UN: Updates H1N1 Vaccine Recommendations
Single doses of H1N1 flu vaccine for adults, adolescents starting at age 10, and pregnant women are among the latest recommendations issued today by the United Nations health agency to combat the pandemic.
The UN World Health
Organization (http://www.who.int/en/) said the Strategic Advisory
Group of Experts (SAGE) on Immunization that advises it on
vaccine policy and strategy, recommended further studies in
children older than six months and younger than 10 years,
since the data are limited.
For pregnant women, SAGE
noted that studies in experimental animals using live
attenuated or inactivated vaccines found no evidence of
direct or indirect harmful effects on fertility, pregnancy,
foetal development, birthing or post-natal development.
“Based on these data and the substantially elevated
risk for a severe outcome in pregnant women infected with
the pandemic virus, SAGE recommended that any licensed
vaccine can be used in pregnant women, provided no specific
contraindication has been identified by the [national]
regulatory authority,” WHO said in its update http://www.who.int/csr/disease/swineflu/notes/briefing_20091030/en/index.html.
Globally,
teenagers and young adults continue to account for the
majority of cases, with rates of hospitalization highest in
very young children. Between 1 and 10 per cent of patients
with clinical illness require hospitalization, and of these
from 10 to 25 per cent require admission to an intensive
care unit, with from 2 to 9 per cent dying.
Overall,
from 7 to 10 per cent of all hospitalized patients are
pregnant women in their second or third trimester and they
are 10 times more likely to need care in intensive care
units than the general population.
Taking note of
findings by the United States Centers for Disease Control
and Prevention that live attenuated seasonal and live
attenuated pandemic vaccines should not be administered
simultaneously, the experts said the vaccines could be
co-administered provided one or both are inactivated. They
found no evidence that such co-administration would increase
the risk of adverse events.
The experts found no
indication of unusual adverse reactions results in from
early monitoring of the various pandemic vaccines so far,
since those that have occurred are well within the range of
seasonal vaccines, which
have an excellent safety profile. Although early
results are reassuring, monitoring for adverse events should
continue.
With regard to the southern hemisphere 2010
winter season, SAGE recommended two options: a trivalent
vaccine effective against H1N1, seasonal H3N2 and influenza
B, and a bivalent vaccine against H3N2 and influenza B,
which might need to be supplemented with a separate
monovalent H1N1vaccine.
ENDS