STBBI prevention guide: STBBI management
This guide includes an overview of practices for the treatment and follow-up of sexually transmitted and blood-borne infections (STBBI) by healthcare professionals practicing in public health or primary care settings.
Last partial content update: November 2025
Content about vaccination and HIV pre- and post-exposure prophylaxis (HIV PrEP and HIV PEP) were moved to the new biomedical prevention page of the STBBI prevention guide.
U=U messaging was edited to align with the content in other Canada.ca pages.
Linked resources were updated.
This information is captured in the table of updates to the guides.
On this page
- Management of STI syndromes
- Treatment of diagnosed STBBI
- Follow-up
- Reporting and partner notification
- References
Management of STI syndromes
A syndromic approach refers to the management of an individual based on signs and symptoms, prior to laboratory confirmation of the etiologic agent(s). Some syndromes are commonly associated with sexually transmitted infections (STI) and the determination of the most likely etiologic agent(s) should be based on the evaluation of the likelihood that the individual acquired an STI.
Laboratory testing should be done to confirm infection when there are signs and symptoms that are consistent with an STI or the individual has a sexual partner who has been diagnosed with an STI. Refer to the STI-associated Syndromes guide for an overview of the management of the following STI-associated syndromes: anogenital ulcers, cervicitis, epididymitis, pelvic inflammatory disease (PID), proctitis, urethritis and vaginitis.
Individuals who require advanced diagnostics or hospitalization should be cared for in consultation with an experienced colleague or referred to a specialist.
Treatment of diagnosed STBBI
Treatment objectives depend on the specific pathogen and whether the infection is curable (e.g. bacterial, HCV) or chronic and manageable (e.g. HSV, HBV, HIV).
For confirmed cases of sexually transmitted and blood-borne infections (STBBI), refer to the etiology-specific guide(s) for guidance on:
- Management and treatment
- Test of cure (TOC) and follow-up
- Reporting requirements
- Notification and treatment of partners
Suppressive therapy
Suppressive therapies are available for some viral STBBI.
Encourage individuals taking suppressive therapies to adhere to these therapies as prescribed and to use barriers (e.g., condoms and dental dams) consistently and correctly to reduce the risk of acquiring or transmitting STBBI.
HIV treatment as prevention
Early diagnosis and treatment can lead to reduced morbidity and mortality associated with HIV infection and disease progression. The goal of antiretroviral therapy (ART) is to achieve and maintain a suppressed viral load to improve the overall health of people living with HIV. Another advantage of effective ART is the prevention of HIV transmission, including vertical transmission.
HIV treatment is a rapidly evolving and complex area, with changes in recommended regimens occurring as new research and evidence becomes available. Consider consulting a colleague experienced in HIV/AIDS care or an infectious diseases specialist for guidance on treatment. Consult Canadian, provincial or territorial guidelines for prescribing information and indications for HIV treatment. Consult your provincial or territorial drug formulary regarding coverage.
U=U
Undetectable = Untransmittable (U = U)Footnote 1Footnote 2Footnote 3 communicates the scientific consensus that HIV cannot be sexually transmitted when a person living with HIV takes and adheres to ART and maintains a suppressed viral load of less than 200 copies per millilitre of blood.
To confirm that a person has achieved and maintains a suppressed viral load, the viral load is usually measured every 4-6 months as part of clinical care.
U=U applies only to sexual transmission of HIV. It does not apply to sharing drug use equipment, or during pregnancy, breastfeeding or chestfeeding.
Health professionals can increase the uptake of HIV treatment, prevent new infections, and reduce HIV-related stigma by communicating the benefits of HIV treatment as part of general sexual health messaging.
Suppressive therapy for genital herpes
Refer to the Genital herpes guide for indications and recommendations for treatment and suppressive therapy.
Daily suppressive antiviral therapy reduces the length, frequency and severity of genital herpes recurrencesFootnote 4Footnote 5Footnote 6Footnote 7 and decreases asymptomatic viral shedding and transmission, but does not eradicate the virus.
Additional resources
- Canada.ca
- Canada Communicable Disease Report (CCDR)
- Canadian AIDS Treatment Information Exchange (CATIE)
Antimicrobial resistance (AMR)
AMR is a global public health challenge. Practice antimicrobial stewardship when treating STBBI. The following practices can limit the development and spread of AMR infections:
- Promote safer practices
- Normalize and increase screening
- Increase detection by testing all affected sites (genital and extra-genital)
- Treat individuals and their sex partner(s) according to current guidelines
- Consider testing and waiting for test results, in order to provide etiology-guided treatment, when the person's clinical condition allows, they are willing to abstain from sex, they are likely to return for follow up and/or test turnaround time is rapid
- Follow up with a TOC, as appropriate (Refer to etiology-specific guides)
- Conduct pre-travel counselling and take a travel history
Neisseria gonorrhoeae and Mycoplasma genitalium have demonstrated resistance to multiple classes of antibiotics. In Canada, an accurate picture of drug resistance is difficult because of a shift towards testing using nucleic acid amplification tests (NAAT) rather than culture; as a result, fewer samples are tested for antimicrobial susceptibilityFootnote 8. Refer to the Gonorrhea guide and Mycoplasma genitalium guide for recommendations on diagnostic testing and treatment.
Additional resources
- Canada.ca
- Canada Communicable Disease Report (CCDR)
Co-infections
Transmission routes are similar for many STBBI; co-infection is common and can have treatment and follow-up implications.
In people living with HIV, co-infection with HBV, HCV or syphilis may impact the course of disease. As well, there may be special considerations for treatment and monitoring to ensure treatment effectiveness and to prevent long-term complicationsFootnote 9.
Partner treatment
For sexual contacts of those with a confirmed bacterial STI, consider providing empiric treatment as a public health preventive measure, to prevent the development of an infection. If empiric treatment is provided, advise the person to abstain from sex until their test results have been received.
If testing confirms an STBBI, consult etiology specific guides for treatment and follow-up recommendations of sexual partners.
Expedited partner treatment
Some jurisdictions offer expedited partner treatment (EPT). Check with provincial or territorial health authority and professional association(s) regarding policies and guidelines for EPT. EPT could involve providing:
- A prescription or medications for partner(s) without requiring assessment by a healthcare provider
- Test kits for sexual partner(s) to mail back
- Information sheets, referral instructions
- Telemedicine consultations
Potential advantages of EPT include:
- Increased proportion of treated partners, particularly among priority populations
- Timely treatment of partners
- Reduced transmission
- Reduced reinfections
- Treatment of undiagnosed STBBI
- Prevention of morbidity and complications
Challenges related to EPT include:
- A therapeutic relationship is not established
- Difficulty verifying treatment completion
- Potential for negative partner reaction
- Partners not seeking testing and care
- Loss of counselling opportunity
- Possible allergic or adverse drug reactionsFootnote 10Footnote 11
Follow-up
Ideally, follow-up should be conducted by the healthcare provider who diagnosed and treated the person, to ensure:
- Resolution of symptoms
- Follow-up testing
- Follow-through on partner notification and treatment
If the same healthcare provider is not available, individuals should be directed to appropriate resources, counselled on when to follow up and on symptoms that may indicate treatment failure.
Follow-up testing is needed if baseline testing might have occurred during the window period.
A TOC may be recommended depending on the pathogen and treatment regimen. For some pathogens a TOC is always recommended and for others, a TOC is recommended only in specific situations. In syphilis cases, post-treatment serologic testing is needed to assess treatment response and should be performed at the recommended intervals for stage of infection.
Offer repeat screening for STBBI based on ongoing risk factors and continued potential for exposure. Repeat screening is generally recommended 3 to 6 months after treatment for a bacterial STI, due to the potential for reinfection.
Refer to etiology-specific guides for information on follow-up.
Reporting and partner notification
STBBI reporting requirements and confidentiality
STBBI reporting requirements vary by province and territory. Inform individuals that provincial or territorial public health acts and the Child Protection Act supersede healthcare provider-client confidentiality and require the release of personal information without consent of the individual for all reportable STBBI and in suspected child abuse.
Assure the person that the information will be reported to authorities only as required by law and will otherwise remain confidential. Advise the person that those who receive and process this personal information are bound by ethical, legal and professional obligations to protect confidentiality.
Partner notification
Healthcare providers are required to maintain confidentiality related to the person: no information related to the person can be released to the partner(s) without consent.
Partner notification is a secondary prevention process through which sexual partners and other contacts potentially exposed to an STBBI are identified, located, assessed, counselled, screened and treated. Partner notification has public health benefits (e.g. disease surveillance and control) and for many STBBI it reduces the potential of reinfection. Partner notification can be an effective means of finding persons with an STBBI or at risk of acquiring an STBBIFootnote 12Footnote 13.
While partner notification is sometimes seen as a conflict between societal and individual rights, its aim is to assist in honouring the rights of the sex partners to know whether they have been exposed to an STBBI and to make informed decisions about their health.
Partner notification practices vary by province and territory. More than one strategy can be used to notify different partners. Partner notification strategies include:
- Self-referral: The person accepts full responsibility for informing their partners of the possibility of exposure to an STBBI and for referring them to appropriate services.
- Healthcare provider or public health referral: With the consent of the person, the healthcare provider or public health professional takes responsibility for confidentially notifying partners of the possibility of their exposure to an STBBI. In general, healthcare provider referral ensures more partners are notified, counselled and assessedFootnote 12Footnote 13.
- Contract referral: The healthcare provider negotiates a time frame with the person (usually 24–48 hours) to inform their partner(s) of their exposure and to refer them to appropriate services, after which time, if not done, the healthcare provider or public health professional will notify the partner(s)Footnote 13.
Barriers to partner notification
If the person does not wish to notify partners or if partners have not come forward, consider the following partner notification barriers. If needed, report to public health authorities.
| Potential barrier | Barrier reduction strategies |
|---|---|
| Actual or fear of physical or emotional abuse |
|
| Fear of losing a partner due to an STBBI diagnosis (blame or guilt) |
|
| Fear of legal procedures |
|
| Fear of re-victimization (victims of sexual assault or sexual abuse) |
|
| Anonymous partnering |
|
Additional resources
- Canada.ca
- Canada Communicable Disease Report (CCDR)
- Canadian Child Welfare Research Portal
- Canadian Medical Association Journal (CMAJ)
- Canadian Public Health Association (CPHA)
- Department of Justice
- HIV Legal Network
- National Collaborating Centre for Infectious Diseases
- Partner notification for sexually-transmitted Infections: Policy options
- Anonymous partner notification for sexually-transmitted Infections: Information sheet
- Internet partner notification for sexually-transmitted Infections: Information sheet
- A review of evidence on partner notification practices for chlamydia
References
- Footnote 1
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LeMessurier J, Traversy G, Varsaneux O, et al. Risk of sexual transmission of human immunodeficiency virus with antiretroviral therapy, suppressed viral load and condom use: A systematic review. CMAJ. 2018;190(46):E1350-E1360.
- Footnote 2
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Djiadeu P, Begum H, Sabourin S, Gadient S, Archibald C, LeBlanc M-A, Chittle A, Fleurant A, Cox J. Risk of sexual transmission of HIV in the context of viral load suppression. Can Commun Dis Rep 2023;49(11/12):457–64. https://doi.org/10.14745/ccdr.v49i1112a01
- Footnote 3
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Eisinger RW, Dieffenbach CW, Fauci AS. HIV viral load and transmissibility of HIV infection: Undetectable equals untransmittable. JAMA. 2019;321(5):451-452.
- Footnote 4
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Heslop R, Roberts H, Flower D, Jordan V. Interventions for men and women with their first episode of genital herpes. Cochrane Database of Systematic Reviews. 2016(8).
- Footnote 5
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Casper C, Wald A. Condom use and the prevention of genital herpes acquisition. Herpes. 2002;9(1):10-14.
- Footnote 6
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Corey L, Wald A, Patel R, et al. Once-daily valacyclovir to reduce the risk of transmission of genital herpes. N Engl J Med. 2004;350(1):11-20. doi: 10.1056/NEJMoa035144 [doi].
- Footnote 7
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Carney O, Ross E, Ikkos G, Mindel A. The effect of suppressive oral acyclovir on the psychological morbidity associated with recurrent genital herpes. Genitourin Med. 1993;69(6):457-459. doi: 10.1136/sti.69.6.457 [doi].
- Footnote 8
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Martin I, Jayaraman G, Wong T, Liu G, Gilmour M, Canadian Public Health Laboratory Network. Trends in antimicrobial resistance in neisseria gonorrhoeae isolated in canada: 2000-2009. Sex Transm Dis. 2011;38(10):892-898. doi: 10.1097/OLQ.0b013e31822c664f [doi].
- Footnote 9
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Dore GJ, Cooper DA. The impact of HIV therapy on co-infection with hepatitis B and hepatitis C viruses. Curr Opin Infect Dis. 2001;14(6):749-755.
- Footnote 10
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Ferreira A, Young T, Mathews C, Zunza M, Low N. Strategies for partner notification for sexually transmitted infections, including HIV. Cochrane Database of Systematic Reviews. 2013(10).
- Footnote 11
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Golden MR, Whittington WL, Handsfield HH, et al. Effect of expedited treatment of sex partners on recurrent or persistent gonorrhea or chlamydial infection. N Engl J Med. 2005;352(7):676-685.
- Footnote 12
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Centers for Disease Control and Prevention. Program operations guidelines for STD prevention. Atlanta, GA: US Department of Health and Human Services. 2001:S1-S39.
- Footnote 13
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Mathews C, Coetzee N, Zwarenstein M, et al. Strategies for partner notification for sexually transmitted diseases. Cochrane Database of Systematic Reviews. 2001(4).
- Footnote 14
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Department of Justice Canada. Criminal justice System's response to non-disclosure of HIV. 2017:1-59.