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Antipseudomonal Drug Exposure Associated with MDR Organisms in the Liver and Lung Transplant Population

BACKGROUND: Multi-drug resistant (MDR) Gram-negative bacteria (GNB) are an emerging complication in transplant recipients. This study describes the prevalence of and risk factors for MDR-GNB infection/colonization in the liver and lung transplant population. METHODS: Cross-sectional study with neste...

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Autores principales: Mulugeta, Surafel G, Veve, Michael P, Jantz, Arin S, Lanfranco, Odaliz Abreu, Davis, Susan L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631527/
http://dx.doi.org/10.1093/ofid/ofx163.1269
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author Mulugeta, Surafel G
Veve, Michael P
Jantz, Arin S
Lanfranco, Odaliz Abreu
Davis, Susan L
author_facet Mulugeta, Surafel G
Veve, Michael P
Jantz, Arin S
Lanfranco, Odaliz Abreu
Davis, Susan L
author_sort Mulugeta, Surafel G
collection PubMed
description BACKGROUND: Multi-drug resistant (MDR) Gram-negative bacteria (GNB) are an emerging complication in transplant recipients. This study describes the prevalence of and risk factors for MDR-GNB infection/colonization in the liver and lung transplant population. METHODS: Cross-sectional study with nested case-case–control included adult liver or lung transplant candidates/recipients from 1/10-7/16. Patients with a positive GNB culture were classified as MDR- or Susceptible (S)-cases; MDR was defined as in vitro resistance to ≥ 3 antibiotic classes. Patients without a positive GNB culture were controls. Primary variable of interest: antibiotic days of therapy (DOT) during time at risk. Patient and isolate characteristics were collected and compared. RESULTS: We included 150 patients: 110 (73%) liver, 40 (27%) lung. Median (IQR) patient age and Charlson comorbidity index were 59 years (52–63) and 5 points (3–6). Isolated organisms: 31 (34%) E. coli, 28 (31%) K. pneumoniae, 33 (36%) others. Resistance to cefepime, piperacillin/tazobactam, and ertapenem: 38%, 27%, and 14%. 61 (41%) MDR-GNB, 21 (14%) S-GNB, 68 (45%) controls. Median (IQR) cumulative antibiotic DOT was: MDR-case – 24.5 days (6–46.5), S-case – 5 days (2–24, P = 0.017 vs. MDR), controls – 0 days (0–10, P < 0.001 vs. MDR). Median (IQR) antipseudomonal (AP) DOT was: MDR-case – 7 days (1–16), S-case – 1 day (0–8, P = 0.055 vs. MDR), controls – 0 days (0–1, P < 0.001 vs. MDR); AP exposure was independently associated with MDR-GNB infection/colonization after correcting for severity of disease pre-transplant (adjOR: 2.9, 95% CI: 1.6–5.3) (Table 1). CONCLUSION: MDR-GNB represent a significant burden to the liver and lung transplant population. A detailed antibiotic history, including AP DOT, may help with risk assessment to guide empiric therapy selection. DISCLOSURES: S. L. Davis, Allergan: Grant Investigator and Scientific Advisor, Consulting fee and Research grant; Merck: Grant Investigator and Scientific Advisor, Consulting fee and Research grant
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spelling pubmed-56315272017-11-07 Antipseudomonal Drug Exposure Associated with MDR Organisms in the Liver and Lung Transplant Population Mulugeta, Surafel G Veve, Michael P Jantz, Arin S Lanfranco, Odaliz Abreu Davis, Susan L Open Forum Infect Dis Abstracts BACKGROUND: Multi-drug resistant (MDR) Gram-negative bacteria (GNB) are an emerging complication in transplant recipients. This study describes the prevalence of and risk factors for MDR-GNB infection/colonization in the liver and lung transplant population. METHODS: Cross-sectional study with nested case-case–control included adult liver or lung transplant candidates/recipients from 1/10-7/16. Patients with a positive GNB culture were classified as MDR- or Susceptible (S)-cases; MDR was defined as in vitro resistance to ≥ 3 antibiotic classes. Patients without a positive GNB culture were controls. Primary variable of interest: antibiotic days of therapy (DOT) during time at risk. Patient and isolate characteristics were collected and compared. RESULTS: We included 150 patients: 110 (73%) liver, 40 (27%) lung. Median (IQR) patient age and Charlson comorbidity index were 59 years (52–63) and 5 points (3–6). Isolated organisms: 31 (34%) E. coli, 28 (31%) K. pneumoniae, 33 (36%) others. Resistance to cefepime, piperacillin/tazobactam, and ertapenem: 38%, 27%, and 14%. 61 (41%) MDR-GNB, 21 (14%) S-GNB, 68 (45%) controls. Median (IQR) cumulative antibiotic DOT was: MDR-case – 24.5 days (6–46.5), S-case – 5 days (2–24, P = 0.017 vs. MDR), controls – 0 days (0–10, P < 0.001 vs. MDR). Median (IQR) antipseudomonal (AP) DOT was: MDR-case – 7 days (1–16), S-case – 1 day (0–8, P = 0.055 vs. MDR), controls – 0 days (0–1, P < 0.001 vs. MDR); AP exposure was independently associated with MDR-GNB infection/colonization after correcting for severity of disease pre-transplant (adjOR: 2.9, 95% CI: 1.6–5.3) (Table 1). CONCLUSION: MDR-GNB represent a significant burden to the liver and lung transplant population. A detailed antibiotic history, including AP DOT, may help with risk assessment to guide empiric therapy selection. DISCLOSURES: S. L. Davis, Allergan: Grant Investigator and Scientific Advisor, Consulting fee and Research grant; Merck: Grant Investigator and Scientific Advisor, Consulting fee and Research grant Oxford University Press 2017-10-04 /pmc/articles/PMC5631527/ http://dx.doi.org/10.1093/ofid/ofx163.1269 Text en © The Author 2017. 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
Mulugeta, Surafel G
Veve, Michael P
Jantz, Arin S
Lanfranco, Odaliz Abreu
Davis, Susan L
Antipseudomonal Drug Exposure Associated with MDR Organisms in the Liver and Lung Transplant Population
title Antipseudomonal Drug Exposure Associated with MDR Organisms in the Liver and Lung Transplant Population
title_full Antipseudomonal Drug Exposure Associated with MDR Organisms in the Liver and Lung Transplant Population
title_fullStr Antipseudomonal Drug Exposure Associated with MDR Organisms in the Liver and Lung Transplant Population
title_full_unstemmed Antipseudomonal Drug Exposure Associated with MDR Organisms in the Liver and Lung Transplant Population
title_short Antipseudomonal Drug Exposure Associated with MDR Organisms in the Liver and Lung Transplant Population
title_sort antipseudomonal drug exposure associated with mdr organisms in the liver and lung transplant population
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631527/
http://dx.doi.org/10.1093/ofid/ofx163.1269
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