ADVERTISEMENT

COVID-19 Pandemic: Transmissions, Deaths, Treatments, Vaccines, Interventions and More...

Status
Not open for further replies.
LMAO
You and Proud are Imbeciles.

Any American with an ounce of common sense knows the mass fatalities in the United States are a direct result of Trump doing nothing in January while ignoring all US Department of Intelligence reports of the upcoming Pandemic crisis.
I think the bigger cause of high infection and fatality rates in the Northeast is the lack of early testing, and overly restrictive CDC testing criteria which allow significant community spread to go undetected.

As I noted earlier in this thread (and as @RU848789 has also reported), NY and NJ would have had to close down prior to the first reported case, in order to have hit the timelines of the West coast.
 
Read an article about the mayor of Belleville NJ (not sure if it was on nj.com or abc7news.com but he got sick in November with the classic Covid symptoms but did not require hospitalization after attending a convention in AC and subsequently he is now positive with the long term antibodies of Covid so that clearly changes the timeline of when Covid was here; If anyone can find article and link!!
 
  • Like
Reactions: biker7766
Read an article about the mayor of Belleville NJ (not sure if it was on nj.com or abc7news.com but he got sick in November with the classic Covid symptoms but did not require hospitalization after attending a convention in AC and subsequently he is now positive with the long term antibodies of Covid so that clearly changes the timeline of when Covid was here; If anyone can find article and link!!
Lots of anecdotal evidence of this. There was a particularly ad flu going around in November / December. Could it have actually been the new virus?
 
  • Like
Reactions: RUPete and scripts
Read an article about the mayor of Belleville NJ (not sure if it was on nj.com or abc7news.com but he got sick in November with the classic Covid symptoms but did not require hospitalization after attending a convention in AC and subsequently he is now positive with the long term antibodies of Covid so that clearly changes the timeline of when Covid was here; If anyone can find article and link!!
https://www.google.com/amp/s/www.nj...-1st-confirmed-case-in-us.html?outputType=amp
 
Lots of anecdotal evidence of this. There was a particularly ad flu going around in November / December. Could it have actually been the new virus?

Long story, but I was hospitalized in December and almost died. Was in critical condition. Almost all of my symptoms were consistent with COVID, with the exception of my pericardial effusion - which there have been some cases in COVID patients. I got a pericardial window and drained a boatload of fluid to save my life. CT scans showed ground glass opacity.

I was very excited to get an antibody test - I got one last Saturday and I was negative. I would have bet anything I had it. But sadly, I did not. Wish I did so I would have potential for immunity.
 
Thread on Twitter about Covid definitively not arriving in USA until Jan/Feb from a Scientist/virologist of some sort. I don't know if he's right because I'm certainly not a scientist, but he's very convincing.



Click the "show this thread" link at underneath the original tweet when Twitter launches to see the whole story he presents.
 
Last edited:
Long story, but I was hospitalized in December and almost died. Was in critical condition. Almost all of my symptoms were consistent with COVID, with the exception of my pericardial effusion - which there have been some cases in COVID patients. I got a pericardial window and drained a boatload of fluid to save my life. CT scans showed ground glass opacity.

I was very excited to get an antibody test - I got one last Saturday and I was negative. I would have bet anything I had it. But sadly, I did not. Wish I did so I would have potential for immunity.
I dunno if that is something that you want to wish for as the after effects are unclear and potentially damaging.
 
I dunno if that is something that you want to wish for as the after effects are unclear and potentially damaging.

I don't think he is wishing to catch Covid. I'm guessing that he wished that whatever he had in December was Covid, since he has already gone though the illness and recovered, and if it was Covid he is potentially immune now.

Likewise, I had an upper respiratory illness in early March. At the time, only lower respiratory symptoms were considered Covid, so I wasn't tested. But now they include upper respiratory symptoms. So I am hoping that I had a very mild case of Covid, and am now recovered and immune. I'd rather be immune instead of worrying about catching it in the future.
 
Martenson presents a mixture of useful info and biased info. His pro HCQ bias is almost off the charts. He almost never discusses any of the inconclusive or bad clinical trials (and there are more of them than the couple of potentially positive ones). And his slides on Lupus from that Italian site are just bad science, since he uses a completely unsubstantiated comment as if it's accepted/reviewed data and ignores the wealth of info showing that lupus patients on HCQ are not being protected against getting COVID (see my post linked below), which is why the Lupus Foundation of America said, "There is no evidence that taking hydroxychloroquine (Plaquenil) is effective in preventing a person from contracting the coronavirus."

https://rutgers.forums.rivals.com/t...social-distancing.191275/page-89#post-4531982

Furthermore, most medical experts and clinicians I've seen weighing in on HCQ have been at best neutral on it and at worst think it's ineffective and possibly unsafe to boot. Perhaps the latest medical literature review and analysis on this published today, excerpted below, will convince doctors that this drug should really not be used until we see the results from ongoing controlled clinical trials. We'll see.

https://faseb.onlinelibrary.wiley.com/doi/full/10.1096/fj.202000919

As hospitals around the globe have filled with patients with COVID‐19, front line providers remain without effective therapeutic tools to directly combat the disease. The initial anecdotal reports out of China led to the initial wide uptake of HCQ and to a lesser extent CQ for many hospitalized patients with COVID‐19 around the globe. As more data have become available, enthusiasm for these medications has been tempered. Well designed, large randomized controlled trials are needed to help determine what role, if any, these medications should have in treating COVID‐19 moving forwards.

While HCQ has in vitro activity against a number of viruses, it does not act like more typical nucleoside/tide antiviral drugs. For instance, HCQ is not thought to act on the critical viral enzymes including the RNA‐dependent RNA polymerase, helicase, or proteases. Despite in vitro activity against influenza, in a large high quality randomized controlled trial, it showed no clinical benefit, suggesting that similar discordance between in vitro and in vivo observations is possible for SARS‐CoV and SARS‐CoV‐273 (Table 3).

Additionally, HCQ and especially CQ have cardiovascular and other risks, particularly when these agents are used at high doses or combined with certain other agents. While large scale studies have demonstrated that long‐term treatment with CQ or HCQ does not increase the incidence of infection, caution should be exercised in extrapolating safety from the studies of chronic administration to largely healthy individuals to estimate the risk associated with short‐course treatment in acutely and severely ill patients. Furthermore, the immunologic actions that make HCQ an important drug for the treatment of auto‐immune diseases might have unintended consequences when it is used for patients with COVID‐19. The effects of this immune modulation on patients with COVID‐19 are unknown at this time, including a potential negative impact on antiviral innate and adaptive immune responses which need to be considered and studied.

For all these reasons, and in the context of accumulating preclinical and clinical data, we recommend that HCQ only be used for COVID‐19 in the context of a carefully constructed randomized clinical trial. If this agent is used outside of a clinical trial, the risks and benefits should be rigorously weighed on a case‐by‐case basis and reviewed in light of both the immune dysfunction induced by the virus and known antiviral and immune modulatory actions of HCQ.

I agree that Martenson seems to have a bias in favor of HCQ but I'm trying to keep an open mind. Results to date from various studies are far from conclusive. Yes, there are side effects (remdesivir has side effects too) and it's pretty apparent that patients who have already reached the critical/ventilator state don't benefit from the drug. However, the evidence for remdesivir in those patients is not compelling either (perhaps studies in progress will change that). This makes sense since you need to inhibit viral replication earlier in the disease process. Now, perhaps some (many? who knows) of those critical cases are patients who are unable to clear virus and still have heavy viral loads - if that is the case, perhaps antivirals would be effective in those cases even at a late stage. We'll see.

I've seen contradictory reports about HCQ from ER doctors. Saw some posts on twitter where NYC doctors were saying they were seeing plenty of patients with covid who were already on HCQ for RA or other conditions. Then there are the reports Martenson talked about where doctors in Europe supposedly found lower rates of covid in those same patient groups. I don't know where the truth lies at this point (no one does) but am not ready to completely dismiss the possibility that HCQ might be useful especially early in the disease.

Browsed through the article you linked - hadn't seen that one yet so thanks for finding it. Will have to read in more detail later today.
 
  • Like
Reactions: ewc128
Long story, but I was hospitalized in December and almost died. Was in critical condition. Almost all of my symptoms were consistent with COVID, with the exception of my pericardial effusion - which there have been some cases in COVID patients. I got a pericardial window and drained a boatload of fluid to save my life. CT scans showed ground glass opacity.

I was very excited to get an antibody test - I got one last Saturday and I was negative. I would have bet anything I had it. But sadly, I did not. Wish I did so I would have potential for immunity.

Was wondering if you were going to post your story - thanks! For those who don't know, the long version is far more harrowing than the short version above. "Greg" and I have emailed a few times about this and we both thought it sounded like COVID, although there are clearly some other nasty viruses out there and people do die from the flu - although you also tested negative for the flu, correct? Would have much rather had COVID and now have immunity. Stay safe, my friend.
 
I don't think he is wishing to catch Covid. I'm guessing that he wished that whatever he had in December was Covid, since he has already gone though the illness and recovered, and if it was Covid he is potentially immune now.

Likewise, I had an upper respiratory illness in early March. At the time, only lower respiratory symptoms were considered Covid, so I wasn't tested. But now they include upper respiratory symptoms. So I am hoping that I had a very mild case of Covid, and am now recovered and immune. I'd rather be immune instead of worrying about catching it in the future.

I know what he was saying, but we're hearing now the after effects might be long lasting, the flu I doubt so much.
 
  • Like
Reactions: Upstream
Was wondering if you were going to post your story - thanks! For those who don't know, the long version is far more harrowing than the short version above. "Greg" and I have emailed a few times about this and we both thought it sounded like COVID, although there are clearly some other nasty viruses out there and people do die from the flu - although you also tested negative for the flu, correct? Would have much rather had COVID and now have immunity. Stay safe, my friend.
Do you buy any credence into studies like this:

https://www.sciencetimes.com/articl...ients-losing-13-years-lives-average-study.htm

I'm a bit skeptical how they came to these conclusions.
 
I know what he was saying, but we're hearing now the after effects might be long lasting, the flu I doubt so much.

While hospitalized, they tested me for every single virus they could. All at RWJ with their infectious disease folks there. Negative for all flus.

They knew at the time it was a virus and the pericardial effusion was caused by my body’s reaction to it. It was very very bad.

And yes, I really hoped for antibodies for all of the reasons above.
 
Was wondering if you were going to post your story - thanks! For those who don't know, the long version is far more harrowing than the short version above. "Greg" and I have emailed a few times about this and we both thought it sounded like COVID, although there are clearly some other nasty viruses out there and people do die from the flu - although you also tested negative for the flu, correct? Would have much rather had COVID and now have immunity. Stay safe, my friend.
Lot of issues I've read with the quick approvals and antibody tests for false positives and then giving someone the wrong impression that they've had the virus. Would those same antibody tests have issues with false negatives or no?
 
  • Like
Reactions: LETSGORU91
While hospitalized, they tested me for every single virus they could. All at RWJ with their infectious disease folks there. Negative for all flus.

They knew at the time it was a virus and the pericardial effusion was caused by my body’s reaction to it. It was very very bad.

And yes, I really hoped for antibodies for all of the reasons above.
Fair enough and I wasn't challenging you on anything really, just a lot of speculation is being thrown out there on what this virus can do to you, especially in regards with lungs, look at the case of the Broadway actor in NYC who had to have his leg amputated and now they're finding out his lungs are severly damaged.

Either way I'm glad you're on the rebound.
 
Long story, but I was hospitalized in December and almost died. Was in critical condition. Almost all of my symptoms were consistent with COVID, with the exception of my pericardial effusion - which there have been some cases in COVID patients. I got a pericardial window and drained a boatload of fluid to save my life. CT scans showed ground glass opacity.

I was very excited to get an antibody test - I got one last Saturday and I was negative. I would have bet anything I had it. But sadly, I did not. Wish I did so I would have potential for immunity.
I would probably try to get another antibody test - different test, though. I assume that requires a prescription?

There is a lot that isn't known about covid, especially with antibody production/immunity, how long that lasts, etc. Maybe you had it and your antibody level has already dropped to a point where the test couldn't measure it. Also, some studies have shown that some covid survivors just don't produce many (or any? not sure) antibodies so you could be one of those.
 
https://www.medrxiv.org/content/10.1101/2020.04.27.20073379v1
Retrospective study by folks not trying to sabotage HCQ on behalf of their Gilead sponsors (VA study). Even though retrospective, and therefore very limited, for me the most positive part is the IL-6 numbers. It shows HCQ attenuates the cytokine storm.


ABSTRACT
Importance: Coronavirus disease 2019 (COVID-19) is a pandemic with no specific drugs and high mortality. The most urgent thing is to find effective treatments. Objective: To determine whether hydroxychloroquine application may be associated with a decreased risk of death in critically ill COVID-19 patients and what is potential mechanism. Design, Setting and Patients: This retrospective study included all 568 critically ill COVID-19 patients who were confirmed by pathogen laboratory tests despite antiviral treatment and had severe acute respiratory distress syndrome, PAO2/FIO2 <300 with need of mechanical ventilation in Tongji Hospital, Wuhan, between February 1 of 2020 to April 8 of 2020. All 568 patients received comparable basic treatments including antiviral drugs and antibiotics, and 48 of them additionally received oral hydroxychloroquine (HCQ) treatment (200 mg twice a day for 7-10 days). Primary endpoint is mortality of patients, and inflammatory cytokines levels were compared between hydroxychloroquine and non-hydroxychloroquine (NHCQ) treatments. MAIN OUTCOMES AND MEASURES: In-hospital death and hospital stay time (day) were obtained, level of inflammatory cytokine (IL-6) was measured and compared between HCQ and NHCQ treatments. RESULTS: The median age of 568 critically ill patients is 68 (57, 76) years old with 37.0% being female. Mortalities are 18.8% (9/48) in HCQ group and 45.8% (238/520) in NHCQ group (p<0.001). The time of hospital stay before patient death is 15 (10-21) days and 8 (4 - 14) days for the HCQ and NHCQ groups, respectively (p<0.05). The level of inflammatory cytokine IL-6 was significantly lowered from 22.2 (8.3-118.9) pg/mL at the beginning of the treatment to 5.2 (3.0-23.4) pg/ml (p<0.05) at the end of the treatment in the HCQ group but there is no change in the NHCQ group. CONCLUSIONS AND RELEVANCE: Hydroxychloroquine treatment is significantly associated with a decreased mortality in critically ill patients with COVID-19 through attenuation of inflammatory cytokine storm. Therefore, hydroxychloroquine should be prescribed for treatment of critically ill COVID-19 patients to save lives.
 
Last edited:
  • Like
Reactions: T2Kplus10
https://www.medrxiv.org/content/10.1101/2020.04.27.20073379v1
Retrospective study by folks not trying to sabotage HCQ on behalf of their Gilead sponsors (VA study). Even though retrospective, and therefore very limited, for me the most positive part is the IL-6 numbers. It shows HCQ attenuates the cytokine storm.


ABSTRACT
Importance: Coronavirus disease 2019 (COVID-19) is a pandemic with no specific drugs and high mortality. The most urgent thing is to find effective treatments. Objective: To determine whether hydroxychloroquine application may be associated with a decreased risk of death in critically ill COVID-19 patients and what is potential mechanism. Design, Setting and Patients: This retrospective study included all 568 critically ill COVID-19 patients who were confirmed by pathogen laboratory tests despite antiviral treatment and had severe acute respiratory distress syndrome, PAO2/FIO2 <300 with need of mechanical ventilation in Tongji Hospital, Wuhan, between February 1 of 2020 to April 8 of 2020. All 568 patients received comparable basic treatments including antiviral drugs and antibiotics, and 48 of them additionally received oral hydroxychloroquine (HCQ) treatment (200 mg twice a day for 7-10 days). Primary endpoint is mortality of patients, and inflammatory cytokines levels were compared between hydroxychloroquine and non-hydroxychloroquine (NHCQ) treatments. MAIN OUTCOMES AND MEASURES: In-hospital death and hospital stay time (day) were obtained, level of inflammatory cytokine (IL-6) was measured and compared between HCQ and NHCQ treatments. RESULTS: The median age of 568 critically ill patients is 68 (57, 76) years old with 37.0% being female. Mortalities are 18.8% (9/48) in HCQ group and 45.8% (238/520) in NHCQ group (p<0.001). The time of hospital stay before patient death is 15 (10-21) days and 8 (4 - 14) days for the HCQ and NHCQ groups, respectively (p<0.05). The level of inflammatory cytokine IL-6 was significantly lowered from 22.2 (8.3-118.9) pg/mL at the beginning of the treatment to 5.2 (3.0-23.4) pg/ml (p<0.05) at the end of the treatment in the HCQ group but there is no change in the NHCQ group. CONCLUSIONS AND RELEVANCE: Hydroxychloroquine treatment is significantly associated with a decreased mortality in critically ill patients with COVID-19 through attenuation of inflammatory cytokine storm. Therefore, hydroxychloroquine should be prescribed for treatment of critically ill COVID-19 patients to save lives.

There is a lot of data (mostly anecdotal) in support of HCQ, and a lot of data (mostly anecdotal) against HCQ. I am not very troubled by the cardiovascular adverse events, since HCQ has know cardiovascular side effects (and the primary reason HCQ exists is to reduce the CV AEs of chloroquine). But I also don't think that HCQ is a magic pill to cure covid, otherwise we would have seen dramatic improvements where it was administered.

But we certainly need data from controlled trials to show if HCQ shows some benefit, and should be included as part of the standard of care.
 
I was sick back in December. So was my Mom.
I just had the antibody test done through Quest. Came back negative.
 
I would probably try to get another antibody test - different test, though. I assume that requires a prescription?

There is a lot that isn't known about covid, especially with antibody production/immunity, how long that lasts, etc. Maybe you had it and your antibody level has already dropped to a point where the test couldn't measure it. Also, some studies have shown that some covid survivors just don't produce many (or any? not sure) antibodies so you could be one of those.


All of that makes sense to me. Antibody tests are now available at many urgent cares in NJ. I simply walked into the Medemerge in Green Brook last Saturday and was out in about an hour. Very easy, no prescription or anything. It was a blood test - one vile. Doc told me they originally had one in stock that was more of a "pregnancy test style" but that was pulled by the FDA 24 hours after the clinic received the tests so they're getting refunded.

Maybe I'll take another test when a different test is available. It's a bit more important for me as I'm still running the restaurants and making deliveries to first responders/hospitals. I am extremely vigilant and feel like I'm doing everything I can to stay clean, but antibodies would have made me feel better.
 
  • Like
Reactions: MulletCork
https://www.medrxiv.org/content/10.1101/2020.04.27.20073379v1
Retrospective study by folks not trying to sabotage HCQ on behalf of their Gilead sponsors (VA study). Even though retrospective, and therefore very limited, for me the most positive part is the IL-6 numbers. It shows HCQ attenuates the cytokine storm.


ABSTRACT
Importance: Coronavirus disease 2019 (COVID-19) is a pandemic with no specific drugs and high mortality. The most urgent thing is to find effective treatments. Objective: To determine whether hydroxychloroquine application may be associated with a decreased risk of death in critically ill COVID-19 patients and what is potential mechanism. Design, Setting and Patients: This retrospective study included all 568 critically ill COVID-19 patients who were confirmed by pathogen laboratory tests despite antiviral treatment and had severe acute respiratory distress syndrome, PAO2/FIO2 <300 with need of mechanical ventilation in Tongji Hospital, Wuhan, between February 1 of 2020 to April 8 of 2020. All 568 patients received comparable basic treatments including antiviral drugs and antibiotics, and 48 of them additionally received oral hydroxychloroquine (HCQ) treatment (200 mg twice a day for 7-10 days). Primary endpoint is mortality of patients, and inflammatory cytokines levels were compared between hydroxychloroquine and non-hydroxychloroquine (NHCQ) treatments. MAIN OUTCOMES AND MEASURES: In-hospital death and hospital stay time (day) were obtained, level of inflammatory cytokine (IL-6) was measured and compared between HCQ and NHCQ treatments. RESULTS: The median age of 568 critically ill patients is 68 (57, 76) years old with 37.0% being female. Mortalities are 18.8% (9/48) in HCQ group and 45.8% (238/520) in NHCQ group (p<0.001). The time of hospital stay before patient death is 15 (10-21) days and 8 (4 - 14) days for the HCQ and NHCQ groups, respectively (p<0.05). The level of inflammatory cytokine IL-6 was significantly lowered from 22.2 (8.3-118.9) pg/mL at the beginning of the treatment to 5.2 (3.0-23.4) pg/ml (p<0.05) at the end of the treatment in the HCQ group but there is no change in the NHCQ group. CONCLUSIONS AND RELEVANCE: Hydroxychloroquine treatment is significantly associated with a decreased mortality in critically ill patients with COVID-19 through attenuation of inflammatory cytokine storm. Therefore, hydroxychloroquine should be prescribed for treatment of critically ill COVID-19 patients to save lives.
I mentioned this in another thread. My company is one of the biggest producers of HCQ. We have received over 500 calls from hospitals and HCPs asking for more info on the product. Who to use it with, who to avoid, how to lower the risk of AEs. etc. HCPs are having success with the product. It's not a cure, but very helpful with the right patients.
 
I agree that Martenson seems to have a bias in favor of HCQ but I'm trying to keep an open mind.
I enjoy listening to Chris's podcasts, so I have to disagree with assessment. He has no bias whatsoever. What he has been saying all along is as an anti-viral it should be evaluated earlier in the disease progression and with proper clinical trials to determine it's effectiveness as a treatment. Everyone is so politically charged over this it clouds people's judgement. Personally, I am waiting on some clinical trials that have just started on HCQ as a PEP, a PREP and as a treatment for those early in the disease progression. That is where I would expect it's greatest benefit if there is any. To date, that data does not exist. To make any judgement on HCQ without that is premature. That is all Chris has been saying as well.
 
Last edited:
  • Like
Reactions: MulletCork
I enjoy listening to Chris's podcasts, so I have to disagree with assessment. He has no bias whatsoever. What he has been saying all along is as an anti-viral it should be evaluated earlier in the disease progression and with proper clinical trials to determine it's effectiveness as a treatment. Everyone is so politically charged over this it clouds people's judgement. Personally, I am waiting on some clinical trials that have just started on HCQ as a PEP, a PREP and as a treatment for those early in the disease progression. That is where I would expect it's greatest benefit if there is any. To date, that data does not exist. To make any judgement on HCQ without that is premature. That is all Chris has been saying as well.
I've been watching his reports every day and have found them extremely valuable. He was on target with this from day 1 while everyone else downplayed the risk of the virus. He's got a medical background and obviously spends a lot of time scouring the literature which saves me a lot of time (plus despite my interest in medicine, I don't have any formal training).

We'll have to agree to disagree on the bias. Well, maybe it's not really bias but it does appear that way to me. He seems to emphasize the reports that show HCQ in a positive light and downplay the ones that are more negative. That's my impression anyway. I don't think it invalidates what he is saying (otherwise I wouldn't still be watching everyday). I tend to agree with his view that if HCQ has any benefit, it will be early in the disease course and possibly as a post-exposure treatment. Maybe as pre-exposure prophylaxis too. Most studies so far have been on very sick patients and it's pretty clear that HCQ isn't doing much if anything for them. You're right though about the political aspect, there's been a lot of push-back ever since Trump started talking about it and that is unfortunate.

I also read through the report that @RU848789 posted and have to say, the results there are far from conclusive. As you note...the jury is still out and the drug may have a role for the early stage or even pre-symptom period. Hopefully it does.
 
I've been watching his reports every day and have found them extremely valuable. He was on target with this from day 1 while everyone else downplayed the risk of the virus. He's got a medical background and obviously spends a lot of time scouring the literature which saves me a lot of time (plus despite my interest in medicine, I don't have any formal training).

We'll have to agree to disagree on the bias. Well, maybe it's not really bias but it does appear that way to me. He seems to emphasize the reports that show HCQ in a positive light and downplay the ones that are more negative. That's my impression anyway. I don't think it invalidates what he is saying (otherwise I wouldn't still be watching everyday). I tend to agree with his view that if HCQ has any benefit, it will be early in the disease course and possibly as a post-exposure treatment. Maybe as pre-exposure prophylaxis too. Most studies so far have been on very sick patients and it's pretty clear that HCQ isn't doing much if anything for them. You're right though about the political aspect, there's been a lot of push-back ever since Trump started talking about it and that is unfortunate.

I also read through the report that @RU848789 posted and have to say, the results there are far from conclusive. As you note...the jury is still out and the drug may have a role for the early stage or even pre-symptom period. Hopefully it does.
Did you see the retrospective study on HCQ released today? No media mention whatsoever as opposed to the crap from the VA retrospective study. Politics as usual.

I mentioned it in this post https://rutgers.forums.rivals.com/t...social-distancing.191275/page-92#post-4536710
 
I enjoy listening to Chris's podcasts, so I have to disagree with assessment. He has no bias whatsoever. What he has been saying all along is as an anti-viral it should be evaluated earlier in the disease progression and with proper clinical trials to determine it's effectiveness as a treatment. Everyone, especially Numbers, is so politically charged over this it clouds people's judgement. Personally, I am waiting on some clinical trials that have just started on HCQ as a PEP, a PREP and as a treatment for those early in the disease progression. That is where I would expect it's greatest benefit if there is any. To date, that data does not exist. To make any judgement on HCQ without that is premature. That is all Chris has been saying as well.

Politics has nothing to do with my criticism of HCQ. The science just isn't there to support its overuse in COVID to date. Martenson has some good content but he's very biased towards HCQ, as I posted last night. How can he claim to be balanced on the lupus angle and include that crap excerpt from some Italian blog (can't even tell what it is, but you also posted it), as if it's valid and not include the guidance from the Lupus Foundation of America, who represent the health of lupus patients, who say there's no evidence HCQ prevents contracting COVID-19? Or include the study that I linked 2 days ago that showed that lupus patients on HCQ actually have disproportionately high rates of COVID (not a good sign for its use as a preventative)? If you don't think that's biased I don't know what to tell you. I'm just asking for balance and good sources and he provided neither.

My main point all along is not that I "know" it doesn't work in some particular settings - it's that the data, to date, absolutely do not support it being used anywhere near as heavily as it has been and it's absolutely not a "cure," as many have called it. I would have simply preferred to wait for the results of the controlled clinical trials going on before ramping up use through the roof, for political reasons. You can go on believing Chris Martenson (a smart guy, but who has never done any clinical research I know of), the far right wing AAPS, and Dr. Raoult, whose original "gamechanging" study has been discredited, and some Italian guy, while I'll take Derek Lowe, Anthony Fauci, and the FASEB paper I linked last night, which did the most thorough literature review, to date, on HCQ and recommended that "HCQ only be used for COVID‐19 in the context of a carefully constructed randomized clinical trial."

Edit for @wisr01 - also, dug up my first couple of posts on HCQ and clearly I was excited in the first post, but then a day or so later, skepticism started creeping in, given the way the research was being presented/hawked, which seemed more than a bit unseemly.

So my skepticism and desire to find out if this would hold up to scrutiny and be a "gamechanger" or just another false "cure" claim (it certainly hasn't been a gamechanger or anywhere near a cure) preceded any knowledge of the politics of anyone involved.

I think your singling me out as follows: "Everyone, especially Numbers, is so politically charged over this it clouds people's judgement," was more than a bit unfair given my posting history on this.

The only "political" angle I've taken, which almost everyone in the scientific community agrees with, is that Trump simply had no place lauding the drug the next day and for weeks afterwards, as he has zero expertise in medical matters. That was completely inappropriate and never should've happened.

Follow up on some earlier posts by @RUfubar and me and others...

Now for some possibly good news. Breaking results on hydroxychloroquine (malaria treatment) in combo with azithromycin (antibiotic often used in pneumonias) show significant reduction in viral load in patients in a study in France. Don't think this is a peer reviewed yet, but it is a placebo controlled field study and these can be very important in emergencies like this.

https://twitter.com/RiganoESQ/status/1239780304082124800

In addition, remdesivir is showing some promising results as are some other anti-viral compounds and remdesivir completes a major phase III clinical trial on 4/3.

https://emedicine.medscape.com/article/2500114-treatment

And lastly, the first patient was enrolled today in a vaccine clinical trial, which will last 6 weeks (this is a preliminary trial just to gauge whether it's worth going to larger trials).

https://www.livescience.com/first-person-coronavirus-vaccine-clinical-trial.html

Dr. Raoult issued the actual paper on HCQ/Azithromycin today (first link) and Mr. Rigano did a spot on Fox tonight (2nd link). Still some skepticism in the medical community, and I have to admit that Mr. Rigano, who is a lawyer, and an advisor to the Stanford School of Medicine, comes off like a salesman in the Fox video, but if Dr. Raoult is correct, this is a game changer.

The data are stunning - 100% virologically cured with the combo by Day 6 vs. 57% cured with just HCQ and 12% in the control. Was a small study (42 patients) though and 6 patients dropped out, which is why some are concerned. However, it should be simple to replicate this on a larger scale and it needs to be done ASAP. I also imagine doctors and patients are going to be demanding these drugs based on this and fortunately both are generic, but I don't know the supply chain landscape.

As an aside it's also way premature to be calling this the 2nd ever 100% virus cure based on that limited of a data set, which is why there's skepticism. It took Pharmasett (and then Gilead who bought them when Merck stupidly failed to buy them) quite some time to make those claims for sofosbuvir curing Hep C, which it has. As an aside, the two active ingredients for Merck's HCV antiviral Zepatier were first scaled up and optimized, before manufacturing and launch, in my group in 2014-2016, but alas, we got to market too late.

https://drive.google.com/file/d/186Bel9RqfsmEx55FDum4eneY_IlWSHnGbj/view
 
Last edited:
I've been watching his reports every day and have found them extremely valuable. He was on target with this from day 1 while everyone else downplayed the risk of the virus. He's got a medical background and obviously spends a lot of time scouring the literature which saves me a lot of time (plus despite my interest in medicine, I don't have any formal training).

We'll have to agree to disagree on the bias. Well, maybe it's not really bias but it does appear that way to me. He seems to emphasize the reports that show HCQ in a positive light and downplay the ones that are more negative. That's my impression anyway. I don't think it invalidates what he is saying (otherwise I wouldn't still be watching everyday). I tend to agree with his view that if HCQ has any benefit, it will be early in the disease course and possibly as a post-exposure treatment. Maybe as pre-exposure prophylaxis too. Most studies so far have been on very sick patients and it's pretty clear that HCQ isn't doing much if anything for them. You're right though about the political aspect, there's been a lot of push-back ever since Trump started talking about it and that is unfortunate.

I also read through the report that @RU848789 posted and have to say, the results there are far from conclusive. As you note...the jury is still out and the drug may have a role for the early stage or even pre-symptom period. Hopefully it does.


I lived in Nigeria for five years in my pre and early teens (parents worked for the United Nations). My parents, siblings and I took chloroquine like you take ibuprofen today. People would pop em in their mouths like nothing. Malaria was so rampant, any time you get a fever, the response was "give em chloroquine"!

Not saying take chloroquine NOW or anything like that. But just pointing out that chloroquine is not a new drug. The side effects of it are pretty known already.
 
  • Like
Reactions: MulletCork
Did you see the retrospective study on HCQ released today? No media mention whatsoever as opposed to the crap from the VA retrospective study. Politics as usual.

I mentioned it in this post https://rutgers.forums.rivals.com/t...social-distancing.191275/page-92#post-4536710
Yes, was about to post it - without having gone through it, this looks to be the most positive data analysis yet on HCQ, but on the surface, Raoult's study looked good, too, before it was more deeply analyzed, so I'll wait for people with more medical expertise than I have to dig into this one. In addition, both the VA study and this study were retrospective and uncontrolled and neither has been peer reviewed yet, so I don't put a lot of stock in either, yet. Don't watch much TV so have no idea what's covered vs. not, but it's been talked about a lot on line. As always, let's see what the controlled, randomized, double-blind studies show. Do you happen to know when any of these will be completed?
 
Long story, but I was hospitalized in December and almost died. Was in critical condition. Almost all of my symptoms were consistent with COVID, with the exception of my pericardial effusion - which there have been some cases in COVID patients. I got a pericardial window and drained a boatload of fluid to save my life. CT scans showed ground glass opacity.

I was very excited to get an antibody test - I got one last Saturday and I was negative. I would have bet anything I had it. But sadly, I did not. Wish I did so I would have potential for immunity.
Either way, I’m glad you’re doing okay.
 
Status
Not open for further replies.
ADVERTISEMENT
ADVERTISEMENT