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Chronic diarrhea

 

Diarrhea lasting more than 2 weeks considered chronic.

 

The outcome of 

diarrhea depends on its cause and ranges from benign conditions such as 
toddler's diarrhea, to severe congenital diseases such as microvillus 
inclusion disease that can lead to irreversible intestinal failure and 
ultimately death.

 
 

Common causes :

 

1- infancy ; 

 

Post gastroenteritis malabsorption syndrome , cows milk / soy protein 
intolerance , secondary disaccharidase  deficiency  , cystic fibrosis .

 

2- childhood :

 

Chronic non  specific diarrhea , secondary disaccharidaes deficiency ,

 

Giardiasis ,  Post gastroenteritis malabsorption syndrome, celiac disease , 
cystic  fibrosis .

 

3- adolescence :

 

Irritable bowel syndrome , inflammatory bowel disease , giardiasis , 
lactose intolerance .

 

Postenteritis syndrome is a clinical-pathologic condition in which 
small intestinal mucosal damage persists after acute gastroenteritis. 
Sensitization to food antigens, secondary disaccharidase deficiency, or 
an infection or reinfection with an enteric pathogen is responsible for 
postenteritis syndrome. A change of the gut microflora due to the 
infectious agent and/or antibiotic therapy can contribute to 
postenteritis diarrhea.

 

Other rare causes

 

Defects in the genes of the Na+/H+ and the Cl−/HCO3− exchangers 
are responsible for congenital Na+ and Cl− diarrhea, respectively.

 

congenital chloride diarrhea; The consequent defect in bicarbonate 
secretion leads to metabolic alkalosis and acidification of the intestinal 
content

 

Patients with congenital sodium diarrhea show similar clinical 
features because of a defective Na+/H+ exchanger in the small and 
large intestine, leading to massive Na+ fecal loss and severe acidosis.

 
 

Evaluation of children having chronic diarrhea .

 

Phase 1 : history and physical examination . If the child have history of 
excessive drink of carbonated drink or fruit juice more than 150 ml/kg/24 
h. with normal growth and height , this is chronic non specific diarrhea 

 

If the patient ingest non absorbable nutrient in excessive amount such as 
sorbitol, dietary adjustment need to be made.

 


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Then do stool exam ; bacterial culture should be done, gross examination 
of stool; if blood  or mucous in stool it indicates inflammation of colon. 

 

Carbohydrate malabsorption; by analysis of stool for ph if less than 5 or 
the presence  of reducing substance .

 

The stool should be sent for electrolyte and osmolality if secretary 
diarrhea is considered. Stool should be examined for ova and parasite 
such as giardia and ameba.

 

phase 2 : if phase 1 has failed to revile a cause pass to phase 2.

 

-sweat chloride test to rule out cystic fibrosis.

 

-72 hours stool collection for fat determination.

 

-stool should be checked for Mg sulfate or phenolphthalein if the diarrhea 
secondary to ingestion of laxative ( factitious diarrhea ).

 

Phase 3  investigations :

 

Endoscopic studies for small bowel and colonic biopsies

 

-barium study and barium enema to rule out anatomic lesion.

 

 Phase 4 ;

 

Hormonal study for vasoactive intestinal poly peptide and gastrin assay. 

 
 
 


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Chronic 

 

diarrhea 

 

Wt   and  ht is 

normal  and no fat 

in the stool 

 

Wt   loss 

 

Stool show fat 

 

Chronic non 

specific diarrhea

Diarrhea related to 

carbohydrate 

intake 

 

Low fat intake 

 

Excessive intake of 

carbonated fluid  

 

Excessive intake of 

fruit juice 

 

Increase fat intake 

to 40% 

 

Decrease fluid 

intake to less than 

90 cc / kg /24 h 

 

Decrease intake of 

fruit juice 

 

Carbohydrate 

malabsorption 

 

Sucrose 

intolerance  

 

Lactose 

intolerance  

 

Monosaccharide 

(glucose – 

galactose ) 

Excessive sorbitol 

ingestion 

 

Decrease sucrose intake , 

add sucrosidase 

 

Decrease lactose intake , 

add lactase tablet  

 

Fructose is beast 

alternative (formula 

contain fructose )

 

Decrease sorbitol intake white 

grape juice is beast

 alternative 

 

If no improvement 

give sucrose free diet 

 

If no improvement give 

lactose free diet 

 

Malabssorption 

syndrome 

 

Diagnostic test 

 

Specific treatment 

 


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Treatment :

 

 

chronic non specific diarrhea.; 

 

occur in generally well appearing toddler 1-3 year of age ( toddler 
diarrhea ) the diarrhea is often brown and watery , at times containing un 
digested food particles , if the child fluid intake more than 150 cc/kg/ 24 
h  fluid intake should be reduced to 90 cc/kg/24 h , parent note that  
patient irritable in the first two days of fluid restriction however this  
result in decrease stool frequency and volume .

 

if the history suggest the child take more fruit juice reduction in the 
offending juice correct diarrhea . sorbitol sugar is found in apples , pear  
can cause diarrhea in toddler , white grape juice is best alternative  . 

 

if the child fat intake is restricted by the parent the fat intake can increase 
to 40% of the total calorie . in addition to treat the cause, during treatment 
of chronic diarrhea should focus on providing adequate nutritional 
support, also take attention to type and volume of fluid when used in 
treatment, when use antibiotic therapy in bacterial overgrowth it should 
be of broad spectrum; such as metronidazole, tetracycline, 
chloramphenicol and ampicillin and for 2 weeks course, i.v. nutrition and 
complete bowel rest for secretary diarrhea and lope amide and 
somatostatin in primary villous atrophy.

 

 

In Rotavirus-induced severe and protracted diarrhea, oral 
administration of human immunoglobulins (300 mg/kg) should be 
considered.

 

 

Zinc supplementation is an important factor in both prevention and 
therapy of chronic diarrhea, because it promotes ion absorption, 
restores epithelial proliferation, and stimulates immune response.

 
 
 

Disaccharidase deficiency :

 

The disaccharidases are located on the brush border membrane surface of 
small bowel , the most common is lactase deficiency, occasionally  
congenital deficiency occur . but most often is the result from diffuse 
acquired lesions of the intestinal epithelium such as infection or celiac 

disease .                                                 

 

 

In older children and 
adults late onset genetic lactase deficiency is the most common cause .

 

Clinical manifestation .

 

Watery osmotic diarrhea with stool PH less than 5.6 , contain excess 
sugar and excoriate the buttocks , patient may bloating and borborygmi.

 

If the Disaccharide involved is a reducing sugar (lactose ) the standard 
clinitest examination will be 2 + or greater in most cases.  Disaccharidase 
activity can be assayed in mucosal biopsy , breath hydrogen excretion 


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after an oral sugar load is a useful non invasive technique for detecting  
disaccharide intolerance . 

 

Treatment :

 

Consist of removal of milk from the diet , in most cases the elimination  
need not be total . a lactase preparation is available as a tablet ingested 
with meal . yogurt contains bacteria that produce lactase enzyme . thus  
frequently tolerated by lactase deficient individual .

 

       

 

Glucose – galactose  malabsorption :

 

More than 30 different mutation of the sodium / glucose transporter gene 
have been identified to cause this rare autosomal recessive congenital 
disorder . this transporter couples glucose and galactose to the sodium 
gradient across intestinal and renal brush border . renal tubular epithelium

  

is affected to a lesser degree . 

 

Clinical manifestation :

 

Osmotic diarrhea followed ingestion of glucose , breast milk or 
conventional formula soon after birth because most dietary sugar  are 
polysaccharides or disaccharides with glucose and galactose moieties . 
the patient may be bloated and if diarrhea persist dehydration and 
acidosis can be sever , resulting in death , the stool is acidic and contain 
sugar. the finding of  positive reducing substance in a watery stool and 
slight glycosuria despite low blood sugar level is highly suggestive of  

 

Glucose – galactose  malabsorption . and it also easily identified by using 
breath hydrogen test , after ingestion of 0.5 g/kg glucose the breath 
hydrogen rise to more than 20 PPM .

 

Treatment : Vigorous restriction of glucose and galactose . fructose the 
only carbohydrate that can be given safely should be added to 
carbohydrate – free formula in a concentration of 6 – 8% . diarrhea 
immediately ceases when infants are given such a formula .

 
 

Arco dermatitis enteropathica :

 

It is due to zinc deficiency , early in life the patient experience rash 
around mucocutaneous junctions ( mouth and anus ) and on the 
extremities , alopecia , chronic diarrhea and sometime if not treated the 
patient fail to thrive .serum zinc and alkaline phosphatase are low , 
intestinal biopsy show Paneth cell inclusion that disappear after 
treatment.

 

Treatment :

 

Oral zinc sulfate 1-2 mg elemental zinc /kg / 24 h .causes rapid healing of 
skin lesion and improvement of diarrhea.

 
 

Cows milk protein intolerance :

 


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It present early in life with watery diarrhea and sometime with streak of 
blood in the stool the infant may develop eczema , recurrent otitis media , 
respiratory wheeze and failure to thrive if not treated .

 

Treatment :

 

By avoiding the offending milk , prolong breast feeding decrease the 
incidence of cows milk protein intolerance . sodium cromoglycate also 
useful in treatment . 
 

 

 




رفعت المحاضرة من قبل: Hatem Saleh
المشاهدات: لقد قام عضو واحد فقط و 70 زائراً بقراءة هذه المحاضرة








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