Clinical evaluation of the newly formatted lateral‐flow device for invasive pulmonary aspergillosis
Pulmonary aspergillosis
DOI:
10.1111/myc.12704
Publication Date:
2017-09-18T15:06:45Z
AUTHORS (6)
ABSTRACT
The study evaluated the newly formatted Aspergillus-specific lateral-flow-device (LFD), and compared its performance to original prototype "old" LFD test using BALF samples from 28 patients (14 with probable/proven invasive pulmonary aspergillosis [IPA] 14 no evidence for IPA). A total of 10/14 (71%) IPA resulted positive new LFD, including 8/9 true-positive 2/5 false-negative results old LFD. All without negative LFD; specificity was significantly improved
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