Context: False-positive cultures for Mycobacterium tuberculosis have been found in nearly all DNA fingerprinting studies, but the effectiveness of interventions to reduce cross-contamination has not been evaluated.

Objective: To evaluate whether changes in laboratory policies and procedures reduced the rate of false-positive cultures.

Design: Retrospective study of isolates with matching DNA fingerprints.

Setting: A mycobacteriology laboratory serving an urban tuberculosis control program and public hospital system.

Patients: All M tuberculosis isolates processed from July 1994 to December 1999.

Methods: Isolates were fingerprinted using IS6110; pTBN12 was used to fingerprint isolates having fewer than 6 copies of IS6110. We further evaluated all patients having only one positive culture whose DNA fingerprint matched that of another isolate processed in the laboratory within 42 days.

Interventions: We changed laboratory policy to reduce the number of smear-positive specimens processed and changed laboratory procedures to minimize the risk of cross-contamination during batch processing.

Main Outcome Measure: The rate of false-positive cultures.

Results: Of 13 940 specimens processed during the study period, 630 (4.5%) from 184 patients and 48 laboratory proficiency specimens grew M tuberculosis. There were no cases (0/184) of probable or definite cross-contamination, compared with the 4% rate (8/199) identified in our previous study (P =.008). We also fingerprinted a convenience sample of isolates from other laboratories in Denver; 13.6% (3/22) of these were false-positive, a rate similar to the 11.9% rate (5/42) identified for other laboratories in our previous study (P =.84).

Conclusions: Laboratory cross-contamination decreased significantly after relatively simple, inexpensive changes in laboratory policies and practices. Cross-contamination continued to occur in other laboratories in Denver.

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Source
http://dx.doi.org/10.5858/2001-125-1213-TEOCILDOI Listing

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