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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.
RapidMLAMSRAGP

Pre-biologic infection screening and vaccination

Essential points for quick revision.

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Active infection before immunosuppression

Sepsis, active tuberculosis, uncontrolled hepatitis, disseminated zoster or another serious infection can deteriorate rapidly if biologic or targeted treatment is started, and a negative screening assay does not overrule compatible symptoms.

Action: Defer the planned immunosuppressant, investigate and treat the infection urgently, notify rheumatology and infection specialists, and restart the initiation pathway only after active disease is controlled and any prophylaxis, vaccine or monitoring plan is explicit.

Synopsis

Complete a reproducible infection and immunisation safety assessment before biologic or targeted therapy, interpret tuberculosis and hepatitis results correctly, and time vaccines without leaving active rheumatic disease untreated.

  • Start with active infection: history, examination and symptom-directed tests come before latent-screen panels; a patient with sepsis or active TB does not proceed to biologic dosing.
  • Tuberculosis assessment combines exposure and residence history, symptoms, IGRA and chest imaging when indicated. Immunosuppression can produce a false-negative or indeterminate IGRA.
  • A positive latent-TB screen requires exclusion of active disease and referral to the TB service for preventive treatment and biologic timing; do not improvise a universal delay.

Key red flags

Cough, weight loss, fever, night sweats, haemoptysis, lymphadenopathy or TB exposure requires active-tuberculosis assessment regardless of an earlier negative IGRA.

Possible active tuberculosis

Persistent cough, weight loss, sweats, fever, lymph nodes or organ-specific symptoms with epidemiological risk requires microbiological and imaging assessment, not a latency label.

Investigation priorities

01
First-line clinical infection assessmentFirst stepFirst line

Identify an active focus that makes immediate immunosuppression unsafe.

Management branches

First gateExclude active infection before latent screening

Biologic or targeted treatment is planned and the patient enters the safety pathway.

  1. Take a structured symptom, exposure, travel, recurrent-infection, device, wound, dental and vaccine history and examine any likely focus.
  2. Investigate and treat active infection first, deferring immunosuppression when sepsis, active TB, uncontrolled hepatitis or significant untreated infection is credible.

Key medicines

Isoniazid plus rifampicin for latent TBA NICE adult preventive option is isoniazid 300 mg orally once daily plus rifampicin 600 mg once daily for three months, with weight adjustment and pyridoxine prescribed when neuropathy risk warrants it under the TB service.
Isoniazid for latent TBGive isoniazid 300 mg orally once daily for six months, with weight adjustment and pyridoxine for relevant neuropathy risk, as an alternative NICE preventive regimen selected by the TB service.
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Sources and review status7 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.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom