Home Infectious Disease Approach to trichomoniasis

Approach to trichomoniasis

Assessment of Trichomoniasis

ℹ️
Key Point: Trichomoniasis is often asymptomatic in both men and women, making systematic screening essential in high-risk populations including Aboriginal and Torres Strait Islander communities.

Clinical Presentation

Women

  • Vaginal discharge (frothy, yellow-green, malodorous) - 50-75% of cases
  • Vulvar irritation, pruritus, or burning
  • Dysuria and urinary frequency
  • Dyspareunia
  • Strawberry cervix (punctate haemorrhages) - pathognomonic but only 2% of cases
  • Asymptomatic - up to 50% of infected women

Men

  • Urethral discharge (usually scanty, clear/white)
  • Dysuria
  • Urethral irritation or tingling
  • Post-void dribbling
  • Asymptomatic - up to 90% of infected men
  • Complications: epididymitis, prostatitis (rare)
⚠️
Clinical Pearl: High index of suspicion required due to frequent asymptomatic presentation. Consider in all patients with urogenital symptoms and sexual risk factors.

Risk Factors

High-Risk Populations
  • Multiple sexual partners or new sexual partner
  • Previous STI history
  • Aboriginal and Torres Strait Islander people
  • Young people aged 15-29 years
  • Sex workers
  • Men who have sex with women (MSW) in high-prevalence areas
  • Partners of infected individuals
  • Incarcerated populations
  • Drug users

Diagnostic Investigations

  • Essential
    Nucleic Acid Amplification Test (NAAT)
    First-line diagnostic test. Available at all Australian pathology laboratories. Superior sensitivity and specificity compared to microscopy or culture. Can be performed on urine, vaginal swab, or cervical swab.
  • Available
    Wet Mount Microscopy
    Point-of-care test if available. Look for motile trichomonads. Sensitivity only 60-70% in women, 40-60% in men. Must be examined within 10 minutes of collection.
  • Available
    Culture
    Traditional gold standard but slower turnaround (2-7 days). Less sensitive than NAAT but useful for antimicrobial resistance testing if treatment failure occurs.
  • Essential
    Comprehensive STI Screen
    Test for chlamydia, gonorrhoea, syphilis, HIV, and hepatitis B as co-infections are common. Consider herpes simplex testing if ulcerative lesions present.
  • Available
    Vaginal pH Testing
    pH >4.5 supportive of trichomoniasis but non-specific. Can help differentiate from candidiasis (pH typically <4.5).

Specimen Collection

1
Women
Self-collected vaginal swab (preferred) or clinician-collected vaginal/cervical swab. First-catch urine acceptable but less sensitive than vaginal specimens.
2
Men
First-catch urine (preferred) or urethral swab. Collect at least 2 hours after last urination. Urethral swabs more sensitive but less acceptable to patients.
3
Transport
Transport specimens at room temperature within 24 hours. For remote areas, NAAT specimens stable for 48-72 hours at room temperature.

Differential Diagnosis

Bacterial Vaginosis
Fishy odour, thin grey discharge, clue cells on microscopy
Vulvovaginal Candidiasis
Thick white discharge, intense pruritus, pH <4.5
Chlamydia/Gonorrhoea
Often asymptomatic, may present with similar urogenital symptoms
Non-specific Urethritis
Male urethral symptoms without identifiable pathogen
🚨
Critical: Always test sexual partners and consider expedited partner therapy. Untreated partners are the primary cause of reinfection.

Testing in Special Populations

🤰 Pregnancy
NAAT Testing Safe and preferred. Associated with preterm birth, low birth weight, and PROM if untreated.
Screening Consider routine screening in high-risk pregnancies, especially ATSI women.
🏴 ATSI Communities
Enhanced Screening Higher prevalence rates. Consider annual screening for sexually active individuals.
Point-of-Care Utilise rapid NAAT where available to improve treatment completion rates.
👶 Adolescents
Confidential Testing Can consent to STI testing from age 14+ in most states. Ensure privacy and confidentiality.
Self-Collection Vaginal self-swabs preferred to reduce examination anxiety and improve acceptability.

Treatment of Trichomoniasis

First-Line Antimicrobial Therapy

Recommended: Metronidazole is the first-line treatment for trichomoniasis with excellent efficacy and PBS availability.
💊
Metronidazole
Flagyl® · Metrogyl® · First-line therapy
Adult Dose 2g single dose OR 400mg BD for 7 days
Paediatric 15mg/kg/dose BD (max 400mg BD) for 7 days
Route Oral
Frequency Single dose or twice daily
Duration Single dose or 7 days
Renal Adj. No adjustment required
Hepatic Adj. Reduce dose 50% in severe impairment
PBS Status ✓ PBS General Benefit
⚠️
Alcohol Interaction: Advise patients to avoid alcohol during treatment and for 48 hours after completion due to disulfiram-like reaction.

Alternative Antimicrobial Therapy

💊
Tinidazole
Fasigyn® · Alternative nitroimidazole
Adult Dose 2g single dose OR 500mg BD for 5 days
Paediatric 50mg/kg single dose (max 2g) for children >12 years
Route Oral
Frequency Single dose or twice daily
Duration Single dose or 5 days
Renal Adj. No adjustment required
Hepatic Adj. Reduce dose in severe impairment
PBS Status ⚡ PBS Restricted Benefit

Treatment Considerations

1
Partner Treatment
Treat all sexual partners simultaneously to prevent reinfection. Contact tracing for partners within 60 days of diagnosis.
2
Sexual Abstinence
Abstain from sexual activity until both patient and partner(s) complete treatment and are asymptomatic for 1 week.
3
Co-infection Screening
Test for other STIs including chlamydia, gonorrhoea, syphilis, HIV, and hepatitis B as appropriate.

Treatment Failure and Resistance

🚨
Treatment Failure: Consider resistance if symptoms persist after appropriate treatment. Exclude reinfection first.
💊
High-Dose Metronidazole
For treatment failure
Adult Dose 400mg TDS for 7 days OR 2g daily for 3-5 days
Duration 7 days (first attempt) or 3-5 days (second attempt)
Monitoring Monitor for peripheral neuropathy with prolonged use
PBS Status ✓ PBS General Benefit

Special Populations

🤰 Pregnancy
Metronidazole Safe in all trimesters. Use 400mg BD for 7 days (avoid single high dose)
Tinidazole Avoid in first trimester; safe in second and third trimesters
👶 Paediatrics
Metronidazole 15mg/kg BD for 7 days (max 400mg BD). Safe from birth
Consideration Investigate for sexual abuse in prepubertal children
👴 Elderly
Dosing Standard adult doses appropriate. Monitor for side effects
Interactions Check for warfarin interactions - may need INR monitoring
🫘 Renal Impairment
Metronidazole No dose adjustment required for mild-moderate impairment
Dialysis Removed by dialysis - give after dialysis session
🔥 Hepatic Impairment
Metronidazole Reduce dose by 50% in severe hepatic impairment
Monitoring Monitor for accumulation and adverse effects
🛡️ Immunocompromised
Treatment Standard regimens effective. May need longer courses
Follow-up More frequent follow-up and test of cure recommended

Monitoring Parameters

Baseline
Clinical Assessment: Symptom severity, partner status, co-infections
Baseline Tests: STI screen, consider pregnancy test
During Treatment
Adherence: Counsel on completion of full course
Alcohol Avoidance: Emphasise no alcohol during and 48 hours after treatment
1 Week Post-Treatment
Clinical Review: Symptom resolution, partner treatment confirmation
Sexual Activity: Safe to resume if asymptomatic and partner treated
4-6 Weeks
Test of Cure: Only if symptoms persist or high-risk patients
Repeat STI Screening: 3 months for high-risk patients

PBS Status Summary

References

  • 01
    World Health Organization. Global health sector strategy on sexually transmitted infections 2016-2021: toward ending STIs. Geneva: WHO Press; 2016. Available at: https://www.who.int/publications/i/item/WHO-RHR-16.09
  • 02
    Kissinger P. Trichomonas vaginalis: a review of epidemiologic, clinical and treatment issues. BMC Infectious Diseases. 2015;15:307. doi:10.1186/s12879-015-1055-0
  • 03
    Australian Government Department of Health. National Notifiable Diseases Surveillance System Annual Report 2022. Canberra: Commonwealth of Australia; 2023. Available at: https://www.health.gov.au/resources/publications/nndss-annual-report-2022
  • 04
    Workowski KA, Bachmann LH, Chan PA, et al. Sexually Transmitted Infections Treatment Guidelines, 2021. MMWR Recommendations and Reports. 2021;70(4):1-187. doi:10.15585/mmwr.rr7004a1
  • 05
    Schwebke JR, Burgess D. Trichomoniasis. Clinical Microbiology Reviews. 2004;17(4):794-803. doi:10.1128/CMR.17.4.794-803.2004
  • 06
    Australian Sexual Health Alliance. Australian STI Management Guidelines for use in Primary Care. Sydney: ASHA; 2018. Available at: http://www.sti.guidelines.org.au
  • 07
    Van Der Pol B, Williams JA, Orr DP, et al. Prevalence, incidence, natural history, and response to treatment of Trichomonas vaginalis infection among adolescent women. Journal of Infectious Diseases. 2005;192(12):2039-2044. doi:10.1086/498217
  • 08
    Silver BJ, Guy RJ, Kaldor JM, et al. Trichomonas vaginalis as a cause of perinatal morbidity: a systematic review and meta-analysis. Sexually Transmitted Diseases. 2014;41(6):369-376. doi:10.1097/OLQ.0000000000000134
  • 09
    Australian Government Department of Health. Pharmaceutical Benefits Scheme Online. Available at: https://www.pbs.gov.au/browse/body-system
  • 10
    Cudmore SL, Delgaty KL, Hayward-McClelland SF, et al. Treatment of infections caused by metronidazole-resistant Trichomonas vaginalis. Clinical Microbiology Reviews. 2004;17(4):783-793. doi:10.1128/CMR.17.4.783-793.2004
  • 11
    Australian Institute of Health and Welfare. The health and welfare of Australia's Aboriginal and Torres Strait Islander peoples 2015. Cat. no. IHW 147. Canberra: AIHW; 2015.
  • 12
    Shafii T, Radolf JD, Sanchez PJ, et al. Mucopurulent cervicitis, urethritis, and vulvovaginitis. Infectious Disease Clinics of North America. 2013;27(4):793-819. doi:10.1016/j.idc.2013.08.004
  • 13
    Muzii L, Marana R, Caruana P, et al. Postoperative enteric infections after hysterectomy: role of prophylactic treatment. Clinical and Experimental Obstetrics & Gynecology. 2000;27(1):37-39.
  • 14
    Soper DE, Bump RC, Hurt WG. Bacterial vaginosis and trichomoniasis vaginitis are risk factors for cuff cellulitis after abdominal hysterectomy. American Journal of Obstetrics and Gynecology. 1990;163(3):1016-1021. doi:10.1016/0002-9378(90)91118-S
  • 15
    Australian Commission on Safety and Quality in Health Care. NSQHS Standards. Sydney: ACSQHC; 2017. Available at: https://www.safetyandquality.gov.au/standards/nsqhs-standards
Medication PBS Status Authority Required Cost to Patient
Metronidazole 400mg tablets