High risk of post‐infectious irritable bowel syndrome in patients with Clostridium difficile infection

Summary Background Infectious enteritis is a commonly identified risk factor for irritable bowel syndrome (IBS). The incidence of Clostridium difficile infection (CDI) is on the rise. However, there is limited information on post‐infectious IBS (PI‐IBS) development following CDI and the host‐ and in...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2016-09, Vol.44 (6), p.576-582
Hauptverfasser: Wadhwa, A., Al Nahhas, M. F., Dierkhising, R. A., Patel, R., Kashyap, P., Pardi, D. S., Khanna, S., Grover, M.
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container_end_page 582
container_issue 6
container_start_page 576
container_title Alimentary pharmacology & therapeutics
container_volume 44
creator Wadhwa, A.
Al Nahhas, M. F.
Dierkhising, R. A.
Patel, R.
Kashyap, P.
Pardi, D. S.
Khanna, S.
Grover, M.
description Summary Background Infectious enteritis is a commonly identified risk factor for irritable bowel syndrome (IBS). The incidence of Clostridium difficile infection (CDI) is on the rise. However, there is limited information on post‐infectious IBS (PI‐IBS) development following CDI and the host‐ and infection‐related risk factors are not known. Aim To determine the incidence and risk factors for PI‐IBS following CDI. Methods A total of 684 cases of CDI identified from September 2012 to November 2013 were surveyed. Participants completed the Rome III IBS questionnaire and details on the CDI episode. Predictive modelling was done using logistic regression to evaluate risk factors for PI‐IBS development. Results A total of 315 CDI cases responded (46% response rate) and 205 were at‐risk (no pre‐CDI IBS) for PI‐IBS development. A total of 52/205 (25%) met the Rome III criteria for IBS ≥6 months following CDI. IBS‐mixed was most common followed by IBS‐diarrhoea. In comparison to those without subsequent PI‐IBS, greater percentage of PI‐IBS patients had CDI symptoms >7 days, nausea, vomiting, abdominal pain during CDI, anxiety and a higher BMI. Using logistic regression, CDI symptoms >7 days [Odds ratio (OR): 2.96, P = 0.01], current anxiety (OR: 1.33, P 
doi_str_mv 10.1111/apt.13737
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F. ; Dierkhising, R. A. ; Patel, R. ; Kashyap, P. ; Pardi, D. S. ; Khanna, S. ; Grover, M.</creator><creatorcontrib>Wadhwa, A. ; Al Nahhas, M. F. ; Dierkhising, R. A. ; Patel, R. ; Kashyap, P. ; Pardi, D. S. ; Khanna, S. ; Grover, M.</creatorcontrib><description>Summary Background Infectious enteritis is a commonly identified risk factor for irritable bowel syndrome (IBS). The incidence of Clostridium difficile infection (CDI) is on the rise. However, there is limited information on post‐infectious IBS (PI‐IBS) development following CDI and the host‐ and infection‐related risk factors are not known. Aim To determine the incidence and risk factors for PI‐IBS following CDI. Methods A total of 684 cases of CDI identified from September 2012 to November 2013 were surveyed. Participants completed the Rome III IBS questionnaire and details on the CDI episode. Predictive modelling was done using logistic regression to evaluate risk factors for PI‐IBS development. Results A total of 315 CDI cases responded (46% response rate) and 205 were at‐risk (no pre‐CDI IBS) for PI‐IBS development. A total of 52/205 (25%) met the Rome III criteria for IBS ≥6 months following CDI. IBS‐mixed was most common followed by IBS‐diarrhoea. In comparison to those without subsequent PI‐IBS, greater percentage of PI‐IBS patients had CDI symptoms &gt;7 days, nausea, vomiting, abdominal pain during CDI, anxiety and a higher BMI. Using logistic regression, CDI symptoms &gt;7 days [Odds ratio (OR): 2.96, P = 0.01], current anxiety (OR: 1.33, P &lt; 0.0001) and a higher BMI (OR: 1.08, P = 0.004) were independently associated with PI‐IBS development; blood in the stool during CDI was protective (OR: 0.44, P = 0.06). Conclusions In this cohort study, new‐onset IBS is common after CDI. Longer CDI duration, current anxiety and higher BMI are associated with the diagnosis of C. difficile PI‐IBS. This chronic sequela should be considered during active management and follow‐up of patients with CDI.</description><identifier>ISSN: 0269-2813</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1111/apt.13737</identifier><identifier>PMID: 27444134</identifier><language>eng</language><publisher>England</publisher><subject>Abdominal Pain - complications ; Abdominal Pain - epidemiology ; Abdominal Pain - microbiology ; Adult ; Clostridioides difficile - physiology ; Clostridium Infections - complications ; Clostridium Infections - epidemiology ; Cohort Studies ; Diarrhea - epidemiology ; Diarrhea - microbiology ; Female ; Humans ; Incidence ; Irritable Bowel Syndrome - epidemiology ; Irritable Bowel Syndrome - microbiology ; Logistic Models ; Male ; Middle Aged ; Risk Factors</subject><ispartof>Alimentary pharmacology &amp; therapeutics, 2016-09, Vol.44 (6), p.576-582</ispartof><rights>2016 John Wiley &amp; Sons Ltd</rights><rights>2016 John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4157-c877a738fc1a5262888951a5477a811d006d003fc4fe68bbce058424ca72e2623</citedby><cites>FETCH-LOGICAL-c4157-c877a738fc1a5262888951a5477a811d006d003fc4fe68bbce058424ca72e2623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fapt.13737$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fapt.13737$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1416,1432,27922,27923,45572,45573,46407,46831</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27444134$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wadhwa, A.</creatorcontrib><creatorcontrib>Al Nahhas, M. F.</creatorcontrib><creatorcontrib>Dierkhising, R. A.</creatorcontrib><creatorcontrib>Patel, R.</creatorcontrib><creatorcontrib>Kashyap, P.</creatorcontrib><creatorcontrib>Pardi, D. S.</creatorcontrib><creatorcontrib>Khanna, S.</creatorcontrib><creatorcontrib>Grover, M.</creatorcontrib><title>High risk of post‐infectious irritable bowel syndrome in patients with Clostridium difficile infection</title><title>Alimentary pharmacology &amp; therapeutics</title><addtitle>Aliment Pharmacol Ther</addtitle><description>Summary Background Infectious enteritis is a commonly identified risk factor for irritable bowel syndrome (IBS). The incidence of Clostridium difficile infection (CDI) is on the rise. However, there is limited information on post‐infectious IBS (PI‐IBS) development following CDI and the host‐ and infection‐related risk factors are not known. Aim To determine the incidence and risk factors for PI‐IBS following CDI. Methods A total of 684 cases of CDI identified from September 2012 to November 2013 were surveyed. Participants completed the Rome III IBS questionnaire and details on the CDI episode. Predictive modelling was done using logistic regression to evaluate risk factors for PI‐IBS development. Results A total of 315 CDI cases responded (46% response rate) and 205 were at‐risk (no pre‐CDI IBS) for PI‐IBS development. A total of 52/205 (25%) met the Rome III criteria for IBS ≥6 months following CDI. IBS‐mixed was most common followed by IBS‐diarrhoea. In comparison to those without subsequent PI‐IBS, greater percentage of PI‐IBS patients had CDI symptoms &gt;7 days, nausea, vomiting, abdominal pain during CDI, anxiety and a higher BMI. Using logistic regression, CDI symptoms &gt;7 days [Odds ratio (OR): 2.96, P = 0.01], current anxiety (OR: 1.33, P &lt; 0.0001) and a higher BMI (OR: 1.08, P = 0.004) were independently associated with PI‐IBS development; blood in the stool during CDI was protective (OR: 0.44, P = 0.06). Conclusions In this cohort study, new‐onset IBS is common after CDI. Longer CDI duration, current anxiety and higher BMI are associated with the diagnosis of C. difficile PI‐IBS. This chronic sequela should be considered during active management and follow‐up of patients with CDI.</description><subject>Abdominal Pain - complications</subject><subject>Abdominal Pain - epidemiology</subject><subject>Abdominal Pain - microbiology</subject><subject>Adult</subject><subject>Clostridioides difficile - physiology</subject><subject>Clostridium Infections - complications</subject><subject>Clostridium Infections - epidemiology</subject><subject>Cohort Studies</subject><subject>Diarrhea - epidemiology</subject><subject>Diarrhea - microbiology</subject><subject>Female</subject><subject>Humans</subject><subject>Incidence</subject><subject>Irritable Bowel Syndrome - epidemiology</subject><subject>Irritable Bowel Syndrome - microbiology</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Risk Factors</subject><issn>0269-2813</issn><issn>1365-2036</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1O3DAUha0KVAbaRV-g8hIWAf8ldjaV0KgFJCRY0LXlODZzIYlTO9PR7HiEPmOfpIYAogssWbbs7x4f34PQF0qOaR4nZpyOKZdcfkALyquyYIRXO2hBWFUXTFG-h_ZTuiOEVJKwj2iPSSEE5WKBVudwu8IR0j0OHo8hTX8f_sDgnZ0grBOGGGEyTedwEzauw2k7tDH0DsOARzOBG6aENzCt8LLLxRFaWPe4Be_BQveIzVLDJ7TrTZfc5-f1AP388f1meV5cXp1dLE8vCytoKQurpDSSK2-pKVnFlFJ1mbciHytK2_yFPLm3wrtKNY11pFSCCWskc5nnB-jbrDuum961NhuMptNjhN7ErQ4G9P83A6z0bfitRa2Y4jQLHD4LxPBr7dKke0jWdZ0ZXO6IptkGq0lZ84wezaiNIaXo_OszlOjHZHRORj8lk9mvb329ki9RZOBkBja5b9v3lfTp9c0s-Q_vwZtK</recordid><startdate>201609</startdate><enddate>201609</enddate><creator>Wadhwa, A.</creator><creator>Al Nahhas, M. F.</creator><creator>Dierkhising, R. A.</creator><creator>Patel, R.</creator><creator>Kashyap, P.</creator><creator>Pardi, D. S.</creator><creator>Khanna, S.</creator><creator>Grover, M.</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201609</creationdate><title>High risk of post‐infectious irritable bowel syndrome in patients with Clostridium difficile infection</title><author>Wadhwa, A. ; Al Nahhas, M. F. ; Dierkhising, R. A. ; Patel, R. ; Kashyap, P. ; Pardi, D. S. ; Khanna, S. ; Grover, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4157-c877a738fc1a5262888951a5477a811d006d003fc4fe68bbce058424ca72e2623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Abdominal Pain - complications</topic><topic>Abdominal Pain - epidemiology</topic><topic>Abdominal Pain - microbiology</topic><topic>Adult</topic><topic>Clostridioides difficile - physiology</topic><topic>Clostridium Infections - complications</topic><topic>Clostridium Infections - epidemiology</topic><topic>Cohort Studies</topic><topic>Diarrhea - epidemiology</topic><topic>Diarrhea - microbiology</topic><topic>Female</topic><topic>Humans</topic><topic>Incidence</topic><topic>Irritable Bowel Syndrome - epidemiology</topic><topic>Irritable Bowel Syndrome - microbiology</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wadhwa, A.</creatorcontrib><creatorcontrib>Al Nahhas, M. F.</creatorcontrib><creatorcontrib>Dierkhising, R. A.</creatorcontrib><creatorcontrib>Patel, R.</creatorcontrib><creatorcontrib>Kashyap, P.</creatorcontrib><creatorcontrib>Pardi, D. S.</creatorcontrib><creatorcontrib>Khanna, S.</creatorcontrib><creatorcontrib>Grover, M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wadhwa, A.</au><au>Al Nahhas, M. F.</au><au>Dierkhising, R. A.</au><au>Patel, R.</au><au>Kashyap, P.</au><au>Pardi, D. S.</au><au>Khanna, S.</au><au>Grover, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High risk of post‐infectious irritable bowel syndrome in patients with Clostridium difficile infection</atitle><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle><addtitle>Aliment Pharmacol Ther</addtitle><date>2016-09</date><risdate>2016</risdate><volume>44</volume><issue>6</issue><spage>576</spage><epage>582</epage><pages>576-582</pages><issn>0269-2813</issn><eissn>1365-2036</eissn><abstract>Summary Background Infectious enteritis is a commonly identified risk factor for irritable bowel syndrome (IBS). The incidence of Clostridium difficile infection (CDI) is on the rise. However, there is limited information on post‐infectious IBS (PI‐IBS) development following CDI and the host‐ and infection‐related risk factors are not known. Aim To determine the incidence and risk factors for PI‐IBS following CDI. Methods A total of 684 cases of CDI identified from September 2012 to November 2013 were surveyed. Participants completed the Rome III IBS questionnaire and details on the CDI episode. Predictive modelling was done using logistic regression to evaluate risk factors for PI‐IBS development. Results A total of 315 CDI cases responded (46% response rate) and 205 were at‐risk (no pre‐CDI IBS) for PI‐IBS development. A total of 52/205 (25%) met the Rome III criteria for IBS ≥6 months following CDI. IBS‐mixed was most common followed by IBS‐diarrhoea. In comparison to those without subsequent PI‐IBS, greater percentage of PI‐IBS patients had CDI symptoms &gt;7 days, nausea, vomiting, abdominal pain during CDI, anxiety and a higher BMI. Using logistic regression, CDI symptoms &gt;7 days [Odds ratio (OR): 2.96, P = 0.01], current anxiety (OR: 1.33, P &lt; 0.0001) and a higher BMI (OR: 1.08, P = 0.004) were independently associated with PI‐IBS development; blood in the stool during CDI was protective (OR: 0.44, P = 0.06). Conclusions In this cohort study, new‐onset IBS is common after CDI. Longer CDI duration, current anxiety and higher BMI are associated with the diagnosis of C. difficile PI‐IBS. This chronic sequela should be considered during active management and follow‐up of patients with CDI.</abstract><cop>England</cop><pmid>27444134</pmid><doi>10.1111/apt.13737</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Abdominal Pain - complications
Abdominal Pain - epidemiology
Abdominal Pain - microbiology
Adult
Clostridioides difficile - physiology
Clostridium Infections - complications
Clostridium Infections - epidemiology
Cohort Studies
Diarrhea - epidemiology
Diarrhea - microbiology
Female
Humans
Incidence
Irritable Bowel Syndrome - epidemiology
Irritable Bowel Syndrome - microbiology
Logistic Models
Male
Middle Aged
Risk Factors
title High risk of post‐infectious irritable bowel syndrome in patients with Clostridium difficile infection
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