Journal article

Non-invasive risk-assessment and bleeding prophylaxis with IVIG in pregnant women with a history of fetal and neonatal alloimmune thrombocytopenia: management to minimize adverse events


Authors listWienzek-Lischka, Sandra; Sawazki, Angelika; Ehrhardt, Harald; Sachs, Ulrich J.; Axt-Fliedner, Roland; Bein, Gregor

Publication year2020

Pages355-363

JournalArchives of Gynecology and Obstetrics

Volume number302

Issue number2

ISSN0932-0067

eISSN1432-0711

Open access statusHybrid

DOI Linkhttps://doi.org/10.1007/s00404-020-05618-y

PublisherSpringer


Abstract
Introduction In pregnant women with a history of fetal and neonatal alloimmune thrombocytopenia (FNAIT), prenatal intervention in subsequent pregnancies may be required to prevent fetal bleeding. Several invasive and non-invasive protocols have been published: amniocentesis for fetal genotyping, fetal blood sampling for the determination of fetal platelet count, intrauterine platelet transfusions, and weekly maternal i.v. immunoglobulin (IVIG) infusion with or without additional corticosteroid therapy. This is the first retrospective study that report the experience with a non-invasive protocol focused on side effects of maternal IVIG treatment and neonatal outcome. Methods Pregnant women with proven FNAIT in history and an antigen positive fetus were treated with IVIG (1 g/kg/bw) every week. To identify potential IVIG-related hemolytic reactions isoagglutinin titer of each IVIG lot and maternal blood count were controlled. IVIG-related side effects were prospectively documented and evaluated. Furthermore, ultrasound examination of the fetus was performed before starting IVIG administration and continued regularly during treatment. Outcome of the index and subsequent pregnancy was compared. Corresponding data of the newborns were analyzed simultaneously. Results IVIG was started at 20 weeks of gestation (median). Compared to the index pregnancy, platelet counts of the newborns were higher in all cases. No intracranial hemorrhage occurred (Index pregnancies: 1 case). Platelet counts were 187 x 10(9)/l (median, range 22-239, 95% CI) and one newborn had mild bleeding. No severe hemolytic reaction was observed and side effects were moderate. Conclusion Among pregnant women with FNAIT history, the use of non-invasive fetal risk determination and maternal IVIG resulted in favorite outcome of all newborns. Invasive diagnostic or therapeutic procedures in women with a history of FNAIT should be abandoned.



Citation Styles

Harvard Citation styleWienzek-Lischka, S., Sawazki, A., Ehrhardt, H., Sachs, U., Axt-Fliedner, R. and Bein, G. (2020) Non-invasive risk-assessment and bleeding prophylaxis with IVIG in pregnant women with a history of fetal and neonatal alloimmune thrombocytopenia: management to minimize adverse events, Archives of Gynecology and Obstetrics, 302(2), pp. 355-363. https://doi.org/10.1007/s00404-020-05618-y

APA Citation styleWienzek-Lischka, S., Sawazki, A., Ehrhardt, H., Sachs, U., Axt-Fliedner, R., & Bein, G. (2020). Non-invasive risk-assessment and bleeding prophylaxis with IVIG in pregnant women with a history of fetal and neonatal alloimmune thrombocytopenia: management to minimize adverse events. Archives of Gynecology and Obstetrics. 302(2), 355-363. https://doi.org/10.1007/s00404-020-05618-y



Keywords


ADVERSE EVENTSANTENATAL MANAGEMENTFetal and neonatal alloimmune thrombocytopenia (FNAIT)INTRAVENOUS IMMUNOGLOBULIN TREATMENTIVIGNon-invasive bleeding prophylaxis

Last updated on 2025-10-06 at 11:12