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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Partner notification and test-of-cure principles

Obstetrics and gynaecology · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
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Some exposures have expiring interventions

A recent substantial HIV exposure, possible pregnancy after unprotected sex, sexual assault, severe STI complication or safeguarding concern cannot wait for routine partner-notification administration.

Action: Assess immediate safety, arrange HIV PEP as soon as possible and no later than 72 hours when indicated, offer time-sensitive emergency contraception, and use urgent SARC or acute-clinical pathways alongside later notification work.

Synopsis

Prevent onward transmission and reinfection through confidential, organism-specific partner notification while distinguishing eradication testing from later reinfection screening and routine follow-up.

  • Partner notification is a clinical intervention: identify potentially exposed partners, agree a safe notification method, support testing and treatment, and document outcomes while protecting the index patient's identity.
  • Use infection-specific lookback periods and exposure-site questions from current BASHH guidance; one universal number is inaccurate across chlamydia, gonorrhoea, trichomoniasis and syphilis.
  • Offer patient referral, provider referral or a negotiated conditional approach according to preference, safety, likelihood of completion and local sexual-health capability.
  • A test of cure asks whether treatment eradicated the diagnosed infection; a later retest mainly seeks reinfection and is not interchangeable with symptom review.
  • Chlamydia test of cure is reserved for pregnancy, persistent symptoms, suspected poor adherence or another defined concern and must be delayed long enough to avoid residual DNA.
  • Gonorrhoea test of cure is recommended for pregnancy, pharyngeal infection, persistent symptoms, unknown susceptibility or treatment other than ceftriaxone under the 2025 guideline.
  • Resolved trichomoniasis does not require routine test of cure, but current partners should receive treatment and persistent or recurrent symptoms need correctly timed retesting.
  • Syphilis follow-up uses serial quantitative RPR or VDRL interpreted by stage, baseline titre, treatment and reinfection risk; treponemal tests often remain positive for life.
  • Recheck pregnancy, HIV and hepatitis window periods, vaccination and prevention needs while preserving a non-judgemental approach to relationship structure and partner number.

Key red flags

A qualifying HIV exposure within 72 hours needs immediate specialist risk assessment because delaying PEP reduces the opportunity for benefit.

Pelvic pain, fever, pregnancy-related pain or bleeding, neurological or ocular symptoms, or disseminated rash requires clinical escalation before administrative follow-up.

Disclosure of coercion, violence, exploitation, stalking or fear that notification will trigger harm requires a tailored safeguarding plan and must not default to patient referral.

A child, person lacking decision-making capacity or adult at risk requires statutory safeguarding processes alongside confidential sexual-health care.

Suspected gonorrhoea treatment failure or resistant infection requires prompt culture, susceptibility testing and specialist or public-health involvement.

Investigation priorities

01
Organism- and site-specific NAATFirst step

Test an index patient or contact at every exposed site and perform correctly timed molecular follow-up.

Management branches

PlanBuild a safe partner map

A transmissible STI is diagnosed or strongly suspected and partner action is required.

  1. Explain confidentiality, identify exposed partners and sites within the current disease-specific lookback, and assess risk of violence or unwanted disclosure.
  2. Agree patient, provider or conditional referral and record how the service can contact partners without revealing the index patient's identity.
  3. Specify testing, epidemiological-treatment and abstinence advice separately for each organism instead of using a generic STI script.
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Sources and review status5 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Apply principles in context and verify current guidance when a decision affects care. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • BASHH chlamydia guideline 2026
  • BASHH gonorrhoea guideline 2025
  • BASHH trichomoniasis guideline 2021
  • BASHH syphilis guideline 2024
  • BASHH post-exposure prophylaxis guideline

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom