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I have been increasingly horrified by the lengths some specialists go in diagnosis hunting when somatization seems rather likely in explaining at least some of the symptoms of patients. They'll order tests on 1 in a trillion diagnoses, perform nerve blocks and even neurolysis in absurd frequencies, and in general subject these patients to quite a bit of discomfort, pain, and not least, medical risk in treatment of pain issues. Even when
An example, girl with intractable pelvic pain treated with an absurd amount of PO as well as regular nerve blocks. Extensive gynecological workup is negative. Also 'passes out' from pain with no change in vitals. Now being worked up for primary autoimmune autonomic dysfunction as a cause of her pain. Despite...no change in vitals corresponding to pain, no vasoactive changes, and normal EMG... Oh, did I mention severe enmeshment, appearance of mother to relish the role of caregiver, and...drumroll please...rape history? They regularly make it to scheduled appointments with pain docs and neurologists, but miss 3/4 of scheduled appointments with counselor and pain psychologist.
Another, child with MS (very real) who has an essentially normal neurologic exam with the exception of vibratory sense dysfunction and no thalamic or sensory cortical lesions on MRI who presents with severe gait disturbance with narrow-based gait and 'collapses' which only happen while assisted with walking and never involve traumatic falls.
Now, don't get me wrong, we hardly want to miss diagnoses.
There was another kid I saw who had a likely spinal concussion. He clearly had some psychosocial issues and was engaging in pain behaviors as well. Injured on the job while working to help support family while dad was being treated for cancer, higher expectations than siblings, problems with peers, etc. Somatization was being floated around in him despite a classic physical exam for myelopathy with findings that a 17 year old wouldn't know how to fake. I was the only one not considering it seriously for a while, and was the only psych dude involved.
I've been where that kid was myself, except I don't actually have any psychosocial issues or pain behavior. So I know what it's like to have doubters around when there really is a bonafide somatic issue going on. And how it can delay diagnosis and intervention.
But it seems like there are many cases where psychiatric history and evaluation make it clear that there is a strong likelihood of somatoform disorder either as primary or as a comorbidity of somatic illness. To me it seems silly that we wait for the exhaustion of tests before we start to consider it. Whatever happened to clinical likelihood?
While I'm not denying the importance of a good medical workup for somatic complaints, regardless of how outlandish, it seems to me that proper care for these patients would involve concurrent psychiatric evaluation and treatment/management.
I don't see why intervention, pain medication, and extensive workups can't also go hand in hand with therapy, coping skills teaching, and/or psychiatric medication. Why would you delay what could be at worst helpful adjunctive treatment allowing these people to live as full lives as possible, and at best could be curative?
Granted I'm also in the minority in that I think all people with chronic debilitating medical conditions should have a psychiatrist as part of their primary management team (even though i don't and have never seen one lol). My mantra is there is no such thing as a chronic pain patient without psych issues.
An example, girl with intractable pelvic pain treated with an absurd amount of PO as well as regular nerve blocks. Extensive gynecological workup is negative. Also 'passes out' from pain with no change in vitals. Now being worked up for primary autoimmune autonomic dysfunction as a cause of her pain. Despite...no change in vitals corresponding to pain, no vasoactive changes, and normal EMG... Oh, did I mention severe enmeshment, appearance of mother to relish the role of caregiver, and...drumroll please...rape history? They regularly make it to scheduled appointments with pain docs and neurologists, but miss 3/4 of scheduled appointments with counselor and pain psychologist.
Another, child with MS (very real) who has an essentially normal neurologic exam with the exception of vibratory sense dysfunction and no thalamic or sensory cortical lesions on MRI who presents with severe gait disturbance with narrow-based gait and 'collapses' which only happen while assisted with walking and never involve traumatic falls.
Now, don't get me wrong, we hardly want to miss diagnoses.
There was another kid I saw who had a likely spinal concussion. He clearly had some psychosocial issues and was engaging in pain behaviors as well. Injured on the job while working to help support family while dad was being treated for cancer, higher expectations than siblings, problems with peers, etc. Somatization was being floated around in him despite a classic physical exam for myelopathy with findings that a 17 year old wouldn't know how to fake. I was the only one not considering it seriously for a while, and was the only psych dude involved.
I've been where that kid was myself, except I don't actually have any psychosocial issues or pain behavior. So I know what it's like to have doubters around when there really is a bonafide somatic issue going on. And how it can delay diagnosis and intervention.
But it seems like there are many cases where psychiatric history and evaluation make it clear that there is a strong likelihood of somatoform disorder either as primary or as a comorbidity of somatic illness. To me it seems silly that we wait for the exhaustion of tests before we start to consider it. Whatever happened to clinical likelihood?
While I'm not denying the importance of a good medical workup for somatic complaints, regardless of how outlandish, it seems to me that proper care for these patients would involve concurrent psychiatric evaluation and treatment/management.
I don't see why intervention, pain medication, and extensive workups can't also go hand in hand with therapy, coping skills teaching, and/or psychiatric medication. Why would you delay what could be at worst helpful adjunctive treatment allowing these people to live as full lives as possible, and at best could be curative?
Granted I'm also in the minority in that I think all people with chronic debilitating medical conditions should have a psychiatrist as part of their primary management team (even though i don't and have never seen one lol). My mantra is there is no such thing as a chronic pain patient without psych issues.