1/
My appraisal of the Danish mask study (DANMASK-19): This was a negative trial - masks were not shown to prevent #COVID19.

Could chance or bias make this outcome more likely?
Does this mean we don’t need to wear masks?

Let’s take a deeper look.

#HowIReadThisPaper

(Thread)
2/
Before beginning, if you have not already done so, I implore you - read the paper!

acpjournals.org/doi/10.7326/M2…

Then, come back, and please comment, add what I have missed, and correct me where I am wrong.

Critical appraisal is a group effort.
3/
First, let’s agree on what was tested:

The hypothesis was that the recommendation to wear masks (added to other public health measures) would reduce the incidence of COVID19 among wearers from 2% to 1% over 1 month, in a setting where mask use was uncommon (Denmark).
4/
6,024 adults were randomized; half were told to wear masks when out of the house.

The primary outcome was a composite of a self-reported positive #SARSCoV2 home antibody test, OP or nasal PCR, or hospital-based diagnosis at 1 month.

The funding source is not worrisome.
5/
Next, let’s estimate the likelihood of finding a difference in the primary outcome.

Finding a large effect size (a 50% relative reduction in incident COVID19 among mask wearers), when the outcome is already rare, is very difficult.

How do we know the outcome was rare?
6/
Only ~2% of patients were diagnosed with COVID19 during the study period.

As @DrTomFrieden notes in the editorial, this rate was much lower than the US & the UK: acpjournals.org/doi/10.7326/M2…

Even if that was an underestimate of transmission in the community…
7/
...surveillance data from Denmark confirm that the daily number of new confirmed cases (left) and the total number of patients hospitalized with COVID19 (right) were both decreasing during the study period:

ourworldindata.org/coronavirus/co…

sst.dk/en/english/cor…
8/
How do we know that a 50% effect size is large?

For comparison, 50% is the lower limit of vaccine efficacy the FDA recommended for COVID vaccines seeking licensure:
fda.gov/regulatory-inf…

This study tested whether a recommendation provided at least that much protection.
9/
On the basis of these observations, failure to find a benefit of masks seems likely.

Next, let’s investigate sources of chance.

The primary outcome point estimate (OR = 0.82) suggests an 18% reduction in the odds of infection, but the 95% confidence interval spans 0.54-1.23.
10/
The width of the confidence interval is larger than the magnitude of the effect estimate itself.

This indicates that there is a lot of uncertainty in the estimate of the effect, and is another possible explanation for the failure to demonstrate a >50% relative reduction.
11/
This is also apparent in the subgroup analyses.

On visual inspection, we see the point estimates for most subgroups were to the left of unity, but had CIs that crossed one.

This is compatible with a modest (<50%) effect size, estimated with low precision (due to low power):
12/
Although there were no significant interactions, the point estimates suggest a stronger effect in those who:
-Wore glasses (↑ protection)
-Were outside longer (↑ exposure)
-Lived in the capital region (↑ prevalence)

If true, these would be consistent with what we expect.
13/
Next, let’s examine sources of bias.

There are at least two sources of bias towards underdiagnosis of COVID19 in this trial:

One is self-report of the primary outcome. Figure 1 shows that ~20% of people in both groups did not report outcome data.
14/
Another source of bias towards underdiagnosis is the time lag of seroconversion.

We know it takes ~2 weeks to generate Ig’s.

For a study lasting 1 month, this means any infections in the last two weeks could have been missed if patients hadn't yet formed Ig's.
15/
In addition, there are at least two more sources of bias towards a null finding in this study:
-Low adherence to the mask recommendation
-Low positive predictive value (PPV) of serology

Let’s examine each of them.
16/
Fewer than half of people in the mask group reported wearing masks as recommended (46%).

Low uptake of the intervention diminishes our ability to detect any benefit of masking that may exist.
17/
Regarding serology and PPV: table 2 reveals that most (~75%) infections were diagnosed via a positive IgM or IgG.

This is problematic because the false-positive rate of any test increases rapidly when outcomes are rare and specificity is much lower than 100%.

How rapidly?
18/
At a prevalence of 2% and a sens/spec of 82.5% / 99.5% for the antibody assay used in this study, the PPV is 77%.

However, using the specificity reported by the FDA of 97.5%, just 2% lower, the PPV falls to 40%.

accessdata.fda.gov/cdrh_docs/pres…
19/
A PPV of <50% means we would expect the majority of all infections diagnosed by serology to be false positives.

False positives are likely to be distributed evenly, thus biasing towards the null.

For more on PPV pitfalls, see this thread:
20/
Let’s close with summarizing what this study adds and some suggestions for how these issues could be addressed in future studies.

Replication in a higher-transmission setting & powering for a more modest effect size are good starting points.

But...
21/
~15% of people in the mask group reported experiencing adverse reactions from others because of their masks, and 1/3 of those who did not wear masks as directed cited their work as the reason.

Social & behavioral incentives were not aligned with mask use in this study.
22/
This raises the Q of whether an individual-level RCT is the best way to study a population-level recommendation.

An argument made eloquently by @MonicaGandhi9 and others is that a community-level cluster RCT could better align social & behavioral incentives with mask use.
23/
The authors note this study did not test masks for source control, which is likely to have an even greater impact on transmission.

That impact, coupled with low risk of harm from masks, is the basis for @CDC's continued recommendation for their use:

cdc.gov/coronavirus/20…
24/
Bottom line: Rare outcomes, powering for a big effect, & multiple sources of chance & bias increased the likelihood of a negative study.

DANMASK-19 didn’t show a large benefit for wearers, but a meaningful public health benefit likely still exists. Keep wearing masks.

(End)

• • •

Missing some Tweet in this thread? You can try to force a refresh
 

Keep Current with Rahul Ganatra

Rahul Ganatra Profile picture

Stay in touch and get notified when new unrolls are available from this author!

Read all threads

This Thread may be Removed Anytime!

PDF

Twitter may remove this content at anytime! Save it as PDF for later use!

Try unrolling a thread yourself!

how to unroll video
  1. Follow @ThreadReaderApp to mention us!

  2. From a Twitter thread mention us with a keyword "unroll"
@threadreaderapp unroll

Practice here first or read more on our help page!

More from @rbganatra

25 Jul
1/
#SARSCoV2 #COVID19 got you down? Me too.

Ready for some good news? Here it is: #Dexamethasone (dex) works.

But when, how much, and for which patients?

Here’s #HowIReadThisPaper on Horby et al: the RECOVERY trial prelim report: nejm.org/doi/full/10.10…

(Thread)
2/
Already read the paper, just want the appraisal? Go here:

Haven’t read it yet? Here are the highlights.

Based on my very informal poll, here’s how twitter respondents indicated they are using dex in COVID19 patients as of mid-July 2020:
3/
Background: COVID19 can induce a deadly hyper-inflammatory host response.

Prior observational data (↓quality, ↑risk of confounding by indication) suggested ↑mortality from steroids in influenza: pubmed.ncbi.nlm.nih.gov/30798570/

The role of steroids in treating COVID19 is unknown.
Read 17 tweets
25 Jul
1/
My appraisal of the RECOVERY trial: This was a (very) positive study.

How could chance or bias affect the validity of these results?
What was missing?
How should we apply these results?

Let’s take a deeper look.

#HowIReadThisPaper
2/
Regarding bias: Strict inclusion/exclusion criteria can introduce selection bias by creating a highly selected study population.

This was NOT so in RECOVERY.

In figure 1, we see that 83% of recruited* patients were ultimately included.

(*assuming “recruited” = “screened”)
3/
Amazingly, ~15% of all patients hospitalized for COVID19 in the UK during the study period were included in this trial.

No other Tx trial for COVID19 even comes close to that level of representation.

→These results should generalize broadly to hospitalized patients.
Read 15 tweets
30 May
1/
How common is loss of smell (anosmia) in #SARSCoV2 #COVID19, and how useful is it for ruling the diagnosis in or out? Let’s take a look at the data.

Here’s a quick #HowIReadThisPaper on two @AnnalsofEM papers addressing this question:

Chua et al

&

Peyroney et al

(Thread)
2/
First, a question:

Let’s assume you have a limited supply of swabs and need to prioritize which patients to test for COVID19.

In which skilled nursing facility (SNF) setting would you expect anosmia to be more useful in identifying patients who will test positive?
3/
Chua et al annemergmed.com/article/S0196-…

Question: What are the test characteristics of acute olfactory loss (hyposmia or anosmia for <14d) for Dx of COVID19, using oropharyngeal PCR as the gold standard?

Design: single-center cross-sectional study via chart review (retrospective)
Read 17 tweets
23 May
1/
Should we use #Lopinavir-ritonavir (LPV/r) + #Ribavirin (RBV) +/- #Interferon beta-1b (IFN) to treat #SARSCoV2 #COVID19? Let’s take a look at the data.

Here’s: #HowIReadThisPaper on @TheLancet trial of triple therapy for COVID19

Hung et al: thelancet.com/journals/lance…
2/
First, let’s assess our baseline beliefs about triple therapy:

Before reading this study, when considering triple therapy as a treatment for patients with COVID19, I think the most important component is likely to be:
3/
Background: A 2003 case series suggested ↓mortality (vs historical controls) in SARS patients treated with LPV/r + RBV :

ncbi.nlm.nih.gov/pmc/articles/P…

In 2015, LPV/r and IFN led to ↓viral load and improved clinical outcomes in animal models of MERS:

pubmed.ncbi.nlm.nih.gov/26198719/
Read 30 tweets
10 May
1/
Should we use #Remdesivir (RDV) to treat #SARSCoV2? #COVID19 Let’s take a look at the data.

Here’s: #HowIReadThisPaper on the @Lancet trial of RDV for COVID19 in humans

Wang et al: thelancet.com/journals/lance…

(Thread)
2/
First, let’s assess our baseline beliefs about RDV.

Before reading this study, when considering remdesivir as a treatment for patients with severe #COVID19, I think the:
3/
Background: There are currently no effective antivirals for patients with severe COVID19.

RDV, a nucleotide analogue, has broad antiviral activity against many coronaviruses in vitro.

This is the first published clinical trial of RDV for #COVID19 in humans.
Read 30 tweets
29 Apr
1/
What is the risk of macrovascular thrombosis among critically ill patients with #SARSCoV2 #COVID19? Let’s take a look at the data.

Here’s #HowIReadThisPaper on a @ThromboisRese1 case series examining this question:

Klok et al: thrombosisresearch.com/article/S0049-…

(Thread)
2/
Background: #COVID19 can cause inflammation, hypoxemia, and disseminated intravascular coagulation (DIC), which all increase risk for venous (DVT, PE) and arterial (CVA, MI) thrombosis.

Currently, the risk of thrombosis in patients critically ill with COVID19 is unknown.
3/
Question: What is the cumulative incidence of venous and arterial thrombosis among critically ill patients with #COVID19?

Date published: 10 April 2020

Funding: None specified
Read 28 tweets

Did Thread Reader help you today?

Support us! We are indie developers!


This site is made by just two indie developers on a laptop doing marketing, support and development! Read more about the story.

Become a Premium Member ($3/month or $30/year) and get exclusive features!

Become Premium

Too expensive? Make a small donation by buying us coffee ($5) or help with server cost ($10)

Donate via Paypal Become our Patreon

Thank you for your support!

Follow Us on Twitter!