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Recommendations for Diagnosis and Management of Autoimmune Pancreatitis in Childhood
- Scheers, Isabelle;
- Palermo, Joseph J;
- Freedman, Steven;
- Wilschanski, Michael;
- Shah, Uzma;
- Abu-El-Haija, Maisam;
- Barth, Bradley;
- Fishman, Douglas S;
- Gariepy, Cheryl;
- Giefer, Matthew J;
- Heyman, Melvin B;
- Himes, Ryan W;
- Husain, Sohail Z;
- Lin, Tom K;
- Liu, Quin;
- Lowe, Mark;
- Mascarenhas, Maria;
- Morinville, Veronique;
- Ooi, Chee Y;
- Perito, Emily R;
- Piccoli, David A;
- Pohl, John F;
- Schwarzenberg, Sarah J;
- Troendle, David;
- Werlin, Steven;
- Zimmerman, Bridget;
- Uc, Aliye;
- Gonska, Tanja
- et al.
Published Web Location
https://doi.org/10.1097/mpg.0000000000002028Abstract
OBJECTIVES:Autoimmune pancreatitis (AIP) represents a complex immune-mediated pancreas disorder. Pediatric AIP (P-AIP) is rare. We have recently summarized the characteristic features of P-AIP. We now aim to develop recommendation statements to standardize the diagnostic and therapeutic approach to P-AIP and facilitate future research in the field. METHODS:A panel of pediatric gastroenterologists participating in the International Study Group of Pediatric Pancreatitis: In search for a cuRE was formed to discuss and then vote on 15 recommendation statements. A consensus of at least 80% was obtained following 3 voting rounds and revision of the statements. RESULTS:We have now generated 15 statements to help standardize the approach to diagnosis and management of P-AIP. CONCLUSIONS:The first P-AIP recommendation statements developed by the International Study Group of Pediatric Pancreatitis: In search for a cuRE group are intended to bring standardization to the diagnosis and treatment of this rare childhood disorder. These statements may help guide a uniform approach to patient care and facilitate future research studies.
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