Relationship between conventional culture and flow cytometry for the diagnosis of urinary tract infection

Abstract Background Urine culture is the gold standard for the diagnosis of urinary tract infections (UTI). The use of flow cytometry analyzers (FCA) prior to culture allows for the quantification and recognition of cell components in urine to be automated and makes it possible to relate these data to the urine pathogens subsequently identified in cultures. Methods Urine samples were assessed with the Sysmex UF-1000i analyzer. Those that met the criteria for culture (> 25 leukocytes/μL or > 385 bacteria/μL) were subjected to quantitative urine culture on chromogenic agar. Counts of red blood cells (RBC), white blood cells (WBC), epithelial cells (EC), and the kind of microorganisms identified in cultures were evaluated. Results A total of 17,483 samples were processed by FCA. Of these, 9057 met the criteria for culture. Urine cultures were reduced by 48.2%. The most common urine pathogen was Escherichia coli (60.3%). Negative urine cultures were significantly ( p E. coli , Klebsiella spp. and Proteus spp. , but urine with Enterococcus spp. had a lower WBC than negative urine. Contaminated urine had a significantly ( p E. coli , Klebsiella spp. and Proteus spp. , but no differences were found for Enterococcus spp . ( p  = 0.729). Negative urine cultures had significantly ( p p E. coli and Klebsiella spp. , in comparison with cultures with Enterococcus spp. ( p  = 0.091) and Proteus spp. ( p  = 0.251). Conclusion The use of the Sysmex UF-1000i flow cytometer for screening urine samples allows for a reduction in the number of urine cultures. WBC values correlate well with the main urine pathogens related to UTI. The results observed for Enterococcus spp. suggest a low impact of these pathogens as a cause of UTI.