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1602. Clostridium difficile Infection as a Predictor of Acute Graft vs. Host Disease Among Allogenic Stem Cell Transplant Recipients

BACKGROUND: Clostridium difficile infection (CDI) is a major cause of infectious diarrhea especially among allogenic stem cell transplant (SCT) recipients. The relationship between CDI and acute Graft vs. Host Disease (aGvHD) has been a topic of great interest for some time, as either of the two con...

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Autores principales: Jabr, Ra’Ed, Shune, Leyla, Atrouni, Wissam El, Telfah, Mohammad, Gao, Guangyi, He, Jianghua, Clough, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253480/
http://dx.doi.org/10.1093/ofid/ofy210.1430
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author Jabr, Ra’Ed
Shune, Leyla
Atrouni, Wissam El
Telfah, Mohammad
Gao, Guangyi
He, Jianghua
Clough, Lisa
author_facet Jabr, Ra’Ed
Shune, Leyla
Atrouni, Wissam El
Telfah, Mohammad
Gao, Guangyi
He, Jianghua
Clough, Lisa
author_sort Jabr, Ra’Ed
collection PubMed
description BACKGROUND: Clostridium difficile infection (CDI) is a major cause of infectious diarrhea especially among allogenic stem cell transplant (SCT) recipients. The relationship between CDI and acute Graft vs. Host Disease (aGvHD) has been a topic of great interest for some time, as either of the two conditions may affect the other. We studied the temporal relation of CDI on aGvHD in the first 100 days posttransplant in a large cohort of allogeneic SCT recipients. METHODS: We conducted an analysis of retrospective data extracted from the medical records of adult patients (more than 18 years of age) who underwent their first allogenic SCT between January 1, 2010 and December 30, 2016 at the University of Kansas Health System. Patients were followed for CDI events between day −10 to day +100 of allogenic transplant. Diagnosis and staging of aGvHD were determined based on standardized aGvHD grading scale utilizing clinical and pathological information between day 0 and day +100. Analysis included descriptive statistics, multivariable logistic regression, and survival analysis with CDI as a time-dependent variable. RESULTS: A total of 656 allogenic SCT recipients were included in the analysis. Of the total sample, 419 (64%) developed aGvHD within the first 100 days. CDI was observed in 112 (17%) of all allogenic SCT recipients, 72 (64%) of CDI cases developed prior to the onset of aGvHD. Fidaxomicin was used in the treatment of 57 (50%), whereas, vancomycin was used in 53 (47%) of CDI cases. On unadjusted analysis, CDI was associated with aGvHD (P = 0.0036), high grade aGvHD (P = 0.0132), and GI aGvHD (P = 0.0003). On multivariate survival analysis, the following predictors were associated with aGvHD: CDI (adjusted Hazard Ratio (aHR) = 1.44, P = 0.0047), matched unrelated donor vs. matched related donor transplant type (aHR = 1.40, P = 0.0023), myeloablative vs. reduced intensity conditioning (aHR = 1.87, P < 0.0001). This was consistent with the stepwise logistic regression model. CONCLUSION: Allogenic SCT recipients with CDI have a higher risk of aGvHD compared with those without CDI. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62534802018-11-28 1602. Clostridium difficile Infection as a Predictor of Acute Graft vs. Host Disease Among Allogenic Stem Cell Transplant Recipients Jabr, Ra’Ed Shune, Leyla Atrouni, Wissam El Telfah, Mohammad Gao, Guangyi He, Jianghua Clough, Lisa Open Forum Infect Dis Abstracts BACKGROUND: Clostridium difficile infection (CDI) is a major cause of infectious diarrhea especially among allogenic stem cell transplant (SCT) recipients. The relationship between CDI and acute Graft vs. Host Disease (aGvHD) has been a topic of great interest for some time, as either of the two conditions may affect the other. We studied the temporal relation of CDI on aGvHD in the first 100 days posttransplant in a large cohort of allogeneic SCT recipients. METHODS: We conducted an analysis of retrospective data extracted from the medical records of adult patients (more than 18 years of age) who underwent their first allogenic SCT between January 1, 2010 and December 30, 2016 at the University of Kansas Health System. Patients were followed for CDI events between day −10 to day +100 of allogenic transplant. Diagnosis and staging of aGvHD were determined based on standardized aGvHD grading scale utilizing clinical and pathological information between day 0 and day +100. Analysis included descriptive statistics, multivariable logistic regression, and survival analysis with CDI as a time-dependent variable. RESULTS: A total of 656 allogenic SCT recipients were included in the analysis. Of the total sample, 419 (64%) developed aGvHD within the first 100 days. CDI was observed in 112 (17%) of all allogenic SCT recipients, 72 (64%) of CDI cases developed prior to the onset of aGvHD. Fidaxomicin was used in the treatment of 57 (50%), whereas, vancomycin was used in 53 (47%) of CDI cases. On unadjusted analysis, CDI was associated with aGvHD (P = 0.0036), high grade aGvHD (P = 0.0132), and GI aGvHD (P = 0.0003). On multivariate survival analysis, the following predictors were associated with aGvHD: CDI (adjusted Hazard Ratio (aHR) = 1.44, P = 0.0047), matched unrelated donor vs. matched related donor transplant type (aHR = 1.40, P = 0.0023), myeloablative vs. reduced intensity conditioning (aHR = 1.87, P < 0.0001). This was consistent with the stepwise logistic regression model. CONCLUSION: Allogenic SCT recipients with CDI have a higher risk of aGvHD compared with those without CDI. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6253480/ http://dx.doi.org/10.1093/ofid/ofy210.1430 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Jabr, Ra’Ed
Shune, Leyla
Atrouni, Wissam El
Telfah, Mohammad
Gao, Guangyi
He, Jianghua
Clough, Lisa
1602. Clostridium difficile Infection as a Predictor of Acute Graft vs. Host Disease Among Allogenic Stem Cell Transplant Recipients
title 1602. Clostridium difficile Infection as a Predictor of Acute Graft vs. Host Disease Among Allogenic Stem Cell Transplant Recipients
title_full 1602. Clostridium difficile Infection as a Predictor of Acute Graft vs. Host Disease Among Allogenic Stem Cell Transplant Recipients
title_fullStr 1602. Clostridium difficile Infection as a Predictor of Acute Graft vs. Host Disease Among Allogenic Stem Cell Transplant Recipients
title_full_unstemmed 1602. Clostridium difficile Infection as a Predictor of Acute Graft vs. Host Disease Among Allogenic Stem Cell Transplant Recipients
title_short 1602. Clostridium difficile Infection as a Predictor of Acute Graft vs. Host Disease Among Allogenic Stem Cell Transplant Recipients
title_sort 1602. clostridium difficile infection as a predictor of acute graft vs. host disease among allogenic stem cell transplant recipients
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253480/
http://dx.doi.org/10.1093/ofid/ofy210.1430
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