Irritable Bowel Syndrome (IBS) At a Glance
Rakesh Kumar Jha, Yanli Zou, Jin Li and Bing Xia
Cite this article as: BJMP 2010;3(4):a342
|
Abstract Irritable bowel syndrome (IBS) is a common disorder characterized by abdominal pain and altered bowel habit. Hence, IBS is associated with a significantly impaired health-related quality of life (HRQOL) and reduced work productivity around the world. The incidence of IBS is rising dramatically worldwide. Currently, 7 – 10 % of people have IBS worldwide and it is 1.5 times more prevalent in younger women than in men. Much research has been undertaken during the past several decades, which has lead to deep understanding about IBS, particularly the pathogenesis and management. This review summarizes the epidemiology, underlying pathophysiology, diagnosis and treatment about IBS that has been published in recent years. We hope this review can help to provide some reference in clinical practice for physicians in the management of IBS. Keywords: IBS, Spastic Bowel syndrome, Nervous Bowel, Irritable colon, Splenic Flexure Syndrome, Functional Bowel Disease |
Introduction :
Irritable bowel syndrome (IBS) is a common disorder characterized by abdominal pain and altered bowel habit for at least three months.(1)
IBS is further defined depending on the predominant bowel symptom: IBS with constipation (IBS-C) or IBS with diarrhoea (IBS-D). Those not classified as either IBS-C or IBS-D are considered as mixed IBS (IBS-M). Alternating IBS (IBS-A) defines patients whose bowel habits oscillate from diarrhoea to constipation and vice versa.
Synonyms: Spastic Bowel syndrome, Nervous Bowel, Irritable colon, mucous colitis, Splenic Flexure Syndrome, Functional Bowel Disease.(2)
Epidemiology:
IBS is a prevalent and expensive condition that is associated with a significantly impaired health-related quality of life (HRQOL) and reduced work productivity. IBS care consumes over $ 20 billion in both direct and indirect expenditures. Moreover, patients with IBS consume over 50% more health care resources than matched controls without IBS.(1)Based on strict criteria, 7 – 10 % of people have IBS worldwide. Community-based data indicate that diarrhoea-predominant IBS (IBS-D) and mixed IBS (IBS-M) subtypes are more prevalent than constipation-predominant IBS (IBS-C), and that switching among subtype groups may occur. IBS is 1.5 times more common in women than in men, is more common in lower socioeconomic groups, and is more commonly diagnosed
in patients younger than 50 years of age. Prevalence estimates of IBS range from 1 % to more than 20% in North America(7%).(1) In Asia the prevalence is about 5%.(3,4,5)Recently, a School-Based Study in china reported the prevalence of IBS in adolescents and children was 13.25% and the ratio of boys to girls was 1:1.8.(6) Most patient with IBS in India are middle-aged men (mean age 39.4 years).(7)
Underlying pathophysiology:
Given the lack of definitive organic markers for IBS, the absence of a consolidated hypothesis regarding its underlying pathophysiology is not surprising. Nevertheless, important advances in research made during the past 50 years have brought us closer than ever to understanding the numerous existing aetiological factors involved in this multifaceted disorder, including environmental factors, genetic factors, previous infection, food intolerance, and abnormal serotonergic signaling in the GI tract.
Environmental factors :
The biopsychosocial model proposed by Engel(8) takes into account the interplay between biologic, psychological, and social factors. This model proposes that there is an underlying biologic predisposition for IBS that may be acted on by environmental factors and psychological stressors, which contribute to disease development, the patient's perception of illness, and impact on treatment outcomes. Different studies have shown that stress can result in release of stress-related hormones that affect colonic sensorimotor function (eg, corticotropin-releasing factor [CRF] and inflammatory mediators [eg, interleukin (IL)-1]), leading to inflammation and altering GI motility and sensation.
Genetics factors :
Twin studies have shown that IBS is twice as prevalent in monozygotic twins than in dizygotic twins.(9,10,11) IBS may be associated with selected gene polymorphisms, including those in IL-10, G-protein GNb3, alpha adrenoceptor, and serotonin reuptake transporter (SERT).
Post-infectious IBS (PI-IBS):
Culture positive gastroenteritis is a very strong risk factor for IBS. Different prospective studies show IBS symptoms developed in 7% to 32% of patients after they recovered from bacterial gastroenteritis.(12,13,14) Specific risk factors for the development of PI-IBS have been identified, including younger age, female sex, presence of severe infectious gastroenteritis for a prolonged period, use of antibiotics to treat this infection, and presence of concomitant psychological disorders (eg, anxiety).(12,13,15,16)
Small Intestinal bacterial overgrowth
Pimentel and colleagues(17,18) have shown that, when measured by the lactose hydrogen breath test (LHBT), small intestinal bacterial overgrowth (SIBO) has been detected in 78% to 84% of patients with IBS. Hence, a higher than usual population of bacteria in the small intestine has been proposed as a potential aetiological factor in IBS. While another study involving a review for the presence of gastrointestinal-related symptoms (including IBS) has shown that asensitivity of the LHBT for SIBO has been shown to be as low as 16.7%, and specificity approximately 70% and the test alone for small intestinal bacterial overgrowth were poor. Hence, combination with scintigraphy resulted in 100% specificity to assess the treatment responce, because double peaks in serial breath hydrogen concentrations may occur as a result of lactulose fermentation by cecal bacteria. (19,20)
Food intolerance :
Approximately 60% of IBS patients believe and different studies show that allergy to certain foods could trigger IBS symptoms. Recent research involving exclusion of foods patients had immunoglobulin (Ig) G antibodies, which are associated with a more delayed response after antigen exposure than IgE antibodies, resulted in significantly better symptom improvement than in patients in the non-exclusion group.(21)
Serotonin signaling in Gastrointestinal (GI) tract:
Normal gut physiology is predicated to be an interaction between the GI musculature and the autonomic nervous system (ANS), and central nervous system (CNS) by the neurotransmitter serotonin (5-hydroxytryptamine [5-HT]) . Impairment in this interaction affects GI motility, secretion, and visceral sensitivity leading to the symptoms associated with IBS .(22)
Preliminary steps toward making a positive diagnosis of IBS:
A careful history and physical examination are frequently helpful in establishing the diagnosis. A variety of criteria have been developed to identify a combination of symptoms to diagnose IBS. Different guidelines from different studies help in making a positive diagnosis of IBS based primarily on the pattern and nature of symptoms, without the need for excessive laboratory testing. In 1978, Manning and colleagues (23,24) proposed diagnostic criteria for IBS that were found to have a reasonable sensitivity of 78% and a specificity of 72%.(1) In 1984, Kruis and colleagues developed another diagnostic criteria with a high sensitivity of 77% and a specificity 89%. Likewise, in 1990 Rome I (25) criteria came with a sensitivity of 71% and specificity of 85%. RomeII(1999)(26) and Rome III(2006)(27) have not been evaluated yet. None of the symptom based diagnostic criteria have been evaluated and ideal reliability found.(1)
Summary of diagnostic criteria used to define IBS:(1)
In 1978, Manning defined IBS as a collection of symptoms, given below, but did not describe their duration. The number of symptoms that need to be present to diagnose IBS was also not reported in the paper, but a threshold of three positive is the most commonly used:
a) Abdominal pain relieved by defecation
b) More frequent stools with onset of pain
c) Looser stools with onset of pain
d) Mucus per rectum
e) Feeling of incomplete emptying
f) Patient-reported visible abdominal distension
Kruis in 1984, defined IBS by a logistic regression model that describes the probability of IBS. Symptoms need to be present for more than two years. Symptoms are as follows:
a) Abdominal pain, flatulence, or bowel irregularity
b) Description of character and severity of abdominal pain
c) Alternating constipation and diarrhea
Signs that exclude IBS (each determined by the physician) :
a) Abnormal physical findings and/or history pathognomonic for any diagnosis other than IBS
b) Erythrocyte sedimentation rate >20 mm/2 h
c) Leukocytosis >10,000/cc
d) Anaemia (Hemoglobin < 12 for women or < 14 for men)
e) Impression, the physician could perform a PR and see blood or the patient may report it.
Again in 1990, Rome I defined IBS as abdominal pain or discomfort relieved with defecation, or associated with a change in stool frequency or consistency, PLUS two or more of the following symptoms on at least 25% of occasions or days for three months:
a) Altered stool frequency
b) Altered stool form
c) Altered stool passage
d) Passage of mucus
e) Bloating or distension
Rome II, in 1999, redefined the criteria as abdominal discomfort or pain that has two of three features for 12 weeks (need not be consecutive) in the last one year.
a) Relieved with defecation
b) Onset associated with a change in frequency of stool
c) Onset associated with a change in form of stool
Recently , Rome III (2006) defined IBS as recurrent abdominal pain or discomfort three days per month in the last three months associated with two or more of:
a) Improvement with defecation
b) Onset associated with a change in frequency of stool
c) Onset associated with a change in form of stool
The role of routine diagnostic investigation in patients with IBS:
Routine diagnostic investigation is based on the age of the patient, family history of selected organic diseases including colorectal cancer, inflammatory bowel disease(IBD), coeliac sprue and the presence of ‘alarm’ features(table1), such as rectal bleeding, weight loss, iron deficiency anaemia and nocturnal symptoms.(1) In patient with typical IBS symptoms and no alarm features, routine diagnostic investigation (complete blood count, serum chemistry, thyroid function tests, stool for ova and parasites and abdominal imaging) is not recommended(1) because of a low likelihood of uncovering organic disease.
Table-1 Lists of alarm features:
Rectal bleeding Weight loss Iron deficiency anaemia Nocturnal symptoms: abdominal pain family history of of selected organic diseases: colorectalcancer, Inflammatory Bowel Disease(IBD), celiac sprue |
Summary of diagnostic investigation in patient with IBS : (1,2)
Diagnostic Investigations :
Routine serologic screening for coeliac sprue for patients with IBS-D and IBS-M.
Lactose Breath test done in lactose maldigestion despite dietary modification.
Colonoscopic Imaging done in IBS patient (>50 yrs age) with alarm feature to rule out organic diseases and screening of colorectal cancer.
Colonoscopy with random biopsies taken in IBS-D to rule out microscopic colitis.
Management of IBS:
The goal of IBS management is to provide relief of symptoms and improve overall well-being.(28) Most studies use a combination therapy including patient education and psychological therapies, diet and fibre therapy along with different types of new emerging pharmacological therapies.
Patient education and psychological therapies:
The majority of patients with IBS have anxiety, depression and features of somatization. Psychological therapies, including cognitive behavioral therapy, dynamic psychotherapy, hypnotherapy(1) shed new light on the management of patients with IBS. The outcome of psychological therapies is improved when delivered by a trained professional (physician, occupational therapist, nurse).(29) A study by Guthrie(30) showed that psychological therapy is feasible and effective in two thirds of patients with IBS who do not respond to standard medical treatment.
Role of diet in IBS:
The concept of food intolerance and the consequent elimination of certain foods from the diet benefit symptoms of IBS. However, there is no sufficient evidence to support this.(1)
Therapeutic effect of dietary fibre, bulking agents and laxatives: The quality of evidence supporting the recommended use of dietary fibre or bulking agents to regularize bowel function is poor.(31) Ispaghula husk (Psyllium hydrophilic mucilloid ) and calcium polycarbophil are moderately effective and can be given a conditional recommendation because of the weakest type of evidence.(1) Polyethylene glycol(PEG) laxative has a role in improving stool frequency but no effect on abdominal pain. Different clinical studies and expert opinion suggest that increased fibre intake may cause bloating, abdominal distension and flatulence.(32) So gradual adjustment of dose is advised for the use of these agents.
Therapeutic effect of antispasmodic agents including peppermint oil:
Certain antispasmodics (hyoscine, cimetropium,and pinaverium and peppermint oil) may provide short-term relief of abdominal pain/discomfort in IBS.(33,34)Evidence for safety and tolerability
Agent |
Mechanism of action |
Targeted disorder |
Clinical status |
Crofelemer |
CFTR |
IBS-D |
Phase2b complete |
Linaclotide |
Guanylate cyclase-c agonist |
IBS-C |
Phase 3 |
Arverapamil |
Calcium channel blocker |
IBS-D |
Phase 3 |
Asimadoline |
Kappa opioid agonist |
IBS |
Phase 2b complete |
Mitemcinal |
Motilin receptor agonist |
IBS-C |
Phase 2 |
Ramosetron |
5-HT 3 antagonist |
IBS-D |
Phase 3 |
TD-5108 |
5-HT 4 agonist |
IBS-C |
Phase 2 |
DDP-773 |
5-HT 3 agonist |
IBS-C |
Phase 2 |
DDP-225 |
5-HT 3 antagonist and NE reuptake inhibition |
IBS-D |
Phase 2 |
BMS-562086 |
Corticotropin-releasing hormone antagonist |
IBS-D |
Phase 2 |
GW876008 |
Corticotropin-releasing hormone antagonist |
IBS |
Phase 2 |
GTP-010 |
Glucagon-like peptide |
IBS pain |
Phase 2 |
AGN-203818 |
Alpha receptor agonist |
IBS pain |
Phase 2 |
Solabegron |
Beta-3 receptor agonist |
IBS |
Phase 2 |
Espindolol (AGI-011) |
Beta receptor antagonist |
IBS (all subtypes) |
Phase 2 |
Dextofisopam |
2,3 benzodiazepinereceptors |
IBS-D and IBS-M |
Phase 3 |
Table 1: Source: ACG Task Force on IBS(2009)
of these agents are very limited.The commonest adverse effects are dry mouth,dizziness and blurred vision.(34-36)
Therapeutic effect of anti-diarrhoeal medications:
The anti-diarrhoeal agent ‘Loperamide’ is effective at slowing down colonic transit and improving stool consistency for the treatment of IBS-D with no severe adverse effects.(37) But safety and tolerability datas are still lacking in many studies.
Therapeutic effect of antibiotics:
Many studies show well tolerance of a short term course of non-absorbable antibiotics (Rifaximin) is most effective for improvement of global symptoms in IBS-D and IBS patient with the predominant symptom of bloating and other associated symptoms, such as diarrhoea and abdominal pain.(38-40) While, the Unted States Food and Drug Administration (FDA or USFDA) approved Rifaximin for treatment of traveler’s diarrhoea. Other antibiotics, Neomycin(41), Clarithromycin and Metronidazole(42) have been well evaluated for the management of IBS.
Therapeutic effect of Probiotics:
Probiotics have a large number of properties that can benefit IBS. Bifidobacteria is the active agent in probiotic combination therapy.Whereas many studies show Lactobacilli to have no impact on symptoms.(43) But one Korean study concluded that the composite probiotics containing Bifidobacterium bifidum BGN4, Lactobacillus acidophilus AD031, and other species are safe and effective, especially in patients who excrete normal or loose stools.(44) Recently, P Moayyedi and colleague in their systematic review recommend that probiotics appear to be efficacious in IBS patients ,but the magnitude of benefit and the most effective species and strain are uncertain. (45)
Therapeutic effect of the 5HT3 receptor antagonists:
Alosetron (5-HT3 receptor antagonists), with dosage of 0.5 to 1 mg daily, is more effective and the commonest drug used for treatment of patients with IBS-D in spite of serious side effects including constipation and colon ischemia.The balance model of benefits and harms for ‘Alosetron’ is most encouraging in women who have not responded to conventional therapies.(46,47)
Therapeutic effect of 5-HT4 receptor agonists:
Tegaserod (5-HT4 receptor agonist) is more effective for the treatment of IBS-C mostly in female and IBS-M. The side effects reported among the patient receiving Tegaserod are diarrhoea (commonest), cardiovascular events i.e. myocardial infarction, unstable angina, or stroke.(48,49) Currently Tegaserod is available from FDA through an emergency investigational new drug protocol. Other 5-HT4 agonists (Cisapride,Renzapride) have not demonstrated improvement compared with placebo.(50,51)
Therapeutic effect of the selective C-2 chloride channel activators:
Lubiprostone (selective C-2 chloride channel activator) is effective for relieving symptoms of IBS-C, mostly in women, and has less frequent side-effects including nausea(8%), diarrhea(6%) and abdominal pain(5%).(52)
Therapeutic effect of antidepressants :
Patients with prominent symptom of abdominal pain in IBS that fails to respond to peripherally acting agents often are considered for treatment with antidepressants (TCAs and SSRIs), however, limited data on safety and tolerability of these agents is shown.(53) Antidepressants have the combined effect of both central and peripheral mechanism in IBS.(54) SSRIs are better tolerated than TCAs and have a prokinetic effect hence work better in IBS-C.(53,55) whereas TCAs are of greater benefit for IBS-D.
Therapeutic effect of herbal therapies and acupuncture:
Unique Chinese herbal mixtures show a benefit in IBS management.(56) Traditional Chinese herbal remedies are routinely used in China to treat the condition, but so far have not been generally accepted by conventional Western medicine.(56,57) Bensoussan and colleague in one randomized, double-blind, placebo-controlled trial concluded that the Chinese herbal formulations appear to offer improvement in symptoms for some patients with IBS.(57) A systematic review of different trials of acupuncture was inconclusive because of heterogenous outcomes.(58,59) Hence further work is needed before any recommendations on acupuncture or herbal mixtures therapy.
Emerging therapies :
The improved understanding of underlying mechanisms in IBS is beneficial for the development of new pharmacological treatment options.
A brief overview of emerging agents in IBS therapy summarized in Table 1 (1)
Conclusion:
IBS is a true medical disorder that has significant impact on those in agony with regard to symptom severity, disability, and impaired quality of life, which exceeds that of most GI disorders. Advances in research over the past several decades have paved the way for an ameliorable understanding of the underlying pathophysiology and standardized symptom-based approaches that can be implemented in making a positive diagnosis and development of innovative treatment options for multiple IBS symptoms. Although many unanswered questions remain, the progress is promising and it has equipped physicians better to efficiently diagnose IBS and choose from a growing armamentarium of treatment options.
Competing Interests None declared Author Details RAKESH KUMAR JHA , MBBS, MD Department of Internal Medicine ( Gastroenterology ),Zhongnan Hospital, Wuhan University School of Medicine,Donghu Road 169,Wuhan 430071 Hubei Province, P.R. of China YANLI ZOU Yanli, MD Department of Internal Medicine ( Gastroenterology ),Zhongnan Hospital, Wuhan University School of Medicine,Donghu Road 169,Wuhan 430071 Hubei Province, P.R. of China JIN LI Jin, MD , Ph.D. Zhongnan Hospital, Wuhan University School of Medicine Donghu Road 169,Wuhan 430071 Hubei Province, P.R. of China BING XIA , MD, Ph.D Director of Department of Gastroenterology,Director of Department of Internal Medicine Chair of Clinical Center for Intestinal & Colorectal Diseases of Hubei Province, Zhongnan Hospital, Wuhan University School of Medicine,Wuhan 430071, Hubei, PR China CORRESPONDENCE: Prof. BING XIA , MD, PhD, Director of Department of Gastroenterology,Director of Department of Internal Medicine,Chair of Clinical Center for Intestinal & Colorectal Diseases of Hubei Province Zhongnan Hospital, Wuhan University School of Medicine Donghu Road 169,Wuhan 430071 Hubei Province, P.R. of China Email: bingxia2004@yahoo.com.cn |
References
- Brandt LJ, Chey WD, Foxx-Orenstein AE et al. An Evidence-Based Systematic Review on the Management of Irritable Bowel Syndrome. Am J Gastroenterology2009;104:S1 – S35
- Avunduk C. Irritable bowel syndrome. Manual of gastroenterology:diagnosis and therapy 2002;3:223-227
- Lule GN, Amayo EO. Irritable bowel syndrome in Kenyans. East AfrMed J 2002;79:360–363
- Saito YA, Schoenfeld P, Locke GR. The epidemiology of irritable bowel syndrome in North America: a systematic review. Am J Gastroenterol2002;97:1910–1915
- Ringel Y, Sperber AD, Drossman DA. Irritable bowel syndrome. Annu Rev Med2001;5:319–338
- Liu Dong, Li Dingguo, Xu Xiaoxing et al.An Epidemiologic Study of Irritable Bowel Syndrome in Adolescents and Children in China: A School-Based Study.Pediatrics 2005;116;e393-e396.
- Ghoshal UC, Abraham P, Bhatt C, et al. Epidemiological and clinical profile of irritable bowel syndrome in India: report of the Indian Society of Gastroenterology Task Force. Indian J Gastroenterol 2008;27:22-28.
- Engel GL. The need for a new medical model: a challenge for biomedicine. Science 1977;196:129-136.
- Falk P. Is IBS a genetic disorder? FBG Newsletter 2003:10-15.
- Levy RL, Jones KR, Whitehead WE, et al. Irritable bowel syndrome in twins: heredity and social learning both contribute to etiology. Gastroenterology 2001;121:799-804.
- Morris-Yates A, Talley NJ, Boyce PM, et al. Evidence of a genetic contribution to functional bowel disorder. Am J Gastroenterol 1998;93:1311-1317.
- Barbara G, De Giorgio R, Stanghellini V, et al. A role for inflammation in irritable bowel syndrome? Gut 2002;51(suppl 1):i41-i44.
- Mach T. The brain-gut axis in irritable bowel syndrome--clinical aspects. Med Sci Monit 2004;10:RA125-RA131
- Spiller RC, Jenkins D, Thornley JP, et al. Increased rectal mucosal enteroendocrine cells, T lymphocytes, and increased gut permeability following acute Campylobacter enteritis and in post-dysenteric irritable bowel syndrome. Gut 2000;47:804-811
- Barbara G, De Giorgio R, Stanghellini V, et al. New pathophysiological mechanisms in irritable bowel syndrome. Aliment Pharmacol Ther 2004;20:1-9.
- Dunlop SP, Jenkins D, Neal KR, et al. Relative importance of enterochromaffin cell hyperplasia, anxiety, and depression in postinfectious IBS. Gastroenterology 2003;125:1651-1659
- Pimentel M, Chow EJ, Lin HC. Eradication of small intestinal bacterial overgrowth reduces symptoms of irritable bowel syndrome. Am J Gastroenterol 2000;95:3503-3506.
- Pimentel M, Chow EJ, Lin HC. Normalization of lactulose breath testing correlates with symptom improvement in irritable bowel syndrome. A double-blind, randomized, placebo-controlled study. Am J Gastroenterol 2003;98:412-419.
- Riordan S, McIver C, Walker B, et al.. The lactulose breath hydrogen test and small intestinal bacterial overgrowth. Am J Gastroenterol 1996;9:1795-1803.
- O'Leary C, Quigley EM. Small bowel bacterial overgrowth, celiac disease, and IBS: what are the real associations? Am J Gastroenterol 2003;98:720-722.
- Atkinson W, Sheldon TA, Shaath N, et al. Food elimination based on IgG antibodies in irritable bowel syndrome: a randomised controlled trial. Gut 2004;53:1459-1464.
- Coates MD, Mahoney CR, Linden DR, et al. Molecular defects in mucosal serotonin content and decreased serotonin reuptake transporter in ulcerative colitis and irritable bowel syndrome. Gastroenterology 2004;126:1657-1664
- Manning AP, Thompson WG, Heaton KW, et al. Towards positive diagnosis of the irritable bowel. BMJ 1978;2:653-654
- Lembo TJ, Fink RN. Clinical assessment of irritable bowel syndrome. J Clin Gastroenterol 2002;35:S31-S36.
- Thompson WG, Creed FH, Drossman DA. Functional bowel disorders and functional abdominal pain. Gastroenterol Int. 1992;5:75-91.
- Thompson WG, Longstreth GF, Drossman DA, et al. Functional bowel disorders and functional abdominal pain. Gut 1999;45(suppl II):II43-II47.
- Drossman DA. The functional gastrointestinal disorders and the Rome III process. Gastroenterology 2006;130:1377-1390
- Brandt LJ, Bjorkman D, Fennerty MB, et al. Systematic review on the management of irritable bowel syndrome in North America. Am J Gastroenterol 2002;97:S7-S26.
- Tries J, Plummer MK, Wisconsin OTR. Biofeedback and bowel disorders: Teaching yourself to live without the problem. Available at: http://www.aboutibs.org/Publications/Biofeedback.html Accessed May 26, 2006.
- Guthrie E. Brief Psychotherapy with Patients with Refractory Irritable Bowel Syndrome. British Journal of Psychotherapy 1991; 8: 175–188.
- Soltofit J, Gudmand-Hoyer E, Krag B et al. A double-blind trial of the effect of wheat bran on symptoms of irritable bowel syndrome. Lancet 1976;I:270-2.
- Snook J, Shepherd HA. Bran. supplementation in the treatment of irritable bowel syndrome. Aliment Pharmacology Ther 1994;8:511-4
- Nigam P , Kapoor KK , Rastog CK et al. Different therapeutic regimens in irritable bowel syndrome . J Assoc Physicians India 1984 ; 32 : 1041 – 4 .
- Passaretti S , Guslandi M , Imbibo BP et al. Effects of cimetropium bromide on gastrointestinal transit time in patients with irritable bowel syndrome. Aliment Pharmacol Ther 1989 ; 3 : 276 .
- Schafer VE , Ewe K. The treatment of irritable colon. Efficacy and tolerance of buscopan plus, buscopan, paracetamol and placebo in ambulatory patients with irritable colon . Fortschr Med 1990 ; 108 : 488 – 92 .
- Glende M , Morselli-Labate AM , Battaglia G e t al. Extended analysis of a double blind, placebo-controlled, 15-week study with otilinium bromide in irritable bowel syndrome . Eur J Gastroenterol Hepatol 2002 ; 14 : 1331 – 8 .
- Hovdenak N . Loperamide treatment of the irritable bowel syndrome . Scand J Gastroenterol 1987 ; 130 : 81 – 4 .
- Ringel Y , Palsson OS , Zakko SF et al. Predictors of clinical response from a phase 2 multi-center efficacy trial using rifaximin, a gut-selective, nonabsorbed antibiotic for the treatment of diarrhea associated irritable bowel sydnrome . Gastroenterology 2008 ; 134 (suppl 1) : A550 (T1141) .
- Lembo A , Zakko SF , Ferreira NL et al. T1390 Rifaximin for the treatment of diarrhea associated irritable bowel syndrome: short term treatment leading to long term sustained response . Gastroenterology 2008 ; 134 (suppl 1) : A 545 (T1390) .
- Pimentel M , Park S , Kong S et al. A 10-day course of rifaximin, a nonabsorbable antibiotic, produces a durable improvement in all symptoms of irritable bowel syndrome: a double-blind randomized controlled study .Gastroenterology 2006 ; 130 : A134 .
- Pimentel M , Chow EJ , Lin HC . Normalization of lactulose breath testing correlates with symptom improvement in irritable bowel syndrome. A double-blind, randomized, placebo-controlled study . Am J Gastroenterol 2003 ; 98 : 412 – 9 .
- Nayak AK , Karnad DR , Abraham P , et al. Metronidazole relieves symptoms in irritable bowel syndrome: the confusion with so-called ‘ chronic amebiasis ’ . Indian J Gastroenterol 1997 ; 16 : 137 – 9 .
- Guyonnet D , Chassany O , Ducrotte P et al. Effect of a fermented milk containing Bifidobacterium animalis DN-173 010 on the health-related quality of life and symptoms in irritable bowel syndrome in adults in primary care: a multicentre, randomized, double blind, controlled trial . Aliment Pharmacol Ther 2007;26:475 – 86 .
- Kyoung Sup Hong,Hyoun Woo Kang,Jong Pil Im et al. Effect of Probiotics on Symptoms in Korean Adults with Irritable Bowel Syndrome. Gut Liver 2009;3(2):101-107.
- P Moayyedi, A C Ford, N J Talley et al. The efficacy of probiotics in the treatment of irritable bowel syndrome: a systematic review. Gut 2010;59:325-332.
- Chang L , Ameen VZ , Dukes GE e t al. A dose-ranging, phase II study of the efficacy and safety of alosetron in men with diarrhea-predominant IBS . Am J Gastroenterol 2005 ; 100 : 115 – 23 .
- Krause R , Ameen V , Gordon SH e t al. A randomized, double-blind, placebo-controlled study to assess efficacy and safety of 0.5 mg and 1 mg alosetron in women with severe diarrhea-predominant IBS . Am J Gastroenterol 2007 ; 102 : 1709 – 19 .
- Ford AC , Brandt L , Foxx-Orenstein A et al. Efficacy of 5HT4-agonists in non-diarrhea predominant irritable bowel syndrome: systematic review and meta-analysis . Am J Gastroenterol 2008 ; 103 (suppl 1) : S478 (1222)
- Chey WD , Pare P , Viegas A e t al. Tegaserod for female patients suffering from IBS with mixed bowel habits or constipation: a randomized controlled trial . Am J Gastroenterol 2008 ; 103 : 1217 – 25 .
- Ziegenhagen DJ , Kruis W . Cisapride treatment of constipation-predominant irritable bowel syndrome is not superior to placebo . J Gastroenterol Hepatol 2004 ; 19 : 744 – 9 .
- George AM , Meyers NL , Hickling RI .Clinical trial: Renzapride therapy for constipation-predominant irritable bowel syndrome — multicentre, randomized, placebo-controlled, double-blind study in primary healthcare setting . Aliment Pharmacol Ther 2008;27:830–7 .
- Drossman DA , Chey WD , Panas R e t al. Lubiprostone significantly improves symptom relief rates in adults with irritable bowel syndrome and constipation (IBS-C): data from two twelve-week, randomized, placebocontrolled, double-blind trials . Gastroenterology 2007 ; 132 : 2586 – 7 .
- Talley NJ . SSRIs in IBS: sensing a dash of disappointment . Clin Gastroenterol Hepatol 2003 ;1:155- 9 .
- Clouse RE . Managing functional bowel disorders from the top down: lessons from a well-designed treatment trial . Gastroenterology 2003 ; 125 : 249 – 53 .
- Gorard DA , Libby GW , Farthing MJG. Influence of antidepressants on whole gut orocaecal transit times in health and irritable bowel syndrome . Aliment Pharmacol Ther 1994 ; 8 : 159 – 66 .
- Madisch A , Holtmann G ,Plein K et al.Treatment of irritable bowel syndrome with herbal preparations: results of a double-blind, randomized, placebocontrolled, multi-centre trial. Aliment Pharmcol Ther 2004; 19 : 271 – 9 .
- Alan Bensoussan, Nick J. Talley, Michael Hing , et al. Treatment of irritable bowel syndrome with Chinese herbal medicine. JAMA 1998;280:1585-1589.
- Fireman Z, Segal A, Kopelman Y, Sternberg A, Carasso R. Acupuncture Treatment for Irritable Bowel Syndrome. Digestion 2001;64:100-103
- Julie A Reynolds, J Martin Bland, Hugh MacPherson. Acupuncture for irritable bowel syndrome – an exploratory randomised controlled trial. ACUPUNCTURE IN MEDICINE 2008;26(1):8-16.
The above article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.