in your
point 1) you wrote that there is a 20:1 ratio of studies showing HCQ and AZTH has no positive impact for all spectrum of disease, setting aside zinc for what you wrote in point 2). you left out the third variable I’ve seen regularly in the studies that did not show a positive impact for HCQ + antibiotic, the dosing of the pair. Typically I’ve seen HCQ given at 2X the dosing in Zelenko and HF’s papers.
Dosing is 2X is not a subtle difference. When you include a requirement of the same dosing, do you stand by that 20:1 claim re studies finding no efficacy to efficacy? Are there any examples you have of published studies with HCQ & antibiotic at dosage at the same level (or even close to) as Zelenko & HF that did not show efficacy?
If there are not examples that clearly are a preponderance in numbers to the ~700 HCQ in the HF study that saw the 50% reduction, you’ve actually made an argument for my suggestion that HCQ is still a treatment meriting strong interest (am getting to your statements in your second point now...)
as to your
point 2), I saw strong assertions, “the definitive jury is out,” in your comments that the risk of heart adverse events is at a harm to benefit ratio that makes HCQ, HCQ/AZTH is not looking good. What I did not see was any data.
I’ve seen a very compelling case from Yale epidemiologist MD/PHD Harvey Risch that this is by no means the case. Note the extremely large set of applicable data, 320,000 patients in a Oxford University study, at the end that showed a 1/10,000 fatality risk re such heart issues with these meds. that is roughly 1% the fatality rate of corona patients, and when you consider only patients at high high risk would get this treatment, this implies a harm to benefit ratio of something like 1 to 500
“Third, concerns have been raised by the FDA and others about risks of cardiac arrhythmia, especially when hydroxychloroquine is given in combination with azithromycin. The FDA based its comments on data in its FDA Adverse Event Reporting System. This reporting system captured up to a thousand cases of arrhythmias attributed to hydroxychloroquine use. In fact, the number is likely higher than that, since the reporting system, which requires physicians or patients to initiate contact with the FDA, appreciably undercounts drug side effects.
But what the FDA did not announce is that these adverse events were generated from tens of millions of patient uses of hydroxychloroquine for long periods of time, often for the chronic treatment of lupus or rheumatoid arthritis. Even if the true rates of arrhythmia are ten-fold higher than those reported, the harms would be minuscule compared to the mortality occurring right now in inadequately treated high-risk COVID-19 patients. This fact is proven by an Oxford University study of more than 320,000 older patients taking both hydroxychloroquine and azithromycin, who had arrhythmia excess death rates of less than 9/100,000 users, as I discuss in my May 27 paper cited above. A new paper in the
American Journal of Medicine by established cardiologists around the world fully agrees with this.“
https://www.newsweek.com/key-defeat...inion-1519535?amp=1&__twitter_impression=true