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Irritable Bowel Syndrome Overview

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Irritable Bowel Syndrome Treatment




Author: Mohammad F El-Baba, MD, Department of Pediatrics, Assistant Professor, Children's Hospital of Michigan and Wayne State University

Mohammad F El-Baba is a member of the following medical societies: American Gastroenterological Association and North American Society for Pediatric Gastroenterology and Nutrition

Editors: Hisham Nazer, MBBCh, FRCP, Professor of Pediatrics, University of Jordan; Consulting Staff, Department of Pediatric Gastroenterology, Bushnaq Medical Centre, Jordan; Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine.com, Inc; David Piccoli, MD, Chief, Division of Gastroenterology and Nutrition, Department of Pediatrics, The Children's Hospital of Philadelphia; Professor, University of Pennsylvania School of Medicine; Steven M Schwarz, MD, FAAP, FACN, AGAF, Professor of Pediatrics, State University of New York, Downstate Medical Center College of Medicine; Professor of Clinical Pediatrics, St George's University School of Medicine; Distinguished Lecturer, New York Medical College, School of Public Health; Chair and Consulting Staff, Department of Pediatrics, Long Island College Hospital; Carmen Cuffari, MD, Associate Professor, Department of Pediatrics, Division of Gastroenterology/Nutrition, Johns Hopkins University School of Medicine

Author and Editor Disclosure

Synonyms and related keywords: irritable bowel syndrome, mucus colitis, spastic colon, irritable colon, functional bowel disease, IBS, functional gastrointestinal disorders, functional GI disorders

Background

Irritable bowel syndrome (IBS) is defined as chronic or recurrent abdominal pain, altered bowel habits, and bloating, with the absence of structural or biochemical abnormalities to explain these symptoms. IBS is part of a broader group of disorders known as functional gastrointestinal disorders. It is the most common gastrointestinal diagnosis among gastroenterology practices in the United States and is one of the top 10 reasons for visits to primary care physicians. IBS is recognized in children, and many patients trace the onset of their symptoms to childhood. Children who have a history of recurrent abdominal pain are at increased risk of IBS during adolescence and young adulthood.

Pathophysiology

IBS has no identifiable cause, and laboratory testing is unrevealing. Over the last 5 decades, the understanding of IBS has evolved from a disorder of motor activities in the upper and lower gastrointestinal tracts to a more integrated understanding of visceral hypersensitivity and brain-gut interaction.

Gastrointestinal motility abnormalities

Studies evaluating the motor response of the colon to meals, pain, and stress suggest a difference between control subjects and patients with IBS. Pretreatment with anticholinergic medication in IBS was demonstrated to reduce meal-stimulated pain and diarrhea. The finding of an abnormal, 3-cycle-per-minute, slow-wave activity in the colon of patients with IBS was not confirmed by other studies and was noted in some individuals without IBS.

Abnormal small-bowel motility has also been reported by some investigators. Intestinal transit has been demonstrated to be delayed in patients with constipation-predominant IBS. In contrast, the transit was accelerated in patients with diarrhea-predominant IBS. Clustered contractions in the duodenum and jejunum and prolonged propagated contractions in the ileum were noted more frequently in patients with IBS. Small-bowel motility studies have demonstrated more abnormal findings in patients with IBS in conscious states than during sleep, suggesting that the condition may result in part from CNS input.

Nongastrointestinal smooth-muscle abnormalities

Bladder dysfunction was identified in 50% of patients with IBS and in only 13% of control subjects. One study found patients with IBS to have a higher incidence of orthostatic hypotension. A clinical study demonstrated a greater reduction of forced expiratory volumes in 1 second (FEV1) induced by methacholine in patients with IBS than in control subjects.

Visceral hypersensitivity

Most patients with functional disorders appear to have inappropriate perception of physiologic events and altered reflex responses in different gut regions. Patients with IBS undergoing balloon distension studies of the colorectum demonstrated awareness of distension and pain at pressures and volumes that were significantly lower than in control subjects. The development of chronic hyperalgesia within the gastrointestinal tract can be explained by the development of hyperexcitability of neurons in the dorsal horn in response to peripheral tissue irritation or to descending influences from the brain stem. Multiple factors are proposed to alter neuroreceptors and afferent spinal neuron functions. These factors include genetic, inflammatory, local nerve mechanical irritation, motility, and psychological factors.

Brain-gut interaction

The brain-gut axis is a bidirectional pathway that links higher cortical centers with visceral afferent sensation and intestinal motor function. Regulation of these connections occurs via numerous neurotransmitters found in the brain and gut, including cholecystokinin, vasoactive intestinal peptide, substance P, 5-hydroxytryptamine (5-HT), and many others. These transmitters act at different sites in the brain and gut and lead to varied effects on gastrointestinal motility, pain control, emotional behavior, and immunity. The 5-HT receptors are implicated in the mechanisms controlling gastrointestinal functions.

Dysregulation of the brain-gut system is becoming an acceptable theory to explain the functional gastrointestinal disorders. Furthermore, several studies have hypothesized that specific 5-HT receptor antagonists may be beneficial in IBS. Recently, a number of newer noninvasive imaging techniques (eg, positron emission tomography, functional MRI) have been applied to assess brain-gut interactions in healthy patients and in those with IBS.

Psychosocial factors in irritable bowel syndrome

Numerous studies have found an increased prevalence of abnormal psychiatric disorders, including anxiety, major depression, personality disorders, and hysteria, in adult patients with IBS, especially patients referred to medical facilities. These psychological disturbances are not believed to cause or induce the symptoms of IBS, but they are thought to influence the patient's perception of the symptoms and affect the clinical outcome. Stressful events are known to affect gastrointestinal functions and may lead to exacerbation of symptoms in patients with IBS. In addition, antidepressant or antipsychotic therapy is helpful in some patients with IBS. A recent meta-analysis has confirmed the relative efficacy of antidepressant medications in irritable bowel syndrome, particularly in predominantly diarrheic patients experiencing severe pain. Recent studies have reported an increased frequency of prior sexual or physical abuse in patients with IBS and other functional gastrointestinal disorders.

Dietary factors

Some studies have proposed that carbohydrate intolerance may produce significant symptoms in patients with IBS. Ingestion of lactose, sorbitol, or fructose is associated with increased gastrointestinal symptoms. Likewise, a food allergy may play a minor role in triggering or exacerbating symptoms in some patients with IBS.

Gastrointestinal infection and irritable bowel syndrome

Some investigations found a correlation between the development of IBS and a prior severe gastrointestinal infection, especially in patients with higher scores for anxiety. Symptoms compatible with IBS will affect 10-15% of patients after acute infectious gastroenteritis. Recent studies have demonstrated low-grade lymphocytic infiltration in the intestinal mucosa, increased permeability, and increases in inflammatory components including enterochromaffin and mast cells.

Some studies have shown that small intestinal bacterial overgrowth is common in subjects with IBS. A double-blind placebo-controlled study by Pimentel et al (2003) showed that normalization of lactulose breath testing with neomycin correlated with symptom improvement in patients with IBS.

Frequency

United States

Symptoms consistent with IBS are present in 10-20% of adolescents and adults. Less than one third of patients seek medical advice. In the pediatric population, IBS symptoms are reported in 14% of high school students and 6% of middle school students. One third of patients with IBS trace their symptoms to childhood.

International

Prevalence in developing countries is probably lower than in Western countries, but this may be explained by a combination of reduced availability of medical care and different cultural approaches to illness.

Mortality/Morbidity

IBS is not a life-threatening condition, but it can have a serious impact on a patient's daily activities and quality of life. Greater impairments in quality of life are reported in patients with IBS who sought medical care compared to those who did not consult their physicians for IBS symptoms. It is a major cause of absenteeism at the workplace and at school. Abdominal pain in patients with IBS is responsible for significant school absences in 4-5% of middle and high school students.

Race

IBS is not well characterized outside Western countries. According to reported studies, the disease prevalence is lower in Hispanic and Asian populations than in Caucasian populations, and whites are more likely to have IBS than blacks.

Sex

  • Women are 2-3 times more likely than men to have IBS.
  • In pediatric patients, both sexes are affected equally.

Age

  • IBS is a disorder of young people. One half of patients experience symptom onset when younger than 35 years, and 40% of patients are aged 35-50 years when symptoms begin.
  • IBS is recognized in children. Symptoms consistent with IBS are reported in 16% of students aged 11-17 years.
  • IBS is not described in preschool-aged and younger children because the diagnosis depends on the child's ability to report detailed symptoms.



History

IBS has a broad range of symptoms; the most common are abdominal pain and altered bowel movements. Although symptoms may vary among patients, a pattern usually develops for each patient. The presence of characteristic symptoms in an otherwise healthy individual is sufficient to make a diagnosis of IBS in most individuals.

  • The characteristics of abdominal pain vary between patients and even within an individual patient.
    • The pain can be dull, achy, colicky, or sharp.
    • Pain can occur anywhere in the abdomen but is commonly located in the hypogastric or periumbilical regions.
    • The pain has no specific pattern but may be aggravated by stress and food and partially relieved after defecation.
  • Altered bowel habits include constipation, diarrhea, or alternating constipation with diarrhea.
    • Stools usually are of small volume and pasty. Constipation is associated with small, hard, pelletlike stools. Diarrhea characteristically occurs during waking hours and often is precipitated by meals.
    • Mucus can be a component of the stool in as many as 50% of patients with IBS.
    • In some patients, defecation is associated with a sense of incomplete evacuation that can lead to repeated trips to the bathroom and prolonged straining.
  • Symptoms of abdominal distension (ie, bloating, increased belching, flatulence) frequently are reported by patients with IBS. They are less common in children than adults.
  • Other gastrointestinal symptoms (ie, heartburn, dyspepsia, nausea, vomiting) are reported in 25-50% of adult patients with IBS. Dyspeptic symptoms are present in as many as 30% of pediatric patients with IBS.
  • Extraintestinal symptoms are also reported. Patients with IBS frequently report dysmenorrhea, urinary frequency, incomplete bladder emptying, back pain, and headache. These complaints are common in adults but rare in children.
  • Patients may relate a history of inciting events.
    • Exacerbation of IBS symptoms is sometimes reported to follow stressful experiences, ingestion of specific foods, or consumption of alcohol or caffeine.
    • Menses may exacerbate IBS symptoms in women.
    • In children, symptom precipitants include school-related problems, overeating, or eating problems.
  • The following clinical features should alert the physician to the possibility of a disorder other than IBS:
    • Frequent awakening by symptoms
    • Steady progressive course
    • Fever
    • Weight loss
    • Arthritis
    • Rectal bleeding
    • Persistent vomiting
  • The diagnosis of IBS requires the identification of the symptoms characteristic of IBS and the exclusion of other medical conditions with similar clinical presentations. Symptom-based criteria have been established for the diagnosis of IBS, which includes the Manning or, more recently, the Rome criteria. The pediatric working team adopted the Rome II criteria in the adult population because these criteria seemed to apply equally well to children. Rome II criteria apply to children old enough to provide an accurate pain history of at least 12 weeks, which need not to be consecutive, in the preceding 12 months. The history can include the following:
    • The abdominal discomfort or pain has 2 out of 3 features, ie, (1) relief with defecation, (2) onset associated with a change in frequency of stool, and (3) onset associated with a change in the form of stool.
    • No structural or metabolic abnormalities exist to explain the symptoms.

Physical

  • Physical examination findings generally are unremarkable. The patient may appear tense and anxious with sweaty palms. Abdominal tenderness may be present. Tender and palpable sigmoid is found in some patients.
  • Findings against the diagnosis of IBS include the following:
    • Abdominal rigidity
    • Rebound tenderness
    • Lymphadenopathy
    • Hepatosplenomegaly
    • Positive fecal bleeding test result

Causes

IBS has no identifiable cause (see Pathophysiology).



Crohn Disease
Endometriosis
Giardiasis
Human Immunodeficiency Virus Infection
Lactose Intolerance
Malabsorption Syndromes
Sprue
Ulcerative Colitis
Zollinger-Ellison Syndrome

Other Problems to be Considered

Antibiotic-associated diarrhea



Lab Studies

  • No specific laboratory markers exist for IBS. Patients who have characteristic symptoms and meet the Rome criteria for IBS (see History) do not require a thorough diagnostic evaluation. A more aggressive approach is recommended for individuals with atypical symptoms, those with a rapidly progressive course, or when the index of suspicion for an organic disease is high.
  • In classic cases, a limited screen for organic disease is reassuring and should consist of the following:
    • Complete blood count
    • Erythrocyte sedimentation rate
    • Stool studies for ova and parasites
    • Stool cultures and stool Clostridium difficile toxin assay, if clinically indicated
    • A breath hydrogen test or a trial of dietary lactose restriction to exclude lactose intolerance
  • The following laboratory tests are indicated in special instances:
    • Lead level assessment
    • Celiac serologic tests
    • Serum immune markers for inflammatory bowel disease
    • Thyroid function tests
    • Tests for Helicobacter pylori (ie, serum antibody titers, urea breath test)

Imaging Studies

  • Plain abdominal radiography is recommended for patients with pain-predominant symptoms. Perform plain abdominal radiography during a pain episode to exclude intermittent obstruction.
  • Upper gastrointestinal study with small-bowel follow through is a useful study if Crohn disease or celiac sprue is suggested.
  • Barium enema can be useful for patients in whom Hirschsprung disease or congenital structural anomalies of the colon are suspected. Barium enema is also indicated in older patients (>50 y) because of the increased likelihood of colonic neoplasms.
  • Gastric scintigraphy is indicated for selected patients to evaluate for gastroparesis.
  • Abdominal ultrasonography is suggested for patients in whom biliary disease is suspected. It has high sensitivity and specificity for gallstones. It can also detect gallbladder wall thickening.

Other Tests

  • Gastrointestinal manometry can assist in evaluating patients in whom gastroparesis or intestinal pseudoobstruction is suspected.
  • Anorectal manometry is useful to screen patients in whom Hirschsprung disease is suspected.

Procedures

  • Sigmoidoscopy or complete colonoscopy is useful to evaluate for inflammatory conditions such as ulcerative colitis and microscopic colitis.
  • Upper endoscopy with small-intestinal biopsies is recommended in patients in whom peptic ulcer disease, Helicobacter pylori infection, Crohn disease, celiac disease, or other malabsorption conditions are suspected.



Medical Care

IBS is a chronic illness and has no cure. Treatment may be challenging and even frustrating to the physician, the patient, and the patient's family. The most important component of treatment is to establish an effective and therapeutic relationship with the patient and his or her family. Educate the child and parents that IBS is a chronic illness that cannot be cured. At the same time, reassure them that it is not a life-threatening condition and it does not lead to physical impairment. Tell the patient and the family that the symptoms are real and respond to their worries and concerns. Reassurance is more effective if offered after a careful history and physical examination and a conservative diagnostic evaluation.

Most patients have mild symptoms and maintain normal daily activities and regular school attendance. Address the possible dietary and psychosocial triggering factors. Counseling, dietary modifications, and lifestyle changes usually are effective and sufficient for treatment.

A smaller proportion of patients have moderate-to-severe symptoms with some disruption of their activities and school performance. This group of patients may benefit from pharmacotherapy and behavioral treatment. Referral to a psychologist may be required.

Consultations

  • Consider further evaluation and a referral to a pediatric gastroenterologist if findings from the patient's history, physical examination, or screening laboratory tests are suggestive of organic disease.

Diet

  • Dietary modification
    • Some patients with IBS report exacerbation of their symptoms after ingestion of certain foods. Elimination of certain foods, such as sorbitol, fructose, and gas-forming legumes, achieves relief in some patients with IBS, especially those with excess gas. Attempt lactose restriction in patients with documented lactose malabsorption.
    • Foods associated with increased flatulence include onions, beans, celery, carrots, prunes, bananas, raisins, brussel sprouts, wheat germ, and bagels.
  • Fiber supplements
    • A high-fiber diet or supplement is useful in patients with constipation-predominant IBS. Several studies have demonstrated that fiber enhances water-retentive properties of stool, increases stool weight, and accelerates colonic transit.
    • In general, dietary fibers are less soluble and more effective as bulking agents, whereas synthetic fibers are more soluble and increase water retention.
    • The recommended daily intake of fiber (in grams) for children is estimated by adding 5 to their age in years.



Pharmacotherapy is recommended for patients with moderate-to-severe symptoms that cause disruptions in activity. Treatment is symptomatic and is directed at the most predominant symptom (eg, dietary fiber supplementation and stool softeners for constipation, antidiarrheals for diarrhea, smooth muscle relaxants for pain). A better understanding of the pathophysiology of IBS and the role of neurotransmitters and receptors involved in the gastrointestinal sensory and motor functions have provided opportunities for the development of newer therapeutic agents. The role of serotonin in the pathophysiology of IBS has drawn much attention, and agonists and antagonists at 5-hydroxytryptamine (5-HT) receptors have been approved for the treatment of subgroups of patients with IBS.

Drug Category: Antispasmodic and anticholinergic agents

These are the most frequently used medications (ie, hyoscyamine, dicyclomine) in the United States for the treatment of pain episodes in patients with IBS. Results from adult studies on the efficacy of these medications have provided conflicting data. The meta-analysis of the use of smooth muscle relaxants (eg, cimetropium, otilonium bromide, pinaverium, mebeverine, trimebutine) by Poynard et al showed efficacy over placebo in IBS. These drugs have calcium channel–blocking properties or antimuscarinic activities. No pediatric data exist with which to evaluate their efficacy or adverse effects.

Drug NameHyoscyamine (Levsin, Levbid)
DescriptionBlocks action of acetylcholine at parasympathetic sites in smooth muscle, secretory glands, and CNS, which in turn has antispasmodic effects.
Adult DoseLevsin: 0.125-0.25 mg (1-2 tab) PO/SL q4h prn; not to exceed 12 tab per d
Levbid: 0.375-0.75 mg PO bid
Pediatric Dose<2 years: 0.125-mg/mL gtt; repeat q4h PO prn
The following is an approximate dosage guide:
2.3 kg (5 lb): 3 gtt; not to exceed 18 gtt per d
3.4 kg (7.5 lb): 4 gtt; not to exceed 24 gtt per d
5 kg (11 lb): 5 gtt; not to exceed 30 gtt per d
7 kg (15 lb): 6 gtt; not to exceed 36 gtt per d
10 kg (22 lb): 8 gtt; not to exceed 48 gtt per d
15 kg (33 lb): 11 gtt; not to exceed 66 gtt per d
2-12 years: Use 1.25-5 mL of elixir (0.03125-0.125 mg) PO q4h prn; not to exceed 30 mL/d
The following is an approximate dosage guide:
10 kg (22 lb): 1.25 mL
20 kg (44 lb): 2.5 mL
40 kg (88 lb): 3.75 mL
50 kg (110 lb): 5 mL
>12 years: Administer as in adults
ContraindicationsDocumented hypersensitivity; obstructive uropathy; narrow-angle glaucoma; myasthenia gravis; obstructive GI tract disease
InteractionsEffects decrease when used concurrently with antacids; toxicity increases when used concurrently with phenothiazines, amantadine, haloperidol, MAOIs, or TCAs
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsCaution in elderly patients; some products contain sodium metabisulfite, which can cause allergic reactions

Drug NameDicyclomine (Bentyl)
DescriptionTreats GI motility disturbances. Blocks action of acetylcholine at parasympathetic sites in secretory glands, smooth muscle, and CNS.
Reports show that administration of dicyclomine syrup in infants has been followed by serious respiratory symptoms, seizures, syncope, pulse rate fluctuations, and coma. Death has been reported.
Adult Dose20-40 mg PO qid; discontinue if not effective within 2 wk or if 80 mg qd is associated with adverse effects
Pediatric Dose<6 months: Contraindicated
>6 months to 2 years: 5-10 mg PO tid/qid 15 min ac; not to exceed 40 mg/d
>2 years to 12 years: 10 mg PO tid
>12 years: Administer as in adults
ContraindicationsDocumented hypersensitivity; obstructive uropathy; obstructive disease of GI tract; severe ulcerative colitis; toxic megacolon; reflux esophagitis; glaucoma; myasthenia gravis; infants <6 mo
InteractionsEffects decrease when used concurrently with antacids; coadministration with anticholinergic drugs (eg, antihistamines, TCAs) may increase toxicity
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsMay cause blurred vision or change in vision, severe constipation, urinary retention, and psychosis
Caution with hepatic or renal insufficiency, cardiovascular disease, urinary tract obstruction, ulcerative colitis, GI obstruction, hyperthyroidism, and hypertension

Drug Category: Antidiarrheal agents

These agents are used to treat diarrhea adjunctly with rehydration therapy to correct fluid and electrolyte depletion. They are usually helpful when diarrhea is the predominant symptom. Studies of the opiate agent loperamide show that it improves stool consistency, decreases stool frequency, and reduces abdominal pain. Cholestyramine acts by binding bile acids and can be helpful in some patients with IBS. Alosetron and tegaserod are 5-HT4 receptor partial agonists that bind with high affinity at human 5-HT4 receptors. The activation of 5-HT4 receptors in the gastrointestinal tract stimulates the peristaltic reflex and intestinal secretion and inhibits visceral sensitivity. In vivo studies showed that tegaserod enhanced basal motor activity and normalized impaired motility throughout the gastrointestinal tract. In addition, studies demonstrated that tegaserod moderated visceral sensitivity during colorectal distension in animals.

Tegaserod was temporarily withdrawn from the US market in March 2007; however, as of July 27, 2007, restricted use of tegaserod is now permitted via a treatment IND protocol. The treatment IND allows tegaserod treatment of irritable bowel syndrome (IBS) with constipation or chronic idiopathic constipation (CIC) in women younger than 55 years who meet specific guidelines. Its use is further restricted to those in critical need who have no known or preexisting heart disease.
 
Earlier this year, tegaserod marketing was suspended because of a meta-analysis of safety data pooled from 29 clinical trials that involved more than 18,000 patients. The results showed an excess number of serious cardiovascular adverse events, including angina, myocardial infarction, and stroke, in those taking tegaserod compared with placebo. In each study, patients were assigned at random to either tegaserod or placebo. Tegaserod was taken by 11,614 patients, and placebo was taken by 7,031 patients. The average age of patients in these studies was 43 years, and most patients (ie, 88%) were women. Serious and life-threatening cardiovascular adverse effects occurred in 13 patients (0.1%) treated with tegaserod; among these, 4 patients had a heart attack (1 died), 6 had unstable angina, and 3 had a stroke. Among the patients taking placebo, only 1 (0.01%) had symptoms suggesting the beginning of a stroke that went away without complication.
 
For more information, see the FDA MedWatch Product Safety Alert.

Drug NameLoperamide (Imodium)
DescriptionSynthetic opioid; does not have central nervous action in therapeutic doses. Acts by slowing intestinal motility and enhancing water and electrolyte absorption. Reduces diarrhea and pain in patients with diarrhea-predominant IBS.
Adult Dose2-12 mg/d PO divided bid/tid; necessary doses differ greatly between individuals
Pediatric Dose<2 years: Not recommended
>2 years: 0.08-0.24 mg/kg/d PO divided bid/tid; not to exceed 2 mg/dose
ContraindicationsDocumented hypersensitivity; diarrhea resulting from infections; pseudomembranous colitis
InteractionsPhenothiazines, TCAs, and CNS depressants may increase toxicity
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsCaution in severe ulcerative colitis or antibiotic-induced pseudomembranous colitis; monitor for CNS toxicity in patients with hepatic insufficiency because of decreased clearance

Drug NameCholestyramine (Prevalite, Questran)
DescriptionBinds endogenous bile acids and can improve diarrhea in patients with unexplained diarrhea or idiopathic bile acid malabsorption.
Adult Dose3-4 g PO bid/qid mixed with fluid or food
Pediatric Dose240 mg/kg/d PO divided tid ac as slurry in water, juice, or milk
ContraindicationsDocumented hypersensitivity; complete biliary obstruction
InteractionsInhibits absorption of numerous drugs including warfarin, thyroid hormone, amiodarone, NSAIDs, methotrexate, digitalis glycosides, glipizide, phenytoin, imipramine, niacin, methyldopa, tetracyclines, clofibrate, hydrocortisone, and penicillin G
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsCaution in constipation and phenylketonuria

Drug NameAlosetron (Lotronex)
DescriptionPotent and selective antagonist of serotonin 5-HT3 receptor type. 5-HT3 receptors are extensively located on enteric neurons of GI tract, and stimulation causes hypersensitivity and hyperactivity of intestine. Alosetron blocks these receptors and, thus, is effective in controlling IBS symptoms.
Only approved for treatment in women with severe, chronic, diarrhea-predominant IBS that has failed to respond to conventional IBS therapy. Less than 5% of IBS is considered severe, and only a fraction of severe cases are diarrhea-predominant IBS. Limiting use to this severely affected population is intended to maximize the benefit-to-risk ratio. Previously removed from US market but reintroduced with new restrictions approved by FDA on June 7, 2002. Restricted because serious and unpredictable GI adverse events (some of which resulted in death) were reported in association with its use following original approval in February 2000.
Adult DoseWomen: 1 mg PO qd for 4 wk initially; may increase to 1 mg PO bid if qd dose inadequate for controlling symptoms; discontinue if inadequate response to 1 mg bid after 4 wk
Men: Not established
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity; history of constipation, intestinal obstruction, stricture, toxic megacolon, GI perforation, adhesions, ischemic colitis, impaired intestinal circulation, thrombophlebitis, hypercoagulable state, Crohn disease, ulcerative colitis, or diverticulitis
InteractionsSubstrate of CYP450 isoenzymes 2C9, 3A4 (minor), and 1A2 (minor); coadministration with isoenzyme inhibitors (eg, cimetidine, fluvoxamine, fluoxetine, sertraline, metronidazole, omeprazole, co-trimoxazole) may decrease elimination and increase risk of toxicity; coadministration with isoenzyme inducers (eg, phenobarbital, fluconazole, carbamazepine, phenytoin) may increase clearance
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsDiscontinue immediately if serious GI adverse events occur (eg, ischemic colitis, serious complications of constipation); these adverse effects have resulted in hospitalization, blood transfusion, surgery, and death
Constipation is a dose-related adverse effect; elderly patients are more prone to GI risks; caution in hepatic insufficiency (decrease dose); pharmacists may only dispense prescriptions that display a prescribing program sticker affixed by an enrolled physician, and they must distribute a copy of the FDA-approved medication guide with each prescription; to enroll in the prescribing program call GlaxoSmithKline at 1-888-825-5249 or visit www.lotronex.com

Drug NameTegaserod hydrogen maleate (Zelnorm)
DescriptionAvailable in US by restricted treatment IND for irritable bowel syndrome with constipation (IBS-C) or chronic idiopathic constipation (CIC) in women younger than 55 years who meet specific guidelines. Used for the short-term treatment of women with irritable bowel syndrome in which constipation is the predominant symptom. Serotonin type 4 receptor partial agonist with no affinity for 5-HT3 receptors. May trigger peristaltic reflex via 5-HT4 activation, which enhances basal motor activity and normalizes impaired GI motility. Research studies have shown inhibitory activity of drug on visceral activity in GI tract.
Adult DoseWomen: 6 mg PO bid 30 min ac for 4-6 wk; in patients who respond to treatment, an additional 4-6 wk of therapy may be considered
Men: Not established
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity; severe renal impairment; moderate or severe renal impairment; history of bowel obstruction, symptomatic gallbladder disease, suspected sphincter of Oddi dysfunction, or abdominal adhesions
InteractionsNone reported
PregnancyB - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
PrecautionsDiarrhea may occur; do not give to patients with diarrhea; discontinue if new or sudden worsening of abdominal pain or diarrhea occurs; ischemic colitis and other forms of intestinal ischemia have been rarely reported (causality has not been established); discontinue immediately if symptoms of ischemic colitis (eg, rectal bleeding, bloody diarrhea, new or worsening abdominal pain) occur and evaluate immediately; do not resume treatment if findings consistent with ischemic colitis

Drug Category: Antidepressant drugs

A number of studies have shown that TCAs (ie, imipramine, amitriptyline) can be useful in the treatment of IBS in some patients. In addition to their antidepressant effects, TCAs have neuromodulatory and analgesic properties, which can be achieved at lower doses than those required for treatment of depression. Because of their inhibitory effect on gut motor function, TCAs may benefit patients with IBS with predominant diarrhea or pain. TCAs particularly benefit patients with IBS who have well-defined depression or panic attacks.

Drug NameAmitriptyline (Elavil)
DescriptionInhibits reuptake of serotonin and/or norepinephrine at presynaptic neuronal membrane, which increases concentration in CNS.
Adult Dose10-50 mg/d PO qhs; administered at lower doses than required for depression
Pediatric Dose0.2-0.4 mg/kg/d PO qhs
ContraindicationsDocumented hypersensitivity; MAOIs within 14 d; history of seizures, cardiac arrhythmias, glaucoma, or urinary retention
InteractionsPhenobarbital may decrease effects; coadministration with CYP2D6 enzyme system inhibitors (eg, cimetidine, quinidine) may increase levels; inhibits hypotensive effects of guanethidine; may interact with thyroid medications, alcohol, CNS depressants, barbiturates, and disulfiram
PregnancyD - Unsafe in pregnancy
PrecautionsCardiovascular disease; seizure disorder; urinary retention; adverse effects include sedation, urinary retention, constipation, dry mouth, dizziness, and arrhythmias; monitor ECG and BP at start of therapy and with dose changes

Drug NameImipramine (Tofranil)
DescriptionInhibits reuptake of norepinephrine or serotonin (5-HT) at presynaptic neuron.
Adult Dose10-50 mg/d PO qhs; administered at lower doses than required for depression
Pediatric Dose0.2-0.4 mg/kg/d PO qhs
ContraindicationsDocumented hypersensitivity; narrow-angle glaucoma; in acute recovery phase following myocardial infarction; MAOIs within 14 d
InteractionsIncreases toxicity of sympathomimetic agents such as isoproterenol and epinephrine by potentiating effects and inhibiting antihypertensive effects of clonidine
PregnancyD - Unsafe in pregnancy
PrecautionsMay impair mental or physical abilities required for performance of potentially hazardous tasks; caution in cardiovascular disease, conduction disturbances, seizure disorders, urinary retention, hyperthyroidism, or concurrent thyroid replacement therapy
Monitor ECG and BP at start of therapy and with dose changes

Drug Category: Laxatives and stool softeners

Can be useful in patients with constipation-predominant IBS. Osmotic laxatives (eg, magnesium hydroxide, lactulose, sorbitol) or stool lubricants (eg, mineral oil) are usually required for long-term therapy for children with moderate-to-severe constipation. Long-term studies have shown that these medications are safe and equally effective. Stimulant laxatives may be necessary intermittently and for short periods, but avoid prolonged use.

Drug NameMineral oil (Milkinol)
DescriptionAn emollient laxative that does not appear to have any pharmacologic action on the GI tract. Acts by lubrication. When taken for 2-3 d, penetrates and softens stool and may interfere with absorption of water. Generally is well tolerated and without major adverse effects. Onset of action is approximately 6-8 h. Indigestible; limited absorption.
Adult Dose15-45 mL PO qd or divided tid
60-150 mL PR as single dose
Pediatric Dose5-20 mL PO qd or divided tid
For chronic functional constipation: Up to 1.5-5 mL/kg/d
For disimpaction: Up to 30 mL per y of age bid; not to exceed 240 mL/d
30-60 mL PR as single dose
ContraindicationsDocumented hypersensitivity; GERD, esophageal dysmotility, and dysphagia because of risk of aspiration and lipid pneumonitis; patients who are bedridden; infants <1 y; use with caution in children <5 y to minimize risk of aspiration
InteractionsDecreases effect of docusate sodium and may decrease absorption of coumarin, oral contraceptives, and fat-soluble vitamins
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsChildren <5 y; prolonged administration may produce a deficiency of fat-soluble vitamins; do not administer with food or meals (may cause aspiration, leading to lipid pneumonitis)



Prognosis

  • IBS is a chronic disorder that cannot be cured and usually persists in a waxing and waning fashion. Many children and adolescents who are diagnosed with IBS continue to experience symptoms into adulthood, and many adult patients with IBS trace their symptoms to childhood. The intensity of pain for a particular patient may vary with time, but the nature of symptoms usually remains unchanged.
  • The quality of life for many patients with IBS can be enhanced with ongoing education, reassurance, psychosocial support, and appropriate pharmacotherapy when indicated.

Patient Education

  • Educate patients and their families about the pathophysiology, diagnosis, and treatment of IBS symptoms. Patients who were given detailed discussions about their diagnosis and treatment were found to have reduced symptom intensity and fewer return visits to physicians.
  • For excellent patient education resources, visit eMedicine's Esophagus, Stomach, and Intestine Center. Also, see eMedicine's patient education article, Irritable Bowel Syndrome.



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Irritable Bowel Syndrome excerpt

Article Last Updated: Jul 31, 2007