Impact of a Rapid Molecular Test for Klebsiella pneumoniae Carbapenemase and Ceftazidime-Avibactam Use on Outcomes After Bacteremia Caused by Carbapenem-Resistant Enterobacterales.

TitleImpact of a Rapid Molecular Test for Klebsiella pneumoniae Carbapenemase and Ceftazidime-Avibactam Use on Outcomes After Bacteremia Caused by Carbapenem-Resistant Enterobacterales.
Publication TypeJournal Article
Year of Publication2022
AuthorsSatlin MJ, Chen L, Gomez-Simmonds A, Marino J, Weston G, Bhowmick T, Seo SK, Sperber SJ, Kim AC, Eilertson B, Derti S, Jenkins SG, Levi MH, Weinstein MP, Tang Y-W, Hong T, Juretschko S, Hoffman KL, Walsh TJ, Westblade LF, Uhlemann A-C, Kreiswirth BN
JournalClin Infect Dis
Volume75
Issue12
Pagination2066-2075
Date Published2022 Dec 19
ISSN1537-6591
KeywordsAnti-Bacterial Agents, Azabicyclo Compounds, Bacteremia, Bacterial Proteins, beta-Lactamase Inhibitors, beta-Lactamases, Carbapenems, Ceftazidime, Drug Combinations, Humans, Klebsiella Infections, Klebsiella pneumoniae, Microbial Sensitivity Tests
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 β-lactam/β-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.

DOI10.1093/cid/ciac354
Alternate JournalClin Infect Dis
PubMed ID35522019
PubMed Central IDPMC10200298
Grant ListR01 AI090155 / AI / NIAID NIH HHS / United States
P30CA008748 / CA / NCI NIH HHS / United States
P30 CA008748 / CA / NCI NIH HHS / United States
UL1 TR002384 / TR / NCATS NIH HHS / United States
UL1TR002384 / TR / NCATS NIH HHS / United States
Related Faculty: 
Lars Westblade, Ph.D.

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