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1162. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified Through the Emerging Infections Program (EIP), United States, 2016–2017
BACKGROUND: Pseudomonas aeruginosa is intrinsically resistant to many commonly used antimicrobials and carbapenems are often required to treat infections. We describe the epidemiology and crude incidence of carbapenem-resistant P. aeruginosa(CRPA) in the EIP catchment area. METHODS: From August 1, 2...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253167/ http://dx.doi.org/10.1093/ofid/ofy210.995 |
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author | Grass, Julian Bulens, Sandra Bamberg, Wendy Janelle, Sarah J Stendel, Patrick Jacob, Jesse T Bower, Chris Sukumaran, Stephen Wilson, Lucy E Vaeth, Elisabeth Li, Linda Lynfield, Ruth Vagnone, Paula Snippes Dobbins, Ginette Phipps, Erin C Hancock, Emily B Dumyati, Ghinwa Tsay, Rebecca Pierce, Rebecca Cassidy, P Maureen West, Nicole Kainer, Marion A Muleta, Daniel Mounsey, Jacquelyn Campbell, Davina Stanton, Richard Karlsson, Maria S Walters, Maroya Spalding |
author_facet | Grass, Julian Bulens, Sandra Bamberg, Wendy Janelle, Sarah J Stendel, Patrick Jacob, Jesse T Bower, Chris Sukumaran, Stephen Wilson, Lucy E Vaeth, Elisabeth Li, Linda Lynfield, Ruth Vagnone, Paula Snippes Dobbins, Ginette Phipps, Erin C Hancock, Emily B Dumyati, Ghinwa Tsay, Rebecca Pierce, Rebecca Cassidy, P Maureen West, Nicole Kainer, Marion A Muleta, Daniel Mounsey, Jacquelyn Campbell, Davina Stanton, Richard Karlsson, Maria S Walters, Maroya Spalding |
author_sort | Grass, Julian |
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 epidemiology and crude incidence of carbapenem-resistant P. aeruginosa(CRPA) in the EIP catchment area. METHODS: From August 1, 2016 through July 31, 2017, we conducted laboratory- and population-based surveillance for CRPA in selected metropolitan areas in Colorado, Georgia, Maryland, Minnesota, New Mexico, New York, Oregon, and Tennessee. We defined an incident 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. A random sample of isolates was screened at CDC for carbapenemases using the modified carbapenem inactivation method (mCIM) and real-time PCR. RESULTS: During the 12-month period, we identified 3,042 incident cases among 2,154 patients. The crude incidence rate was 21.2 (95% CI, 20.4–21.9) per 100,000 persons and varied by site (range: 7.7 in Oregon to 31.1 in Maryland). The median age of patients was 64 years (range: <1–101) and 41.2% were female. Nearly all (97.1%) had at least one underlying condition and 10.2% had cystic fibrosis (CF); 17.8% of cases were from CF patients. For most cases, isolates were from the lower respiratory tract (49.2%) or urine (35.3%) and occurred in patients with recent hospitalization (87.2%) or indwelling devices (70.3%); 8.7% died. At the clinical laboratory, 84.7% of isolates were susceptible to an aminoglycoside and 66.4% to ceftazidime or cefepime. Among the 391 isolates tested, nine (2.3%) were mCIM-positive; one had a carbapenemase detected by PCR (bla(VIM-4)). CONCLUSION: The burden of CRPA varied by EIP site. Most cases occurred in persons with healthcare exposures and underlying conditions. The majority of isolates were susceptible to at least one first-line antimicrobial. Carbapenemase producers were rare; a more specific phenotypic definition would greatly facilitate surveillance for these isolates. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-6253167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62531672018-11-28 1162. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified Through the Emerging Infections Program (EIP), United States, 2016–2017 Grass, Julian Bulens, Sandra Bamberg, Wendy Janelle, Sarah J Stendel, Patrick Jacob, Jesse T Bower, Chris Sukumaran, Stephen Wilson, Lucy E Vaeth, Elisabeth Li, Linda Lynfield, Ruth Vagnone, Paula Snippes Dobbins, Ginette Phipps, Erin C Hancock, Emily B Dumyati, Ghinwa Tsay, Rebecca Pierce, Rebecca Cassidy, P Maureen West, Nicole Kainer, Marion A Muleta, Daniel Mounsey, Jacquelyn Campbell, Davina Stanton, Richard Karlsson, Maria S Walters, Maroya Spalding 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 epidemiology and crude incidence of carbapenem-resistant P. aeruginosa(CRPA) in the EIP catchment area. METHODS: From August 1, 2016 through July 31, 2017, we conducted laboratory- and population-based surveillance for CRPA in selected metropolitan areas in Colorado, Georgia, Maryland, Minnesota, New Mexico, New York, Oregon, and Tennessee. We defined an incident 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. A random sample of isolates was screened at CDC for carbapenemases using the modified carbapenem inactivation method (mCIM) and real-time PCR. RESULTS: During the 12-month period, we identified 3,042 incident cases among 2,154 patients. The crude incidence rate was 21.2 (95% CI, 20.4–21.9) per 100,000 persons and varied by site (range: 7.7 in Oregon to 31.1 in Maryland). The median age of patients was 64 years (range: <1–101) and 41.2% were female. Nearly all (97.1%) had at least one underlying condition and 10.2% had cystic fibrosis (CF); 17.8% of cases were from CF patients. For most cases, isolates were from the lower respiratory tract (49.2%) or urine (35.3%) and occurred in patients with recent hospitalization (87.2%) or indwelling devices (70.3%); 8.7% died. At the clinical laboratory, 84.7% of isolates were susceptible to an aminoglycoside and 66.4% to ceftazidime or cefepime. Among the 391 isolates tested, nine (2.3%) were mCIM-positive; one had a carbapenemase detected by PCR (bla(VIM-4)). CONCLUSION: The burden of CRPA varied by EIP site. Most cases occurred in persons with healthcare exposures and underlying conditions. The majority of isolates were susceptible to at least one first-line antimicrobial. Carbapenemase producers were rare; a more specific phenotypic definition would greatly facilitate surveillance for these isolates. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6253167/ http://dx.doi.org/10.1093/ofid/ofy210.995 Text en © The Author(s) 2018. 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 Bulens, Sandra Bamberg, Wendy Janelle, Sarah J Stendel, Patrick Jacob, Jesse T Bower, Chris Sukumaran, Stephen Wilson, Lucy E Vaeth, Elisabeth Li, Linda Lynfield, Ruth Vagnone, Paula Snippes Dobbins, Ginette Phipps, Erin C Hancock, Emily B Dumyati, Ghinwa Tsay, Rebecca Pierce, Rebecca Cassidy, P Maureen West, Nicole Kainer, Marion A Muleta, Daniel Mounsey, Jacquelyn Campbell, Davina Stanton, Richard Karlsson, Maria S Walters, Maroya Spalding 1162. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified Through the Emerging Infections Program (EIP), United States, 2016–2017 |
title | 1162. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified Through the Emerging Infections Program (EIP), United States, 2016–2017 |
title_full | 1162. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified Through the Emerging Infections Program (EIP), United States, 2016–2017 |
title_fullStr | 1162. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified Through the Emerging Infections Program (EIP), United States, 2016–2017 |
title_full_unstemmed | 1162. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified Through the Emerging Infections Program (EIP), United States, 2016–2017 |
title_short | 1162. Epidemiology of Carbapenem-Resistant Pseudomonas aeruginosa Identified Through the Emerging Infections Program (EIP), United States, 2016–2017 |
title_sort | 1162. epidemiology of carbapenem-resistant pseudomonas aeruginosa identified through the emerging infections program (eip), united states, 2016–2017 |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253167/ http://dx.doi.org/10.1093/ofid/ofy210.995 |
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