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 DEFINITION
 EPIDEMOLOGY
 ETIOPATHOGENESIS
 CLINICAL FEATURES
 DIAGNOSIS
 RED FLAG SIGNS
 INVESTIGATIONS
 TREATMENT
It is a functional bowel disorder characterized by
abdominal pain or discomfort and altered bowel
movements in the absence of detectable structural
abnormalities
Chronic, recurrent ,relapsing and often lifelong
Often overlap with other functional disorders like
fibromyalgia, headache, backache and genitourinary
symptoms
 Prevalence : 1-20% worldwide (10% to 20% - US and Europe
5% - Asian countries)
 Incidence : 1-2% per year
 2-3 times more common in women
 Most patients have their first symptoms before 45 years of age
INDIA
 Prevalence is 4-8%
 More common in men
 Etiology is uncertain and maybe multifactorial
 Pathogenesis in IBS is poorly understood
GI Motor Abnormalities
Visceral Hypersensitivity
Brain gut axis Dysregulation
Abnormal Psychological features
Postinfectious IBS
Risk factors- young females,prololged duration of initial illness,
toxicity of infecting bacterial strain
Microbes involved in initial infection – Campylobacter
,salmonella and shigella
Immune activation and low grade mucosal inflammation
Altered gut flora
Abnormal serotonin pathways
 Serotonin plays an important role in regulation of GI motility
and visceral perception
 IBS –D patients show increased 5HT containing
enterochromaffin cells in colon
• Abdominal pain
and discomfort
• Altered bowel
habits
• Gas and flatulence
• Upper GI
symptoms
Abdominal pain or discomfort
 A prerequisite for the diagnosis of IBS
 It is episodic and crampy & highly variable in intensity and
location
 Sleep deprivation and malnutrition is uncommon
 Pain exacerbated by eating and emotional stress and improved by
passing stools or flatus
 In females symptoms worsen during premenstrual and menstrual
phases
Altered bowel habits-
 Alteration in bowel habits most consistent clinical feature
 Most common pattern is constipation alternating with diarrhea
 At first constipation is episodic but later becomes continuous and
unresponsive to laxatives
 Stools are usually hard with narrowed caliber
 Sense of incomplete evacuation
 Pts. with diarrhea have a stool volume <200ml and maybe associated
with passage of mucus but not blood
 Nocturnal diarrhea not seen
Gas and flatulence-
 Pts complain of abdominal distention and increased belching or
flatulence
Upper GI symptoms-
 25-50% complain of dyspepsia, heartburn, nausea and vomiting
 Indian patients have more of upper GI symptoms
 IBS-D (Diarrhoea predominant)
 IBS-C (Constipation predominant)
 IBS-M (Mixed diarrhoea and constipation)
 Usefulness of subtypes debatable
 Within 1 yr 75% change subtypes & 29% switch between IBS-C and IBS-D
 No clear diagnostic markers exist for IBS
 So diagnosis depends on positive clinical features and ruling out
organic diseases by careful clinical examination and investigations
 Diagnosis can be made confidently in most patients using
Rome III criteria + absence of red flag signs + supportive symptoms
which include defecation straining, urgency or a feeling of incomplete
bowel movement ,passing mucus and bloating
 Sensitivity 17%
 Specificity 95%
RED FLAG
 Unintentional and unexplained wt. loss
 Rectal bleeding
 Family h/o bowel/ovarian cancer
 A change in bowel habit to loose and/or more frequent stools persisting for more
than 6 wks in a person aged over 60yrs.
 Anemia
 Abdominal masses
 Rectal masses
 Inflammatory markers for IBD
To rule out organic causes
 CBC
 ESR
 CRP
 Stool examination for ova and parasites
 Antibodies for Coeliac Disease
 Hydrogen breath test
 Sigmoidoscopy when more than 50 years/ red flag signs present
 Younger individual with mild symptoms – minimal diagnostic evaluation,
 Older – undergo more thorough evaluations
 IBD
 COLORECTAL CANCER
 COLONIC TB
 FRUCTOS/LACTOSE INTOLERENCE’
 CELIAC SPRUE
 Endocrinopathies- HYPOTHYROIDISM ,HYPERTHYROIDUSM
 INFECTIOUS COLITIS
 ACUTE INTERMITTENT PORPHYRIA and LEAD POISONING
 PHYCOLOGICAL –ANXIETY,DEPRESSION
 Patient education and counselling
 Dietary alteration
 Pharmacotherapy
 Psychotherapy
 Reassuring the patient is the most successful form of treatment for
IBS
 Many are concerned that they have developed cancer – more anxiety
-more colonic symptoms
 Explain functional nature of disorder and how to avoid obvious food
precipitants
 Emphasise on expected chronicity of symptoms with periodic
exacerbations
 Eliminate food stuffs that appear to produce symptoms
 Consume high fibre diet – IBS-C
 Exclude wheat ,diary and gluten –Pain and bloating
 Avoid legumes and excess dietary fibre - IBS-D
 Diet low in FODMAPs
(Fermentable Oligosaccharides, Disaccharides, Monosaccharides And
Polyols)
 FODMAPs areshort chain carbs poorly absorbed in small intestine and
fermented by bacteria in colon to produce gas
Antidiarrheal agents
 Delay faecal transit , increase colonic segmentaion contractions and reduce rectal
perception
Serotonin receptor agonist and antagonist
 5 HT3 receptor agonist –5 HT release increases secretions and reduces GI
transit time and cause constipation and hence useful in IBS-D. Eg:- Alosetron
 s/e-Causes ischemic colitis and severe constipation
 5 HT4 agonist – are prokinetic eg Tegaserod- Suspended due to CVS events.
Stool bulking agents
 Fibre speeds up colonic transit and prevent excessive hydration and
dehydration of stool
Chloride channel activators
 Chloride secretion induce passive movement of Na and water into bowel lumen
and improve bowel function
Guanylate Cyclase-C Agonist
 Activation of GC-C generates cGMP which triggers secretion of fluid, sodium
and bicarbonate
 Antidepressant drugs
 TCAs reduce visceral hypersensitivity
 Their antimuscarinic effects cause constipation. Useful in IBS-D
 SSRIs are secretagogues and stimulate GI motility. Helpful in IBS-C
Modulation of gut flora- Rifamixin , probiotics
Antispasmodics
 provide temporary relief for painful cramps related to intestinal spasm
 Inhibit gastrocolic reflux and reduce postprandial pain
 s/e –xerostomia, urinary retention ,blurred vision ,drowsiness
 Psychological therapy is effective in two thirds of patients with IBS who do not
respond to standard medical treatment
 Cognitive behavioral therapy
 Hypnotherapy
 Dynamic therapy
 Chronic relapsing condition with considerable financial burden and
impacts overall quality of life
 At present only symptomatic therapy available
 Drugs don’t alter the clinical course
 Treatment should be tailored to the individual patient and should be a
combination of therapies
 No serious complications
 Haemorrhoids - aggravated by constipation and diarrhoea
 Vitamin and mineral deficiencies – because of avoiding certain foods
THANK YOU

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Irritable bowel syndrome

  • 2.  DEFINITION  EPIDEMOLOGY  ETIOPATHOGENESIS  CLINICAL FEATURES  DIAGNOSIS  RED FLAG SIGNS  INVESTIGATIONS  TREATMENT
  • 3. It is a functional bowel disorder characterized by abdominal pain or discomfort and altered bowel movements in the absence of detectable structural abnormalities Chronic, recurrent ,relapsing and often lifelong Often overlap with other functional disorders like fibromyalgia, headache, backache and genitourinary symptoms
  • 4.  Prevalence : 1-20% worldwide (10% to 20% - US and Europe 5% - Asian countries)  Incidence : 1-2% per year  2-3 times more common in women  Most patients have their first symptoms before 45 years of age INDIA  Prevalence is 4-8%  More common in men
  • 5.  Etiology is uncertain and maybe multifactorial  Pathogenesis in IBS is poorly understood GI Motor Abnormalities Visceral Hypersensitivity Brain gut axis Dysregulation Abnormal Psychological features
  • 6. Postinfectious IBS Risk factors- young females,prololged duration of initial illness, toxicity of infecting bacterial strain Microbes involved in initial infection – Campylobacter ,salmonella and shigella Immune activation and low grade mucosal inflammation Altered gut flora Abnormal serotonin pathways  Serotonin plays an important role in regulation of GI motility and visceral perception  IBS –D patients show increased 5HT containing enterochromaffin cells in colon
  • 7. • Abdominal pain and discomfort • Altered bowel habits • Gas and flatulence • Upper GI symptoms
  • 8. Abdominal pain or discomfort  A prerequisite for the diagnosis of IBS  It is episodic and crampy & highly variable in intensity and location  Sleep deprivation and malnutrition is uncommon  Pain exacerbated by eating and emotional stress and improved by passing stools or flatus  In females symptoms worsen during premenstrual and menstrual phases
  • 9. Altered bowel habits-  Alteration in bowel habits most consistent clinical feature  Most common pattern is constipation alternating with diarrhea  At first constipation is episodic but later becomes continuous and unresponsive to laxatives  Stools are usually hard with narrowed caliber  Sense of incomplete evacuation  Pts. with diarrhea have a stool volume <200ml and maybe associated with passage of mucus but not blood  Nocturnal diarrhea not seen
  • 10. Gas and flatulence-  Pts complain of abdominal distention and increased belching or flatulence Upper GI symptoms-  25-50% complain of dyspepsia, heartburn, nausea and vomiting  Indian patients have more of upper GI symptoms
  • 11.  IBS-D (Diarrhoea predominant)  IBS-C (Constipation predominant)  IBS-M (Mixed diarrhoea and constipation)  Usefulness of subtypes debatable  Within 1 yr 75% change subtypes & 29% switch between IBS-C and IBS-D
  • 12.  No clear diagnostic markers exist for IBS  So diagnosis depends on positive clinical features and ruling out organic diseases by careful clinical examination and investigations  Diagnosis can be made confidently in most patients using Rome III criteria + absence of red flag signs + supportive symptoms which include defecation straining, urgency or a feeling of incomplete bowel movement ,passing mucus and bloating
  • 13.  Sensitivity 17%  Specificity 95%
  • 14. RED FLAG  Unintentional and unexplained wt. loss  Rectal bleeding  Family h/o bowel/ovarian cancer  A change in bowel habit to loose and/or more frequent stools persisting for more than 6 wks in a person aged over 60yrs.  Anemia  Abdominal masses  Rectal masses  Inflammatory markers for IBD
  • 15. To rule out organic causes  CBC  ESR  CRP  Stool examination for ova and parasites  Antibodies for Coeliac Disease  Hydrogen breath test  Sigmoidoscopy when more than 50 years/ red flag signs present  Younger individual with mild symptoms – minimal diagnostic evaluation,  Older – undergo more thorough evaluations
  • 16.  IBD  COLORECTAL CANCER  COLONIC TB  FRUCTOS/LACTOSE INTOLERENCE’  CELIAC SPRUE  Endocrinopathies- HYPOTHYROIDISM ,HYPERTHYROIDUSM  INFECTIOUS COLITIS  ACUTE INTERMITTENT PORPHYRIA and LEAD POISONING  PHYCOLOGICAL –ANXIETY,DEPRESSION
  • 17.  Patient education and counselling  Dietary alteration  Pharmacotherapy  Psychotherapy
  • 18.  Reassuring the patient is the most successful form of treatment for IBS  Many are concerned that they have developed cancer – more anxiety -more colonic symptoms  Explain functional nature of disorder and how to avoid obvious food precipitants  Emphasise on expected chronicity of symptoms with periodic exacerbations
  • 19.  Eliminate food stuffs that appear to produce symptoms  Consume high fibre diet – IBS-C  Exclude wheat ,diary and gluten –Pain and bloating  Avoid legumes and excess dietary fibre - IBS-D  Diet low in FODMAPs (Fermentable Oligosaccharides, Disaccharides, Monosaccharides And Polyols)  FODMAPs areshort chain carbs poorly absorbed in small intestine and fermented by bacteria in colon to produce gas
  • 20.
  • 21. Antidiarrheal agents  Delay faecal transit , increase colonic segmentaion contractions and reduce rectal perception Serotonin receptor agonist and antagonist  5 HT3 receptor agonist –5 HT release increases secretions and reduces GI transit time and cause constipation and hence useful in IBS-D. Eg:- Alosetron  s/e-Causes ischemic colitis and severe constipation  5 HT4 agonist – are prokinetic eg Tegaserod- Suspended due to CVS events.
  • 22. Stool bulking agents  Fibre speeds up colonic transit and prevent excessive hydration and dehydration of stool Chloride channel activators  Chloride secretion induce passive movement of Na and water into bowel lumen and improve bowel function Guanylate Cyclase-C Agonist  Activation of GC-C generates cGMP which triggers secretion of fluid, sodium and bicarbonate
  • 23.  Antidepressant drugs  TCAs reduce visceral hypersensitivity  Their antimuscarinic effects cause constipation. Useful in IBS-D  SSRIs are secretagogues and stimulate GI motility. Helpful in IBS-C Modulation of gut flora- Rifamixin , probiotics Antispasmodics  provide temporary relief for painful cramps related to intestinal spasm  Inhibit gastrocolic reflux and reduce postprandial pain  s/e –xerostomia, urinary retention ,blurred vision ,drowsiness
  • 24.  Psychological therapy is effective in two thirds of patients with IBS who do not respond to standard medical treatment  Cognitive behavioral therapy  Hypnotherapy  Dynamic therapy
  • 25.  Chronic relapsing condition with considerable financial burden and impacts overall quality of life  At present only symptomatic therapy available  Drugs don’t alter the clinical course  Treatment should be tailored to the individual patient and should be a combination of therapies  No serious complications  Haemorrhoids - aggravated by constipation and diarrhoea  Vitamin and mineral deficiencies – because of avoiding certain foods