Indications for Vaccination
Routine
- Annual influenza vaccination is indicated for everyone older than 6 months
- Influenza vaccines are again trivalent as B Yamagata strains have not been seen since 2020-21.
- Enhanced vaccines are recommended for those >65: High dose (HD-IIV3), adjuvanted (aIIV3) or recombinant (RIV3) are all considered enhanced vaccines
- ACIP states that solid organ transplant recipients aged 18 through 64 years on immunosuppressive medication regimens may receive either HD-IIV3 or aIIV3 as an acceptable option to IIV-3 or RIV3
- Children 6 months-8 years old should receive two doses as a primary series the first time they get flu vaccine. In subsequent years children receive one dose
- Some people are at significantly higher risk of influenza complications.
- All children aged 6 through 59 months.
- All persons aged ≥50 years.
- Adults and children who have chronic pulmonary (including asthma), cardiovascular (excluding isolated hypertension), renal, hepatic, neurologic, hematologic, or metabolic disorders (including diabetes mellitus).
- Persons who are immunocompromised due to any cause (including but not limited to immunosuppression caused by medications or HIV infection).
- Persons who are or will be pregnant during the influenza season.
- Children and adolescents (aged 6 months through 18 years) who are receiving aspirin- or salicylate-containing medications and who might be at risk for experiencing Reye syndrome after influenza virus infection.
- Residents of nursing homes and other long-term care facilities.
- American Indian or Alaska Native persons.
- Persons who are extremely obese (body mass index ≥40 for adults).
- For most persons who need only 1 dose of influenza vaccine, vaccination should ideally be offered during September or October. Vaccination should continue after October and throughout the season as long as influenza viruses are circulating and unexpired vaccine is available. Earlier vaccination should be considered for children who will need two doses and for pregnant people in the third trimester in order to provide transplacental antibody protection to their infants during the influenza season
Travel
- In temperate regions, influenza in seasonal, typically October-May in the Northern hemisphere and April-September in the Southern Hemisphere
- Vaccination is recommended in September through October, as well as throughout the influenza season if not already vaccinated.
- Timing of influenza vaccine may be altered for those traveling to the Southern Hemisphere. Southern hemisphere vaccine formulation may be different and is usually not available in the north
- Influenza may circulate year round in tropical regions
- Consider pre-departure vaccination for US residents not vaccinated during the previous northern winter who are at higher risk for complications traveling during the southern winter (April–September) to the Southern Hemisphere or to the tropics at any time of year, or on a cruise ship or organized tourist group to any location at any time of year
- All persons (regardless of risk status) who are vaccinated in preparation for travel before the upcoming influenza season’s vaccine is available should receive the current vaccine the following fall or winter.
- Additional information on global influenza surveillance by region is available at FluNet (WHO).
Dose and Schedule
Tradename (Manufacturer) |
Vaccine (type, CDC acronym) | Age | Dose and Route | Primary Schedule - routine | Subsequent Booster |
Standard dose inactivated egg-based | |||||
Afluria Trivalent, |
Standard dose, Egg-based, IIV3 | ≥ 6 months |
6 months-35 months 7.5 µg/0.25mL IM ≥ 3 years 15 µg/0.5 mL IM |
2 doses initially if 6 months -8 years Otherwise, single dose |
Annual |
FluarixTrivalent, FluLavalTrivalent, FluzoneTrivalent |
Standard dose, Egg-based, IIV3 | ≥ 6 months | 15 µg/0.5 mL IM |
2 doses initially if 6 months -8 years Otherwise, single dose |
Annual |
Standard dose cell-based | |||||
FlucelvaxTrivalent | Cell-based, Egg-free, ccIIV3 | ≥ 6 months | 15 µg/0.5 mL IM |
2 doses initially if 6 months -8 years Otherwise, single dose |
Annual |
Enhanced |
|||||
FlublokTrivalent | Recombinant, Egg-free, RIV3 | ≥ 18 years | 45 µg/0.5 mL IM | Single dose | Annual |
Fluzone High-DoseTrivalent | High dose, Egg-based, HD-IIV3 | ≥ 65 years | 60 µg/0.5 mL IM | Single dose | Annual |
FluadTrivalent | Adjuvanted, Egg-based, aIIV3 | ≥ 65 years | 15 µg/0.5 mL IM | Annual | |
Live attenuated | |||||
FluMistTrivalent | Attenuated live virus, Egg-based, LAIV3 | 2 years-49 years | 106.5–7.5 fluorescent focus units/0.2 mL intranasal |
2 doses initially if 6 months -8 years Otherwise, single dose |
Annual |
Efficacy, Duration of Protection
Standard Vaccines
- Efficacy varies by season; 0-60%. Average ~55% Clin Infect Dis 2023; 768: 540
- Protection lasts around 6 months but wanes after ~4 months.
- Waning at largely in those >60
-
Seasonal flu vaccine ineffective against H5N1 and other avian influenza type
- seasonal vaccine recommended for persons at high-risk of H5N1 to reduce incidence of co-infection between avian and non-avian Influenza A
Enhanced Vaccines
- Clinical trial data are limited and not entirely consistent
- Observational data are more available but subject to bias and unmeasured confounders
- Generally studies have shown modest increased efficacy relative to standard vaccines in the range of 17-30% increase in relative efficacy
- For more detail see CDC. Prevention and Control of Seasonal Influenza
Choice, Interchangeability
- IIV3 products are largely interchangeable
- LAIV3 has the narrowest age range of suitable patients
- All 3 enhanced vaccines (aIIV3, HD-IIV3, RIV3) suitable for older adults. No adequate head to head comparisons
Contraindications
- Allergic reactions to eating eggs, including anaphylaxis no longer need to be considered in the choice of influenza vaccines. As of 2023, ACIP recommends that all persons with egg allergy should receive an age appropriate influenza vaccine that is either egg-based or non-egg based. CDC review of the evidence.
- All vaccines should be administered in a setting where anaphylaxis can be recognized and managed
- History of anaphylaxis to any influenza vaccine is a contraindication to future use of all egg-based vaccines and LAIV
- For LAIV, the following are considered contraindications:
- Children who are receiving aspirin or salicylate containing medications
- Children aged 2 through 4 years who have received a diagnosis of asthma or wheezing in the last 12 months
- Children and adults who are immunocompromised due to any cause
- Close contacts and caregivers of severely immunosuppressed persons who require a protected environment.
- Pregnancy
- Persons with active CSF leak or Persons with cochlear implants
- Receipt of influenza antiviral medication within the previous 48 hours for oseltamivir and zanamivir, previous 5 days for peramivir, and previous 17 days for baloxavir
Precautions
- Moderate or severe acute illness with or without fever is a general precaution for vaccination
- A history of Guillain-Barré syndrome (GBS) within 6 weeks of a previous dose of any type of influenza vaccine is considered a precaution
- A history of a severe allergic reaction (e.g., anaphylaxis) to any egg-based IIV or LAIV of any valency is a precaution for the use of ccIIV3 or RIV3.
- Fluzone, quadrivalent: syncope has been reported immediately following vaccination
- Procedures should be in place to avoid injury from fainting.
- For LAIV, Asthma in persons aged ≥5 years, moderate or severe current illness, and underlying conditions that increase the risk of influenza complications are precautions
- History of egg allergy:
- Allergic reactions to eating eggs, including anaphylaxis, is no longer factor. See above.
Adverse Effects
- Local reactions including pain, redness or swelling
Drug Interactions
- Influenza antiviral medications impair the replication of LAIV leading to decreased efficancy
Special Populations
Pregnancy, Breastfeeding
- Pregnancy is associated with an increased risk of complications from influenza and influenza vaccination is recommended during pregnancy
- Influenza vaccination during pregnancy is associated with a decreased risk of respiratory illness and influenza during pregnancy and in the immediate post partum period
- Influenza vaccination during pregnancy is associated with decreased risk of respiratory illness or influenza in neonates
- Breastfeeding is not a contraindication or precaution
Immunocompromised / HIV
- HIV is associated with decreased efficacy of influenza vaccines in patients with significant CD4 cell suppression
- Other types of immunosuppression may decrease efficacy. For a complete discussion see Clin Infect Dis. 2014 Feb;58(3):e44
- Immunocompromised patients should not receive LAIV3
Serologic Testing
- Serologic testing has no role
Comments
- Current full-length ACIP documents for each individual vaccine
- Full FDA PI for each US approved vaccine
-
FluMist will be available for self or caregiver administration for the 2025-26 influenza season
- U.S. CDC recommendations for Prevention and Control of Seasonal Influenza
- Influenza: U.S. CDC vaccine information resources