Report from CMHS Meeting on ECT
Held January 17, 1997 Wyndham Bristol Hotel, Washington, D.C.
For many years, ECT survivors, doctors, researchers and
advocates have tried to call attention to the many issues
surrounding ECT. And for that same amount of time groups that oppose
any regulation of ECT, such as the American Psychiatric Association
and National Alliance for the Mentally Ill, have resorted to name
calling and other tactics in an effort to deflect attention from the
real issues. (Letters
obtained under the Freedom of Information Act that protest CMHS's
efforts)
But now, the United States government is listening. In fact, they
have done more than listen, they've encouraged open
communication and a thorough investigation
into the complaints of the thousands of ECT patients across the
country.
The Center for Mental
Health Services, part of the US Department of Health and Human
Services, has been conducting a review
of electroconvulsive therapy. Despite efforts from NAMI and other
groups, CMHS is including ECT survivor issues in the study. This
study is not yet finished, but CMHS has said it will include the
results of a recent meeting in Washington, DC in that report.
A group of consumer/survivors met with officials from CMHS on
January 17, and spent the day discussing the issues surrounding ECT.
Our voices represented a variety of viewpoints, but we were able to
reach a consensus on three key points.
1. The research into the after effects of ECT, and how ECT
recipients feel about their treatment, is lacking substantially. And
the little research that does exist is full of bias from the perspective
of ECT doctors, who often fail to acknowledge problems exist. Our
task force agreed that more research is needed in the areas of
patient attitudes and effects of ECT on the brain.
2. CMHS and the newly-formed Coalition of ECT Recipients will
co-propose a study to investigate patient attitudes, to be funded by
CMHS/NIMH. This study will be led by the Coalition, although
methodologists from outside the field of mental health will be
brought in to assure the study is unbiased.
3. The results of this meeting should have a prominent place in
the CMHS review.
As this exciting project develops, I will give updates here.
Other areas of concern and discussion:
- FDA negligence in the regulation of ECT devices. Researcher
Doug Cameron explained why the device currently in use does not
fall under the FDA guidelines. He illustrated why this is NOT
the procedure that was grandfathered in under the current Act.
Although the APA and shock industry says that today's ECT is
gentler, Cameron has shown through intensive
research that today's machines actually deliver more
electricity, not less. We agreed that the FDA should investigate
this.
- Fraud and deception. Cameron is in the process of showing that
the memory studies are based on fraud. I will be adding more
information about this as it becomes available, but it basically
breaks down to the researchers using a smaller amount of
electricity than the amount used in clinical practice. (The
difference between threshold and supra threshold; more on this
later.)
- Pre and post testing. Most of us agreed that extensive testing
of all ECT patients should be mandated by law. This would
include proper memory testing, and MRIs, all before and after
the series.
- Informed consent. Participants felt that patients are being
given improper consent, relying on materials that the industry
uses as public relations, rather than true, solid information.
What would constitute real informed consent? The Washington
Post printed an article September 24, 1996, noting that the
"model consent form drafted by the APA and copied by
hospitals says that 'perhaps 1 in 200' patients report lasting
memory problems....Harold A. Sackeim...member of the APA's 6
member shock therapy task force says that the 1 in 200 number is
not derived from any scientific studies. It is, Sackeim said,
'an impressionistic number' provided by...ECT advocate Max Fink
in 1979. The figure will likely be deleted from future APA
reports, Sackeim said."
- Mandatory reporting laws: A federal law should be enacted that
would require each state's mental health department to maintain
statistics on ECT treatments, similar
to the California law.
- Involuntary ECT. With two dissenting, the rest of us agreed
that ECT should never be given against a person's will. If they
say no to ECT, that should be the patient's choice. Since
Medicaid and Medicare both allow payment for ECT, this has
escalated its use and escalated the use of forced shock,
especially on older women.
The government paying for forced ECT is another concern.
- Conflict of interest in the industry. The top
"experts" on ECT have financial interests via owning
the machinery companies, as well as companies that make
accessories (mouth guards, videos, etc.). This has led to a very
imbalanced effort in the area of public information and
research.
- Use of ECT on children. This involves the issue of involuntary
ECT, since children cannot legally consent. There are *still*
reports of parents having their kids shocked to try and get them
to "give up" their homosexuality, even though the
psychiatric industry no longer lists homosexuality as a mental
illness in its DSM. The use of ECT on children was outlawed in
Texas, but ECT enthusiasts suggested that in order to get around
this, doctors send the children to nearby Louisiana by ambulance
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