Positive red cell antibody screen (red cell alloimmunisation) in a pregnant woman
BioMG follows French guidelines. Adapt it to the guidelines and the tests available where you practise.
Positive antibody screen in pregnancy: identify, quantify, refer
- State on the prescription: gestational age, RhD group, anti-D immunoglobulin injection (date, dose), previous transfusions.
Immunohaematology tests (if the laboratory has not already done them)
- Antibody identification
- Titration of the identified antibody
- Quantification of the antibody (anti-D, anti-c, anti-E, anti-Kell…)if neededAntibodies that can cause major fetomaternal incompatibility (anti-D, anti-c, anti-E, anti-Kell, etc.): quantification by antibody level, not combinable with titration under the fee schedule [2]; for anti-D, the SFTS recommends quantification techniques beyond standard titration [3].
- RH-Kell phenotype of the partner (antigen targeted by the antibody: c, E, Kell…)if neededRisk antibody other than anti-D: fetomaternal incompatibility is excluded only if the partner does not carry the antigen; if he carries it in the heterozygous state, doubt persists [4]. As long as the partner's phenotype or the fetal genotype is not informative, the pregnancy is monitored as incompatible [4].
- Fetal RhD genotyping on maternal blood (RhD-negative woman, from 11 weeks of gestation)if neededRhD-negative woman whose partner is RhD positive or of unknown group; a negative or indeterminate result is checked on a second sample, at least 15 days later and after 15 weeks [2,5].
- Fetal C, c, E or Kell genotyping on maternal blood (if anti-c, anti-E or anti-Kell with a heterozygous partner or one of unknown phenotype)if needednon-French guidelineRisk antibody other than anti-D, with a heterozygous partner or one of unknown phenotype: as long as this result is missing, the pregnancy is monitored as incompatible; the technique is available in France for C, c, E and Kell [4]. The Netherlands (2025) prefers it to the father's phenotype for anti-c and anti-Kell, and the UK (2025) proposes it [6,7]. In France, it has no fee-schedule code apart from RhD [2], and the expert centre following the pregnancy can arrange it.
- Partner's RhD blood group (if he has no blood group card)if neededRhD-negative woman: the partner's RhD group is to be documented; if he has no blood group card, prescribe it [5].
Do not order
- Concluding oneself that it is "passive anti-D" after an anti-D immunoglobulin injection, without identification or quantification: any positive irregular antibody screen during pregnancy requires identification and titration [8], and the SFTS recommends for anti-D quantification techniques beyond standard titration, with an interpretive comment from the laboratory specialist [3].
- Irregular antibody screen to look for anti-A or anti-B antibodies: they are excluded from the regulatory irregular antibody screen of pregnancy [8].
Sources (15)
- Laget L, Cortey A. Suivi immuno-hématologique des femmes enceintes. La Revue du Praticien. 2018;68(5):541-6.
- Assurance maladie. Nomenclature des actes de biologie médicale (NABM), version 105 : actes 1131, 1141, 1149, 1150 (RAI) et 4085, 4086 (génotypage RHD fœtal).
- Toly-Ndour C, Piccione E, Magdelaine C, et al.; groupe de travail Allo-immunisation fœtomaternelle anti-érythrocytaire de la Société francophone de transfusion sanguine (SFTS). Recommandations pour la prise en charge immuno-hématologique de la grossesse. Transfus Clin Biol. 2026 (en ligne le 25 août 2026).
- Laget L, Cortey A. Suivi immuno-hématologique des femmes enceintes. Rev Prat. 2018;68(5):541-546.
- Collège national des gynécologues et obstétriciens français (CNGOF). Prévention de l'allo-immunisation Rhésus D chez les patientes de groupe Rhésus D négatif. Mise à jour de décembre 2017 des RPC du CNGOF de 2005.
- Nederlandse Vereniging voor Obstetrie en Gynaecologie (NVOG). Kwaliteitsnorm Erytrocytenimmunisatie in de zwangerschap, 17 juin 2025.
- Australian Red Cross Lifeblood. British Society for Haematology (BSH) « Guideline for the investigation and management of red cell antibodies in pregnancy », 28 mai 2025. Résumé de : Regan F, Veale K, Robinson F, et al. Transfus Med. 2025;35(1):3-23 (PMID 39912875).
- Code de la santé publique, article R2122-2 (examens prénataux obligatoires), version en vigueur (décret n° 2003-462 du 21 mai 2003).
- Toly-Ndour C, Mourtada H, Huguet-Jacquot S, Maisonneuve E, Friszer S, Pernot F, et al. Clinical input of anti-D quantitation by continuous-flow analysis on autoanalyzer in the management of high-titer anti-D maternal alloimmunization. Transfusion. 2018;58(2):294-305.
- Ghesquière L, Leroy J, Deken V, Tournier A, Vaast P, Subtil D, et al. Anti-RH1 alloimmunization: at what maternal antibody threshold is there a risk of severe fetal anemia? Transfusion. 2023;63(3):629-637.
- Franchinard L, Maisonneuve E, Friszer S, Toly Ndour C, Huguet-Jacquot S, Maurice P, et al. Perinatal risk factors associated with severity of haemolytic disease of the foetus and newborn due to Rhc maternal-foetal incompatibility: a retrospective cohort study. Vox Sang. 2022;117(4):570-579.
- Mustafa HJ, Sambatur EV, Shamshirsaz AA, Johnson S, Moise KJ Jr, Baschat AA, et al. Monitoring and management of hemolytic disease of the fetus and newborn based on an international expert Delphi consensus. Am J Obstet Gynecol. 2025;232(3):280-300.
- Gemeinsamer Bundesausschuss (G-BA). Richtlinie über die ärztliche Betreuung während der Schwangerschaft und nach der Geburt (Mutterschafts-Richtlinie), version du 21 septembre 2023, dernière modification du 16 juillet 2026, en vigueur depuis le 25 août 2026.
- Worcestershire Acute Hospitals NHS Trust. Obstetric Pathway: Pregnant Women with Red Cell Antibodies (WAHT-TP-094), approuvé le 15 novembre 2019. Protocole hospitalier local, appliquant les recommandations britanniques antérieures à celle de 2025.
- American College of Obstetricians and Gynecologists. ACOG Clinical Practice Update: Paternal and Fetal Genotyping in the Management of Alloimmunization in Pregnancy. Obstet Gynecol. 2024;144(2):e47-e49.