A personalized approach to the treatment of newborns with Rh factor hemolytic disease who underwent intrauterine hemotransfusion
https://doi.org/10.21508/1027-4065-2026-71-3-26-33
Abstract
The widespread use of intrauterine blood transfusions to correct severe anemia associated with Rh-related hemolytic disease of the fetus and newborn significantly impacts the preand postnatal presentation of the disease, complicating the assessment of its severity and the selection of treatment methods. Objective . To define a personalized approach to treating newborns with Rh-related hemolytic disease who have undergone intrauterine blood transfusions, based on clinical and laboratory parameters and treatment outcomes. Materials and Methods . 92 newborns born between 28–38 weeks with Rh-related hemolytic disease (ICD-10: P55.0) were examined. They were divided into three groups based on the frequency of intrauterine blood transfusions. Group 1 consisted of 42 infants who had received one blood transfusion, Group 2 included 38 infants who had received two blood transfusions, and Group 3 included 12 infants who had received three or more blood transfusions. Results . Fetal hemoglobin levels and the incidence of a positive Coombs test significantly decreased with increasing frequency of intrauterine blood transfusions ( p <0.05). Reticulocyte levels were lower in Group 3 infants compared to Groups 1 and 2 ( p <0.05). The rate of exchange transfusions did not differ statistically between groups, ranging from 42.8% to 50%. Red blood cell replacement transfusions were administered to a third of the children in Group 3, 5.3% in Group 2, and 19.1% in Group 1, with statistically significant differences between Groups 2 and 3 ( p =0.023). Fatal outcomes occurred only in Group 3 and were due to the development of cardiovascular failure during the exchange transfusion. Conclusions . A personalized approach to treating newborns with Rh-specific hemolytic disease requires consideration of risk factors for postnatal immune hemolysis, including the direct Coombs test, fetal hemoglobin levels, and reticulocyte counts.
About the Authors
I. I. BocharovaRussian Federation
129110, Moscow
101000, Moscow
M. N. Shakaya
Russian Federation
129110, Moscow
A. A, Yakubina
Russian Federation
129110, Moscow
L. A. Dalnikovskaya
Russian Federation
129110, Moscow
S. V. Novikova
Russian Federation
129110, Moscow
101000, Moscow
E. N. Ilyashenko
Russian Federation
129110, Moscow
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Review
For citations:
Bocharova I.I., Shakaya M.N., Yakubina A.A., Dalnikovskaya L.A., Novikova S.V., Ilyashenko E.N. A personalized approach to the treatment of newborns with Rh factor hemolytic disease who underwent intrauterine hemotransfusion. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 2026;71(3):26-33. (In Russ.) https://doi.org/10.21508/1027-4065-2026-71-3-26-33
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