PostEverything Perspective
Suicide is on the rise. Depression therapy is limited. Let’s try psychedelics.
If dying patients have the 'right to try' drugs not approved by the FDA, why not those contemplating suicide?
Ira
Byock is a palliative care physician and chief medical officer of the
Institute for Human Caring of Providence St. Joseph Health in Torrance,
Calif. His books include "The Best Care Possible."
An
unnerving aspect of our times is the rise of unthinkable events such as
mass shootings and rampant opioid overdoses. To that list we can add rising rates of suicide.
Each year 45,000 Americans take their own lives. Many reasons drive
them, but a final, common pathway involves feeling helpless and
hopeless. Traditional psychotherapy and medications go only so far in
treating these hallmarks of severe depression. But novel therapies
exist, with the potential to effectively treat depression and save the
lives of people contemplating suicide: It’s time to seriously consider
psychedelics.
President Trump recently signed into law
a bill intended to grant patients who are expected to die access to
medications that might extend their lives. The federal law follows
similar “right to try” initiatives in more than 30 states that let
incurably ill patients try drugs not approved by the Food and Drug
Administration. The FDA’s own Expanded Access
program (also called Compassionate Use) does so, as well. Why not
extend these provisions to prevent suicide by people suffering from
persistent depression?
As Michael Pollan details in his book, “How to Change Your Mind:
What the New Science of Psychedelics Teaches Us About Consciousness,
Dying, Addiction, Depression, and Transcendence,” plant-based
psychedelics have been used for millennia by indigenous people for
mind-altering benefits. In 1938, Swiss chemist Albert Hofmann
synthesized LSD, and a few years later he discovered its profound
psychoactive properties. In the 1950s, the Sandoz company made the drug
available to psychiatrists interested in treating ailments such as
depression, anxiety and addictions. By the time LSD and similar drugs
were outlawed in the 1970s, more than 1,000 medical papers had been
published documenting the drugs’ therapeutic potential. In recent years,
the FDA has permitted a few new clinical trials of psychedelic-assisted
therapies, using improved methodologies. The results have been
striking. When prescribed to carefully screened patients, under the care
and monitoring of health professionals, these medications appear to be
highly beneficial and safe.
Psychedelics
are not intoxicants in the usual sense; they do not dull a person’s
senses or induce sleepiness. Side effects include temporary changes in
sensory perception and diminished coordination and fine-motor function.
These occur mostly during the first few hours of a session. The drugs
are not toxic to the brain or other organs. “Bad trips,” the terrifying
episodes of panic that occasionally occurred during recreational use of
these drugs, are exceedingly rare when the psychedelics LSD or
psilocybin are administered in monitored, supportive settings and
patients are prepared in pre-session counseling.
In
contrast to currently approved antidepressants, which must be taken
daily and typically require weeks to take effect (or not), psychedelics
are administered in medically supervised settings, usually during one or
two six-hour sessions, and their therapeutic effects are immediate. In
clinical studies, as many as 80 percent of patients experienced substantial relief from depression,
including those whose illness had persisted through multiple courses of
treatments. The neuropharmacological and psychological mechanisms for
the improvements in people’s mental health are also different from those
of existing antidepressants. Research subjects commonly described a
shift to a more positive worldview, accompanied by a deepened sense of
meaning and connection to others, and an enhanced appreciation for the
intrinsic value of their lives. Notably, the benefits often endure for
many months after even a single treatment.
At
present, the main barriers to expanded research and therapeutic use of
these medications are regulatory. LSD and psilocybin remain Schedule I
drugs, which makes clinical use illegal and research burdensome. But
building on successful preliminary studies, the FDA may permit the start
of a few Phase III clinical trials of psilocybin — a critical step to
approval. If successful, within a handful of years, doctors may be able
to administer psychedelics again.
Another
route to legality may shorten the wait for suffering patients, however:
including the drugs in the “right to try” and Expanded Access programs.
Psychedelics fit the criteria. People living with incurable conditions —
cancers and neurodegenerative conditions, such as ALS — often
experience anxieties, grief and depression associated with the
progressive debility and impending death. Many contemplate suicide.
Indeed, terminal illness defines the one category for which ending one’s
life is gaining social acceptance. In seven states and the District of
Columbia, doctors can legally prescribe lethal medications to dying
patients who want the option of ending their lives. Since Oregon’s Death With Dignity Act
was enacted in 1997, roughly two-thirds of people who requested lethal
prescriptions were motivated by feelings of being a burden, loss of
control, lack of enjoyment of life, and a sense that life was not worth
living. Clinical studies of psychedelics-assisted therapies for people
who are dying and experiencing emotional and existential suffering have
shown notably positive results.
I
am troubled by the normalization of physician-hastened death as a
solution to suffering, yet it is fair to ask: If dying people have a
right to die and take drugs to hasten death, shouldn’t they also have a
right to try drugs that might alleviate their distress?
And
if larger-scale studies confirm the benefits of psychedelic-assisted
therapies, why wouldn’t we cautiously expand access to those treatments
to non-physically-ill sufferers? Treatment-resistant depression is,
after all, a life-threatening condition that can end in suicide.
Currently, in Holland, Belgium, Switzerland and Canada, people with
persistent suffering who are not terminally ill, including those with depression,
may qualify for assisted suicide and euthanasia. Although this seems
chilling to me, I’m in the minority. When the New York Times published
an online debate
on the issue, a large majority of commenters felt that the option of
hastening death should be available for people regardless of their
physical condition.
Perhaps we could save the
lives of some suffering people who see no escape from their despair. It
would be wrong to dismiss the opportunity of this cultural moment. It
would be right to try.
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