Diagnosis

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Type & screen performed when   during 1st trimester, include weak D test  
Repeat screening when   20-24 weeks  
If AB screen is positive   must then identify & determine in clinically significant IgG AB  
If IgG AB present   paternal phenotype to determine homo or heterozygous  
IgG AB are   D, E, c, C, K  
Titer clinically significant ABs   titer >32 is significant; 2 tube increase in titer from previous titier is significant; reagent red cells must be of same phenotype form one titer to the next  
Titer clinically significant ABs cont   if initial titer >32, 2nd titer at 18-20 weeks; if titer still >32, then amnio or percutaneous umbilical cord sampling done between 20-24 weeks; 16 or less then repeat monthly at 18-20 weeks  
Amniocentesis & Cordocentesis (PUBS)   performed no later than 24 weeks  
Amniotic fluid   measurement of bilirubin conc. obtained spechtophoto & plotted over time; if conc. increases then hemolysis is worsening  
PUBS   obtained by cannulating umbilical vein using ultrasound  
PUBS cont   blood tested for Hgb, Hct, DAT, checked for NRBCs, allows for direct transfusion  
Intrauterine transfusion   performed mostly by cordocentesis; risk of trauma to placenta may cause increase AB titiers because of antigenic challege to mother from FHM  
Plasma exchange & Intravenous immune globulin   done during 2nd & 3rd trimester; used to delay severe HDN until fetus is large enough for IUT  
Early delivery   not as necessary now with IUT  


   

 
 

 
 

 

 
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