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Clinical Impact of Ceftriaxone Resistance in Escherichia coli Bloodstream Infections: A Multicenter Prospective Cohort Study
BACKGROUND: Ceftriaxone-resistant (CRO-R) Escherichia coli bloodstream infections (BSIs) are common. METHODS: This is a prospective cohort of patients with E coli BSI at 14 United States hospitals between November 2020 and April 2021. For each patient with a CRO-R E coli BSI enrolled, the next conse...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645644/ https://www.ncbi.nlm.nih.gov/pubmed/36381622 http://dx.doi.org/10.1093/ofid/ofac572 |
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author | Tamma, Pranita D Komarow, Lauren Ge, Lizhao Garcia-Diaz, Julia Herc, Erica S Doi, Yohei Arias, Cesar A Albin, Owen Saade, Elie Miller, Loren G Jacob, Jesse T Satlin, Michael J Krsak, Martin Huskins, W Charles Dhar, Sorabh Shelburne, Samuel A Hill, Carol Baum, Keri R Bhojani, Minal Greenwood-Quaintance, Kerryl E Schmidt-Malan, Suzannah M Patel, Robin Evans, Scott R Chambers, Henry F Fowler, Vance G van Duin, David |
author_facet | Tamma, Pranita D Komarow, Lauren Ge, Lizhao Garcia-Diaz, Julia Herc, Erica S Doi, Yohei Arias, Cesar A Albin, Owen Saade, Elie Miller, Loren G Jacob, Jesse T Satlin, Michael J Krsak, Martin Huskins, W Charles Dhar, Sorabh Shelburne, Samuel A Hill, Carol Baum, Keri R Bhojani, Minal Greenwood-Quaintance, Kerryl E Schmidt-Malan, Suzannah M Patel, Robin Evans, Scott R Chambers, Henry F Fowler, Vance G van Duin, David |
author_sort | Tamma, Pranita D |
collection | PubMed |
description | BACKGROUND: Ceftriaxone-resistant (CRO-R) Escherichia coli bloodstream infections (BSIs) are common. METHODS: This is a prospective cohort of patients with E coli BSI at 14 United States hospitals between November 2020 and April 2021. For each patient with a CRO-R E coli BSI enrolled, the next consecutive patient with a ceftriaxone-susceptible (CRO-S) E coli BSI was included. Primary outcome was desirability of outcome ranking (DOOR) at day 30, with 50% probability of worse outcomes in the CRO-R group as the null hypothesis. Inverse probability weighting (IPW) was used to reduce confounding. RESULTS: Notable differences between patients infected with CRO-R and CRO-S E coli BSI included the proportion with Pitt bacteremia score ≥4 (23% vs 15%, P = .079) and the median time to active antibiotic therapy (12 hours [interquartile range {IQR}, 1–35 hours] vs 1 hour [IQR, 0–6 hours]; P < .001). Unadjusted DOOR analyses indicated a 58% probability (95% confidence interval [CI], 52%–63%) for a worse clinical outcome in CRO-R versus CRO-S BSI. In the IPW-adjusted cohort, no difference was observed (54% [95% CI, 47%–61%]). Secondary outcomes included unadjusted and adjusted differences in the proportion of 30-day mortality between CRO-R and CRO-S BSIs (−5.3% [95% CI, −10.3% to −.4%] and −1.8 [95% CI, −6.7% to 3.2%], respectively), postculture median length of stay (8 days [IQR, 5–13 days] vs 6 days [IQR, 4–9 days]; P < .001), and incident admission to a long-term care facility (22% vs 12%, P = .045). CONCLUSIONS: Patients with CRO-R E coli BSI generally have poorer outcomes compared to patients infected with CRO-S E coli BSI, even after adjusting for important confounders. |
format | Online Article Text |
id | pubmed-9645644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96456442022-11-14 Clinical Impact of Ceftriaxone Resistance in Escherichia coli Bloodstream Infections: A Multicenter Prospective Cohort Study Tamma, Pranita D Komarow, Lauren Ge, Lizhao Garcia-Diaz, Julia Herc, Erica S Doi, Yohei Arias, Cesar A Albin, Owen Saade, Elie Miller, Loren G Jacob, Jesse T Satlin, Michael J Krsak, Martin Huskins, W Charles Dhar, Sorabh Shelburne, Samuel A Hill, Carol Baum, Keri R Bhojani, Minal Greenwood-Quaintance, Kerryl E Schmidt-Malan, Suzannah M Patel, Robin Evans, Scott R Chambers, Henry F Fowler, Vance G van Duin, David Open Forum Infect Dis Major Article BACKGROUND: Ceftriaxone-resistant (CRO-R) Escherichia coli bloodstream infections (BSIs) are common. METHODS: This is a prospective cohort of patients with E coli BSI at 14 United States hospitals between November 2020 and April 2021. For each patient with a CRO-R E coli BSI enrolled, the next consecutive patient with a ceftriaxone-susceptible (CRO-S) E coli BSI was included. Primary outcome was desirability of outcome ranking (DOOR) at day 30, with 50% probability of worse outcomes in the CRO-R group as the null hypothesis. Inverse probability weighting (IPW) was used to reduce confounding. RESULTS: Notable differences between patients infected with CRO-R and CRO-S E coli BSI included the proportion with Pitt bacteremia score ≥4 (23% vs 15%, P = .079) and the median time to active antibiotic therapy (12 hours [interquartile range {IQR}, 1–35 hours] vs 1 hour [IQR, 0–6 hours]; P < .001). Unadjusted DOOR analyses indicated a 58% probability (95% confidence interval [CI], 52%–63%) for a worse clinical outcome in CRO-R versus CRO-S BSI. In the IPW-adjusted cohort, no difference was observed (54% [95% CI, 47%–61%]). Secondary outcomes included unadjusted and adjusted differences in the proportion of 30-day mortality between CRO-R and CRO-S BSIs (−5.3% [95% CI, −10.3% to −.4%] and −1.8 [95% CI, −6.7% to 3.2%], respectively), postculture median length of stay (8 days [IQR, 5–13 days] vs 6 days [IQR, 4–9 days]; P < .001), and incident admission to a long-term care facility (22% vs 12%, P = .045). CONCLUSIONS: Patients with CRO-R E coli BSI generally have poorer outcomes compared to patients infected with CRO-S E coli BSI, even after adjusting for important confounders. Oxford University Press 2022-10-27 /pmc/articles/PMC9645644/ /pubmed/36381622 http://dx.doi.org/10.1093/ofid/ofac572 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://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 (https://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 | Major Article Tamma, Pranita D Komarow, Lauren Ge, Lizhao Garcia-Diaz, Julia Herc, Erica S Doi, Yohei Arias, Cesar A Albin, Owen Saade, Elie Miller, Loren G Jacob, Jesse T Satlin, Michael J Krsak, Martin Huskins, W Charles Dhar, Sorabh Shelburne, Samuel A Hill, Carol Baum, Keri R Bhojani, Minal Greenwood-Quaintance, Kerryl E Schmidt-Malan, Suzannah M Patel, Robin Evans, Scott R Chambers, Henry F Fowler, Vance G van Duin, David Clinical Impact of Ceftriaxone Resistance in Escherichia coli Bloodstream Infections: A Multicenter Prospective Cohort Study |
title | Clinical Impact of Ceftriaxone Resistance in Escherichia coli Bloodstream Infections: A Multicenter Prospective Cohort Study |
title_full | Clinical Impact of Ceftriaxone Resistance in Escherichia coli Bloodstream Infections: A Multicenter Prospective Cohort Study |
title_fullStr | Clinical Impact of Ceftriaxone Resistance in Escherichia coli Bloodstream Infections: A Multicenter Prospective Cohort Study |
title_full_unstemmed | Clinical Impact of Ceftriaxone Resistance in Escherichia coli Bloodstream Infections: A Multicenter Prospective Cohort Study |
title_short | Clinical Impact of Ceftriaxone Resistance in Escherichia coli Bloodstream Infections: A Multicenter Prospective Cohort Study |
title_sort | clinical impact of ceftriaxone resistance in escherichia coli bloodstream infections: a multicenter prospective cohort study |
topic | Major Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645644/ https://www.ncbi.nlm.nih.gov/pubmed/36381622 http://dx.doi.org/10.1093/ofid/ofac572 |
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