Clinical Pathway for Pancreatic Enzyme Replacement Therapy (PERT) in Children with Suspected or Confirmed Exocrine Pancreatic Insufficiency (EPI)
Child with Confirmed EPI
- Initiate PERT
- Titrate PERT dose
-
Symptoms Suggestive of EPI
- Poor weight gain/linear growth
- Steatorrhea
- Loose/frequent stools after meals
or snacks - Foul smelling stools
- Flatulence
- Abdominal pain associated with eating
- Voracious appetite
- Rectal prolapse
Team Assessment
-
History and Physical Exam
- Assess prenatal testing, newborn screen, sweat test
- Feeding history, growth pattern
- Surgical history suggestive for acquired EPI
- Conditions with high risk for EPI
- Symptoms of fat malabsorption
- Previous enzyme replacement therapy
- Child presents with any of the following:
- 2 positive PI CF variants
- Meconium ileus
- Rectal prolapse
- Poor weight gain
- Steatorrhea
Initiate PERT at First Visit
Do not initiate PERT
Screen for Exocrine Pancreatic Insufficiency
- Obtain Fecal Elastase
- Requires a single spot stool sample
- Perform on solid stool
- Results inaccurate if:
- Stool sample is loose/watery
- Test is performed in term infants < 72 hrs of age or preterm infants < 2 wks of age
- Low result must be confirmed with repeat testing
Normal Fecal Elastase
> 500 mcg/g
> 500 mcg/g
Borderline Fecal Elastase
200-500 mcg/g
200-500 mcg/g
Abnormal Fecal Elastase
< 200 mcg/g
< 200 mcg/g
- PERT not indicated; discontinue if previously initiated
- Consider subspecialist for evaluation
- Pulmonary/CF Center
- GI
- Repeat fecal elastase to confirm diagnosis
- Refer to subspecialist for evaluation
- Pulmonary/CF Center
- GI
- Refer to clinical nutrition as indicated
- Consider RUQ ultrasound
- Additional testing by subspecialist
- Consider PERT while awaiting
subspecialist evaluation
- Repeat fecal elastase unless genetic variants consistent with CF and EPI
- Refer to subspecialist for evaluation
- Pulmonary/CF Center
- GI
- Refer to clinical nutrition as indicated
- Consider RUQ ultrasound
- Additional testing by subspecialist
-
Monitor
- Growth
- Fat malabsorption
-
Monitor
- Growth
- Fat malabsorption
- Repeat fecal elastase in 1 yr or sooner if clinical symptoms
-
Monitor
- Growth
- Fat malabsorption
-
Annually as clinically indicated
- Fecal elastase
- Fat-soluble vitamin levels
- Vitamin A
- 25-OH vitamin D
- Vitamin E
- PT/INR as a measure of vitamin K
Consider Titrating PERT Dose
Refer to clinical nutrition as indicated
Refer to clinical nutrition as indicated
Evidence
- CF Diagnosis Clinical Care Guidelines
- Pancreatic insufficiency in Cystic Fibrosis
- Enteral Tube Feeding in Cystic Fibrosis Clinical Care Guidelines
- Pancreatic Enzymes in Cystic Fibrosis Clinical Care Guidelines
- Exocrine Pancreatic Insufficiency in Children – Challenges in Management
- ESPGHAN and NASPGHAN Report on the Assessment of Exocrine Pancreatic Function and Pancreatitis in Children
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