A study by Johns Hopkins researchers shows that a fifth of U.S. neurologists appear unaware of serious drug safety risks associated with various anti-epilepsy drugs, potentially jeopardizing the health of patients who could be just as effectively treated with safer alternative medications.
The findings suggest that the U.S. Food and Drug Administration needs a better way to communicate information to specialists about newly discovered safety risks, the researchers say, since the warnings are in many cases not getting through to doctors making important prescribing decisions.
And, the researchers add, while their new study, reported online in the journal Epilepsy and Behavior, was focused on neurologists and anti-epilepsy drugs, they believe their findings are applicable to a wide spectrum of medical specialists and medications.
“There is poor communication from the FDA to specialists, and there’s some risk to patients because of this,” says study leader Gregory L. Krauss, M.D., a professor of neurology at the Johns Hopkins University School of Medicine.
“Unless it’s a major change requiring the FDA to issue a black box warning on a product, important information appears to be slipping through the cracks.
“We need a more systematic and comprehensive method so that doctors receive updated safety warnings in a format that guarantees they will see and digest what they need to protect patients.”
Krauss and his colleagues surveyed 505 neurologists from across the nation in different types of medical practices.
They asked about several new safety risks for antiseizure drugs recently identified by the FDA: increased suicidal thoughts or behavior with newer agents; high risks for birth defects and cognitive impairment in offspring of mothers taking divalproex (sold by the brand name Depakote); and risks for serious hypersensitivity reactions in some patients of Asian descent starting treatment with carbamazepine (Tegretol).
One in five of the neurologists surveyed said they knew of none of the risks.
Those neurologists who treat two hundred epilepsy patients a year or more were most likely to know all of the risks.
Krauss says he was most struck by the lack of understanding of the risk to certain Asian patients who take carbamazepine to control their seizures.
The FDA in 2007 recommended that before initiating the drug in patients of Asian heritage, neurologists should screen to see if those patients have a specific haplotype, a specific section of DNA found in a few percent of Asian people, before prescribing the drug.
The researchers found that 70 percent of the neurologists who responded knew of the recommendation.
While 147 neurologists (29.1 percent) reported initiating carbamazepine treatment in Asian patients, only 33 of them (22.5 percent) said they performed haplotype screening.
Eighteen neurologists reported that their Asian patients developed carbamazepine-related hypersensitivity reactions — severe skin rashes that can lead to scarring, blisters in the mouth and shredding of the skin – during this time period.
“If their doctors were more educated about the risks,” Krauss says, “these patients may have avoided these severe hypersensitivity reactions.”
Krauss says doctors may not do the screening because it is difficult to find laboratories able to perform the haplotyping, and he notes that it may make more sense to prescribe an alternate drug to Asian patients.
The researchers found that 80 percent of respondents knew that the FDA had newly warned that the risk of suicide with newer drugs is 4.3 per 1,000, double what had previously been believed.
Seventy percent said they counseled patients about the risk.
As for pregnancy risks related to divalproex, fewer than half of the respondents knew that a warning had been issued noting high risks of birth defects and of developmental risks in offspring (an 8 to 9 point drop in IQ).
While 93 percent of respondents reported counseling women planning pregnancies about the birth defect risks of divalproex, Krauss says safer drugs should be used if possible during pregnancy.
Krauss says part of the problem is the absence of a single place for neurologists to find updated risk information.
Neurologists get safety information from scattered sources; only a few get emails from the FDA, while others get the information from neurology societies, from continuing medical education courses or from newly published journal articles.
“The FDA needs to do better getting the warnings to prescribing doctors,” he says.
“There has to be a direct way to communicate risks without overwhelming physicians with messages.”
Resource:
http://www.medicalnewstoday.com/releases/264882.php
Another article of interest: Many Neurologists Unaware of Safety Risks Related to Anti-Epilepsy Drugs http://www.sciencedaily.com/releases/2013/08/130814192251.htm?utm_source=feedburner&utm_medium=email&utm_campaign=Feed%3A+sciencedaily%2Fhealth_medicine%2Fepilepsy+%28ScienceDaily%3A+Health+%26+Medicine+News+–+Epilepsy+Research%29
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Years ago I was on multi meds 4. Back in the 70s and 80s they did not look into the effect. They check the levels in the blood. I payed the price of a NON ALCOHOL. fatty liver. Now they should be checking the enzymes levels in the lower organs along with the levels of the meds in the blood.
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Comment by Mark D Geist — July 13, 2023 @ 10:26 AM
Oh how awful, Mark!
I was of the original Dilantin era, so I was real rat bait.
Now I get blood work, every six months.
(And I’m NOT on Dilantin. After I lost my hair and developed galloping gum rot.)
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Comment by Phylis Feiner Johnson — July 13, 2023 @ 10:34 AM
The 4 drugs I was in where Dilantin tegratol and mysalen and depakeen. They did a job on me years ago.
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Comment by Mark D Geist — July 13, 2023 @ 1:34 PM
So which is better? The devil you know? Or the devil you don’t know? 😦
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Comment by Phylis Feiner Johnson — July 13, 2023 @ 1:50 PM
With the current heat waves going around, I have to wonder if any of the AED meds cause dehydration. Certainly some antidepressants do.
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Comment by HoDo — July 13, 2023 @ 10:41 AM
I would certainly think so. The question of course is, WHICH AEDs?
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Comment by Phylis Feiner Johnson — July 13, 2023 @ 10:46 AM
Here’s a start: https://www.epilepsy.com/connect/forum-archive/medication-issues/dehydration-and-seizures
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Comment by HoDo — July 13, 2023 @ 11:12 AM
According to VerywellHealth, https://www.verywellhealth.com/anti-epileptic-drugs-4686301, Dilantin for sure. Other AEDs that affect the sodium balance are Topamax, Oxcarbazepine, Zonisamine, and Rufinamide.
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Comment by HoDo — July 13, 2023 @ 11:23 AM
TEGRETOL was always good to take in the NO R months, to keep brain chemistry calmer, SO THEY SAY, & i did have less petit mal seizures triggered by the HEAT & HUMIDITY. I better though drink MORE water / H20 for my brain to stay hydrated. That was in the 1970’s & early 80’s until I was taken off DILANTIN & my seizures then decreased after being taken off of dilantin. Magnesium Stearate can also trigger seizures which is in ALL GENERIC NAME AED’s & most BRAND NAMES, which is why I am always taking MAGNESIUM L-THERONATE that does get into the BBB/Blood Brain Barrier. I sleep better as well. So How many neurologists know about that or even care to let you know IF they do know it ? IF you do not do things yourself to help YOURSELF 1st before they care to tell you, you will wait for a long time having MORE seizures while you wait for them to tell you something. They could care less that over 95% of any AED has ALUMINUM in the drug you are taking.
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Comment by James D — July 14, 2023 @ 8:00 AM
Reblogged this on Disablities & Mental Health Issues.
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Comment by Kenneth — July 13, 2023 @ 11:54 AM
This is scary when most of us depend on our doctors to prescribe us medications. I always do my research and maybe I am a little overly-anxious about it as well. 🙂
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Comment by Emily Louise — July 13, 2023 @ 1:18 PM
Being your own advocate is always the best way to go. No one knows your brain/body or cares as much as you.
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Comment by Phylis Feiner Johnson — July 13, 2023 @ 1:23 PM
Carbatrol caused many issues for me. Years ago I read all the side effects I was having and intermittent seizures. It was the Carbatrol. I now take Lacosamide and have been doing pretty well, but I don’t like the side effects I am reading.
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Comment by Doreen — July 13, 2023 @ 5:02 PM