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PERSISTENT DIARRHEA
CHRONIC DIARRHEA
Moderator Presented by
Dr. Sumit Das Dr. Fahad Muhamed Shareef A T
Ass. Prof. PG in Pediatrics
Dept. of Pediatrics
• Diarrhea
– 3 times in 24 hours
– Consistency important over frequency
• Acute Diarrhea
• Persistent Diarrhea
• Chronic Diarrhea
TERMS & DEFINITIONS
PERSISTENT DIARRHEA
• Starts as acute, lasts at least 14 days with
the exclusion of chronic or recurrent
diarrheal conditions
– Celiac disease Tropical Sprue
– Biochemical Congenital
– Metabolic
?WHY
• 10% of total diarrhea
• 35% of diarrheal deaths
• For every 100 children, 7 suffers
• PD in Malnutrition – 20%
• 60% < 6 months
• 90% < 1 year
RISK FACTORS & CAUSES
• Repeated enteric infections
• Malabsorption of CHO & fats
• Malnutrition
• Very young age
• Recent introduction of animal milk
• Irrational usage of antibiotics
• Lack of breast feeding/ bottle feeding
• Improper therapy of ADD
• Protein dietary intolerance
PATHOGENESIS
“PSIMI”
Mucosal injury d/t invasive pathogens
Malabsorption of macro & mircronutrients
Prolongation of mucosal injury & delayed intestinal repair
mechanisms (ineff. villous repair)
Sequential infection with multiple pathogens
Increased absorption of foreign proteins
Malnutrition
PRESENTATION
• Several loose stools
• Dehydration absent
• If present, inc stool output
dec oral intake
• Features of PEM
Clinical Evaluation
• History & Physical Examn.
• Should be excluded from Chronic
diarrhoea
• To R/o associated systemic infections
– CBC
– URE & C/S
– CXR
• Stool microscopy
• Stool pH & reducing substance
• Nutritional management is the cornerstone
– Dietary management
– Supplemental vitamins & minerals
• Two third cases – OPD
• Assess dehydration
• Hospitalization necessary or not
• Avoid unnecessary antibiotics
TREATMENT
When to hospitalize?
• Age < 4 mon & not breast fed
• Dehydration
• Severe malnutrition
– W/L < 70%
– W/A < 60%
– Pedal edema
• Systemic infection
Dietary Management
< 6 months
• Encourage exclusive breast feeding
• Reestablish breast feeding
• Replace animal milks with curds or lactose
free formula
• Cooked rice may be mixed if necessary
>6 months
• Continue Breast feeding
• Mixed diet
• Initiate DIET A
• DIET B
• DIET C
Milk cereal mixtures
v/s
milk free diet
• Highly palatable
• Provide good quality protein
• Some micronutrients
• Faster weight gain
• No significant increase in stool output
• No increasing risk of dehydration
Principles
• Total elimination of milk not necessary
• Limit intake to 2g/kg/day lactose (50-60
ml)
• Start feeding asap
• 6-7 feeds per day
• Start with 110kcal/kg and inc to 150kcal/kg
over 2 weeks
• If enteral intake diff, start NG feed
DIET A
reduced lactose diet (65-70%)
Ingredients Measures Wt/Vol
Milk 1/3 katori 50ml
Sugar 1.5 tsp 7g
Oil 1 tsp 4.5g
Puffed rice powder 2 tsp 6.0g
Water 2/3 katori 100ml
Calories/100g 85 kcal
Proteins/100g 2.0g
How to prepare
DIET B
lactose free with reduced starch(15-20%)
Ingredients Measures Wt/Vol
Egg white 3 tsp Half egg white
Puffed rice powder 3 tsp 9.0g
Glucose 1.5 tsp 7g
Oil 1.5 tsp 7g
Water 3/4 katori 120ml
Calories/100g 90 kcal
Proteins/100g 2.4g
How to prepare
DIET C
Monosaccharide based
Ingredients Measures Wt/Vol
Egg white 3 tsp Half egg white
Or Chicken puree 5 tsp 15 g
Glucose 1.5 tsp 7 g
Oil 1.5 tsp 7 g
Water 1 katori 150ml
Calories/100g 67 kcal
Proteins/100g 3 g
How to prepare
Supplementation
• 2 x RDA of multivitamins and minerals for
2-4 weeks
• At least Vit A (single dose) & Zinc 10-
20mg (2 weeks)
• In severe malnutrition,
– 50% Mg sulfate 0.2ml/kg/dose twice a day for
3 days
– Potassium 5-6meq/kg/day
Monitoring response
• Dec in no. of diarrheal stools
– <= 2 liquid stools/day for 2 consec. Days
• Adeq. Food intake
• Weight gain
Most children lose wt in the initial 1-2 days
and then show a steady gain
When to change diet
• Marked increase in stool freq (10/day)
• Return of signs of dehydration
• Failure to establish wt gain by day 7
 after discharge little milk after 10 days
No signs of lactose intolerance
Milk qty increased and normal diet ovr a
week
PARENTERAL NUTRITION
• PD with oral intolerance after 10 days
• Severe forms of IBD+ resistant colitis
• Severe NEC
COMPLICATIONS
PARTIAL PARENTERAL NUTRITION
• Isolyte P - 250ml 25%D – 150ml
• A.A – 100ml NaHCO3 – 20ml
• KCl – 5ml MVI – 2ml
• 50-60 ml/kg/d
Antimicrobial Therapy
• Gross blood in stools
• Asso systemic infection
• Severe malnutrition
• Screen for UTI and treat
• Group B Salmonella isolated in stool
PREVENTION
• Improving nutritional status
• Prevention and rational treatment of acute
diarrhea
• Promote exclusive breast feeding
• Ensure safe complemetary feeding
practices
• Zinc supplementaton
• Avoid irrational & unnecessary use of
antibiotics
CHRONIC DIARRHEA
• Diarrhea for >= 14 days with exclusion of
persistent diarrhea.
• Infections
• Malabsorption
• Metabolic
• Miscellaneous
INFECTIONS
• Tuberculosis
• Eosinophilic gastroenteritis
• IBD
• NEC
• Henoch Scholein
MALABSORPTION
• Pancreatic diseases
• Liver diseases
• Intestinal diseases
INTESTNAL MALABSORPTION
• CELIAC DISEASE (TVA)
• GIARDIASIS
• BACTERIAL OVERGROWTH
• MALNUTRITION PVA
• TROPICAL SPRUE
• ABETALIPOPROTEINEMIA
• LYMPHANGIECTASIA
• ENZYME DEF.
Miscellaneous
• TODDLER’S DIARRHEA
• CHRONIC NON SPECIFIC DIARRHEA
• IRRITABLE BOWEL SYNDROME
• AUTOIMMUNE ENTEROPATHY
• MOTILITY DOSORDERS
• ENDOCRINE
• NEOPLASTIC DISORDERS
• MANCHAUSEN BY PROXY
Clinical evaluation
• Onset
– At birth chloride diarrhea, microvillous inclusion dis.
– 6 mon autoimmune enteropathy
– Infant Hirschsprung’s dis
– Abrupt Infections
– Gradual Rest
• Weight loss : Malabsorption,neoplasm
• Dietary history
– Lactose intolerance, cow’s protein, soy protein, egg protein
– Overfeeding, chewing gum diarrhea, Non specific diarrhea
• Treatment history
– Antibiotics, prpnl, digitalis, cholestyramine, Munchausen
• Family history : IBD, IBS
STOOL CHARACTERISTICS
• Blood Dysentry
• Oil/ food particlesMalabsorption, maldigestion
• White/ tan colour Celiac disease, absence of bile
• Loose & bulky Celiac disease
• Greasy & yellowish exocrine pancreatic insuff
• Liquid as water Cong. Chloride diarrhea
• Plain x-ray abdomen
• Ultrasonography
• Colonoscopy
• Capsule endoscopy
STEP 1 Intestinal microbiology
• Stool cultures
• Microscopy for parasites
• Viruses
• Stool electrolytes
• H2 breath test
Screening test for celiac disease (transglutaminase 2 autoantibodies)
Noninvasive tests for:
• Intestinal function
• Pancreatic function and sweat test
• Intestinal inflammation
Tests for food allergy
• Prick/patch tests
DIAGNOSTIC WORK UP
TEST NORMAL VALUES IMPLICATION
α1-Antitrypsin concentration <0.9 mg/g stool
Increased intestinal permeability
and protein loss
Steatocrit <2.5% (>2 yr old) Fecal fat loss
Fecal reducing substances Absent Carbohydrate malabsorption
Elastase concentration >200 µg/g stool Exocrine pancreatic dysfunction
Chymotrypsin concentration
>7.5 U/g
>375 U/24 h
Exocrine pancreatic dysfunction
Fecal occult blood Absent
Fecal blood loss, distal intestinal
inflammation
Calprotectin concentration 100 µg/g stool Intestinal inflammation
Fecal leukocytes <5/microscopic field Colonic inflammation
Nitric oxide in rectal dyalisate <5 µM of NO2
−/NO3
− Rectal inflammation
Dual sugar (cellobiose/mannitol)
absorption test
Urine excretion ratio:
0.010 ±0.018
Increased intestinal permeability
NON INVASIVE TESTS
STEP 2 INTESTINAL MORPHOLOGY
• Standard jejunal/colonic histology
• Morphometry
• PAS staining
• Electron microscopy
STEP 3 SPECIAL INVESTIGATIONS
Intestinal immunohistochemistry
Anti-enterocyte antibodies
Serum chromogranin and catecholamines
Autoantibodies
75SeHCAT measurement
Brush border enzymatic activities
Motility and electrophysiological studies
TREATMENT
• General supportive measures
– Replacement of fluids & electrolytes
• Nutritional rehabilitation
• Elimination diet
• Treat the cause
CELIAC DISEASE
• Immunologically mediated small intestinal
enteropathy
• Sensitivity to gluten
• Multiple associations
• Classic form :
– 6m- 24m
– Chronic diarrhea, anorexia,vomiting
– Abd pain & distension
– Poor weight gain & wieght loss
• Older children
– Diarrhea, nausea, vomiting
– Abd pain, bloating,
– Weight loss & constipation
• Extraintestinal symptoms
• In Late presentation
• Short stature, IDA
• DH, delayed puberty
• Hepatitis, osteopenia
• Arthritis, Epilepsy
• DIAGNOSIS
• Serology
– Anti-gliadin IgA & IgG
– Anti-reticulin IgA
– Anti- endomysial Ig A - high
– Anti-TTG high
• Intestinal biopsy & HPE
– Villous atrophy wt crypt hyperplasia
– Abnormal surface epithelium
– Full clinical & histological remission
• TREATMENT
• Strict gluten free diet
PERSISTENT v/s CHRONIC
• Onset
• Age group
• Wt. loss
• Dehydration
• Recurrence
• Etiology
persistent diarrhea & Chronic diarrhea

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persistent diarrhea & Chronic diarrhea

  • 1. PERSISTENT DIARRHEA CHRONIC DIARRHEA Moderator Presented by Dr. Sumit Das Dr. Fahad Muhamed Shareef A T Ass. Prof. PG in Pediatrics Dept. of Pediatrics
  • 2. • Diarrhea – 3 times in 24 hours – Consistency important over frequency • Acute Diarrhea • Persistent Diarrhea • Chronic Diarrhea TERMS & DEFINITIONS
  • 3. PERSISTENT DIARRHEA • Starts as acute, lasts at least 14 days with the exclusion of chronic or recurrent diarrheal conditions – Celiac disease Tropical Sprue – Biochemical Congenital – Metabolic
  • 4. ?WHY • 10% of total diarrhea • 35% of diarrheal deaths • For every 100 children, 7 suffers • PD in Malnutrition – 20% • 60% < 6 months • 90% < 1 year
  • 5. RISK FACTORS & CAUSES • Repeated enteric infections • Malabsorption of CHO & fats • Malnutrition • Very young age • Recent introduction of animal milk • Irrational usage of antibiotics • Lack of breast feeding/ bottle feeding • Improper therapy of ADD • Protein dietary intolerance
  • 6. PATHOGENESIS “PSIMI” Mucosal injury d/t invasive pathogens Malabsorption of macro & mircronutrients Prolongation of mucosal injury & delayed intestinal repair mechanisms (ineff. villous repair) Sequential infection with multiple pathogens Increased absorption of foreign proteins Malnutrition
  • 7. PRESENTATION • Several loose stools • Dehydration absent • If present, inc stool output dec oral intake • Features of PEM
  • 8. Clinical Evaluation • History & Physical Examn. • Should be excluded from Chronic diarrhoea • To R/o associated systemic infections – CBC – URE & C/S – CXR • Stool microscopy • Stool pH & reducing substance
  • 9. • Nutritional management is the cornerstone – Dietary management – Supplemental vitamins & minerals • Two third cases – OPD • Assess dehydration • Hospitalization necessary or not • Avoid unnecessary antibiotics TREATMENT
  • 10. When to hospitalize? • Age < 4 mon & not breast fed • Dehydration • Severe malnutrition – W/L < 70% – W/A < 60% – Pedal edema • Systemic infection
  • 11. Dietary Management < 6 months • Encourage exclusive breast feeding • Reestablish breast feeding • Replace animal milks with curds or lactose free formula • Cooked rice may be mixed if necessary
  • 12. >6 months • Continue Breast feeding • Mixed diet • Initiate DIET A • DIET B • DIET C
  • 13. Milk cereal mixtures v/s milk free diet • Highly palatable • Provide good quality protein • Some micronutrients • Faster weight gain • No significant increase in stool output • No increasing risk of dehydration
  • 14. Principles • Total elimination of milk not necessary • Limit intake to 2g/kg/day lactose (50-60 ml) • Start feeding asap • 6-7 feeds per day • Start with 110kcal/kg and inc to 150kcal/kg over 2 weeks • If enteral intake diff, start NG feed
  • 15. DIET A reduced lactose diet (65-70%) Ingredients Measures Wt/Vol Milk 1/3 katori 50ml Sugar 1.5 tsp 7g Oil 1 tsp 4.5g Puffed rice powder 2 tsp 6.0g Water 2/3 katori 100ml Calories/100g 85 kcal Proteins/100g 2.0g How to prepare
  • 16. DIET B lactose free with reduced starch(15-20%) Ingredients Measures Wt/Vol Egg white 3 tsp Half egg white Puffed rice powder 3 tsp 9.0g Glucose 1.5 tsp 7g Oil 1.5 tsp 7g Water 3/4 katori 120ml Calories/100g 90 kcal Proteins/100g 2.4g How to prepare
  • 17. DIET C Monosaccharide based Ingredients Measures Wt/Vol Egg white 3 tsp Half egg white Or Chicken puree 5 tsp 15 g Glucose 1.5 tsp 7 g Oil 1.5 tsp 7 g Water 1 katori 150ml Calories/100g 67 kcal Proteins/100g 3 g How to prepare
  • 18. Supplementation • 2 x RDA of multivitamins and minerals for 2-4 weeks • At least Vit A (single dose) & Zinc 10- 20mg (2 weeks) • In severe malnutrition, – 50% Mg sulfate 0.2ml/kg/dose twice a day for 3 days – Potassium 5-6meq/kg/day
  • 19. Monitoring response • Dec in no. of diarrheal stools – <= 2 liquid stools/day for 2 consec. Days • Adeq. Food intake • Weight gain Most children lose wt in the initial 1-2 days and then show a steady gain
  • 20. When to change diet • Marked increase in stool freq (10/day) • Return of signs of dehydration • Failure to establish wt gain by day 7  after discharge little milk after 10 days No signs of lactose intolerance Milk qty increased and normal diet ovr a week
  • 21. PARENTERAL NUTRITION • PD with oral intolerance after 10 days • Severe forms of IBD+ resistant colitis • Severe NEC COMPLICATIONS PARTIAL PARENTERAL NUTRITION • Isolyte P - 250ml 25%D – 150ml • A.A – 100ml NaHCO3 – 20ml • KCl – 5ml MVI – 2ml • 50-60 ml/kg/d
  • 22. Antimicrobial Therapy • Gross blood in stools • Asso systemic infection • Severe malnutrition • Screen for UTI and treat • Group B Salmonella isolated in stool
  • 23.
  • 24. PREVENTION • Improving nutritional status • Prevention and rational treatment of acute diarrhea • Promote exclusive breast feeding • Ensure safe complemetary feeding practices • Zinc supplementaton • Avoid irrational & unnecessary use of antibiotics
  • 25.
  • 26. CHRONIC DIARRHEA • Diarrhea for >= 14 days with exclusion of persistent diarrhea. • Infections • Malabsorption • Metabolic • Miscellaneous
  • 27. INFECTIONS • Tuberculosis • Eosinophilic gastroenteritis • IBD • NEC • Henoch Scholein MALABSORPTION • Pancreatic diseases • Liver diseases • Intestinal diseases
  • 28. INTESTNAL MALABSORPTION • CELIAC DISEASE (TVA) • GIARDIASIS • BACTERIAL OVERGROWTH • MALNUTRITION PVA • TROPICAL SPRUE • ABETALIPOPROTEINEMIA • LYMPHANGIECTASIA • ENZYME DEF.
  • 29. Miscellaneous • TODDLER’S DIARRHEA • CHRONIC NON SPECIFIC DIARRHEA • IRRITABLE BOWEL SYNDROME • AUTOIMMUNE ENTEROPATHY • MOTILITY DOSORDERS • ENDOCRINE • NEOPLASTIC DISORDERS • MANCHAUSEN BY PROXY
  • 30. Clinical evaluation • Onset – At birth chloride diarrhea, microvillous inclusion dis. – 6 mon autoimmune enteropathy – Infant Hirschsprung’s dis – Abrupt Infections – Gradual Rest • Weight loss : Malabsorption,neoplasm • Dietary history – Lactose intolerance, cow’s protein, soy protein, egg protein – Overfeeding, chewing gum diarrhea, Non specific diarrhea • Treatment history – Antibiotics, prpnl, digitalis, cholestyramine, Munchausen • Family history : IBD, IBS
  • 31. STOOL CHARACTERISTICS • Blood Dysentry • Oil/ food particlesMalabsorption, maldigestion • White/ tan colour Celiac disease, absence of bile • Loose & bulky Celiac disease • Greasy & yellowish exocrine pancreatic insuff • Liquid as water Cong. Chloride diarrhea
  • 32.
  • 33. • Plain x-ray abdomen • Ultrasonography • Colonoscopy • Capsule endoscopy
  • 34. STEP 1 Intestinal microbiology • Stool cultures • Microscopy for parasites • Viruses • Stool electrolytes • H2 breath test Screening test for celiac disease (transglutaminase 2 autoantibodies) Noninvasive tests for: • Intestinal function • Pancreatic function and sweat test • Intestinal inflammation Tests for food allergy • Prick/patch tests DIAGNOSTIC WORK UP
  • 35. TEST NORMAL VALUES IMPLICATION α1-Antitrypsin concentration <0.9 mg/g stool Increased intestinal permeability and protein loss Steatocrit <2.5% (>2 yr old) Fecal fat loss Fecal reducing substances Absent Carbohydrate malabsorption Elastase concentration >200 µg/g stool Exocrine pancreatic dysfunction Chymotrypsin concentration >7.5 U/g >375 U/24 h Exocrine pancreatic dysfunction Fecal occult blood Absent Fecal blood loss, distal intestinal inflammation Calprotectin concentration 100 µg/g stool Intestinal inflammation Fecal leukocytes <5/microscopic field Colonic inflammation Nitric oxide in rectal dyalisate <5 µM of NO2 −/NO3 − Rectal inflammation Dual sugar (cellobiose/mannitol) absorption test Urine excretion ratio: 0.010 ±0.018 Increased intestinal permeability NON INVASIVE TESTS
  • 36. STEP 2 INTESTINAL MORPHOLOGY • Standard jejunal/colonic histology • Morphometry • PAS staining • Electron microscopy STEP 3 SPECIAL INVESTIGATIONS Intestinal immunohistochemistry Anti-enterocyte antibodies Serum chromogranin and catecholamines Autoantibodies 75SeHCAT measurement Brush border enzymatic activities Motility and electrophysiological studies
  • 37. TREATMENT • General supportive measures – Replacement of fluids & electrolytes • Nutritional rehabilitation • Elimination diet • Treat the cause
  • 38. CELIAC DISEASE • Immunologically mediated small intestinal enteropathy • Sensitivity to gluten • Multiple associations • Classic form : – 6m- 24m – Chronic diarrhea, anorexia,vomiting – Abd pain & distension – Poor weight gain & wieght loss
  • 39. • Older children – Diarrhea, nausea, vomiting – Abd pain, bloating, – Weight loss & constipation • Extraintestinal symptoms • In Late presentation • Short stature, IDA • DH, delayed puberty • Hepatitis, osteopenia • Arthritis, Epilepsy
  • 40. • DIAGNOSIS • Serology – Anti-gliadin IgA & IgG – Anti-reticulin IgA – Anti- endomysial Ig A - high – Anti-TTG high • Intestinal biopsy & HPE – Villous atrophy wt crypt hyperplasia – Abnormal surface epithelium – Full clinical & histological remission • TREATMENT • Strict gluten free diet
  • 41. PERSISTENT v/s CHRONIC • Onset • Age group • Wt. loss • Dehydration • Recurrence • Etiology

Editor's Notes

  1. Mix milk, sugar, rice together….. Add boiled water and mix well. Add oil
  2. Whip the egg white well. Add puffed rice powder, glucose, oil and mix well. Add boiled water and mix rapidly to avoid clumping
  3. Boil chicken, remove bones and make chicken puree. Mix chicken puree with glucose and oil. Add boiled water to make a smoothi flowing feed