Environmental Science & Engineering - www.esemag.com - March 2003
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When pharmaceuticals arrive at the tap
The new issue emerging in environmental
science is the contamination
of ground and surface
water bodies with pharmaceutical
and personal care products,
or PPCPs.
When people take medications, or
use personal care products such as
medicated shampoo or sunscreen, a
considerable amount of the biologically
active chemical eventually enters the
wastewater stream after passing
through, or flowing off the body. The
same holds true for veterinary medicines
and animal care products. PPCPs
have been found in studies of ground
and surface waters in Canada,
Germany, and the United States, and
can be expected to appear in most
developed areas.
In Canada, surface waters near
wastewater treatment plants were
found contaminated with painkillers,
anti-inflammatory drugs, anti-seizure
medications, and blood cholesterol
drugs (Stevenson, 2002). Drugs found
in German rivers include carbamazepine,
an anti-convulsant, and
diclofenac, an anti-inflammatory, at
concentrations up to 1 part per billion
(Potera, 2000). Under landfills, where
water leaching downward can carry
drugs along with it, far higher concentrations
have been found, posing a risk
to nearby sub-surface waters. In the
United States, attention has also
focused on animal feed lots, where animal
wastes, contaminated with antibiotics,
have led to contamination of
local surface waters (Kolpin et al.,
2002).
Around the world, more than 60
chemicals have been discovered in
water sources, including anti-cancer
medications, anti-asthma medications,
anti-cholesterol drugs, hypnotics,
antibiotics, antiseptics, X-ray contrast
agents, sunscreen agents, caffeine, and
synthetic musk fragrance chemicals
(Potera, 2002).
The most troubling findings in the
growing body of PPCP research is that
some of these drugs are making it into
fresh water systems, and are detectable
at the tap. In a study by Glen Boyd at
Tulane University, for example, several
PPCPs were detected in local tap
water samples including the pain killer
naproxen, the sex hormone estrone,
and a breakdown product of anti-cholesterol
drugs (Potera, 2000). Though
the chemicals were found at very low
levels - they were barely detectable -
scientists consider them of concern
because, by design, pharmaceuticals
are intended to exert their effects at
very low concentrations.
In response to the growing concern,
in September, 2001, Health Canada
enacted a two-year program to study
new environmental assessment regulations
for PPCPs. And as of September
13, 2001, companies seeking approval
to import or manufacture new products
regulated under Canada’s Food and
Drugs Act have to notify the Minister
of the Environment under the New
Substances Notification Regulations
of the Canadian Environmental
Protection Act (Health Canada, 2001).
Health Canada’s two-year research
project is half over, and calls for concrete
regulatory action are likely as
advocates of the precautionary principle
team up with planners of the "we
must act even in uncertainty" mindset.
But like other low-concentration, poorly
understood environmental contamination
issues, managing the risk of
PPCPs poses several challenges, that,
if not handled carefully, could ultimately
result in less safety and less
environmental quality for Canadians.
Policy challenges
PPCPs pose several policy challenges
common to managing uncertain,
low-level environmental risks.
First, there is the challenge of determining
whether or not PPCPs actually
pose a risk to plant, animal, or human
health. Though unpleasant to contemplate,
all of Earth’s organisms evolved
and spend their lives being exposed to
very low concentrations of thousands
of potentially harmful chemicals, both
natural and artificial. Preventing all
such exposures would be impossible,
even if society had unlimited resources
to throw at the problem. Thus, one
question that must be answered with
PPCPs is: "Does the dose make a poison?"
On this front, expert opinion
suggests that the dosages are too low to
be considered risky, but some theories
suggest that even very low exposure
levels could ultimately cause harm,
particularly for pharmaceuticals
(Stevenson, 2002).
Second, there is the challenge of
addressing newly discovered, still uncertain,
and probably low-level risks
without shifting resources away from
the management of older, bigger, better
established risks. As public health
researchers at Harvard University have
shown, there is a real cost to be paid
when management of lower-level,
more uncertain risk is allowed to consume
resources that could be used to
address higher-level, more certain
risks. As researchers Tammy Tengs and
John D. Graham observe, the United
States spent about $21.4 (US) billion
in 1994 on 185 life-saving interventions,
averting about 57,000 deaths.
But spending that same amount of
money, prioritized to produce maximum
return on investment, would have
saved an additional 60,000 people
(Tengs and Graham, 1996).
And one cannot forget that the single
biggest protector of safety, health,
and environmental quality is societal
and individual wealth (Bloom and
Canning, 2000). Resources taken out
of the productive economy and shifted
into the regulatory economy are not
risk-neutral. Indeed, by reducing economic
growth, regulatory diversion of
resources constitutes a risk-increasing
factor that may offset the perceived
benefit of regulating a low-level risk
such as PPCP exposure.
Third, there is the challenge of figuring
out the proper point at which the
problem can best be managed. Without
eliminating the use of pharmaceuticals
and chemicals altogether, one cannot
prevent the release of PPCPs into the
environment through the diverse set of
waste streams discussed above. That
means that management of PPCP contamination
and exposure has to be handled
downstream, at the point of drinking
water and wastewater treatment.
But even that would only be a partial
solution as water treatment does
not account for PPCPs that find their
way into surface and subsurface
sources through landfill leaching, animal feedlots, or pet wastes, which contain
veterinary PPCPs with similar
characteristics to PPCPs of human origin.
Water purification at the point of
consumption could remove PPCPs
from the tap entirely, but this would
not address potential impacts of
PPCPs on wildlife, or on people who
periodically consume the wildlife,
such as hunters or fishers.
Additionally, one could envision a
system in which all unused PPCPs
were returned to pharmacies, which
would ensure their environmentally
safe disposal, but such a system would
also address only a small fraction of
the problem.
All of these approaches would
address only a portion of the sources of
PPCP contamination, but each would
impose significant costs, draining
resources away from the health-protective
productive economy. Which takes
us to the last question: Who should pay
for PPCP management?
Ideally, to create the right incentives
for reducing pollution, the cost of
remediation should rest on the polluter,
but this straightforward approach has
problems. Under this principle, consumers
would be responsible for the
added costs of downstream waste
water remediation, and the costs allocated
according to use, perhaps collected
as a fee attached to drugs and
personal care products. But this is
problematic in terms of ability to pay,
and fundamental ethics.
The basic ethic of the "polluter
pays" principle presumes that the polluter
has a meaningful ability to
change his or her behavior in response
to the incentives, which is unlikely in
the case of many medicines. Shifting
the fee up the ladder of production to
the producers of PPCPs wouldn’t really
circumvent this dilemma, as such
costs will ultimately be passed onto the
already cost-burdened pharmaceutical
user as well, or, in the case of insured
pharmaceuticals, onto the general taxpayer.
The costs of additional drinking
water or wastewater purification would
ultimately be paid by consumers, but
this diffuse cost recovery would not
give incentives to some of the larger
PPCP releasers (landfills and feedlots)
to institute technological controls that
might prevent the entry of PPCPs into
the environment.
Conclusion
PPCPs are a newly-discovered form
of pollution that poses several difficult
challenges to policymakers, but one is
paramount: while the risk is known to
be low-level and is still highly uncertain,
remedies have known drawbacks
that can easily make the public, or subpopulations,
less well off. Such drawbacks
include the potential for diverting
resources from more certain risks
of higher magnitudes, or for reducing
after-tax income of the general population,
or already-cash-strapped subpopulations,
a phenomenon that clearly
puts those populations at greater risk
from a broad range of adverse health
consequences. Individuals who are
highly risk-averse might choose to
limit water intake to only purified
sources, but this addresses only a small
part of the overall policy challenge.
Policymakers are likely to be pressured
to act to somehow ensure that
PPCPs do not cause environmental
harm, or pose a hazard to the health of
even sensitive individuals in the population.
But in circumstances such as these,
where risks are poorly defined and
interventions likely to be costly and
only marginally effective, policymakers
would do well to consider the work
of policy analyst Aaron Wildavsky,
who showed that such high-uncertainty/
low-level risk situations lend themselves
to watchfulness and research,
but not interceptive action (Wildavsky,
1991). They should pay particular
attention to the work of Harvard’s
Tammy Tengs and John Graham, who
point out that prioritization is key to
maximizing public safety (Tengs and
Graham, 1996). And they should study
the work of toxicologist Bruce Ames
and others who point out that truly, it’s
the dose that makes the poison (Ames
and Gold, 1998). Scrutiny of the work
of these well-respected students of
health, safety, and environmental quality
would suggest that at present, the
best response to the PPCP situation, as
with many other environmental problems,
is to watch and wait until one can
see the whites of its eyes.
Kenneth Green, D. Env. (keng@fraserinstitute.ca) is Chief Scientist
and Director of the Centre for Studies
in Risk, Regulation and Environment
at The Fraser Institute. He most recently
wrote Global Warming: Understanding
the Debate. This article first
appeared in Fraser Forum (www.fraserinstitute.ca) and is reprinted here
with permission.
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