Management of Influenza B Infection
For patients with suspected or confirmed influenza B, start oseltamivir 75 mg orally twice daily for 5 days immediately if they are hospitalized, severely ill, or have high-risk conditions—regardless of symptom duration or vaccination status. 1
Who Requires Immediate Antiviral Treatment
Mandatory Treatment Groups
- All hospitalized patients with suspected or confirmed influenza B, regardless of illness duration prior to hospitalization 1
- Severely ill or progressively worsening patients of any age, regardless of illness duration 1
- Children younger than 2 years (especially infants <6 months who have the highest hospitalization rates) 1, 2
- Adults ≥65 years of age 1, 2
- Pregnant women and those within 2 weeks postpartum 1, 2
High-Risk Conditions Requiring Treatment
- Chronic pulmonary disease (asthma, COPD, cystic fibrosis, bronchiectasis) 1, 2
- Chronic cardiac disease (congenital heart disease, heart failure, coronary artery disease) 1, 2
- Immunocompromising conditions (HIV, chemotherapy, long-term corticosteroids, transplant recipients, asplenia) 1, 2
- Chronic renal disease (including dialysis and transplantation) 1, 2
- Diabetes mellitus requiring medication 2
- Chronic liver disease (cirrhosis) 2
- Neurological disorders (cerebral palsy, epilepsy, stroke) 2
- Morbid obesity (BMI ≥40) 1
- Residents of long-term care facilities 2
Optional Treatment for Otherwise Healthy Outpatients
Consider treatment for previously healthy outpatients if they present within 48 hours of symptom onset, particularly if they live with high-risk household contacts 1, 2
Timing of Antiviral Initiation
The 48-Hour Window
Maximum benefit occurs when oseltamivir is started within 48 hours of symptom onset, reducing illness duration by approximately 1–1.5 days in otherwise healthy adults and 17.6–29.9 hours in children 2, 3, 4
Critical Exception: Treatment Beyond 48 Hours
Do not withhold oseltamivir in high-risk, severely ill, or hospitalized patients presenting after 48 hours, as substantial mortality benefit persists even when treatment is initiated up to 96 hours after symptom onset (odds ratio for death = 0.21) 1, 2, 5
Do Not Wait for Laboratory Confirmation
Start treatment empirically based on clinical suspicion during influenza season without awaiting test results in high-risk patients, as delays reduce effectiveness 1, 2
Oseltamivir Dosing
Adult and Adolescent Dosing (≥13 years)
- Treatment: 75 mg orally twice daily for 5 days 1, 2, 6
- Prophylaxis: 75 mg orally once daily for 10 days (post-exposure) or up to 6 weeks (seasonal) 2, 6
Pediatric Weight-Based Dosing (Treatment: twice daily for 5 days)
- ≤15 kg: 30 mg twice daily 1, 2, 6
- >15–23 kg: 45 mg twice daily 1, 2, 6
- >23–40 kg: 60 mg twice daily 1, 2, 6
- >40 kg: 75 mg twice daily 1, 2, 6
Infants <12 Months
- 9–11 months: 3.5 mg/kg per dose twice daily 6
- 0–8 months: 3 mg/kg per dose twice daily 6
- Preterm infants: Dose varies by postmenstrual age (1.0–3.0 mg/kg twice daily) 6
Renal Dose Adjustments
- CrCl >30–60 mL/min: 30 mg twice daily (treatment) or 30 mg once daily (prophylaxis) 2
- CrCl 10–30 mL/min: 30 mg once daily (treatment) or 30 mg every other day (prophylaxis) 1, 2
- Hemodialysis: 30 mg immediately, then 30 mg after each dialysis session 2
Expected Clinical Benefits
Symptom Reduction
- Illness duration shortened by 1–1.5 days when started within 48 hours 2, 3, 4
- Symptom severity reduced by 30–38% 2
- Faster return to normal activities 3
Complication Prevention
- 50% reduction in pneumonia risk in patients with laboratory-confirmed influenza 2
- 34% reduction in otitis media in children 2
- 35% reduction in secondary complications requiring antibiotics 7
- Significant mortality benefit in hospitalized patients (OR = 0.21 for death within 15 days) 2, 5
Important Influenza B–Specific Considerations
Oseltamivir appears somewhat less effective against influenza B compared to influenza A, with observational studies showing children with influenza A resolved fever and stopped viral shedding more quickly than those with influenza B 2. However, oseltamivir remains the first-line treatment for influenza B because it is active against both influenza A and B, whereas adamantanes (amantadine, rimantadine) have no activity against influenza B 1, 8, 9, 4.
Zanamivir (inhaled) is equally effective against influenza A and B and may be preferred in confirmed influenza B epidemics, but it is contraindicated in patients with underlying airway disease (asthma, COPD) due to risk of bronchospasm 10, 8, 9. For patients with chronic respiratory conditions and influenza B, oseltamivir is the safer choice 2.
Managing Bacterial Superinfection
When to Add Antibiotics
Empirically treat bacterial coinfection in addition to oseltamivir if the patient presents with: 1, 5
- Initial severe disease (extensive pneumonia, respiratory failure, hypotension, persistent fever)
- Clinical deterioration after initial improvement
- Failure to improve after 3–5 days of antiviral treatment
- New consolidation on chest imaging or purulent sputum production
Antibiotic Selection
- Non-severe pneumonia: Oral amoxicillin-clavulanate or doxycycline 5, 6
- Severe pneumonia: IV β-lactam (cefuroxime, cefotaxime, or amoxicillin-clavulanate) PLUS macrolide (azithromycin or clarithromycin) 5, 6
- Coverage targets: Streptococcus pneumoniae, Staphylococcus aureus, Haemophilus influenzae 6
Prophylaxis Indications
Post-Exposure Prophylaxis (75 mg once daily for 10 days)
Initiate within 48 hours of exposure for: 2
- Household contacts of influenza-infected persons, especially high-risk individuals
- Unvaccinated healthcare workers caring for high-risk patients during outbreaks
- Severely immunocompromised patients (e.g., transplant recipients) after household exposure
Institutional Outbreak Control
All eligible residents of nursing homes or chronic care facilities should receive prophylaxis regardless of vaccination status, continued for ≥2 weeks or until 1 week after outbreak ends 1, 2
Common Adverse Effects
- Nausea and vomiting are the most common side effects, occurring in 10–15% of patients (vs. 9% with placebo) 2, 6, 3
- Taking oseltamivir with food reduces gastrointestinal side effects 2, 6
- Diarrhea may occur in infants <1 year 2, 6
- No established causal link between oseltamivir and neuropsychiatric events despite early concerns 2, 6
Critical Pitfalls to Avoid
- Do not withhold oseltamivir while waiting for laboratory confirmation in high-risk patients during influenza season 1, 2
- Do not refuse treatment to high-risk patients presenting >48 hours after symptom onset, as mortality benefit persists up to 96 hours 1, 2, 5
- Do not use corticosteroids as adjunctive therapy for influenza unless indicated for other reasons (e.g., COPD exacerbation), as they increase mortality and bacterial superinfection risk 1, 7
- Do not use amantadine or rimantadine for influenza B, as they have no activity against influenza B viruses 1, 8, 9, 4
- Do not use zanamivir in patients with asthma or COPD, as it can trigger bronchospasm 10, 8, 9
- Do not routinely use higher doses or extended duration of oseltamivir, as randomized trials show no survival benefit 1, 2
When to Consider Antiviral Resistance Testing
Consider resistance testing for: 1
- Patients who develop laboratory-confirmed influenza while on or immediately after oseltamivir prophylaxis
- Immunocompromised patients with persistent viral replication (>7–10 days) who remain ill during or after treatment
- Patients with severe influenza who do not improve with treatment and have evidence of persistent viral replication
If oseltamivir resistance is suspected or confirmed, switch to zanamivir (if no contraindications) or IV peramivir 1, 7