Results 41 to 50 of about 190,669 (229)
Objective: To describe serious hemodynamic changes secondary to anemia in the case of restrictive foramen ovale (FO). Case: A 43-year-old pregnant woman, G4P0030, underwent fetal echocardiography at 35 weeks of gestation and was found to have (1 ...
Suchaya Luewan+3 more
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Objective We present a case of fetal severe anemia associated with Jra alloimmunization, which was managed using Doppler measurement of the peak systolic velocity of the fetal middle cerebral artery (MCA-PSV) and intrauterine transfusion (IUT) of Jr(a ...
Masatake Toshimitsu+4 more
openalex +2 more sources
Plasmapheresis for the Treatment of Anti-M Alloimmunization in Pregnancy
Intrauterine transfusion is the standard antenatal treatment for a fetus with severe anemia. Plasmapheresis is an alternative treatment for cases with a history of severe hemolytic disease of the fetus and newborns at less than 20 weeks of gestation ...
Yohei Maki+6 more
doaj +1 more source
INTRODUCTION This case report traces the diagnostic and therapeutic process of the Immuno-Transfusion Service in a case of fetal anaemia characterized by various inconsistencies between clinical and laboratory data.
Eleonora Donno+11 more
doaj +1 more source
Background Intrauterine blood transfusions (IUBTs) are critical for treating fetal anemia but may expose fetuses to toxic metals. This study assessed mercury (Hg), cadmium (Cd), lead (Pb), and arsenic (As) levels in red blood cell (RBC) transfusion bags ...
Iman Al‐Saleh+4 more
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The selection and preparation of red cell components for intrauterine transfusion: A national survey
The practice regarding the selection and preparation of red blood cells (RBCs) for intrauterine transfusion (IUT) is variable reflecting historical practice and expert opinion rather than evidence‐based recommendations.
Melanie Bodnar+12 more
semanticscholar +1 more source
Foetal Haemoglobin as a Marker of Bone Marrow Suppression Secondary to Anti-Kell Alloimmunisation
Anti-Kell alloimmunisation is a potentially severe minor blood group type incompatibility, not only as a cause of haemolytic disease of the foetus and newborn, but also due to the destruction of red blood cells (RBC) and mature form in the bone marrow ...
Rodrigo Alfredo Morales Painamil+7 more
doaj +1 more source
Severe hereditary spherocytosis presenting with non-immune fetal hydrops
Background: Hereditary spherocytosis (HS) is characterized by spherocytes on the peripheral smear and heterogeneous clinical presentation (mild, moderate, moderate/severe, and severe) depending upon the severity of hemolytic anemia, jaundice, and ...
Snehal Mallakmir+3 more
doaj +1 more source
The aim of our study was to evaluate the middle cerebral artery velocimetry before and after intrauterine blood transfusion in immune hydrops fetalis.
Ahmet Yalınkaya+5 more
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Twin Anemia Polycythemia Sequence: Knowledge and Insights After 15 Years of Research
. Twin anemia polycythemia sequence (TAPS) is a chronic form of unbalanced feto-fetal transfusion through minuscule placental anastomoses in monochorionic twin pregnancies, leading to anemia in the donor twin and polycythemia in the recipient twin.
Lisanne S.A. Tollenaar+8 more
doaj +1 more source