Friday, October 27, 2006

Pancreatitis Pediatric

Pancreatitis Pediatric

There are many causes of pancreatitis in childhood:



  • viral etiology including:

..........1. mumps ,

..........2. infectious mononucleosis ,

..........3. influenza A,

..........4. german measles , and

..........5. Coxsackie B virus .

These would produce a clinical picture of acute pancreatitis with severe epigastric pain , severe enough to cause the child to assume a sitting position , radiating to the back , persistent vomiting and fever .If the pancreatitis is due to a viral uncomplicated infection , the prognosis is good .

Other causes include

  • abdominal trauma ,
  • obstruction of the pancreatic drainage system by biliary duct sludging or pancreatic protein precipitations ,
  • hereditary ( familial cases have been reported ) ,
  • drugs , and
  • numerous systemic diseases which make diagnosing a cause for pancreatitis quite difficult unless other manifestations of the systemic disease are apparent at the same time or prior to the attack .

If your child has had two episodes of pancreatitis , a gastroenterology consult is necessary. A search for other possibilities such as:

  • hyperlipidemia ,
  • hyperparathyroidism ,
  • ascariasis and
  • cystic fibrosis is warranted .

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Diagnosing Pediatric Pancreatitis

  • Plain abdominal X-rays maybe done ,
  • an abdomial ultrasound and or
  • an ERCP to exclude pancreatic drainage system obstruction
  • (please discuss the need for all these investigations with the gastroenterologist as some may not be indicated in individual cases ).

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Management of an acute episode may include:

  • taking nothing by mouth ,
  • nasogastric suction ,
  • pain medication ,
  • IV nutrition ( TPN ),
  • very rarely would surgery be required .
  • If the cause is unknown , there is little you can do to prevent recurrent pancreatitis.
  • A care plan is necessary to be discussed with both the pediatrician and gastroenterologist on when to bring your child for follow-up and when hospitalization is required.

Pain Management in Pediatric Pancreatitis

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Pediatric Pain Update: Presentations at the Fourth International Symposium
on Pediatric Pain in Helsinki
Charles B. Berde, MD, PhD

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Department of Anaesthesia, Harvard Medical School andChildren’s Hospital, Boston, Massachusetts, USA

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The Pediatric Special Interest Group of the IASP sponsored a Fourth International Symposium on Pediatric Pain in Helsinki in early July, 1997. The meeting was well organized, and well attended by a diverse audience. Review and summary of the abstracts presented at this meeting afford an opportunity to review the state of the field.

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At the time of the first symposium in Seattle in 1988, much effort was exerted in demonstrating that infants feel pain, that they can safely receive anesthesia and analgesia, and that pain can be assessed at all in preverbal subjects. In many respects, the field has matured since then.

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McClain and Lee reported on the impact of family stress on the intensity and duration of chronic pain in children. Wheeler et al. reported on a large experience with pancreatitis in children, treated mostly with parenteral opioids. There is a need for better study of the effectiveness of therapies for both acute and chronic pancreatitis, and better clarification of the risks and benefits of opioids for long-term pain. It remains an open question whether newer opioids, agonist-antagonists, or kappa-receptor-selective opioids have any clear benefit over traditional mu agonists, with their known effects on the sphincter of Oddi.

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Conclusion
The abstracts presented at this meeting demonstrate the continued active interest in the field of children’s pain, improvements in the quality of study design and in measurement tools, and impressive advances from the developmental neurobiologists in understanding the ontogeny of pain responses. The meeting organizers did a great job of presenting this rapidly advancing field and are to be commended.



Conditions Associated with Acute and Chronic Pancreatitis in Childhood

  1. Infections
  2. Ascaris lumbricoides (duct obstruction)
  3. Campylobacter fetus
  4. Clonorchis sinensis (duct obstruction)
  5. Coxsackie B virus
  6. Cytomegalovirus
  7. Echovirus Enterovirus
  8. Epstein-Barr virus Escherichia coli-verotoxin-producing
  9. Hepatitis A and B
  10. Human immunodeficiency virus
  11. Influenza A and B
  12. Legionnaire disease
  13. Leptospirosis
  14. Malaria
  15. Measles
  16. Mumps
  17. Mycoplasma
  18. Rubella
  19. Rubeola
  20. Typhoid fever
  21. Varicella
  22. Yersinia
  23. Trauma
  24. Abdominal radiotherapy
  25. Accidental blunt injury
  26. Burns
  27. Child abuse
  28. Endoscopic retrograde cholangiopancreatography or other ductal imaging using contrast
  29. Surgical trauma
  30. Total body cast
  31. Anatomic
  32. Absence or anomalous insertion of the common bile duct or pancreatic duct
  33. Ampullary disease: diverticulum, stenosis
  34. Annular pancreas
  35. Anomalous choledochopancreaticoductal junction
  36. Aplasia of the pancreas
  37. Biliary tract malformations
  38. Choledochal cyst
  39. Choledochocele
  40. Cholelithiasis
  41. Duodenal obstruction (diverticulum, hematoma, tumor, stricture)
  42. Duodenal ulcer-perforated
  43. Duplication cyst (duodenum, gastropancreatic, common bile duct)
  44. Dysplasia of the pancreas
  45. Gastric trichobezoar
  46. Heterotopic pancreas
  47. Hypoplasia of the pancreas
  48. Pancreas divisum
  49. Pancreatic pseudocyst
  50. Sclerosing cholangitis
  51. Sphincter of Oddi dysfunction
  52. Tumors of the pancreas
  53. Idiopathic
  54. Systemic/Metabolic/Hereditary
  55. Alpha-1-antitrypsin deficiency
  56. Anorexia nervosa
  57. Autoimmune diseases
  58. Brain tumor
  59. Bulimia
  60. Collagen vascular diseases
  61. Congenital partial lipodystrophy
  62. Crohn's disease
  63. Cystic fibrosis
  64. Dermatomyositis
  65. Diabetes mellitus (ketoacidosis)
  66. Glycogen storage disease types Ia, Ib
  67. Head trauma
  68. Hemochromatosis
  69. Hemolytic-uremic syndrome
  70. Henoch-Schonlein purpura
  71. Hereditary pancreatitis
  72. Hyperalimentation
  73. Hypercalcemia
  74. Hyperlipidemia types I, IV, and V
  75. Hyperparathyroidism
  76. Hypertriglyceridemia
  77. Hypothermia
  78. Inborn errors of metabolism (organic acidemias, cytochrome c oxidase deficiency)
  79. Juvenile tropical pancreatitis
  80. Kawasaki disease
  81. Malnutrition with or without refeeding
  82. Periarteritis nodosa
  83. Peritonitis
  84. Renal failure with uremia
  85. Reye syndrome
  86. Sarcoidosis
  87. Septic shock
  88. Systemic lupus erythematosus
  89. Transplantation (bone marrow, heart, kidney, liver, pancreas)
  90. Ulcerative colitis
  91. Wilson disease

To view information on other digestive disease, click on Digestive Diseases Library.

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