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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.

Vaginal discharge differential diagnosis

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

RapidFull
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Discharge can accompany time-critical disease

Haemodynamic disturbance, pregnancy with pain or bleeding, severe pelvic tenderness, fever, peritonism, rapidly spreading vulval inflammation or toxic shock features require urgent assessment rather than a routine vaginitis pathway.

Action: Check observations and pregnancy status, assess abdominal and pelvic red flags, begin sepsis or ectopic-pregnancy escalation where indicated, and involve acute gynaecology or emergency care without waiting for routine swab results.

Synopsis

Distinguish physiological discharge from vaginal, cervical, upper-genital-tract and non-infective disease while recognising pregnancy complications, pelvic infection, safeguarding concerns and malignancy promptly.

  • Normal discharge varies with ovulation, pregnancy, sexual arousal and exogenous hormones; it is usually clear or white and is not accompanied by itch, strong odour, bleeding or pelvic pain.
  • Localise the syndrome before naming an organism: vulval itch and soreness suggest candidiasis or dermatosis, malodour suggests bacterial vaginosis or trichomoniasis, and mucopurulent contact bleeding suggests cervicitis.
  • Bacterial vaginosis typically causes thin homogeneous discharge, a fishy odour and vaginal pH above 4.5 with little inflammation; symptoms alone do not prove the diagnosis.
  • Vulvovaginal candidiasis more often causes itch, soreness, erythema, fissuring and non-offensive discharge with pH at or below 4.5; asymptomatic Candida colonisation does not require treatment.
  • Take an exposure-sensitive sexual history and offer site-appropriate NAAT for chlamydia and gonorrhoea; add a validated trichomonas test when the phenotype or exposure makes it plausible.
  • Pregnancy testing, consented examination and targeted microscopy, pH or swabs are selected according to symptoms; a normal external examination does not exclude cervical or upper-tract infection.
  • Persistent or recurrent discharge after negative infection tests should trigger review for irritant dermatitis, a retained foreign body, genitourinary syndrome of menopause, fistula or neoplasia rather than repeated empirical antimicrobials.

Key red flags

A positive pregnancy test with unilateral pain, shoulder-tip pain, bleeding, syncope or peritoneal signs requires urgent assessment for ectopic pregnancy.

Fever, vomiting, marked lower abdominal pain, cervical excitation, adnexal tenderness or peritonism suggests pelvic inflammatory disease or a surgical emergency.

Hypotension, tachycardia, rash, confusion, severe myalgia or a retained tampon raises concern for toxic shock or sepsis and needs emergency care.

Postmenopausal, persistent blood-stained, offensive or watery discharge, especially with a visible lesion or pelvic mass, needs an expedited cancer pathway.

Severe vulval pain, necrosis, rapidly extending erythema, urinary retention or immunosuppression warrants same-day specialist examination.

Investigation priorities

01
Urine or serum hCGFirst step

Identify pregnancy before interpreting pain, bleeding or selecting medicines.

Management branches

TriageExclude pregnancy and severe infection

Discharge is accompanied by pain, bleeding, fever, systemic symptoms or clinical deterioration.

  1. Record observations, assess abdomen and obtain hCG promptly when pregnancy is possible.
  2. Escalate haemodynamic compromise, peritonism, suspected ectopic pregnancy, sepsis or necrotising vulval infection immediately.
  3. When PID is clinically likely, collect appropriate microbiology but do not delay empirical treatment for laboratory confirmation.
LocalisationMatch phenotype to anatomical site

The patient is stable and requires a focused diagnostic assessment.

  1. Separate physiological variation from vulval inflammation, vaginal dysbiosis, cervicitis, upper-tract disease and a non-infective structural cause.
  2. Offer consented external, speculum or bimanual examination only where findings will alter the pathway, with a chaperone and option to stop.
  3. Select pregnancy, pH, microscopy, culture and site-specific NAAT according to the resulting hypotheses rather than ordering an undifferentiated panel.
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Sources and review status6 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 bacterial vaginosis guideline
  • BASHH vulvovaginal candidiasis guideline
  • BASHH pelvic inflammatory disease guideline
  • BASHH chlamydia guideline 2026
  • BASHH gonorrhoea guideline 2025
  • NICE NG12 suspected cancer recommendations

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