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I wanted to get peoples thoughts on the DSM as a document. Love it or hate it, and why. Thanks.
i like it except for the personality disorders. A lot of them are culutrally biased and do not work well for those who come from different culutures. i also think they need to implement the "spectrum" scale to rate the level of each disorder rather than just saying you meet the criteria. overall i like it.Psyclops said:I wanted to get peoples thoughts on the DSM as a document. Love it or hate it, and why. Thanks.
i don't have a particular study but i am quite positive it is culturally biased, there is a lot of research and interest in the area (not just personality disorders, i mean everything)Psyclops said:I would also be interested in knowing more about the culture bias, I'm not familiar with it. But I do agree with you Axis II is a mess. I personally am not a fan either. I think it does a poor job of focusing on the eitiology of disorders, I think that is a result of it being an atheoretical document created by the other APA. Only classifying things by thier symptomology although doesn't seem to be the best in my opinion.
clinpsychgirl said:I agree that the categorization of what constitutes a mental disorder is somewhat problematic...
However, I think DSM categorication is helpful when used in conjuction with the development of (evidence-based) treatment protocols. The symptom guidlines allows for a systematic method to measure treatment outcome (by measuring symptom reduction).
i like it except for the personality disorders. A lot of them are culutrally biased and do not work well for those who come from different culutures.
that spoke about how certain depressed patients show a faster response to norepinefrine agonists (or reuptake inhibitors not sure which) and others show a faster response to serotonergic agents. That would suggest to me that there might be a couple of ways to reach the same disorder. I.e., two etiologies.
To me, if you'd like to measure symptom reduction, that alone tells me you are considering symptomatology a continuous variable (which of course, it is).
JatPenn said:To me, if you'd like to measure symptom reduction, that alone tells me you are considering symptomatology a continuous variable (which of course, it is). So why not have a classification system where symptoms are measured on a dimensional scale and disorders are determined based on symptom severity profiles?
Psyclops said:I wanted to get peoples thoughts on the DSM as a document. Love it or hate it, and why. Thanks.
Psyclops said:The dimensional model certainly makes sense to me if you intend to be measureing and treating overt abnormal behavior or merely intrapsychic issues that are leading to some form of distress. I think one of the problems lies in that it is constructed by psychiatrists who naturally follow the medical model. As long as they continue to be the major contributors to the main classiffication system for psychopathology that will be the cases. That being said, I think there will be a big overhaul to Axis-2 come DSM-V. Will it be a dimensional model? That remains to be seen.
JatPenn said:Unfortunately, I think we'll need to wait for VI to see any considerable overhaul. From what I understand, V is just about ready to be published.
LM02 said:Nope - DSM-V is scheduled for 2011, and the task forces are scheduled to start the meat of their work in 2007.
Psyclops said:Psychanon,
Good post, but I have to disagree with you that making inferences about etiology based on responses to tx is backwards.
Psyclops said:I agree, clinical applicability is something that should be strived for, and qestioned vis-a-vis the DSM. I think you only have to look at the SCID to find that it lacks clinical utility. I think that the SCID is another document that lacks utility if it is used as it was intended. It certainly is a valiant effort, and in the right spirit (standardised diagnostic tool) but in practice it is unwieldy, confusing, and far too rigid. Of course there will always be give and take in utility.
I certainly don't think that we should be striving for a "good enough" system. And diagnoses such as adjustment disorder, in my opinion, a joke. Another thing to think about is how much useful are the diagnostic codes. What does a DSM diagnotic code really tell you about an incoming patient, especially if it something like adjustment disorder?
Neuro-Dr said:The point of making an atheoretical model for psychopathology is to allow for a common language to be used across disciplines (psychiatry, social work, LMFT, etc.). In addition an attempt was made to move away from rediculous beliefs like the "schizophrenic mother". While this annoys some people who believe that the person should be considered as a whole. nothing changes the fact that you are still a person even if depressed, anxious, what have you.
A model based on onset, duration, prognosis and sx presentation also allows for the clean-up of errors caused by sx alone. I can't tell you how many times I have seen people give onset schizophrenia to someonw in there late 40's when dopaminergic tracts are already dying out. I have seen people blow psychotic disorders becasue they believed olfactory hallucinations are common in schizophrenia. People who use dysthymia as depression light and other aggregious errors that demonstrate their limited understanding of psychopathology.
Contrary to popular belief, the accuracy of medical dx is about 67% and psych is 65%, so there is not a great deal more innacuracy. In addition, those of you who like research, what are you basing your inclusion criteria on? Is someone depressed because they watch a sad movie, have an MMPI-2 scale 2 of 65 or higher, BDI of 12, say they are sad or do you want to use a standard set of criteria. This is the major issue..do we really expect all of these patients to present and respond to treatment the same? Show the same changes on fMRI?
Using rating scales is completely problematic, those who have tried to use even decent measures like the BDI show horrible reliability over sessions, even with the same rater.
While problematic, the DSM-IV-TR is still the most useful resource in the MH field. Most of the errors I have seen clinicians make involve the "broken leg" theory of psychology rather than application of the DSM, they do far more damage with there views that neurological conditions such as autism are due to parenting styles, poor diets (leaky gut syndrome) and other non-science based evidence.
Having said all this, I'm glad someone brought the topic up, because these types of debates are productive.
Neuro-Dr said:The answer is actuarial. Those cut points determined a different outcome, response to treatment, long term prognosis, etc. These points of differential where not picked out of a hat. The reason why we have brief psychotic disorder, schizophrenaform and schizophrenia is becasue the cut points of 1 month and 6 months were associated with higher percentages of variable outcomes.
As for MDD, the same was true, that when sx of 6 but not 5 were put together it changed the duration of the episodes, lielihood of reoccurance, response to treatment. I'm not saying that the changes were so dramatic as to always be of clinical relevance, but nor were they arbitrary.
Neuro-Dr said:I can't say that I'm positive that I know what "snarky" means. But, if you ever want data regarding what someone says you should feel free to ask for it.
With regard to the accuracy of medical and MH dx - ther references are from Monahan's 1982 prediction data and Lawler 2003.
For the DSM stats, you can use the sourcebook or refer to the appendices regarding the field trials of 6,000 patients and over 100 sites sponsored by the NIMH, NIDA, and NIAAA. These are the work groups used in every DSM printed since III, I think. As to whether they seperately published the findings, they say "no", but I can't say that no one ever has.
The psychotic quote cam from Benazzi 2003, that linked schizophreniform more to a mood disorder tham schizophrenia. With mood disorders the data is rather pervasive, there are numerous publications indicating factors such as early onset, frequency of episodes, partial recovery from episode are all major indicators of prognosis.
I think you wanted to know why associated findings such as sleep, appetite, attention and concentration were included and why you need 5 (I said 6 in the previous post). The prognosis and onset indicators change with these factors:
for instance (Vermetten, Geuze & Mertens 2004) - insomnia of more than 1 year's duration predicted depression at 40% with insomnia predating the depressive episode at 38% and anxiety at 38%. Increase stage 2 sleep was also predictive of onset depressive episodes at higher rates. Possibly these findings could indicate a link betwee 5HT and sleep onset and depression. In bipolar, the relation to sleep should be obvious, but the duration may be related to "kindling" in the ventral-tegmental dopaminergic tracts.
With appetite, remember that you are looking at a qualifier for "with vegitative signs" or "catatonic features" - it is not necessarily that the appetite itself changes the prognosis, but rather leads to the qualifier. These have different treatments (Peselow, Sanfilipo & Defiglia 1992) - there are probably more curent references, but this is for illustration.
Is that enough - I know I painted some broad strokes, but I hope this shows where I'm going with this.