Risk Factors for Rapid Progression From Acute Recurrent to Chronic Pancreatitis in Children: Report From INSPPIRE. Issue 2 (August 2019)
- Record Type:
- Journal Article
- Title:
- Risk Factors for Rapid Progression From Acute Recurrent to Chronic Pancreatitis in Children: Report From INSPPIRE. Issue 2 (August 2019)
- Main Title:
- Risk Factors for Rapid Progression From Acute Recurrent to Chronic Pancreatitis in Children
- Authors:
- Liu, Quin Y.
Abu-El-Haija, Maisam
Husain, Sohail Z.
Barth, Bradley
Bellin, Melena
Fishman, Douglas S.
Freedman, Steven D.
Gariepy, Cheryl E.
Giefer, Matthew J.
Gonska, Tanja
Heyman, Melvin B.
Himes, Ryan
Lin, Tom K.
Maqbool, Asim
Mascarenhas, Maria
McFerron, Brian A.
Morinville, Veronique D.
Nathan, Jaimie D.
Ooi, Chee Y.
Perito, Emily R.
Pohl, John F.
Rhee, Sue
Schwarzenberg, Sarah J.
Shah, Uzma
Troendle, David
Werlin, Steven L.
Wilschanski, Michael
Zimmerman, M. Bridget
Lowe, Mark E.
Uc, Aliye - Abstract:
- ABSTRACT: Objective: The aim of the study was to determine the rate of progression from acute recurrent pancreatitis (ARP) to chronic pancreatitis (CP) in children and assess risk factors. Study Design: Data were collected from the IN ternational S tudy group of P ediatric P ancreatitis: I n search for a cuRE (INSPPIRE) cohort. Kaplan-Meier curves were constructed to calculate duration of progression from initial attack of acute pancreatitis (AP) to CP. Log-rank test was used to compare survival (nonprogression) probability distribution between groups. Cox proportional hazard regression models were fitted to obtain hazard ratio (with 95% confidence interval [CI]) of progression for each risk variable. Results: Of 442 children, 251 had ARP and 191 had CP. The median time of progression from initial attack of AP to CP was 3.79 years. The progression was faster in those ages 6 years or older at the first episode of AP compared to those younger than 6 years (median time to CP: 2.91 vs 4.92 years; P = 0.01). Children with pathogenic PRSS1 variants progressed more rapidly to CP compared to children without PRSS1 variants (median time to CP: 2.52 vs 4.48 years; P = 0.003). Within 6 years after the initial AP attack, cumulative proportion with exocrine pancreatic insufficiency was 18.0% (95% CI: 12.4%, 25.6%); diabetes mellitus was 7.7% (95% CI: 4.2%, 14.1%). Conclusions: Children with ARP rapidly progress to CP, exocrine pancreatic insufficiency, and diabetes. The progression toABSTRACT: Objective: The aim of the study was to determine the rate of progression from acute recurrent pancreatitis (ARP) to chronic pancreatitis (CP) in children and assess risk factors. Study Design: Data were collected from the IN ternational S tudy group of P ediatric P ancreatitis: I n search for a cuRE (INSPPIRE) cohort. Kaplan-Meier curves were constructed to calculate duration of progression from initial attack of acute pancreatitis (AP) to CP. Log-rank test was used to compare survival (nonprogression) probability distribution between groups. Cox proportional hazard regression models were fitted to obtain hazard ratio (with 95% confidence interval [CI]) of progression for each risk variable. Results: Of 442 children, 251 had ARP and 191 had CP. The median time of progression from initial attack of AP to CP was 3.79 years. The progression was faster in those ages 6 years or older at the first episode of AP compared to those younger than 6 years (median time to CP: 2.91 vs 4.92 years; P = 0.01). Children with pathogenic PRSS1 variants progressed more rapidly to CP compared to children without PRSS1 variants (median time to CP: 2.52 vs 4.48 years; P = 0.003). Within 6 years after the initial AP attack, cumulative proportion with exocrine pancreatic insufficiency was 18.0% (95% CI: 12.4%, 25.6%); diabetes mellitus was 7.7% (95% CI: 4.2%, 14.1%). Conclusions: Children with ARP rapidly progress to CP, exocrine pancreatic insufficiency, and diabetes. The progression to CP is faster in children who were 6 years or older at the first episode of AP or with pathogenic PRSS1 variants. The factors that affect the aggressive disease course in childhood warrant further investigation. Abstract : Supplemental Digital Content is available in the text … (more)
- Is Part Of:
- Journal of pediatric gastroenterology and nutrition. Volume 69:Issue 2(2019)
- Journal:
- Journal of pediatric gastroenterology and nutrition
- Issue:
- Volume 69:Issue 2(2019)
- Issue Display:
- Volume 69, Issue 2 (2019)
- Year:
- 2019
- Volume:
- 69
- Issue:
- 2
- Issue Sort Value:
- 2019-0069-0002-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-08
- Subjects:
- diabetes mellitus -- natural history -- pancreatic insufficiency -- pediatric pancreatitis -- PRSS1
Children -- Nutrition -- Periodicals
Pediatric gastroenterology -- Periodicals
Infants -- Nutrition -- Periodicals
Nutrition disorders in children -- Periodicals
Child Nutrition -- Periodicals
Digestive System -- growth & development -- Periodicals
Gastrointestinal Diseases -- Periodicals
Infant Nutrition -- Periodicals
Nutrition Disorders -- Periodicals
Child
618.923 - Journal URLs:
- http://www.jpgn.org ↗
http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=toc&D=yrovft&AN=00005176-000000000-00000 ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/MPG.0000000000002405 ↗
- Languages:
- English
- ISSNs:
- 0277-2116
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5030.175000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 14181.xml