Thoughts on Competence, Healing and the Passage of Time (Acceptance and Commitment Therapy)

http://www.psychotherapy.net/article/Acceptance-and-Commitment-Therapy-ACT

I was struck – again, as I often am – by the claim of effectiveness. Persons with psychosis exposed to four hours of ACT, if not healed, functioning better, at least by one measure.  The patients in the ACT “arm” of the study: their re-admission rate was halved.   The citation was in the Psychotherapy,net article, and here, you can read it for yourself:

http://www.actmindfully.com.au/upimages/bach&hayes-_act_schizophrenia.pdf

As I read it I wondered: Why haven’t these wonderful results ended up in my local inpatient psychiatric facility? What happened between 2002, when the article was published, and now, 2016?  This should be a big deal if it can be replicated!

You, reader, please look at the article. Maybe I missed something.

I did notice that they asked for volunteers, which is always a bias – the bane of the age of the Institutional Review Board (IRB), which requires your informed consent before participating in any trial. We could leave that aside, as across studies, that is a constant.  Nonetheless, the researchers were refused by four of every five patients they asked.  That seems a selection bias of some importance.  And they sought to exclude those who had psychosis and substance abuse, those who had developmental disabilities.  Could that be the reason why this hasn’t been disseminated?  Too narrow a group, uncommon in the general milieu of your average state inpatient psychiatric hospital?

Another question is how has ACT avoided the near universal cycle – the phases the “big” psychotherapies go through in their journey – from idea to hypothesis to experiment to revision to experiments on a larger scale (proliferation) to model to growth (dissemination) to popularity (even enthusiastic popularity!). With results like that cited above, where is the growth and popularity?

Mind you, ACT’s root dates from 1986. And it has a “pedigree.”  Descending from B.F. Skinner’s work in behavioral psychology.  DBT started around the late 1980s – and in the same location, the University of Washington (Seattle, WA).

Or could it be this, noted in one line in the article? That the treatment was delivered by “a psychology intern who had been trained to the point of competence by the developer of the treatment approach.”

How much difference does it make if your clinical supervisor is the developer of the therapy model and you are “trained to the point of competence?”

The popularization of psychotherapy in the 1960s and the 1970s, with headlines in Time for Gestalt Therapy and Transactional Analysis – the unlimited, pervasive and ongoing jokes and cartoons about Psychoanalysis – none of that has happened or is happening with EMDR or ACT or DBT or MI or CBT.

Even though Steven Hayes (the developer of ACT) and ACT were written up in a six page article in Time magazine in 2006.

Serious therapies for serious people, our acronym laden therapies we get training in today, with limited claims – except for their curative powers. Those psychotherapies of the ‘60s and ‘70s did make vast claims as well: they claimed that “Therapy was too good to be limited to the sick.”

Today let’s aim to get reasonably good training, attend workshops, aim for adherence and combine our competence in our selected therapies along with our healing, aim for the alleviation of misery and perhaps better than “just normal” as a result of our efforts.

Postscript:   http://www.stevenchayes.com/

See what Steven Hayes has to say for himself about his major influence – B.F. Skinner – experiences that were linked to Gestalt Therapy at Esalen at Big Sur, California – and what motivates him.

Modern Depression

Note:  This blog post includes a case study for illustrative purposes.  Various efforts have been pursued to adhere to ethical guidelines in using case material.

An article in the Wall Street Journal (May 28/29, 2016) woke me up to the latest book by Peter Kramer, M.D., perhaps best known for his 1994 book, Listening to Prozac.   The new book, Ordinarily Well: The Case for Antidepressants (2016), both revisits some of the themes addressed in Listening to Prozac, and adds yet again to the defense of biological psychiatry by noting what is the author’s view: that after twenty years, the number of cases of advanced depression appears to have been greatly reduced by the use of anti-depressants.  By the way, Dr. Kramer is not against psychotherapy, is for good evidence, and takes note of the fact that some recent studies and meta-studies have questioned the efficacy of anti-depressants.

Here’s a quote from the article:

“[When I was in training in the early 1970s] I saw men and women who suffered depression at the deepest level.  On general hospital wards, such patients were not rare.  Thin, stooped, immobile suffering souls, they had the classic depressive habitus, the attitude or physique of the disease.  They spoke slowly and repetitively.  They were hard to interview.”

In the article Dr. Kramer goes on to note that at the time, his clinical supervisors, his training, all directed him to apply psychotherapy as the first line of treatment.  Only after a great deal of time and lack of response to psychotherapy were the medications of the day used.  Concerning today’s psychiatric ‘landscape,’ he goes on to note that not only he, but a number of experts in depression who he interviewed in preparing his latest book, have noted the diminishing numbers of such immobilized melancholics in our current time.  His thesis is that the broad prescribing of anti-depressants – on the whole, the Selective Serotonin Re-uptake Inhibitors (SSRI) – has greatly changed the epidemiology of the worst sort of depression.

After reading the article, I reflected on my encounters with such debilitated individuals and, accounting for only outpatient settings (I am not including day hospitalization treatment), I could only recall two.

Since I began working in an integrated care setting I’ve seen one of those two suffering individuals. That person reminded me that the isolating effect of such an advanced stage of the illness can baffle the sufferer and the helpers.  As I reviewed the chart prior to meeting the patient, I saw that over five years each of five different primary care providers – all of them seeing the patient only one time – had noted the patient’s depression.  Each had made an attempt to address the depressive illness in the provider’s own way: a prescription for a low dose of an SSRI or a referral to psychiatric care  – or both.  None had diagnosed Major Depression, Moderate (or Severe): the diagnosis was “Depression,” which coded as 311 under the DSM-IV – Depressive D/O Not Otherwise Specified.  Not a diagnosis that usually shouts out the worst of depressive suffering.

Only the most recent encounter gave me some insight into the level of depression. The provider had used an evidence based practice – she had used the Personal Health Questionnaire  (PHQ-9) – and the overall score was very elevated and there was also a positive for the suicidal ideation item (#9). 

Nonetheless, I was not prepared for the extent of the patient’s retrograde depression: the monosyllabic replies, the latency of response, the effort needed on my part to draw out the simplest details, the blankness of expression, the downturned eyes, the entire lack of the gestural postures that add to our verbal expressions – no shrugs, no shaking the head “no,” just quietly sitting there.  No spontaneous narrative.  And, no, the patient could not recall feeling much better than this the past couple of years. No fidgeting or tearing up.  Nothing.

It took a great deal of time, but I managed to draw out that this person took various responsibilities seriously. Those extended into the future and seemed sufficiently strong commitments that I could relieve myself of concern that the patient would attempt suicide (and there was no intent or plan).  Other risk factors were nil or minimal.  The patient agreed the medical provider and I could help the patient with a more comprehensive treatment plan (including a higher dosing of the SSRI and telephone coaching by this clinical social worker) and, no, having made it through so far without hospitalization, that option was declined. With this we began our attempt to revive the human being in our care. 

Not fancy, but what we do is extend the effort, in each individual’s treatment, to achieve efficacy.  The big picture is that our training should include a good grasp of the simple (and the cheap) to change the course of the worst illnesses.

Cultural Compentency

It seems in Japan they have some notions about hospitalization that are very different from ours.  http://www.economist.com/node/876845 and http://www.economist.com/node/876845.  I first learned of this several years ago when I was planning for travel outside the country.  I was researching and came across a checklist that took me to the US State Department website.  Chock full of information it is, of course, with the now common warnings you’d expect concerning war and terrorism in many countries, as well as health warnings.  Think Zika virus.  And just last year Ebola.

But it was their more mundane and ordinary cautions that caught my eye: what if you had a medical emergency in one of these countries?  What if you had a psychiatric emergency?  Here’s another angle on Japan. http://www.japanpsychiatrist.com/Abstracts/TravelMed.pdf

Something that caught my eye in this article was that a medical doctor could essentially declare themselves a psychiatrist after one year of training, not the four that is common in the USA.  And with seeming little oversight or clinical supervision or training.

I think I am warming up to our clinical training and licensing practices – in comparison.