Recommendations pertaining to the use of viral vaccines: Influenza: 2011
For a review of the 2010 influenza season please refer to the website of the National Institute for
Communicable Diseases of the National Health Laboratory Service: www.nicd.ac.za
Recommended vaccine formulation
The following strains have been recommended by the World Health Organization for the 2011 Southern
Hemisphere influenza season and are the same as the recommendations for the 2010 season:-
• an A/California/7/2009 (H1N1) - like virus
• an A/Perth/16/2009 (H3N2) - like virus *
• a B/Brisbane/60/2008 - like virus
* (A/Wisconsin/15/2009 and A/Victoria/210/2009 are A/Perth/16/2009 – like viruses)
Vaccines should contain 15μg of each haemagglutinin antigen in each 0.5ml dose. Indications
1. Persons (adults or children) who are at high risk for influenza and its complications because of
underlying medical conditions and who are receiving regular medical care for conditions such as
chronic pulmonary and cardiac diseases, chronic renal diseases, diabetes mellitus and similar
metabolic disorders, individuals who are immunosuppressed (including HIV infected persons with CD4 counts above 100 cells per µℓ), individuals who are morbidly obese (BMI≥40);
2. Pregnant women – irrespective of stage of pregnancy
3. Residents of old-age homes, chronic care and rehabilitation institutions;
4. Children on long-term aspirin therapy;
5. Medical and nursing staff responsible for the care of high-risk cases;
6. Adults and children who are family contacts of high-risk cases;
7. All persons over the age of 65 years;
8. Any persons wishing to protect themselves from the risk of contracting influenza, especially in industrial
settings, where large-scale absenteeism could cause significant economic losses.
Adults: Whole or split-product or subunit vaccine:- 1 dose I.M.
Children (<12 years): Split-product or subunit vaccine:- 1 dose I.M.
Children <9 years who have never been vaccinated should receive 2 doses 1 month apart
Children less than 3 years of age should receive half the adult dose on two occasions separated 1 month apart
Influenza vaccine is not recommended for infants less than 6 months of age
Contraindications
Persons with a history of severe (anaphylactic) hypersensitivity to eggs or other components of the
Persons with acute febrile illnesses should preferably be immunized after symptoms have resolved.
Vaccines should be given sufficiently early to provide protection for the winter. A protective antibody response
Antiviral chemotherapy
At present novel influenza A (H1N1) and H3N2 and B influenza viruses remains largely sensitive to oseltamivir
(as well as zanamivir). The dosages for treatment are provided in the following table:-
Recommended dosage of antiviral agents for treatment Age Group Oseltamivir dosage* Zanamivir dosage*
Two 5 mg inhalations (10 mg total) twice per day
Children
Two 5 mg inhalations (10 mg total) twice per day (only in
*Recommended duration of treatment is 5 days. Zanamivir is only registered for children ≥ 12 years of age. Antiviral chemoprophylaxis
Chemoprophylaxis for contacts of persons with influenza is not recommended. Recent WHO
recommendations advise presumptive treatment using the treatment regimen described above for high risk
(severely immunocompromised) individuals exposed to influenza instead of the previously recommended long-
term lower dose chemoprophylaxis regimen. These individuals require to be very carefully monitored during
influenza outbreak season for early signs and should then be treated immediately on suspicion of infection.
For a more detailed description of antiviral management and prophylaxis of influenza, please refer to the
Healthcare Workers Handbook on Influenza on the NICD website: http://www.nicd.ac.za
EFFECTIVENESS AND GAINS MAINTENANCE IN SOCIALPHOBIA: A NATURALISTIC STUDY OF COGNITIVESofi Marom, Ph.D.,1Ã Eva Gilboa-Schechtman, Ph.D.,2 Idan M. Aderka, M.A.,2 Abraham Weizman, M.D.,1Background: The impact of depression on cognitive behavioral group therapy(CBGT) for social phobia (SP) in a naturalistic outpatient setting was examinedafter treatment termination and at 1-year follow-up. Method
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