Evidence map›Paper›PMID 36261315›Full record

ArticleAnnals of neurology2023

Fewer COVID-19 Neurological Complications with Dexamethasone and Remdesivir.

Alexander Grundmann, Chieh-Hsi Wu, Marc Hardwick, J Kenneth Baillie, Peter J M Openshaw, Malcolm G Semple, Dankmar Böhning, Sarah Pett, Benedict D Michael, Rhys H Thomas and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Annals of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Remdesivir for the treatment of COVID-19.The Cochrane database of systematic reviews · 2023
    Pooled it
  3. Article
  4. Review
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  8. Article
  9. Article
  10. Neurological complications caused by SARS-CoV-2.Clinical microbiology reviews · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 1 country.

Alexander GrundmannClinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Chieh-Hsi WuStatistics, Mathematical Sciences, and Faculty of Social Sciences, University of Southampton, Southampton, UK.
Marc HardwickClinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
J Kenneth BaillieRoslin Institute, University of Edinburgh, Easter Bush, Edinburgh, UK.
Peter J M OpenshawNational Heart and Lung Institute, Imperial College London, London, UK.
Malcolm G SempleNIHR Health Protection Research Unit for Emerging and Zoonotic Infections, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
Dankmar BöhningStatistics, Mathematical Sciences, and Faculty of Social Sciences, University of Southampton, Southampton, UK.
Sarah PettMedical Research Council Clinical Trials Unit, Institute of Clinical Trials and Methodology, University College London, London, UK.
Benedict D MichaelNIHR Health Protection Research Unit for Emerging and Zoonotic Infections, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
Rhys H ThomasTranslational and Clinical Research Institute, University of Newcastle, Newcastle upon Tyne, UK.
Ian GaleaClinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.ORCID 0000-0002-1268-5102
ISARIC4C investigators
University Hospital Southampton NHS Foundation Trust · GBUniversity of Liverpool · GBUniversity of Southampton · GBImperial College Healthcare NHS Trust · GBMRC Clinical Trials Unit at UCL · GBRoslin Institute · GBRoyal Victoria Infirmary · GB

Funding

Medical Research Council MC_PC_19059Medical Research Council MC_PC_20029Medical Research Council MC_PC_20058Medical Research Council MC_UU_00004/04Medical Research Council MR/T028750/1Medical Research Council MR/V007181/1Medical Research Council MR/V03605X/1
6 · The paper itself

Abstract

objectiveThe objective of this study was to assess the impact of treatment with dexamethasone, remdesivir or both on neurological complications in acute coronavirus diease 2019 (COVID-19).

methodsWe used observational data from the International Severe Acute and emerging Respiratory Infection Consortium World Health Organization (WHO) Clinical Characterization Protocol, United Kingdom. Hospital inpatients aged ≥18 years with laboratory-confirmed severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) infection admitted between January 31, 2020, and June 29, 2021, were included. Treatment allocation was non-blinded and performed by reporting clinicians. A propensity scoring methodology was used to minimize confounding. Treatment with remdesivir, dexamethasone, or both was assessed against the standard of care. The primary outcome was a neurological complication occurring at the point of death, discharge, or resolution of the COVID-19 clinical episode.

resultsOut of 89,297 hospital inpatients, 64,088 had severe COVID-19 and 25,209 had non-hypoxic COVID-19. Neurological complications developed in 4.8% and 4.5%, respectively. In both groups, neurological complications were associated with increased mortality, intensive care unit (ICU) admission, worse self-care on discharge, and time to recovery. In patients with severe COVID-19, treatment with dexamethasone (n = 21,129), remdesivir (n = 1,428), and both combined (n = 10,846) were associated with a lower frequency of neurological complications: OR = 0.76 (95% confidence interval [CI] = 0.69-0.83), OR = 0.69 (95% CI = 0.51-0.90), and OR = 0.54 (95% CI = 0.47-0.61), respectively. In patients with non-hypoxic COVID-19, dexamethasone (n = 2,580) was associated with less neurological complications (OR = 0.78, 95% CI = 0.62-0.97), whereas the dexamethasone/remdesivir combination (n = 460) showed a similar trend (OR = 0.63, 95% CI = 0.31-1.15).

interpretationTreatment with dexamethasone, remdesivir, or both in patients hospitalized with COVID-19 was associated with a lower frequency of neurological complications in an additive manner, such that the greatest benefit was observed in patients who received both drugs together. ANN NEUROL 2023;93:88-102.

Indexed as

AlanineAntiviral AgentsCOVID-19COVID-19 Drug TreatmentDexamethasoneAdenosine MonophosphateAdolescentAdultHumansSARS-CoV-2Adenosine MonophosphateAlanineAntiviral AgentsDexamethasoneremdesivir

Identifiers

PMID36261315
PMCPMC9874556
OpenAlexW4306836026

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.