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REPRODUCIBILITY OF LYSIS-CENTRIFUGATION CULTURES FOR QUANTIFICATION OF MYCOBACTERIUM-AVIUM COMPLEX BACTEREMIA
REPRODUCIBILITY OF LYSIS-CENTRIFUGATION CULTURES FOR QUANTIFICATION OF MYCOBACTERIUM-AVIUM COMPLEX BACTEREMIA JOURNAL OF CLINICAL MICROBIOLOGY Havlir, D., Kemper, C. A., Deresinski, S. C. 1993; 31 (7): 1794-1798Abstract
While quantitative mycobacterial blood cultures have been accepted as the standard for evaluating response to various Mycobacterium avium complex (MAC) treatment regimens, variability in this methodology has not been evaluated in a rigorous fashion. We thus studied the reproducibility of quantitative MAC cultures by a lysis-centrifugation culture system within and among five institutions. To measure the intralaboratory variation in mycobacterial colony counts, colony counts from duplicate blood specimens collected from 52 AIDS patients with MAC bacteremia were determined. Colony counts ranged from 0 to 50,000 CFU/ml. Nonparametric analyses revealed there was no significant difference in colony counts between the 52 duplicate specimens. The agreement between the intralaboratory paired specimens, as measured by the intraclass correlation coefficient, was 0.997. To measure the interlaboratory variation, multiple 10-ml aliquots from 12 patients were distributed to five institutions and processed within 24 to 32 h by lysis-centrifugation. For the 12 specimens distributed to the five laboratories, two-way analysis of variance for repeated measures revealed no significant difference in an individual patient's colony counts between laboratories (P > 0.2). We conclude that quantitation of mycobacterial colony counts by the lysis-centrifugation system is reproducible within and between institutions. Clinical trials evaluating response to therapeutic interventions for MAC can use multiple laboratories for quantitation of mycobacteremia. Furthermore, a 24- to 32-h delay in processing appeared to have no impact on reproducibility.
View details for Web of Science ID A1993LJ20100022
View details for PubMedID 8349755
View details for PubMedCentralID PMC265634