1.Identify the problems from the history.
Young college student
Increased frequency of bowel movements
Stools fill up the toilet bowl
Stools float in the bowl
Foul odor and offensive flatus
Long standing problem with bowels movements
Cystic fibrosis
Frequent pulmonary infections
2. Identify the salient findings from physical examination.
Diminished breath sounds with few expiratory wheezes
Loud P2
Clubbing
Decreased subcutaneous fat and muscle mass
Abdomen "doughy" consistency
Stool pasty and malodorous
3.
Based on history and physical examination cite
the major clinical problem (not the diagnosis):
Diarrhea
Steatorrhea/malabsorption
Cystic fibrosis
4. Before we define what is diarrhea, tell me what is normal bowel movements.
Normal stool
Normal bowel frequency ranges from three times a week three times a day
Weight 200 g/d
5. What is the definition for diarrhea?
The definition of diarrhea is somewhat controversial. It depends on the patient’s as well as the physician’s perspective.
Patients usually consider diarrhea as being an increase in the daily frequency, liquidity, or volume of the stool. Also an urgency to defecate.
Scientifically, diarrhea exists if more that 300 gms stool is passed daily on the Western diet.
Clinically, it may be defined as more than 3 bowel movements day.
Relative to what the patient’s “usual” habit has been.
It is important to take a good history
and ask appropriate questions regarding stooling. Don’t just accept the patient’s statement of diarrhea.
6. What is Pseudodiarrhea or hyper defecation:
Increase in frequency without an increase in weight of the stool.
Irritable bowel syndrome
Proctitis
Hyperthyroidism
7. Define Fecal incontinence
Involuntary release of rectal contents
8. How do we clinically classify Diarrhea?
Diarrhea lasting two weeks or less is considered to be Acute Diarrhea
Diarrhea lasting longer than two weeks or is intermittent over months or years is considered Chronic Diarrhea.
9. Which of these diarrhea does our patient have?
Chronic Diarrhea
10. What is the difference between acute and chronic diarrhea?
Acute Diarrhea
lasts two weeks or less
self-limited
requiring no diagnostic work-up
symptomatic treatment only (fluids)
Acute diarrhea should be investigated only if there is
evidence of tissue invasion such as blood or pus in the stool
fever
leukocytosis
severity that produces significant fluid and electrolyte loss
Chronic diarrhea
lasts longer than two weeks
or is intermittent over months or years
This form requires a diagnostic work-up and a treatment strategy
11. What questions would you ask a patient with diarrhea?
Compare the patient’s usual or normal frequency and pattern with that of the current pattern or frequency.
Ask about the characteristics
Watery, bulky, color, presence of blood or pus
Bulky greasy foul smelling stools : Intestinal malabsorption
Change in odor
Change in timing
Frequency, duration
Continuous, intermittent
Time of day or night
Diarrhea alternating with constipation : Irritable bowel syndrome, Cancer colon
Precipitating events such as food or drug
Causes of relief
Improves with fasting : Osmotic diarrhea
Ask about associated symptoms
Fever, nausea, vomiting, abdominal pain, anorexia: Inflammatory diarrhea
Symptoms of autonomic dysfunction: Diabetic diarrhea
Flatulence and bloating : Intestinal mucosal disease
Arthritis, skin lesions, ocular symptoms: Idiopathic inflammatory bowel disease
Edema, Ascites: Protein loosing enteropathy
Ask about predisposing factors such as travel, diet, drug history, family history, other medical surgical problems.
12. Summarize pertinent historical information on our patient with regards to diarrhea.
3-4 bowel movements/ day which he has accepted as normal
Bulky greasy foul smelling stools that float in toilet bowl
Continuous
No identified precipitating or relieving factor
No associated symptoms
History of Cystic fibrosis
13. What physical findings would you look for in the evaluation of a patient with Chronic diarrhea?
Consequences to diarrhea
Edema, Ascites / Protein loosing enteropathy
Signs of Vitamin deficiency of fat-soluble vitamins (A, D, E, K)./ Steatorrhea
Signs of hypovolemia and dehydration
Etiology of diarrhea
CNS disturbances / Altered motility
Signs of autonomic dysfunction / Diabetes
Arthritis, skin lesions, ocular signs: Idiopathic inflammatory bowel disease
14. What are the pertinent physical findings in this patient?
Decreased subcutaneous fat and muscle mass
Tympanitic abdomen
"doughy" consistency
Loud P2 / Pulmonary hypertension
Expiratory wheeze / Consistent with CF
Clubbing / Consistent with CF
15. Classify the chronic diarrhea into subgroups:
Chronic diarrhea can be classified as follows:
Steatorrhea : Passage of stools containing an excessive amount of fat (>7 gm fecal fat/24 hrs or more than 10% of ingested fat)
Intraluminal stage
Deficiency of pancreatic enzymes/Chronic pancreatitis
Bacterial overgrowth in the small bowel/decreased motility in a diabetic
Deficient bile salts/biliary tract disease
Intestinal stage
Damage to the absorptive surface (mucosa)/Celiac disease
Removal stage
Damaged lymphatic channels/Whipple disease
Watery diarrhea
Osmotic diarrhea. A consequence of increased amounts of poorly absorbable, osmotically active solutes in the lumen of the intestine
Disaccharide deficiency/lactase deficiency
Ingestion of drugs such as laxatives and antacids containing magnesium or phosphate
Chewing gum (sorbitol)
Secretary diarrhea: Secretion of electrolytes and water exceed absorption or absorption of electrolytes and water are impaired
Certain laxatives/castor oil
Bacterial toxin/infection
Exudative Inflammation of the bowel mucosa may result in loss of pus, mucus, blood, protein
E. histolytica
Giardia
Intestinal dysmotility
Increased motility/hyperthyroidism
Delayed transit time with bacterial growth/ blind loop syndrome or diabetic neuropathy
16. What investigational options do we have in the workup of patients with Chronic diarrhea, based on the knowledge of subgroups of chronic diarrhea ?
Stool
Blood and leukocytes in stool : Inflammatory diarrhea. Inflammatory colonic disease.
Fecal fat. Steatorrhea (>7 gm fecal fat/24 hrs)
Stool for ova and parasites
Stool for C/S
C. dificile toxin.
Malabsorption
Iron, folate, B12 : Malabsorption
Vitamin deficiency of fat-soluble vitamins (A, D, E, K).
Fecal fat. Steatorrhea (>7 gm fecal fat/24 hrs)
D-xylose absorption test
Bowel changes
EGD: Small intestine biopsy
Colonoscopy indicated if stool is negative for pathogens. Colonic mucosa may have to be looked at endoscopically and biopsied if inflammatory bowel disease is suspected.
.
17. What are the appropriate investigations in this patient?
Stool
Malabsorption studies
18. You have the results of stool for pathogens and fecal fat.
No blood or leukocytes in stools
>11 gm fecal fat/24 hrs,
No pathogens detected in stools.
19. What is D-xylose test?
D-xylose test should be done when there is steatorrhea .
Helps distinguish steatorrhea due to Pancreatic disease from small bowel disease
Normal D-xylose indicates pancreatic disease.
Abnormal D-xylose indicates small bowel disease and small bowel biopsy is indicated.
>25% of ingested dose (25gm) in the 5 hr urine collection.
Understand the mechanism of the D-xylose test.
20. Let us summarize the results of diagnostic tests in this patient?
Stool is negative for blood, pus, pathogens.
Stool fecal fat is >11 gm/24hr.
D-xylose is normal
These findings localize the problem to Pancreas.
21. What is this patient’s diagnosis?
Malabsorption
Secondary to chronic pancreatic insufficiency
Secondary to with cystic fibrosis.
22. What is/are the primary manifestations of pancreatic involvement in cystic fibrosis
23. What is the patho-physiology of pancreatic insufficiency in Cystic fibrosis ?
The disorder is characterized by
Normally, the pancreas secretes in response to secretin.
In cystic fibrosis this response is greatly diminished, resulting in
The pancreatic lesions are in general caused by obstruction of small ducts by secretions and cellular debris although stenosis of large pancreatic ducts is occasionally seen.
24. Describe the pathological findings of Pancreas in Cystic fibrosis.
When severely affected, the pancreas is shrunken, cystic, fibrotic, and fatty.
Histologically
25. What are the Radiological features of Pancreatic disease in Cystic fibrosis?
Calcification, although rare, may be apparent on radiographs.
Ultrasonography, magnetic resonance imaging (MRI), and computed tomographic (CT) scanning all can document the progression of pancreatic disease in cystic fibrosis.
There are three general patterns of abnormality seen on MRI:
26. ERCP: Describe the duodenal aspirate in patient with pancreatic insufficiency due to Cystic fibrosis?
Duodenal aspirates from patients with cystic fibrosis and complete pancreatic achylia are of
CCK and secretin fail to stimulate fluid or enzyme secretion.
Patients without absorptive defects may have normal or even elevated concentrations of pancreatic enzymes, but pancreatic secretions remain scanty and viscid and contain low concentrations of bicarbonate even after stimulation.
27. What would be the indicated treatment for this patient's chronic diarrhea?
Pancreatic enzyme replacement in sufficient daily doses to eliminate diarrhea.
28. What nutritional deficiency might be seen in this patient?
Vitamin deficiency of fat-soluble vitamins (A,D,E,K).
29. What would your diagnosis be if the patient were a 42 y/o /f with a similar problem associated with ingestion of certain graincontaining food? What pathology would be found in this instance? What dietary recommendations would you make for
Celiac disease
Abnormal small bowel biopsy (flat mucosa with varying degrees of villous atrophy and infiltration of the lamina propria with lymphocytes and plasma cells.
Avoid gluten (wheat,oats,barley,rye) in diet.
30. What are the common etiologies for acute diarrhea?
Infectious
Viruses
Bacteria
Toxins S aureus, C difficile, toxigenic E.coli
Invasion Shiegella, Salmonella
Parasites Giardia, Cryptosporidium
Non-infectious.
Drugs
laxatives
antacids
alcohol
antibiotics
chemotherapy
a host of other pharmaceuticals used in everyday practice
Food toxins / Preformed toxins / Starts within several hours following ingestion / Rarely fever
Mushrooms
Seafood
Metabolic causes (hyperthyroidism)
Motor disorders such as irritable bowel syndrome
Redemption of enteral feeding following prolonged fast
Fecal impaction
Onset of chronic diarrhea
31. Who are the People at risk for acute diarrhea?
Developing nations
Who ingest shell fish
Male homosexuals
AIDS
IV drug users
Residential homes/ nursing homes
Day care centers