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[e-drug] DTCA and Canada 1
- From: e-drug@healthnet.org
- Date: Thu, 4 Sep 2003 01:11:48 -0400 (EDT)
E-drug: DTCA and Canada 1
---------------------------------------------
[The following articles on Direct to Consumer Advertising (DTCA) have
been published in the current issue of Canadian Medical Association
Journal. They will be sent as separate messages. BS]
2 September 2003; Vol. 169, No. 5
URL: http://www.cmaj.ca/content/vol169/issue5/index.shtml?etoc
1. Editorial: Ads and prescription pads
[copied as fair use]
CMAJ 2003;169 381
<http://www.cmaj.ca/cgi/content/full/169/5/381?etoc>http://www.cmaj.ca/cgi/content/full/169/5/381?etoc
How does direct-to-consumer advertising (DTCA) affect prescribing? A
survey in primary care environments with and without legal DTCA
Barbara Mintzes, Morris L. Barer, Richard L. Kravitz, Ken Bassett,
Joel Lexchin, Arminee Kazanjian, Robert G. Evans, Richard Pan, and
Stephen A. Marion
CMAJ 2003;169 405-412
http://www.cmaj.ca/cgi/content/abstract/169/5/405?etoc
In 2000, pharmaceutical firms in the United States spent US$2.5
billion on direct-to-consumer advertising (DTCA) - more than 3 times
the amount they had spent in 1996, and 35% more than in the previous
year.1 From a business perspective, this money was well spent: for
example, it has been claimed that each dollar spent on consumer
advertising for the allergy drug Claritin has brought in $3.50 in
increased sales.2 In this issue, Barbara Mintzes and colleagues
report on the effects of DTCA on patients and physicians3 (see pages
405 and 425). It seems that DTCA has a primary and a secondary
effect: patients are susceptible to advertisers' claims, and
physicians are susceptible to patients' requests for advertised drugs.
Is this necessarily a bad thing? Some common illnesses such as asthma
and diabetes are undertreated, whether through underdiagnosis or poor
"compliance," and a substantial proportion of the general adult
population has pharmaceutically treatable risk factors such as
hypertension and hyperlipidemia. An argument can be made that
underprescribing is a medical error (of omission).4
Arguments in favour of DTCA also speak of "empowering" the patient by
means of providing information on the treatment choices available.
Those wonderfully cryptic "reminder" and "help-seeking" ads one sees
on television these days (which slide under the regulatory radar in
Canada by naming either a condition or a treatment but not both
together in what might be construed as a "product claim" - see page
421) may raise awareness of some health problems and reduce stigma,
thus helping to break down resistance against seeking information,
diagnosis and treatment. Insofar as DTCA is informative, who are
physicians and regulators to say it isn't good for patients?
The trouble with DTCA is not that it is directed to patients, who
have every right to know about the therapeutic products potentially
available to them. The problem is simply that it is advertising,
whose purpose is to deliver messages, not information. Those messages
are intended to promote the use of newer, more expensive drugs (even
if older, cheaper, ones work as well) and to increase brand
recognition (but not an awareness of side effects, or of
nonpharmacologic options for treatment and prevention). Their purpose
is to create demand by delivering a double message of anxiety and
hope, encouraging a belief that a condition - hair loss, acne,
shyness, allergies or osteoporosis - is not only "widespread [and]
serious" but "treatable."5 In addition to raising general consumer
awareness, they carve out new and sometimes questionable market
niches (e.g., through a Viagra ad campaign aimed at younger men).1
The fact that DTCA is subject to government regulation and voluntary
standards gives some reassurance, but not much. Advertising standards
are as tricky to interpret and enforce as marketing gurus are
creative; moreover, the very fact that DTCA is subject to government
regulation and advisory-board approval has the paradoxical effect of
increasing its credibility.1
But perhaps the most noteworthy point about DTCA is that word
"consumer." By being marketed in media traditionally used to flog
cars, fast food and shampoo, prescription drugs have become
name-brand commodities, enveloped in the kind of fantasy and desire
that surrounds the purchase of lifestyle products. At the same time,
the constant barrage of DTCA contributes to the "medicalization" of
normal human experience by which the authority of medicine and our
modern inability to accept the normality of illness and death has
turned us into "two-legged bundles of diagnoses."6 Moreover, what
Ivan Illich so forcefully described in 19767 as an iatrogenic
phenomenon has now gone corporate: "The social construction of
disease is being replaced by the corporate construction of disease."5
One launches into such critiques at the risk of sounding hysterical.
And so we hold back from an alarmist stance that assumes that no
patient is capable of responding to an advertisement skeptically. But
consider the following: if US-style, "product claim" DTCA were
permitted in Canada (the only other country that allows it is New
Zealand), pharmaceutical firms might spend about Cdn$360 million a
year and expect drug sales to increase by as much as $1.2 billion.
These additional costs will be added almost entirely to the cost of
medicare. Do we know enough about the RCT-proven benefits of the
advertised drugs to decide whether this is a wise use of our
resources? Those resources might be better spent in providing
unbiased "consumer" information about drugs and alternative non-drug
therapies and prevention. - CMAJ
References
1. US National Institute for Health Care Management. Prescription
drugs and mass media, 2000. Washington: The Institute; 2001.
Available:
www.google.ca/search?q=cache:Mql7xCnuyc4J:www.nihcm.org/DTCbrief.pdf+Prescription+drugs+and+mass+media,+2000.+&hl=en&ie=UTF-8(accessed
2003 Aug 11).
2. Pill pushers. Economist 2001; Apr. 21. p. 58-9.
3. Mintzes B, Barer ML, Kravitz RL, Bassett K, Lexchin J, Kazanjian
A, et al. How does direct-to-consumer advertising (DTCA) affect
prescribing? A survey in primary care environments with and without
legal DTCA. CMAJ 2003;169(5):405-12.
4. Committee on Quality Health Care in America. Crossing the quality
chasm: a new health system for the 21st century. Washington: National
Academy Press; 2001.
5. Moynihan R, Heath I, Henry D. Selling sickness: the pharmaceutical
industry and disease mongering. BMJ 2002;324:886-91.[Free Full Text]
6. Illich I. Death undefeated. BMJ 1995;311:1652-3.[Free Full Text]
7. Illich I. Limits to medicine. In: Medical nemesis: the
expropriation of health. Toronto: McClelland and Stewart; 1976.
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