Obstetric cholestasis is a complication of pregnancy in which pregnancy hormones affect the liver. Cholestasis is a condition where bile cannot flow from the liver to the duodenum. Progressive familial intrahepatic cholestasis type 2 orphanet. Increased susceptibility for intrahepatic cholestasis of. Tabular list of icd10 codes that describe conditions which may be causes of death underlying.
Intrahepatic cholestasis of pregnancy icp is a pregnancyspecific disorders that occurs mainly in the third trimester of pregnancy and is characterized by pruritus and elevated bile acid levels. Learn more about this condition, including its risk factors, symptoms, diagnosis, treatment, and. Click on the image or right click to open the source website in a new browser window. Cholestasis nec icd10cm alphabetical index the icd10cm alphabetical index is designed to allow medical coders to look up various medical terms and connect them with the appropriate icd codes. Causes of intrahepatic cholestasis of pregnancy icp. Icd10 to deaths during pregnancy, childbirth and the puerperium. Colestasis intrahepatica gestacional cig consenso fasgo 2016.
Progressive familial intrahepatic cholestasis orphanet. Progressive familial intrahepatic cholestasis type 2 pfic2, a type of. Intrahepatic cholestasis of pregnancy as an indicator of liver. With cholestasis, the flow of bile is impaired at some point between the liver cells which produce bile and the duodenum the first segment of the small intestine. Search about 1 items found relating to cholestasis nec. Icp is a reversible form of cholestasis impaired bile flow appearing mainly in the late second or third trimester of pregnancy, and tends to dissolve rapidly after delivery 3, 7, 8.
It typically presents with troublesome itching and can lead to complications for both mother and fetus. Intrahepatic cholestasis of pregnancy icp is a reversible type of hormonally influenced cholestasis. When bile flow is stopped, the pigment bilirubin a waste product formed when old or damaged red blood cells are broken down escapes into the bloodstream and accumulates. Please use one of the following formats to cite this article in your essay, paper or report. Risk of stillbirth baby born with no signs of life after 23 completed weeks of pregnancy. Development of the who application of icd10 to deaths during pregnancy, childbirth, and the. Colestasis gravidica gastroenterologia y hepatologia elsevier. Intrahepatic cholestasis of pregnancy icp, also known as obstetric cholestasis, cholestasis of pregnancy, jaundice of pregnancy, and prurigo gravidarum, is a medical condition in which cholestasis occurs during pregnancy. Icd 10 code lookup find diagnosis codes icd 10 cm and procedure codes icd 10 pcs by disease, condition or icd 10 code. Intrahepatic cholestasis of pregnancy icp, also known as obstetric cholestasis, cholestasis of pregnancy, jaundice of pregnancy, and prurigo gravidarum, is a. There are 3 terms under the parent term cholestasis nec in the icd10cm alphabetical index. These images are a random sampling from a bing search on the term intrahepatic cholestasis of pregnancy. Neonatal cholestasis is never physiological but rather is a sign of hepatobiliary andor metabolic disorders, some of which might be fatal if not identified and treated rapidly. One in 10 women with obstetric cholestasis will have their baby before 37 weeks of pregnancy.
Free, official information about 2012 and also 202015 icd9cm diagnosis code 646. However, less than 25% of those presenting with cholestasis will progress to endstage liver disease during childhood. It is clinically and virtually impossible to use this code on a nonfemale patient outside the stated age range. It frequently develops in late pregnancy in individuals who are genetically predisposed. Intrahepatic cholestasis of pregnancy icp is a unique hepatic disorder in pregnancy characterized by mild to severe pruritus and disturbed liver function tests16. Altogether 10,504 women with a history of icp were found. Forty percent to 50% of infants who have the pizz phenotype may have asymptomatic abnormal liver biochemical test results in the first year after birth, and 10 % to 15% will develop neonatal cholestasis.