TABLE 2.
Summary of recommendations
| Category | Recommendation | Grade |
|---|---|---|
| Nutrition and endocrine | 1. Patients with CP are at risk for macro- and micronutrient deficiencies. Patients should be monitored for growth and pubertal delay, dietary intake, and fat-soluble vitamin deficiencies. Growth and intake should be reviewed at every clinic visit, a minimum of every 6 to 12 months. Fat-soluble vitamin laboratory analysis should occur every 12 to 18 months or as clinically indicated | 1B |
| 2. A multidisciplinary approach that includes a clinical pediatric dietitian is needed to adequately monitor nutritional status, evaluate nutrient intake and provide education and recommendations to help prevent both malnutrition and obesity | 1C | |
| 3. There is a clear role for PERT in children with CP who have EPI with steatorrhea, poor growth and/or nutritional deficiencies. PERT dosing for CP-associated EPI is similar to that used in patients with CF | 1B | |
| 4. Children with CP should be screened yearly for pancreatogenic DM with a fasting glucose and HbA1c level | 1C | |
| 5. Consider OGTT if pre-diabetes is present based on abnormal fasting glucose (100–125mg/dL) and/or HbA1c level (5.7%–6.4%). OGTT should be performed annually once a patient is considered to have pre-diabetes | 1C | |
| 6. Chronic pancreatitis patients with diabetes should be referred to a pediatric endocrinologist to optimize glucose management and determine if evaluation for other forms of DM should be considered | 1B | |
| 7. It is important to address clinical symptoms of malabsorption and PERT in children with CP and DM to improve glycemic control | 1C | |
| 8. Insufficient data exists to recommend the use of antioxidants as a treatment to prevent EPI or other disease progression in children with CP | 2C | |
| Pain management | 9. Treatment of pain in pediatric CP requires a multidisciplinary approach, ideally involving a pediatric pain physician, pediatric gastroenterologist, psychologist, nurse, and physical therapist | 1B |
| 10. Cognitive behavioral Therapy (CBT) should be considered in management of pediatric CP pain | 1B | |
| 11. Physical therapy may be considered as an adjunct therapy for pain management in children with CP | 2B | |
| 12. There is insufficient data to recommend PERT as therapy for pain in children without EPI | 1B | |
| 13. There is insufficient data to recommend antioxidants, steroids, leukotriene antagonists, or somatostatins in the management of pain for children with CP | 2C | |
| 14. Analgesic pain management in CP should follow an “analgesic ladder” that incorporates the layering of non-opioid and opioid medications. Ideally this should be directed by a pain specialist working in partnership with a pancreatologist or gastroenterologist | 1B | |
| 15. Neuromodulators may be effective in treating pain in children with CP as part of a multidisciplinary approach | 1C | |
| 16. Celiac plexus block for pain has not been shown to be effective in children with CP and cannot be recommended | 1C | |
| 17. Children with CP suffering from pain refractory to standard medical management should be evaluated at a center with pediatric experience in pain management | 1C | |
| Lifestyle modifications | 18. On the basis of long-term adult data, providers should caution patients about the acute and chronic negative effects of alcohol abuse on pancreatic health | 1B |
| 19. Health-care providers should caution patients about the dose-dependent response of tobacco smoking on the development and progression of CP among adult patients and should advise against smoking | 1A | |
| 20. Data are limited regarding the impact of weight and BMI on CP outcomes, as such, providers should counsel patients and parents about a balanced healthy diet and lifestyle | 1C | |
| 21. Administering a survey tool to assess QOL and/or functional assessment among pediatric patients to assess degree of impairment and drive targeted interventions indicated | 2C | |
| Sequelae of disease | 22. The majority of pancreatic fluid collections will resolve spontaneously with supportive care. Intervention is reserved for complications from mass-effect, infection/necrosis or if spontaneous regression of the collection is thought to be unlikely | 1B |
| 23. Children with CP that continue to exhibit abdominal pain, bloating or other GI concerns deserve an appropriate GI workup to evaluate for other etiologies that may explain their symptoms | 1C |
CP = chronic pancreatitis; DM = diabetes mellitus; EPI = exocrine pancreatic insufficiency; GI = gastrointestinal, OGTT = oral glucose tolerance test; PERT = pancreatic enzyme replacement therapy; QOL = quality of life.