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Elevated serum amylase and lipase in pediatric diabetic ketoacidosis
J Antonio Quiros1, James P Marcin, Nathan Kuppermann
1Division of Gastroenterology, University of California Davis School of Medicine and the UC Davis Children's Hospital, USA.
Insights
Pancreatic enzyme elevations are common in children with diabetic ketoacidosis (DKA) but rarely indicate pancreatitis. These elevations correlate with higher blood urea nitrogen levels, not abdominal pain.
Area of Science:
- Pediatric Endocrinology
- Gastroenterology
- Biochemistry
Background:
- Pancreatic enzyme concentrations are often elevated in pediatric patients experiencing diabetic ketoacidosis (DKA).
- The clinical and biochemical factors linked to these elevations require further investigation.
Purpose of the Study:
- To identify clinical and biochemical characteristics associated with elevated pancreatic enzyme levels in children with DKA.
- To test the hypothesis that pancreatic enzyme elevations correlate with biochemical markers of hypoperfusion.
Main Methods:
- A prospective cohort study was conducted across three university-affiliated children's hospitals.
- Data were collected from 67 children under 18 years old hospitalized with DKA.
- Serum electrolyte, lactate, calcium, phosphate, magnesium, amylase, lipase, and triglyceride levels were monitored at various intervals during the initial 48 hours of DKA treatment.
Main Results:
- Elevated lipase was observed in 31% and elevated amylase in 24% of pediatric DKA patients.
- Pancreatic enzyme levels peaked between 12-24 hours after DKA treatment initiation.
- Elevated blood urea nitrogen (BUN) was associated with increased amylase and lipase levels. Hypophosphatemia was also linked to elevated lipase.
Conclusions:
- Elevations in pancreatic enzymes are frequent in children with DKA, though clinical pancreatitis is uncommon.
- Peak pancreatic enzyme levels occur 12-24 hours post-treatment initiation.
- Pancreatic enzyme elevation in DKA is associated with elevated BUN at presentation but not with abdominal pain.
Objectives:
Pancreatic enzyme concentrations are frequently elevated in children with diabetic ketoacidosis (DKA). We sought to determine the clinical and biochemical characteristics associated with patients with these elevations. Our hypothesis was that pancreatic enzyme elevations would be associated with biochemical markers of hypoperfusion.
Design:
Prospective cohort study.
Setting:
Three university-affiliated children's hospitals.
Patients:
We collected data on consecutive children <18 yrs of age hospitalized with the diagnosis of DKA.
Interventions:
Serum electrolyte and lactate concentrations and venous pH and Pco2 were measured every 3 hrs from hours 0 to 12 and then every 6 hrs until hour 24. Serum calcium, phosphate, and magnesium concentrations were measured every 6 hrs from hours 0 to 24. Serum amylase, lipase, and triglyceride concentrations were measured at hour 0 and then 12, 24, and 48 hrs after the initiation of therapy.
Measurements And Main Results:
We performed multivariable analyses to test for associations between clinical variables and pancreatic enzyme elevation in 67 children with DKA. Lipase was elevated in 21 (31%) and amylase in 16 (24%) of the children. Pancreatic enzyme values peaked 12-24 hrs after admission. There was no significant correlation between pancreatic enzyme elevation and abdominal pain. In multivariable analyses, an elevated blood urea nitrogen (BUN) concentration was associated with elevated serum amylase (odds ratio 1.04 per unit increase; 95% confidence interval, 1.01-1.09; p = .02), and elevated BUN concentrations and hypophosphatemia were associated with elevated serum lipase (odds ratio 1.04 per unit increase; 95% confidence interval, 1.00-1.08; p = .04; and odds ratio 0.35 per unit increase; 95% confidence interval, 0.15-0.81; p = .01, respectively).
Conclusions:
Elevation of pancreatic enzymes is common in children with DKA, but clinical pancreatitis is rare. Pancreatic enzyme levels reach a peak 12-24 hrs after initiation of treatment for DKA. Pancreatic enzyme elevation is associated with increased BUN concentrations at presentation but is not associated with abdominal pain.
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