Testimony to Texas State Legislature
regarding House Bill 2452. Peter Sterling, Ph.D.
As a neuroscientist I have studied the
structure and function of the mammalian brain for more than 30
years. I teach this subject to medical and graduate students at the
University of Pennsylvania where I also conduct an active research
program on this subject. I became concerned abut the effects of
electroconvulsive shock (ECS) on the brain more than 20 years ago
after reading in the public press of a bright, professional woman
whose memory was destroyed by a series of "therapeutic"
ECS treatments. This led me to study the literature on ECS, both the
clinical literature regarding possible efficacy and negative side
-effects and also the experimental literature - - the application of
ECS to animals in order to study the basis for the possible efficacy
and side effects. I have continued to follow this literature over
several decades and here summarize my main conclusions. ECS
unquestionably damages the brain. The damage is due to a variety of
known mechanisms:
1. ECS is designed to evoke a grand mal epileptic seizure
involving massive excitation of cortical neurons that also deliver
excitation to lower brain structures. The seizure causes an acute
rise in blood pressure well into the hypertensive range, and this
frequently causes small hemorrhages in the brain. Wherever a
hemorrhage occurs in the brain, nerve cells die - and nerve cells
are not replaced.
2. ECS ruptures the "blood -brain barrier." This barrier
normally prevents many substances in the blood from reaching the
brain. This protects the brain, which is our most chemically
sensitive organ, from a variety of potential insults. Where this
barrier is breached, nerve cells are exposed to insult and may
also die. Rupture of this barrier also leads to brain edema
(swelling), which, since the brain is enclosed by the rigid skull,
leads to local arrest of blood supply, anoxia and neuron death.
3. Compromised neurons tend to release the neurotransmitter,
glutamate, into the surrounding milieu. This chemical excites
further neuronal activity which releases more glutamate, leading
to "excito-toxicity" - - neurons literally die due to
overactivity. Such excito -toxicity has been recognized relatively
recently and is now a major topic of research. It is known to
accompany seizures and over repeated episodes of ECS may be a
significant contributor to accumulated brain damage.
The degree of damage consequent to ECS varies between
individuals. It can be catastrophic in response to a single series,
or it can appear more gradually following repeated series. This is
much like the damage to boxers - who may occasionally die in the
ring due to massive cerebral hemorrhage, or more commonly accumulate
damage until the impairment becomes obvious. Since any positive
therapeutic effect of ECS is temporary, the treatment is commonly
repeated, so chronic brain damage is inevitable. The key
manifestation of this damage is memory loss.
This is disturbing enough, but there are probably other losses as
well, such as the ability to think clearly, to learn new facts and
so on. It must be particularly incapacitating to individuals who are
already impaired by a mental illness. So, one would expect
physicians to weigh carefully the possible benefits of the therapy
against the cumulative damage that it causes. However, rather than
weigh gain vs. loss, psychiatrists deny the obvious, that there is
cumulative damage. The reason that psychiatrists can remain unaware
of accumulating memory loss is that they do not routinely test for
it. Testing is required when patients take certain drugs, such as
lithium. high blood levels of lithium can be toxic; and lithium can
damage the blood-forming cells in the bone marrow.
Therefore, blood levels of the drug and the state of the bone
marrow are monitored. Memory loss could be monitored just as easily,
by asking patients before ECS about early events in their lives and
then questioning the patients following each series of ECS. When
this was done by Janis (almost 50 years ago), losses were marked and
prolonged. However, no effort has been made since then to do this
simple test. The physician's first injunction is "Do no
harm." Because this treatment clearly does harm, I believe it
to be misguided. Where the treatment is applied without
investigating the degree of harm and monitoring its accumulation, I
believe it to be irresponsible and therefore requiring of
regulation.
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