HONG KONG INSTITUTE OF MEDICAL
LABORATORY SCIENCES
Quality Assurance Programme Limited
In
collaboration with
Public Health Laboratory Services Branch
Centre for Health Protection
External Quality Assessment Programme
in
Neisseria gonorrhoeae Susceptibility Testing
Survey materials
Reference material / well characterised
isolates
No. of survey materials
Two lyophilized cultures of Neisseria
gonorrhoeae
Frequency
Two times a year
Deadline for Return of Result
Two weeks after the dispatch of survey material
Quality Control of Survey Slides
Homogeneity Check
10% of the total no. of ampoules in each batch are randomly selected for homogeneity testing.?To pass the homogeneity test, all the PT
items tested for homogeneity should have ST results 100% matching the expected
sensitivity test results of the lyophilised GC culture being selected as PT
sample. If no growth was found in one ampoule, the intended ST results are
based on other ampoules. If more than two ampoules were found no growth during
the homogeneity test, the whole batch will be discarded.
Stability Check
10% of the ampoules are arranged to be
dispatched to Bacteriology Laboratory, PHLSB for stability checking.?If no growth was found in more than two
ampoules, or the susceptibility categories obtained differs from that in the
homogeneity testing, the survey samples will be recalled.
Test
requested
Antimicrobial susceptibility testing of the organisms to a panel of antimicrobial agents
Request for replacement samples
Participants can request a replacement of survey materials by submitting a formal request. The request form can be downloaded at:
http://www.hkimlsqap.org/Information/Form/Specimen Replacement Form.pdf
Criteria for Performance Evaluation of Neisseria gonorrhoeae
Susceptibility Testing
Timely Reporting
Participants are required to report the results before the due dates. Late return of slides will not be scored.
Scoring of Result
Scoring is expressed as the number of correct
results against the number of scored results. In general, participants' results
will be scored according to the susceptibility categories submitted as follows:
Preliminary Result
Intended results will be posted online 3 weeks after the dispatch of survey materials.
Survey Reports
Final report will be issued to the participants documenting the identities of samples dispatched, intended results, reported results, scores achieved against the antimicrobials used and the respective methods used for susceptibility tests. If there is a statistical difference in the performance for test methods used by each group of participants, this will be discussed. Late or nil return will be marked on the individual report of the participant. Year-end summaries of the total scores will be compiled and released.
Certificate of Participation
A certificate of participation will also be issued indicating the number of survey results returned timely.
Enquiry
Should there be any enquiry on the survey, participants are requested to contact HKIMLSQAP for assistance.
Appeal
Should there be any data discrepancy in the survey report or any
disagreement with the performance evaluation; participant can appeal to the
chairman of HKIMLSQAP for amendment and review.
(852) 2499 0015 [Phone]
(852) 2124 2798 [Fax]
info@hkimlsqap.org [Email]
The Chairman
Quality Assurance Programme Committee
Hong Kong Institute of Medical Laboratory Sciences Quality Assurance Programme Ltd.
Flat 1711, 17/F, Block C,
Last updated on 09 February 2014.