Chronic Fatigue Syndrome

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Whose managing this these days?
I might be getting a referral for this. Person has other mental health to still be worthwhile consult. But is it PCP or Rheum? Whose claimed this? Or we putting it under somatoform?

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Some stuff I picked up.

Obviously check for a B12/folic acid and TSH. Check labs that would be done on an annual physical. You're going to rightfully look like an idiot if you diagnosed the person with Chronic Fatigue when they had an easily identifiable etiology that would've been treatable such as an iron deficiency.

The above should be obvious but I see a lot of doctors miss this.

Now there is where I realistically will be telling something some won't know. If someone suffers from chronic fatigue I also order a serum vitamin D level (a significant portion of the population has a Vitamin D deficiency yet this is hardly ever screened), an Epstein Barr Virus antibody panel, an IL-6 and ANA.

Several patients I've seen have abnormal results with the above labs. The problem being with exception of a Vitamin D deficiency is if the above are abnormal WTF are you going to do? I've had some patients with chronic Epstein Barr and there's no good treatment for it that's generally accepted. I had a patient with chronic EBV and he saw a highly respected infectious disease doctor that told him pretty much nothing could be done on his end. There is some data showing that ultra-high doses of Vitamin C only achievable with IV Vitamin C, not oral, could reduce chronic EBV problems but the data, while published, is sparse and very few people can do this. An abnormally high IL-6 or ANA? What to do? I don't know.

Also as mentioned Lyme Disease. I've seen people suffer from chronic problems even for decades after a Lyme Disease infection that was already treated. What to do? I don't know.

I had a patient with a significant Vitamin D deficiency, chronic fatigue and fibromyalgia, treated with by raising her Vitamin D level that was about a 5 ng/mL to about 70 (literally taking 15,000 IU a day, a dose toxic to most people), low dosage Naltrexone at 4.5 mg daily, and daily NAC. She told me Fibromyalgia pain was reduced about 80%, and fatigue was no longer present, but this is me grasping for straws. There's no good conventional treatment regimen.
 
Some stuff I picked up.

Obviously check for a B12/folic acid and TSH. Check labs that would be done on an annual physical. You're going to rightfully look like an idiot if you diagnosed the person with Chronic Fatigue when they had an easily identifiable etiology that would've been treatable such as an iron deficiency.

The above should be obvious but I see a lot of doctors miss this.

Now there is where I realistically will be telling something some won't know. If someone suffers from chronic fatigue I also order a serum vitamin D level (a significant portion of the population has a Vitamin D deficiency yet this is hardly ever screened), an Epstein Barr Virus antibody panel, an IL-6 and ANA.

Several patients I've seen have abnormal results with the above labs. The problem being with exception of a Vitamin D deficiency is if the above are abnormal WTF are you going to do? I've had some patients with chronic Epstein Barr and there's no good treatment for it that's generally accepted. I had a patient with chronic EBV and he saw a highly respected infectious disease doctor that told him pretty much nothing could be done on his end. There is some data showing that ultra-high doses of Vitamin C only achievable with IV Vitamin C, not oral, could reduce chronic EBV problems but the data, while published, is sparse and very few people can do this. An abnormally high IL-6 or ANA? What to do? I don't know.

Also as mentioned Lyme Disease. I've seen people suffer from chronic problems even for decades after a Lyme Disease infection that was already treated. What to do? I don't know.

I had a patient with a significant Vitamin D deficiency, chronic fatigue and fibromyalgia, treated with by raising her Vitamin D level that was about a 5 ng/mL to about 70 (literally taking 15,000 IU a day, a dose toxic to most people), low dosage Naltrexone at 4.5 mg daily, and daily NAC. She told me Fibromyalgia pain was reduced about 80%, and fatigue was no longer present, but this is me grasping for straws. There's no good conventional treatment regimen.

Your beginning is good (most people with unexplained fatigue who presented for depression I send a CMP, CBC and TSH/FT4 just to screen for common causes of unexplained fatigue).

Vit D meh, most insurances won't even pay for Vit D level testing anymore and I just tell everyone to supplement with 1000U of Vit D3 during the winter especially, you can't really overdo it unless you're taking massive amounts of Vit D. But it's definitely a relatively low risk lab to do.

The other stuff, you're just checking for nonspecific labs a bunch of people are gonna come back positive for unless you're following specific symptoms.
+ "screening" ANA is like the bane of Rheum's existence....15% of totally asymptomatic people can have + ANA screen.
IL-6 elevated is like ESR, it's a pretty nonspecific inflammatory marker.
"Chronic EBV" is like (as you mentioned) "Chronic Lyme"....it's not clear if it's even a real thing. You need to know what you're looking at on an EBV panel to interpret it correctly anyway because basically every adult is going to have a positive VCA IgG and EBNA. There is a very severe disease state called Chronic Active EBV but those people are super sick.

Rather than just gunshot labs if someone's that hung up on fatigue I'd just send them to Rheumatology or ID so they can order whatever labs they want and give the patient anticipatory guidance about the labs they're ordering rather than get the patient all excited about a + ANA that probably means nothing.
 
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The problem being with exception of a Vitamin D deficiency is if the above are abnormal WTF are you going to do? I've had some patients with chronic Epstein Barr and there's no good treatment for it that's generally accepted. I had a patient with chronic EBV and he saw a highly respected infectious disease doctor that told him pretty much nothing could be done on his end. There is some data showing that ultra-high doses of Vitamin C only achievable with IV Vitamin C, not oral, could reduce chronic EBV problems but the data, while published, is sparse and very few people can do this. An abnormally high IL-6 or ANA? What to do? I don't know.
Why are you getting labs if you aren't going to do anything with the results? Sounds like a waste of time and money.
 
Im usually a skeptical guy, but i think there is something to CFS, although not sure exactly what it is. I have 3 patients with it essentially, who have had extensive workups to exclude everything else, they don't have personality disorders/are fairly reasonable people, sleep well, are on no sedating medications, mental health relatively controlled, etc. I tend to see it in young caucasian women. There isnt really anything you can do to manage it, exercise helps but too much worsens the fatigue. I think there may be various poorly defined autoimmune/neurological conditions out there that we dont know about

i am highly skeptical about chronic lyme disease though lol
 
Im usually a skeptical guy, but i think there is something to CFS, although not sure exactly what it is. I have 3 patients with it essentially, who have had extensive workups to exclude everything else, they don't have personality disorders/are fairly reasonable people, sleep well, are on no sedating medications, mental health relatively controlled, etc. I tend to see it in young caucasian women. There isnt really anything you can do to manage it, exercise helps but too much worsens the fatigue. I think there may be various poorly defined autoimmune/neurological conditions out there that we dont know about

i am highly skeptical about chronic lyme disease though lol

There is probably a subset of people who have something that we do not currently have good tests for yet. But then there re a large amount of people who are more conversion/somatic symptom disorder. As for Chronic Lyme's, I've only tested one person with that diagnosis in their chart who did not terribly fail validity testing.
 
To me this is a Rhum consult unless they've had one recently. They tend to be the closest things we have to diagnosticians left and the cross-over with things like Fibromyalgia is significant in CFS.

I have seen one case that I think was this in an adolescent male (so pretty low suspected incidence) but definitely complicated by some neuroatypicality that did not meet full criteria for ASD. Did do a smidge better with higher dosed Strattera and was able to complete some school work following mental health treatment, but far from a full response.
 
To me this is a Rhum consult unless they've had one recently. They tend to be the closest things we have to diagnosticians left and the cross-over with things like Fibromyalgia is significant in CFS.

I have seen one case that I think was this in an adolescent male (so pretty low suspected incidence) but definitely complicated by some neuroatypicality that did not meet full criteria for ASD. Did do a smidge better with higher dosed Strattera and was able to complete some school work following mental health treatment, but far from a full response.

Maybe slightly off-topic but seems relevant; here is a preprint of a book chapter that Fred Wolfe (one of the rheumatologists who initially helped define fibro) wrote a few years ago about the social construction of distress as it relates to fibro.

Relevantly it makes the point that fibro symptoms are really a continuum and are usually present in chronic pain patients who don't actually meet fibro criteria, suggesting it is probably not a distinct entity.
 

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The problem with CFS is it is a diagnosis of exclusion. However, the only treatments are exercise and CBT (essentially), with no proven pharma therapies. The diagnosis itself is not "proven" yet either.

So it seems appropriate that someone (PCP, rheum) works it up thoroughly, but after a clear diagnosis it is treated by therapists + PCP... Or worried well cash-only psychiatry clinics lol.

There is so much overlap with depression and conversion disorder that it makes sense a psychiatrist could see these folks if they wanted to, and probably could be somewhat helpful. 50 years ago these folks would have been given the diagnosis of "hysteria," of which modern criteria for these folks would be conversion disorder (~60%) and somatic symptom disorder (~15-20%).
Rheumatology once?
Rheumatology twice?
Do I hear a third Aye for rheumatology as the keepers of CFS?
 
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Your beginning is good (most people with unexplained fatigue who presented for depression I send a CMP, CBC and TSH/FT4 just to screen for common causes of unexplained fatigue).

Vit D meh, most insurances won't even pay for Vit D level testing anymore and I just tell everyone to supplement with 1000U of Vit D3 during the winter especially, you can't really overdo it unless you're taking massive amounts of Vit D. But it's definitely a relatively low risk lab to do.

The other stuff, you're just checking for nonspecific labs a bunch of people are gonna come back positive for unless you're following specific symptoms.
+ "screening" ANA is like the bane of Rheum's existence....15% of totally asymptomatic people can have + ANA screen.
IL-6 elevated is like ESR, it's a pretty nonspecific inflammatory marker.
"Chronic EBV" is like (as you mentioned) "Chronic Lyme"....it's not clear if it's even a real thing. You need to know what you're looking at on an EBV panel to interpret it correctly anyway because basically every adult is going to have a positive VCA IgG and EBNA. There is a very severe disease state called Chronic Active EBV but those people are super sick.

Rather than just gunshot labs if someone's that hung up on fatigue I'd just send them to Rheumatology or ID so they can order whatever labs they want and give the patient anticipatory guidance about the labs they're ordering rather than get the patient all excited about a + ANA that probably means nothing.
I agree with referral, but disagree with the statement about how totally asymptomatic people have a positive ANA screen, being a reason not to check ANA *in someone symptomatic* and consider the results of that study. While I agree with saying that should be left to rheum, pointing to asymptomatic people being positive and it having little clinical meaning, vs testing in symptomatic people, is sort of the definition of not really understanding pre and post test probabilities and that a positive ANA in someone symptomatic va asymptomatic does not have the same clinical significance. I get that a positive ANA in someone may not have much related clinical significance either.

I get your point that it can frequently be non-specific. But there is a reason it frequently gets ordered in the presence of some symptoms.

But yeah, leave it to rheum.
 
I agree with referral, but disagree with the statement about how totally asymptomatic people have a positive ANA screen, being a reason not to check ANA *in someone symptomatic* and consider the results of that study. While I agree with saying that should be left to rheum, pointing to asymptomatic people being positive and it having little clinical meaning, vs testing in symptomatic people, is sort of the definition of not really understanding pre and post test probabilities and that a positive ANA in someone symptomatic va asymptomatic does not have the same clinical significance. I get that a positive ANA in someone may not have much related clinical significance either.

I get your point that it can frequently be non-specific. But there is a reason it frequently gets ordered in the presence of some symptoms.

But yeah, leave it to rheum.

Never fear, I got the whole pre vs post-test probability thing down. My point is that "Fatigue" as an isolated symptom is generally not symptomatic enough to go fishing with an isolated ANA and a high proportion of the general population will come back positive to begin with. The statement "there is a reason it frequently gets ordered in the presence of some symptoms" is so vague as to be useless. Yes, symptoms of an autoimmune disease...and you should know what you're going to do with a + ANA if it comes back.

Fish up some papers showing that checking an ANA in people with chronic fatigue as an isolated symptoms yields much more than saying "you have a positive ANA" in a bunch of them and we can figure out the pre-test probability of finding something actionable in fatigue + positive ANA.
 
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No one wants to manage it. Therefore, it is a niche if you want to do it in private practice.

It's not a diagnosis of exclusion.
2015 IOM diagnostic criteria for myalgic encephalomyelitis/chronic fatigue syndrome:
Diagnosis requires that the patient have the following three symptoms*:
  1. A substantial reduction or impairment in the ability to engage in pre-illness levels of occupational, educational, social, or personal activities that persists for more than six months and is accompanied by fatigue, which is often profound, is of new or definite onset (not lifelong), is not the result of ongoing excessive exertion, and is not substantially alleviated by rest.
  2. Post-exertional malaise - Worsening of a patient's symptoms and function after exposure to physical or cognitive stressors that were normally tolerated before disease onset.
  3. Unrefreshing sleep.
At least one of the two following manifestations is also required*:
  1. Cognitive impairment - Problems with thinking or executive function exacerbated by exertion, effort, or stress or time pressure.
  2. Orthostatic intolerance - Worsening of symptoms upon assuming and maintaining upright posture. Symptoms are improved, although not necessarily abolished, by lying back down or elevating the feet.
* Frequency and severity of symptoms should be assessed. The diagnosis of ME/CFS should be questioned if patients do not have these symptoms at least half of the time with moderate, substantial, or severe intensity.
Treatment of it feels like it largely falls within the realm of psychiatry. Addressing sleep, depression, anxiety, cognitive difficulties, pain, dizziness. Using behavioral therapies, diet, a graduated exercise program to avoid post-exertional fatigue, and motivational interviewing for those behavioral changes.

I have several carefully selected patients with CFS in my private practice who are doing much better in treatment, mainly because they're highly motivated to get better and I've convinced them to stop looking for an underlying cause for the 100th time (of course, after reviewing/getting labs and tests I think would be indicated myself).
 
Never fear, I got the whole pre vs post-test probability thing down. My point is that "Fatigue" as an isolated symptom is generally not symptomatic enough to go fishing with an isolated ANA and a high proportion of the general population will come back positive to begin with. The statement "there is a reason it frequently gets ordered in the presence of some symptoms" is so vague as to be useless. Yes, symptoms of an autoimmune disease...and you should know what you're going to do with a + ANA if it comes back.

Fish up some papers showing that checking an ANA in people with chronic fatigue as an isolated symptoms yields much more than saying "you have a positive ANA" in a bunch of them and we can figure out the pre-test probability of finding something actionable in fatigue + positive ANA.
An ANA is not needed unless they also have other systemic signs like joint pain, rashes, muscle stiffness, recurrent/persistent fevers, abdominal pain. It's pretty low yield otherwise and the false positives can be misleading and even harmful.
 
Never fear, I got the whole pre vs post-test probability thing down. My point is that "Fatigue" as an isolated symptom is generally not symptomatic enough to go fishing with an isolated ANA and a high proportion of the general population will come back positive to begin with. The statement "there is a reason it frequently gets ordered in the presence of some symptoms" is so vague as to be useless. Yes, symptoms of an autoimmune disease...and you should know what you're going to do with a + ANA if it comes back.

Fish up some papers showing that checking an ANA in people with chronic fatigue as an isolated symptoms yields much more than saying "you have a positive ANA" in a bunch of them and we can figure out the pre-test probability of finding something actionable in fatigue + positive ANA.
By definition CFS is not a question of fatigue as the only symptom, and in reality, how often are you having patients present to psychiatry with literally only overwhelming fatigue as the symptom they are complaining of? I think I can count on 1 hand how many times I have actually seen a patient complaining of fatigue and only fatigue without something identifiable (new parent, cut back on coffee, etc) being the cause of just plain old fatigue. Invariably these patients have other complaints.

I guess I disagree, that in that presence of symptoms, and by the definition of the discussion we are having, the symptoms cannot be better accounted for by a psychiatric diagnosis, such as depression, we are talking about overwhelming fatigue plus other complaints, not otherwise accounted for. That to me begs ruling out autoimmune etiologies in addition to other things. As a psychiatrist, really your job is to 1) help rule out somatic causes of symptoms such as fatigue and 2) diagnose psychiatric causes of symptoms, for which you often have to do Step 1.

Now I know I am telling you what you already know of your job. And your points are good.

But where I disagree, is that in your patient so profoundly fatigued they are seeking psychiatric care, typically because they meet criteria for impairment of major life function(s), where a somatic or psychiatric diagnosis is not immediately apparent, I feel that immune etiologies *must* be investigated.

Now, I am not saying the psychiatrist should be the one to order an ANA.

I've heard different things from rheumatologists. Some say that ordering the "standard panel" for inflammatory disease is not really helpful, they know which ones they want when they see the patient. Others would say, it can speed things up when the blood tests they would most likely order to work up an immune etiology is already ordered and they can review the results with a patient.

I agree that what an ANA does NOT do, is that for the psychiatrist I'm not sure it changes management, does it? You tell me. Sounds like these patients are appropriate referrals to rheum regardless of the blood test results, so ANA doesn't add much there.

My argument is more, the idea that ANA is useless in these patients or that inflammatory disease does not need to be investigated. Which may not be your point, that's fine. But it is my point.

Just, an attitude like why bother with these people. Some of them will have identifiable conditions, some will have inflammatory disease, and some may be diagnosed as CFS, which we can then debate if that is "real". My understanding is that typically it is the rheumatologist that diagnoses that, even if in the long term they do not manage it ongoing.

The impairment is "real." I have no doubt the fatigue is also "real." As to whether we can diagnose it or treat it, I'm not sure.

I think that is more a failure of medicine (we don't know enough, or these issues are more complex or are not appropriate for what a medical approach currently can address) than that this isn't "real."

I almost never find a physician pose the question of whether or not a patient's symptoms are "real" posed in any way that is less than somewhat contemptuous or dismissive or blaming of the patient and it bothers me.

I still disagree that a rheum work up and that will probably include bloodwork, is not indicated. If your point is just the psychiatrist shouldn't order that, again, I do think that is debatable.
 
Basically, someone said when they have fatigue NOS and a psychiatric diagnosis isn't clear, they consider other etiologies and one of which is autoimmune disorders. Which now has led to a debate about the tests, specifically ANA.

Any rheumatologist is going to tell you an ANA is not an end all be all for any rheum diagnosis, diagnosing it or including it. They are still probably going to order it. So you're arguing more to saying it's better rheum does it than making an argument against the test being performed in these hypothetical patients.
 
Now there is where I realistically will be telling something some won't know. If someone suffers from chronic fatigue I also order a serum vitamin D level (a significant portion of the population has a Vitamin D deficiency yet this is hardly ever screened), an Epstein Barr Virus antibody panel, an IL-6 and ANA.

Several patients I've seen have abnormal results with the above labs. The problem being with exception of a Vitamin D deficiency is if the above are abnormal WTF are you going to do? I've had some patients with chronic Epstein Barr and there's no good treatment for it that's generally accepted. I had a patient with chronic EBV and he saw a highly respected infectious disease doctor that told him pretty much nothing could be done on his end. There is some data showing that ultra-high doses of Vitamin C only achievable with IV Vitamin C, not oral, could reduce chronic EBV problems but the data, while published, is sparse and very few people can do this. An abnormally high IL-6 or ANA? What to do? I don't know.
Sorry, but there is no indication for checking for EBV antibodies for patients with chronic fatigue. EBV is known to be a trigger for chronic fatigue syndrome but is not causative. chronic EBV is diagnosed based on EBV DNA levels, not antibodies, and is characterized by fever, lymphadenopathy, and hepatosplenomegaly, not fatigue alone.

It is not unreasonable to check Vitamin D levels, though vitamin D is not associated with chronic fatigue in cohort studies (only retrospective). unfortunately, insurance companies are increasingly not covering vitamin D tests as they don't think it's medically necessary.

There is no indication for checking IL-6 levels.

There is no indication for checking an ANA in patients with fatigue alone. Maybe if there are other findings (blood dyscrasias, rashes, serositis, joint pains etc). It is very common for women to have elevated ANA titres as well, and indiscriminate testing can lead to unnecessary workups.

A sleep study may be more useful than any of the above.

chronic fatigue is my least favorite of the somatoform syndromes to treat. fatigue is an incredibly pervasive and nebulous symptom and these patients tend not to respond well to pharmacological or psychotherapeutic intervention. It is nice when you have a patient whose fatigue completely lifts with psychotherapy but it is also quite rare. Antidepressants (SSRIs/SNRIs/TCAs) tend to worsen fatigue. I have had some success with bupropion. Stimulants rarely help but I will occasionally trial and see if they help and discontinue if they don't (though patients are reluctant to discontinue even when there is no benefit). Sedative hypnotics can worsen fatigue. Co-enzyme q10 can be helpful for cognitive fatigue and possibly NADH. Low dose naltrexone can help with pain symptoms and possibly fatigue. Other treatments for pain symptoms include MBSR, ACT, emotional expression and awareness, pain reprocessing therapy. Minimizing polypharmacy is important.
 
I think the hard part with stuff like this and fibromyalgia, is that its often championed by people with significant BPD and instagram influencers as a trendy thing so they make it look less valid on the surface given the usual suspects who endorse the symptoms. I would wager that for a lot of people its a desire to play the sick role/obtain attention and validation/etc but others im not so sure and these people are often forgot about because of the ridiculousness of the aforementioned people
 
Couple things--

1.I really wish non-psych providers got more into the habit of don't call it psych unless you have done your due diligence in the work up. I've seen tons of patients who have persistent fatigue and were never even evaluated for OSA.

2.It does ring a lot of the other somatic disorders. A huge part of this is yes, the patient is experiencing the distress. What is the cause? We may never know. If we did know, is there anything we can do about it? Don't know. I have encountered patients whether it is c/o fatigue, concentration issues, dizziness, pain down under, frequent urination, GI sx, etc. The brutal reality is our understanding of medicine is and always will be so incomplete. We have to make do with what we can as providers and as patients. I try to counsel patients to not get hung up on chasing a diagnosis or seeking a cure at the expense of putting everything else on hold. It is very possible there will never be a satisfying answer. Yes, you can continue to look but putting everything else on hold worsens things. Do a reasonable amount of exercise, eat healthy, good sleep hygiene, etc etc. If they come up with the excuse that I'm too _____ to do even the smallest things, I tell them, ultimately the decision and consequences are theirs and I'm just here to offer what I can.

As a personal note, I've had persistent fatigue since 10 years of age. Got a reasonable work up earlier in life. No, I did not do the rheum panel or the fancier stuff outside a PCP office. But I continue to pursue other evidence based modalities that can help. Take whatever help you can. Why wouldn't you? I start work around 0730 and by the time 7pm rolls around, if I even sit for too long I can easily fall asleep. Had the sleep work up too. I don't think stims/wake promoting agents is the answer, just would not be my preference either. But I manage to live a decent life. From the start I accepted that there's probably no answer, and to make do. Worked great for me : ).
 
1.I really wish non-psych providers got more into the habit of don't call it psych unless you have done your due diligence in the work up. I've seen tons of patients who have persistent fatigue and were never even evaluated for OSA.

I've had several instances where the non-psych provider diagnosed Conversion Disorder or some other psych disorder, such as Chronic Fatigue without doing the due diligence, or blew off the patient because they had a psych issue.

One of my patients, a prominent academic anesthesiologist, who used to be treated by a highly regarded neurologist in California (but she's now in Missouri) was wrongfully diagnosed with Conversion Disorder after the local neurologist did a test that's nowhere close to 100% accurate, it was negative so he wrote she has conversion disorder and then blew her off.

She showed me the report and I told her that he didn't do the due diligence. She saw another physician who then treated her effectively and and the neurological issue improved. I told her to report the prior local neurologist to the state medical board and she did.
 
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I was reading through this and felt that I should say something. Then I realized that this is the clastic "is this a real disease or isn't it". Our smarter gurus of knowledge will tell you that about 1/3 of such somatic complaints are supratentorial, but 2/3rs are real and we are just too stupid to see the cause because we are not Star Trek and don't know everything right when the plot needs to know the solution. The l'd like to think that if due diligence was performed and there is no recommended treatment, our efforts are better than nothing, "organic" cause or not.
 
A patient has, say a non-psych physical illness, (oversimplified as we know psych illness have physiological etiology, and several "physical" illnesses affect mood), and there's a test that's say 80% accurate (and I know this is oversimplified cause there's validity, reliability, false (+), false (-)).

So if the test is negative that doesn't mean the patient doesn't have it. That does mean, however that with clinical examination and a good history it helps the clinician in a direction.

What's going on with several of our non-psych colleagues in the field are they're utilizing these tests in an all-or-nothing manner, not knowing their nuances and then submitting a diagnosis without also considering room for error and such. Then, if they diagnose say with somatoform or conversion disorder refer them to us, sometimes with an agenda of really not wanting to deal with what could be a difficult case that is really in their boundary and not ours.
 
I had a patient with classic POTS. PCP kept insisting her dizziness on standing up is “anxiety”.. Send her to see cardio.
 
I've had several instances where the non-psych provider diagnosed Conversion Disorder or some other psych disorder, such as Chronic Fatigue without doing the due diligence, or blew off the patient because they had a psych issue.

One of my patients, a prominent academic anesthesiologist, who used to be treated by a highly regarded neurologist in California (but she's now in Missouri) was wrongfully diagnosed with Conversion Disorder after the local neurologist did a test that's nowhere close to 100% accurate, it was negative so he wrote she has conversion disorder and then blew her off.

She showed me the report and I told her that he didn't do the due diligence. She saw another physician who then treated her effectively and and the neurological issue improved. I told her to report the prior local neurologist to the state medical board and she did.
Just like chronic fatigue syndrome, conversion disorder or functional neurological disorder is not a diagnosis of exclusion. It requires positive clinical findings that are incompatible with known medical pathways. Neurologists should know this as some clinics have FND among the top 3 conditions they encounter in clinical practice.
 
Just like chronic fatigue syndrome, conversion disorder or functional neurological disorder is not a diagnosis of exclusion. It requires positive clinical findings that are incompatible with known medical pathways. Neurologists should know this as some clinics have FND among the top 3 conditions they encounter in clinical practice.
Question, how often are psychiatrists called upon to manage FND? Worked with a neurologist who said I'd see it come up at some point in psych and had never even heard of it till that rotation.
 
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