Role of motility in chronic diarrhoea
Patients complaining of ‘chronic diarrhoea’ usually mean the passage of loose, urgent stools. Chronic diarrhoea is a feature of malabsorption; it may also be seen in the ‘dumping syndrome’ which follows gastric surgery, small intestinal bacterial overgrowth, bile salt malabsorption and in malabsorpt...
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Published in | Neurogastroenterology and motility Vol. 18; no. 12; pp. 1045 - 1055 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.12.2006
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Subjects | |
Online Access | Get full text |
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Summary: | Patients complaining of ‘chronic diarrhoea’ usually mean the passage of loose, urgent stools. Chronic diarrhoea is a feature of malabsorption; it may also be seen in the ‘dumping syndrome’ which follows gastric surgery, small intestinal bacterial overgrowth, bile salt malabsorption and in malabsorption of simple sugars including most commonly lactose, fructose and sorbitol. Excessively rapid entry of chyme into the small or large intestine generates propulsive motor patterns leading to accelerated transit. Inflammation is associated with decreased normal mixing motor patterns but increased propulsive motility including high amplitude propagated contractions (HAPCs). Evidence for abnormal small intestinal motility in the diarrhoea associated with irritable bowel syndrome (IBS) is conflicting and any difference appears small. Increased colonic HAPCs with increased propulsion is seen in IBS with diarrhoea (IBS‐D). Stress‐induced colonic motility is increased in IBS‐D with hyper‐responsiveness to corticotrophin releasing factor (CRF). Long‐lasting increases in mucosal serotonin availability may contribute to the chronic diarrhoea seen in IBS‐D and coeliac disease. Treatments for abnormal motility in chronic diarrhoea include those designed to correct specific underlying abnormalities including octreotide, antibiotics, colestyramine, specific food avoidance and anti‐inflammatory agents. There are also treatments aimed primarily at altering motility directly including opiates, 5HT3 receptor antagonists and amitriptyline. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 1350-1925 1365-2982 |
DOI: | 10.1111/j.1365-2982.2006.00836.x |