Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Nov-Dec;41(6):313-317.
doi: 10.5144/0256-4947.2021.313. Epub 2021 Dec 2.

Complications of intravascular intrauterine transfusion for Rh alloimmunization

Affiliations

Complications of intravascular intrauterine transfusion for Rh alloimmunization

Asma Alkhaibary et al. Ann Saudi Med. 2021 Nov-Dec.

Abstract

Background: Intravascular intrauterine transfusion (IUT) is considered a safe procedure, but complications still occur, including fatalities.

Objective: Review the outcomes of Rh alloimmunization, including indications and possible complications.

Design: Retrospective cohort (medical record review).

Setting: Tertiary care center.

Patients and methods: We retrieved the records for all mothers who had an IUT for Rh alloimmunization between January 2009 and August 2019. We collected data on complications, post-transfusion hemoglobin and antibody combinations.

Main outcome measure: Complications of IUT.

Sample size: 119 mothers with 154 fetuses (154 different pregnancies).

Results: The 154 fetuses had 560 intrauterine transfusions. The median pre-IUT hemoglobin was a median of 8.0 g/dL while the median post-IUT hemoglobin 16 g/dL. Immediate procedure-related complications included fetal bradycardia in 2.7%, significant bleeding from the cord puncture site (for more than 2 minutes in 0.9%), and contractions in 0.9%. Eight (5.2%) were delivered by cesarean delivery due to IUT-specific complications such as post-procedure fetal bradycardia. Intrauterine fetal death complicated 8.4% of the pregnancies (13 fetuses). Phototherapy was required in 76 (49.4%), postnatal blood transfusions in 17 (11%), and exchange transfusion in 11 (7.1%). Neonatal death occurred 8 (5.2%). Data were insufficient to assess associations of complications with antibody combinations.

Conclusions: Intrauterine transfusion is an effective treatment with high survival rates (around 90% for cases of Rh alloimmunization).

Limitations: Case series.

Conflict of interest: None.

PubMed Disclaimer

Figures

None
Graphical abstract
Figure 1.
Figure 1.
Percentage of antibody combinations requiring intrauterine transfusion.

References

    1. Kumar S, Regan F.. Management of pregnancies with RhD alloimmunization. Br Med J. 2005. May 28;330(7502):1255–1258. - PMC - PubMed
    1. Liley AW:. Intrauterine transfusion of foetus in haemolytic disease. Br Med J. 1963. Nov 2; 2(5365):1107–1109. - PMC - PubMed
    1. Rodeck CH, Nicolaides KH, Warsof SL, Fysh WJ, Gamsu HR, Kemp JR.. The management of severe rhesus isoimmunization by fetoscopic intravascular transfusion. Am J Obstet Gynecol. 1984;150:769–774. - PubMed
    1. Nicolini U, Nicolaidis P, Fisk NM, Tannirandorn Y, Rodeck CH.. Fetal blood sampling from the intrahepatic vein: analysis of safety and clinical experience with 214 procedures. Obstet Gynecol. 1990;76:47–53. - PubMed
    1. van Kamp IL, Klumper FJ, Oepkes D, Meerman RH, Scherjon SA, Vandenbussche FP, Kanhai HH.. Complications of intrauterine intravascular transfusion for fetal anemia due to maternal red-cell alloimmunization. Am J Obstet Gynecol. 2005;192:171–177. - PubMed