DSM 5 ‘Psychosis Risk Syndrome’-far too risky
By Allen Frances
March 18, 2010
Among all the problematic suggestions for DSM5, the proposal for a ” Psychosis Risk Syndrome” stands out as the most ill conceived and potentially harmful. It aims to solve a pressing problem in psychiatry- the need for early identification and preventive treatment. Psychotic episodes create tremendous short term impairment and may impact negatively on long term prognosis and treatment efficacy. It would save great suffering if we could get there early and do something useful to reduce the lifetime burden of illness before too much damage is done.
But good intentions are not enough. The whole concept of early intervention rests on three fundamental pillars- being able to diagnose the right people and then providing them with a treatment that is effective and safe. “Psychosis Risk Syndrome” fails badly on all three counts: 1) it would misidentify many teenagers who are not really at risk for psychosis; 2) the treatment they would most often receive (atypical antipsychotic medication) has no proven efficacy; but, 3) it does have definite dangerous complications.
First, let’s deal with the misidentification problem. Even in the most expert of hands (ie in very highly selected research clinics), at least two of three people who get the diagnosis do not go on to become psychotic. Of great counterintuitive interest, the longer the research clinic operates the lower becomes its rate of correct identification. With time and spreading reputation, the clinic attracts increasingly heterogeneous referrals- so that it is more difficult to discriminate from among them those who are truly at risk for psychosis.
That would be the misidentification rate once the diagnosis became official and was applied in the real world? No one can say for sure, but two thirds is certainly a lower limit of misidentification. There are several reasons to believe that the ratio of wrong diagnoses would actually be much higher: 1)the raters in general practice would be much less expert than specialists in research clinics; 2) the “patients” would be closer to normal and harder to discriminate; and, 3)drug company marketing would influence parents and clinicians to be especially alert to any strangeness in teenagers. It has been estimated that the false positive rate would jump from about 70 percent in specialty clinics to about 90 percent in general practice.
This means that as many as an astounding nine in ten individuals identified as “risk syndrome” would not really be at risk for developing psychosis.
Those supporting the diagnosis for DSM5 have attempted to fix this overwhelming problem by inserting a definitional criterion that the person must be seeking treatment. They hope this requirement would both reduce the rate of false positives and ensure that those who are misidentified will need some form of treatment. Their preferred treatment for “risk syndrome” is cognitive/behavior therapy which might be helpful (and is unlikely to be harmful) even to those who have been misidentified.
This fix fails badly on both counts- ie in reducing false positives and in guaranteeing safe treatment. Under the best of circumstances, the overwhelming majority of “treatment seekers” will still be false positive. Once the diagnosis is official and marketted, the problem will get much worse as a new army of “treatment seekers” is brought in by their families. Their perceived “strangeness” may come from many causes other than psychotic risk, including:1) drug use; 2) adolescent developmental issues and rebelliousness; 3) culturally dystonic creativity 4) stable schizotypal personality; or, 5)normal eccentricity. A far more efficient signal to noise filter would have been to require that the individual must also have a close family member who has experienced psychotic episodes.
Then we get to the worrying treatment issues. It is the height of unrealistic wishful thinking to assume that most of the misidentified patients will get cognitve therapy. Cognitive theray is in short supply and largely unavailable-especially for this population. On the other hand, antipsychotic medications are fairly ubiquitous and already frequently given for off label indications, particularly to kids on Medicaid.
It has not yet been established that antipsychotic medications are effective in preventing psychotic episodes or in improving life course in those who would meet the criteria for “risk syndrome”. This is an area that to date has received little study and the few existing findings are equivocal.
In contrast, the harmful effects of atypical antipsychotics are extremely well established and frightening. Teenagers starting at an average weight of 110 pounds gained an average of 12 pounds in 12 weeks- and one of the antipsychotics caused an 18 pound weight gain in this period. This raises the risk for diabetes, metabolic syndrome, and a shorter life span.
To sum up: 1) The “risk syndrome” would misidentify many (somewhere between 3-9) kids for every one correctly identified;and, 2) the treatment most likely to be offered has no proven efficacy, but can have extremely dangerous complications. This is a clearly the prescription for an iatrogenic public health disaster.
Read the rest of the article here: http://www.psychologytoday.com/blog/dsm5-in-distress/201003/dsm-5-psychosis-risk-syndrome-far-too-risky