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RESEARCH ARTICLE

Evaluation of self-collected urine dip swab method for detection of Chlamydia trachomatis

Anna-Maria Costa A D , Christopher K. Fairley B , Suzanne M. Garland A C and Sepehr N. Tabrizi A C
+ Author Affiliations
- Author Affiliations

A Department of Microbiology and Infectious Diseases, The Royal Women’s Hospital, Locked Bag 300, Parkville, Vic. 3052, Australia.

B Melbourne Sexual Health Centre, 580 Swanston Street, Carlton, Vic. 3053, Australia.

C Department of Obstetrics and Gynaecology, University of Melbourne, Parkville, Vic. 3052, Australia.

D Corresponding author. Email: annamaria.costa@thewomens.org.au

Sexual Health 6(3) 213-216 https://doi.org/10.1071/SH09013
Submitted: 4 February 2009  Accepted: 12 May 2009   Published: 3 August 2009

Abstract

Background: The present study is an evaluation of a self-collected urine dip (SCUD) swab as an alternative sampling method for the detection of Chlamydia trachomatis (CT) in urine samples that conforms to postal service regulations in Australia. Methods: Sixty urine samples, previously identified as CT positive were used to prepare SCUD swabs in vitro. In addition, replicate SCUD swabs were prepared from known CT positive urine samples and stored at room temperature, or sent through the postal system. All samples were tested for CT and an inhibition control using the Roche TaqMan 48 Real-time polymerase chain reaction system. Results: Overall, 58/60 (97%) SCUD swabs generated positive CT results. Triplicate SCUD swabs prepared from five known positive urine samples and stored up to 7 days at room temperature, showed positive results in all samples. Ten replicates of SCUD swabs from five known CT positive samples were also tested after being posted from different regions in Australia, with a transit time of 2–7 days, back to the Melbourne laboratory. There was 94% positivity of the SCUD swab samples. Conclusion: The present study demonstrated SCUD swabs to be a sensitive and robust method of self-collecting samples for detection of CT subsequent to sending the samples through the postal service.

Additional keywords: self-collected sampling, polymerase chain reaction, TaqMan 48.


Acknowledgements

The authors thank the staff of Molecular Microbiology at the Royal Women’s Hospital and Royal Children’s Hospital and also Stuart Gardiner and Elice Rudland for posting the swabs from different locations around Australia. Thanks also to Elya Moore for assistance with the statistical analysis.


References


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