Infantile-onset inflammatory bowel disease has variable long-term outcomes Front Pediatr. 2023 Mar 1;11:1097779. doi: 10.3389/fped.2023.1097779. eCollection 2023.
Alex Krauthammer 1 2, Ilana Weintraub 1, Ron Shaoul 3, Raffi Lev-Tzion 4, Efrat Broide 5, Michael Wilschanski 6, Aaron Lerner 7, Baruch Yerushalmi 8, Dror S Shouval 9, Hussein Shamaly 10, Yael Haberman-Ziv 1 2, Batia Weiss 1 2 |
Author information 1Pediatric Gastroenterology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel hashomer, Israel. 2Sackler Faculty of Medicine, Tel-Aviv University, Tel Aviv, Israel. 3Pediatric Gastroenterology Unit, Faculty of Medicine, Ruth Rappaport Children's Hospital, Rambam Health Care Campus, Haifa, Israel. 4Paediatric Gastroenterology, Shaare Zedek Medical Centre, Jerusalem, Israel. 5Pediatric Gastroenterology Unit, Shamir Medical Center, Sackler Faculty of Medicine Tel Aviv University, Tel Aviv, Israel. 6Pediatric Gastroenterology Unit, Hadassah Hebrew University Hospital, Jerusalem, Israel. 7Pediatric Gastroenterology and Nutrition Unit, Carmel Medical Center, B, Rappaport School of Medicine, Technion-Israel Institute of Technology, Haifa, Israel. 8Pediatric Gastroenterology Unit, Soroka University Medical Center, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel. 9Institute of Gastroenterology, Nutrition and Liver Diseases, Schneider Children's Medical Center, Sackler Faculty of Medicine Tel-Aviv University, Tel Aviv, Israel. 10Department of Pediatrics, Saint Vincent de Paul-French Hospital, Nazareth, Israel. Abstract Objective and aim: Infantile-onset inflammatory bowel disease (IO-IBD), defined as IBD diagnosed at age 2 years or younger, tends to be more severe and refractory to conventional treatment than IBD diagnosed at a later age. However, data about IO-IBD and its long-term follow up are limited. We thus aimed to evaluate the presentation and long-term outcomes of patients with IO-IBD in a retrospective multicenter study. Methods: Medical records of patients diagnosed with IO-IBD in eight medical centers during 2000-2017 with at least 1-year follow up were reviewed. Demographics and disease characteristics at diagnosis including age of onset, disease phenotype and location, surgeries, medical therapy, and comorbid conditions were recorded. Results: Twenty-three patients with IO-IBD (16 males, 70%) were identified and followed for a median (range) of 51.2 (26.0-110.3) months. The mean ages at presentation and at the last follow up were 14 ± 9.8 and 101 ± 77 months, respectively. Six (26%) patients needed ileostomy already at the time of diagnosis and 20 (87%) were treated with corticosteroids. During long-term follow up, remission was achieved in 16 (73%) patients; of whom, 3 (14%) were without medications and 7 (32%) were in remission with the use of 5-aminosalicylic acid only. One patient needed hemicolectomy and one developed a severe EBV related infection. Conclusion: The majority of patients with IO-IBD achieved long-term remission, despite a severe disease presentation at diagnosis. Surgery rate however is high, mainly during the first months from diagnosis.
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