸形。2例妊娠因致命畸形在20周时终止妊娠;2例患有尿路梗阻性疾病的胎儿进行了胎儿尿液采样,1例插入了膀胱羊膜分流管。产后超声检查证实32例泌尿系统扩张,15例为肾囊性发育不良,5例为肾发育不全/发育不良,6例为合并病变,1例马蹄肾和1例异位肾。5例婴儿被发现正常。有7例死产和7例新生儿死亡。放射性核素扫描显示9例存在梗阻,6例肾功能减退,10例无肾功能。排尿性膀胱尿道造影显示11例有反流,5例婴儿为无反流无梗阻性扩张的肾系统。9例婴儿接受了肾脏手术。本研究得出的结论是,即使在极其繁忙的医院,产前对肾脏疾病的检测也相当准确,尽管样本量很大,但未观察到其他研究报道的某些类型的畸形。

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