Photo: Guy Oliver/IRIN
The doctor will see you now...
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The
majority of Africa ’s private medicine sellers
do not operate out of established pharmacies. Aspirin and cough syrup,
antibiotics and malaria pills are tucked in among the pomade and toothpaste in
run-down `dukas’ and on dusty market stalls; packets of pills are strapped onto
the display boards of itinerant hawkers or pinned to open umbrellas.
These
vendors are controversial. They have no medical training, they sell without
prescription, and with no guarantee the drugs are genuine and still in date.
But they can be a godsend if you live in a village far from the nearest clinic
or pharmacy, or if your child has a fever late in the evening when all the more
official sources of medicines are shut.
Around
10 years ago it was clear that in countries depending on private vendors of
anti-malarials there was a big problem. Although effective artemisinin drugs
were available, most private vendors were still selling older, cheaper drugs
like chloraquine, which were no longer effective. Where they did sell
artemisinin drugs, they were likely - again for cost reasons - to be the simple
variety (monotherapy) that looked very likely to cause a build-up of
resistance, rather than the combined drugs like Coartem, which were more
expensive.
So
a plan was proposed to flood the market with high-quality, combined therapy
drugs at heavily subsidized prices. It was hoped that this would increase
availability in both private outlets and public clinics, reduce prices so that
the best drugs would be as cheap as the less effective ones, and displace the
risky monotherapies, which the World Health Organization (WHO) was hoping to
phase out altogether.
The
plan was put into practice as a pilot project in eight countries, funded mostly
by the UK ’s
Department for International Development and the Bill and Melinda Gates
Foundation, and administered by the Global Fund. Now an independent evaluation
of that pilot has been published and the board of the Global Fund is meeting in
nine days to decide whether AMF has worked as was intended, and whether it
should be continued, scaled up, or abandoned altogether.
Mixed
results
The
results, frankly, were mixed, and varied enormously between countries. The
biggest effect was seen in the private sector, which responded quickly to the
offer of lower priced drugs. In six of the eight countries (but not Niger and Madagascar ) artemisinin-combination
therapies (ACTs) became much more available in the first year of the project
and took a substantially larger share of the market. Again in most countries,
but not all, the high-quality drugs became much cheaper - in the case of Tanzania the
price fell to around one fifth of its former level. But the price fall in Uganda was tiny, and the price in Madagascar
actually rose a little.
One
of its drawbacks is that it has essentially replaced one bad system with
another bad system, albeit with better drugsMuch less dramatic effects were
seen in the public sector, probably because public procurement is much more
cumbersome and slower to respond to price changes. The use of artemisinin
monotherapies did decline, although it was not clear how much of the reduction
was due to AMF, and how much was a response to WHO pressure and regulation.
The
result of the evaluation was welcomed by the scientists who put together the
original plan. A comment in the London-based journal, the Lancet, said AMF “had
transformed access to effective antimalarials” in seven countries that
represent a quarter of the world’s malaria cases.
Others
have been less welcoming. Oxfam has published an extremely critical paper
warning against such a heavy reliance on private providers and saying that even
at subsidized prices, the drugs are still out of reach of the poorest people.
It also points out that many childhood fevers are not caused by malaria, and
that treating fevers indiscrimately with antimalarials is both wasteful and
dangerous.
Diagnosis
vital
Oxfam’s
senior health policy adviser, Mohga Kamal Yanni, said: “A shopkeeper selling
salt, pepper and malaria medicines cannot diagnose or treat a child with
pneumonia. It is dangerous to put the lives of sick children in the hands of a
shopkeeper with no medical training and to pursue a scheme that doesn’t help
those people who need it the most.”
At
the London School of Hygiene and Tropical Medicine, Toby Leslie, a researcher
with the ACT Consortium, is more measured, but agrees that the encouragement to
treat without proper diagnosis is AMF’s weak point. “Undoubtedly it has
improved access to ACTs in most of the countries where it has been tested,” he
told IRIN, “and that’s definitely encouraging.
“But
one of its drawbacks is that it has essentially replaced one bad system with
another bad system, albeit with better drugs. There’s no access to diagnosis,
and what we would once have assumed to be malaria, we now know is often not
malaria. What we need now is what I would call `son of AMF’, with better
targeting. There’s a lot of movement on this, and a lot of voices trying to be
heard. There’s a long way to go, but it would be a shame just to drop the ball,
undermining any gains that have been made.”
Oxfam
is unlikely to be the only group campaigning against a continuation of AMF at
the Global Fund meeting in Geneva .
It has never been popular with the US government, and has not received
any funding from the president’s Malaria Initiative. Campaigners on malaria issues
say the Facility is unlikely to be continued in its present form, but the
subsidy system could continue on a country by country basis.
One
such campaigner told IRIN that the transition would have to be carefully
managed. “With this kind of programme,” she said, “you can’t just have a hard
stop. That would lead to stock-outs, not just in the private, but also in the
public sector. You need a transition period for each of the pilot countries to
figure out the best way forward for them, so that you don’t put people at
risk.”
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