Original
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Editorial |
Volume
356, Number 9229 : 12 August 2000 |
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Donor
responsibilities in rolling back malaria |
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The previous global campaign to eradicate
malaria failed. This WHO-led campaign
lasted from 1955 to 1969. A new campaign,
Roll Back Malaria (RBM), was launched
in October, 1998. It must not be allowed
to fail. Malaria accounts for more than
a million deaths annually. Since the mid-1960s
malaria itself is estimated to have slowed
economic growth in highly malarious areas
by 1·3% per year. If not for this
negative growth, Africa's gross domestic
product would be US$100 billion greater
than it is now.
Can the new campaign succeed? It has,
at least, gained much support. A key feature
of RBM is that it is a partnership--of
four core partners (WHO, UNICEF, the World
Bank, and UNDP) and national governments,
other UN bodies, non-governmental organisations,
and the private sector. By the third global
RBM meeting in March this year, there
were 93 partners. The overall aim is to
halve the burden of malaria by the year
2010 through four critical actions: enabling
everyone at risk to sleep in a mosquito-free
environment, mainly through use of insecticide-treated
bednets; prompt diagnosis and treatment
(within or near the home, as reported
in today's Lancet on p 550, for
example); antimalarial therapy for all
pregnant women at risk of malaria; and
early identification and effective response
to epidemics. Programmes are to be country
specific and implemented through existing
systems.
The African Summit on RBM in April this
year in Abuja, Nigeria, was perhaps the
first time heads of states met to discuss
a specific disease. They resolved to reach
60% coverage for the first three critical
actions by the year 2005. In response
to their call for US$1 billion per year
of new resources for RBM, they received
pledges of an additional $300-500 million
a year from the World Bank, and Can$10
million (US$6·5 million) over 5 years
from the Canadian International Development
Agency. Although well short of requirements,
these offers represent recognition of
the need for budgetary support, not just
technical assistance.
The G8 countries have also pledged support
for malaria control. With such encouraging
starts, why should there be concern now
about the likelihood of failure? Epidemiology,
entomology, genetics, health-care delivery,
and a range of other operational issues
all contribute to the technical complexity
of malaria control, which partners seem
not to appreciate. Why, for example,
has UNICEF proposed support for chloroquine
for Burmese towns along the Thai border?
[note:
This is a region with a large amount of
multidrug resistance in P. falciparum]
Why did USAID threaten Belize
with withdrawal of support if it continued
with use of DDT? Donors may not
see that short-term support or sustainability
through cost recovery are at odds with
scientific reasoning. When USAID
stopped support to Tanzania for bednets
after 5 years, it left a community especially
vulnerable to malaria because the protection
of bednets had reduced immunity to the
infection. And in poor areas
few people can pay towards their bednets,
but nets work much better when used by
the entire community. Grants rather than
loans are needed. Even so, as the World
Bank has admitted, there remains the difficulty
of weak capacity for implementation.
It is time for RBM to switch focus from
the campaigning to implementation of malaria-control
activities. Things must be done right
this time, which means first knowing what
is right and operationally feasible. A
recommendation was made at a meeting of
malaria scientists in June at the Center
for International Development at Harvard
University for all projects to first pass
scientific and operational scrutiny by
an external multidisciplinary expert review
panel, who would assess projects according
to scientific norms. Proposals for projects
would still come from the field, so there
is no danger of detracting from local
ownership or partnerships, a concern that
led to vehement dissent by UNICEF about
having a review panel. That organisation
has yet to approve the consensus document
for guiding RBM drawn up at Harvard.
The RBM partnership is in principle well
founded, but partners must realise that
for the programme to succeed money cannot
be squandered on flawed projects. Scientific
rigour of projects should not take second
place to their political correctness.
RBM should not fear constructive independent
review.
The Lancet
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