Does Doxycycline Protect Against Development of Clostridium difficile Infection?
Background. Receipt of antibiotics is a major risk factor for Clostridium difficile infection (CDI). Doxycycline has been associated with a lower risk for CDI than other antibiotics. We investigated whether doxycycline protected against development of CDI in hospitalized patients receiving ceftriaxo...
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description | Background. Receipt of antibiotics is a major risk factor for Clostridium difficile infection (CDI). Doxycycline has been associated with a lower risk for CDI than other antibiotics. We investigated whether doxycycline protected against development of CDI in hospitalized patients receiving ceftriaxone, a high-risk antibiotic for CDI. Methods. We studied adults admitted to an academic county hospital between 1 June 2005 and 31 December 2010 who received ceftriaxone to determine whether the additional receipt of doxycycline decreased the risk of CDI. Patients were followed from first administration of ceftriaxone to occurrence of CDI or administrative closure 30 days later. Results. Two thousand three hundred five unique patients comprising 2734 hospitalizations were studied. Overall, 43 patients developed CDI within 30 days of ceftriaxone receipt, an incidence of 5.60 cases per 10 000 patient-days. The incidence of CDI was 1.67 cases per 10 000 patient-days in those receiving doxycycline, compared to 8.11 per 10 000 patient-days in those who did not receive doxycycline. In a multivariable model adjusted for age, gender, race, comorbidities, hospital duration, pneumonia diagnosis, surgical admission, and duration of ceftriaxone and other antibiotics, for each day of doxycycline receipt the rate of CDI was 27% lower than a patient who did not receive doxycycline (hazard ratio, 0.73; 95% confidence interval, .56–.96). Conclusions. In this cohort of patients receiving ceftriaxone, doxycycline was associated with lower risk of CDI. Guidelines recommend this combination as a second-line regimen for some patients with community-acquired pneumonia (CAP). Further clinical studies would help define whether doxycycline-containing regimens should be a preferred therapy for CAP. |
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Receipt of antibiotics is a major risk factor for Clostridium difficile infection (CDI). Doxycycline has been associated with a lower risk for CDI than other antibiotics. We investigated whether doxycycline protected against development of CDI in hospitalized patients receiving ceftriaxone, a high-risk antibiotic for CDI. Methods. We studied adults admitted to an academic county hospital between 1 June 2005 and 31 December 2010 who received ceftriaxone to determine whether the additional receipt of doxycycline decreased the risk of CDI. Patients were followed from first administration of ceftriaxone to occurrence of CDI or administrative closure 30 days later. Results. Two thousand three hundred five unique patients comprising 2734 hospitalizations were studied. Overall, 43 patients developed CDI within 30 days of ceftriaxone receipt, an incidence of 5.60 cases per 10 000 patient-days. The incidence of CDI was 1.67 cases per 10 000 patient-days in those receiving doxycycline, compared to 8.11 per 10 000 patient-days in those who did not receive doxycycline. In a multivariable model adjusted for age, gender, race, comorbidities, hospital duration, pneumonia diagnosis, surgical admission, and duration of ceftriaxone and other antibiotics, for each day of doxycycline receipt the rate of CDI was 27% lower than a patient who did not receive doxycycline (hazard ratio, 0.73; 95% confidence interval, .56–.96). Conclusions. In this cohort of patients receiving ceftriaxone, doxycycline was associated with lower risk of CDI. Guidelines recommend this combination as a second-line regimen for some patients with community-acquired pneumonia (CAP). Further clinical studies would help define whether doxycycline-containing regimens should be a preferred therapy for CAP.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/cis457</identifier><identifier>PMID: 22563022</identifier><identifier>CODEN: CIDIEL</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Aged ; and Commentaries ; Anti-Bacterial Agents - therapeutic use ; Antibacterial agents ; Antibiotic Prophylaxis ; Antibiotics ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; ARTICLES AND COMMENTARIES ; Bacterial diseases ; Bacterial diseases of the digestive system and abdomen ; Biological and medical sciences ; Ceftriaxone - therapeutic use ; Clostridium ; Clostridium difficile ; Clostridium difficile - isolation & purification ; Cohort Studies ; Comorbidity ; Diarrhea ; Doxycycline - therapeutic use ; Enterocolitis, Pseudomembranous - drug therapy ; Enterocolitis, Pseudomembranous - microbiology ; Enterocolitis, Pseudomembranous - prevention & control ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Gram-positive bacteria ; Hospital admissions ; Hospitalization ; Human bacterial diseases ; Humans ; Infections ; Infectious diseases ; Male ; Medical sciences ; Middle Aged ; Mortality ; Other diseases. Semiology ; Pharmacology. Drug treatments ; Pneumonia ; Proportional Hazards Models ; Risk factors ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><ispartof>Clinical infectious diseases, 2012-09, Vol.55 (5), p.615-620</ispartof><rights>Copyright © 2012 Oxford University Press on behalf of the Infectious Diseases Society of America</rights><rights>2015 INIST-CNRS</rights><rights>Copyright University of Chicago, acting through its Press Sep 1, 2012</rights><rights>The Author 2012. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-bc245eaef512ad160f263a5332f7be59229df0c2f2e32ddc469ffad20bbf32593</citedby><cites>FETCH-LOGICAL-c458t-bc245eaef512ad160f263a5332f7be59229df0c2f2e32ddc469ffad20bbf32593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/23269463$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/23269463$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,881,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26280232$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22563022$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Doernberg, Sarah B.</creatorcontrib><creatorcontrib>Winston, Lisa G.</creatorcontrib><creatorcontrib>Deck, Daniel H.</creatorcontrib><creatorcontrib>Chambers, Henry F.</creatorcontrib><title>Does Doxycycline Protect Against Development of Clostridium difficile Infection?</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Background. Receipt of antibiotics is a major risk factor for Clostridium difficile infection (CDI). Doxycycline has been associated with a lower risk for CDI than other antibiotics. We investigated whether doxycycline protected against development of CDI in hospitalized patients receiving ceftriaxone, a high-risk antibiotic for CDI. Methods. We studied adults admitted to an academic county hospital between 1 June 2005 and 31 December 2010 who received ceftriaxone to determine whether the additional receipt of doxycycline decreased the risk of CDI. Patients were followed from first administration of ceftriaxone to occurrence of CDI or administrative closure 30 days later. Results. Two thousand three hundred five unique patients comprising 2734 hospitalizations were studied. Overall, 43 patients developed CDI within 30 days of ceftriaxone receipt, an incidence of 5.60 cases per 10 000 patient-days. The incidence of CDI was 1.67 cases per 10 000 patient-days in those receiving doxycycline, compared to 8.11 per 10 000 patient-days in those who did not receive doxycycline. In a multivariable model adjusted for age, gender, race, comorbidities, hospital duration, pneumonia diagnosis, surgical admission, and duration of ceftriaxone and other antibiotics, for each day of doxycycline receipt the rate of CDI was 27% lower than a patient who did not receive doxycycline (hazard ratio, 0.73; 95% confidence interval, .56–.96). Conclusions. In this cohort of patients receiving ceftriaxone, doxycycline was associated with lower risk of CDI. Guidelines recommend this combination as a second-line regimen for some patients with community-acquired pneumonia (CAP). Further clinical studies would help define whether doxycycline-containing regimens should be a preferred therapy for CAP.</description><subject>Adult</subject><subject>Aged</subject><subject>and Commentaries</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Antibacterial agents</subject><subject>Antibiotic Prophylaxis</subject><subject>Antibiotics</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>ARTICLES AND COMMENTARIES</subject><subject>Bacterial diseases</subject><subject>Bacterial diseases of the digestive system and abdomen</subject><subject>Biological and medical sciences</subject><subject>Ceftriaxone - therapeutic use</subject><subject>Clostridium</subject><subject>Clostridium difficile</subject><subject>Clostridium difficile - isolation & purification</subject><subject>Cohort Studies</subject><subject>Comorbidity</subject><subject>Diarrhea</subject><subject>Doxycycline - therapeutic use</subject><subject>Enterocolitis, Pseudomembranous - drug therapy</subject><subject>Enterocolitis, Pseudomembranous - microbiology</subject><subject>Enterocolitis, Pseudomembranous - prevention & control</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gram-positive bacteria</subject><subject>Hospital admissions</subject><subject>Hospitalization</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Other diseases. Semiology</subject><subject>Pharmacology. Drug treatments</subject><subject>Pneumonia</subject><subject>Proportional Hazards Models</subject><subject>Risk factors</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0c9rFDEUB_Agiv2hF-_KgBREGJu8TDKZi1J2tRYK9lDPIZMfNctMsk1mivvfmzJrqz2EBN7nPV74IvSG4E8Ed_RUe1NOblj7DB0SRtuas448L2_MRN0IKg7QUc4bjAkRmL1EBwCMUwxwiK7W0eZqHX_v9E4PPtjqKsXJ6qk6u1E-5Kla2zs7xO1ow1RFV62GmKfkjZ_HynjnvPaDrS6CKz0-hi-v0Aunhmxf7-9j9PPb1-vV9_ryx_nF6uyy1g0TU91raJhV1jECyhCOHXCqGKXg2t6yDqAzDmtwYCkYoxveOacM4L53FFhHj9HnZe527kdrdFkvqUFukx9V2smovPy_EvwveRPvJG06IhgpAz7sB6R4O9s8ydFnbYdBBRvnLAmm0NJGCCj0_RO6iXMK5XuLagXHbVEfF6VTzDlZ97AMwfI-KFmCkktQBb_7d_0H-jeZAk72QGWtBpdUKK2PjoPAQO_d28Vt8hTTY50C7xpO6R8v-6cV</recordid><startdate>20120901</startdate><enddate>20120901</enddate><creator>Doernberg, Sarah B.</creator><creator>Winston, Lisa G.</creator><creator>Deck, Daniel H.</creator><creator>Chambers, Henry F.</creator><general>Oxford University Press</general><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>7T2</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120901</creationdate><title>Does Doxycycline Protect Against Development of Clostridium difficile Infection?</title><author>Doernberg, Sarah B. ; Winston, Lisa G. ; Deck, Daniel H. ; Chambers, Henry F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-bc245eaef512ad160f263a5332f7be59229df0c2f2e32ddc469ffad20bbf32593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Aged</topic><topic>and Commentaries</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Antibacterial agents</topic><topic>Antibiotic Prophylaxis</topic><topic>Antibiotics</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>ARTICLES AND COMMENTARIES</topic><topic>Bacterial diseases</topic><topic>Bacterial diseases of the digestive system and abdomen</topic><topic>Biological and medical sciences</topic><topic>Ceftriaxone - therapeutic use</topic><topic>Clostridium</topic><topic>Clostridium difficile</topic><topic>Clostridium difficile - isolation & purification</topic><topic>Cohort Studies</topic><topic>Comorbidity</topic><topic>Diarrhea</topic><topic>Doxycycline - therapeutic use</topic><topic>Enterocolitis, Pseudomembranous - drug therapy</topic><topic>Enterocolitis, Pseudomembranous - microbiology</topic><topic>Enterocolitis, Pseudomembranous - prevention & control</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gram-positive bacteria</topic><topic>Hospital admissions</topic><topic>Hospitalization</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Other diseases. Semiology</topic><topic>Pharmacology. Drug treatments</topic><topic>Pneumonia</topic><topic>Proportional Hazards Models</topic><topic>Risk factors</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Doernberg, Sarah B.</creatorcontrib><creatorcontrib>Winston, Lisa G.</creatorcontrib><creatorcontrib>Deck, Daniel H.</creatorcontrib><creatorcontrib>Chambers, Henry F.</creatorcontrib><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>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Doernberg, Sarah B.</au><au>Winston, Lisa G.</au><au>Deck, Daniel H.</au><au>Chambers, Henry F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Does Doxycycline Protect Against Development of Clostridium difficile Infection?</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2012-09-01</date><risdate>2012</risdate><volume>55</volume><issue>5</issue><spage>615</spage><epage>620</epage><pages>615-620</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>Background. Receipt of antibiotics is a major risk factor for Clostridium difficile infection (CDI). Doxycycline has been associated with a lower risk for CDI than other antibiotics. We investigated whether doxycycline protected against development of CDI in hospitalized patients receiving ceftriaxone, a high-risk antibiotic for CDI. Methods. We studied adults admitted to an academic county hospital between 1 June 2005 and 31 December 2010 who received ceftriaxone to determine whether the additional receipt of doxycycline decreased the risk of CDI. Patients were followed from first administration of ceftriaxone to occurrence of CDI or administrative closure 30 days later. Results. Two thousand three hundred five unique patients comprising 2734 hospitalizations were studied. Overall, 43 patients developed CDI within 30 days of ceftriaxone receipt, an incidence of 5.60 cases per 10 000 patient-days. The incidence of CDI was 1.67 cases per 10 000 patient-days in those receiving doxycycline, compared to 8.11 per 10 000 patient-days in those who did not receive doxycycline. In a multivariable model adjusted for age, gender, race, comorbidities, hospital duration, pneumonia diagnosis, surgical admission, and duration of ceftriaxone and other antibiotics, for each day of doxycycline receipt the rate of CDI was 27% lower than a patient who did not receive doxycycline (hazard ratio, 0.73; 95% confidence interval, .56–.96). Conclusions. In this cohort of patients receiving ceftriaxone, doxycycline was associated with lower risk of CDI. Guidelines recommend this combination as a second-line regimen for some patients with community-acquired pneumonia (CAP). Further clinical studies would help define whether doxycycline-containing regimens should be a preferred therapy for CAP.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>22563022</pmid><doi>10.1093/cid/cis457</doi><tpages>6</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; Alma/SFX Local Collection |
subjects | Adult Aged and Commentaries Anti-Bacterial Agents - therapeutic use Antibacterial agents Antibiotic Prophylaxis Antibiotics Antibiotics. Antiinfectious agents. Antiparasitic agents ARTICLES AND COMMENTARIES Bacterial diseases Bacterial diseases of the digestive system and abdomen Biological and medical sciences Ceftriaxone - therapeutic use Clostridium Clostridium difficile Clostridium difficile - isolation & purification Cohort Studies Comorbidity Diarrhea Doxycycline - therapeutic use Enterocolitis, Pseudomembranous - drug therapy Enterocolitis, Pseudomembranous - microbiology Enterocolitis, Pseudomembranous - prevention & control Female Gastroenterology. Liver. Pancreas. Abdomen Gram-positive bacteria Hospital admissions Hospitalization Human bacterial diseases Humans Infections Infectious diseases Male Medical sciences Middle Aged Mortality Other diseases. Semiology Pharmacology. Drug treatments Pneumonia Proportional Hazards Models Risk factors Stomach. Duodenum. Small intestine. Colon. Rectum. Anus |
title | Does Doxycycline Protect Against Development of Clostridium difficile Infection? |
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