Literature DB >> 36073943

Effectiveness and Safety of Beta-Lactam Antibiotics with and without Therapeutic Drug Monitoring in Patients with Pseudomonas aeruginosa Pneumonia or Bloodstream Infection.

Ashlan J Kunz Coyne1, Mohammad Alshaer2, Anthony M Casapao3, Veena Venugopalan4, Carmen Isache1, Jason Ferreira1, Christopher A Jankowski1.   

Abstract

This objective of this study was to compare clinical outcomes in hospitalized patients with Pseudomonas aeruginosa pneumonia (PNA) or bloodstream infection (BSI) receiving beta-lactam antibiotic (BLA) infusions with and without the guidance of therapeutic drug monitoring (TDM). A retrospective, parallel cohort study was conducted at two academic medical centers between December 2015 and January 2020, UF Shands Gainesville, which uses BLA TDM for select patients (BLA TDM), and UF Health Jacksonville, which does not use BLA TDM (No-BLA TDM). All hospitalized adult patients with respiratory or blood culture positive for P. aeruginosa who met diagnosis criteria for lower respiratory tract infection with a positive P. aeruginosa respiratory culture and who received ≥48 h of intravenous BLA with in vitro susceptibility within 72 h of positive culture collection were included. The primary outcome was a composite of presumed treatment failure defined as the presence of any of the following from index-positive P. aeruginosa culture collection to the end of BLA therapy: all-cause mortality, escalation of and/or additional antimicrobial therapy for P. aeruginosa infection after 48 h of treatment with susceptible BLA due to worsening clinical status, or transfer to a higher level of care (i.e., the intensive care unit [ICU]). Analyses were adjusted for possible confounding with inverse probability of treatment weighting (IPTW). Two-hundred patients were included (BLA TDM, n = 95; No-BLA TDM, n = 105). In IPTW-adjusted analysis of the primary composite endpoint, BLA TDM demonstrated a significant decrease in presumed treatment failure compared to No-BLA TDM (adjusted odds ratio [aOR] 0.037, 95% confidence interval [CI] [0.013 to 0.107]; P < 0.001). BLA TDM had more 30-, 60- and 90-day infection-related readmissions ([aOR], 11.301, 95% CI (3.595 to 35.516); aOR 10.389, 95% CI [2.496 to 43.239], and aOR 24.970, 95% CI [6.703 to 93.028]) in IPTW analyses. For both unadjusted and IPTW-adjusted cohorts, there was no significant difference in hospital and ICU length of stay, adverse effects while on BLA, or microbiological eradication between BLA TDM and No-BLA TDM. In hospitalized adult patients with P. aeruginosa PNA or BSI, the use of TDM-guided BLA infusions decreased the odds of presumed treatment failure compared to patients receiving BLA infusions without TDM guidance. Future studies should evaluate BLA TDM impact on readmission.

Entities:  

Keywords:  Pseudomonas aeruginosa; beta-lactam antibiotics; beta-lactams; bloodstream infection; pneumonia; therapeutic drug monitoring

Mesh:

Substances:

Year:  2022        PMID: 36073943      PMCID: PMC9578394          DOI: 10.1128/aac.00646-22

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.938


  60 in total

1.  Pharmacodynamics of cefepime in patients with Gram-negative infections.

Authors:  Vincent H Tam; Peggy S McKinnon; Ronda L Akins; Michael J Rybak; George L Drusano
Journal:  J Antimicrob Chemother       Date:  2002-09       Impact factor: 5.790

2.  Therapeutic drug monitoring of beta-lactams in critically ill patients: proof of concept.

Authors:  Jason A Roberts; Marta Ulldemolins; Michael S Roberts; Brett McWhinney; Jacobus Ungerer; David L Paterson; Jeffrey Lipman
Journal:  Int J Antimicrob Agents       Date:  2010-08-03       Impact factor: 5.283

Review 3.  Individualising Therapy to Minimize Bacterial Multidrug Resistance.

Authors:  A J Heffernan; F B Sime; J Lipman; J A Roberts
Journal:  Drugs       Date:  2018-04       Impact factor: 9.546

4.  Too much of a good thing: a retrospective study of β-lactam concentration-toxicity relationships.

Authors:  Sahand Imani; Hergen Buscher; Debbie Marriott; Sheridan Gentili; Indy Sandaradura
Journal:  J Antimicrob Chemother       Date:  2017-10-01       Impact factor: 5.790

Review 5.  Therapeutic drug monitoring of the β-lactam antibiotics: what is the evidence and which patients should we be using it for?

Authors:  Angela Huttner; Stephan Harbarth; William W Hope; Jeffrey Lipman; Jason A Roberts
Journal:  J Antimicrob Chemother       Date:  2015-07-17       Impact factor: 5.790

6.  Optimizing β-lactams treatment in critically-ill patients using pharmacokinetics/pharmacodynamics targets: are first conventional doses effective?

Authors:  Isabelle K Delattre; Fabio S Taccone; Frédérique Jacobs; Maya Hites; Thierry Dugernier; Herbert Spapen; Pierre-François Laterre; Pierre E Wallemacq; Françoise Van Bambeke; Paul M Tulkens
Journal:  Expert Rev Anti Infect Ther       Date:  2017-06-19       Impact factor: 5.091

Review 7.  A guide to therapeutic drug monitoring of β-lactam antibiotics.

Authors:  Andrew J Fratoni; David P Nicolau; Joseph L Kuti
Journal:  Pharmacotherapy       Date:  2021-02-14       Impact factor: 4.705

Review 8.  Therapeutic Strategies for Emerging Multidrug-Resistant Pseudomonas aeruginosa.

Authors:  Ashlan J Kunz Coyne; Amer El Ghali; Dana Holger; Nicholas Rebold; Michael J Rybak
Journal:  Infect Dis Ther       Date:  2022-02-12

9.  Effect of therapeutic drug monitoring-based dose optimization of piperacillin/tazobactam on sepsis-related organ dysfunction in patients with sepsis: a randomized controlled trial.

Authors:  Stefan Hagel; Friedhelm Bach; Thorsten Brenner; Hendrik Bracht; Alexander Brinkmann; Thorsten Annecke; Andreas Hohn; Markus Weigand; Guido Michels; Stefan Kluge; Axel Nierhaus; Dominik Jarczak; Christina König; Dirk Weismann; Otto Frey; Dominic Witzke; Carsten Müller; Michael Bauer; Michael Kiehntopf; Sophie Neugebauer; Thomas Lehmann; Jason A Roberts; Mathias W Pletz
Journal:  Intensive Care Med       Date:  2022-02-01       Impact factor: 41.787

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