Evidence map›Paper›PMID 35962234›Full record

ArticleAdvances in therapy2022

Comparative Effectiveness of Dexamethasone in Hospitalized COVID-19 Patients in the United States.

Casey Kar-Chan Choong, Mark Belger, Alisa E Koch, Kristin J Meyers, Vincent C Marconi, Hamed Abedtash, Douglas Faries, Venkatesh Krishnan

Open access · hybridAbstract read
In one paragraph

Article in Advances in therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 49% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Casey Kar-Chan ChoongEli Lilly and Company, 893 S. Delaware Street, Indianapolis, IN, 46225, USA.ORCID 0000-0001-6476-784X
Mark BelgerEli Lilly and Company, 893 S. Delaware Street, Indianapolis, IN, 46225, USA.
Alisa E KochEli Lilly and Company, 893 S. Delaware Street, Indianapolis, IN, 46225, USA.
Kristin J MeyersEli Lilly and Company, 893 S. Delaware Street, Indianapolis, IN, 46225, USA.
Vincent C MarconiRollins School of Public Health and the Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA, USA.
Hamed AbedtashEli Lilly and Company, 893 S. Delaware Street, Indianapolis, IN, 46225, USA.
Douglas FariesEli Lilly and Company, 893 S. Delaware Street, Indianapolis, IN, 46225, USA.
Venkatesh KrishnanEli Lilly and Company, 893 S. Delaware Street, Indianapolis, IN, 46225, USA. krishnan_gary@lilly.com.
Eli Lilly (United States) · USEmory University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTo compare the mortality of hospitalized patients with COVID-19 between those that required supplemental oxygen and received dexamethasone with a comparable set of patients who did not receive dexamethasone.

methodsWe utilized the Premier Health Database to identify hospitalized adult patients with COVID-19 from July 1, 2020-January 31, 2021. Index date was when patients first initiated oxygen therapy. The primary endpoint was in-hospital mortality for patients receiving dexamethasone versus those not receiving dexamethasone 1-day pre- to 1-day post-index period. Secondary endpoints included 28-day mortality, time to in-hospital mortality, progression to invasive mechanical ventilation or death, time to discharge, and proportion discharged alive by day 28. Twenty-three models using weighting, matching, stratification, and regression were deployed through the concept of frequentist model average (FMA) to estimate the effect of dexamethasone on all-cause mortality up to the 28-day hospitalization period.

resultsA total of 1,208,881 patients with COVID-19 were screened; as an inpatient 255,216 used oxygen, and 251,536 were included in the analysis. In the dexamethasone group, odds of in-hospital mortality were higher than those of the comparator (FMA: odds ratio [OR] 1.15, 95% CI 1.08, 1.22). Using a best fit model, OR for in-hospital mortality was non-significant for the dexamethasone group compared with the comparator (OR 1.02, 95% CI 0.92, 1.14). Dexamethasone treatment was associated with poorer outcomes versus the comparator group across the majority of secondary endpoints, except for number of days in hospital, which was lower in the dexamethasone group versus the comparator group (mean difference - 2.14, 95% CI - 2.43, - 1.47).

conclusionsHospitalized adult patients with COVID-19 who required supplemental oxygen and received dexamethasone did not have a survival benefit versus similar patients not receiving dexamethasone. The dexamethasone group was not associated with favorable responses for outcomes such as progression to death or mechanical ventilation and time to in-hospital death.

Indexed as

COVID-19 Drug TreatmentAdultDexamethasoneHospital MortalityHumansInpatientsOxygenSARS-CoV-2United StatesDexamethasoneOxygenComparisonDexamethasoneEffectivenessPremier Health DatabaseUnited States

Identifiers

PMID35962234
PMCPMC9374287
OpenAlexW4290878780

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.