Influenza treatment
- Patients with suspected influenza should be isolated and respiratory precautions commenced – see here for advice.
- If potential Avian Influenza (e.g. History of travel to SE Asia or S Asia), Discuss urgently with Micro/ID; see Triage of HCID.
- The RECOVERY trial includes patients with influenza. To contact the RECOVERY research team use emergency.research@oxnet.nhs.uk or ext 22003. When prescribing for patients in the trial use the RECOVERY trial PowerPlan on EPR.
Eligibility for treatment
Patient group |
Recommendation |
Uncomplicated (most healthy adults)
|
Do not treat
|
Complicated:
|
If within 48 hours symptom onset: Treat
If 2-5 days after symptom onset: can discuss starting treatment Micro/ID
More than 5 days after symptom onset: Do not treat |
At risk of complicated influenza:
|
If within 48 hours symptom onset: Treat
If 2-5 days after symptom onset: can discuss starting treatment with Micro/ID
More than 5 days after symptom onset: Do not treat |
All use of antivirals must be as per UKHSA guidance on use of antiviral agents for the treatment and prophylaxis of seasonal influenza. Any use outside of this should be discussed with Micro/ID.
Drug Treatment
Preferred
Uncomplicated: No treatment (no evidence of benefit).
Complicated / At risk of complicated: oseltamivir 75mg po bd for 5 days (10 days for immunosuppressed patients)
- For dosing in adult patients 40kg or less: 60mg po bd for 5 days (10 days for immunosuppressed patients)
- For dosing in renal impairment see oseltamivir drug monograph
Treatment of influenza in at risk and severely immunocompromised patients should be started promptly when influenza is suspected rather than waiting for positive test results.
Alternative (complicated influenza in severely immunosuppressed patients)
Zanamivir either inhaled (10mg bd inhaled) or IV (600mg bd iv).
- For IV dosing in renal impairment see Zanamivir drug mongraph
Consider Zanamivir if:
- poor clinical response to oseltamivir
- evidence of gastrointestinal dysfunction
- subtype testing confirms a strain with potential oseltamivir resistance (e.g. A [H1N1] pdm09).