期刊
TRANSFUSION MEDICINE AND HEMOTHERAPY
卷 48, 期 5, 页码 306-315出版社
KARGER
DOI: 10.1159/000518782
关键词
Hemolytic disease of fetus and newborn; Alloimmunization; Cell-free DNA; Middle cerebral artery; Peak systolic velocity; Next-generation sequencing
The laboratory monitoring of mother, fetus, and newborn in hemolytic disease of fetus and newborn at Copenhagen University Hospital in Denmark involves screening and testing measures for pregnant women, including Rh typing and antibody screening, with preventive measures such as Rh immunoglobulin for RhD-negative pregnant women.
Background: Laboratory monitoring of mother, fetus, and newborn in hemolytic disease of fetus and newborn (HDFN) aims to guide clinicians and the immunized women to focus on the most serious problems of alloimmunization and thus minimize the consequences of HDFN in general and of anti-D in particular. Here, we present the current approach of laboratory screening and testing for prevention and monitoring of HDFN at the Copenhagen University Hospital in Denmark. Summary: All pregnant women are typed and screened in the 1st trimester. This serves to identify the RhD-negative pregnant women who at gestational age (GA) of 25 weeks are offered a second screen test and a non-invasive fetal RhD prediction. At GA 29 weeks, and again after delivery, non-immunized RhD-negative women carrying an RhD-positive fetus are offered Rh immunoglobulin. If the 1st trimester screen reveals an alloantibody, antenatal investigation is initiated. This also includes RhD-positive women with alloantibodies. Specificity and titer are determined, the fetal phenotype is predicted by non-invasive genotyping based on cell-free DNA (RhD, K, Rhc, RhC, RhE, ABO), and serial monitoring of titer commences. Based on titers and specificity, monitoring with serial peak systolic velocity measurements in the fetal middle cerebral artery to detect anemia will take place. Intrauterine transfusion is given when fetal anemia is suspected. Monitoring of the newborn by titer and survival of fetal red blood cells by flow cytometry will help predict the length of the recovery of the newborn.
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