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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.

New HIV diagnosis and baseline assessment

Infectious diseases, microbiology and sexual health · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
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Advanced HIV with acute organ disease

Hypoxia, meningism, focal neurology, visual loss, shock, severe wasting, persistent diarrhoea, oesophageal symptoms or CD4 below 200 cells/µL with illness may indicate an opportunistic infection requiring urgent diagnosis before routine ART timing.

Action: Use ABCDE, involve HIV and infection specialists immediately, obtain syndrome-directed samples and imaging, start life-saving opportunistic-infection therapy and decide ART timing specifically, especially for cryptococcal or tuberculosis meningitis.

Synopsis

Confirm HIV sensitively and respectfully, recognise acute and advanced disease, complete the baseline resistance, coinfection and safety assessment and link rapidly to specialist treatment and prevention.

  • Use a laboratory fourth-generation HIV-1/2 antigen–antibody assay as the standard screening test and follow the national confirmatory algorithm after a reactive result.
  • During very early infection, antigen, antibody and rapid tests may be negative; request HIV RNA when acute HIV is strongly suspected.
  • Communicate a new diagnosis privately, non-judgmentally and with a clear same-day linkage plan; assess immediate mental-health and safeguarding needs.
  • Obtain baseline HIV viral load, CD4 count, resistance genotype, full blood count, renal, liver, bone and metabolic profile before or at ART initiation.
  • Test hepatitis B and C, syphilis and exposure-site STIs; assess tuberculosis, toxoplasma and other infections according to history and CD4 count.
  • Check HLA-B*57:01 before abacavir and never use abacavir in a positive patient.
  • Start ART rapidly for nearly everyone, but coordinate timing with treatment of cryptococcal meningitis, TB meningitis and selected unstable opportunistic infections.
  • Explain that sustained undetectable viral load on treatment prevents sexual transmission: undetectable equals untransmittable.

Key red flags

Breathlessness, dry cough and hypoxia with advanced HIV suggests Pneumocystis pneumonia and needs urgent blood gas and imaging.

Headache, confusion or meningism can represent cryptococcal, tuberculous or other CNS infection and requires urgent lumbar-puncture planning.

Visual floaters, field loss or reduced acuity in severe immune suppression requires same-day retinal examination for CMV.

Acute fever, rash, pharyngitis and lymphadenopathy after recent exposure may be primary HIV despite an initially negative antibody test.

Severe weight loss, chronic diarrhoea, oral or oesophageal candidiasis and recurrent infections suggest advanced immune deficiency.

A reactive antenatal or blood-donor screen needs urgent confirmatory testing and supportive specialist communication, not delayed or casual disclosure.

Acute retroviral syndrome

Fever, rash, sore throat, lymphadenopathy, myalgia, diarrhoea, headache or aseptic meningitis occurs weeks after some acquisitions.

Advanced immune deficiency

Wasting, oesophageal candidiasis, chronic diarrhoea, dyspnoea, neurological disease and unusual skin lesions suggest low CD4 count.

Psychosocial crisis

Acute distress, self-harm thoughts, coercion, insecure housing, immigration concern or partner violence requires immediate supportive assessment.

Investigation priorities

01
Fourth-generation HIV antigen–antibody assayFirst step

Screen for established and many early HIV-1 or HIV-2 infections using venous laboratory testing.

Management branches

CONFIRMVerify and communicate diagnosis

An HIV screen is reactive or acute infection remains likely despite negative screening.

  1. Send the national confirmatory differentiation and nucleic-acid tests and urgently request HIV RNA when acute infection is suspected.
  2. Explain that a screening result needs confirmation, maintain privacy and assess immediate emotional safety and support preferences.
  3. Take a focused exposure, previous test, PrEP or PEP, ART, pregnancy and symptom history without assigning blame.
  4. Link directly to an HIV specialist team and ensure the patient knows exactly when, where and how follow-up will occur.

Key medicines

Rapid-start antiretroviral regimenUse the exact specialist-selected once-daily integrase-inhibitor-based combination after baseline specimens, adjusted for resistance, hepatitis B, pregnancy, kidney function and interactions.Do not improvise a partial regimen; check polyvalent cations, rifamycins, anticonvulsants, acid suppressants and whether HBV-active agents must be maintained.
Bictegravir, emtricitabine and tenofovir alafenamideGive one 50 mg/200 mg/25 mg tablet orally once daily when the HIV specialist selects this complete regimen.Not suitable for every renal, pregnancy, resistance or interaction context; review rifamycins, anticonvulsants, polyvalent cations and hepatitis B before stopping.
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Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • BHIVA BASHH BIA Adult HIV Testing Guidelines 2020
  • BHIVA HIV-1 treatment guidelines
  • NICE NG60 HIV testing: increasing uptake among people who may have undiagnosed HIV
  • NHS HIV and AIDS information

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