Indications for Prophylactic Oseltamivir (Tamiflu)
Prophylactic oseltamivir should be given to high-risk patients who are unvaccinated or within 2 weeks of vaccination, household contacts of infected individuals, and during institutional outbreaks, with dosing of 75 mg once daily for adults (10 days post-exposure or up to 6 weeks during community outbreaks) and weight-based dosing for children. 1, 2
High-Risk Patients Requiring Prophylaxis
Unvaccinated or Recently Vaccinated High-Risk Individuals
- High-risk patients who have not received influenza vaccine or were vaccinated less than 2 weeks ago should receive prophylaxis during the period until immunity develops (approximately 2 weeks in adults). 1
- Children under 9 years receiving their first influenza vaccine may require up to 6 weeks of prophylaxis: 4 weeks after the first dose plus 2 additional weeks after the second dose. 1, 2
Specific High-Risk Groups Warranting Prophylaxis
The following populations are at increased risk for influenza complications and should be considered for prophylaxis when unvaccinated or exposed: 3
- Children <5 years (especially <2 years) and adults ≥65 years 3
- Residents of nursing homes and chronic care facilities 3
- Patients with chronic pulmonary disease (including asthma, COPD, cystic fibrosis) 3
- Patients with hemodynamically significant cardiovascular disease 3
- Patients with chronic metabolic diseases (including diabetes mellitus), renal dysfunction, or hepatic disease 3
- Immunocompromised patients (including HIV infection, malignancy, chemotherapy recipients, transplant patients, those on chronic steroids ≥20 mg/day prednisolone equivalent for >1 month) 3, 1
- Pregnant and postpartum women 3
- Children and adolescents <19 years on long-term aspirin therapy (risk of Reye syndrome) 3
- Patients with neurologic/neurodevelopmental conditions (cerebral palsy, epilepsy, stroke, muscular dystrophy, spinal cord injury) 3
- Patients with conditions compromising respiratory function (tracheostomy, mechanical ventilation) 3
- Patients with extreme obesity (BMI ≥40 for adults) 3
Immunocompromised Patients
- Patients with immune deficiencies who are expected to have inadequate antibody response to vaccine should be considered for prophylaxis. 1
- Prophylaxis may be continued for up to 12 weeks during community outbreaks in immunocompromised patients. 1, 4
Household and Close Contact Prophylaxis
Post-Exposure Prophylaxis
- Household contacts and caregivers of high-risk individuals who are unvaccinated should receive prophylaxis during peak influenza activity to reduce viral spread. 1, 2
- Initiate prophylaxis for household or close family contacts of a confirmed influenza patient due to potential exposure to both the index case and common environmental sources. 2
- Standard post-exposure prophylaxis duration is 10 days after last known exposure, initiated within 48 hours of exposure. 2
- Studies demonstrate 82-89% protective efficacy in preventing laboratory-confirmed influenza illness in household contacts. 2
Special Considerations for Infants
- Infants under 6 months (who cannot be vaccinated) should be protected through prophylaxis of their household contacts and caregivers. 1
Healthcare and Institutional Settings
Healthcare Workers and Institutional Staff
- Healthcare workers and institutional staff who are unvaccinated and have frequent contact with high-risk patients should be considered for prophylaxis during community outbreaks. 1
- This includes physicians, nurses, nursing home employees, and home care providers with contact with high-risk persons. 3
Institutional Outbreaks
- Nursing home residents and long-term care facility patients should receive prophylaxis during institutional outbreaks, with studies showing 92% reduction in influenza illness. 1, 5
- Prophylaxis should be provided for control of influenza outbreaks in unimmunized staff and children in institutional settings. 6
Dosing Regimens
Adults
- Standard prophylaxis dose: 75 mg once daily 1, 4
- Duration: At least 10 days post-exposure or up to 6 weeks during community outbreaks 1, 2
- No dose reduction needed based on age alone for elderly patients with normal renal function 1
- Dose adjustment required for renal impairment (creatinine clearance 10-60 mL/min) 4
Pediatric Dosing (Weight-Based)
- ≤15 kg: 30 mg once daily for 10 days
- >15-23 kg: 45 mg once daily for 10 days
- >23-40 kg: 60 mg once daily for 10 days
- >40 kg: 75 mg once daily for 10 days
For infants 3 months to <12 months: 2
- 3 mg/kg once daily for 10 days
For infants <3 months: 2
- Not recommended unless the situation is judged critical
Duration of Prophylaxis by Clinical Scenario
- Post-exposure (household contact): 10 days 2
- Community outbreaks: Up to 6 weeks during periods of influenza activity 1, 2
- Immunocompromised patients during outbreaks: Up to 12 weeks 1, 4
- Seasonal prophylaxis in high-risk unvaccinated: Duration of local influenza activity 5
Important Clinical Caveats
Not a Substitute for Vaccination
- Chemoprophylaxis is not a substitute for vaccination, which remains the primary means of influenza prevention. 2, 6
- Oseltamivir prophylaxis does not interfere with antibody response to influenza vaccine. 2
Timing Considerations
- Prophylaxis is most effective when initiated within 48 hours of exposure to an infected individual. 2
- For recently vaccinated individuals, continue prophylaxis until immunity develops (approximately 2 weeks post-vaccination in adults). 1
Safety Profile
- Oseltamivir is well-tolerated across all age groups with no increased adverse events in elderly compared to younger adults. 1
- Most common side effects are nausea and vomiting, which are mild, transient, and reduced when taken with food. 1, 5
Contraindications and Special Populations
- Children at high risk with contraindications to vaccination should receive prophylaxis throughout the influenza season. 1
- For pregnant women and immunocompromised patients, the benefits of prophylaxis typically outweigh the risks when there is significant exposure. 2
- Efficacy has not been established in immunocompromised patients, but safety has been demonstrated for up to 12 weeks. 4