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Mahesh Shenai, MD
@mahesh_shenai
Neurosurgeon, data analyst. Read beyond the title/ abstract and constructively question. Posts are my personal opinions, not medical advice.Tweets are my own.
Joined August 2021

Mahesh Shenai, MD’s Tweets

Where is the data that supports bivalent efficacy against BA4/5? And if we don't have that data for BA4/5, how do we know it will work against XBB.1.5? Recommendations should be backed by data.
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The new bivalent shot is your best protection against both infection & serious illness Another question: How well do our tests work XBB.1.5? All the evidence says that they should work just fine And last but not least, how well do our treatments work? 6/n
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Excellent thread, finding high C19 seroprevalence in <18yo, concluding strong natural protection against serious C19. Vax/booster recs should be stratified, not universal.
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1/ Our @ukhsa paper on paediatric #SARSCoV2 antibody prevalence in England is now published By Sep 2022, 97.2% of 1-17 year-olds had #SARSCoV2 antibodies Our findings are critical for future #COVID19 vaccine/booster recommendations for kids …🧵 👉sciencedirect.com/science/articl
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🚩Quick takes on MMWR BV study re: ED/UC visits- - Relative VE (vs. prior MV doses) <50% unless > 8 months out. - rVE vs. hospitalization <50% - declined to stratify by age, prior inf, or comorbids (why?) - design precludes calc of absolute risk ⬇️
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twitter.com/mahesh_shenai/ The exclusions are peculiar. -100 case pts that were flu+ -42 pts were flu "indeterminate" -71 with undetermined vax status Total exclusions approximate or exceed size of case and control groups!
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Replying to @VPrasadMDMPH
They specifically excluded control (non C19 pts) that tested + for flu, because those person's were less likely to have received the flu vax, and therefore also the C19 BV vax. This effectively reduces the C19 unvaxxed proportion in the control group, elevating the VE.
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🚩Quick takes on new MMWR: -Small study, limit to >65yo hosp. pts w/ symptoms. -32% excluded=large selec. bias - design precludes calc. of absolute benefit/NNV -each adjustment seems to favor +VE - probable benefit to >65yo, magnitude questionable
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cdc.gov/mmwr/volumes/7 New CDC MMWR re Bivalent VE vs. hosp. in >65 yo pop.=73%. You would think after 3 mos. and MILLIONS of doses, CDC would give robust VEs for many scenarios. Instead, they manage only this study in a population of 798 hospitalized adults >65. Why?
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5d/ The title of the paper is “APPARENT risks of postural orthostatic tachycardia ..." The authors seem to imply uncertainty in their own title! Which I believe is a respectable signal that they suggest the findings should be taken with a degree of caution.
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5c/ A subtle finding of this study is that vax appears to be a greater risk factor than infxn (2.6 x vs. 1.5x) for myocarditis, but the small sample size of post-infectious myocarditis limits its significance. The risk appears to be much higher in males (~3.5) vs. females (~1.4).
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5a/ Some further discussion: The authors are very careful to limit their conclusion THAT VAX MAY LEAD TO POTS, by emphasizing the 5.35x finding in their conclusion. Of course, the authors themselves LIMITED that conclusion, both comparison groups are inherently different.
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4i/ So, -all data limited by ICD accuracy/omission. - the reported 5.35x (infxn:vax) is signif limited by probable selection bias. -the modest 1.10x (post:pre POTS:CPCs) number does not overcome ICD inaccuracies. -The 1.08x (Post:pre infxn POTs:CPCs) was never significant.
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4g/ Authors acknowledge this selection bias, and state “these populations may have inherent differences,the comparisons between populations should be interpreted more cautiously than [within] populations. So the most dramatic result (5.35x) is not as reliable as 1.10x for vax.
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4f/ There may also be selection bias. Look@ Tables 1,2: POTS diagnosis BEFORE vax was 176/100k, whereas BEFORE infxn 987/100k. That is 5.6x difference. In fact, there are many dx that seem unbalanced between the two groups, when one expects pre-exposure groups to be similar.
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4e/ The auths fairly recognize this “non-differential” misclassification bias, stating bias towards the “null” (e.g. understate the rate). This may be true in the absolute rates, but if there is selective bias in the denominators (pre-exposure), the odds may be exaggerated.
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4d/ But, there is another problem here – during the time of study ('20-'22), no POTS specific ICD code existed. Surrogate codes (I49.8 & G90.9) were thus used. The auths. then had to internally validate this method using a small subset of 50 pts, and found an accuracy of 80%.
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4b/ They calculate the ODDS of POTS diagnoses, myocarditis, and then other common primary care dx (CPCs), comparing pre- and post- exposure rates. Dx categories are determined by ICD-9/10 codes from admin DBs, which can be messy. This can lead to misclassification biases.
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4a/ METHODS: The auths set up 2 separate retrospective cohorts @ Cedars-Sinai in LA, [1] vax (with infxn excluded) and the [2] infection (with vax excluded). They then used ICD codes to calculate the frequencies of diagnoses before and after each exposure (per 100k).
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3b/If that doesn’t function correctly, the heart must beat excessively fast (tachycardia) to compensate. It is a condition that was recognized long before COVID-19, and is not unique to it at all. Generally, the cause of POTS is diverse and often unknown in many cases.
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3a/ A brief primer on “POTS” = “postural orthostatic tachycardia syndrome”. When you go from a lying 2 standing, gravity pulls blood to feet and AWAY from your brain. Our bodies have adapted to counter that drop, and maintain BP to brain via the “sympathetic” nervous system.
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2c/ This is somehow being narrated into support for “long-COVID”,eg: twitter.com/BerkeleyJr/sta Instead, at most, it CAUTIOUSLY reports that POTS dx are 🔼 after vax, but at a rate 5x 🔽 than infxn, but almost no differently than diagnoses of other common conditions post-exposure.
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New research confirmed a link between a Covid infection and a debilitating heart condition called POTS, or postural orthostatic tachycardia syndrome, that has been diagnosed in some patients with long Covid. nbcnews.com/health/health-
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2b/ The study uses ICD 9 and 10 codes to identify various diagnoses. Study is subject to misclassification and selection bias, as noted by the authors. As shown below, the promoted 5.35x “topline” result is much less valid than modest OR suggesting vax causes POTS (1.10x)
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sensiblemed.substack.com/p/how-myocardi Excellent essay by , a cardiologist, re: asymmetric & unknown risks of myocarditis. Myocarditis cannot be dismissed, especially by leaders of orgs enforcing mandates, esp w/ young, healthy constituents. Risk/benefit depends on the individual.
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🚩 Interesting "Viewpoint" by FDAs Dr.Marks, re: future C19 vax develop.: - vax has beneficial AND "unanticipated consequences" - immunobridging unreliable - RCTs needed But then, why did his FDA/VRBPAC approve bivalent boosters for all, w/o RCTs?
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youtu.be/NOeDCdWH09o?t= Re: #TwitterFiles2 & dissenters, see this recent Califf/Fauci exchange: (12:38) Califf: "we've got EFFORTS to respond to this...its designed to disrupt & undermine the ability and credibility of govt" (14:15) Fauci:"I'm wondering if they have day jobs."
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