Part
III: Culture
recording and reporting of laboratory results
Tuberculosis laboratories
must establish a uniform procedure for reporting culture results.
If laboratory findings are to be useful, they must be communicated
in ways that make sense to the different authorities: Health
care workers use the findings for the diagnosis and management
of tuberculosis; public health authorities use them for statistical
and epidemiological purposes, while tuberculosis managers use
the information to ensure that bacteriologically proven patients
are receiving appropriate chemotherapy.
Culture
procedures for tuberculosis bacteriology are notoriously time-consuming,
often taking weeks or months to complete. For this reason, interim
reports should be issued. The following schedule is recommended:
- If
the cultures have been contaminated, a report should
be sent out immediately and a repeat specimen requested
- If
cultures are positive and growth has been identified
as M. tuberculosis a report should be sent out immediately
- At
four weeks an interim report (optional) could be sent
out on all negative specimens, stating that another report
will be issued in the event of the specimen becoming positive
later on
- At
eight weeks a final report should be issued containing
all the data previously reported so that earlier interim reports
can be destroyed and only the final report retained in the
patients?
file
Culture reports should be
qualitative (ie. positive or negative) as well as quantitative
(ie. number of colonies isolated). The average number
of colonies on all the bottles/tubes per specimen should be
reported. The following scheme is recommended:
| Reading |
Report |
| No
growth |
Negative |
| 1-19
colonies |
Positive
(number of colonies) |
| 20-100 colonies |
Positive
(1+) |
| 100-200
colonies |
Positive
(2 +) |
| 200-500
colonies (almost confluent growth) |
Positive (3 +) |
| >500
colonies (confluent growth) |
Positive
(4 +) |
| Contaminated
|
Contaminated |
In
high tuberculosis prevalence countries more than 85% of disease
is due to M. tuberculosis and other mycobacteria rarely
are responsible for clinical disease. Also, the robust decontamination
techniques used favour the isolation of M. tuberculosis
while killing some of the more fragile mycobacteria. A positive
culture with the characteristics as described before can, therefore,
fairly safely be labelled as ?tubercle
bacilli?
and the recommended way of reporting is as follows:
?Cultivation
yielded __________ growth of mycobacteria with the characteristics
of tubercle bacilli?
Model
tuberculosis culture reports are presented in Annex 4.
Obviously,
all the technical details of each laboratory test cannot be
recorded on the reports, but they should be precisely outlined
in the laboratory manual and all the results must be noted in
the laboratory register. A copy of the completed final report
should be retained in the laboratory. When reading cultures
the following should be recorded in the laboratory register:
- Growth
rate (slow / rapid)
- Number
of colonies isolated
- Pigment production in the
colonies (none / present and colour)
- Colony
morphology (rough / smooth / shiny / flat)
- Results
of differential tests
A
model laboratory register is presented in Annex 5.
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