Accuracy of the BD MAX™ vaginal panel in the diagnosis of infectious vaginitis
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The aim of this study was to evaluate the BD MAX™ vaginal panel in the diagnosis of bacterial vaginosis (BV), vulvovaginal candidiasis (VVC), and trichomoniasis by comparing it with conventional methods: (i) combination of Hay criteria and presence of clue cells with predominant growth of Gardnerella vaginalis, (ii) yeast culture, and (iii) combination of culture, wet mount microscopic examination, and an alternative molecular assay. One thousand vaginal samples of women ≥ 14 years were analyzed; 5% of the samples belonged to pregnant women. 19.3% were classified as BV, in 33.6% yeasts were recovered and in 1.5% TV was detected. For BV, sensitivity and specificity were of 89.8% and 96.5%, respectively; for VVC, sensitivity and specificity were of 97.4% and 96.8%, respectively, and for T. vaginalis, the sensitivity and specificity were of 100%. The BD MAX™ vaginal panel is highly sensitive and specific and simplifies the identification of infectious vaginitis.
KeywordsBacterial vaginosis Gardnerella vaginalis Vulvovaginal candidiasis Trichomonas vaginalis Vaginitis BD MAX vaginal panel
Compliance with ethical standards
Conflict of interest
A. Canut-Blasco reports personal fees from Pfizer, Merck, Roche, and Werfen unrelated to the current study. All other authors declare that they have no conflict of interest.
For this type of study, formal consent is not required.
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