Sunday’s New York Times carried an editorial
by Mike Osterholm and Mark Olshaker. In it, they decry the budget proposal by
President (cringe) Trump to cut the NIH budget by 18 per cent, the State
Department and AID budget by 28% and to repeal the ACA (luckily that didn’t
happen). All of these proposals will further cripple our ability to prevent or
respond to infectious disease crises both here in the US and abroad.
Osterholm and Olshaker remind us of congress’s failure to
adequately fund the US response to local Zika outbreaks here in the US, and
they wonder what would happen in the face of a real pandemic like the 1918 flu
that infected about 500 million people – frequently young people – adding up to
about one-third of the planet’s population at the time, and killed about 50 million. With the 2017 world population of 7.9
billion, something similar today would
kill 260 million people. Could such a
thing occur? Sure. All we need is for one of the circulating
bird flu strains of the virus become virulent for humans. A few mutations here and there . . .
But, and you won’t be surprised here, a more immediate
threat that is currently ongoing and building is that posed by antibiotic
resistance. And this brings me to where I might have a quibble with the authors
of the Times editorial. They conclude
that only government can produce the drugs and vaccines needed to repulse these
infectious disease threats in the absence of a viable, existing market. Well –
yes if you say that only government funding of competent companies and
scientists can do this. Government
itself has a poor track record in the invention of antibacterial drugs after
say the 1950s. But recent efforts through HHS have provided significant funding
for companies and academics to spur these efforts.

At the same time, government can play a critical role in
providing funding in terms of market entry rewards, patent vouchers and other
key post-market incentives that will essentially create an attractive
marketplace for new antibiotics that will be active in the treatment of
resistant infections.
So here are two solutions to the problem both within reach.
(1) Lets get our scientists trained. (2) Lets provide market incentives for new
antibiotics. All this takes is money,
will and work!
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