Learning Outcomes
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Influenza A viruses are found in many animal hosts and can potentially cause global (pandemic) influenza outbreaks, whereas types B and C only affect humans and do not cause pandemics.
Influenza A viruses are classified by subtype on the basis of the two main surface glycoproteins hemagglutinin (HA) and neuraminidase (NA). Click here for full topic...
Avian influenza ('bird flu') - eg type A subtype H5N1 - is a disease of birds which does not usually infect people, although it is clear that it can in some circumstances. The concern about the current epizootic of H5N1 in bird populations in Asia is that the virus could change to be able to pass from person-to-person and cause a pandemic, because there is no pre-existing immunity in humans to this new virus. It is not clear if, when or how long this process of adaptation would take.
The H5N1 virus could improve its transmissibility among humans via two principal mechanisms:
The first is a "reassortment" event, in which genetic material is exchanged between human and avian viruses during co-infection of a human or pig. Reassortment could result in a fully transmissible pandemic virus, announced by a sudden surge of cases with explosive spread. This was the mechanism leading to the viruses causing the 1957 and 1968 influenza pandemics.
The second mechanism is a more gradual process of adaptive mutation, whereby the capability of the virus to bind to human cells increases during subsequent infections of humans. Very recent genetic analysis of the 1918 influenza virus suggests that the 1918 virus was not a reassortment virus (like those of the 1957 and 1968 pandemics), but more likely an entirely avian-like virus that adapted to humans, ie was able to cross the species barrier. This virus resulted in an unknown number of deaths worldwide but estimated at 50 - 100 million deaths, 8250 deaths in NZ, and shortened life expectancy by 13 years in the USA. The greatest impact was in the 20-40 year age group.
Given the unprecedented number of birds infected with H5N1, the fact that so far there have only been 165 (to the end of January 2006) confirmed human cases shows the low (direct) risk from avian influenza to humans so far. Over half of those with confirmed H5N1 infection have died. However, if the virus mutates to a human form, it is likely to become less lethal - the New Zealand planning model, based on the 1918 pandemic, assumes a 2% case fatality rate.
If avian H5N1 enters NZ via an infected bird there is little direct human health threat as long as the virus does not establish itself in bird populations in NZ. Click here for full topic...
Scenarios used to gauge the potential impact of an influenza pandemic in NZ
estimate a maximum 40% incidence, potentially resulting in 83 influenza
consultations per GP/week (likely more owing to GP sickness) over an 8 week period (compared with a usual death rate of 4,400). Note: that the pandemic is not linear, but rates peak in the middle weeks.
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Transmission of influenza occurs by either droplets or direct contact. Overall "hand hygiene" is the single most important measure to reduce the risk of transmission. Other infection control measures in the surgery include:
H5N1 influenza virus has been shown to have resistance to amantadine, which is unlikely to be effective.
Tamiflu® (oseltamivir) can be used for either treatment or prophylaxis (75mg bd for 5 days for treatment, one cap daily for prophylaxis). Its effectiveness against H5N1 has not been tested in vivo although it has been shown to be effective against the virus in the laboratory. Final policy on priorities for the use of Tamiflu can only be made once the epidemiology of the pandemic strain is understood, but it is currently planned that, in accordance with WHO advice, Tamiflu will be predominantly used for the treatment of cases, although at an early stage when attempts are being made to stamp out small clusters it may be administered to contacts of cases or suspect cases in an effort to reduce spread. The drug is ineffective if given more than 48 hours after infection. Early usage (within 48 hours) is therefore crucial. The drug appears generally safe with the most common side effects being transient nausea, vomiting, abdominal pain, and headache. Based on studies of its use for seasonal influenza, it reduces viral production and shedding, shortening the duration of the illness. Click here for full topic...
Current influenza A vaccines are unlikely to offer protection against a new pandemic strain. Although New Zealand has an agreement in place for access to vaccine against a future pandemic strain, there would be a delay of at least 15-27 weeks between identification of a pandemic and the arrival of a vaccine. 2 doses of vaccine are likely to be required with up to 4 weeks between courses, but trials are still in progress. Vaccine manufacturers are developing a "prototype" vaccine to the current H5N1 virus which may offer some protection against a future pandemic strain. Click here for full topic...
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