Management and Outcomes of a First Recurrence of Clostridium difficile-Associated Disease in Quebec, Canada

Background. During an epidemic of Clostridium difficile-associated disease (CDAD) caused by a strain that is a hyper-producer of toxins A and B, the frequency of a first recurrence after metronidazole treatment of the initial episode doubled in 2003–2004, compared with 1991–2002. Methods. To examine...

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Veröffentlicht in:Clinical infectious diseases 2006-03, Vol.42 (6), p.758-764
Hauptverfasser: Pépin, Jacques, Routhier, Sophie, Gagnon, Sandra, Brazeau, Isabel
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Routhier, Sophie
Gagnon, Sandra
Brazeau, Isabel
description Background. During an epidemic of Clostridium difficile-associated disease (CDAD) caused by a strain that is a hyper-producer of toxins A and B, the frequency of a first recurrence after metronidazole treatment of the initial episode doubled in 2003–2004, compared with 1991–2002. Methods. To examine whether administration of metronidazole as treatment for a first recurrence of CDAD remained appropriate, we reviewed data for patients with CDAD diagnosed in a hospital in Quebec, Canada, during 1991–2005, who experienced a first recurrence. The frequency of a second recurrence within 60 days after the first one was measured using Kaplan-Meier analysis. Cox regression was used for multivariate analysis. Results. A total of 463 patients had a first recurrence of CDAD, of whom 154 (33.3%) experienced a second recurrence. Independent predictors of a second recurrence were age and duration of hospitalization after the first recurrence; this latter finding suggested that many such episodes were reinfections rather than relapses. Neither choice of treatment drug (metronidazole or vancomycin) nor use of the same drug for treatment of first recurrence, as had been used during the initial episode, was associated with increased risk of a second recurrence. However, 51 patients (11.0%) developed at least 1 complication (i.e., shock, need for colectomy, megacolon, perforation, or death within 30 days) during the first recurrence. Older age, a high leukocyte count, and renal failure at first recurrence were strongly associated with a complicated CDAD. Conclusions. Metronidazole is not inferior to vancomycin for treatment of patients with a first recurrence of CDAD, but the risk of complications with any treatment of CDAD may be higher than has previously been documented.
doi_str_mv 10.1086/501126
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During an epidemic of Clostridium difficile-associated disease (CDAD) caused by a strain that is a hyper-producer of toxins A and B, the frequency of a first recurrence after metronidazole treatment of the initial episode doubled in 2003–2004, compared with 1991–2002. Methods. To examine whether administration of metronidazole as treatment for a first recurrence of CDAD remained appropriate, we reviewed data for patients with CDAD diagnosed in a hospital in Quebec, Canada, during 1991–2005, who experienced a first recurrence. The frequency of a second recurrence within 60 days after the first one was measured using Kaplan-Meier analysis. Cox regression was used for multivariate analysis. Results. A total of 463 patients had a first recurrence of CDAD, of whom 154 (33.3%) experienced a second recurrence. Independent predictors of a second recurrence were age and duration of hospitalization after the first recurrence; this latter finding suggested that many such episodes were reinfections rather than relapses. Neither choice of treatment drug (metronidazole or vancomycin) nor use of the same drug for treatment of first recurrence, as had been used during the initial episode, was associated with increased risk of a second recurrence. However, 51 patients (11.0%) developed at least 1 complication (i.e., shock, need for colectomy, megacolon, perforation, or death within 30 days) during the first recurrence. Older age, a high leukocyte count, and renal failure at first recurrence were strongly associated with a complicated CDAD. Conclusions. Metronidazole is not inferior to vancomycin for treatment of patients with a first recurrence of CDAD, but the risk of complications with any treatment of CDAD may be higher than has previously been documented.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1086/501126</identifier><identifier>PMID: 16477549</identifier><identifier>CODEN: CIDIEL</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>Adolescent ; Adult ; Age Factors ; Aged ; Aged, 80 and over ; Anti-Bacterial Agents - therapeutic use ; Articles and Commentaries ; Biological and medical sciences ; Child ; Child, Preschool ; Clostridium ; Clostridium difficile ; Clostridium difficile - isolation &amp; purification ; Clostridium difficile - pathogenicity ; Colitis ; Diarrhea ; Drug Therapy, Combination ; Enterocolitis, Pseudomembranous - drug therapy ; Enterocolitis, Pseudomembranous - epidemiology ; Epidemiology ; Female ; Humans ; Infant ; Infant, Newborn ; Infectious diseases ; Leukocytes ; Male ; Medical sciences ; Middle Aged ; Predisposing factors ; Quebec - epidemiology ; Recurrence ; Relapse ; Retrospective Studies ; Risk Factors ; Toxins ; Treatment Outcome</subject><ispartof>Clinical infectious diseases, 2006-03, Vol.42 (6), p.758-764</ispartof><rights>Copyright 2006 The Infectious Diseases Society of America</rights><rights>2006 by the Infectious Diseases Society of America 2006</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-374f64bde460661fd3d94f6d8a085dd71522c33b82be8869c13f3a839900d3d03</citedby><cites>FETCH-LOGICAL-c521t-374f64bde460661fd3d94f6d8a085dd71522c33b82be8869c13f3a839900d3d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4463709$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4463709$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17665011$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16477549$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pépin, Jacques</creatorcontrib><creatorcontrib>Routhier, Sophie</creatorcontrib><creatorcontrib>Gagnon, Sandra</creatorcontrib><creatorcontrib>Brazeau, Isabel</creatorcontrib><title>Management and Outcomes of a First Recurrence of Clostridium difficile-Associated Disease in Quebec, Canada</title><title>Clinical infectious diseases</title><addtitle>Clinical Infectious Diseases</addtitle><addtitle>Clinical Infectious Diseases</addtitle><description>Background. During an epidemic of Clostridium difficile-associated disease (CDAD) caused by a strain that is a hyper-producer of toxins A and B, the frequency of a first recurrence after metronidazole treatment of the initial episode doubled in 2003–2004, compared with 1991–2002. Methods. To examine whether administration of metronidazole as treatment for a first recurrence of CDAD remained appropriate, we reviewed data for patients with CDAD diagnosed in a hospital in Quebec, Canada, during 1991–2005, who experienced a first recurrence. The frequency of a second recurrence within 60 days after the first one was measured using Kaplan-Meier analysis. Cox regression was used for multivariate analysis. Results. A total of 463 patients had a first recurrence of CDAD, of whom 154 (33.3%) experienced a second recurrence. Independent predictors of a second recurrence were age and duration of hospitalization after the first recurrence; this latter finding suggested that many such episodes were reinfections rather than relapses. Neither choice of treatment drug (metronidazole or vancomycin) nor use of the same drug for treatment of first recurrence, as had been used during the initial episode, was associated with increased risk of a second recurrence. However, 51 patients (11.0%) developed at least 1 complication (i.e., shock, need for colectomy, megacolon, perforation, or death within 30 days) during the first recurrence. Older age, a high leukocyte count, and renal failure at first recurrence were strongly associated with a complicated CDAD. Conclusions. Metronidazole is not inferior to vancomycin for treatment of patients with a first recurrence of CDAD, but the risk of complications with any treatment of CDAD may be higher than has previously been documented.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Articles and Commentaries</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Clostridium</subject><subject>Clostridium difficile</subject><subject>Clostridium difficile - isolation &amp; purification</subject><subject>Clostridium difficile - pathogenicity</subject><subject>Colitis</subject><subject>Diarrhea</subject><subject>Drug Therapy, Combination</subject><subject>Enterocolitis, Pseudomembranous - drug therapy</subject><subject>Enterocolitis, Pseudomembranous - epidemiology</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Infectious diseases</subject><subject>Leukocytes</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Predisposing factors</subject><subject>Quebec - epidemiology</subject><subject>Recurrence</subject><subject>Relapse</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Toxins</subject><subject>Treatment Outcome</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0Etv1DAQB_AIgegD-AQImQOcCNjxI86xbOlD2lJAICEukWOPkds8Fo8jwbevV1l1TxUnWzM_zYz-RfGC0feMavVBUsYq9ag4ZJLXpZINe5z_VOpSaK4PiiPEG5qNpvJpccCUqGspmsPi9sqM5jcMMCZiRkeu52SnAZBMnhhyFiIm8g3sHCOMFrbVVT9hisGFeSAueB9s6KE8QZxsMAkcOQ0IBoGEkXydoQP7jqzyEmeeFU-86RGe797j4sfZp--ri3J9fX65OlmXVlYslbwWXonOgVBUKeYdd02uOG2ols7VTFaV5bzTVQdaq8Yy7rnRvGkozZby4-LtMncTpz8zYGqHgBb63owwzdiqWinKG_VfyOocqhDVHto4IUbw7SaGwcR_LaPtNv92yT_DV7uJczeA27Nd4Bm82QGD1vQ-mtEG3Lt82nZUdq8XN82bh5e9XMwNpineKyEUr-l2Vbm0Ayb4e9828TYnwGvZXvz81V41X9hafv7Yan4H4ritdw</recordid><startdate>20060315</startdate><enddate>20060315</enddate><creator>Pépin, Jacques</creator><creator>Routhier, Sophie</creator><creator>Gagnon, Sandra</creator><creator>Brazeau, Isabel</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><scope>BSCLL</scope><scope>IQODW</scope><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>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20060315</creationdate><title>Management and Outcomes of a First Recurrence of Clostridium difficile-Associated Disease in Quebec, Canada</title><author>Pépin, Jacques ; Routhier, Sophie ; Gagnon, Sandra ; Brazeau, Isabel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-374f64bde460661fd3d94f6d8a085dd71522c33b82be8869c13f3a839900d3d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Factors</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Articles and Commentaries</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Clostridium</topic><topic>Clostridium difficile</topic><topic>Clostridium difficile - isolation &amp; purification</topic><topic>Clostridium difficile - pathogenicity</topic><topic>Colitis</topic><topic>Diarrhea</topic><topic>Drug Therapy, Combination</topic><topic>Enterocolitis, Pseudomembranous - drug therapy</topic><topic>Enterocolitis, Pseudomembranous - epidemiology</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Infectious diseases</topic><topic>Leukocytes</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Predisposing factors</topic><topic>Quebec - epidemiology</topic><topic>Recurrence</topic><topic>Relapse</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Toxins</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pépin, Jacques</creatorcontrib><creatorcontrib>Routhier, Sophie</creatorcontrib><creatorcontrib>Gagnon, Sandra</creatorcontrib><creatorcontrib>Brazeau, Isabel</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pépin, Jacques</au><au>Routhier, Sophie</au><au>Gagnon, Sandra</au><au>Brazeau, Isabel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Management and Outcomes of a First Recurrence of Clostridium difficile-Associated Disease in Quebec, Canada</atitle><jtitle>Clinical infectious diseases</jtitle><stitle>Clinical Infectious Diseases</stitle><addtitle>Clinical Infectious Diseases</addtitle><date>2006-03-15</date><risdate>2006</risdate><volume>42</volume><issue>6</issue><spage>758</spage><epage>764</epage><pages>758-764</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>Background. During an epidemic of Clostridium difficile-associated disease (CDAD) caused by a strain that is a hyper-producer of toxins A and B, the frequency of a first recurrence after metronidazole treatment of the initial episode doubled in 2003–2004, compared with 1991–2002. Methods. To examine whether administration of metronidazole as treatment for a first recurrence of CDAD remained appropriate, we reviewed data for patients with CDAD diagnosed in a hospital in Quebec, Canada, during 1991–2005, who experienced a first recurrence. The frequency of a second recurrence within 60 days after the first one was measured using Kaplan-Meier analysis. Cox regression was used for multivariate analysis. Results. A total of 463 patients had a first recurrence of CDAD, of whom 154 (33.3%) experienced a second recurrence. Independent predictors of a second recurrence were age and duration of hospitalization after the first recurrence; this latter finding suggested that many such episodes were reinfections rather than relapses. Neither choice of treatment drug (metronidazole or vancomycin) nor use of the same drug for treatment of first recurrence, as had been used during the initial episode, was associated with increased risk of a second recurrence. However, 51 patients (11.0%) developed at least 1 complication (i.e., shock, need for colectomy, megacolon, perforation, or death within 30 days) during the first recurrence. Older age, a high leukocyte count, and renal failure at first recurrence were strongly associated with a complicated CDAD. Conclusions. Metronidazole is not inferior to vancomycin for treatment of patients with a first recurrence of CDAD, but the risk of complications with any treatment of CDAD may be higher than has previously been documented.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>16477549</pmid><doi>10.1086/501126</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source Jstor Complete Legacy; Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adolescent
Adult
Age Factors
Aged
Aged, 80 and over
Anti-Bacterial Agents - therapeutic use
Articles and Commentaries
Biological and medical sciences
Child
Child, Preschool
Clostridium
Clostridium difficile
Clostridium difficile - isolation & purification
Clostridium difficile - pathogenicity
Colitis
Diarrhea
Drug Therapy, Combination
Enterocolitis, Pseudomembranous - drug therapy
Enterocolitis, Pseudomembranous - epidemiology
Epidemiology
Female
Humans
Infant
Infant, Newborn
Infectious diseases
Leukocytes
Male
Medical sciences
Middle Aged
Predisposing factors
Quebec - epidemiology
Recurrence
Relapse
Retrospective Studies
Risk Factors
Toxins
Treatment Outcome
title Management and Outcomes of a First Recurrence of Clostridium difficile-Associated Disease in Quebec, Canada
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