CHAPTER 4: NIP A PANDEMIC IN THE BUD
4.1. We have already noted that the processes
of disease transmission and virus mutation which might lead to
an outbreak of pandemic influenza are not adequately understood.
At the most basic level it is impossible to predict whether a
pandemic strain will be a "pure" avian virus, or a reassortment
of human and avian influenza viruses produced in a "mixing
vessel" such as a pig.
4.2. This uncertainty has profound implications
for pandemic planning. Reassortment could lead to a "big
bang"a sudden leap in the development of the virus,
which could, almost overnight, acquire the capacity to pass efficiently
between humans. On this assumption an initial cluster of cases
would rapidly expand into a pandemic. Progressive mutation of
an avian virus, on the other hand, could result in the virus gradually
acquiring the ability to move between humans. Initial clusters,
of which there might be several, would be small and slow-growing,
as longer chains of human infection developed. Clusters would
be harder to spot, but easier to deal with once identified.
4.3. Recent modelling by Professor Neil Ferguson
and others, the results of which were published in Nature
on 8 September,[10] shows
that once an initial outbreak is identified there is a short period
during which a pandemic could be stamped out, by isolation of
known cases, restrictions on movement, and intensive, targeted
prophylactic use of antiviral drugs. This ground-breaking work
has allowed the WHO to establish a rapid response strategy, and
as a direct result of this article Roche Products Ltd, manufacturers
of oseltamivir (Tamiflu) announced the donation of three million
courses of the drug to the WHO to form a rapid response stockpile.
In addition, China has announced that in the event of an outbreak
it would quarantine the affected area, so providing some prospect
that the other prerequisite for successisolationcould
be achieved.
4.4. However, the modelling appears to be based
on the assumption that the outbreak will occur in a rural area;
it is far from clear what would happen were it to occur in a major
conurbation. Furthermore, even in rural areas the practical difficulties
would be enormous. Rapid diagnosis of the initial cluster would
be essentialat our seminar Dr Jeremy Farrar even suggested
that once the number of cases exceeded 50 it would be too late
to prevent a global pandemic. At the same time he painted a vivid
picture of the logistical difficulties involved in getting suspected
cases from rural villages in Vietnam to properly equipped hospitals
where tests could be carried out. Even once a diagnosis is made,
antiviral drugs would have to be distributed rapidly to possibly
remote and inaccessible locations, which would also have to be
sealed off. As Dr Stohr, of the WHO, said, the chances of success
are "not huge":
"The models say it can work; the reality would
say we have areas in Asia where 80 per cent of the country can
only be reached by four-wheeled drive vehicles; where the challenge
is to treat in ten to 15 days 80 per cent of a population with
a drug which has to be taken over a certain period of time; where
you have to have a very high compliance rate; where you have to
practically seal off the territory and make sure nobody gets in
or out. It is a huge challenge." (Q 210)
Commenting on such issues, Dr Nabarro noted that
it might be necessary to draw on "military capability"
to implement the rapid response measures. This seems to us to
be a sensible and proportionate strategy. (Q 308)
4.5. A further limitation of the modelling is
that is does not take account of the different processes by which
a pandemic might emerge: in the words of the Medical Research
Council, "It is less clear how effective these strategies
would be in the face of a gradual evolution of strains with more
efficient human-to-human transmission, and/or diffuse emergence
on a widely dispersed geographic front in remote districts with
poor communications". There is clearly an urgent need for
further work in this area. (p. 138)
4.6. In the longer term it is clear that the
best way to develop a rapid response capability is to invest in
improved surveillance and healthcare facilities in the region.
The priorities for rapid response were summarised by Dr Stohr:
local healthcare workers who are "aware of the clinical science
and
attentive"; hospitals within reach of rural communities;
regional laboratories able to propagate virus samples and diagnose
infection with avian influenza. Much of this investment will thus
involve upgrading generic healthcare facilities and skills; it
should therefore bring enormous collateral benefits to the region,
and the international community, through improving the detection
of all infectious disease threats, as well as improving response
times to a potential influenza pandemic. (Q 202)
Conclusions
4.7. Recent modelling by United Kingdom researchers
suggests that by rapid diagnosis and targeted response it may
be possible to nip a pandemic in the bud. While this research
has profound implications, further refinement of the modelling
is urgently required, and we look to the Medical Research Council
to make this a high priority within its influenza research programme.
4.8. While it may be theoretically possible
to nip a pandemic in the bud, the practical difficulties remain
formidable. We welcome the donation by Roche Products Ltd of three
million courses of oseltamivir to the WHO, and we also welcome
the efforts of the UN and its agencies to improve surveillance
and implement a co-ordinated rapid response strategy. We urge
the Government to give their full backing to these efforts.
4.9. We further believe that substantial investment
by the international community in improving healthcare in south
east Asia represents the best long-term strategy to prevent future
influenza pandemics. We recommend that the Government, in collaboration
with international partners and the World Bank, make such investment
a high priority.
10 Ferguson et al.(2005), Nature 437, pp 209-214. Back
|