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COVID-19 is still going strong, far outstripping my lame intentions to post something weekly. I have been keeping close tabs on all developments, but I feel like I would need to post a few times a week to be useful and I can't seem to make time for that. I do hope to give a COVID-19 summary update at the next Montgomery County Pediatric Society virtual meeting on March 8. In the meantime if you have particular questions please use the Comments section to pose them.

This week the news media finally seemed to start paying attention to disturbing developments in Ebola virus infections in both East and West Africa. It's worth discussion, especially since the world is much better prepared to handle it now than it was during the large outbreak in West Africa a few years ago.

First to East Africa, where we have new cases appearing in the Democratic Republic of Congo. The total number of cases is low, perhaps 6 (it's difficult to be certain of the exact number mostly based on media reports), but what is noteworthy is that the index case may have been infected by semen from an Ebola survivor originally infected in the 2018-20 outbreak in the DRC. Fortunately public health resources are being mobilized rapidly in a locale which like many other countries previously has had significant barriers to public health measures for Ebola control.

In West Africa, Guinea is the epicenter of a new outbreak. This was one of the countries, along with Liberia and Sierra Leone, most affected by the 2014-16 outbreak that spilled over into the US and elsewhere. Here the index case appears to be a nurse who first sought medical attention on January 18, was misdiagnosed for a time, and ultimately died on January 28. She was buried without safety protocols, further exposing others to the virus. As in the DRC, public health interventions are proceeding much more rapidly than in the past. As I write this, the World Health Organization is deploying staff to the area, along with millions of dollars in funding. Importantly, we have 2 main tools today that were not available in past outbreaks.

First, we now have specific treatment for Ebola virus disease in the form of a monoclonal antibody cocktail approved by the FDA a few months ago; results of a large trial were published in the NEJM in December. The trade name is Inmazeb, a bit less of a mouthful than the trio of monoclonal antibodies that make up the pharmaceutical: atoltivimab, maftivimab, and odesivimab-ebgn. It is effective in lessening mortality in infected individuals especially if given early in the disease course. Unfortunately it is administered IV so it is a little more cumbersome especially in resource-poor areas.

Second are Ebola vaccines. The US FDA approved one, called Ervebo, last December. It is a live recombinant vaccine made using a backbone of vesicular stomatitis virus (VSV) with the envelope glycoprotein of the Zaire ebolavirus substituted into the nucleic acid code. (VSV is primarily a disease of cattle, horses, and swine, and outbreaks have occurred in the US. Humans occasionally can be infected, primarily from direct contact with infected animals.) This vaccine is used to immunize contacts of Ebola virus patients in what is termed "ring vaccination;" the technique was highly successful in controlling and eventually eliminating smallpox, for example.

A second vaccine, not reviewed by the FDA, is available for use in other countries. It is actually a combination of 2 vaccines, a first dose Zabdeno which is an adenovirus-vector vaccine and a second dose called Mvabea which contains Vaccinia Ankara Bavarian Nordic virus supplemented with parts of various Ebola and related filoviruses. Because of the requirement for 2 doses, Zabdeno is not that helpful for immediate outbreak control such as with ring vaccination, but it is another tool to help contain the virus in a population.

The WHO announced creation of Ebola vaccine stockpiles just on January 12, 2021, good timing for what we are experiencing now. Immunization programs started in the DRC on February 15; vaccine shipments will arrive in Guinea on February 21 with vaccine campaigns starting on February 22.

Perhaps the US currently is at less risk for imported Ebola because of somewhat limited international travel, but we should not relax. Just as with SARS-CoV-2, any health crisis anywhere in the world affects all of us. Outbreaks in resource-poor populations can be devastating. I'm hopeful all the new advances in Ebola virus disease will prevent a repeat of the tragic 2014-16 West African outbreak.

I guess it might be nice to talk about something besides COVID-19, but diphtheria definitely is not nice. A couple of weeks ago the CDC issued a Level 1 travel alert for Vietnam due to an outbreak of diphtheria in the Central Highlands region. Level 1 is the lowest of 3 travel alert levels, just meaning to keep a watch on things if planning to travel there.

I'm hoping no one feels the need to travel abroad now with our current pandemic possibly ramping up again, but this notice does provide us with a good opportunity to review clinical signs and symptoms of diphtheria, a disease very few of us have seen.

Of course it is a vaccine-preventable disease, so immunization is our primary guard against becoming ill. Remember it is a toxin-mediated disease, with fatalities usually due to myocarditis or to neuritis causing paralysis. In addition to common findings of sore throat and low-grade fever, the characteristic gray pseudomembrane can form in the pharynx or nose and is a big clue for the disease if you know what you are looking for. Respiratory diphtheria is fairly contagious, leading to outbreaks. Antitoxin and antibiotic therapy are mainstays to prevent complications in infected individuals, and antibiotic treatment can reduce transmission to others. The CDC's Yellow Book has a concise summary of features.

Speaking of vaccines, please remember not to let our pandemic delay children being immunized!

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It's always been hard to keep up with the medical literature, especially to figure out what original articles are of high enough quality to warrant a change in your clinical practice. It's not enough to just read the abstract, or to be reassured because the authors are from a reputable institution or the article is published in a reputable journal. I've been teaching Evidence Based Medicine (EBM) in various formats for over 20 years, including a full graduate school course for a while. I've learned a lot, both from reading but also from my students and colleagues, about how to sort through the jungle of words and diagrams in medical articles to pick up those rare pearls of good information.

EBM officially came into being in the early 1990s and, like most things, it has evolved. What hasn't changed much, however, are the forces that result in low quality evidence being published and advertised:

  • Pressure on researchers to "publish or perish." This not only involves job security and academic promotion but also a natural desire to make a name for oneself.
  • Pressure from academic institutions to ask their researchers to "hype" their studies in the hopes of increasing organizational rankings in national publications and also increase charitable donations.
  • Complicity from the lay press, anxious to describe in breathtaking fashion a new study, even if it has no direct relevance to clinical practice or improving lives of their viewers/readers.
  • Efforts from commercial organizations, such as pharmaceutical companies, test developers, and device manufacturers, to sell their products.
  • Predatory journals who will publish anything for a price. (One "gotcha" study showed how one of these journals published a report taken straight from the pages of a "Seinfeld" script - clearly totally bogus and obviously published in such a journal without any editorial review.)
  • Failure of the medical community as a whole to convey the inherent uncertainty in medical science - very few things are absolute "facts."

All of this just got worse in the pandemic era. Individual clinicians, researchers, and organizations seem bent on being the first to report the newest covid finding, and publishers and the lay press are anxious to help them. Unfortunately, things have moved too fast. Just recently, 3 major journals (New England Journal of Medicine, Lancet, and Annals of Internal Medicine) retracted publications due to, in my opinion, sloppy editing - plain rookie mistakes likely due to being in too much of a rush. (Actually as I'm writing this I heard about a potential new retraction with Proceedings of the National Academy of Sciences regarding mode of transmission of SARS-CoV-2). It is even harder now for those of us at the point of care to digest the onslaught of poor science looking for the truly helpful articles. However, there is still hope, and here are some quick guides to survival in the Pandemic Era of Medical Practice (PEMP, I just made up that acronym).

The image above is one I've used many times, most recently at a talk I gave at the AAP NCE meeting last fall. It is my version of the "evidence pyramid," a hierarchy of studies much misunderstood by the general medical public. Simply explained, results utilizing the study design types at the lower end of the pyramid are more likely to be shown to be wrong when subsequent studies, usually from a higher design type in the pyramid, are performed. Also, note that pure bench studies and animal studies aren't even part of the pyramid; those studies would not immediately impact clinical (human) medical practice. Also be aware that a poorly-designed randomized controlled trial (RCT) wouldn't be near the top of the pyramid; bad science can occur at all levels and trumps the pyramid ranking.

The vast majority of design types we are seeing related to COVID-19 are case series, i.e. just a report of what was tried and what happened, usually of a retrospective nature. It's not that these studies are bad, but compared to a randomized, placebo-controlled double blind trial of a new therapy, it just doesn't stand up. The gap between the lower and upper ends of the pyramid are magnified when we are dealing with a completely new disease like COVID-19.

(BTW, if you are wondering about GOBSAT, I wish I had invented the acronym but I didn't. It stands for Good Ol' Boys Sittin' Around a Table, another word for expert opinion. Again, if that is all we have to go on, I'm certainly interested in what experts think, but it's astonishing over the years how often GOBSAT opinions are reversed when better studies are performed.)

So, here's a quick and dirty approach of how I keep up with the flood of medical studies. First, I look at the abstract. If it sounds like something worth reading more, I then go immediately to the Methods section of the article. Yes, I know that section is the most painful of all, but that's where I figure out study design and whether the study may have critical flaws that would affect study results. Also, in spite of modern-day editing, even the best journals still allow conclusions to appear in the abstract that aren't supported by the study itself; usually they just represent the authors' conjectures but aren't labelled as such. If the Methods section doesn't pass muster, I don't read the rest of the article. If, however, the Methods look reasonably sound (remember, this is biology, we can't expect perfection in any study) I look through the results and discussion to see if this is something that would apply to my patients.

One more point that has just surfaced during PEMP. I'm starting to see increased alerts about manuscripts submitted to pre-publication web sites. Prior to the pandemic, these were sites where authors submitted data to be looked at by other scientists. They were not necessarily even submitted to a journal, just a way to increase transparency and actually a good thing. One key important fact is that the documents have not undergone any peer review at all. Unfortunately, now many authors are submitting results of case series and the like to these sites, and the lay press and even otherwise sound academicians are referring to these as "publications" when in fact they are nothing of the sort. As a reviewer for many medical journals and author of a few scientific articles, I can tell you that most articles submitted for publication undergo many, many significant changes before publication. I wouldn't advise clinicians to even look at these postings, they are useful only if someone is trying to design a research study on a similar topic. Some of the web sites include medrxiv.org and biorxiv.org. Again, nothing wrong with these sites other than how they are currently being misused by a few individuals.

So, I would advise you all not to be too discouraged by the confusion and flood of information. Listen to the lay press so you know what your patients and families are hearing, read the key articles, and be prepared to answer questions in your practice.