This impressive book goes into detail concerning the horrifying deterioration in the psychiatric care of the
Severely and Persistently Mentally Ill (SPMI’s - primarily people with
schizophrenia) in the United States that I have personally witnessed since I was a resident in psychiatry
in the late 1970’s in California.
By the time I had started my residency, the passage in California of the
Lanterman Petris Short (LPS) Act in 1972 - followed by the passage of similar laws in many other states - had for the most part cleared up a lot of the abuses in the
state hospital system that anti-psychiatry groups still go on and on about as if they were still common. It
insured that the cases of patients who had been hospitalized involuntarily would be reviewed by the courts within 17 days or
sooner. Psychiatrists in the system could no longer just let patients languish in the hospital forever by merely following what a previous
doctor had said without doing their own personal evaluation, or avoid closely
following the patients’ condition to see if there were any changes.
No longer would
patients linger in hospitals for years because of a misdiagnosis. For example, patients with the very treatable bipolar disorder (in which psychotic episodes are often relatively short-lived) had often been diagnosed with the far less treatable schizophrenia (especially if they were African American) Occasionally someone had been hospitalized for decades because
unscrupulous relatives conspired to steal their money by labeling them with a
mental illness with the help of a gullible or greedy psychiatrist.
After the laws mandating court review were in place, people who were
hospitalized back then often agreed to stay much longer than 17 days - because their paranoid delusions and hallucinations had been somewhat controlled
with anti-psychotic meds. Up until then they had anosognosia - the lack of
awareness that anything might be wrong with them. After they became less delusional,
they began to understand that they needed treatment.
Psych meds often take two to three weeks just to kick in, or need to be changed to something else after that period of time because one agent was ineffective while another might not be - which in a sense would restart the whole clock - so often they had to remain hospitalized for several weeks.
This time frame also allowed psychiatrists in training to see first hand the course of major
psychiatric illnesses and monitor longer term responses to it. It also allowed doctors
time to make a better determination about whether the patient’s primary issue was drug abuse
rather than some other chronic mental illness, and refer drug abusers to
appropriate rehab treatment.
Committed psychotic patients at
that time could be forced to take anti-psychotic meds even if they refused prior to
their court review. That has since changed in most jurisdictions. I cannot for the life of me see the point of committing a patient involuntarily if the doctors cannot then treat them.
Even though the state
hospitals were beginning to discharge their long-term patients under the justification
that the meds would allow for effective outpatient treatment, hospital stays were long enough to allow ward social workers to arrange for placement in
board and care type living situations, get the patients enrolled in Social
Security Disability (SSI) to pay for it, and make follow-up appointments in
community mental health centers so that patients could continue to receive
their medications. Community mental health centers were also far more numerous
and available for this purpose than they are today.
The LPS criteria for
hospitalizing someone against their will were very reasonable: mentally ill and a danger to self, a danger to others, or gravely disabled. The latter meant that due to their
mental illness they were unable to provide for their own food, clothing, and
shelter. A cardboard box on a street did not qualify as the ability to provide
for their own shelter as it seems to today.
A “danger to self” did not just mean suicidal, also as it seems to today; it could refer to dangers to self due to delusions and poor judgment, such as walking naked into someone’s house who might mistake them for a burglar and shoot them. Sometimes doctors considering a “603” 72-hour commitment holds had to pump relatives for information they could use to justify that. I recall one patient’s family finally tell me, after I asked many follow-up questions, that the patient had tried to get out of a moving car.
A “danger to self” did not just mean suicidal, also as it seems to today; it could refer to dangers to self due to delusions and poor judgment, such as walking naked into someone’s house who might mistake them for a burglar and shoot them. Sometimes doctors considering a “603” 72-hour commitment holds had to pump relatives for information they could use to justify that. I recall one patient’s family finally tell me, after I asked many follow-up questions, that the patient had tried to get out of a moving car.
The author of Breakdown, Lynn Nanos, is a social worker who works for a psychiatric emergency services team, and
has seen and documented the monstrous changes in the previously described public
mental health treatment of chronically ill SPMI’s. She provides sad, disturbing,
and hair-raising case studies of suicides and murders of both family members
and strangers due to the premature discharge of dangerous, delusional patients who did not think they were ill and refused treatment.
Due to the mutual
biases of the so-called patients’ rights advocates on the left of the
political spectrum, and tax-phobic politicians and government agencies on the
right of the political spectrum, hospital stays have been whittled down to just
a few days, so that anosognostic patients are either not referred for
psychiatric follow-up at all, or do not show up even if they had been. Many are
discharged with no prescription medication to take after they leave.
Nanos makes the case
that the commonly-heard idea that chronic psychiatric patients are less likely
to commit violence than others is highly misleading. It ignores the significant minority of mentally
ill folks who do have violent
propensities – and who are often more dangerous than others - when their violent episodes could have been
stopped if they had received proper medication. Not to mention that the violence-prone
mentally ill are highly unlikely to participate in the epidemiological studies that are the basis of the misleading argument. Dead family members have lost all of their rights. Many suicides of those who
are “dying with their rights on” could also likely have been prevented.
Many of these
patients now end up in jail. The patients’ “rights” warriors never seem to
inquire as to why this might be the case. Could it be that such patients don’t
realize they are mentally ill and are responding to command hallucinations to
assault others, or are committing nuisance crimes like disturbing the peace or trespassing
because they do not know any better? Even when they kill someone, the not-guilty-by-reason-of-insanity
defense seldom succeeds (particularly after John Hinckley tried to kill
President Reagan, who himself did not appear to think mental illness was real
when his administration attempted in the early 1980’s to kick all the chronic
schizophrenics off SSI until the courts stepped in), and they of course are
sent to jail rather than to a hospital.
According to the
author, private hospitals often tend to favor hospitalizing malingerers who
fake mental illness in order to have a place to stay and receive food, over the
more highly disturbed and potentially violent SPMI’s who really need the beds.
This, along with drastic decreases in the number of available beds, has led to
a situation in which patients are stuck in hospital emergency rooms - manned by staff that are ill-equipped to
handle them - for days at a time until a bed is finally found or until they are in
frustration discharged by the facility to the streets. There are also financial
incentives to treat “easier” patients due to the fact that they have shorter
hospital stays and hospitals are financially incentivized to keep stays short.
Government
agencies often listen to “peer support groups” comprised of individuals who
think the signs and symptoms of schizophrenia and other psychoses are just some
variant of normal.
Nanos makes a good
case for assisted outpatient programs (AOTs), which help patients stay with
treatment despite not being forced to take their medication. Mental health professionals attempt to persuade the
recipients to adhere to their prescribed medications and attend their clinical outpatient
appointments with psychotherapists, psychiatrists, and case managers. All AOT involves
intensive case management services and comprehensive supervision.
In
court-ordered AOT, judges order seriously mentally ill patients to adhere to
their outpatient regimens. AOT’s seem to be even more effective when judges are
involved, probably due to what the author refers to as “black robe syndrome.”
Several
studies indicate that AOT’s, particular those that last 180 days, significantly
reduce violence, readmissions to hospitals, no-shows at outpatient
appointments, arrests, jail time, self-harm, suicide attempts and substance
abuse, while significantly improving the self care of SPMI patients.
Nonetheless, even AOT’s are opposed by various special interests. In Massachusetts,
its opponents even include the National Alliance for the Mentally Ill, which is
supposed to be advocating for these patients.
Unfortunately,
these patients are downright lousy at advocating for themselves, so it’s going
to take a lot of other people speaking up before things go back to the far more
functional way they were just a few decades ago.