Sensitivity of fetal RHD screening for safe guidance of targeted anti-D immunoglobulin prophylaxis: prospective cohort study of a nationwide programme in the Netherlands

BMJ. 2016 Nov 7:355:i5789. doi: 10.1136/bmj.i5789.

Abstract

Objective: To determine the accuracy of non-invasive fetal testing for the RHD gene in week 27 of pregnancy as part of an antenatal screening programme to restrict anti-D immunoglobulin use to women carrying a child positive for RHD DESIGN: Prospectively monitoring of fetal RHD testing accuracy compared with serological cord blood typing on introduction of the test. Fetal RHD testing was performed with a duplex real time quantitative polymerase chain reaction, with cell-free fetal DNA isolated from 1 mL of maternal plasma The study period was between 4 July 2011 and 7 October 2012. The proportion of women participating in screening was determined.

Setting: Nationwide screening programme, the Netherlands. Tests are performed in a centralised setting.

Participants: 25 789 RhD negative pregnant women.

Main outcome measures: Sensitivity, specificity, false negative rate, and false positive rate of fetal RHD testing compared with serological cord blood typing; proportion of technical failures; and compliance to the screening programme.

Results: A fetal RHD test result and serological cord blood result were available for 25 789 pregnancies. Sensitivity for detection of fetal RHD was 99.94% (95% confidence interval 99.89% to 99.97%) and specificity was 97.74% (97.43% to 98.02%). Nine false negative results for fetal RHD testing were registered (0.03%, 95% confidence interval 0.01% to 0.06%). In two cases these were due to technical failures. False positive fetal RHD testing results were registered for 225 samples (0.87%, 0.76% to 0.99%). Weak RhD expression was shown in 22 of these cases, justifying anti-D immunoglobulin use. The negative and positive predictive values were 99.91% (95% confidence interval 99.82% to 99.95%) and 98.60% (98.40% to 98.77%), respectively. More than 98% of the women participated in the screening programme.

Conclusions: Fetal RHD testing in week 27 of pregnancy as part of a national antenatal screening programme is highly reliable and can be used to target both antenatal and postnatal anti-D immunoglobulin use.

Publication types

  • Comparative Study

MeSH terms

  • DNA / isolation & purification
  • Female
  • Fetal Blood / chemistry
  • Humans
  • Netherlands
  • Predictive Value of Tests
  • Pregnancy
  • Pregnancy Complications, Hematologic / blood
  • Prenatal Diagnosis*
  • Prospective Studies
  • Real-Time Polymerase Chain Reaction
  • Rh Isoimmunization / diagnosis*
  • Rh Isoimmunization / genetics
  • Rh Isoimmunization / therapy
  • Rh-Hr Blood-Group System / genetics*
  • Rho(D) Immune Globulin / administration & dosage
  • Rho(D) Immune Globulin / genetics
  • Sensitivity and Specificity

Substances

  • Rh-Hr Blood-Group System
  • Rho(D) Immune Globulin
  • DNA