Home Tag Cholestasis

Articles in Cholestasis

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Uses of Uruso
Uruso drug is made in the form of tablets, the main ingredient is Ursodeoxycholic acid. The drug is used in the treatment of gallstones and to improve liver function.
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Uses of Phytomenadione
Phytomenadione is a medicine belonging to the group of minerals and vitamins. The main ingredient of the medicine is Phytomenadione - a type of vitamin K, prepared in the form of an injectable solution, 10mg/1ml tube. The following article will help you better understand the uses and how to use Phytomenadione properly.
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USES OF TRANSMETIL
Transmetil is a drug that treats the symptoms of cholestasis in cirrhosis, pre-cirrhosis, especially in pregnant women and symptoms of depression. The drug is prepared in the form of enteric-coated tablets, box of 1 blister x 10 tablets. Understanding the effects as well as following the correct indications and dosage of Transmetil will help patients use the drug effectively and safely.
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The "golden" phase of treatment of biliary atresia in infants
Congenital biliary atresia is a rare disease of the liver and biliary tract, characterized by disruption or deficiency of the extrahepatic biliary system, causing obstruction of bile flow. Due to misdiagnosis and late detection, many infants are missed the golden opportunity to have surgery to treat the disease. So when is the best time to treat congenital biliary atresia?
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Distinguish between physiological jaundice and jaundice due to biliary atresia in neonates
Physiological jaundice is a common sign in newborns, caused by broken red blood cells and incomplete liver function of bilirubin metabolism. However, jaundice due to biliary atresia can cause serious complications and leave mental sequelae, even leading to death.
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How is biliary atresia diagnosed?
Congenital biliary atresia is a rare disease of the liver and biliary tract that results from an unexplained inflammatory process that destroys the intrahepatic and extrahepatic bile ducts, impeding the outflow of bile. leading to fibrosis, biliary obstruction and progression of cirrhosis.
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Causes and symptoms of biliary atresia
Congenital biliary atresia is a fairly rare disease of the liver and bile, appearing due to many causes such as bacterial infections, viruses, environmental factors or abnormalities in pregnancy, ...
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Treatment methods for biliary atresia
Biliary atresia is a disease characterized by an obstruction in the flow of bile from the liver to the duodenum (small intestine), which can lead to many dangerous complications such as liver abscess, cirrhosis, liver failure or even is death. Treatment of congenital biliary atresia by surgery is an effective method to treat the disease, reducing the risk of complications.
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Nutrition after treatment for congenital biliary atresia
Biliary atresia in infants is a pathology that causes cholestatic jaundice in young children, if not treated early, it can lead to bad complications such as cirrhosis, liver failure and death. The only treatment for congenital biliary atresia is surgery. Treatment after surgery with care and nutritional supplements is focused to avoid future complications for the child.
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Distinguishing congenital biliary atresia from physiological jaundice, anemia, hepatitis
Jaundice in newborns is a manifestation of one of the diseases such as anemia, hepatitis or physiological jaundice or even congenital biliary atresia. The distinction between these diseases is to determine the direction of treatment for the child.
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Complications after surgery for congenital biliary atresia
Congenital biliary atresia is considered a rare pathology of the liver and biliary tract, characterized by disruption or deficiency of the extrahepatic biliary system, resulting in obstruction of bile flow.
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Cardiology Pediatrics Orthopedics