Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/120841
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Type: Journal article
Title: A reliable and easy to transport quality control method for chlamydia and gonorrhoea molecular point of care testing
Author: Badman, S.G.
Causer, L.M.
Guy, R.
Wand, H.
Donovan, B.
Tabrizi, S.N.
Speers, D.
Shephard, M.D.
Vallely, A.
Whiley, D.
Kaldor, J.
Wilson, D.
Regan, D.
Ward, J.
Fairley, C.K.
Hengel, B.
Tangey, A.
Anderson, D.
Natoli, L.
Atkinson, D.
Citation: Pathology, 2018; 50(3):317-321
Publisher: Elsevier
Issue Date: 2018
ISSN: 0031-3025
1465-3931
Statement of
Responsibility: 
S. G. Badman, L. M. Causer, R. Guy, H. Wand, B. Donovan, S. N. Tabrizi, D. Speers, M. D. Shephard, A. Vallely, D. Whiley
Abstract: Quality control (QC) is an essential component of point-of-care testing programs. In the context of a randomised-controlled trial (TTANGO) using GeneXpert (Xpert) Chlamydia trachomatis and Neisseria gonorrhoeae (CT/NG) point-of-care testing in remote areas of Australia, we aimed to develop and utilise a stable positive control material. Bacterial cultures of CT and NG were resuspended together to provide cycle threshold (Ct) values of approximately 25 cycles for both CT and NG when tested on the Xpert CT/NG assay. These positive control suspensions were dried in aliquots, heat inactivated, and then provided to 12 participating health services as research-only QC samples in kit form. At each service, a QC sample was resuspended and tested each month on the Xpert. QC results, including Xpert Ct values, were analysed from each site over 30 months and we calculated costs per QC sample. Overall, at 12 health services there were 89 QC samples tested (average of 8 tests per site per year). Mean Ct values for the 89 controls samples were 25.25 cycles (SD = 1.15) for CT, 24.04 cycles (SD = 1.400) for one NG target and 23.35 cycles (SD = 1.55) for the other NG target. No significant differences in Ct value for CT or NG controls were observed over a trial period of 30 months. Positive QC samples for research use in a trial of a molecular point-of-care assay were inexpensive to produce and stable when stored at 2-8°C. For routine use, additional requirements such as meeting National Association of Testing Authority (NATA) regulations and Therapeutic Goods Administration (TGA) approval will need to be achieved.
Keywords: TTANGO investigators
Humans
Chlamydia Infections
Gonorrhea
Specimen Handling
Molecular Diagnostic Techniques
Nucleic Acid Amplification Techniques
Quality Control
Point-of-Care Testing
Rights: © 2017 Royal College of Pathologists of Australasia. Published by Elsevier B.V. All rights reserved.
DOI: 10.1016/j.pathol.2017.09.012
Grant ID: http://purl.org/au-research/grants/nhmrc/109902
http://purl.org/au-research/grants/nhmrc/1092503
Published version: http://dx.doi.org/10.1016/j.pathol.2017.09.012
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