The Norwegian experience with nationwide implementation of fetal RHD genotyping and targeted routine antenatal anti‐D prophylaxis. Issue 5 (5th April 2021)

• Record Type: Journal Article
• Authors: Sørensen, Kirsten; Bævre, Mette S.; Tomter, Geir; Llohn, Abid Hussain; Hagen, Kristin G.; Espinosa, Aurora; Jacobsen, Barbora; Arsenovic, Mirajana Grujic; Sørvoll, Ingvild Hausberg; Ulvahaug, Aud Norunn; Sundic, Tatjana; Akkök, Çiğdem Akalın
• Is Part Of: Transfusion medicine. Volume 31:Issue 5(2021)
• Page Start: 314
• Page End: 321
• Publication Date: 2021-04-05
• Subjects: Blood -- Transfusion -- Periodicals; 615.39
• DOI: 10.1111/tme.12772
• Languages: English
• ISSNs: 0958-7578

Abstract

Abstract: Objectives: To reduce the risk of RhD alloimmunization during the last trimester of pregnancy, a targeted routine antenatal anti‐D prophylaxis (RAADP) programme was implemented in Norway in 2016. Here, we present and discuss our experience with the nationwide implementation of the programme, and report sample uptake and preliminary data of de novo anti‐D in pregnancy. Background: The targeted RAADP was advised by the academic community and evaluated by the health authorities. A National Working Group has conducted the implementation in the transfusion services and contributed to organise the administration of the antenatal anti‐D prophylaxis. Fetal RhD type is determined by non‐invasive prenatal testing at gestational week 24, and anti‐D prophylaxis is administrated at gestational week 28 only to women with RhD positive fetuses. Methods: We describe the implementation process of targeted RAADP in Norway. The sample uptake is calculated by comparing the number of fetal RHD screens with the expected number of samples. Results: The sample uptake shows regional variations: 88%–100% after 3 years. Promising decrease in de novo anti‐D detected during pregnancy is observed. Conclusions: Nationwide targeted RAADP is implemented and included in the Norwegian maternity care programme. Compliance to sample uptake should further improve in some regions. A remaining issue to fulfil is the documentation of the accuracy of the fetal RHD ‐typing at all sites. Post‐natal prophylaxis will then be guided by the fetal RHD result. Dedicated registries will ensure data to evaluate the expected reduction in pregnancy‐related RhD immunisations, which is the final success criterion of the programme.