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Irritable Bowel Syndrome

Irritable bowel syndrome (IBS) is a functional bowel disorder characterized by abdominal pain or discomfort and altered bowel habits without detectable structural abnormalities. Key symptoms include abdominal pain relieved by defecation, changes in stool frequency or form, and bloating. IBS can be caused by abnormal gut motility, visceral hypersensitivity, central neural dysregulation, psychological factors, and low-grade mucosal inflammation. Treatment focuses on dietary modifications, medication to address predominant symptoms of diarrhea or constipation, and stress management techniques.

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0% found this document useful (0 votes)
138 views3 pages

Irritable Bowel Syndrome

Irritable bowel syndrome (IBS) is a functional bowel disorder characterized by abdominal pain or discomfort and altered bowel habits without detectable structural abnormalities. Key symptoms include abdominal pain relieved by defecation, changes in stool frequency or form, and bloating. IBS can be caused by abnormal gut motility, visceral hypersensitivity, central neural dysregulation, psychological factors, and low-grade mucosal inflammation. Treatment focuses on dietary modifications, medication to address predominant symptoms of diarrhea or constipation, and stress management techniques.

Uploaded by

Isabel Castillo
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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INTERNAL MEDICINE

Irritable Bowel Syndrome EXEMIUS


DR. CHRISTINE B. SUBIA December 2019 2021
IRRITABLE BOWEL SYNDROME  If predominant symptom is constipation may have weeks or
 Functional bowel disorder characterized by abdominal pain or months of constipation interrupted with brief periods of
discomfort and altered bowel habits in the absence of diarrhea.
detectable structural abnormalities.  Diarrhea from IBS consists of small volumes of loose
 No clear diagnostic markers stools( <200 mL).
 10–20% of adults and adolescents have symptoms consistent  Diarrhea may be aggravated by emotional stress or eating.
with ibs
 Female predominance. Gas and Flatulence
 IBS symptoms tend to come and go over time and often  Frequently complain: abdominal distention and increased
overlap with other functional disorders such as fibromyalgia, belching or flatulence visible distention with increase in
headache, backache, and gut sx. abdominal girth. Common in:
 Females
 Higher overall Somatic
 Patients with IBS tend to reflux gas from the distal to the more
proximal intestinebelching.
 Patient with bloating:
 Lower thresholds for pain
 More desire to defecate
 25 and 50%- dyspepsia, heartburn, nausea, and vomiting
 The prevalence of IBS is higher among patients with
dyspepsia (31.7%)

PATHOPHYSIOLOGY
1. Abnormal gut motor and sensory activity
CLINICAL FEATURES 2. Central neural dysfunction
 Affects all ages 3. Psychological disturbances
 Most patients have their first symptoms before age 45 4. Mucosal inflammation
 Women 2-3x as often as men and make up 80% of the 5. Stress
population with severe IBS. 6. Luminal factors
 Pain or abdominal discomfort- is a key symptom for the
diagnosis of IBS. Gastrointestinal Motor Abnormalities
 Sx should improved with defecation and/or have their onset  Increased rectosigmoid motor activity for up to 3 h after
associated with a change in frequency or form of stool. eating.
 Painless diarrhea or constipation does not fulfill the diagnostic  Inflation of rectal balloons both in IBS-D and IBS-C patients
criteria. leads to marked and prolonged distention-evoked contractile
 Supportive symptoms that are not part of the diagnostic activity
criteria include defecation straining, urgency or a feeling of
incomplete bowel movement, passing mucus, and bloating Visceral Hypersensitivity
 Patients frequently exhibit exaggerated sensory responses to
Abdominal Pain visceral stimulation
 Abdominal pain or discomfort  prerequisite clinical feature  >2x-perceptions of food intolerance
of IBS.  Postprandial pain has been temporally related to entry of the
 Highly variable in intensity and location. food bolus into the cecum in 74% of patients
 Episodic and crampy, but it may be superimposed on a 1. Increased end-organ sensitivity with recruitment of “silent”
background of constant ache. nociceptors
 Pain may be mild enough to be ignored or it may interfere with 2. Spinal hyperexcitability with activation of NO and possibly
daily activities. other neurotransmitters
 Usually during waking hours. 3. Endogenous (cortical and brainstem) modulation of caudad
 Severe IBS: frequently wake repeatedly during the night. nociceptive
 Pain is often exacerbated by eating or emotional stress 4. Transmission over time, the possible development of
 Improved by passage of flatus or stools. longterm hyperalgesia due to development of neuroplasticity
 Female worsening symptoms during the premenstrual and Central Neural Dyregulation
menstrual phases.

Altered Bowel Habits


 Alteration in bowel habits is the most consistent clinical
feature in IBS.
 The most common pattern is constipation alternating with
diarrhea, usually with one of these symptoms predominates
 Stools are usually hard with narrowed calibre
 Sense of incomplete evacuation

TRANSCRIBER Team Rocket


INTERNAL MEDICINE
Irritable Bowel Syndrome EXEMIUS
DR. CHRISTINE B. SUBIA December 2019 2021
 Strongly suggested by the clinical association of emotional DIARRHEA: Major complaint
disorders and stress with symptom exacerbation and the  Lactase deficiency
therapeutic response to therapies that act on cerebral cortical  Laxative abuse
sites.  Malabsorption
 Preferential activation of the prefrontal lobe contains a  Celiac sprue
vigilance network within the brain that increases alertness  Hyperthyroidism
 IBD
Abnormal Physiological Features  Infectious diarrhea
 80% of IBS patient has psychiatric features
 Psychological factors influence pain thresholds in IBS patients CONSTIPATION: Major complaint
 Abuse associated with greater pain reporting, psychological  Side effect of many different drugs(anticholinergic,
distress, and poor health outcome antihypertensive, and antidepressants)
 MRI: greater activation of the posterior and middle dorsal  Endocrinopathies (hypothyroidism and hypoparathyroidism)
cingulate cortexCNS–enteric nervous system dysregulation
DIAGNOSTICS
POST-INFECTIOUS IBS  Complete blood count
Risk factors for developing postinfectious IBS:  Sigmoidoscopic examination
 Prolonged duration of initial illness  Stool exam
 Toxicity of infecting bacterial strain  Sigmoid colon biopsy to rule out microscopic colitis.
 Smoking  Age >40 years aircontrast barium enema or colonoscopy
 Mucosal markers of inflammation  Primary sx are diarrhea and increased gas, the possibility of
 Female gender lactase deficiency should be ruled out with a hydrogen breath
 Depression test or with evaluation after a 3-week lactose-free diet
 Hypochondriasis  Celiac sprue-serology testing
 Adverse life events in the preceding 3 months  Dyspepsiaupper GI radiographs or
 Campylobacter, Salmonella, and Shigella esophagogastroduodenoscopy

Immune activation and mucosal inflammation TREATMENT


 IBS px’s show persistent signs of low-grade mucosal PATIENT COUNSELING AND DIETARY ALTERATIONS
inflammation with activated lymphocytes, mast cells, and  Reassurance and careful explanation
enhanced expression of proinflammatory cytokines.  Aggravating: substances (such as coffee, disaccharides,
 These abnormalities may contribute to abnormal epithelial legumes, and cabbage
secretion and visceral hypersensitivity  Excessive fructose and artificial sweeteners, such as sorbitol or
 Mucosal inflammation can lead to increased expression of mannitol, may cause diarrhea, bloating, cramping, or
TRPV1 in the enteric nervous system flatulence.

Altered Gut Flora STOOL-BULKING AGENTS


IBS patients had:  High-fiber diets and bulking agents, such as bran or
 Decreased proportions of the genera Bifidobacterium and hydrophilic colloid, are frequently used in treating IBS.
Lactobacillus  Fiber supplementation with psyllium has been shown to
 Increased ratios of Firmicutes:Bacteroidetes. reduce perception of rectal distention, indicating that fiber
may have a positive effect on visceral afferent function.
APPROACH TO THE PATIENT: Irritable Bowel Syndrome  Fiber should be started at a nominal dose and slowly titrated
Clinical features suggestive of IBS include the following: up as tolerated over the course of several weeks to a targeted
 Recurrence of lower abdominal pain with altered bowel habits dose of 20–30 g of total dietary and supplementary fiber per
over a period of time without progressive deterioration day.
 Onset of symptoms during periods of stress or emotional
upset
 Absence of other systemic symptoms such as fever and weight
loss, and small-volume stool without any evidence of blood

DIFFERENTIAL DIAGNOSIS
 Epigastric or periumbilical area: biliary tract disease, PUD,
intestinal ischemia, and carcinoma of the stomach and
pancreas
 Lower abdomen: diverticula, IBD or carcinoma of the colon
 Postprandial pain+ accompanied by bloating, nausea, and
vomiting- gastroparesis or PGO
 Intestinal infestation with Giardia lamblia or other parasites
may cause similar symptoms.

TRANSCRIBER Team Rocket


INTERNAL MEDICINE
Irritable Bowel Syndrome EXEMIUS
DR. CHRISTINE B. SUBIA December 2019 2021
ANTISPASMODICS
 Anticholinergic drugs may provide temporary relief for
symptoms such as painful cramps related to intestinal spasm.
 Most effective when prescribed in anticipation of
predictable pain
 Postprandial pain is best managed by giving
antispasmodics 30 min before meals so that effective blood
levels are achieved shortly before the anticipated onset of pain

ANTI-DIARRHEAL AGENTS
 Peripherally acting opiate-based agents are the initial therapy
of choice for IBS-D.
 Increases in segmenting colonic contractions, delays in fecal
transit, increases in anal pressures, and reductions in rectal
perception.
 Loperamide, 2–4 mg every 4–6 h up to a maximum of 12 g/d-
when diarrhea is severe in IBS
 These agents are most useful if taken before anticipated
stressful events that are known to cause diarrhea.

ANTI-DEPRESSANT DRUG
 Mood-elevating effects have several physiologic effects that
suggest they may be beneficial in IBS
 TCA’s- slows jejunal migrating motor complex transit
propagation and delays orocecal and whole-gut transit,
indicative of a motor inhibitory effect
 (SSRI) Paroxetine - accelerates orocecal transit, raising the
possibility that this drug class may be useful in IBS-C patients.

ANTI-FLATULENCE THERAPY
 Patients should be advised to eat slowly and not chew gum or
drink carbonated beverages.
 If bloating is accompanied by diarrhea and worsens after
ingesting dairy products, fresh fruits, vegetables, or juices,
further investigation or a dietary exclusion trial may be
worthwhile.
 Avoiding flatogenic foods, exercising, losing excess weight, and
taking activated charcoal are safe but unproven remedies

MODULATION OF GUT FLORA


 Nonabsorbed oral antibiotic Rifaximin is the most thoroughly
studied antibiotic for the treatment of IBS
 Rifaximin at a dose of 550 mg two times daily for 2 weeks
experienced substantial improvement of global IBS symptoms
 10 probiotic studies in IBS patients found significant relief of
pain and bloating with the use of:
 Bifidobacterium breve
 B. longum
 Lactobacillus acidophilus

TRANSCRIBER Team Rocket

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