Seminars in Hematology
Volume 42, Issue 3 , Pages 169-178, July 2005

Red Blood Cell Alloimmunization in Pregnancy

  • Kenneth J. Moise Jr

      Affiliations

    • Corresponding Author InformationAddress correspondence to Kenneth J. Moise Jr, MD, Director, Division of Maternal-Fetal Medicine, University of North Carolina School of Medicine, 214 MacNider Bldg CB#7516, Chapel Hill, NC 27599-7516

Division of Maternal-Fetal Medicine, University of North Carolina School of Medicine, Chapel Hill, NC

Red blood cell (RBC) alloimmunization in pregnancy continues to occur despite the widespread use of both antenatal and postpartum Rhesus immune globulin (RhIG), due mainly to inadvertent omissions in administration as well as antenatal sensitization prior to RhIG given at 28 weeks’ gestation. Additional instances are attributable to the lack of immune globulins to other RBC antigens. Evaluation of the alloimmunized pregnancy begins with the maternal titer. Once a critical value [32 for anti-Rh(D) and other irregular antibodies; 8 for anti-K and –k] is reached, fetal surveillance using serial Doppler ultrasound measurements of the peak velocity in the fetal middle cerebral artery (MCA) is standard. In the case of a heterozygous paternal phenotype, amniocentesis can be performed to detect the antigen-negative fetus that requires no further evaluation. MCA velocities greater than 1.5 multiples of the median necessitate cordocentesis, and if fetal anemia is detected, intrauterine transfusion therapy is initiated. A perinatal survival of greater than 85% with normal neurologic outcome is now expected. Future therapies will target specific immune manipulations in the pregnant patient.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0037-1963(05)00060-0

doi:10.1053/j.seminhematol.2005.04.007

Seminars in Hematology
Volume 42, Issue 3 , Pages 169-178, July 2005