首页> 外文期刊>International Journal of Reproduction, Contraception, Obstetrics and Gynecology >Analysis of frequency of congenital fetal anomalies diagnosed on antenatal ultrasound in a tertiary care hospital of Balochistan
【24h】

Analysis of frequency of congenital fetal anomalies diagnosed on antenatal ultrasound in a tertiary care hospital of Balochistan

机译:och路支省一家三级医院产前超声诊断出先天性胎儿异常的频率分析

获取原文
       

摘要

Background: The objective of our study is to check the incidence of various congenital fetal anomalies in antenatal period by ultrasonography in a subset of population. Methods: This cross sectional study was conducted in the department of Radiology, Bolan Medical Complex Hospital Quetta from November 2017 to October 2018. Total of 1323 second and third trimester pregnancies were analyzed for a period of one year. 34 fetal anomalies were detected making the prevalence of 2.5%. Information obtained from history, clinical examination and Ultrasound examination were recorded. The data was analyzed in SPSS 20.These patients were also interviewed for folic acid supplementation and consanguineous marriage. Results: 1323 patients were examined with congenital abnormalities detected in 34 fetuses. Among 34 fetuses, 20 were male and 14 were female fetuses. Out of 34, mother of 24 fetuses verified that they did not take folic acid supplementation. Consanguineous marriage recognized as the important risk factor as found in 22 congenital abnormal fetus. CNS anomalies were the most commonly occurring anomalies with prevalence of (0.9%) followed by gastrointestinal tract anomalies (0.3%) and Urinary tract anomalies (0.3%). Conclusions: The fetus prognosis largely depends on early detection of its any congenital anomaly on antenatal ultrasound as they can result in abortions, still births and other fetal defects. So antenatal ultrasound is very important and safe method for early detection and management of fetal anomalies.
机译:背景:我们的研究目的是通过超声检查一部分人群中产前期各种先天性胎儿异常的发生率。方法:这项横断面研究于2017年11月至2018年10月在奎达博兰医疗综合医院放射科进行。共分析了1323例中,晚期妊娠,为期一年。检测到34例胎儿异常,患病率为2.5%。记录从病史,临床检查和超声检查中获得的信息。在SPSS 20中对数据进行了分析。还对这些患者进行了叶酸补充和近亲结婚的访谈。结果:检查了1323例先天性异常,其中34例胎儿。在34胎中,男性20例,女性14例。在34名胎儿中,有24名胎儿的母亲证实他们没有服用叶酸。在22位先天性异常胎儿中,近亲结婚被认为是重要的危险因素。 CNS异常是最常见的异常,患病率为(0.9%),其次是胃肠道异常(0.3%)和泌尿道异常(0.3%)。结论:胎儿的预后很大程度上取决于在产前超声上早期发现其任何先天性异常,因为它们可能导致流产,死产和其他胎儿缺陷。因此,产前超声检查是早期发现和处理胎儿异常的非常重要且安全的方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号