Cargando…

1270. Early Real-world Evidence in the Use of Eravacycline for the Management of Draconian Infections

BACKGROUND: Eravacycline (ERV) is a next-generation tetracycline approved for complicated intra-abdominal infections (cIAI) with in-vitro activity to multidrug-resistant organisms such as carbapenem resistant Enterobacteriaceae, extended spectrum beta-lactamase, and carbapenem-resistant Acinetobacte...

Descripción completa

Detalles Bibliográficos
Autores principales: Carr, Amy, El Ghali, Amer, Kaur, Parminder, Minor, Sarah B, Casapao, Anthony M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776886/
http://dx.doi.org/10.1093/ofid/ofaa439.1454
_version_ 1783630785081769984
author Carr, Amy
El Ghali, Amer
Kaur, Parminder
Minor, Sarah B
Casapao, Anthony M
author_facet Carr, Amy
El Ghali, Amer
Kaur, Parminder
Minor, Sarah B
Casapao, Anthony M
author_sort Carr, Amy
collection PubMed
description BACKGROUND: Eravacycline (ERV) is a next-generation tetracycline approved for complicated intra-abdominal infections (cIAI) with in-vitro activity to multidrug-resistant organisms such as carbapenem resistant Enterobacteriaceae, extended spectrum beta-lactamase, and carbapenem-resistant Acinetobacter baumannii (CRAB). The purpose of this study was to identify the utility of ERV in clinical practice. METHODS: Retrospective case series was conducted on patients at AdventHealth that received at least two doses of ERV. Primary endpoint for the study was clinical success while on ERV, meeting none of the following criteria: changing therapy, mortality, or lack of improvement from sign/symptoms. RESULTS: Of 23 patients, 74% were males with a mean age of 55 ±18 years and mean body weight of 79 ±27 kg. Mean APACHE II and Charleson scores were 20 (±11) and 6 (±4), respectively. 91% received ERV for an off-label indication or organism. Infection types were respiratory (44%), cIAI (35%), skin (9%), and other (13%). All patients had positive cultures, while 61% were treated as a polymicrobial infection and 17% had bacteremia. Microorganisms included A. xylosoxidans, S. maltophilia, CRAB, and K pneumoniae. 48% had ERV susceptibilities from .06-4 mcg/mL, including two MIC ≥32mcg/mL for S. maltophilia. 70% were given another antibiotic prior to ERV with a median duration of 5 (1-35) days. Median duration of ERV was 8 (3-30) days. 83% percent received ERV in combination with another antibiotic. During treatment, 26% had a Child-Pugh Class C at baseline and 30% had elevated liver function tests. No adverse drug reactions were reported. Upon discharge, 35% continued ERV. Clinical success was observed in 57% (12/21) of patients. Clinical outcome by infection type is summarized in Figure 1. Of 9 cases of clinical failure, 14% were changed to alternative, 19% died while on ERV, and 10% failed to resolve signs/symptoms. Two cases of M. abscessus infections had insufficient follow-up to assess clinical outcome. Figure 1. Eravacycline Clinical Outcome by Infection Type [Image: see text] CONCLUSION: Initial real-world experience with ERV differs significantly from the trials regarding severity of illness, types of infection, and clinical outcomes. Further evaluation is necessary for using ERV as combination therapy and in off-label indications. DISCLOSURES: All Authors: No reported disclosures
format Online
Article
Text
id pubmed-7776886
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77768862021-01-07 1270. Early Real-world Evidence in the Use of Eravacycline for the Management of Draconian Infections Carr, Amy El Ghali, Amer Kaur, Parminder Minor, Sarah B Casapao, Anthony M Open Forum Infect Dis Poster Abstracts BACKGROUND: Eravacycline (ERV) is a next-generation tetracycline approved for complicated intra-abdominal infections (cIAI) with in-vitro activity to multidrug-resistant organisms such as carbapenem resistant Enterobacteriaceae, extended spectrum beta-lactamase, and carbapenem-resistant Acinetobacter baumannii (CRAB). The purpose of this study was to identify the utility of ERV in clinical practice. METHODS: Retrospective case series was conducted on patients at AdventHealth that received at least two doses of ERV. Primary endpoint for the study was clinical success while on ERV, meeting none of the following criteria: changing therapy, mortality, or lack of improvement from sign/symptoms. RESULTS: Of 23 patients, 74% were males with a mean age of 55 ±18 years and mean body weight of 79 ±27 kg. Mean APACHE II and Charleson scores were 20 (±11) and 6 (±4), respectively. 91% received ERV for an off-label indication or organism. Infection types were respiratory (44%), cIAI (35%), skin (9%), and other (13%). All patients had positive cultures, while 61% were treated as a polymicrobial infection and 17% had bacteremia. Microorganisms included A. xylosoxidans, S. maltophilia, CRAB, and K pneumoniae. 48% had ERV susceptibilities from .06-4 mcg/mL, including two MIC ≥32mcg/mL for S. maltophilia. 70% were given another antibiotic prior to ERV with a median duration of 5 (1-35) days. Median duration of ERV was 8 (3-30) days. 83% percent received ERV in combination with another antibiotic. During treatment, 26% had a Child-Pugh Class C at baseline and 30% had elevated liver function tests. No adverse drug reactions were reported. Upon discharge, 35% continued ERV. Clinical success was observed in 57% (12/21) of patients. Clinical outcome by infection type is summarized in Figure 1. Of 9 cases of clinical failure, 14% were changed to alternative, 19% died while on ERV, and 10% failed to resolve signs/symptoms. Two cases of M. abscessus infections had insufficient follow-up to assess clinical outcome. Figure 1. Eravacycline Clinical Outcome by Infection Type [Image: see text] CONCLUSION: Initial real-world experience with ERV differs significantly from the trials regarding severity of illness, types of infection, and clinical outcomes. Further evaluation is necessary for using ERV as combination therapy and in off-label indications. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2020-12-31 /pmc/articles/PMC7776886/ http://dx.doi.org/10.1093/ofid/ofaa439.1454 Text en © The Author 2020. 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 Poster Abstracts
Carr, Amy
El Ghali, Amer
Kaur, Parminder
Minor, Sarah B
Casapao, Anthony M
1270. Early Real-world Evidence in the Use of Eravacycline for the Management of Draconian Infections
title 1270. Early Real-world Evidence in the Use of Eravacycline for the Management of Draconian Infections
title_full 1270. Early Real-world Evidence in the Use of Eravacycline for the Management of Draconian Infections
title_fullStr 1270. Early Real-world Evidence in the Use of Eravacycline for the Management of Draconian Infections
title_full_unstemmed 1270. Early Real-world Evidence in the Use of Eravacycline for the Management of Draconian Infections
title_short 1270. Early Real-world Evidence in the Use of Eravacycline for the Management of Draconian Infections
title_sort 1270. early real-world evidence in the use of eravacycline for the management of draconian infections
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776886/
http://dx.doi.org/10.1093/ofid/ofaa439.1454
work_keys_str_mv AT carramy 1270earlyrealworldevidenceintheuseoferavacyclineforthemanagementofdraconianinfections
AT elghaliamer 1270earlyrealworldevidenceintheuseoferavacyclineforthemanagementofdraconianinfections
AT kaurparminder 1270earlyrealworldevidenceintheuseoferavacyclineforthemanagementofdraconianinfections
AT minorsarahb 1270earlyrealworldevidenceintheuseoferavacyclineforthemanagementofdraconianinfections
AT casapaoanthonym 1270earlyrealworldevidenceintheuseoferavacyclineforthemanagementofdraconianinfections