APPROACH
TO CHRONIC
DIARRHEA
Dr Toqeer Hussain
PGT MEDICINE
SKBZ CMH MEDICINE
CHRONIC DIARRHEA
🠶 Diarrhea is defined as passage of abnormally
liquid or unformed stools at an increased
frequency.
🠶 Chronic Diarrhea- lasting > 4 weeks .
🠶Most of the causes are Non infectious.
🠶Stool weight more than 200 g daily in western diet.
CLASSIFICATIO
N
🠶1.Secretory diarrhea.
🠶2.Osmotic diarrhea.
🠶3. Steatorrheal
diarrhea.
🠶4.Inflammatory
diarrhea.
🠶5. Dysmotility causes.
🠶6.Factitial diarrhea.
🠶7.Iatrogenic causes.
🠶Also classified –
🠶1. Small bowel
diseases.
🠶2. Colonic diseases.
🠶3. Malabsorption.
SECRETORY DIARRHEA
🠶 Due to derangements in fluid and electrolyte
transport across the entero colnic mucosa.
🠶 Net secretion of anions ( chloride or
bicarbonate ), potassium or net inhibition of
sodium absorption .
🠶 Lack of sufficient absorptive surface area
limits electrolyte absorption ( sodium )
🠶 Characterized by – watery ,large volume fecal output ,
painless and persist with fasting
Secretory diarrhea
1. Exogenous stimulant laxative
2. Chronic ethanol ingestion
3. Other drugs and toxins
4. Endogenous laxatives ( Dihydroxy bile acids)
5. Idiopathic secretory diarrhea
6. Bowel resection or fistula or disease.
7. Partial bowel obstruction / impaction
8. Hormone producing tumors ( VIPoma, Carcinoid ,Gastrinoma, ,
somatostatinoma)
9. Addison ‘s disease
10. Congenital electrolyte absorption defects.
11. Certain bacterial infection.( cholera ,E.coli )
12. Diverticulitis
13. Endocrinopathies – Hyperthyroidism, Mastocytosis,
Medullary Carcinoma thyroid , pheochromocytoma
14. Ileal bile acid malabsorption
15. IBD – Crohn ‘s disease, Microscopic colitis ,
colitis
16. Neoplasia – Colon cancer, lymphoma, Villous
adenoma in rectum
17.Vaculitis.
OSMOTIC DIARRHEA
🠶Osmotic diarrhea occurs when ingested poorly
absorbed osmotically active solutes draw
enough fluid into the lumen to exceed the
reabsorptive capacity of the colon.
🠶Fecal water output increases in proportion to
solute load.
🠶Characteristically ceases with fasting or
with discontinuation of the causative
agent.
🠶Causes include :
🠶1. Osmotic laxatives
🠶2. Ions – Magnesium, sulphate, phosphate
🠶3. Lactase and disaccharide deficiencies
🠶4. Non absorbable carbohydrates – sorbitol, lactulose,
mannitol, polyethylene glycol .
🠶5. Foods – FODMAPs – Fermentable oligosaccharides,
disaccharides, monosaccharides, and polyols.
STEATORRHEAL CAUSES
🠶Fat malabsorption lead to greasy , foul smelling,
difficult flush diarrhea.
🠶Associated with weight loss and nutritional deficiencies
due mal absorption of amino acids and vitamins.
🠶Quantitatively steatorrhea is defined as stool fat
exceeding 7g/day.
🠶Causes
–
🠶 1. Intraluminal mal digestion : Pancreatic exocrine
insufficiency Bacterial overgrowth
Bariatric surgery Liver disease.
Inadequate luminal bile acid sequestration
CAUSES
2. Mucosal malabsorption :
Celiac sprue
Whipple’s disease.
Infections – Giardia abeta lipoproteinemia
Mesenteric Ischemia.
Short bowel syndrome
Small intestinal bacterial over growth
3. Post mucosal obstruction – Primary or Secondary
INFLAMMATORY DIARRHEA
🠶 Accompanied by fever, pain, bleeding.
🠶 Mechanism – Exudation of fluid
Fat mal absorption
Disrupted fluid / electrolyte
absortption Hyper secretion or hyper
motility
Stool analysis – presence of leukocytes or leukocyte
derived proteins
– Calprotectin.
1.Idiopathic inflammatory bowel disease -Crohn ‘s disease and Chronic
ulcerative colitis*
2. Lymphocytic and collagenous colitis
3. Immune related mucosal diseases – primary and secondary
immunodeficiency, food allergy , eosinophilic gastroenteritis
4. Infections – Tuberculosis, yersiniosis , Amebiasis, Strongyloidasis
Pseudomembranous colitis, Cytomegalovirus, HSV
5. Radiation colitis
6. Gastrointestinal malignancies – Colon cancer, lymphoma,
7.Diverticulitis
8. Ischemic colitis
DYSMOTOLITY CASUES
🠶 Rapid transit – mal digestion
🠶Hypermotility – intestinal hurry
🠶Irritable bowel syndrome
🠶Visceral neuromyopathies
🠶Drugs ( prokinetic agents )
🠶Post vagotomy and Post
sympathectomy
🠶Diabetic autonomic neuropathy
🠶Hyperthyroidism
IATROGENIC CAUSES
🠶Cholecystectom
y
🠶Ileal resection
🠶Bariatric surgery
🠶Vagotomy
🠶Fundoplicatio.
FACTITIAL CASUES
🠶Munchausen
syndrome
🠶Eating disorders
APPROACH
🠶 HISTORY :
1.Duration - > 4 weeks
2.Onset – congenital, abrupt, gradual
3. Pattern – Continuous , intermittent
4. Severity
5.Dry mouth , increased thirst, decreased urine out put ,
weakness
- Dehydration
6.Abdominal pain – location, relation to meal, relation to
bowel movements, aggravating or relieving factors
7. Fever
8.Weight loss
9.
Flatulance
10.Bloating or gaseous distension
11.Abdominal cramps
12.Systemic diseases: endocrine, collagen
vascular , neoplastic , immunologic
13.Extra intestinal manifestations- skin
changes, arthralgia, oral apthous ulcer.
14.Fecal incontinence/ urgency- present or
absent , Relationship of defecation to meals /
15. Aggravating factors – diet, stress
16.Alleviating factors –diet, drugs
17.Previous evaluation.
18.Family history – IBD or Sprue
19.Stool characteristics : watery, bloody,
oil/food particles, frequency, volume,
20.Epidemiology
21.Iatrogenic factors – drugs, laxative abuse,
radiation, previous abdominal surgery.
22. Diet history
PHYSICAL EXAMINATION
FINDINGS POTENTIAL IMPLICATION
Orthostasis, Hypotension Dehydration, Neuropathy
Muscle wasting , edema Malnutrition
Urticaria pigmentosa,
dermatographism
Mast cell disease
Pinch purpura, macroglossia Amyloidosis
Hyperpigmentation Addison’s disease
Migratory necrotizing erythema Glucagonoma
Flushing, wheezing, right sided heart
murmur
Carcinoid syndrome
Dermatitis herpetiformis Celiac disease
Thyroid nodule , lymphadenopathy Medullary carcinoma of thyroid
Tremor
, lid lag Hyperthyroidism
Hepatomegaly Endocrine tumor, Amyloidosis
Abdominal bruits Chronic mesenteric ischemia
Arthritis IBD, Whipple’s disease
Lymphadenopathy HIV infection, Lymphoma, cancer
Anal sphincter weakness Fecal incontinence
STOOL ANALYSIS
🠶Random sample / timed sample
🠶Daily stool weight
🠶1.Stool Na, K,
🠶2.Stool pH – acidic ( < 6 ) increased
carbohydrate fermentation in colon
🠶3.Occult blood
🠶4.White blood cells
🠶5. Stool water analyzed for Laxatives -Mg,
PO4, SO4,Bisacodyl
🠶6. Osmotic gap –
< 50 Osm/ Kg – Secretory diarrhea
> 100 Osm/ Kg – Osmotic diarrhea
🠶7.Fat contents –
Steatorrhea – excessive loss of fat in stool
 7 gm or > 9 % of intake for 24 hours.
 > 14 gm /24 hr – fat mal absorption
8.Lactoferrin or Calprotectin
9.Chemical test – Carbohydrates -Anthrone reagent
Alpha 1 anti trypsin clearance to detect protein
losing
enteropathy.
DIAGNOSTIC APPROACH TO THE PATIENT WITH
CHRONIC SECRETORY DIARRHEA
DIAGNOSTIC APPROACH TO THE
PATIENT WITH OSMOTIC
DIARRHEA
DIAGNOSTIC APPROACH TO THE PATIENT
WITH CHRONIC INFLAMMATORY
DIARRHEA
DIAGNOSTIC APPROACH TO THE PATIENT
WITH CHRONIC FATTY DIARRHEA
TREATMENT
🠶Fluid and electrolyte replenishment- oral
rehydration therapy or intravenous fluid therapy.
🠶Empirical therapy :
🠶1.Therapuetic trials of pancreatic enzyme
replacement and conjugated bile acid
supplementation.
🠶2. Opiates – codeine, opium or morphine
🠶3. Octreotide – Carcinoid syndrome ,
endocrinopathies, dumping syndrome,
chemotherapy induced diarrhea and AIDS.
🠶4. Clonidine – diabetic diarrhea
🠶5.Crofelemer – non infectious diarrhea in AIDS
patients on ART
🠶6. Probiotics by modifying the colonic flora
stimulate local immunity and speed resolution in
traveler ‘s diarrhea ,antibiotic associated
diarrhea.
🠶7. Other non specific agents :
Herbal remedies – golden seal,
barberry,arrowroot Stool modifying agents-
psyllium
THANK YOU

APPROACH TO CHRONIC DIAHRRIA.pptx.......

  • 1.
    APPROACH TO CHRONIC DIARRHEA Dr ToqeerHussain PGT MEDICINE SKBZ CMH MEDICINE
  • 2.
    CHRONIC DIARRHEA 🠶 Diarrheais defined as passage of abnormally liquid or unformed stools at an increased frequency. 🠶 Chronic Diarrhea- lasting > 4 weeks . 🠶Most of the causes are Non infectious. 🠶Stool weight more than 200 g daily in western diet.
  • 3.
    CLASSIFICATIO N 🠶1.Secretory diarrhea. 🠶2.Osmotic diarrhea. 🠶3.Steatorrheal diarrhea. 🠶4.Inflammatory diarrhea. 🠶5. Dysmotility causes. 🠶6.Factitial diarrhea. 🠶7.Iatrogenic causes.
  • 4.
    🠶Also classified – 🠶1.Small bowel diseases. 🠶2. Colonic diseases. 🠶3. Malabsorption.
  • 5.
    SECRETORY DIARRHEA 🠶 Dueto derangements in fluid and electrolyte transport across the entero colnic mucosa. 🠶 Net secretion of anions ( chloride or bicarbonate ), potassium or net inhibition of sodium absorption . 🠶 Lack of sufficient absorptive surface area limits electrolyte absorption ( sodium ) 🠶 Characterized by – watery ,large volume fecal output , painless and persist with fasting
  • 6.
    Secretory diarrhea 1. Exogenousstimulant laxative 2. Chronic ethanol ingestion 3. Other drugs and toxins 4. Endogenous laxatives ( Dihydroxy bile acids) 5. Idiopathic secretory diarrhea 6. Bowel resection or fistula or disease. 7. Partial bowel obstruction / impaction 8. Hormone producing tumors ( VIPoma, Carcinoid ,Gastrinoma, , somatostatinoma) 9. Addison ‘s disease 10. Congenital electrolyte absorption defects. 11. Certain bacterial infection.( cholera ,E.coli )
  • 7.
    12. Diverticulitis 13. Endocrinopathies– Hyperthyroidism, Mastocytosis, Medullary Carcinoma thyroid , pheochromocytoma 14. Ileal bile acid malabsorption 15. IBD – Crohn ‘s disease, Microscopic colitis , colitis 16. Neoplasia – Colon cancer, lymphoma, Villous adenoma in rectum 17.Vaculitis.
  • 8.
    OSMOTIC DIARRHEA 🠶Osmotic diarrheaoccurs when ingested poorly absorbed osmotically active solutes draw enough fluid into the lumen to exceed the reabsorptive capacity of the colon. 🠶Fecal water output increases in proportion to solute load. 🠶Characteristically ceases with fasting or with discontinuation of the causative agent.
  • 9.
    🠶Causes include : 🠶1.Osmotic laxatives 🠶2. Ions – Magnesium, sulphate, phosphate 🠶3. Lactase and disaccharide deficiencies 🠶4. Non absorbable carbohydrates – sorbitol, lactulose, mannitol, polyethylene glycol . 🠶5. Foods – FODMAPs – Fermentable oligosaccharides, disaccharides, monosaccharides, and polyols.
  • 10.
    STEATORRHEAL CAUSES 🠶Fat malabsorptionlead to greasy , foul smelling, difficult flush diarrhea. 🠶Associated with weight loss and nutritional deficiencies due mal absorption of amino acids and vitamins. 🠶Quantitatively steatorrhea is defined as stool fat exceeding 7g/day.
  • 11.
    🠶Causes – 🠶 1. Intraluminalmal digestion : Pancreatic exocrine insufficiency Bacterial overgrowth Bariatric surgery Liver disease. Inadequate luminal bile acid sequestration
  • 12.
    CAUSES 2. Mucosal malabsorption: Celiac sprue Whipple’s disease. Infections – Giardia abeta lipoproteinemia Mesenteric Ischemia. Short bowel syndrome Small intestinal bacterial over growth 3. Post mucosal obstruction – Primary or Secondary
  • 13.
    INFLAMMATORY DIARRHEA 🠶 Accompaniedby fever, pain, bleeding. 🠶 Mechanism – Exudation of fluid Fat mal absorption Disrupted fluid / electrolyte absortption Hyper secretion or hyper motility Stool analysis – presence of leukocytes or leukocyte derived proteins – Calprotectin.
  • 14.
    1.Idiopathic inflammatory boweldisease -Crohn ‘s disease and Chronic ulcerative colitis* 2. Lymphocytic and collagenous colitis 3. Immune related mucosal diseases – primary and secondary immunodeficiency, food allergy , eosinophilic gastroenteritis 4. Infections – Tuberculosis, yersiniosis , Amebiasis, Strongyloidasis Pseudomembranous colitis, Cytomegalovirus, HSV 5. Radiation colitis 6. Gastrointestinal malignancies – Colon cancer, lymphoma, 7.Diverticulitis 8. Ischemic colitis
  • 15.
    DYSMOTOLITY CASUES 🠶 Rapidtransit – mal digestion 🠶Hypermotility – intestinal hurry 🠶Irritable bowel syndrome 🠶Visceral neuromyopathies 🠶Drugs ( prokinetic agents ) 🠶Post vagotomy and Post sympathectomy 🠶Diabetic autonomic neuropathy 🠶Hyperthyroidism
  • 16.
  • 17.
  • 18.
    APPROACH 🠶 HISTORY : 1.Duration- > 4 weeks 2.Onset – congenital, abrupt, gradual 3. Pattern – Continuous , intermittent 4. Severity 5.Dry mouth , increased thirst, decreased urine out put , weakness - Dehydration 6.Abdominal pain – location, relation to meal, relation to bowel movements, aggravating or relieving factors 7. Fever 8.Weight loss
  • 19.
    9. Flatulance 10.Bloating or gaseousdistension 11.Abdominal cramps 12.Systemic diseases: endocrine, collagen vascular , neoplastic , immunologic 13.Extra intestinal manifestations- skin changes, arthralgia, oral apthous ulcer. 14.Fecal incontinence/ urgency- present or absent , Relationship of defecation to meals /
  • 20.
    15. Aggravating factors– diet, stress 16.Alleviating factors –diet, drugs 17.Previous evaluation. 18.Family history – IBD or Sprue 19.Stool characteristics : watery, bloody, oil/food particles, frequency, volume, 20.Epidemiology 21.Iatrogenic factors – drugs, laxative abuse, radiation, previous abdominal surgery. 22. Diet history
  • 21.
    PHYSICAL EXAMINATION FINDINGS POTENTIALIMPLICATION Orthostasis, Hypotension Dehydration, Neuropathy Muscle wasting , edema Malnutrition Urticaria pigmentosa, dermatographism Mast cell disease Pinch purpura, macroglossia Amyloidosis Hyperpigmentation Addison’s disease Migratory necrotizing erythema Glucagonoma
  • 22.
    Flushing, wheezing, rightsided heart murmur Carcinoid syndrome Dermatitis herpetiformis Celiac disease Thyroid nodule , lymphadenopathy Medullary carcinoma of thyroid Tremor , lid lag Hyperthyroidism Hepatomegaly Endocrine tumor, Amyloidosis Abdominal bruits Chronic mesenteric ischemia Arthritis IBD, Whipple’s disease Lymphadenopathy HIV infection, Lymphoma, cancer Anal sphincter weakness Fecal incontinence
  • 23.
    STOOL ANALYSIS 🠶Random sample/ timed sample 🠶Daily stool weight 🠶1.Stool Na, K, 🠶2.Stool pH – acidic ( < 6 ) increased carbohydrate fermentation in colon 🠶3.Occult blood 🠶4.White blood cells 🠶5. Stool water analyzed for Laxatives -Mg, PO4, SO4,Bisacodyl
  • 24.
    🠶6. Osmotic gap– < 50 Osm/ Kg – Secretory diarrhea > 100 Osm/ Kg – Osmotic diarrhea 🠶7.Fat contents – Steatorrhea – excessive loss of fat in stool  7 gm or > 9 % of intake for 24 hours.  > 14 gm /24 hr – fat mal absorption 8.Lactoferrin or Calprotectin 9.Chemical test – Carbohydrates -Anthrone reagent Alpha 1 anti trypsin clearance to detect protein losing enteropathy.
  • 25.
    DIAGNOSTIC APPROACH TOTHE PATIENT WITH CHRONIC SECRETORY DIARRHEA
  • 26.
    DIAGNOSTIC APPROACH TOTHE PATIENT WITH OSMOTIC DIARRHEA
  • 27.
    DIAGNOSTIC APPROACH TOTHE PATIENT WITH CHRONIC INFLAMMATORY DIARRHEA
  • 28.
    DIAGNOSTIC APPROACH TOTHE PATIENT WITH CHRONIC FATTY DIARRHEA
  • 29.
    TREATMENT 🠶Fluid and electrolytereplenishment- oral rehydration therapy or intravenous fluid therapy. 🠶Empirical therapy : 🠶1.Therapuetic trials of pancreatic enzyme replacement and conjugated bile acid supplementation. 🠶2. Opiates – codeine, opium or morphine 🠶3. Octreotide – Carcinoid syndrome , endocrinopathies, dumping syndrome, chemotherapy induced diarrhea and AIDS.
  • 30.
    🠶4. Clonidine –diabetic diarrhea 🠶5.Crofelemer – non infectious diarrhea in AIDS patients on ART 🠶6. Probiotics by modifying the colonic flora stimulate local immunity and speed resolution in traveler ‘s diarrhea ,antibiotic associated diarrhea. 🠶7. Other non specific agents : Herbal remedies – golden seal, barberry,arrowroot Stool modifying agents- psyllium
  • 32.