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DC Field | Value | Language |
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dc.contributor.author | Chen, Chieh-Lung | - |
dc.contributor.author | Tseng, How-Yang | - |
dc.contributor.author | Chen, Wei-Cheng | - |
dc.contributor.author | dkk. | - |
dc.date.accessioned | 2025-01-06T02:38:16Z | - |
dc.date.available | 2025-01-06T02:38:16Z | - |
dc.date.issued | 2024-06 | - |
dc.identifier.issn | 1684-1182 | - |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/9509 | - |
dc.description.abstract | Background: The optimal timing for applying the BioFire FilmArray Pneumonia Panel (FAPP) in intensive care unit (ICU) patients with hospital-acquired pneumonia (HAP) or ventilator-associated pneumonia (VAP) remains undefined, and there are limited data on its impact on antimicrobial stewardship. Methods: This retrospective study was conducted at a referral hospital in Taiwan from November 2019 to October 2022. Adult ICU patients with HAP/VAP who underwent FAPP testing were enrolled. Patient data, FAPP results, conventional microbiological testing results, and the real-world impact of FAPP results on antimicrobial therapy adjustments were assessed. Logistic regression was used to determine the predictive factors for bacterial detection by FAPP. Results: Among 592 respiratory specimens, including 564 (95.3%) endotracheal aspirate specimens, 19 (3.2%) expectorated sputum specimens and 9 (1.5%) bronchoalveolar lavage specimens, from 467 patients with HAP/VAP, FAPP testing yielded 368 (62.2%) positive results. Independent predictors for positive bacterial detection by FAPP included prolonged hospital stay (odds ratio [OR], 3.14), recent admissions (OR, 1.59), elevated C-reactive protein levels (OR, 1.85), Acute Physiology and Chronic Health Evaluation II scores (OR, 1.58), and septic shock (OR, 1.79). Approximately 50% of antimicrobial therapy for infections caused by Gram-negative bacteria and 58.4% for Gram-positive bacteria were adjusted or confirmed after obtaining FAPP results. Conclusions: This study identified several factors predicting bacterial detection by FAPP in critically ill patients with HAP/VAP. More than 50% real-world clinical practices were adjusted or confirmed based on the FAPP results. Clinical algorithms for the use of FAPP and antimicrobial stewardship guidelines may further enhance its benefits. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Journal of Microbiology, Immunology and Infection | en_US |
dc.relation.ispartofseries | Original Article;480-489 | - |
dc.subject | Critically ill | en_US |
dc.subject | Intensive care unit | en_US |
dc.subject | Hospital-acquired pneumonia | en_US |
dc.subject | Ventilator-associated pneumonia | en_US |
dc.subject | Multiplex polymerase chain reaction | en_US |
dc.subject | Antimicrobial stewardship | en_US |
dc.title | Application of a multiplex molecular pneumonia panel and real-world impact on antimicrobial stewardship among patients with hospital-acquired and ventilatorassociated pneumonia in intensive care units | en_US |
dc.type | Article | en_US |
Appears in Collections: | Vol. 57 No. 3 (2024) |
Files in This Item:
File | Description | Size | Format | |
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480-489.pdf | 1.64 MB | Adobe PDF | View/Open |
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