Believers that #LongCovid is "all in your mind" because there are on specific biomarkers or routine diagnostic tests are "normal" need to look at other autoimmune/inflammatory disorders. In #MultipleSclerosis, or example, it took decades to refine the diagnostic criteria. 1/🧵
First, before MRI/CT scans were invented, many #MS pts were misdiagnosed with psych disorders, including hysteria. Spinal taps in MS patients did not always reveal abnormalities. Many patients had various non-specific white matter lesions in MRI, but some had few or none. 2/🧵
Some #MS pts had optic neuritis, but many did not. Some had a lesion in the cervical cord, and many did not. How do you make sense of it all? It took many years and several revisions to come with the diagnostic criteria that we use today to diagnose MS and MS variants. 3/🧵
Rheumatoid #arthritis is another example: many are RF-positive, and some are RF-negative. #Sjogrens syndrome is another diagnostic dilemma, especially if anti-SSA and anti-SSB antibodies are negative. The point is: autoimmune/inflammatory disorders are COMPLEX! 4/🧵
#LongCovid has significant autoimmune/inflammatory basis, but needs to be defined better by subtypes (neurologic, cardiovascular, pulmonary, psychiatric, mixed, etc.) Specialized tests should be developed (serum cytokine panel? T-cell immunologic panel? Cardiac MRI?) 5/🧵
#LongCovid is not one disease and not one disease process, but should be viewed as an umbrella that, depending on the subtype, should lead to these subtypes' specific diagnostic tests. Treatment, which has to be developed, may have to be tailored to the subtypes as well. 6/🧵
Nobody should expect #LongCovid to be diagnosed or treated based on simple & cheap diagnostics or therapies. It's going to be complex, tedious & expensive - exactly what our #healthcare dislikes! It will take innovation, creation & thinking outside the box to yield results. 7/7
P.S. First post should read "Believers that #LongCovid is "all in your mind" because there are NO specific biomarkers..."
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🧵The new generation of doctors should be trained in compassion & non-biased approach in patients with chronic illness. Many of us have been trained to think "it's just anxiety" or "they're somatizing" when faced with a difficult patient. We were primed to dismiss & gaslight. 1/n
I remember attendings teaching us that if a nonparalyzed pt is in a wheelchair w/ sunglasses on for light sensitivity, that's a bad sign (ie a sign that they have psych problems, not real physical illness). I didn't know then that they would be my patients with #Dysautonomia. 2/n
I now teach medical students who work with me to never assume that the patient's complaints are due to a psychological problem: do the workup thoroughly, and if you still don't know what's wrong, tell them so and then refer them to someone else. Don't dismiss, label or judge. 3/n
A 🧵on an article that I won't repost here that claims there are "both sides" to #MECFS and #LongCovid with the sides being "psychological" vs. "physical." As a neurologist specializing in post-infectious syndromes, with #MECFS being a common subtype, I see a lot of confusion. 1/
This confusion is especially prominent by physicians and non-physicians who do not see patients with these disorders. It's natural for people to want to reduce the complexities of disabling chronic illness to easily quantifiable, diagnosable and treatable disorders, but... 2/
Many disorders in medicine and neurology are not simple and are not explained by one abnormal blood test or imaging: equally not simple are psychiatric disorders, most of which do not have no objective biomarker and most of which rely on subjective diagnostic criteria. 3/
The authors from the @Brain1878 study with a false claim that #POTS is psychogenic respond to all of the letters with more false claims. I'll try to outline them here 🧵: 1. They say, "the underlying cause of POTS remains elusive, and regrettably, there is no effective 1/n
@Brain1878 treatment."
- No, the cause is not elusive, there are multiple causes and multiple treatments.
"Working hypothesis largely overlooked the role of cortical neurons."
-No, I published a paper with a working hypothesis that POTS is a CNS disorder. link.springer.com/article/10.100…
@Brain1878 "Our hope is that novel finding of POTS will spark the development of new treatment approaches."
-No, when you say that POTS is psychogenic, you close the door on any and all new treatment approaches. You commit the patient to CBT and SSRIs that do not work for #POTS. 3/n
Very happy to share our new study on #immunotherapy in #POTS. We conclude that patients w/ severe, treatment-refractory POTS experienced significant improvement with subcutaneous immunoglobulin or PLEX. Randomized controlled trials are needed. #MedTwitter link.springer.com/epdf/10.1007/s