Abstract

One of the affected organs in cystic fibrosis (CF) is the pancreas, mainly translated into exocrine pancreatic insufficiency. Although rare, acute pancreatitis (AP) has been described, mostly in pancreatic sufficient patients. Objectives. Estimating AP prevalence in CF pediatric population of the I.N.S.M.C. „AlessandrescuRusescu” CF centre. Material and methods. 5 year retrospective study (2011-2016) including INSMC CF centre pediatric population aged 3-18 years. PA diagnosis was established on the presence of minimum 2 criteria between: characteristic abdominal pain, x3 normal value for age elevation of amylase/lipase, medical imaging evaluation suggestive for AP. Patients were evaluated with different criteria including PIP score of predicting AP risk. Outcomes. 48 patients were included with a slight female predominance (54%). 3 of them presented diagnostic criteria for AP (6,25%), all heaving pancreatic insufficiency and high PIP score (low risk of developing AP); 2 of them have low compliance with pancreatic enzymes substitution therapy; one of them presented recurrent episodes of AP. Conclusions. AP is a rare CF complication. It can be easily missed due to a large number of abdominal pain and emesis causes in CF patients. Although it is usually associated with pancreatic sufficiency, all our patients were pancreatic insufficient.

Highlights

  • Pancreatita acută (PA) diagnosis was established on the presence of minimum 2 criteria between: characteristic abdominal pain, x3 normal value for age elevation of amylase/lipase, medical imaging evaluation suggestive for acute pancreatitis (AP)

  • Patients were evaluated with different criteria including PIP score of predicting AP risk

  • Outcomes. 48 patients were included with a slight female predominance (54%). 3 of them presented diagnostic criteria for AP (6,25%), all heaving pancreatic insufficiency and high PIP score; 2 of them have low compliance with pancreatic enzymes substitution therapy; one of them presented recurrent episodes of AP

Read more

Summary

Clinical studies

Valentina-Daniela COMĂNICI1,2, Ioana Florentina CODREANU1,2, Anca BĂLĂNESCU1, Alina Angelica BELIVACĂ1, Iustina Violeta STAN1,2, Mihai CRAIU1,2, Mirela-Elena RITIVOIU1,2, Dumitru MATEI1,2 1 UMF „Carol Davila“, București, România 2 Departamentul Pediatrie INSMC „Alessandrescu Rusescu“, București, România

Objectives
Conclusions
MATERIALE ŞI METODE
Patologie asociată
Limitări ale studiului
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.