Multidisciplinary approach to the treatment of pediatric pancreaticobiliary disorders

• Published in: Journal of pediatric surgery 1997-02, Vol.32 (2), p.158-165
• Main Authors: Tagge, Edward P, Tarnasky, Paul R, Chandler, John, Tagge, Derya U, Smith, Charles, Hebra, Andre, Hawes, Robert H, Cotton, Peter B, Othersen, H.Biemann
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Biliary Tract - injuries; Biliary Tract Diseases - diagnosis; Biliary Tract Diseases - surgery; Biliary Tract Surgical Procedures - methods; Child; Child, Preschool; Cholangiopancreatography, Endoscopic Retrograde; Cholecystectomy, Laparoscopic; Choledochal Cyst - diagnosis; Choledochal Cyst - surgery; Cholelithiasis - diagnosis; Cholelithiasis - surgery; Chronic Disease; Female; Humans; Infant; Male; Pancreatitis - diagnosis; Pancreatitis - surgery; Retrospective Studies; Treatment Outcome
• ISSN: 0022-3468; 1531-5037
• DOI: 10.1016/S0022-3468(97)90171-8

A multidisciplinary approach using traditional open surgery, endoscopic retrograde cholangiopancreatography (ERCP) and laparoscopic surgery has revolutionized the care of the adult with pancreaticobiliary disease. This study focuses on a similar collaborative effort to diagnose and treat children with pancreaticobiliary disorders. Charts of all patients treated on the pediatric surgery service between June 1990 and May 1995, who also underwent ERCP, were abstracted for disease process, presenting symptoms, laboratory evaluation, surgical or endoscopic procedures, and eventual outcome. Twenty-six children were identified, ranging from 6 months to 19 years of age. Pancreaticobiliary disorders included pancreas divisum (n = 1), choledochal cyst (n = 4), pancreaticobiliary trauma (n = 4), cholelithiasis and choledocholithiasis (n = 17). The pancreaticobiliary tree was successfully visualized by ERCP in 25 of 26 (96%) patients. Fifteen of these patients also underwent attempted therapeutic endoscopic procedures, with 13 (87%) performed successfully. Three patients with choledochal cyst had stents placed preoperatively for cholangitis, all of whom have undergone successful choledochal cyst excision. Two trauma patients underwent attempted stenting of a bile leak and bile duct stricture, respectively, both of which were unsuccessful, necessitating surgical correction. Seventeen patients with cholelithiasis underwent ERCP to rule out choledocholithiasis. Ten patients were found to have common duct stones, and all stones were endoscopically extracted, including those in a 6-month-old child. Overall survival rate was 96% (25 of 26), with the one death occurring in a trauma patient unrelated to his pancreaticobiliary disorder. A multidisciplinary approach using traditional open surgery, ERCP and laparoscopic surgery can successfully treat even young children with pancreaticobiliary disorders. In experienced hands, diagnostic ERCP and therapeutic endoscopic intervention can be performed successfully in most pediatric patients, greatly simplifying the surgical management of these potentially complex problems.