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Much
of medicine is based on what is considered the strongest possible
evidence: The placebo-controlled trial. A paper published in the
October 19 issue of Annals
of Internal Medicine --
entitled "What's In Placebos: Who Knows?" calls into
question this foundation upon which much of medicine rests, by
showing that there is no standard behind the standard -- no standard
for the placebo.
The
thinking behind relying on placebo-controlled trials is this: to be
sure a treatment itself is effective, one needs to compare people
whose only difference is whether or not they are taking the drug.
Both groups should equally think they are on the drug -- to protect
against effects of factors like expectation. So study participants
are allocated "randomly" to the drug or a "placebo"
-- a pill that might be mistaken for the active drug but is inert.
But,
according to the paper's author, Beatrice Golomb, MD, PhD, associate
professor of medicine at the University of California, San Diego
School of Medicine, this standard has a fundamental problem, "there
isn't anything actually known to be physiologically inert. On top of
that, there are no regulations about what goes into placebos, and
what is in them is often determined by the makers of the drug being
studied, who have a vested interest in the outcome. And there has
been no expectation that placebos' composition be disclosed. At least
then readers of the study might make up their own mind about whether
the ingredients in the placebo might affect the interpretation of the
study." Golomb
pointed out these limitations to the placebo in a pair of letters to
the journal Nature 15
years ago.
"A
positive or negative effect of the placebo can lead to the misleading
appearance of a negative or positive effect of the drug," she
said. "And an effect in the same direction as the drug can lead
a true effect of the drug to be lost. These concerns aren't just
theoretical. Where the composition has been disclosed, the
ingredients of the placebo have in some instances had a likely impact
on the result of the study -- in either direction (obscuring a real
effect, or creating a spurious one). In the cases we know about, this
is not because of any willful manipulation, but because it can in
fact be difficult to come up with a placebo that does not have some
kind of problem."
Since
15 years have elapsed, the situation might have improved. Therefore,
Golomb and her colleagues analyzed just how often randomized trials
published in the past two years in each of the top four general
medical journals actually disclosed the makeup of placebos.
The
answer is not reassuring, according to the researchers, who found
that the placebo ingredients for pills were disclosed in fewer than
10 percent of cases. (The nature of the "control" was
significantly more likely to be stated for other types of treatments
-- like injections, acupuncture, or surgery -- where people are more
likely to question what "placebo" actually means.)
"How
often study results are affected by what's in the placebo is hard to
say -- because, as this study showed, most of the time we have no
idea what the placebo is," Golomb concluded.
Journal
Reference:
Beatrice
A. Golomb, Laura C. Erickson, Sabrina Koperski, Deanna Sack, Murray
Enkin, Jeremy Howick. What's
in Placebos: Who Knows? Analysis of Randomized, Controlled
Trials. Annals
of Internal Medicine,
2010; 153: 532-535 [link]
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