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Interventions for post-infectious irritable bowel syndrome: a systematic review of treatment efficacy
Tropical Diseases, Travel Medicine and Vaccines volume 1, Article number: 1 (2015)
Post-infectious irritable bowel syndrome (PI-IBS) due to traveler’s diarrhea is the second most common illness seen in post-travel clinics, yet its optimal management remains unknown. We performed a systematic review to evaluate treatment efficacy in PI-IBS.
We searched Medline, EMBASE, LILACS, CINAHL, CAB abstracts, and the Cochrane Library to February 3, 2014 for intervention studies of the pharmacologic and non-pharmacologic management of PI-IBS and examined the evidence according to a modified Grading of Recommendations Assessment, Development, and Evaluation (GRADE) scale.
Of 336 records, 9 studies were included. Eight studies of pharmacologic interventions examined 5 agents (mesalazine or mesalamine, ondansetron, prednisolone, cholestyramine, and metronidazole). One study examined the non-pharmacologic intervention of different infant nutritional formulas following acute gastroenteritis. The quality of the evidence to date was low, with small sample size (fewer than 50 participants) and short duration of follow-up. Overall, the efficacy of pharmacological treatment ranged from no benefit (ondansetron and prednisolone) to moderately beneficial (cholestyramine and metronidazole). The evidence for mesalazine was equivocal: one study showed benefit, two others showed none.
Heterogeneity in outcome measures and low strength of evidence preclude recommendations on the optimal management of PI-IBS by a specific agent. More comparative intervention research into PI-IBS treatment is needed for consistent best practice in PI-IBS management. Clinicians may elect to pursue therapeutic trials of mesalazine, cholestyramine, or metronidazole in individual patients, but should be aware that data supporting the efficacy of these agents is limited.
Traveler’s diarrhea (TD) is a frequent cause of illness in returning travelers, and it is most often attributable to bacterial causes [1–3]. It has been well documented that acute gastroenteritis and dysentery due to TD are associated with increased risk of developing post-infectious irritable bowel syndrome (PI-IBS) in both adults and children [4, 5]. Half of all travelers to the developing world experience diarrhea while abroad or upon return, and at least 10 % of those will develop PI-IBS . During 2009–2011, PI-IBS was the second most common diagnosis among returning tourist travelers and the third most common diagnosis among all non-immigrant travelers evaluated at Canadian post-travel clinics . PI-IBS results in abdominal discomfort, bloating, and diarrhea that persist for years despite clearance of the initial inciting pathogens [7, 8]. It has been postulated that PI-IBS may be caused by altered motility, increased intestinal permeability, and persistent intestinal inflammation, but the exact mechanisms of disease still need to be elucidated [7–10]. Diagnosis is typically made by documenting a history of gastroenteritis or dysentery and a new onset of IBS according to Rome criteria [7–10].
However, despite the relative frequency of PI-IBS, little synthesized evidence surrounding its management exists: there are no management guidelines or expert recommendations, and there is a distinct paucity of literature exploring treatment options. Therefore, there is a clear need for effective management guidelines [11, 12].
In order to determine the optimal evidence-based management of PI-IBS, we conducted a systematic review of the pharmacologic and non-pharmacologic interventions which have been evaluated to date for treatment of PI-IBS.
The search was conducted in two steps and in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines (PRISMA checklist included as Additional file 1: Appendix 1) . First, we searched Medline, Excerpta Medica database (EMBASE), Literature in the Health Sciences in Latin America and the Caribbean (LILACS), Cumulative Index to Nursing and Allied Health Literature (CINAHL), Commonwealth Agricultural Bureaux (CAB) abstracts, and the Cochrane Library from inception to February 3, 2014 using combinations of the following search terms: “Post-infectious irritable bowel syndrome”, “post-infectious irritable bowel”, “post-infectious diarrhea”, “post-infectious constipation”, “post-infectious abdominal pain”, “post-infectious motility”, “post-infective irritable bowel”, and “post-diarrhea”. We restricted the search to English language papers and to studies conducted on humans. Additional file 1: Appendix 2 includes the Medline search. Second, we hand-searched reference lists and cited bibliographies from literature identified in the electronic database search but not meeting inclusion criteria for the systematic review for relevant papers, as well as the Public Health Agency of Canada/Committee to Advise on Tropical Medicine and Travel (http://www.phac-aspc.gc.ca/tmp-pmv/catmat-ccmtmv/index-eng.php) and Centers for Disease Control Websites (http://www.cdc.gov) for position and technical papers [14, 15].
We included all systematic reviews, randomized controlled trials (RCTs), clinical trials, cohort studies, observational studies, case–control studies, and larger case series (N > 5 participants) assessing or reporting the efficacy, safety, or tolerability of pharmacologic and non-pharmacologic interventions used in the management of post-infectious irritable bowel syndrome. For RCTs, we included placebo, comparator, or intervention trials and those with “no treatment” arms. Due to an anticipated paucity of high-quality studies, we included any trial fulfilling inclusion criteria, regardless of its definition of PI-IBS. We excluded case reports or small case series (N < =5 participants).
We extracted all of the following possible outcomes, if and where reported: global symptom severity (efficacy); severity of abdominal pain (efficacy); frequency of diarrhea (efficacy); stool form and consistency as defined by the Bristol stool classification scale  (efficacy); severity of bloating (efficacy); subjective and objective tolerability of the drug; subjective and objective tolerability of the non-pharmacologic intervention; cost of intervention; duration of symptoms (efficacy); functional disability (efficacy); and adverse outcomes (safety). Data including intervention details, number of men and women in each group, average participant age, comorbidities (if reported), initial infectious organism (if reported), and article descriptors (e.g. title, authors) were extracted by two reviewers (ET, JO) and verified by one reviewer (AB) and stored in an MS Access database.
Quality and Strength of the evidence: We evaluated the studies included using a modified version of Grading of Recommendations Assessment, Development, and Evaluation (GRADE) . GRADE is a system of rating evidence for systematic reviews and guideline development, which rates evidence from low to high quality . It defines criteria for rating the quality of evidence for an intervention on specific outcomes based on: limitations, inconsistency, indirectness, imprecision, and publication bias. The quality of evidence for each treatment was evaluated across these criteria as appropriate given the number of studies per treatment and outcome.
Synthesis of intervention efficacy: We summarized the evidence using descriptive measures for each intervention type/agent. Meta-analysis of treatment efficacy was planned if at least five efficacy measures for the same treatment were available.
The literature search returned 336 studies, of which 9 were included (Fig. 1): 8 evaluated pharmacologic interventions, and one evaluated a non-pharmacologic intervention. Of the 327 excluded articles, 222 were excluded at the title stage due to irrelevance to either IBS or PI-IBS. An additional 26 articles were excluded at the abstract stage due to irrelevance to either IBS or PI-IBS, despite titles suggestive of bowel syndrome-oriented primary research. Exclusion at the full text stage (N = 79) fell into 1 of 5 broad categories: review article with no primary data cited (N = 32); original research into the epidemiology, pathogenesis, diagnosis, or prognosis or PI-IBS, but without an evaluated treatment intervention (N = 12); therapeutic trial for IBS, without mention of PI-IBS (N = 9); therapeutic trial for prevention of traveler’s diarrhea (N = 8), and other (N = 18). Articles in the “other” category were excluded for various reasons such as publication only in a foreign language, publication in the form of an editorial or letter, or publication of a non-research article that had been updated subsequently by the same authors.
Study characteristics, quality of the evidence, and outcome measures of the included trials are shown in Table 1. Amongst the 8 studies examining pharmacological interventions, 5 different therapies were evaluated: mesalazine or mesalamine [18–20], ondansetron , prednisolone , cholestyramine [23, 24], and metronidazole . We had an insufficient number of studies examining the same intervention on the same outcome measure to complete a full GRADE assessment. Thus, we used a modified GRADE rating consisting of only the limitations and indirectness categories (Table 2). The literature included in this study varied from low to moderate quality of evidence, due to reasons such as nature of study (N = 5), unclear allocation concealment and randomization method (N = 9) and differences in population of interest (N = 3, Table 1).
Across the eight pharmacologic interventions, the efficacy of outcome ranged from no improvements to moderate reduction in bowel symptoms. Efficacy of mesalazine (N = 3) ranged from no improvement (bowel symptoms or quality of life, N = 2) to reducing daily stool frequency by 1.33 and a Bristol stool score  improvement by 2.17 (N = 1). Ondansteron (N = 1) did not provide any significant improvements to drinking capacity, gastric volume, and gastric emptying, but did improve the nausea score by 51 % compared to the placebo. Prednisolone (N = 1) did not show any improvements in abdominal pain, stool looseness, urgency, frequency, or global wellness score compared to the placebo. Treatment of post-infectious bile malabsorption with cholestyramine (N = 2) demonstrated 70.8–75.9 % decrease in stool frequency, from 7.2–7.83 stools per day to 1.89–2.1 stools per day. Metronidazole (N = 1) resulted in improvement in stool scores (urgency and frequency), pain response, and total symptom score.
Bafutto, et al.  conducted a non-randomized interventional trial that compared the treatment response of PI-IBS patients and non-infective IBS patients, both diagnosed based on Rome III criteria, after 30 days of mesalazine therapy. In the PI-IBS group, the average stool frequency score decreased significantly from 2.44 at baseline to 1.11 on the 30th day after therapy (P < 0.0001). Stool form and consistency, as determined by the Bristol stool scale, improved significantly from 3.28 at baseline to 1.11 on the 30th day (P < 0.0001). Significant improvements in the same measures were also noted in the non-infective IBS group following mesalazine treatment.
The other two studies [19, 20] showed no significant change in symptoms following mesalazine treatment. Hanevik et al.  conducted an open pilot study of 18 patients with PI-IBS who were randomized to either mesalazine treatment or a non-treatment control group. There were no significant improvements in symptom scores in either group. Similarly, Tuteja et al.  conducted a pilot study with 17 patients with PI-IBS who were randomized to mesalazine treatment or placebo and found that mesalazine did not improve global symptoms, abdominal pain, bloating, stool urgency, frequency, or consistency, or quality of life score. These studies had longer treatment periods than the study by Bafutto et al.: six weeks  and three months , respectively.
In a double-blind, randomized controlled trial, Dizdar et al.  randomized fifteen patients with PI-IBS to placebo or ondansetron treatment. The subjects were given 1 dose of ondansetron or placebo, fasted overnight, given a second dose of ondansetron or placebo, and then fed a meat soup test meal (Toro clear meat soup; Rieber & Son A/S, Bergen, Norway) in order to assess the drinking capacity, gastric volume, and gastric emptying via ultrasound. Symptoms were measured at the maximal drinking capacity after the ingestion of the soup. There was no significant improvement in abdominal pain, nausea, fullness, satiety, drinking capacity, 3D gastric volumes, or gastric emptying after the ondansetron treatment. However, the postprandial nausea score was significantly lower in the group that received ondanesteron than in the placebo group (27.47 ± 21.89 vs 41.40 ± 23.04 respectively, P < 0.005).
In a double-blind, randomized controlled study by Dunlop et al. , twenty-nine PI-IBS patients were randomized to placebo or prednisolone and treated for 6 weeks. This study used cell counts from rectal biopsies as the primary and secondary outcome measures, but also included symptom scores as outcome measures. There was a decrease in gastrointestinal symptoms, consisting of abdominal pain, fecal looseness, urgency, and frequency, after the prednisolone treatment (P = 0.01). However, this decrease was not significantly different from the symptom reduction observed in the placebo group (P < 0.02). There was no statistically significant improvement in depression, anxiety, or global well-being score in the prednisolone treatment group. Patients receiving placebo demonstrated significantly greater improvement in the constipation syndrome score (1.0 ± 0.33) as compared to those receiving prednisolone (−0.4 ± 0.55) (P = 0.035).
Two retrospective studies of patients with post-infectious bile acid malabsorption, a subset of PI-IBS, were included. In both studies, patients with post-infective bile acid malabsorption were identified based on results of a 75SeHCAT bile acid retention scan (a clinical test used to diagnose bile malabsorption) and a positive stool culture or clinical record of severe infectious gastroenteritis. In both studies, patients were allowed to titrate their own dose of cholestyramine, so the dose between patients varied from 2–16 g/day. Both studies were small, containing no more than 25 participants each. Menon et al.  reported that out of 25 patients, 7 patients stopped cholestyramine treatment due to constipation or no improvement in symptoms. However, 18 patients had a significant decrease in the frequency of bowel movements from 7.83 before the cholestyramine treatment to 1.89 stools/day afterwards (P = 0.001). The 18 patients who showed initial response had a sustained response to cholestyramine for over a year. Niaz et al.  reported a decrease in stool frequency from 7.2 stools/day one week before cholestyramine treatment to 2.1 stools/day after two weeks of cholestyramine treatment (P < 0.001).
Thakur et al.  recruited 17 patients with PI-IBS, 24 patients with IBS-constipation (IBS-c) subtype, and 35 patients with IBS-diarrhea (IBS-d) subtype based on Rome II criteria and a history of acute gastroenteritis. The participants took metronidazole orally for seven days, and then returned on day twenty-eight for reassessment. There was a significant improvement in pain, modified stool score (stool frequency and consistency), and total symptom scores at days 7 and 28 compared to baseline. Stool symptoms continued to improve between day 7 and 28 in the PI-IBS group even though patients were no longer taking the medication. However, these improvements were not quantified in the manuscript. Both IBS-d and PI-IBS groups showed improved total symptom score and pain response compared to IBS-c (P < 0.05). In terms of stool symptoms, both the IBS-c and IBS-d groups improved in the first seven days, but unlike the PI-IBS group, these improvements were not sustained to 28 days.
Infant formula 
The sole trial of non-pharmacologic interventions for PI-IBS investigated the response to three different dietary treatments in lactose intolerant infants with chronic post-infectious diarrhea . This was a randomized intervention trial with no control arm, in which 29 infants were randomized to receive one of three dietary formulas (10 Pregestimil, 9 Portagen, and 10 soy). The three formulas differed primarily in carbohydrate, protein, and fat content, with Pregestimil having the highest carbohydrate content, but least amount of protein and fat. The average age of the infants was 4.8 months, and there were 17 males and 12 females. All infants were clinically diagnosed with acute gastroenteritis and diarrhea for more than 3 weeks, and the primary outcome of the study was improvement in diarrhea in 7 days. Infants receiving the Pregestimil formula demonstrated improved clinical symptoms, shorter time to improvement, and a lower rate of worsening diarrhea. Nine out of 10 infants had clinical improvement on Pregestimil (95 % CI: 0.71–1.09), 4 out of 9 infants improved on Portagen (95 % CI: 0.34–0.54), and only 1 out of 10 infants improved on soy (95 % CI: 0.04–0.16).
This systematic review of therapeutic interventions for PI-IBS demonstrated a lack of consistent, high-quality evidence to support an optimal management regimen for adults and children. Our search yielded 9 studies, of which one focused solely on various infant formulas and found that progestimil, a high carbohydrate and low protein and fat formula, lead to improvement in diarrhea in infants with PI-IBS and lactose intolerance. Eight others evaluated the effect of various medications on the symptoms of PI-IBS in adult patients. Treatment with either cholestyramine or metronidazole yielded moderate improvement in gastrointestinal symptoms in patients with PI-IBS. Treatment with ondansetron or prednisolone yielded no significant reduction in stool frequency, consistency, or pain, while treatment with mesalazine yielded variable results.
Very few randomized controlled trials have been conducted to evaluate interventions for PI-IBS. The available evidence is of low quality, and based on the frequency of PI-IBS in travelers returned from abroad, there is a need for higher quality research in this area. All of the studies available on management of PI-IBS deal with very small sample sizes (N < 50), which may not be large enough to capture the true effect of an intervention. Lack of homogeneity amongst reported outcome measures and the small number of studies hindered the pooling of results and meta-analysis. The follow-up periods in these studies were usually quite short, often less than 1 month. For a condition lasting an average of 2–3 years, this is insufficient to determine whether a treatment has had a lasting impact.
Current management practices for PI-IBS are largely based on the studies of patients with non-infectious IBS, and the treatments are mostly focused on symptom alleviation [8, 11]. For instance, patients are prescribed opiates for diarrhea, antispasmodics for abdominal discomfort, and tricyclic antidepressants for pain management . In addition, soluble fiber and peppermint oil have been demonstrated to mitigate symptoms in randomized clinical trials of patients with IBS . However, it must be noted that PI-IBS is a clinically distinct subgroup of IBS, with a specific inciting event and unique histologic and clinical features. PI-IBS necessarily follows an enteric infection, usually bacterial, and typically results in more serotonin-producing enterochromaffin cells (EC cells) and a higher number of mast cells in the gut [28, 29]. Patients with PI-IBS typically manifest more frequent diarrhea than constipation, and have fewer psychiatric comorbidities than do those with non-infectious IBS [28, 29]. These characteristics may have implications for treatment and its effect in patients with PI-IBS.
Depending on the severity of a patient’s PI-IBS symptoms, interventions such as mesalazine, cholestyramine, or metronidazole may be considered in therapeutic trials in individual patients. These interventions are based on biological plausibility, clinical research, and the current understanding of PI-IBS pathogenesis, which extends from in vitro and in vivo models of this syndrome. While some of the interventions described showed no benefit, including prednisolone and ondansetron, or had conflicting results in different studies (mesalazine), given the low quality of the available studies it is difficult to conclusively judge the effectiveness of these interventions. Patients should be informed of the available options, but also educated regarding the lack of evidence supporting those options and allowed to make their own treatment decisions. Patients should also be educated regarding the chronic nature of PI-IBS and encouraged to monitor their symptoms for patterns of worsening and improvement in order to identify potential triggers. Primary care physicians could aid patients through awareness of the risk factors for development of PI-IBS, and monitoring patients following episodes of acute gastroenteritis for development of PI-IBS. Counselling around the risk of PI-IBS in the pre-travel consultation setting may encourage greater attention to food and water precautions during travel, and through promotion of awareness, indirectly help to manage patient expectations should PI-IBS arise post-travel.
Limitations to our review include the use of keyword searches instead of medical sub-heading (MeSH) searches. Use of MeSH on databases like MEDLINE or EMBASE may be more sensitive than simple keyword searching. However, there was no MeSH term for PI-IBS, and an initial trial of MeSH related to IBS and management on MEDLINE and EMBASE yielded results that were neither sensitive nor specific. PI-IBS may not be included in the MeSH thesaurus because it is a relatively recently studied phenomenon, the term is conversational in that it has not been defined in the medical language, and PI-IBS is not yet considered sufficiently different from general IBS. Restriction of our search to English language articles may have compromised the sensitivity of our search strategy, and may have introduced bias to our results. We felt these risks would be low as PI-IBS is vastly over-represented in non-immigrant/non-‘visiting friends and relatives’ travelers traveling from developed to developing world settings , and due to the concentration of PI-IBS expertise in European, Australian, and North American centers. Other limitations include the lack of standardization of the definition of PI-IBS. Some of the included trials used Rome criteria to define PI-IBS, and not all provided evidence for exclusion of other causes of chronic gastrointestinal symptoms following travelers’ diarrhea, such as persistent infection, co-infection, or underlying gastrointestinal disease, all of which may have affected performance of the investigational therapeutic. Finally, heterogeneity in mechanism of action of the tested therapeutics and end-points made pooled analysis of the results impossible.
This knowledge synthesis has important consequences for individual patients, as well as for healthcare systems. Chronic diarrhea places a strain on healthcare resources as up to half of travelers returning from tropical and sub-tropical destinations develop infectious diarrhea [1–4, 6], and an estimated 10 % of those will go on to develop PI-IBS . Despite the prevalence of PI-IBS, this systematic review found only 8 pharmacological and 1 non-pharmacological intervention trials specific to the management of PI-IBS. While interventions such as metronidazole, mesalazine, or cholestyramine may provide symptomatic relief, additional primary research into the pharmacologic management of PI-IBS is needed, as it is a clinically distinct subgroup of IBS with different underlying pathogenesis, and the evidence to support specific pharmacologic maneuvers, including those listed above, is extremely limited. Major research gaps in the management of PI-IBS exist, and priority should be given to evaluation of interventions that provide sustained symptomatic relief and target the underlying pathogenesis, thereby reducing morbidity, and improve the long-term prognosis of this disease. While non-pharmacologic interventions such as dietary restrictions, soluble fiber, and behavioural modifications are favored in the management of IBS, we found no evidence that these strategies extend to the PI-IBS population. A fulsome discussion of the risks, chronicity, and limited management options of PI-IBS should be entertained in the pre-travel setting so as to encourage adherence by travelers to food and water precautions while abroad, and prompt treatment of TD should it arise.
Commonwealth agricultural bureaux
Cumulative index to nursing and allied health literature
Excerpta medica database
Grading of recommendations assessment, development, and evaluation
Irritable bowel syndrome
Irritable bowel syndrome with constipation
Irritable bowel syndrome with diarrhea
Literature in the health sciences in latin America and the Caribbean
Post-infectious irritable bowel syndrome
Preferred reporting items for systematic reviews and meta-analyses
Randomized controlled trial
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Ilnyckyj A, Balachandra B, Elliott L, Choudhri S, Duerksen DR. Post-traveler’s diarrhea irritable bowel syndrome: a prospective study. Am J Gastroenterol. 2003;98(3):596–9.
Zboromyrska Y, Hurtado JC, Salvador P, Alvarez-Martínez MJ, Valls ME, Mas J, et al. Aetiology of traveller’s diarrhoea: evaluation of a multiplex PCR tool to detect different enteropathogens. Clin Microbiol Infect. 2014;20(10):O753–9.
Connor BA, Riddle MS. Post-infectious sequelae of travelers’ diarrhea. J Travel Med. 2013;20(5):303–12.
Stermer E, Lubezky A, Potasman I, Paster E, Lavy A. Is traveler’s diarrhea a significant risk factor for the development of irritable bowel syndrome? A prospective study. Clin Infect Dis. 2006;43(7):898–901.
Thabane M, Simunovic M, Akhtar-Danesh N, Garg AX, Clark WF, Collins SM, et al. An outbreak of acute bacterial gastroenteritis is associated with an increased incidence of irritable bowel syndrome in children. Am J Gastroenterol. 2010;105(4):933–9.
Boggild AK, Geduld J, Libman M, Ward BJ, McCarthy AE, Doyle P, et al. Travel-acquired infections and illnesses in Canadians: surveillance report from CanTravNet surveillance data, 2009–2011. Open Med. 2014;8(1):e20–32.
Spiller R, Campbell E. Post-infectious irritable bowel syndrome. Curr Opin Gastroenterol. 2006;22(1):13–7.
DuPont AW. Postinfectious irritable bowel syndrome. Clin Infect Dis. 2008;46(4):594–9.
Dupont HL. Gastrointestinal infections and the development of irritable bowel syndrome. Curr Opin Infect Dis. 2011;24(5):503–8.
Ghoshal UC, Ranjan P. Post-infectious irritable bowel syndrome: the past, the present and the future. J Gastroenterol Hepatol. 2011;26 Suppl 3:94–101.
Barbara G, Stanghellini V, Cremon C, De Giorgio R, Corinaldesi R. Almost all irritable bowel syndromes are post-infectious and respond to probiotics: controversial issues. Dig Dis. 2007;25(3):245–8.
Barbara G, Cremon C, Pallotti F, De Giorgio R, Stanghellini V, Corinaldesi R. Postinfectious irritable bowel syndrome. J Pediatr Gastroenterol Nutr. 2009;48 Suppl 2:S95–7.
Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151(4):264–9. W64.
Government of Canada PHAC. CATMAT - Travel Health - Public Health Agency of Canada [Internet]. 2006 [cited 2014 Jun 14]. Available from: http://www.phac-aspc.gc.ca/tmp-pmv/catmat-ccmtmv/index-eng.php.
Department of Health and Human Services. Center for Disease Control and Prevention [Internet]. [cited 2014 Jun 14]. Available from: http://www.cdc.gov.
Lewis SJ, Heaton KW. Stool form scale as a useful guide to intestinal transit time. Scand J Gastroenterol. 1997;32(9):920–4.
Guyatt G, Oxman AD, Akl EA, Kunz R, Vist G, Brozek J, et al. GRADE guidelines: 1. Introduction-GRADE evidence profiles and summary of findings tables. J Clin Epidemiol. 2011;64(4):383–94.
Bafutto M, de Almeida JR, Leite NV, Oliveira EC, Gabriel-Neto S, Rezende-Filho J. Treatment of postinfectious irritable bowel syndrome and noninfective irritable bowel syndrome with mesalazine. Arq Gastroenterol. 2011;48(1):36–40.
Hanevik K, Dizdar V, Langeland N, Eide GE, Hausken T. Tolerability and effect of mesalazine in postinfectious irritable bowel syndrome. Aliment Pharmacol Ther. 2011;34(2):259–60.
Tuteja AK, Fang JC, Al-Suqi M, Stoddard GJ, Hale DC. Double-blind placebo-controlled study of mesalamine in post-infective irritable bowel syndrome--a pilot study. Scand J Gastroenterol. 2012;47(10):1159–64.
Dizdar V, Gilja OH, Hausken T. Increased visceral sensitivity in Giardia-induced postinfectious irritable bowel syndrome and functional dyspepsia. Effect of the 5HT3-antagonist ondansetron. Neurogastroenterol Motil. 2007;19(12):977–82.
Dunlop SP, Jenkins D, Neal KR, Naesdal J, Borgaonker M, Collins SM, et al. Randomized, double-blind, placebo-controlled trial of prednisolone in post-infectious irritable bowel syndrome. Aliment Pharmacol Ther. 2003;18(1):77–84.
Menon S, Jones BJM. Postinfective bile acid malabsorption: is this a long-term condition? Eur J Gastroenterol Hepatol. 2011;23(4):308–10.
Niaz SK, Sandrasegaran K, Renny FH, Jones BJ. Postinfective diarrhoea and bile acid malabsorption. J R Coll Physicians Lond. 1997;31(1):53–6.
Thakur T, Altekar SB, Bapat MR, Rathi PM, Joshi A, Abraham P. Post-infectious irritable bowel syndrome: Role of metronidazole. Ann Gastroenterol. 2009;22(2):102–5.
Lifshitz F, Fagundes-Neto U, Ferreira VC, Cordano A, Hda Ribeiro C. The response to dietary treatment of patients with chronic post-infectious diarrhea and lactose intolerance. J Am Coll Nutr. 1990;9(3):231–40.
Ford AC, Talley NJ, Spiegel BMR, Foxx-Orenstein AE, Schiller L, Quigley EMM, et al. Effect of fibre, antispasmodics, and peppermint oil in the treatment of irritable bowel syndrome: systematic review and meta-analysis. BMJ. 2008;337:a2313.
Dunlop SP, Jenkins D, Spiller RC. Distinctive clinical, psychological, and histological features of postinfective irritable bowel syndrome. Am J Gastroenterol. 2003;98(7):1578–83.
Bhuiyan MR, Majumder TK, Raihan AA, Roy PK, Farha N, Kamal M. Histopathological alterations in post-infectious irritable bowel syndrome in Bangladeshi population. Mymensingh Med J. 2010;19(2):275–81.
Thabane M, Kottachchi DT, Marshall JK. Systematic review and meta-analysis: the incidence and prognosis of post-infectious irritable bowel syndrome. Aliment Pharmacol Ther. 2007;26:535–44.
This study was unfunded. SM is supported by a Canadian Institutes of Health Research Fellowship.
The authors declare that they have no competing interests.
ET, JO, and AVP contributed to data collection, analysis, and interpretation, and to writing the manuscript. SM contributed to data analysis and interpretation, and to writing the manuscript. AKB conceived the study, and contributed to data collection, analysis, and interpretation, and to writing the manuscript. All authors critically appraised the manuscript.
Emma Torbicki and Justin Oh contributed equally to this work.
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Torbicki, E., Oh, J., Mishra, S. et al. Interventions for post-infectious irritable bowel syndrome: a systematic review of treatment efficacy. Trop Dis Travel Med Vaccines 1, 1 (2015). https://doi.org/10.1186/s40794-015-0002-9
- Chronic diarrhea
- Knowledge synthesis
- Traveler’s diarrhea
- Travel medicine