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Necrotizing enterocolitis following intrauterine blood transfusion
Journal of Pediatric Surgery, 1991Intravascular intrauterine transfusion allows a more sophisticated and exact approach to the management of severe Rh hemolytic disease. This technique involves direct manipulation of the fetal umbilical vessels; its hazards include umbilical cord trauma and thrombosis or emboli. The consequences of such events in utero are largely unknown. In this case
Catherine A. Musemeche, Marleta Reynolds
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Fetal Diagnosis and Therapy, 2013
Twin anemia-polycythemia sequence (TAPS) is a rare condition which may occur either spontaneously in uncomplicated monochorionic twin pregnancies or may develop after laser treatment in twin-twin transfusion syndrome. TAPS is characterized by a large intertwin discordance in hemoglobin levels without discordance in amniotic fluid levels, and may lead ...
Genova, L.+6 more
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Twin anemia-polycythemia sequence (TAPS) is a rare condition which may occur either spontaneously in uncomplicated monochorionic twin pregnancies or may develop after laser treatment in twin-twin transfusion syndrome. TAPS is characterized by a large intertwin discordance in hemoglobin levels without discordance in amniotic fluid levels, and may lead ...
Genova, L.+6 more
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Neonatal Hepatitis and Excessive Hepatic Iron Deposition Following Intrauterine Blood Transfusion [PDF]
The management of hemolytic disease has undergone a number of significant changes over the past few decades. Intrauterine transfusion therapy, particularly intravascular transfusions, have significantly reduced the morbidity and mortality associated with isoimmunization.
Keith Eddleman+2 more
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Transfusion and Apheresis Science, 2011
We report the case of a 36-year old pregnant woman with a Kell alloimmunization (anti-K1), probably secondary to a previous blood transfusion, and a severe hemolytic disease of the fetus. Once the first fetal blood transfusion by cordocentesis was performed, we started treatment with repeated plasmapheresis to maintain anti-K1 titer below 1:32.
P. Pecos+5 more
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We report the case of a 36-year old pregnant woman with a Kell alloimmunization (anti-K1), probably secondary to a previous blood transfusion, and a severe hemolytic disease of the fetus. Once the first fetal blood transfusion by cordocentesis was performed, we started treatment with repeated plasmapheresis to maintain anti-K1 titer below 1:32.
P. Pecos+5 more
openaire +4 more sources
Maternal Blood Donation for Intrauterine Transfusion [PDF]
Pregnancy affected by erythrocyte alloimmunization often requires intrauterine transfusion for fetal survival. Because blood donated by a random donor has been associated with an increased risk of disease transmission, maternal blood donation has been advocated as an alternative blood source for intrauterine transfusion.
Kenneth J. Moise+3 more
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Fetal Blood Sampling and Intrauterine Transfusion [PDF]
Fetal blood sampling via cordocentesis, alternatively called percutaneous umbilical blood sampling, has improved the accuracy of diagnosis of fetal disorders, including hydrops, neonatal alloimmune thrombocytopenia, and genetic diseases. The ability to access the fetal vasculature allows timely intrauterine treatment, most commonly red blood cell or ...
George R. Saade, Karin A. Fox
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Survey of intrauterine red blood cell (RBC) transfusion practices in the United States
Transfusion, 2022A paucity of data exists about the current practice of fetal red blood cell (RBC) transfusion in the United States (US). This investigation describes intrauterine transfusion (IUT) RBC product selection and processing practices at different US ...
S. Bakhtary+8 more
semanticscholar +1 more source
Journal of pediatric hematology/oncology, 2022
Management of hemolytic disease of the fetus and newborn relies on monitoring of maternal antibody titers, fetal ultrasound, and fetal middle cerebral artery peak systolic velocity studies and is generally treated by intrauterine transfusion (IUT).
Alan J. Lee, A. Leonard, K. Markham
semanticscholar +1 more source
Management of hemolytic disease of the fetus and newborn relies on monitoring of maternal antibody titers, fetal ultrasound, and fetal middle cerebral artery peak systolic velocity studies and is generally treated by intrauterine transfusion (IUT).
Alan J. Lee, A. Leonard, K. Markham
semanticscholar +1 more source
P‐TS‐4 | ABO/Rh‐Type Discrepancy in a Neonate Receiving Intrauterine Transfusion
Transfusion, 2023diagnosis of hemorrhage, hemorrhage-related diagnosis (GI bleed/trauma with signs of hemorrhage) or an admission hemoglobin of
N. Donahue, K. Krum
semanticscholar +1 more source
Pediatric Blood & Cancer, 2023
To the Editor: Hyperhemolysis syndrome (HS) is among the most feared transfusion complications in sickle cell disease (SCD). HS manifests with destruction of both transfused and recipient red blood cells (RBCs), profound anemia below the pre-transfusion ...
E. Abels+5 more
semanticscholar +1 more source
To the Editor: Hyperhemolysis syndrome (HS) is among the most feared transfusion complications in sickle cell disease (SCD). HS manifests with destruction of both transfused and recipient red blood cells (RBCs), profound anemia below the pre-transfusion ...
E. Abels+5 more
semanticscholar +1 more source