M Abu-El-Haija et al. JPGN 2018; 67: 131-43. This working group made ~27 recommendations (summarized in Table 1) and indicated the quality of evidence supporting the recommendation as well as the agreement among team members –virtually all received at least 12 of 13 votes.
Here are the ones that grabbed my attention:
For Acute Pancreatitis (AP):
1a & 1aa. Children with mild AP should be started on a regular diet –preferably via mouth as compared to nasogastric route
1b. Enteral nutrition (EN) should be attempted in children with severe AP within 72 hours from presentation, once deemed hemodynamically stable.
1.4 Even in severe AP, jejunal tube feeding should be reserved for those unable to tolerate oral or NG tube feeding
For Acute Recurrent Pancreatitis (ARP):
2.1a & 2.1b. Children should receive a regular-fat diet in between bouts of ARP and a regular-fat diet can safely be started within 1 week after the onset of a bout of AP (except in those with very elevated triglycerids (>1000 mg/dL)
2.2a & 2.3a. PERT is NOT recommended in children with ARP without eocrine pancreatic insufficiency (EPI). Antioxidants are NOT recommended (insufficient supporting evidence)
For Chronic Pancreatitis (CP):
3.1b & 3.12a. Recommends routine followup every 3-6 months and a regular diet
3.3a, 3.4a, & 3.5a Monitoring: recommends checking fat-soluble vitamin levels every 6 to 12 months, checking for EPI with elastase (or 72 hr fecal fat) every 6-12 months, and BMD (bone mineral density) if CP and malnutrition (especially if Vit D deficiency or hx/o fractures)
My take: This report provides a methodical approach for the care of children with these pancreatic disorders.
Another study (MJ Giefer et al. J Pediatr 2017; 186: 95-100) from the INSPPIRE group provides data on early-onset pancreatitis. Specifically, the group presents clinical information on 342 children with acute recurrent pancreatitis or chronic pancreatitis regarding disease burden and associations with genetic mutations.
Genetic disease is much more common in younger ages:
In subset younger than 6 years, 72 of 102 had genetic diseases identified: PRSS1 in 42, CFTR in 27, SPINK1 in 12, and CTRC in 8.
In subset 6-11 years of age, 52 of 90 had genetic diseases identified: PRSS1 in 20, CFTR in 23, SPINK1 in 22, and CTRC in 1.
In subset greater than 12 years of age, 39 of 72 had genetic diseases identified: PRSS1 in 13, CFTR in 24, SPINK1 in 6, and CTRC in 1.
Testing for newer susceptibility genes were not evaluated as they had not become commercially available: carboxypeptidase 1, claudin 2, carboxylesterlipase, and carboxyesterlipase-hybrid
SPINK1 is noted to be present in 1-3% of general population; CTRC mutation occur in 0.7% of healthy controls.
Obstructive causes were common. Pancreas divisum was identified in 38 patients but there was not a great deal of difference among the age groups; similarly, other obstructive causes were identified in about one-third of patients and included sphincter of Oddi dysfunction (n=9), gallstones (n=17), pancreaticobiliary malunion (n=12), biliary cyst (n=11), pancreatic stricture (n=2), annular pancreas (n=3), and duodenal diverticulum.
Exocrine insufficiency noted in 52 (no strong age predilection)
Diabetes in 18 (11 of the cases occurred in those >12 years)
Constant moderate pain noted in 82 (25 in group <6, 27 in 6-12 group, and 30 in group >12 years)
Constant severe pain noted in 18 (4 in group <6, 5 in 6-12 group, and 9 in group >12 years)
Average number of hospitalizations in past year was 1 in those ≤12 and 2 in those older than 12.
My take: PRSS1 and CTRC mutations are associated with early onset pancreatitis.
Our group received a very helpful update on pancreatitis from Maisam Abu-El-Haija (GI) and Jaime Nathan (surgery). My notes may include some errors in transcription and errors of omission. Some pictures of the slides are included below as well.
About 30% of acute pancreatitis patients have a 2nd bout of pancreatitis. Obesity is a risk factor for recurrence.
There has been a recent increase in incidence of acute pancreatitis.
Cincinnati has a gene panel to examine the four most common mutations which cause hereditary pancreatitis (PRSS1, SPINK1, CFTR, and CRTC) along with 6 other relevant genes. (28 day turnaround) In addition, there is a pancreatitis insufficiency panel.
Discussed screening for pancreatic insufficiency. Directly measuring pancreatic enzymes are more sensitive for early insufficiency, but may be unnecessary if good growth and normal stool elastase.
There are NO proven medical/dietary therapies to prevent recurrent or chronic pancreatitis and eliminate pain symptoms.
The INSPPIRE Group (CE Gariepy et al. JPGN 2017; 64: 95-103) has published consensus recommendations for acute recurrent pancreatitis (ARP) and chronic pancreatitis (CP).
While the authors acknowledge the need for high-level evidence/further research, they provide a large number of consensus recommendations. These recommendations are succinctly summarized in Table 1 and Table 2. From a reader’s perspective, my preference would have been to separate the recommendations for ARP and CP rather than to intermix them (though many of the recommendations are the same for both conditions).
ARP specific recommendations:
“Initial evaluation should include AST,ALT, GGT, Total bilirubin (fractionate if elevated), fasting lipids, and total serum calcium.”
Evaluate for fat-soluble vitamin deficiency, and pancreatic exocrine insufficiency at least annually
ARP and CP recommendations:
Consider ammonia and urine organic acids if there is a concern for undiagnosed metabolic disease.
Check for celiac disease.
Check for O&P if immunosuppressed, travel to endemic areas of Ascaris, or if peripheral eosinophilia.
Evaluation of genetic causes: should include sweat chloride test and PRSS1 gene testing. Consider SPINK1, CFTR, and CTRC evaluation.
Evaluate with MRCP (not ultrasound) acutely if GGT >2 x ULN or if direct bilirubin is elevated.
Non-acutely, MRCP recommended to evaluate pancreatic ductal abnormalities. “When available, secretin-enhanced MRCP …should be obtained.” sMRCP can provide dynamic images of the pancreatic duct allowing differentiation of fixed from nonfixed lesions; this technique has not been widely adopted by pediatric radiologists compared with adult radiologists.
CP specific recommendations:
Evaluate for fat-soluble vitamin deficiency, pancreatic exocrine insufficiency, and pancreatic endocrine insufficiency at least annually
The authors did not recommend checking serum IgG4 in the absence of associated systemic disease or suggestive imaging for autoimmune pancreatitis.
Briefly noted: J-H Choi et al. Clin Gastroenterol Hepatol; 2017: 15: 86-92. This study indicated that vigorous hydration with lactated ringer’s (LR) reduces risk of pancreatitis after ERCP. A potential inference would be that LR would be an optimal fluid for pancreatitis more broadly. (Related: Why an ERCP Study Matters to Pediatric Care | gutsandgrowth)