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Impact of a Rapid Molecular Test for Klebsiella pneumoniae Carbapenemase and Ceftazidime-Avibactam Use on Outcomes After Bacteremia Caused by Carbapenem-Resistant Enterobacterales.
Satlin, Michael J; Chen, Liang; Gomez-Simmonds, Angela; Marino, Jamie; Weston, Gregory; Bhowmick, Tanaya; Seo, Susan K; Sperber, Steven J; Kim, Angela C; Eilertson, Brandon; Derti, Sierra; Jenkins, Stephen G; Levi, Michael H; Weinstein, Melvin P; Tang, Yi-Wei; Hong, Tao; Juretschko, Stefan; Hoffman, Katherine L; Walsh, Thomas J; Westblade, Lars F; Uhlemann, Anne-Catrin; Kreiswirth, Barry N.
Afiliación
  • Satlin MJ; Division of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, New York, USA.
  • Chen L; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.
  • Gomez-Simmonds A; Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, New Jersey, USA.
  • Marino J; Department of Medical Sciences, Hackensack Meridian School of Medicine, Nutley, New Jersey, USA.
  • Weston G; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
  • Bhowmick T; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.
  • Seo SK; Division of Infectious Diseases, Department of Medicine, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York, USA.
  • Sperber SJ; Division of Allergy, Immunology, and Infectious Diseases, Department of Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
  • Kim AC; Infectious Diseases Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Eilertson B; Division of Infectious Diseases, Hackensack Meridian School of Medicine, Nutley, New Jersey, USA.
  • Derti S; Division of Infectious Diseases, Department of Medicine, Hackensack University Medical Center, Hackensack, New Jersey, USA.
  • Jenkins SG; Division of Infectious Diseases, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Manhasset, New York, USA.
  • Levi MH; Division of Infectious Diseases, Department of Medicine, State University of New York Downstate, Brooklyn, New York, USA.
  • Weinstein MP; Division of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, New York, USA.
  • Tang YW; Division of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, New York, USA.
  • Hong T; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.
  • Juretschko S; Department of Pathology, Albert Einstein College of Medicine, Bronx, New York, USA.
  • Hoffman KL; Division of Allergy, Immunology, and Infectious Diseases, Department of Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
  • Walsh TJ; Department of Pathology and Laboratory Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
  • Westblade LF; Department of Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Uhlemann AC; Department of Pathology, Hackensack University Medical Center, Hackensack, New Jersey, USA.
  • Kreiswirth BN; Department of Pathology, Northwell Health, Manhasset, New York, USA.
Clin Infect Dis ; 75(12): 2066-2075, 2022 12 19.
Article en En | MEDLINE | ID: mdl-35522019
ABSTRACT

BACKGROUND:

Patients with bacteremia due to carbapenem-resistant Enterobacterales (CRE) experience delays until appropriate therapy and high mortality rates. Rapid molecular diagnostics for carbapenemases and new ß-lactam/ß-lactamase inhibitors may improve outcomes.

METHODS:

We conducted an observational study of patients with CRE bacteremia from 2016 to 2018 at 8 New York and New Jersey medical centers and assessed center-specific clinical microbiology practices. We compared time to receipt of active antimicrobial therapy and mortality between patients whose positive blood cultures underwent rapid molecular testing for the Klebsiella pneumoniae carbapenemase (KPC) gene (blaKPC) and patients whose cultures did not undergo this test. CRE isolates underwent antimicrobial susceptibility testing by broth microdilution and carbapenemase profiling by whole-genome sequencing. We also assessed outcomes when ceftazidime-avibactam and polymyxins were used as targeted therapies.

RESULTS:

Of 137 patients with CRE bacteremia, 89 (65%) had a KPC-producing organism. Patients whose blood cultures underwent blaKPC PCR testing (n = 51) had shorter time until receipt of active therapy (median 24 vs 50 hours; P = .009) compared with other patients (n = 86) and decreased 14-day (16% vs 37%; P = .007) and 30-day (24% vs 47%; P = .007) mortality. blaKPC PCR testing was associated with decreased 30-day mortality (adjusted odds ratio .37; 95% CI .16-.84) in an adjusted model. The 30-day mortality rate was 10% with ceftazidime-avibactam monotherapy and 31% with polymyxin monotherapy (P = .08).

CONCLUSIONS:

In a KPC-endemic area, blaKPC PCR testing of positive blood cultures was associated with decreased time until appropriate therapy and decreased mortality for CRE bacteremia, and ceftazidime-avibactam is a reasonable first-line therapy for these infections.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Infecciones por Klebsiella / Bacteriemia Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Infecciones por Klebsiella / Bacteriemia Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos