Influenza primary prevention: Difference between revisions
Jump to navigation
Jump to search
Line 6: | Line 6: | ||
==Primary Prevention== | ==Primary Prevention== | ||
===Vaccination=== | ===Vaccination=== | ||
{| style="border: 0px; font-size: | {| style="border: 0px; font-size: 85%; margin: 3px; width:300px;" align=right | ||
! style="background: #4479BA; color:#FFF;" |Contraindications for Live Attenuated Influenza Vaccine | ! style="background: #4479BA; color:#FFF;" |Contraindications for Live Attenuated Influenza Vaccine | ||
|- | |- |
Revision as of 18:41, 24 October 2014
Influenza Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Influenza primary prevention On the Web |
American Roentgen Ray Society Images of Influenza primary prevention |
Risk calculators and risk factors for Influenza primary prevention |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Alejandro Lemor, M.D. [2]
Overview
Primary Prevention
Vaccination
Contraindications for Live Attenuated Influenza Vaccine |
---|
|
|
|
|
|
|
|
- Vaccination against influenza with a flu vaccine is strongly recommended for high-risk groups, such as children and the elderly.
- Routine annual influenza vaccination is recommended for all persons aged ≥6 months who do not have contraindications.
- Vaccination optimally should occur before onset of influenza activity in the community.
- Health care providers should offer vaccination soon after vaccine becomes available (by October, if possible).
- Vaccination should be offered as long as influenza viruses are circulating. *
- Children aged 6 months through 8 years who require 2 doses should receive their first dose as soon as possible after vaccine becomes available, and the second dose ≥4 weeks later.
- For 2014–15, U.S.-licensed influenza vaccines will contain the same vaccine virus strains as those in the 2013–14 vaccine. Trivalent influenza vaccines will contain hemagglutinin (HA) derived from an A/California/7/2009 (H1N1)-like virus, an A/Texas/50/2012 (H3N2)-like virus, and a B/Massachusetts/2/2012-like (Yamagata lineage) virus. Quadrivalent influenza vaccines will contain these antigens, and also a B/Brisbane/60/2008-like (Victoria lineage) virus.
Chemoprophylaxis Adapted from CDC [1]
- Annual influenza vaccination is the best way to prevent influenza because vaccination can be given well before influenza virus exposures occur, and can provide safe and effective immunity throughout the influenza season.
- antiviral medications are approximately 70% to 90% effective in preventing influenza and are useful adjuncts to influenza vaccination.
- CDC does not recommend widespread or routine use of antiviral medications for chemoprophylaxis so as to limit the possibilities that antiviral resistant viruses could emerge. Indiscriminate use of chemoprophylaxis might promote resistance to antiviral medications, or reduce antiviral medication availability for treatment of persons at higher risk for influenza complications or those who are severely ill.
- In general, CDC does not recommend seasonal or pre-exposure antiviral chemoprophylaxis, but antiviral medications can be considered for chemoprophylaxis in certain situations.
- The following are examples of situations where antiviral medications can be considered for chemoprophylaxis to prevent influenza:
- Prevention of influenza in persons at high risk of influenza complications during the first two weeks following vaccination after exposure to an infectious person.
- Prevention for people with severe immune deficiencies or others who might not respond to influenza vaccination, such as persons receiving immunosuppressive medications, after exposure to an infectious person.
- Prevention for people at high risk for complications from influenza who cannot receive influenza vaccine due to a contraindication after exposure to an infectious person.
- Prevention of influenza among residents of institutions, such as long-term care facilities, during influenza outbreaks in the institution.
- An emphasis on close monitoring and early initiation of antiviral treatment if fever and/or respiratory symptoms develop is an alternative to chemoprophylaxis after a suspected exposure for some persons.
- To be effective as chemoprophylaxis, an antiviral medication must be taken each day for the duration of potential exposure to a person with influenza and continued for 7 days after the last known exposure. For persons taking antiviral chemoprophylaxis after inactivated influenza vaccination, the recommended duration is until immunity after vaccination develops (antibody development after vaccination takes about two weeks in adults and can take longer in children depending on age and vaccination history).
- Antiviral chemoprophylaxis generally is not recommended if more than 48 hours have elapsed since the first exposure to an infectious person.
- Patients receiving antiviral chemoprophylaxis should be encouraged to seek medical evaluation as soon as they develop a febrile respiratory illness that might indicate influenza.