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Isolated fetal pyelectasis and the risk of Down syndrome: a meta‐analysis
Author(s) -
Orzechowski K. M.,
Berghella V.
Publication year - 2013
Publication title -
ultrasound in obstetrics and gynecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.202
H-Index - 141
eISSN - 1469-0705
pISSN - 0960-7692
DOI - 10.1002/uog.12516
Subject(s) - medicine , obstetrics , meta analysis , fetus , trisomy , pregnancy , aneuploidy , gynecology , biology , chromosome , biochemistry , genetics , gene
Objectives We performed a meta‐analysis to examine the performance of second‐trimester (14–24 weeks' gestation) isolated fetal pyelectasis as a marker for trisomy 21 and to calculate its associated weighted pooled likelihood ratios . Methods PubMed , Ovid MEDLINE and Cochrane databases were searched using the terms ‘pyelectasis’ and ‘pelviectasis’. Studies were included if fetuses with isolated pyelectasis were reported separately from fetuses with other soft markers of aneuploidy and/or structural anomalies and if knowledge of the fetal karyotype was unknown at the time of ultrasound examination . Results Individual study statistics were pooled as weighted positive and negative likelihood ratios with 95% CIs , using a random‐effects model. Ten observational studies were included (2148 cases of isolated pyelectasis). Isolated fetal pyelectasis was defined in seven out of 10 studies as a renal pelvis anteroposterior diameter of ≥ 4 mm. Isolated fetal pyelectasis was associated with pooled positive and negative likelihood ratios of 2.78 (95% CI , 1.75–4.43) and 0.99 (95% CI , 0.98–1.00), respectively . Conclusions The detection of isolated fetal pyelectasis on mid‐trimester ultrasound is associated with an increased likelihood of trisomy 21. If the finding of isolated fetal pyelectasis is used to adjust the trisomy 21 risk from maternal serum screening tests, a positive likelihood ratio of 2.78 should be used in the calculation. Copyright © 2013 ISUOG. Published by John Wiley & Sons Ltd .

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