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Rh disease (also known as rhesus isoimmunization, Rh (D) disease, or rhesus incompatibility, and blue baby disease) is a type of hemolytic disease of the fetus and newborn (HDFN). HDFN due to anti-D antibodies is the proper and currently used name for this disease as the Rh blood group system actually has more than 50 antigens and not only the ...
Front cover of a PCHR from the late 1990s. The paper based child health record as used by the UK National Health Service [1] is popularly known as the "Red Book." It is given to the parents on or just after the birth of their child, and is used by parents to record standard health details such as height and weight as well as developmental milestones such as first words and first time walking. [2]
One study done by Moran et al., found that titers are not reliable for anti-E. Their most severe case of hemolytic disease of the newborn occurred with titers 1:2. Moran states that it would be unwise routinely to dismiss anti-E as being of little clinical consequence.
the Queensland Children's Early Warning Tool (Q-CEWT), which has variations depending on the specific child's age, the Queensland Neonatal Early Warning Tool (Q-NEWT). Q-ADDS was developed as a research project by the University of Queensland for Queensland Health to standardise 25 existing observation charts.
Individuals with a positive RhD status have RhD antigens expressed on the cell membrane of their red blood cells, whereas Rhesus D antigens are absent for individuals with a negative RhD status. Rhesus factor testing is usually performed on pregnant women to determine the RhD blood group of the mother and the fetus.
The name rhesus factor (Rh) goes back to the use of erythrocytes extracted from the blood of rhesus monkeys for obtaining the first blood serum. The Rh blood group system is a human blood group system. It contains proteins on the surface of red blood cells. After the ABO blood group system, it is most likely to be involved in transfusion reactions.
A rise in the retic count can mean that an infant may not need additional transfusions. [33] Low retic is observed in infants treated with IUT and in those with HDN from anti-Kell. [13] Neutrophils - as Neutropenia is one of the complications of HDN, the neutrophil count should be checked. [5] [6]
A rise in the reticulocyte count can mean that an infant may not need additional transfusions. [18] Low reticulocyte count is observed in infants treated with IUT and in those with HDN from anti-Kell [16] Neutrophils - as Neutropenia is one of the complications of HDN, the neutrophil count should be checked. [9] [10]