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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MDPI AG,
2024-01-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_dbd469b9dfa844daad1c79010e86543f | ||
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. |