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486. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified through the Emerging Infections Program (EIP), United States, 2016–2018
BACKGROUND: Pseudomonas aeruginosa is intrinsically resistant to many commonly used antimicrobials, and carbapenems are often required to treat infections. We describe the crude incidence, epidemiology, and molecular characteristics of carbapenem-resistant P. aeruginosa (CRPA) in the EIP catchment a...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811195/ http://dx.doi.org/10.1093/ofid/ofz360.559 |
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author | Grass, Julian E Bulens, Sandra N Bamberg, Wendy M Janelle, Sarah J Schutz, Kyle Jacob, Jesse T Bower, Chris W Blakney, Rebekah Wilson, Lucy E Vaeth, Elisabeth Li, Linda Lynfield, Ruth Snippes Vagnone, Paula Dobbins, Ginette Phipps, Erin C Hancock, Emily B Dumyati, Ghinwa Tsay, Rebecca Cassidy, P Maureen West, Nicole Kainer, Marion A Mounsey, Jacquelyn Stanton, Richard A McAllister, Gillian A Campbell, Davina Lutgring, Joseph D Karlsson, Maria Walters, Maroya S |
author_facet | Grass, Julian E Bulens, Sandra N Bamberg, Wendy M Janelle, Sarah J Schutz, Kyle Jacob, Jesse T Bower, Chris W Blakney, Rebekah Wilson, Lucy E Vaeth, Elisabeth Li, Linda Lynfield, Ruth Snippes Vagnone, Paula Dobbins, Ginette Phipps, Erin C Hancock, Emily B Dumyati, Ghinwa Tsay, Rebecca Cassidy, P Maureen West, Nicole Kainer, Marion A Mounsey, Jacquelyn Stanton, Richard A McAllister, Gillian A Campbell, Davina Lutgring, Joseph D Karlsson, Maria Walters, Maroya S |
author_sort | Grass, Julian E |
collection | PubMed |
description | BACKGROUND: Pseudomonas aeruginosa is intrinsically resistant to many commonly used antimicrobials, and carbapenems are often required to treat infections. We describe the crude incidence, epidemiology, and molecular characteristics of carbapenem-resistant P. aeruginosa (CRPA) in the EIP catchment area. METHODS: From August 1, 2016 through July 31, 2018, we conducted laboratory- and population-based surveillance for CRPA in selected areas in eight sites. We defined a case as the first isolate of P. aeruginosa resistant to imipenem, meropenem, or doripenem from the lower respiratory tract, urine, wounds, or normally sterile sites identified from a resident of the EIP catchment area in a 30-day period. Patient charts were reviewed. Analysis excluded cystic fibrosis patients. A random sample of isolates was collected. Real-time PCR to detect carbapenemase genes and whole-genome sequencing are in progress. RESULTS: We identified 4,209 cases in 3373 patients. The annual incidence was 14.50 (95% CI, 14.07–14.94) per 100,000 persons and varied among sites from 4.89 in OR to 25.21 in NY. The median age of patients was 66 years (range: < 1–101), 42.1% were female, and nearly all (97.5%) had an underlying condition. Most cases were identified from urine (42.8%) and lower respiratory tract (35.7%) cultures. Nearly all (93.3%) occurred in patients with inpatient healthcare facility stay, surgery, chronic dialysis, or indwelling devices in the prior year; death occurred in 7.2%. Among 937 isolates tested, 847 (90.4%) underwent PCR; six (0.7%) harbored a carbapenemase, from four sites (CO, MD, NY, and OR): bla(VIM) (3), bla(KPC) (2), and bla(IMP) (1). Of 612 (65.3%) isolates sequenced, the most common ST types were ST235 (9.2%) and ST298 (4.9%). CONCLUSION: Carbapenemases were rarely the cause of carbapenem resistance but were found at EIP sites with high and low CRPA incidence. The emergence of mobile carbapenemases in P. aeruginosa has the potential to increase the incidence of CRPA. Increased detection and early response to carbapenemase-producing CRPA is key to prevent further emergence. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-6811195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68111952019-10-29 486. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified through the Emerging Infections Program (EIP), United States, 2016–2018 Grass, Julian E Bulens, Sandra N Bamberg, Wendy M Janelle, Sarah J Schutz, Kyle Jacob, Jesse T Bower, Chris W Blakney, Rebekah Wilson, Lucy E Vaeth, Elisabeth Li, Linda Lynfield, Ruth Snippes Vagnone, Paula Dobbins, Ginette Phipps, Erin C Hancock, Emily B Dumyati, Ghinwa Tsay, Rebecca Cassidy, P Maureen West, Nicole Kainer, Marion A Mounsey, Jacquelyn Stanton, Richard A McAllister, Gillian A Campbell, Davina Lutgring, Joseph D Karlsson, Maria Walters, Maroya S Open Forum Infect Dis Abstracts BACKGROUND: Pseudomonas aeruginosa is intrinsically resistant to many commonly used antimicrobials, and carbapenems are often required to treat infections. We describe the crude incidence, epidemiology, and molecular characteristics of carbapenem-resistant P. aeruginosa (CRPA) in the EIP catchment area. METHODS: From August 1, 2016 through July 31, 2018, we conducted laboratory- and population-based surveillance for CRPA in selected areas in eight sites. We defined a case as the first isolate of P. aeruginosa resistant to imipenem, meropenem, or doripenem from the lower respiratory tract, urine, wounds, or normally sterile sites identified from a resident of the EIP catchment area in a 30-day period. Patient charts were reviewed. Analysis excluded cystic fibrosis patients. A random sample of isolates was collected. Real-time PCR to detect carbapenemase genes and whole-genome sequencing are in progress. RESULTS: We identified 4,209 cases in 3373 patients. The annual incidence was 14.50 (95% CI, 14.07–14.94) per 100,000 persons and varied among sites from 4.89 in OR to 25.21 in NY. The median age of patients was 66 years (range: < 1–101), 42.1% were female, and nearly all (97.5%) had an underlying condition. Most cases were identified from urine (42.8%) and lower respiratory tract (35.7%) cultures. Nearly all (93.3%) occurred in patients with inpatient healthcare facility stay, surgery, chronic dialysis, or indwelling devices in the prior year; death occurred in 7.2%. Among 937 isolates tested, 847 (90.4%) underwent PCR; six (0.7%) harbored a carbapenemase, from four sites (CO, MD, NY, and OR): bla(VIM) (3), bla(KPC) (2), and bla(IMP) (1). Of 612 (65.3%) isolates sequenced, the most common ST types were ST235 (9.2%) and ST298 (4.9%). CONCLUSION: Carbapenemases were rarely the cause of carbapenem resistance but were found at EIP sites with high and low CRPA incidence. The emergence of mobile carbapenemases in P. aeruginosa has the potential to increase the incidence of CRPA. Increased detection and early response to carbapenemase-producing CRPA is key to prevent further emergence. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6811195/ http://dx.doi.org/10.1093/ofid/ofz360.559 Text en © The Author(s) 2019. 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 Grass, Julian E Bulens, Sandra N Bamberg, Wendy M Janelle, Sarah J Schutz, Kyle Jacob, Jesse T Bower, Chris W Blakney, Rebekah Wilson, Lucy E Vaeth, Elisabeth Li, Linda Lynfield, Ruth Snippes Vagnone, Paula Dobbins, Ginette Phipps, Erin C Hancock, Emily B Dumyati, Ghinwa Tsay, Rebecca Cassidy, P Maureen West, Nicole Kainer, Marion A Mounsey, Jacquelyn Stanton, Richard A McAllister, Gillian A Campbell, Davina Lutgring, Joseph D Karlsson, Maria Walters, Maroya S 486. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified through the Emerging Infections Program (EIP), United States, 2016–2018 |
title | 486. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified through the Emerging Infections Program (EIP), United States, 2016–2018 |
title_full | 486. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified through the Emerging Infections Program (EIP), United States, 2016–2018 |
title_fullStr | 486. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified through the Emerging Infections Program (EIP), United States, 2016–2018 |
title_full_unstemmed | 486. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified through the Emerging Infections Program (EIP), United States, 2016–2018 |
title_short | 486. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified through the Emerging Infections Program (EIP), United States, 2016–2018 |
title_sort | 486. epidemiology of carbapenem-resistant pseudomonas aeruginosa identified through the emerging infections program (eip), united states, 2016–2018 |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811195/ http://dx.doi.org/10.1093/ofid/ofz360.559 |
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