Description
Book SynopsisThis book offers a comprehensive overview of the latest standard medical procedures and surgical techniques for biliary atresia (BA), as well as the perioperative care, long-term follow-up and transitions. Experts on pediatrics in such fields as hepatology, surgery, pathology, and liver transplantation present their research findings and analyses of this rare and intractable disease of unknown etiology. In Japan, shared experience and sound understanding based on conferences and guidelines have led to standardization of management and clinical care and, as a result, better outcomes.
Providing insights into improving surgical outcomes, and including special chapters focusing on social support systems for patients and families as well as recent advances in early diagnosis, this book a valuable resource for medical professionals around the globe who are involved in treating biliary atresia. It is especially useful for pediatric hepatologists, pediatric surgeons and transplant surgeons.
Table of ContentsBiliary Atresia: A Historical OverviewHistory of The Japanese Biliary Atresia Society (JABS)Japanese Biliary Atresia Registry (JBAR)Pathogenesis: Overview Pathogenesis: Genetics/EpigeneticsPathogenesis: Viral InfectionPathogenesis: Maternal Microchimerism Epidemiology: Incidence and Gender RatioEpidemiology: Ethnic Variations/Family Histories/HeredityEpidemiology: Gestational Age/Birth Weight /Associated AnomaliesClassifications Mass Screening Stool Color Card System Prenatal Diagnosis and Signs/SymptomsIntracranial HemorrhagePathology Biomarkers Differential Diagnosis Diagnostic Modalities Preoperative Management and Direct CholangiographyOperative Procedures: Open Kasai ProcedureOperative Procedures: Laparoscopic Kasai ProcedureOperative Procedures: Re-do Kasai ProcedureOperative Procedures: Cadaveric Liver TransplantationOperative Procedures: Living Donor Liver TransplantationMedical Treatment: UDCA/Steroid Medical Treatment: Kampo MedicinePrevention/Treatment of Postoperative CholangitisNutritional Support Protocols of Follow-up ManagementPrognostic IndicatorsLong-term Complications: Gastro-Esophageal VaricesLong-term Complications: Hypersplenism Long-term Complications: Cholangitis/Gall StonesLong-term Complications: Hepatopulmonary SyndromeLong-term Complications: Portopulmonary HypertensionLong-term Complications: Liver Cirrhosis/Hepatic Encephalopathy Long-Term Results, GeneralLong-Term Results, Deformity of Intrahepatic Bile DuctsLong-Term Results, Social Performance Long-Term Results, Liver Transplantation Biliary Atresia and Pregnancy/Delivery Biliary Atresia and Malignancy Future Prospects Transition in Biliary Atresia Society of Patients and Families Clinical Guidelines for Biliary Atresia
