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提高超声对孤立性胎儿肢体异常的检测能力。

Improving the ultrasound detection of isolated fetal limb abnormalities.

作者信息

Andrikopoulou Maria, Vahanian Sevan A, Chavez Martin R, Murphy Jean, Hanna Nazeeh, Vintzileos Anthony M

机构信息

a Department of Obstetrics and Gynecology , Winthrop University Hospital , Mineola , NY , USA.

b Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology , Winthrop University Hospital , Mineola , NY , USA.

出版信息

J Matern Fetal Neonatal Med. 2017 Jan;30(1):46-49. doi: 10.3109/14767058.2016.1160048. Epub 2016 Mar 29.

Abstract

OBJECTIVE

The prenatal detection rate of isolated fetal limb abnormalities ranges from 4 to 29.5%. Our aim was to determine the accuracy of a detailed ultrasound protocol in detecting isolated fetal limb abnormalities Methods: This is a retrospective study of infants born at our institution with isolated limb defects from 2009 to 2014. Antepartum and postpartum records were reviewed for genetic testing results. We routinely image both upper and lower extremities, including all long bones, hands, feet, fingers and toes. Posturing, muscular tone and movement are also noted.

RESULTS

During the study period, there were 52 neonates born with isolated fetal limb abnormalities who had received a fetal anatomic survey in our ultrasound unit and 15 930 sonograms performed with normal findings; 36 out of the 52 had been prenatally diagnosed (detection rate 69%). The specificity of the protocol was 100% as there were no false positive cases, the positive predictive value was 100% and negative predictive value 99.8%. Forty-three of 52 neonates had normal genetic testing either prenatally or postnatally; 9 neonates did not undergo genetic testing. The average additional time required for this detailed protocol was <5 min for second trimester sonogram.

CONCLUSION

A minimal investment in time for detailed evaluation of fetal limbs more than doubles the previously reported prenatal detection rate.

摘要

目的

孤立性胎儿肢体异常的产前检出率为4%至29.5%。我们的目的是确定详细超声检查方案在检测孤立性胎儿肢体异常方面的准确性。方法:这是一项对2009年至2014年在我们机构出生的患有孤立性肢体缺陷婴儿的回顾性研究。回顾产前和产后记录以获取基因检测结果。我们常规对上下肢进行成像,包括所有长骨、手、脚、手指和脚趾。同时记录姿势、肌肉张力和活动情况。

结果

在研究期间,有52例出生时患有孤立性胎儿肢体异常的新生儿在我们的超声科室接受了胎儿解剖学检查,共进行了15930次超声检查且结果正常;52例中有36例在产前被诊断出来(检出率69%)。该方案的特异性为100%,因为没有假阳性病例,阳性预测值为100%,阴性预测值为99.8%。52例新生儿中有43例产前或产后基因检测正常;9例新生儿未进行基因检测。孕中期超声检查采用该详细方案平均额外所需时间<5分钟。

结论

对胎儿肢体进行详细评估只需投入极少的时间,就能使先前报道的产前检出率提高一倍多。

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