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Bezlotoxumab for Prevention of Recurrent Clostridium difficile Infection in Patients at Increased Risk for Recurrence
by
Gerding, Dale N
, Kumar, Princy N
, Guris, Dalya
, Rahav, Galia
, Dubberke, Erik R
, Ellison, Misoo C
, Yacyshyn, Bruce
, Kao, Dina
, Eves, Karen
, Dorr, Mary Beth
, Hanson, Mary E
, Kelly, Ciaran P
, Lee, Christine
in
and Commentaries
2018
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Bezlotoxumab for Prevention of Recurrent Clostridium difficile Infection in Patients at Increased Risk for Recurrence
by
Gerding, Dale N
, Kumar, Princy N
, Guris, Dalya
, Rahav, Galia
, Dubberke, Erik R
, Ellison, Misoo C
, Yacyshyn, Bruce
, Kao, Dina
, Eves, Karen
, Dorr, Mary Beth
, Hanson, Mary E
, Kelly, Ciaran P
, Lee, Christine
in
and Commentaries
2018
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Do you wish to request the book?
Bezlotoxumab for Prevention of Recurrent Clostridium difficile Infection in Patients at Increased Risk for Recurrence
by
Gerding, Dale N
, Kumar, Princy N
, Guris, Dalya
, Rahav, Galia
, Dubberke, Erik R
, Ellison, Misoo C
, Yacyshyn, Bruce
, Kao, Dina
, Eves, Karen
, Dorr, Mary Beth
, Hanson, Mary E
, Kelly, Ciaran P
, Lee, Christine
in
and Commentaries
2018
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Bezlotoxumab for Prevention of Recurrent Clostridium difficile Infection in Patients at Increased Risk for Recurrence
Journal Article
Bezlotoxumab for Prevention of Recurrent Clostridium difficile Infection in Patients at Increased Risk for Recurrence
2018
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Overview
Abstract
Background
Bezlotoxumab is a human monoclonal antibody against Clostridium difficile toxin B indicated to prevent C. difficile infection (CDI) recurrence (rCDI) in adults at high risk for rCDI. This post hoc analysis of pooled monocolonal antibodies for C.difficile therapy (MODIFY) I/II data assessed bezlotoxumab efficacy in participants with characteristics associated with increased risk for rCDI.
Methods
The analysis population was the modified intent-to-treat population who received bezlotoxumab or placebo (n = 1554) by risk factors for rCDI that were prespecified in the statistical analysis plan: age ≥65 years, history of CDI, compromised immunity, severe CDI, and ribotype 027/078/244. The proportion of participants with rCDI in 12 weeks, fecal microbiota transplant procedures, 30-day all cause and CDI-associated hospital readmissions, and mortality at 30 and 90 days after randomization were presented.
Results
The majority of enrolled participants (75.6%) had ≥1 risk factor; these participants were older and a higher proportion had comorbidities compared with participants with no risk factors. The proportion of placebo participants who experienced rCDI exceeded 30% for each risk factor compared with 20.9% among those without a risk factor, and the rCDI rate increased with the number of risk factors (1 risk factor: 31.3%; ≥3 risk factors: 46.1%). Bezlotoxumab reduced rCDI, fecal microbiota transplants, and CDI-associated 30-day readmissions in participants with risk factors for rCDI.
Conclusions
The risk factors prespecified in the MODIFY statistical analysis plan are appropriate to identify patients at high risk for rCDI. While participants with ≥3 risk factors had the greatest reduction of rCDI with bezlotoxumab, those with 1 or 2 risk factors may also benefit.
Clinical Trials Registration
NCT01241552 (MODIFY I) and NCT01513239 (MODIFY II).
Subgroup analyses from MODIFY confirmed that prior Clostridium difficile infection (CDI), age ≥65 years, infection with 027/078/244 strain, compromised immunity, and severe CDI are risk factors for recurrent CDI. Bezlotoxumab reduced CDI recurrence in participants with ≥1 risk factor compared with placebo.
Publisher
Oxford University Press
Subject
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