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Treatment of Carbapenem-Resistant Enterobacteriaceae Infections with Ceftazidime-Avibactam
BACKGROUND: CRE is an urgent threats to public health with a high mortality estimated at >30–50%. Until recently, polymyxin-based antibiotics were the only available options. However, a new therapeutic option has become available: ceftazidime-avibactam. We sought to describe outcomes from these i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632115/ http://dx.doi.org/10.1093/ofid/ofx163.644 |
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author | Rahmati, Elham Blodget, Emily She, Rosemary C Abbott, Jennifer Cupo Bonomo, Robert A Spellberg, Brad |
author_facet | Rahmati, Elham Blodget, Emily She, Rosemary C Abbott, Jennifer Cupo Bonomo, Robert A Spellberg, Brad |
author_sort | Rahmati, Elham |
collection | PubMed |
description | BACKGROUND: CRE is an urgent threats to public health with a high mortality estimated at >30–50%. Until recently, polymyxin-based antibiotics were the only available options. However, a new therapeutic option has become available: ceftazidime-avibactam. We sought to describe outcomes from these infections treated with ceftazidime-avibactam. METHODS: From 9/2015 to 12/ 2016, we reviewed charts of 11 patients infected with CRE who received ceftazidime-avibactam at USC (Los Angeles, CA). Sixteen isolates analyzed. All isolates were resistant to meropenem (MIC ≥ 16). Carbapenemase production confirmed by detection of bla(KPC). Clinical success defined as clinical improvement, lack of recurrence, and survival in 90 days. Recurrence defined as clinical signs of infection and recovery of CRE after ≥ 7 days of treatment. RESULTS: The median age was 49 (35-89); 73% (7/11) female; and 27% (3/11) solid organ transplants. All CRE infections caused by Klebsiella pneumoniae. All sequence type 258, 7/11 harboring bla(KPC-2) and 4/11 bla(KPC-3). Nine capsular type wzi-154 and 2 wzi-29. qSOFA score was 0 (0–2) predicting mortality of 3%. Seven had intraabdominal infections; 2 pyelonephritis, 1 skin and soft-tissue infection, and 1 primary bacteremia. There were five episodes of secondary bacteremia. The patients were treated for a median duration of 15 (3-43) days. All received other antibiotics prior to ceftazidime-avibactam. Eighty-seven percent (9/11) treated with monotherapy and 13% (2/11) in conjunction with colistemethate sodium. 27% (3/11) were receiving CRRT or hemodialysis during treatment. No incidents of renal toxicity observed using RIFLE criteria. Clinical success was 73% (8/11); 30 day survival rate 82% (9/11); 90 day survival rate 73% (8/11); and in hospital mortality 27% (3/11). Patients receiving CRRT or hemodialysis had 75% (3/4) mortality (P = 0.02). Recurrence occurred in 18% (2/11). Decreased sensitivity to ceftazidime-avibactam noted in one patient. 27% (3/11) had CRE isolated after ≥ 7 days treatment. CONCLUSION: In CRE-infected patient treated with ceftazidime-avibactam, the overall mortality rate was 27% with the highest mortality among those receiving renal replacement therapy which was comparable to a prior studies. Additional research is needed to optimize the use of ceftazidime-avibactam to treat CRE infections. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-5632115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56321152017-11-07 Treatment of Carbapenem-Resistant Enterobacteriaceae Infections with Ceftazidime-Avibactam Rahmati, Elham Blodget, Emily She, Rosemary C Abbott, Jennifer Cupo Bonomo, Robert A Spellberg, Brad Open Forum Infect Dis Abstracts BACKGROUND: CRE is an urgent threats to public health with a high mortality estimated at >30–50%. Until recently, polymyxin-based antibiotics were the only available options. However, a new therapeutic option has become available: ceftazidime-avibactam. We sought to describe outcomes from these infections treated with ceftazidime-avibactam. METHODS: From 9/2015 to 12/ 2016, we reviewed charts of 11 patients infected with CRE who received ceftazidime-avibactam at USC (Los Angeles, CA). Sixteen isolates analyzed. All isolates were resistant to meropenem (MIC ≥ 16). Carbapenemase production confirmed by detection of bla(KPC). Clinical success defined as clinical improvement, lack of recurrence, and survival in 90 days. Recurrence defined as clinical signs of infection and recovery of CRE after ≥ 7 days of treatment. RESULTS: The median age was 49 (35-89); 73% (7/11) female; and 27% (3/11) solid organ transplants. All CRE infections caused by Klebsiella pneumoniae. All sequence type 258, 7/11 harboring bla(KPC-2) and 4/11 bla(KPC-3). Nine capsular type wzi-154 and 2 wzi-29. qSOFA score was 0 (0–2) predicting mortality of 3%. Seven had intraabdominal infections; 2 pyelonephritis, 1 skin and soft-tissue infection, and 1 primary bacteremia. There were five episodes of secondary bacteremia. The patients were treated for a median duration of 15 (3-43) days. All received other antibiotics prior to ceftazidime-avibactam. Eighty-seven percent (9/11) treated with monotherapy and 13% (2/11) in conjunction with colistemethate sodium. 27% (3/11) were receiving CRRT or hemodialysis during treatment. No incidents of renal toxicity observed using RIFLE criteria. Clinical success was 73% (8/11); 30 day survival rate 82% (9/11); 90 day survival rate 73% (8/11); and in hospital mortality 27% (3/11). Patients receiving CRRT or hemodialysis had 75% (3/4) mortality (P = 0.02). Recurrence occurred in 18% (2/11). Decreased sensitivity to ceftazidime-avibactam noted in one patient. 27% (3/11) had CRE isolated after ≥ 7 days treatment. CONCLUSION: In CRE-infected patient treated with ceftazidime-avibactam, the overall mortality rate was 27% with the highest mortality among those receiving renal replacement therapy which was comparable to a prior studies. Additional research is needed to optimize the use of ceftazidime-avibactam to treat CRE infections. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2017-10-04 /pmc/articles/PMC5632115/ http://dx.doi.org/10.1093/ofid/ofx163.644 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 Rahmati, Elham Blodget, Emily She, Rosemary C Abbott, Jennifer Cupo Bonomo, Robert A Spellberg, Brad Treatment of Carbapenem-Resistant Enterobacteriaceae Infections with Ceftazidime-Avibactam |
title | Treatment of Carbapenem-Resistant Enterobacteriaceae Infections with Ceftazidime-Avibactam |
title_full | Treatment of Carbapenem-Resistant Enterobacteriaceae Infections with Ceftazidime-Avibactam |
title_fullStr | Treatment of Carbapenem-Resistant Enterobacteriaceae Infections with Ceftazidime-Avibactam |
title_full_unstemmed | Treatment of Carbapenem-Resistant Enterobacteriaceae Infections with Ceftazidime-Avibactam |
title_short | Treatment of Carbapenem-Resistant Enterobacteriaceae Infections with Ceftazidime-Avibactam |
title_sort | treatment of carbapenem-resistant enterobacteriaceae infections with ceftazidime-avibactam |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632115/ http://dx.doi.org/10.1093/ofid/ofx163.644 |
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