Abstract

ObjectivesThe clinical course and progression of acute pancreatitis are poorly understood to date, necessitating more studies of clinical profiles during the disease. Moreover, understanding the etiologies and clinical presentations of acute pancreatitis (AP) in children can contribute to early diagnosis and, hence, earlier interventions. Therefore, this article aims to study the clinical profiles of children with acute pancreatitis (AP) in relation to complications and other variables.Study designWe retrospectively studied 56 patients who presented with AP to the pediatric department in Salmaniya Medical Complex between January 2006 and December 2017. Cases of chronic pancreatitis and ages above 12 years were excluded. The data concerned demographics, etiology, clinical data, hospital course, and outcomes.ResultsThe study included 56 patients aged a mean of 8.46 years (male:female - 33:23). The average hospital stay was 7.68 days. Patients received parenteral feeds a mean of 2.77 days. All patients had an ultrasound, nine required CT scans (16.1%), and five MRIs (8.9%). There were 18 local complications (32.1%): pseudocysts (n=3, 5.36%), cholangitis (n=2, 3.6%), and edema (n=13, 23.2%). There were 23 intensive care unit (ICU) admissions (41.1%). No mortalities occurred but there were six recurrences (10.7%). Symptoms of abdominal pain, vomiting, fever, and nausea occurred in 100%, 57.1%, 35.7%, and 23.2% of patients, respectively. Etiologies were 41.1% biliary, 23.2% idiopathic, 19.6% traumatic, and 8.93% drug-induced. Leukocytes were elevated in 20 patients (35.7%), c-reactive protein (CRP) in five (8.93%), serum amylase in 45 (80.4%), and urinary amylase in all 56 patients (100%).ConclusionMost pediatric AP cases were attributed to biliary causes followed by trauma. Age was significantly correlated with complication rates (P=0.013). Abdominal pain was a more common symptom than vomiting. Leukocytosis was associated with ICU admissions. There was no significant relation between c-reactive protein, serum amylase, or urinary amylase, and complications or ICU admissions. Pediatric AP was self-limiting and there were no fatalities.

Highlights

  • Acute pancreatitis (AP) can be defined by the presence of characteristic abdominal pain, an increase in pancreatic enzymes by a factor of 3, and suggestive imaging findings

  • Leukocytes were elevated in 20 patients (35.7%), c-reactive protein (CRP) in five (8.93%), serum amylase in 45 (80.4%), and urinary amylase in all 56 patients (100%)

  • acute pancreatitis (AP) in the pediatric age group has a good prognosis and a low mortality rate, yet there is a risk of recurrence in 15% to 35% of patients (North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN) [6]

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Summary

Introduction

Acute pancreatitis (AP) can be defined by the presence of characteristic abdominal pain, an increase in pancreatic enzymes by a factor of 3, and suggestive imaging findings. According to the ‘Atlanta’ and ‘International Study Group of Paediatric Pancreatitis: In Search of a Cure’ (INSPPIRE) criteria, the diagnosis of AP is made when two of these three features are present [1,2]. There has been an increasing trend in pancreatitis among pediatric populations over the years. This increase has been linked to a greater understanding of etiologies and advancements in diagnostic modalities [3,4]. AP in the pediatric age group has a good prognosis and a low mortality rate, yet there is a risk of recurrence in 15% to 35% of patients (North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN) [6]

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