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Medicine and the Media
Medicine, the media and monetary interests: the need for
transparency and professionalism
Ray Moynihan and Melissa Sweet
MJA 2000; 173: 631-634
→ Other articles have cited this article
Abstract -
Breakthroughs and boosterism -
The news business -
Cosy relationships -
The buck stops...where? -
Cash for comment -
Evidence-based journalism -
References -
Authors' Details
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- Emerging evidence suggests that media coverage of medicine is
increasingly promotional in nature.
- Recent Australian examples include misleading newspaper articles
on an experimental cancer vaccine and a high profile television
current affairs segment on a new influenza drug, which failed to
disclose the industry ties of a key expert featured in the report.
- There are widening concerns that this problem in medical journalism
may be exacerbated by the growing commercialisation of medical and
scientific research, and the increasing ties between researchers,
doctors and pharmaceutical or biotechnology companies.
- Closer links between industry and medicine are being explicitly
encouraged both in academia and the health care sector for the mutual
benefits they bring. However, these partnerships are the cause of
growing unease within medicine.
- In the United States, rigorous legislation governing research
protocols is being proposed, and in Australia new ethical guidelines
covering industry-profession relationships are being
promulgated.
- If one of the media's roles is informing the community about the
business of health and medicine in a fair and accurate way, a cultural
change in medical journalism is required.
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In November 1999, one of Australia's high circulation newspapers
published a prominent story about a new cancer vaccine that had
"tripled life expectancy in trials".1 In May 2000 the Australian
Press Council upheld a complaint from a leading cancer expert that
this report, versions of which were published in sister newspapers
across the country, was both misleading and inaccurate.2 While the
Australian Press Council made no judgement about the scientific
evidence supporting the new vaccine, the finding served as a timely
reminder of the need for more scepticism in medical journalism. Yet
just two months later, in July 2000, the same vaccine received another
round of positive publicity in the nation's leading newspapers,
publicity echoing promotional material from the vaccine's
proponents.3
If one of the media's roles is to inform the community in a fair and
accurate way, the reporting of medicine or medical research too often
falls short of the mark. A recent study of newspaper and television
coverage of medications over a five-year period found many stories
tended to overstate therapy benefits, played down potential harms
and failed to disclose the relevant industry ties of cited experts
(Box).4 The misleading nature of
much medical reporting requires urgent attention from both
journalists and health professionals.
Concern about media reporting raising false hopes, undue anxiety or
unnecessary alarm is not new.5 However, the increasing
commercialisation of scientific research, and the expanding role of
the stockmarket in medicine, are creating powerful new forces. Like
many new therapeutic advances, the experimental cancer vaccine
featured in the Australian media is promoted by a biotechnology
company listed on the stock-exchange: for these companies positive
stories may boost share prices and negative stories may send them
plummeting.
Closer involvement between industry and science, which is being
explicitly encouraged in a bipartisan way in Australia,6 may well carry
the clear benefits of increased research funding or enhanced
commercial opportunities for effective new treatments -- but at what
cost? Within medical circles, and in the wider community, there is
growing unease that overly cosy relationships may be affecting
research integrity and professional independence.7,8 It may be time
for the media to offer more critical analysis of the business of
medicine, and less thinly disguised promotion of the latest
"breakthroughs".
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At the international Berzelius Symposium, Medicine and the
Media, convened in Stockholm in September this year by the
Swedish Society of Medicine, many contributions focused on the
increasing commercialisation of medical and scientific research.
While some conference participants expressed optimism about a
growing sophistication in media coverage of medicine, others
expressed concern about promotional "boosterism", particularly in
media coverage of genetics and biotechnology.9
At the conference, Lars Holmgren, from the Karolinska Institute,
Sweden, focused on the now-infamous front-page story in the New
York Times on Sunday, 3 May 1998. It began with the paragraph:
"Within a year, if all goes well, the first cancer patient will be
injected with two new drugs that can eradicate any type of cancer, with
no obvious side effects and no drug resistance -- in mice."10 The article
referred to two agents, endostatin and angiostatin, which have shown
significant promise in treating cancer in mice by blocking
angiogenesis. It had an international impact, provoking widespread
follow-up in other media outlets, and leading to many inquiries from
anxious cancer patients about a treatment that had not yet been
trialled in humans.
As Holmgren explained, the front-page story also had a dramatic
impact on the shares of the company developing the agent, which
increased in value severalfold the next day. An investigation by the
Los Angeles Times11 later showed that the
shares in this and other biotechnology companies have since risen and
fallen in response to continuing public relations activities and
media stories, both positive and negative.12
In a provocative conclusion, Holmgren suggested that the trend
towards researchers seeking to attract investors through publicity
in the mass media -- often ahead of publication in scientific journals
-- had become so prevalent that the high-tech stock index, the Nasdaq,
had become a more reliable indicator of scientific developments than
journals themselves!
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If "good news" medical stories are valuable for listed companies,
they are also big business for commercial media and increasingly
entrepreneurial public broadcasters. Television news and current
affairs programs routinely broadcast formulaic "breakthrough"
medical stories, and often heavily promote them. As the southern
hemisphere flu season got under way this year, a top-rating
television current affairs program broadcast an item about Glaxo
Wellcome's new influenza product Relenza (zanamivir), described as
a "wonder drug" with "miraculous results".13 While brief mentions were
made of concerns about cost-effectiveness and a paucity of
sufficient trial data in high-risk patients, the presenter's
voiceover was upbeat, and reinforced by comments that the drug had
been hailed as "the greatest breakthrough ever" in the treatment of
influenza. During the day of the broadcast and the following day's
trading, the price of shares in Glaxo's Australian partner, Biota,
jumped almost 15%.
While the television segment was extremely good news for company
investors, it serves as another stark example of the malaise
affecting much of medical reporting. Like many previous items about
zanamivir, the drug's modest benefits were not
mentioned.14 Similarly, the evidence
of rare but potential serious harm associated with the new drug for
those with pre-existing illnesses like asthma were
ignored.15
Perhaps most importantly, the television program failed to inform
its audience of the links between Glaxo Wellcome and one of the key
experts who repeatedly appeared in the segment, despite the
company's support for the expert's research on zanamivir being
clearly disclosed in the scientific literature.16 Instead, the
program chose to describe the specialist as an "independent
professor" from an academic institution. This clear failure to
reveal the relevant industry ties of a key source is not an isolated
instance.4
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While many media stories are failing to report on the potential
conflicts of interest of their "experts", the growing ties between
industry and academic medicine are generating considerable
disquiet. In an editorial in the New England Journal of
Medicine in May this year, Marcia Angell, the journal's editor,
detailed the dangers of the increasingly "cosy relations" between
medical scientists and the drug and device manufacturers providing
funds for research, consultancies for advice, and free trips to speak
at international conferences.7
As an example of the problem, Angell cited the difficulties in finding
independent reviewers to write about the treatment of depression,
because so many US psychiatrists have links to companies selling
antidepressants. "The problem is by no means unique to psychiatry,"
she wrote. Nor is the problem unique to the United States. Two years ago
a leading Australian academic complained publicly of the difficulty
in finding independent specialists to sit on regulatory committees,
because so many were consultants to drug companies.17
The reason for concerns about the increasingly intricate ties
between researchers and industry is not simply academic. Evidence
suggests that a range of physician-company interactions (like
attending company-sponsored education, or accepting sponsored
trips) can carry negative impacts on behaviour.18 As Angell
pointed out, "there is now considerable evidence that researchers
with ties to drug companies are indeed more likely to report results
that are favourable to the products of those companies than
researchers without such ties."7
An obvious concern is that corporate funding may sometimes cause
bias. More subtly, according to Angell, ties may influence
scientific judgements in ways that are difficult to identify. The
bottom line is that companies are seen to be buying the goodwill of
researchers, "which is a very valuable commodity for drug and device
manufacturers".7
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The goodwill of researchers and opinion leaders is a particularly
valuable commodity precisely because it can be exploited by a company
using the media to promote a new product direct to the public. Having a
new product endorsed in newspapers or on television by a purportedly
independent authority figure is invaluable. Clearly, the
mainstream media must urgently institute routine disclosure of the
potential conflicts of medical and health experts, just as medical
journals have required for some time. Amendments to journalist codes
of ethics may be one route towards this outcome. Similarly, it may be
appropriate for media to disclose when a public relations company or
another vested interest has been responsible for orchestrating a
story.19
Community concerns about the ties between doctors and the
pharmaceutical industry led the Royal Australasian College of
Physicians this year to disseminate new ethical guidelines that
cover these relationships.20 Largely accepting the
benefits of close commercial relationships, including company
funding of research, paid consultancies and sponsored travel, the
guidelines recognise the possibility that these relationships may
cause conflicts between physicians' responsibilities to their
patients, and their own personal gain. Essentially endorsing the
multiplicity of industry-professional ties, the guidelines argue
that openness to public scrutiny is a sufficient safeguard.
But self-regulatory professional guidelines that carry no real
penalties are not considered enough in some quarters. Responding to
Angell's editorial, the United States Secretary for Health and Human
Services, Donna Shalala, recently announced a list of wide-ranging
measures to improve ethical conduct in research.21 Included is
the possibility of new legislation which would impose fines of up to
$US250 000 per clinical investigator and up to $1 million per research
institution for violations of ethical research conduct -- such as
failing to obtain proper informed consent from research
participants.
Shalala argued that several recent incidents in the United States,
including the much-publicised death of a subject in a gene therapy
trial,22 had shaken public
confidence in research ethics. One of the reasons that protection for
human subjects needed to be strengthened was, according to her
editorial, that academic investigators increasingly have
commercial links with trial sponsors or personally hold patents over
the therapies being trialled, creating potential conflicts of
interest and major ethical dilemmas.
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The recent Australian Broadcasting Authority inquiry into
commercial radio, known as the "cash for comment" inquiry, has helped
raise awareness of the extent of hidden corporate payments to
broadcasters and the way in which those payments can undermine and
distort public debate. In a similar distortion of public debate,
overly promotional media coverage of healthcare products may help
foster false public expectations of benefits, encourage
unnecessary or potentially harmful use, and add to healthcare costs.
As well, there are concerns such coverage may promote
overmedicalisation and discourage the use of effective non-medical
interventions.
In light of the revelations which emerged from the "cash for comment"
inquiry,23 a rigorous and
wide-ranging investigation of the nature and extent of commercial
links between the medical profession and the pharmaceutical,
biotechnology and medical technology companies may now be timely in
Australia. In a spirit of openness and disclosure, such an inquiry
could also examine the ties between journalists and the medical
companies whose products they are charged with reporting on.
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Enhanced transparency about industry ties is only one strategy for
improving the way the media covers medicine. In our view, journalists
and media managers could benefit greatly from a heightened
understanding of the move towards an evidence-based approach in
healthcare. As a recent article in the Australian journalists'
professional magazine, The Walkley, noted,24 the media
could learn from the questions which are being asked by proponents of
evidence-based medicine (eg: What is the evidence to support the
claim being made? How strong is the evidence? How does it fit with the
existing body of evidence? Are there other, valid conclusions which
could be drawn? Have the results been published in a reputable
peer-reviewed journal? What interest might the doctor/researcher
have in promoting this view?).
Strategies for quality improvement will require debates within
media organisations, journalist professional bodies and the wider
research community. Valuable assistance in those debates may soon
come from a group of researchers who are now conducting a randomised
controlled trial of various educational interventions for
journalists covering health and medicine.25 Similarly, many
researchers and journalists, as well as the Australasian Medical
Writers Association, are working on educational and other resources
designed to improve medical reporting.26,27 In Sweden, for
example, medical journalists are encouraged to follow a number of
ethical guidelines, including do not arouse false hopes and fears;
try to present risks and benefits together; emphasise the uncertain
and temporal nature of knowledge.28
Critical, informed and independent journalism will become even more
crucial in light of increasing commercialisation, combined with the
major, complex changes arising from the new biotechnologies. Media
organisations currently face a fundamental choice about how they
cover the issue of human health: to act as "cheer squads" for the new
products, or to seek out truly independent evaluation of promotional
claims in order to better inform the public about the limitations,
uncertainties, dangers and costs, as well as the genuine health
benefits, of new medical therapies and technologies.
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1Telegraph, 19 November 1999: 3.
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The Australian Press Council. Adjudication No. 1081. Re: The
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Greenblat A. Cancer drug fires up AVT. The Age 20 July 2000:
B3; and The Sydney Morning Herald, 20 July 2000: 23.
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Greenberg DS. Stricter regulation proposed for US gene therapy
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September 2000. Stockholm.
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Authors' Details | |
Ray Moynihan, BA, Journalist, Australian Financial
Review, Harkness Fellow in Health Policy, 1998-1999.
Melissa Sweet, BA, MA, Journalist, The Bulletin and
Australian Doctor.
Reprints will not be available from the authors. Correspondence: Mr R
Moynihan, 76 Francis Street, Bondi, NSW 2026.
ray_128AThotmail.com
©MJA 2000
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| What the media didn't say |
The relative-risk "gee-whizz" effect |
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A retrospective analysis of 207 United States newspaper (n = 180)
and television (n = 37) stories in the period 1994-1998 about three
preventive medications (pravastatin, a cholesterol-lowering drug; alendronate,
a bisphosphonate for treatment and prevention of osteoporosis; and aspirin,
as used to prevent cardiovascular disease) revealed that:
- 53% of 207 stories did not mention potential harms.
- 70% of 207 stories did not mention drug costs.
- 83% of 124 stories which quantified benefits used a "relative"
frame only -- an approach that is potentially misleading.
- 60% of 85 stories that cited at least one expert or study with a relevant
"industry tie" failed to disclose that tie.
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A story reported a randomised controlled trial
of alendronate as producing an "almost miraculous" 50% reduction
in the incidence of fractured hip. Sounds good? The story did not report
the actual rate of fractured hip in untreated patients (2%) or treated patients
(1%). The relative-risk reduction of 50% sounds much more impressive than
the absolute-risk reduction of 1% -- and, of course, both figures must be
weighed against other information, such as the costs and side effects of
treatment.4 |
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