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RESEARCH ARTICLE

Genital Chlamydia trachomatis infection

Evan Freeman A , Basil Donovan B C and Katherine Brown D E
+ Author Affiliations
- Author Affiliations

A NSW Public Health Officer Training Program, NSW Department of Health

B National Centre in HIV Epidemiology and Clinical Research, The University of New South Wales

C The Sydney Sexual Health Centre, Sydney Hospital

D South Eastern Sydney Illawarra Area Health Service

E The University of Wollongong

NSW Public Health Bulletin 21(12) 268-269 https://doi.org/10.1071/NB10053
Published: 8 March 2011

Chlamydia trachomatis is one of three species of Chlamydiae that commonly cause disease in humans. It is responsible for ano-genital and conjunctival (conjunctivitis and trachoma) infections. Infant conjunctivitis and pneumonia can result from maternal genital infection.1 C. trachomatis serovars D–K are responsible for most sexually-acquired genital infections. Serovar L2 causes a severe proctolitis or genital ulcer lymphadenopathy syndrome known as lymphogranuloma venereum which is beginning to reappear in Australia among men who have sex with men.2

Chlamydia is a notifiable condition in New South Wales (NSW) under the Public Health Act 1991. There were 14 947 laboratory-confirmed cases notified in 2009. Known as the ‘silent disease’, it is the most reported sexually transmissible infection (STI) in Australia, the United States, the United Kingdom and Canada. Due to the mainly asymptomatic nature of chlamydia, chronic infection and re-infection are common,3 highlighting the importance of screening.4 People aged less than 25 years have the highest rates of infection.


Symptoms

Most infected people are asymptomatic (70% of women and 90% of men). Symptoms that may occur during acute infections include urethral discharge and discomfort on urination (dysuria). Men may also develop painful swollen testes (epididymitis). Women occasionally report dysuria or bleeding between periods. Deep pain during sexual intercourse and lower abdominal pain in women suggest pelvic inflammatory disease from ascending infection. Pelvic inflammatory disease increases the risk of subsequent ectopic pregnancy and infertility.3 Either gender can develop reactive arthritis, associated with mucocutaneous lesions.


Testing

Ano-genital tract infection can be detected using self-collected vaginal or anal swabs or a urine specimen. Self-collected specimens have lowered the barriers to testing. A clinician may collect a cervical swab if a woman has symptoms or as part of a pap test. A variety of nucleic acid amplification tests are also used, with sensitivities in the range of 85–97% and specificities exceeding 99%.


Treatment

Uncomplicated ano-genital infection is treated with a single oral dose of azithromycin.1 Complicated infections (pelvic inflammatory disease and epididymitis) and lymphogranuloma venereum require treatment with doxycycline for a minimum of 14 days; other antibiotics are also often required.5


Re-infection and contact tracing

While cure rates are high (>95%), re-infection rates are also high (approximately 30%). Therefore, people treated for chlamydia should be retested after 12 weeks of treatment. As infected sexual partners are typically asymptomatic, they often do not present for contact testing and treatment. The value and legality of dispensing a second dose of azithromycin for the patient to deliver to their partner(s) (patient-delivered partner therapy) has been recommended for review in Australia.6


The Australian Collaboration for Chlamydia Enhanced Sentinel Surveillance (ACCESS) Project

The Commonwealth-funded ACCESS Project has been established in response to increasing numbers of chlamydia notifications, with the possibility that much of the increase could be due to increased testing.7 Priority populations requiring ongoing surveillance include Aboriginal and Torres Strait Islanders, young heterosexuals, men who have sex with men, and sex workers. An early impression determined through this pilot sentinel surveillance is that rates of chlamydia may not be rising as quickly as the notification data suggest.


Fast-track treatment: using patient-delivered partner therapy to reduce chlamydia prevalence

Patient-delivered partner therapy has been considered because of the increasing number of diagnoses and the concern that current clinical treatment systems are not slowing the spread of disease. This process includes the patient providing advice to their partner about the nature of chlamydial infection, testing and treatment.

It is believed to work best when clients are selected; avoiding high-risk populations where other STIs and bloodborne viruses may be of concern (e.g. injecting drug users and men who have sex with men). The Centers for Disease Control and Prevention in the United States has included this option within its current guidelines for STI management.



References

[1]  Heymann DL, editor. Control of Communicable Diseases Manual. 19th ed. Washington: American Public Health Association; 2008.

[2]  Stark D, van Hal S, Hillman R, Harkness J, Marriott D. Lymphogranuloma venereum in Australia: anorectal Chlamydia trachomatis serovar L2b in men who have sex with men. J Clin Microbiol 2007; 45 1029–31.
Lymphogranuloma venereum in Australia: anorectal Chlamydia trachomatis serovar L2b in men who have sex with men.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2s7jsVeqsg%3D%3D&md5=6adb45d503770ea56321795a25d7774cCAS | 17251405PubMed |

[3]  Cretikos M, Davies S, Brotherton A. Chlamydia, gonorrhoea and syphilis. N S W Public Health Bull 2006; 17 86–7..
| 17036087PubMed |

[4]  Geisler WM, Wang C, Morrison SG, Black CM, Bandea CI, Hook EW. The natural history of untreated Chlamydia trachomatis infection in the interval between screening and returning for treatment. Sex Transm Dis 2008; 35 119–23.
The natural history of untreated Chlamydia trachomatis infection in the interval between screening and returning for treatment.Crossref | GoogleScholarGoogle Scholar | 17898680PubMed |

[5]  Centers for Disease Control and Prevention. Updated recommended treatment regimens for gonococcal infections and associated conditions – United States, April 2007. Available from: http://www.cdc.gov/std/treatment/2006/updated-regimens.htm (Cited 1 February 2010.)

[6]  McNulty A, Teh MF, Freedman E. Patient delivered partner therapy for chlamydial infection—what would be missed? Sex Transm Dis 2008; 35 834–6.
Patient delivered partner therapy for chlamydial infection—what would be missed?Crossref | GoogleScholarGoogle Scholar | 18580822PubMed |

[7]  Chen MY, Fairley CK, Donovan B. Nowhere near the point of diminishing returns: correlations between chlamydia testing and notification rates in New South Wales. Aust N Z J Public Health 2005; 29 249–53.
Nowhere near the point of diminishing returns: correlations between chlamydia testing and notification rates in New South Wales.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXitlWjsb4%3D&md5=e070329fdc90708029dc6e5a39beb7afCAS | 15991773PubMed |