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182. Piperacillin/tazobactam (P/T) versus meropenem (Mero) for treatment of extended-spectrum beta-lactamase (ESBL)-producing E.coli and K. pneumoniae bloodstream infections (BSIs)

BACKGROUND: A recent study of Mero vs. P/T for the treatment of BSIs caused by ceftriaxone-resistant Enterobacterales, including ESBL-producing organisms, revealed discouraging outcomes for patients (pts) receiving P/T. The purpose of this study is to evaluate clinical outcomes in pts treated with P...

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Autores principales: Cox, Alexandra L, Beardsley, James R, Williamson, John C, Stone, Tyler J, DeWitt, Michael E, Palavecino, Elizabeth, Luther, Vera, Taylor, Alex D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677261/
http://dx.doi.org/10.1093/ofid/ofad500.255
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author Cox, Alexandra L
Beardsley, James R
Williamson, John C
Stone, Tyler J
DeWitt, Michael E
Palavecino, Elizabeth
Luther, Vera
Taylor, Alex D
author_facet Cox, Alexandra L
Beardsley, James R
Williamson, John C
Stone, Tyler J
DeWitt, Michael E
Palavecino, Elizabeth
Luther, Vera
Taylor, Alex D
author_sort Cox, Alexandra L
collection PubMed
description BACKGROUND: A recent study of Mero vs. P/T for the treatment of BSIs caused by ceftriaxone-resistant Enterobacterales, including ESBL-producing organisms, revealed discouraging outcomes for patients (pts) receiving P/T. The purpose of this study is to evaluate clinical outcomes in pts treated with P/T versus Mero for BSIs caused by ESBL-producing E. coli or K. pneumoniae. METHODS: This is a single health-system, retrospective, observational study. Adult inpatients with blood cultures positive for ESBL-producing E. coli or K. pneumoniae during 2016-2020 were identified by a report from an automated broth microdilution system. Pts with an isolate susceptible to both P/T and Mero who received either P/T or Mero within 24 hours of culture collection and for a duration of least 48 hours were included. Pts who had neutropenia, expired or transitioned to comfort care within 48 hours of study drug initiation, did not have source control by day 5, had a polymicrobial infection, or had a concurrent infection caused by another gram-negative organism were excluded. Pts were screened for eligibility and then randomly selected until a target of 25 pts meeting study criteria in the Mero and the P/T groups were included. The primary outcome was all-cause mortality at 30 days. Secondary outcomes included length of hospital stay, clinical and microbiological resolution by day 5, and time to clinical and microbiological resolution. RESULTS: Forty-nine pts met study criteria and were included after one pt was excluded from P/T group due to a polymicrobial infection. Overall, the median age was 67 [53, 76], 29 (59%) pts were female, and 21 (43%) pts were admitted to an ICU at culture draw or within 24 hours. Forty-three of the 49 (88%) infections were caused by E.coli, and 38 (78%) infections originated from a urinary source. Results of the analysis are shown in table 1 and figures A-C. [Figure: see text] [Figure: see text] CONCLUSION: In this real-world study of pts with ESBL-producing BSIs that were predominantly from a urinary source, pts treated with P/T and Mero had similar outcomes. These results demonstrate the need for additional randomized, controlled trials, in a variety of settings to further assess outcomes in this pt population. DISCLOSURES: Tyler J. Stone, PharmD, ViiV Healthcare: Employee
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spelling pubmed-106772612023-11-27 182. Piperacillin/tazobactam (P/T) versus meropenem (Mero) for treatment of extended-spectrum beta-lactamase (ESBL)-producing E.coli and K. pneumoniae bloodstream infections (BSIs) Cox, Alexandra L Beardsley, James R Williamson, John C Stone, Tyler J DeWitt, Michael E Palavecino, Elizabeth Luther, Vera Taylor, Alex D Open Forum Infect Dis Abstract BACKGROUND: A recent study of Mero vs. P/T for the treatment of BSIs caused by ceftriaxone-resistant Enterobacterales, including ESBL-producing organisms, revealed discouraging outcomes for patients (pts) receiving P/T. The purpose of this study is to evaluate clinical outcomes in pts treated with P/T versus Mero for BSIs caused by ESBL-producing E. coli or K. pneumoniae. METHODS: This is a single health-system, retrospective, observational study. Adult inpatients with blood cultures positive for ESBL-producing E. coli or K. pneumoniae during 2016-2020 were identified by a report from an automated broth microdilution system. Pts with an isolate susceptible to both P/T and Mero who received either P/T or Mero within 24 hours of culture collection and for a duration of least 48 hours were included. Pts who had neutropenia, expired or transitioned to comfort care within 48 hours of study drug initiation, did not have source control by day 5, had a polymicrobial infection, or had a concurrent infection caused by another gram-negative organism were excluded. Pts were screened for eligibility and then randomly selected until a target of 25 pts meeting study criteria in the Mero and the P/T groups were included. The primary outcome was all-cause mortality at 30 days. Secondary outcomes included length of hospital stay, clinical and microbiological resolution by day 5, and time to clinical and microbiological resolution. RESULTS: Forty-nine pts met study criteria and were included after one pt was excluded from P/T group due to a polymicrobial infection. Overall, the median age was 67 [53, 76], 29 (59%) pts were female, and 21 (43%) pts were admitted to an ICU at culture draw or within 24 hours. Forty-three of the 49 (88%) infections were caused by E.coli, and 38 (78%) infections originated from a urinary source. Results of the analysis are shown in table 1 and figures A-C. [Figure: see text] [Figure: see text] CONCLUSION: In this real-world study of pts with ESBL-producing BSIs that were predominantly from a urinary source, pts treated with P/T and Mero had similar outcomes. These results demonstrate the need for additional randomized, controlled trials, in a variety of settings to further assess outcomes in this pt population. DISCLOSURES: Tyler J. Stone, PharmD, ViiV Healthcare: Employee Oxford University Press 2023-11-27 /pmc/articles/PMC10677261/ http://dx.doi.org/10.1093/ofid/ofad500.255 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Cox, Alexandra L
Beardsley, James R
Williamson, John C
Stone, Tyler J
DeWitt, Michael E
Palavecino, Elizabeth
Luther, Vera
Taylor, Alex D
182. Piperacillin/tazobactam (P/T) versus meropenem (Mero) for treatment of extended-spectrum beta-lactamase (ESBL)-producing E.coli and K. pneumoniae bloodstream infections (BSIs)
title 182. Piperacillin/tazobactam (P/T) versus meropenem (Mero) for treatment of extended-spectrum beta-lactamase (ESBL)-producing E.coli and K. pneumoniae bloodstream infections (BSIs)
title_full 182. Piperacillin/tazobactam (P/T) versus meropenem (Mero) for treatment of extended-spectrum beta-lactamase (ESBL)-producing E.coli and K. pneumoniae bloodstream infections (BSIs)
title_fullStr 182. Piperacillin/tazobactam (P/T) versus meropenem (Mero) for treatment of extended-spectrum beta-lactamase (ESBL)-producing E.coli and K. pneumoniae bloodstream infections (BSIs)
title_full_unstemmed 182. Piperacillin/tazobactam (P/T) versus meropenem (Mero) for treatment of extended-spectrum beta-lactamase (ESBL)-producing E.coli and K. pneumoniae bloodstream infections (BSIs)
title_short 182. Piperacillin/tazobactam (P/T) versus meropenem (Mero) for treatment of extended-spectrum beta-lactamase (ESBL)-producing E.coli and K. pneumoniae bloodstream infections (BSIs)
title_sort 182. piperacillin/tazobactam (p/t) versus meropenem (mero) for treatment of extended-spectrum beta-lactamase (esbl)-producing e.coli and k. pneumoniae bloodstream infections (bsis)
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677261/
http://dx.doi.org/10.1093/ofid/ofad500.255
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