Prediction of fetal anemia in pregnancies with red-cell alloimmunization: comparison of middle cerebral artery peak systolic velocity and amniotic fluid OD450
Authors: Bullock, R.1; Martin, W. L.1; Coomarasamy, A.1; Kilby, M. D.1
Source: Ultrasound in Obstetrics and Gynecology, Volume 25, Number 4, April 2005 , pp. 331-334(4)
Publisher: John Wiley & Sons, Ltd.
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Abstract:
ObjectiveTo compare the accuracy of Doppler velocimetry (middle cerebral artery peak systolic velocity, MCA-PSV) and amniocentesis (amniotic fluid delta optical density 450 (OD450)) for the detection of fetal anemia against the gold standard of fetal blood sampling (FBS).MethodsThirty-eight pregnancies were identified to be at risk of fetal anemia from immune causes between January 2000 and May 2002. In a cross-sectional diagnostic accuracy study, MCA-PSV and amniotic fluid delta OD450 values were plotted on reference charts and compared to an FBS obtained within the subsequent 7 days. Receiveroperating characteristics (ROC) curves were used and the area under the curve (AUC) calculated to compare the overall accuracy of the two tests. Sensitivity, specificity and likelihood ratios for positive (LR+) and negative (LR-) test results were generated for specific thresholds of MCA-PSV and delta OD450.ResultsFor MCA-PSV (n = 38), the AUC was 0.71 (95% CI 0.570.85) and for amniotic fluid delta OD450 (n = 22) it was 0.68 (95% CI 0.490.87) compared with FBS within 7 days. Sensitivity, specificity and LR+, LR- for MCA-PSV were 64%, 81%, 3.4 and 0.5, respectively, and 53%, 71%, 1.9 and 0.7 for amniotic fluid OD450, respectively.ConclusionMCA-PSV and OD450 have similar test accuracy in detecting fetal anemia. MCA-PSV is non-invasive and therefore presents no risk of miscarriage or preterm labor and thus is a preferable method of screening for fetal anemia. Copyright © 2005 ISUOG. Published by John Wiley & Sons, Ltd.Keywords: fetal anemia; MCA Doppler; non-invasive monitoring; rhesus disease
Document Type: Research article
DOI: 10.1002/uog.1886
Affiliations: 1: Division of Reproductive and Child Health, Birmingham Women's Hospital, Birmingham, UK
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