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 Pancreatitis: In search for a cuRE was formedtodiscussandthenvoteon15recommendationstatements.Aconsensusof atleast80%wasobtainedfollowing3votingroundsandrevisionofthestatements. 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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 232-236 |
| Number of pages | 5 |
| Journal | Journal of pediatric gastroenterology and nutrition |
| Volume | 67 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jan 1 2018 |
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Keywords
- Autoimmune pancreatitis
- Children
- Idiopathic duct–centric pancreatitis
- Lymphoplasmacytic sclerosing pancreatitis
- Pancreatitis
- Recommendations
Cite this
Recommendations for diagnosis and management of autoimmune pancreatitis in childhood : Consensus from INSPPIRE. / 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.
In: Journal of pediatric gastroenterology and nutrition, Vol. 67, No. 2, 01.01.2018, p. 232-236.Research output: Contribution to journal › Review article
}
TY - JOUR
T1 - Recommendations for diagnosis and management of autoimmune pancreatitis in childhood
T2 - Consensus from INSPPIRE
AU - Scheers, Isabelle
AU - Palermo, Joseph J.
AU - Freedman, Steven
AU - Wilschanski, Michael
AU - Shah, Uzma
AU - Abu-El-Haija, Maisam
AU - Barth, Bradley
AU - Fishman, Douglas S.
AU - Gariepy, Cheryl
AU - Giefer, Matthew J.
AU - Heyman, Melvin B.
AU - Himes, Ryan W.
AU - Husain, Sohail Z.
AU - Lin, Tom K.
AU - Liu, Quin
AU - Lowe, Mark
AU - Mascarenhas, Maria
AU - Morinville, Veronique
AU - Ooi, Chee Y.
AU - Perito, Emily R.
AU - Piccoli, David A.
AU - Pohl, John F.
AU - Schwarzenberg, Sarah J.
AU - Troendle, David
AU - Werlin, Steven
AU - Zimmerman, Bridget
AU - Uc, Aliye
AU - Gonska, Tanja
PY - 2018/1/1
Y1 - 2018/1/1
N2 - 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 formedtodiscussandthenvoteon15recommendationstatements.Aconsensusof atleast80%wasobtainedfollowing3votingroundsandrevisionofthestatements. 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.
AB - 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 formedtodiscussandthenvoteon15recommendationstatements.Aconsensusof atleast80%wasobtainedfollowing3votingroundsandrevisionofthestatements. 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.
KW - Autoimmune pancreatitis
KW - Children
KW - Idiopathic duct–centric pancreatitis
KW - Lymphoplasmacytic sclerosing pancreatitis
KW - Pancreatitis
KW - Recommendations
UR - http://www.scopus.com/inward/record.url?scp=85055614942&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85055614942&partnerID=8YFLogxK
U2 - 10.1097/MPG.0000000000002028
DO - 10.1097/MPG.0000000000002028
M3 - Review article
C2 - 29746340
AN - SCOPUS:85055614942
VL - 67
SP - 232
EP - 236
JO - Journal of Pediatric Gastroenterology and Nutrition
JF - Journal of Pediatric Gastroenterology and Nutrition
SN - 0277-2116
IS - 2
ER -