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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Veröffentlicht in:Clinical infectious diseases 2012-09, Vol.55 (5), p.615-620
Hauptverfasser: Doernberg, Sarah B., Winston, Lisa G., Deck, Daniel H., Chambers, Henry F.
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container_title Clinical infectious diseases
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creator Doernberg, Sarah B.
Winston, Lisa G.
Deck, Daniel H.
Chambers, Henry F.
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.
doi_str_mv 10.1093/cid/cis457
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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 &amp; purification ; Cohort Studies ; Comorbidity ; Diarrhea ; Doxycycline - therapeutic use ; Enterocolitis, Pseudomembranous - drug therapy ; Enterocolitis, Pseudomembranous - microbiology ; Enterocolitis, Pseudomembranous - prevention &amp; 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. 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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). 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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. 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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.</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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identifier ISSN: 1058-4838
ispartof Clinical infectious diseases, 2012-09, Vol.55 (5), p.615-620
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language eng
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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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