TOC |
ID
Pandemic (H1N1) 2009 influenza vaccine
Updated 2009 Sep 28 05:14 PM: topic created 2009 Sep 24
REF:
http://dynaweb.ebscohost.com/Detail.aspx?id=474412&sid=dd350d47-a4ae-4fa1-9aeb-dd9689dcbe70@sessionmgr4
Overview:
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vaccination efforts should begin as soon as vaccine is available
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key target groups to receive pandemic (H1N1) 2009 influenza vaccine include
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pregnant women
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people who live with or care for infants < 6 months old
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health care and emergency medical services personnel
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persons aged 6 months through 24 years
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people aged 25-64 years who have medical conditions that put them at higher
risk for influenza-related complications
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both live, attenuated and inactivated influenza A (H1N1) 2009 monovalent
vaccine formulations will be available
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inactivated vaccine dosing
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single 0.5 mL dose for adults and children e 10 years old
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two 0.5 mL doses about 1 month apart for children ages 36 months to 9 years
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two 0.25 mL doses about 1 month apart for children ages 6-36 months
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live attenuated vaccine dosing
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single 0.2 mL dose for adults and children e 10 years old
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two 0.2 mL doses about 1 month apart for children ages 2-9 years
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each 0.2 mL dose given as 0.1 mL per nostril
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pandemic (H1N1) 2009 influenza vaccine does not replace need for seasonal
influenza vaccine
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simultaneous administration of inactivated seasonal and pandemic influenza
vaccines are permissible at different anatomic sites; simultaneous administration
of live, attenuated vaccines not recommended
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efficacy
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single dose of inactivated pandemic (H1N1) 2009 vaccine in healthy adults
appears immunogenic with mostly mild adverse effects
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single dose of inactivated pandemic (H1N1) 2009 vaccine appears immunogenic
in most healthy children aged 10-17 years
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side effects expected to be similar to seasonal influenza vaccine and include
mostly mild local and systemic reactions
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possibly very low risk of Guillain-Barre syndrome (GBS) after influenza
vaccination
9-29-2009