Recommendations for Diagnosis and Management of Autoimmune Pancreatitis in Childhood: Consensus From INSPPIRE
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...
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| Published in | Journal of pediatric gastroenterology and nutrition Vol. 67; no. 2; pp. 232 - 236 |
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| Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format | Journal Article Conference Proceeding |
| Language | English |
| Published |
United States
by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology
01.08.2018
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| Online Access | Get full text |
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| Abstract | 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 PancreatitisIn 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 PancreatitisIn 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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| AbstractList | 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.
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.
We have now generated 15 statements to help standardize the approach to diagnosis and management of P-AIP.
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. OBJECTIVESAutoimmune 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. METHODSA 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. RESULTSWe have now generated 15 statements to help standardize the approach to diagnosis and management of P-AIP. CONCLUSIONSThe 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. 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 PancreatitisIn 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 PancreatitisIn 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. |
| Author | Werlin, Steven Gonska, Tanja Barth, Bradley Zimmerman, Bridget Scheers, Isabelle Ooi, Chee Y Gariepy, Cheryl Himes, Ryan W Abu-El-Haija, Maisam Fishman, Douglas S Pohl, John F Heyman, Melvin B Shah, Uzma Husain, Sohail Z Piccoli, David A Morinville, Veronique Lowe, Mark Uc, Aliye Freedman, Steven Liu, Quin Troendle, David Giefer, Matthew J Perito, Emily R Wilschanski, Michael Lin, Tom K Mascarenhas, Maria Schwarzenberg, Sarah J Palermo, Joseph J |
| AuthorAffiliation | University of Texas Southwestern Medical School, Dallas Baylor College of Medicine, Houston, TX The Childrenʼs Hospital of Philadelphia, Philadelphia, PA Harvard Medical School, Massachusetts General Hospital for Children, Boston, MA Discipline of Paediatrics, School of Womenʼs and Childrenʼs Health Medicine, University of New South Wales and Sydney Childrenʼs Hospital Randwick, Sydney, Australia Nationwide Childrenʼs Hospital, Columbus, OH Washington University School of Medicine, St-Louis, MO Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA Hadassah Hebrew University Hospital, Jerusalem, Israel University of California at San Francisco, San Francisco, CA University of Minnesota, Masonic Childrenʼs Hospital, Minneapolis, MN Medical College of Wisconsin, Milwaukee, WI Montreal Childrenʼs Hospital, McGill University, Montreal, QC, Canada Cedars-Sinai Medical Center, Los Angeles, CA Childrenʼs Hospital of Pittsburgh of UPMC, Pittsburgh, PA Hospital for Sick Children, Toronto, On |
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| Cites_doi | 10.1097/MPG.0000000000001371 10.1038/ajg.2017.85 10.1016/j.pan.2015.03.011 10.1016/j.jpeds.2014.11.019 10.1053/j.gastro.2015.03.010 10.1053/j.gastro.2015.04.051 10.1007/s00535-014-0942-2 10.1097/MPG.0000000000000417 10.1016/S0016-5085(00)70264-2 10.1007/s00428-009-0747-5 10.1097/MPA.0b013e3182142fd2 10.1007/s00247-008-1132-2 10.1016/S0016-5107(04)02393-4 10.1097/MPG.0000000000000692 10.1097/MPA.0b013e318233bec5 |
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| Snippet | OBJECTIVES:Autoimmune pancreatitis (AIP) represents a complex immune-mediated pancreas disorder. Pediatric AIP (P-AIP) is rare. We have recently summarized the... Autoimmune pancreatitis (AIP) represents a complex immune-mediated pancreas disorder. Pediatric AIP (P-AIP) is rare. We have recently summarized the... OBJECTIVESAutoimmune pancreatitis (AIP) represents a complex immune-mediated pancreas disorder. Pediatric AIP (P-AIP) is rare. We have recently summarized the... |
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| Title | Recommendations for Diagnosis and Management of Autoimmune Pancreatitis in Childhood: Consensus From INSPPIRE |
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