Optimized Antibiotic Management of Critically Ill Patients with Severe Pneumonia Following Multiplex Polymerase Chain Reaction Testing: A Prospective Clinical Exploratory Trial

Molecular diagnostic testing is assumed to enable fast respiratory pathogen identification and contribute to improved pneumonia management. We set up a prospective clinical trial at a tertiary hospital intensive care unit including adult patients suspected of severe pneumonia from whom a lower respi...

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Main Authors: Alexia Verroken (Author), Julien Favresse (Author), Ahalieyah Anantharajah (Author), Hector Rodriguez-Villalobos (Author), Xavier Wittebole (Author), Pierre-François Laterre (Author)
Format: Book
Published: MDPI AG, 2024-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Alexia Verroken  |e author 
700 1 0 |a Julien Favresse  |e author 
700 1 0 |a Ahalieyah Anantharajah  |e author 
700 1 0 |a Hector Rodriguez-Villalobos  |e author 
700 1 0 |a Xavier Wittebole  |e author 
700 1 0 |a Pierre-François Laterre  |e author 
245 0 0 |a Optimized Antibiotic Management of Critically Ill Patients with Severe Pneumonia Following Multiplex Polymerase Chain Reaction Testing: A Prospective Clinical Exploratory Trial 
260 |b MDPI AG,   |c 2024-01-01T00:00:00Z. 
500 |a 10.3390/antibiotics13010067 
500 |a 2079-6382 
520 |a Molecular diagnostic testing is assumed to enable fast respiratory pathogen identification and contribute to improved pneumonia management. We set up a prospective clinical trial at a tertiary hospital intensive care unit including adult patients suspected of severe pneumonia from whom a lower respiratory tract sample could be obtained. During control periods (CPs), routine testing was performed, and during intervention periods (IPs), this testing was completed with the FilmArray Pneumonia Panel <i>plus</i> test (FA-PNEU) executed 24/7. The main objective was to measure the impact of FA-PNEU results in terms of reduced time to targeted antimicrobial treatment administration. Over a 10-month period, analysis was performed on 35 CP and 50 IP patients. The median time to targeted antimicrobial treatment administration was reduced to 4.3 h in IPs compared to 26.4 h in CPs, with 54% of IP patients having FA-PNEU results that led to a treatment modification, of which all but one were targeted. Modifications included 10 (37%) de-escalations, 7 (25.9%) escalations, 3 (11.1%) regimen switches, and 7 (25.9%) complete antimicrobial discontinuations. FA-PNEU results were available with a 42.3 h gain compared to routine identification. This prospective study confirmed retrospective data demonstrating the benefit of FA-PNEU testing in severe pneumonia management of critically ill patients through improved antimicrobial use. 
546 |a EN 
690 |a severe pneumonia 
690 |a molecular testing 
690 |a FilmArray Pneumonia 
690 |a antibiotic management 
690 |a critically ill 
690 |a antimicrobial stewardship 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antibiotics, Vol 13, Iss 1, p 67 (2024) 
787 0 |n https://www.mdpi.com/2079-6382/13/1/67 
787 0 |n https://doaj.org/toc/2079-6382 
856 4 1 |u https://doaj.org/article/dbd469b9dfa844daad1c79010e86543f  |z Connect to this object online.