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Biofire pneumonia panel in lung donors: faster detection but limited pathogens
Authors:Anh Nguyen  Joy Chen  Erin Isaza  Niel Panchal  Fred Deiter  Jonathan Hoover  Binh Trinh  Steve R. Hays  Jeffrey A. Golden  Jonathan P. Singer  Marek Brzezinski  John R. Greenland  Jasleen Kukreja
Affiliation:1. Department of Surgery, School of Medicine, University of California San Francisco, San Francisco, California, USA;2. Department of Medicine, School of Medicine, University of California San Francisco, San Francisco, California, USA;3. Department of Anesthesia and Perioperative Care, School of Medicine, University of California San Francisco, San Francisco, California, USA
Abstract:

Background

Culture of bronchoalveolar lavage (BAL) specimens takes time to report. We tested whether a molecular diagnostic test could accelerate donor lung assessment and treatment.

Methods

We compared BioFire Film Array Pneumonia Panel (BFPP) with standard of care (SOC) tests on lung allograft samples at three time points: (1) donor BAL at organ recovery, (2) donor bronchial tissue and airway swab at implantation, and (3) first recipient BAL following lung implantation. Primary outcomes were the difference in time to result (Wilcoxon signed-ranked tests) and the agreement in results between BFPP and SOC assays (Gwet's agreement coefficient).

Results

We enrolled 50 subjects. In donor lung BAL specimens, BFPP detected 52 infections (14 out of 26 pathogens in the panel). Viral and bacterial BFPP results were reported 2.4 h (interquartile range, IQR 2.0–6.4) following BAL versus 4.6 h (IQR 1.9–6.0, p = 0.625) for OPO BAL viral SOC results and 66 h (IQR 47–87, p < .0001) for OPO BAL bacterial SOC results. Although there was high overall agreement of results between BAL–BFPP versus OPO BAL–SOC tests (Gwet's AC p < .001 for all), the level of agreement differed among 26 pathogens designed in BFPP and differed by types of specimens. BFPP could not detect many infections identified by SOC assays.

Conclusions

BFPP decreased time to detection of lung pathogens among donated lungs, but it cannot replace SOC tests due to the limited number of pathogens in the panel.
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Keywords:molecular diagnostic  lung transplant  pathogen detection
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