antivirals in the treatment of uncomplicated flu in the community

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Use of Antivirals in the Treatment of adults and children in community/A&E with uncomplicated influenza

1. Uncomplicated influenza:

  • influenza presenting with fever, coryza, generalised symptoms (headache, malaise, myalgia, arthralgia) and sometimes gastrointestinal symptoms, but without any features of complicated influenza.

2. Complicated influenza:

  • influenza requiring hospital admission and/or with symptoms and signs of lower respiratory tract infection (hypoxaemia, dyspnoea, lung infiltrate), central nervous system involvement and/or a significant exacerbation of an underlying medical condition

Prescribing in primary care:

  • GPs may only prescribe antiviral medicines for the prophylaxis and treatment of influenza under the General Medical Services (GMS) regulations when the Chief Medical Officer (CMO) has confirmed that influenza is circulating in the community. The CMO announcement is issued to the NHS through the Central Alerting System (CAS)
  • GPs have the discretion to prescribe antiviral medicines for people who are not in the specified at-risk groups but who are considered to be at risk of complications if not treated with an antiviral medicine.

All patients should be advised of the symptoms of complicated influenza and told to seek medical help should their condition worsen. The following recommendations for adults refer to dosages in Box 1. For paediatric dosing seek specialist advice Previously healthy people (excluding pregnant women): No antiviral treatment, or if physician feels patient is at serious risk of developing serious complications from influenza, then oseltamivir PO.

Consider if Risk factors for complicated influenza:

  • a. Neurological, hepatic, renal, pulmonary and chronic cardiac disease.
  • b. Diabetes mellitus.
  • c. Severe immunosuppression.
  • d. Age over 65 years.
  • e. Pregnancy (including up to 2 weeks post-partum).
  • f. Children under 6 months of age.
  • g. Morbid obesity (BMI >=40)

At risk population, including pregnant women (but excluding the severely immunosuppressed):

  • oseltamivir (PO). Do not wait for laboratory confirmation
    • treatment should be started as soon as possible, ideally within 48 hours of onset. There is evidence that treatment may reduce the risk of mortality even if started up to 5 days after onset.
    • starting treatment more than 48 hours after onset is an off-label use of oseltamivir and clinical judgement should be exercised (1)

Severely immunosuppressed patients:

  • some influenza subtypes are associated with a greater risk of developing oseltamivir resistance; the risk of resistance is higher in people who are severely immunosuppressed who are given antivirals, and the selection of first line antivirals in severely immunosuppressed individuals should take account of the dominant circulating strain of influenza
  • oseltamivir PO is the first line treatment, unless the dominant circulating strain has a higher risk for developing oseltamivir resistance, for example influenza A(H1N1)pdm09, in which case use zanamivir (inhaled (INH))
    • when oseltamivir is indicated, the manufacturer recommends a longer treatment course of 75mg PO twice daily for 10 days for immunosuppressed patients
    • treatment should start as soon as possible. If clinical condition does not improve, continue with Zanamivir, take a specimen for resistance testing and consider other possible causes for a failure to improve

Suspected or confirmed oseltamivir resistant influenza in a patient who requires treatment:

  • Zanamivir (INH). Treatment should be started as soon as possible. Management of patients for whom zanamivir is indicated, who are unable to self-administer inhaled zanamivir: Some patients who would normally receive inhaled zanamivir are unable to use it, either due to underlying severe respiratory disease or inability to effectively self-administer the Diskhaler (R) (this includes children under 5, for whom zanamivir is unlicensed).

Patients who are severely immunosuppressed and cannot take inhaled zanamivir should receive oseltamivir PO. As they are at increased risk of developing oseltamivir resistant influenza, they should be reviewed clinically to assess response to therapy. Patients who have suspected or confirmed oseltamivir resistant infection and cannot take inhaled zanamivir should be considered for IV zanamivir; this would be outside the marketing authorisation.

BOX 1:

Dosage in adults for treatment of uncomplicated influenza:

Oseltamivir 75mg PO twice daily for 5 days

Zanamivir 10mg INH twice daily for 5 days

**Note: dose adjustments are required for obesity, renal dysfunction **

 

Recommended oseltamivir treatment dosing in relation to renal function (adults and those aged 13 years or over):

Source: Summary of Product Characteristics updated Feb 2019 (*). The recommendations for haemo-dialysis, haemo(dia)filtration and established renal failure are based on expert opinion (++)

Seek specialist advice for the use of antivirals for complicated influenza management.

Seek specialist advice for use of antivirals in children with influenza

For guidance for use of antivirals in prophylaxis of influenza then see linked item

Seek specialist advice for the use of antivirals in severe immunosuppression

Notes:

  • Severe immunosuppression: Examples of severe immunosuppression relevant to this guidance are given below. Degrees of immunosuppression are difficult to quantify and individual variation exists, therefore this list is not comprehensive:
    • a. Severe primary immunodeficiency
    • b. Current or recent (within 6 months) chemotherapy or radiotherapy for malignancy
    • c. Solid organ transplant recipients on immunosuppressive therapy
    • d. Bone marrow transplant recipients currently receiving immunosuppressive treatment, or within 12 months of receiving immunosuppression
    • e. Patients with current graft-versus-host disease
    • f. Patients currently receiving high dose systemic corticosteroids (equivalent to >=40 mg prednisolone per day for >1 week in an adult, or >=2mg/kg/day for >=1 week in a child), and for at least 3 months after treatment has stopped.
    • g. HIV infected patients with severe immunosuppression (CD4<200/µl or <15% of total lymphocytes in an adult or child over 5; CD4< 500/µl or <15% of total lymphocytes in a child aged 1 to 5; expert clinical opinion in a child aged under 1)
    • h. 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

Reference:

Last edited 10/2019 and last reviewed 01/2020

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