Lost in transition? Loss of follow-up and quality of life in adults after resection of choledochal malformation in childhood
Reem Abo-Namous, Joachim F. Kuebler, Andrej Potthoff, Omid Madadi-Sanjani, Marie Uecker, Jens Dingemann, Claus Petersen, Benno Ure, Nagoud Schukfeh

TL;DR
This study examines long-term outcomes and quality of life in adults who had childhood surgery for choledochal malformation, finding many are lost to follow-up but report good quality of life.
Contribution
The study provides long-term follow-up data on CM patients in Germany, highlighting the need for transition programs due to ongoing complications and cancer risks.
Findings
Most patients (78%) stopped gastroenterologic follow-up after CM resection.
Patients reported HRQOL scores comparable to the healthy population.
Some patients experienced severe long-term complications like bile duct stenosis and portal vein thrombosis.
Abstract
Choledochal malformation (CM) is a rare disease that can lead to malignancy and potential long-term sequelae despite surgical resection. There is no long-term follow-up data on patients after CM resection in Germany. We aimed to determine the long-term outcome of our patients with a duration of follow-up >10 years and focused on long-term sequelae and health-related quality of life (HRQOL). All patients who had undergone CM-resection in our department from 01/1978 to 06/2009 were contacted. Patients were interviewed about postoperative complications and their present medical attendance. HRQOL was determined using Pediatric Quality of Life Inventory 4.0 (PedsQL), version for adults. The PedsQL scales the HRQOL from 0 to 100, with higher scores indicating a better HRQOL. Scores were compared to those published for a healthy population. Out of 56 patients who were contacted, 23 (41 %)…
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Taxonomy
TopicsPediatric Hepatobiliary Diseases and Treatments · Gallbladder and Bile Duct Disorders · Intestinal Malrotation and Obstruction Disorders
