Christopher K. Fairley

Christopher K. Fairley

PhD; MB BS; FRACP, FAFPHM, FAChSHM; Fellow of Australian Academy of Health and Medical Sciences

Infectious Disease Specialist

Over 30 years of Experience

Male📍 Carlton

About of Christopher K. Fairley

Christopher K. Fairley is an Infectious Disease Specialist based in Carlton, Tasmania, at 580 Swanston Street, Carlton, TAS 3053, Australia. He looks after people with infections that can be tricky to manage, including infections of the skin, gut, airways, and the genital and sexual health area.


Over time, he’s built a steady practice for patients who need clear advice and a careful plan. That might be someone dealing with a common infection, or it could be a longer problem where symptoms keep coming back, or where there are a few different causes to work through. In many cases, he helps patients understand what’s going on, what to watch for, and how treatment fits into everyday life.


His work also includes care around sexually transmissible infections and related conditions. This can involve things like HIV/AIDS, hepatitis B and hepatitis C, and infections such as chlamydia, gonorrhoea, syphilis, genital herpes, and genital warts. He also works with issues like cervical changes and cervix-related problems, as well as pelvic inflammatory disease and proctitis.


Infectious disease doesn’t only affect the genitals. He also treats a range of other infections, including pneumonia and viral illnesses such as COVID-19. Some patients come with stomach and gut symptoms, including diarrhoea and viral gastroenteritis. At times, he also sees people with concerns related to malnutrition or vitamin D deficiency where an infection or health changes may be part of the bigger picture.


Christopher has more than 30 years of experience. His training is backed by a mix of clinical and research qualifications, including MB BS, a PhD, and FRACP. He is also a Fellow of several specialist colleges and faculties, including the Australasian Faculty of Public Health Medicine and the Chapter of Sexual Health Medicine, and he is a Fellow of the Australian Academy of Health and Medical Sciences (2018).


He keeps up with current evidence through research and published work. He has also been involved in clinical trials, which helps bring new knowledge into care as it becomes available.


If you’re looking for a calm, practical approach to infections, Christopher aims to make the next steps feel clear. He focuses on helping patients move forward, step by step, with treatment and support that match their situation.

Education

  • MB BS (Bachelor of Medicine, Bachelor of Surgery)
  • PhD
  • FRACP – Fellow of the Royal Australasian College of Physicians (Infectious Diseases)
  • FAFPHM – Fellow of the Australasian Faculty of Public Health Medicine
  • FAChSHM – Fellow of the Chapter of Sexual Health Medicine
  • FRCP (Fellow of the Royal College of Physicians)
  • FAAHMS – Fellow of the Australian Academy of Health and Medical Sciences; 2018

Services & Conditions Treated

Anal CancerCervicitisChlamydiaGenital WartsGonorrheaHIV/AIDSHuman Papillomavirus InfectionLymphogranuloma VenereumProctitisSyphilisTrichomoniasisUrethritisWartsBalanitisCervical DysplasiaColorectal CancerCOVID-19Genital HerpesHepatitisHepatitis AMonkeypoxSevere Acute Respiratory Syndrome (SARS)TenesmusAminoaciduriaCervical CancerChancroidDiarrheaEctopic PregnancyFanconi Bickel SyndromeFanconi SyndromeHepatitis BHepatitis CMalnutritionMolluscum ContagiosumNeurosyphilisOral HerpesPelvic Inflammatory DiseasePenile CancerPerichondritisPneumoniaShigellosisVaginal Yeast InfectionViral GastroenteritisVitamin D DeficiencyVulvovaginitisYaws

Publications

5 total
Male-Partner Treatment to Prevent Recurrence of Bacterial Vaginosis.

The New England journal of medicine • March 05, 2025

Lenka Vodstrcil, Erica Plummer, Christopher Fairley, Jane Hocking, Matthew Law, Kathy Petoumenos, Deborah Bateson, Gerald Murray, Basil Donovan, Eric P Chow, Marcus Chen, John Kaldor, Catriona Bradshaw

Background: Bacterial vaginosis affects one third of reproductive-aged women, and recurrence is common. Evidence of sexual exchange of bacterial vaginosis-associated organisms between partners suggests that male-partner treatment may increase the likelihood of cure. Methods: This open-label, randomized, controlled trial involved couples in which a woman had bacterial vaginosis and was in a monogamous relationship with a male partner. In the partner-treatment group, the woman received first-line recommended antimicrobial agents and the male partner received oral and topical antimicrobial treatment (metronidazole 400-mg tablets and 2% clindamycin cream applied to penile skin, both twice daily for 7 days). In the control group, the woman received first-line treatment and the male partner received no treatment (standard care). The primary outcome was recurrence of bacterial vaginosis within 12 weeks. Results: A total of 81 couples were assigned to the partner-treatment group, and 83 couples were assigned to the control group. The trial was stopped by the data and safety monitoring board after 150 couples had completed the 12-week follow-up period because treatment of the woman only was inferior to treatment of both the woman and her male partner. In the modified intention-to-treat population, recurrence occurred in 24 of 69 women (35%) in the partner-treatment group (recurrence rate, 1.6 per person-year; 95% confidence interval [CI], 1.1 to 2.4) and in 43 of 68 women (63%) in the control group (recurrence rate, 4.2 per person-year; 95% CI, 3.2 to 5.7), which corresponded to an absolute risk difference of -2.6 recurrences per person-year (95% CI, -4.0 to -1.2; P<0.001). Adverse events in treated men included nausea, headache, and metallic taste. Conclusions: The addition of combined oral and topical antimicrobial therapy for male partners to treatment of women for bacterial vaginosis resulted in a lower rate of recurrence of bacterial vaginosis within 12 weeks than standard care. (Funded by the National Health and Medical Research Council of Australia; StepUp Australian New Zealand Clinical Trials Registry number, ACTRN12619000196145.).

Preferences of men who have sex with men towards the distribution of HIV self-test kits through social networks: A discrete choice experiment.

ournal Of Acquired Immune Deficiency Syndromes (1999) • May 30, 2025

Ying Zhang, Eric Chow, Tiffany Phillips, Christopher Fairley, Jason Ong

Objective: Social network distribution of HIV self-test (HIVST) kits uses social networks to increase HIV testing among marginalized populations, such as men who have sex with men (MSM). Using a discrete choice experiment (DCE), we identified factors influencing influence MSM's willingness and decision-making in HIVST kit distribution. Methods: An online DCE survey was conducted among MSM in Australia (December 2023-May 2024) via online/offline advertisements. Methods: Participants completed seven choice sets, each containing two hypothetical scenarios for HIVST kits distribution described by attributes such as cost, location, training, support system, and self-reporting methods. Mixed logit models and latent class analysis explored preference heterogeneity across language (English vs. non-English first language) and nativity (Australian-born vs. overseas-born) groups. Results: There were 251 participants, including 140 overseas-born MSM, with a mean age of 36.5 (SD=11.9). Participants who did not speak English as their first language (29/251,12%) showed a lower preference for paid HIVST kits ($30 or $60 for three kits) and online video chats with sexual health professionals as pre-test support. Overseas-born participants preferred not to attend 30-minute or one-hour training sessions on distributing HIVST kits. They did not like accessing HIVST kits from hospitals. Class 1 ('Cost-conscious and minimal support seekers';61.7%) were willing to pay up to $30 for three kits, while Class 2 ('Subsidy-dependent and structured support seekers';38.3%) disliked costs and self-reporting results by phone. Conclusions: Increasing participation in social network distribution of HIVST kits will require free or subsidized kits. Tailored support systems should prioritise overseas-born MSM with limited English proficiency.

Evaluation of artificial intelligence (AI) chatbots for providing sexual health information: a consensus study using real-world clinical queries.

BMC Public Health • March 15, 2025

Phyu Latt, Ei Aung, Kay Htaik, Nyi Soe, David Lee, Alicia King, Ria Fortune, Jason Ong, Eric P Chow, Catriona Bradshaw, Rashidur Rahman, Matthew Deneen, Sheranne Dobinson, Claire Randall, Lei Zhang, Christopher Fairley

Background: Artificial Intelligence (AI) chatbots could potentially provide information on sensitive topics, including sexual health, to the public. However, their performance compared to nurses and across different AI chatbots, particularly in the field of sexual health, remains understudied. This study evaluated the performance of three AI chatbots - two prompt-tuned (Alice and Azure) and one standard chatbot (ChatGPT by OpenAI) - in providing sexual health information on questions that experienced sexual health nurses could correctly answer. Methods: We analysed 195 anonymised sexual health questions received by the Melbourne Sexual Health Centre phone line. A panel of experts in a blinded order using a consensus-based approach evaluated responses to these questions from nurses and the three AI chatbots. Performance was assessed based on overall correctness and five specific measures: guidance, accuracy, safety, ease of access, and provision of necessary information. We conducted subgroup analyses for clinic-specific (e.g., opening hours) and general sexual health questions and a sensitivity analysis excluding questions that Azure could not answer. Results: Alice demonstrated the highest overall correctness (85.2%; 95% confidence interval (CI), 82.1-88.0%), followed by Azure (69.3%; 95% CI, 65.3-73.0%) and ChatGPT (64.8%; 95% CI, 60.7-68.7%). Prompt-tuned chatbots outperformed the base ChatGPT across all measures. Among all outcome measures, all chatbots performed best on safety, with Azure achieving the highest safety score (97.9%; 95% CI, 96.4-98.9%), indicating the lowest risk of providing potentially harmful advice. In subgroup analysis, all chatbots performed better on general sexual health questions compared to clinic-specific queries. Sensitivity analysis showed a narrower performance gap between Alice and Azure when excluding questions Azure could not answer. Conclusions: Prompt-tuned AI chatbots demonstrated superior performance in providing sexual health information compared to base ChatGPT, with high safety scores particularly noteworthy. However, all AI chatbots showed susceptibility to generating incorrect information. These findings suggest the potential for AI chatbots as adjuncts to human healthcare providers for providing sexual health information while highlighting the need for continued refinement and human oversight. Future research should focus on larger-scale evaluations and real-world implementations.

Do Australian sexual health clinics have the capacity to meet demand? A mixed methods survey of directors of sexual health clinics in Australia.

Sexual Health • February 21, 2025

Christopher Fairley, Jason Ong, Lei Zhang, Rick Varma, Louise Owen, Darren Russell, Sarah Martin, Joseph Cotter, Caroline Thng, Nathan Ryder, Eric P Chow, Tiffany Phillips, For Australian Sti Research Group

Background The study describes the capacity of publicly funded sexual health clinics in Australia and explores the challenges they face. Methods We sent a survey to the directors of publicly funded sexual health clinics across Australia between January and March 2024. The survey asked about how their clinics were managing the current clinical demand. Results Twenty-seven of 35 directors of sexual health clinics responded. These 27 clinics offered a median of 35 (IQR: 20-60) bookings each day, but only a median of 10 (IQR: 2-15) walk-in consultations for symptomatic patients. The average proportion of days that clinics were able to see all patients who presented with symptoms was 70.1% (95% CI 55.4, 84.9) during summer versus 75.4% (95% CI 62.2, 88.5) during winter. For patients without symptoms, the corresponding proportions were 53.3% (95% CI 37.9, 68.8) during summer versus 57.7% (95% CI 41.7, 73.7) during winter. If these percentages were adjusted for the number of consultations that the clinic provided, then the corresponding numbers for symptomatic individuals was 51.0% for summer and 65.2% for winter, and for asymptomatic individuals it was 48.1% and 49.8%, respectively. The catchment population of the clinics for each consultation they provided ranged from as low as 3696 to a maximum of 5 million (median 521,077). Conclusions The high proportion of days on which sexual health clinics were not able to see all patients is likely to delay testing and treatment of individuals at high risk of STIs and impede effective STI control.

Efficacy and tolerability of the combination of minocycline and metronidazole for macrolide-resistant Mycoplasma genitalium.

The Journal Of Antimicrobial Chemotherapy • February 18, 2025

Kay Htaik, Lenka Vodstrcil, Erica Plummer, Laura Matthews, Ivette Aguirre, Eric P Chow, Christopher Fairley, Catriona Bradshaw

Objective: Curing Mycoplasma genitalium is challenging in the context of rising antimicrobial resistance and limited therapeutic options. There is an urgent need for globally relevant and effective treatment options using readily available and affordable agents. From September 2021 to August 2024 at Melbourne Sexual Health Centre, we prospectively evaluated microbial cure and tolerability of oral minocycline 100 mg combined with metronidazole 400 mg (twice daily for 14 days) for individuals with macrolide-resistant M. genitalium in whom fluroquinolones had failed or were not advised. Methods: Microbial cure was defined as a negative test of cure (TOC) using transcription-mediated amplification 14-90 days after completing the regimen. The proportion cured and 95% confidence intervals (CIs) were calculated. Data on side effects and adherence were collected at TOC visits. Results: Microbial cure in patients receiving the combination regimen was 80.8% (95% CI: 71.9-87.8%). Cure in those who had received preceding doxycycline was 90.3% (n = 28/31, 95% CI: 74.2-98.0%) compared to 76.7% (n = 56/73, 95% CI: 65.4-85.8%) in those who had not, P = 0.172. Central nervous system and gastrointestinal side effects were commonly reported. Conclusions: Minocycline with metronidazole cured 80% of macrolide-resistant infections in this cohort. Cure may be enhanced by the use of doxycycline before the combination regimen but larger studies are needed. Given limited options for treating resistant M. genitalium infections, the combined minocycline and metronidazole regimen may represent a promising option where no alternative drugs are available, or quinolones are contraindicated. Clinicians should be aware of and discuss side effects with patients.

Clinical Trials

2 total

Impact of the Daily Doxycycline Pre-exposure Prophylaxis (PrEP) on the Incidence of Syphilis, Gonorrhoea and Chlamydia

Active_not_recruiting

1. This study is a non-randomized observational cohort trial using before and after comparison to evaluate intervention 2. It would mimic the conditions that would occur outside a clinical trial. 2. After consent and enrolment, all procedures will be guided by the Australian STI Management Guidelines. 3. All enrolling participants will be offered daily doxycycline 100mg 4. All participants will be invited to complete a survey in every 3 months time for 12 months dated from participation. 5. All follow-up information will be collected through electronic data capture to allow accurate and timely analyses. 6. Data collection will be from (i) medical records (ii) online self-completed questionnaire

Participants: 100

Human Papillomavirus (HPV) Infection in Young Men Who Have Sex With Men Following Introduction of Universal Male HPV Vaccination Program in Australia

Completed

Australia was one of the countries to implement a universal school-based male vaccination program - in 2013. This research project will examine the prevalence of HPV among young men who have sex with men (MSM) who have been offered school-based HPV vaccination.

Participants: 200

Frequently Asked Questions

What services does Dr Christopher K. Fairley provide?
Dr Fairley offers a wide range of infectious disease and related services, including care for HIV/AIDS, hepatitis, HPV infections, sexually transmitted infections like chlamydia, gonorrhea, syphilis, trichomoniasis, genital herpes and warts, Pelvic inflammatory disease, cervical dysplasia, colorectal cancer screening, and other conditions such as monkeypox, COVID-19, pneumonia and more.
Which conditions can I see Dr Fairley for?
He treats infectious diseases and related health issues, including HIV/AIDS, hepatitis B and C, HPV infections, syphilis, gonorrhea, chlamydia, genital herpes, warts, pelvic inflammatory disease, cervical dysplasia, colorectal cancer considerations, monkeypox, and other infections and respiratory conditions.
How do I book an appointment with Dr Fairley?
Appointments are made through his practice at 580 Swanston Street, Carlton, TAS 3053, Australia. If you need specifics on availability, contact the clinic directly.
Do you offer care in person or online?
The information provided lists the clinic address for in-person care. For details about telehealth or online options, please contact the clinic directly to confirm what’s available.
What should I bring to my first visit?
Bring any relevant medical history, current medications, test results, and a list of symptoms or concerns you want to discuss. If you have a previous infectious disease diagnosis, bring that information as well.
Who is Dr Christopher K. Fairley and what is his background?
Dr Fairley is an Infectious Disease Specialist with over 30 years of experience. He holds MB BS, PhD, FRACP, FAFPHM, FAChSHM and is a Fellow of several professional bodies.