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 working with poultry, travel to USA, SE or South Asia), Discuss urgently with Micro/ID; see Triage of HCID For ED HCID triage poster, see here.
- The REMAP CAP trial includes randomisation of patients to oseltamivir. When prescribing for patients in the trial use the REMAP CAP trial PowerPlan on EPR.
- Be aware if testing (particularly by PCR), if vaccinated within 14 days with Live Attenuated Influenza Vaccine (LAIV), may produce a false positive – if clinically consistent with influenza, then manage as such.
- Please ensure vaccination history taken. Note that children in risk groups can be offered vaccination from 6 months of age
For neonatal exposure, discuss with Paeds ID.
Eligibility for treatment
Risk factors for severe influenza and hospitalisation (at risk population)
- Chronic neurological, hepatic, renal, respiratory and cardiovascular diseases requiring frequent hospitalisation/follow up
- Potential Immunosuppression*
- Children under 6 months of age in unvaccinated mothers
- Prematurity within last 6 months
*see NICE TA 168 includes:-
- Primary immunodeficiency - not on replacement therapy
- Current or recent (within 6 months) chemotherapy or radiotherapy for malignancy,
- Solid organ transplant recipient currently receiving immunosuppressive treatment
- Bone marrow transplant recipient currently receiving immunosuppressive treatment or within 12 months of receiving immunosuppression,
- Patients with current Graft vs host disease (GVHD),
- Patients currently receiving high dose systemic corticosteroids 2mg/kg/day or more for 1 week or longer, and for at least 3 months after this length of treatment has stopped
- People living with HIV with severe immunosuppression on discussion with Paeds ID team.
- Patients currently or recently (within 6 months) on other types of highly immunosuppressive therapy or where the patient’s specialist regards them as severely immunosuppressed
Non-severe influenza, previously healthy patient
No antiviral treatment required
Severe influenza OR Non-severe and at risk population
Start within 48 hours of illness onset for the greatest benefit. Evidence beyond 48 hours of onset is limited.
First line treatment: Oseltamivir po, see dosing table below, for 5 days (10 days for immunosuppressed and/or critically ill patients in PCC, discuss with Paeds ID)
Oseltamivir treatment dose:
|
Age |
Oseltamivir treatment dose |
|
Infants under 12 months |
3mg/kg BD (max. per dose 30mg) |
|
1–12 years (10-15kg) |
30mg BD |
|
1–12 years (more than 15kg to 23kg) |
45mg BD |
|
1–12 years (more than 23kg to 40kg) |
60mg BD |
|
1–12 years (more than 40kg) |
75mg BD |
|
13–17 years (up to 41kg) |
60mg BD |
|
13–17 years (41kg and above) |
75mg BD |
Dosing in Renal impairment: Discuss with pharmacist
Where oseltamivir is not tolerated or there is a poor clinical response: Discuss with Paeds ID.
Note: Treatment may also be considered to reduce transmission to severely immunosuppressed household contacts