NEW YORK | Mon Oct 18, 2010 5:18pm EDT
NEW YORK (Reuters Health) - Despite carrying monikers like 'fake' or 'dummy' or 'sham,' some placebo pills may be potent enough to taint medical research results, hints a new review of more than 150 clinical trials.
This time researchers aren't just talking about a 'placebo effect' on the mind, but rather physiological effects of the pills' constituents on the body. What's more, they found that less than one out of every 10 studies published in four top medical journals actually divulged what ingredients were used in placebo pills.
"We've been trained to associate placebos with being inert," lead researcher Dr. Beatrice Golomb of the University of California, San Diego, told Reuters Health. "But there isn't evidence that anything is truly physiologically inert."
"This really does question the primary foundation on which medical care is based," added Golomb.
A standard method used to deduce whether or not an experimental drug is effective is to compare it to one that looks, smells and tastes the same yet lacks active ingredients: a placebo. By keeping patients unaware of which pill they consume, a research team can learn if the differences in observed outcomes are due to the medication itself or simply the power of suggestion.
At least that's the ideal. However, in looking at older studies of heart disease, Golomb noticed that placebos often consisted of things like olive or corn oil, which are now known to lower cholesterol levels -- potentially diluting the experimental treatment's perceived benefits.
Some earlier clinical trials of cancer and HIV treatments, she found, used placebo pills composed of lactose sugar and found relatively few gastrointestinal problems in the experimental group: AIDS and cancer patients can be at an increased risk for lactose intolerance.
And these were just the rare studies that included the recipe. Further, she noted that the company producing the experimental drug often supplies the study placebo as well.
"This led me to wonder," said Golomb. "What rules are there about what goes into placebos?"
She contacted the U.S. Food and Drug Administration and learned that, in fact, there were no rules.
So Golomb and her colleagues decided to dig deeper. They reviewed 167 placebo-controlled trials published in highly respected medical journals in 2008 and 2009 and found that placebo components were very rarely described.
Only about 8 percent of the trials shared the contents of the pills. Studies were a little more open regarding placebo injections and other treatments with about one in every four divulging the information, report the researchers in the Annals of Internal Medicine.
"We can only hope that this hasn't seriously systematically affected medical treatment," noted Golomb.
But she and her team suggest that it is a very real possibility, with potentially serious consequences. "An ineffective treatment might appear effective, or an effective treatment might appear ineffective in trials," senior researcher Jeremy Howick of the University of Oxford, in England, told Reuters Health in an email. "This is obviously harmful for public health since it could lead to use and payment for ineffective treatments, or failure to recognize effective ones."
"Placebos are best viewed as treatments in their own right," he added.
*We welcome comments that advance the story directly or with relevant tangential information. We try to block comments that use offensive language or appear to be spam and review comments frequently to ensure they meet our standards. If you see a comment that you believe is irrelevant or inappropriate, you can flag it to our editors by using the report abuse links. Views expressed in the comments do not represent those of Reuters.
No comments:
Post a Comment