Hello everyone, thank you for the invitation. Today I will share with you the problem of neonatal hemolytic disease and some confusions about newborn babies suffering from hemolytic disease. If you are not familiar with it yet If you understand, it doesn’t matter, because I will share it with you next. I hope it can help everyone and solve everyone’s problems. Let’s get started!
Contents of this article
- Is neonatal hemolytic disease a genetic disease
- What does a complete set of hemolytic tests include
- What will happen to children with hemolytic >
- What should I do if my newborn baby has hemolytic disease***
1. Neonatal hemolytic disease is a genetic disease
It is not a genetic disease. Genetic diseases refer to abnormalities in the genetic material of parents, which are manifested in the process of gestating the next generation, resulting in a series of clinical manifestations of the disease. The common cause of neonatal hemolytic disease is that the mother and fetus have different blood types. The fetus\’s blood type antigens enter the mother\’s body through the placenta, produce antibodies, and then enter the fetus\’ body to produce an antigen-antibody reaction, resulting in a disease in which red blood cells are massively destroyed.
2. What does the full set of hemolysis examinations include
Hemolysis examination items include , 1. Routine blood tests, such as a decrease in red blood cells and hemoglobin, and an increase in peripheral blood nucleated red blood cells, all indicate that hemolysis may occur. Second, serum bilirubin, mainly unconjugated bilirubin, increases. Dynamic changes in bilirubin levels in patients with hemolytic jaundice. 3. Blood type, A, B, oxygen hemolytic disease, the mother is oxygen type, and the newborn is type A or B.
3. What will happen to children with hemolytic disease
Hemolytic disease in newborn babies Various symptoms may occur, the most common of which are jaundice, hepatosplenomegaly, and anemia. Mild symptoms progress slowly and have little impact on the general condition. Severe cases progress quickly, leading to lethargy, anorexia, and even bilirubin encephalopathy or death. Most newborns will develop jaundice after birth, but when jaundice appears too early, the onset is too fast, longer than 24 hours or on the second day, hemolysis may occur.
4. What to do if a newborn baby has hemolytic disease***
Infant hemolytic disease should be something that parents need to pay attention to during a pre-marital physical examination On the other hand, this situation should be considered to be caused by RH type hemolysis. Hemolytic disease of newborns often causes pathological jaundice. First, hormones are used to prevent the reaction of antigens and antibodies, and then the disease cells are removed. For jaundice, light therapy is used, and the baby is allowed to spend more time in the sun after discharge. Just bask in the sun and breastfeed on time.
This is the end of my sharing on neonatal hemolytic disease and hemolytic disease in newborn babies. We\’d be delighted if your issue was resolved.
