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Clinical Decision Support Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Not linked to any defined compartments |
This is the narrative for the resource. See also the XML, JSON or Turtle format. This example conforms to the profile Citation.
Generated Narrative
Resource "citation-example-systematic-meta-review"
url: http://hl7.org/fhir/Citation/citation-example-systematic-meta-review
identifier: FEvIR Object Identifier: 27121
title: SMR Sterne JAC JAMA 32876694
status: active
description: A systematic review included in the Steroids SMR Project
copyright: https://creativecommons.org/licenses/by-nc-sa/4.0/
author: Brian S. Alper:
- | Style | Text |
* | Computable Publishing (citation-summary-style#comppub) | Association Between Administration of Systemic Corticosteroids and Mortality Among Critically Ill Patients With COVID-19: A Meta-analysis [Journal Article]. Contributors: The WHO Rapid Evidence Appraisal for COVID-19 Therapies (REACT) Working Group Authors and Members of the Writing Committee: Jonathan A. C. Sterne, MA, MSc, PhD; Srinivas Murthy, MD, MSc; Janet V. Diaz, MD; Arthur S. Slutsky, CM, MD; Jesús Villar, MD, PhD; Derek C. Angus, MD, MPH; Djillali Annane, MD, PhD; Luciano Cesar Pontes Azevedo, MD, PhD; Otavio Berwanger, MD, PhD; Alexandre B. Cavalcanti, MD, PhD; Pierre-Francois Dequin, MD, PhD; Bin Du, MD; Jonathan Emberson, PhD; David Fisher, MSc; Bruno Giraudeau, PhD; Anthony C. Gordon, MBBS, MD; Anders Granholm, MD; Cameron Green, MSc; Richard Haynes, DM; Nicholas Heming, MD, PhD; Julian P. T. Higgins, BA, PhD; Peter Horby, PhD; Peter Jüni, MD; Martin J. Landray, PhD; Amelie Le Gouge, MSc; Marie Leclerc, MSc; Wei Shen Lim, BMedSci, BMBS, DM; Flávia R. Machado, MD, PhD; Colin McArthur, MBChB; Ferhat Meziani, MD, PhD; Morten Hylander Møller, MD, PhD; Anders Perner, MD, PhD; Marie Warrer Petersen, MD; Jelena Savović, BPharm, MSc, PhD; Bruno Tomazini, MD; Viviane C. Veiga, MD, PhD; Steve Webb, MBBS, MPH, PhD; John C. Marshall, MD. In: JAMA, PMID 32876694. Accessed February 15, 2021. Available at: http://doi.org/10.1001/jama.2020.17023. |
- | Type | Classifier |
* | FEvIR Platform Use (CitationClassificationType#fevir-platform-use) | Project Specific (CitationArtifactClassifier#project-specific) |
statusDate
activity: ROB assessment ()
actual: true
period: ?? --> 2021-06-07
statusDate
activity: Author contact ()
actual: true
period: 2021-06-07 --> (ongoing)
citedArtifact
identifier: id: 32876694, pii: 2770279, id: 10.1001/jama.2020.17023, id: PMC7489434
relatedIdentifier: id: CRD42020197242
dateAccessed: 2021-02-15
Titles
- Type Language Text * primary-human-use () English (Tags for the Identification of Languages#en) Association Between Administration of Systemic Corticosteroids and Mortality Among Critically Ill Patients With COVID-19: A Meta-analysis. Abstracts
- Type Text * Primary human use (CitedArtifactAbstractType#primary-human-use) <AbstractText Label="Importance">Effective therapies for patients with coronavirus disease 2019 (COVID-19) are needed, and clinical trial data have demonstrated that low-dose dexamethasone reduced mortality in hospitalized patients with COVID-19 who required respiratory support.</AbstractText><AbstractText Label="Objective">To estimate the association between administration of corticosteroids compared with usual care or placebo and 28-day all-cause mortality.</AbstractText><AbstractText Label="Design, Setting, and Participants">Prospective meta-analysis that pooled data from 7 randomized clinical trials that evaluated the efficacy of corticosteroids in 1703 critically ill patients with COVID-19. The trials were conducted in 12 countries from February 26, 2020, to June 9, 2020, and the date of final follow-up was July 6, 2020. Pooled data were aggregated from the individual trials, overall, and in predefined subgroups. Risk of bias was assessed using the Cochrane Risk of Bias Assessment Tool. Inconsistency among trial results was assessed using the I2 statistic. The primary analysis was an inverse variance-weighted fixed-effect meta-analysis of overall mortality, with the association between the intervention and mortality quantified using odds ratios (ORs). Random-effects meta-analyses also were conducted (with the Paule-Mandel estimate of heterogeneity and the Hartung-Knapp adjustment) and an inverse variance-weighted fixed-effect analysis using risk ratios.</AbstractText><AbstractText Label="Exposures">Patients had been randomized to receive systemic dexamethasone, hydrocortisone, or methylprednisolone (678 patients) or to receive usual care or placebo (1025 patients).</AbstractText><AbstractText Label="Main Outcomes and Measures">The primary outcome measure was all-cause mortality at 28 days after randomization. A secondary outcome was investigator-defined serious adverse events.</AbstractText><AbstractText Label="Results">A total of 1703 patients (median age, 60 years [interquartile range, 52-68 years]; 488 [29%] women) were included in the analysis. Risk of bias was assessed as "low" for 6 of the 7 mortality results and as "some concerns" in 1 trial because of the randomization method. Five trials reported mortality at 28 days, 1 trial at 21 days, and 1 trial at 30 days. There were 222 deaths among the 678 patients randomized to corticosteroids and 425 deaths among the 1025 patients randomized to usual care or placebo (summary OR, 0.66 [95% CI, 0.53-0.82]; P < .001 based on a fixed-effect meta-analysis). There was little inconsistency between the trial results (I2 = 15.6%; P = .31 for heterogeneity) and the summary OR was 0.70 (95% CI, 0.48-1.01; P = .053) based on the random-effects meta-analysis. The fixed-effect summary OR for the association with mortality was 0.64 (95% CI, 0.50-0.82; P < .001) for dexamethasone compared with usual care or placebo (3 trials, 1282 patients, and 527 deaths), the OR was 0.69 (95% CI, 0.43-1.12; P = .13) for hydrocortisone (3 trials, 374 patients, and 94 deaths), and the OR was 0.91 (95% CI, 0.29-2.87; P = .87) for methylprednisolone (1 trial, 47 patients, and 26 deaths). Among the 6 trials that reported serious adverse events, 64 events occurred among 354 patients randomized to corticosteroids and 80 events occurred among 342 patients randomized to usual care or placebo.</AbstractText><AbstractText Label="Conclusions and Relevance">In this prospective meta-analysis of clinical trials of critically ill patients with COVID-19, administration of systemic corticosteroids, compared with usual care or placebo, was associated with lower 28-day all-cause mortality.</AbstractText> publicationForm
PublishedIns
- Type Identifier Title PublisherLocation * Periodical (PublishedInType#D020492) ISSN Type: 1538-3598, ISOAbbreviation: JAMA, ISSN Linking: 0098-7484, Medline Title Abbreviation: JAMA, NLM Unique ID: 7501160 JAMA United States periodicRelease
citedMedium: Internet (journal-issue-medium#Internet)
volume: 324
issue: 13
DateOfPublications
- Date Year Month Day * 2020-10-06 2020 10 06 language: English (Tags for the Identification of Languages#en)
pageString: 1330-1341
webLocation
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url: https://jamanetwork.com/journals/jama/fullarticle/2770279
classification
type: Steroids SMR project use ()
classifier: primary article (), Unclear risk of bias ()
WhoClassifieds
- Person FreeToShare * : Brian S. Alper false classification
type: UC Description ()
classifier: To assess systemic corticosteroids on 28-day mortality in critically ill patients with COVID-19 ()
WhoClassifieds
- Person Organization FreeToShare * : Dr. Ethan Molitch : University of Chicago true classification
type: Knowledge Artifact Type (CitedArtifactClassificationType#knowledge-artifact-type)
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classifier: Print (CitationArtifactClassifier#Print)
classification
type: Chemical (CitedArtifactClassificationType#chemical)
classifier: Adrenal Cortex Hormones (chemical-substances#0; #D000305), Glucocorticoids (chemical-substances#0; #D005938), Dexamethasone (chemical-substances#7S5I7G3JQL; #D003907), Hydrocortisone (chemical-substances#WI4X0X7BPJ; #D006854), Methylprednisolone (chemical-substances#X4W7ZR7023; #D008775)
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type: MeSH heading (CitedArtifactClassificationType#mesh-heading)
classifier: Adrenal Cortex Hormones (#D000305; #Q000627 "therapeutic use"; [not stated]#Y), Betacoronavirus (#D000073640), COVID-19 (#D000086382), Cause of Death (#D002423), Coronavirus Infections (#D018352; #Q000188 "drug therapy"; [not stated]#Y; #Q000401 "mortality"; [not stated]#N), Critical Illness (#D016638), Dexamethasone (#D003907; #Q000627 "therapeutic use"; [not stated]#N), Glucocorticoids (#D005938; #Q000627 "therapeutic use"; [not stated]#Y), Humans (#D006801), Hydrocortisone (#D006854; #Q000627 "therapeutic use"; [not stated]#N), Methylprednisolone (#D008775; #Q000627 "therapeutic use"; [not stated]#N), Pandemics (#D058873), Pneumonia, Viral (#D011024; #Q000188 "drug therapy"; [not stated]#Y; #Q000401 "mortality"; [not stated]#N), Randomized Controlled Trials as Topic (#D016032), SARS-CoV-2 (#D000086402)
classification
type: Publication type (CitedArtifactClassificationType#publication-type)
classifier: Journal Article (#D016428), Meta-Analysis (#D017418), Research Support, Non-U.S. Gov't (#D013485)
classification
type: Supplemental MeSH for Protocol (CitedArtifactClassificationType#supplemental-mesh-protocol)
classifier: COVID-19 drug treatment (#C000705127)
classification
type: Citation subset (CitedArtifactClassificationType#citation-subset)
classifier: AIM (elements_descriptions.html#citationsubset#AIM), IM (elements_descriptions.html#citationsubset#IM)
classification
type: Funding ()
classifier: The World Health Organization (Conflict of interest statements included notes on several fundings for co-investigators as well, albeit not directly funding this meta-analysis) ()
WhoClassifieds
- Person Organization FreeToShare * : Erfan Shamsoddin : COVID-19 Knowledge Accelerator true contributorship
complete: true
entry
collectiveName: WHO Rapid Evidence Appraisal for COVID-19 Therapies (REACT) Working Group
entry
name: Jonathan A C Sterne
initials: JAC
affiliationInfo
affiliation: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, England.
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affiliation: NIHR Bristol Biomedical Research Centre, Bristol, England.
telecom: jonathan.sterne@bristol.ac.uk
correspondingContact: true
entry
name: Srinivas Murthy
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- Affiliation * Department of Pediatrics, University of British Columbia, Vancouver, Canada. entry
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- Affiliation * Clinical Unit, Health Emergencies Programme, World Health Organization, Geneva, Switzerland. entry
name: Arthur S Slutsky
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- Affiliation * Applied Health Research Centre, Li Ka Shing Knowledge Institute of St Michael's Hospital, Department of Medicine, University of Toronto, Toronto, Ontario, Canada. entry
name: Jesús Villar
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affiliation: Research Unit, Hospital Universitario Dr Negrín, Las Palmas de Gran Canaria, Spain.
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affiliation: CIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain.
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name: Derek C Angus
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- Affiliation * Department of Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania. entry
name: Djillali Annane
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- Affiliation * Department of Intensive Care, Raymond Poincaré Hospital (APHP), School of Medicine Simone Veil, University Paris Saclay-UVSQ, Paris, France. entry
name: Luciano Cesar Pontes Azevedo
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affiliation: Hospital Sírio-Libanês, São Paulo, Brazil.
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affiliation: Emergency Medicine Department, University of São Paulo School of Medicine, São Paulo, Brazil.
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- Affiliation * Academic Research Organization, Hospital Israelita Albert Einstein, São Paulo, Brazil. entry
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- Affiliation * HCor Research Insitute, São Paulo, Brazil. entry
name: Pierre-Francois Dequin
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affiliation: Médecine Intensive-Réanimation, INSERM CIC1415, CHRU de Tours, Tours, France.
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affiliation: CRICS-TriGGERSep Network, Centre d'Etude des Pathologies Respiratoires, Université de Tours, Tours, France.
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name: Bin Du
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name: Jonathan Emberson
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affiliation: MRC Population Health Research Unit, University of Oxford, Oxford, England.
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- Affiliation * MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, Faculty of Population Health Sciences, University College London, London, England. entry
name: Bruno Giraudeau
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name: Anthony C Gordon
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- Affiliation * Division of Anaesthetics, Pain Medicine and Intensive Care, Imperial College London, London, England. entry
name: Anders Granholm
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- Affiliation * Department of Intensive Care, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark. entry
name: Cameron Green
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- Affiliation * Australian and New Zealand Intensive Care Research Centre, School of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia. entry
name: Richard Haynes
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affiliation: Nuffield Department of Population Health, University of Oxford, Oxford, England.
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affiliation: MRC Population Health Research Unit, University of Oxford, Oxford, England.
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name: Nicholas Heming
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- Affiliation * Department of Intensive Care, Raymond Poincaré Hospital (APHP), School of Medicine Simone Veil, University Paris Saclay-UVSQ, Paris, France. entry
name: Julian P T Higgins
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affiliation: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, England.
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affiliation: NIHR Bristol Biomedical Research Centre, Bristol, England.
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affiliation: NIHR Applied Research Collaboration West, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, England.
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name: Peter Horby
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- Affiliation * Nuffield Department of Medicine, University of Oxford, Oxford, England. entry
name: Peter Jüni
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- Affiliation * Applied Health Research Centre, Li Ka Shing Knowledge Institute of St Michael's Hospital, Department of Medicine, University of Toronto, Toronto, Ontario, Canada. entry
name: Martin J Landray
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affiliation: Nuffield Department of Population Health, University of Oxford, Oxford, England.
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affiliation: MRC Population Health Research Unit, University of Oxford, Oxford, England.
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affiliation: NIHR Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, England.
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name: Amelie Le Gouge
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- Affiliation * CIC INSERM 1415-CHRU de Tours, Tours, France. entry
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- Affiliation * CIC INSERM 1415-CHRU de Tours, Tours, France. entry
name: Wei Shen Lim
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- Affiliation * Respiratory Medicine Department, Nottingham University Hospitals NHS Trust, Nottingham, England. entry
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affiliation: Department of Critical Care Medicine, Auckland City Hospital, Auckland, New Zealand.
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affiliation: Hôpitaux Universitaires de Strasbourg, Service de Médecine Intensive Réanimation, Nouvel Hôpital Civil, Strasbourg, France.
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affiliation: INSERM UMR 1260, Regenerative Nanomedicine, FMTS, Strasbourg, France.
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- Affiliation * Department of Intensive Care, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark. entry
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- Affiliation * Department of Intensive Care, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark. entry
name: Jelena Savovic
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affiliation: Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, England.
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name: Bruno Tomazini
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affiliation: Hospital Sírio-Libanês, São Paulo, Brazil.
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affiliation: Department of Surgery, School of Medicine, University of São Paulo, São Paulo, Brazil.
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name: Viviane C Veiga
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- Affiliation * BP-A Beneficência Portuguesa de São Paulo, São Paulo, Brazil. entry
name: Steve Webb
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affiliation: Australian and New Zealand Intensive Care Research Centre, School of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia.
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affiliation: St John of God Healthcare, Subiaco, Australia.
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name: John C Marshall
initials: JC
AffiliationInfos
- Affiliation * Li Ka Shing Knowledge Institute, St Michael's Hospital, University of Toronto, Toronto, Ontario, Canada. Summaries
- Type Source Value * Author string (ContributorSummaryType[5.0.0-snapshot1]#author-string) articleCopy () The WHO Rapid Evidence Appraisal for COVID-19 Therapies (REACT) Working Group Authors and Members of the Writing Committee: Jonathan A. C. Sterne, MA, MSc, PhD; Srinivas Murthy, MD, MSc; Janet V. Diaz, MD; Arthur S. Slutsky, CM, MD; Jesús Villar, MD, PhD; Derek C. Angus, MD, MPH; Djillali Annane, MD, PhD; Luciano Cesar Pontes Azevedo, MD, PhD; Otavio Berwanger, MD, PhD; Alexandre B. Cavalcanti, MD, PhD; Pierre-Francois Dequin, MD, PhD; Bin Du, MD; Jonathan Emberson, PhD; David Fisher, MSc; Bruno Giraudeau, PhD; Anthony C. Gordon, MBBS, MD; Anders Granholm, MD; Cameron Green, MSc; Richard Haynes, DM; Nicholas Heming, MD, PhD; Julian P. T. Higgins, BA, PhD; Peter Horby, PhD; Peter Jüni, MD; Martin J. Landray, PhD; Amelie Le Gouge, MSc; Marie Leclerc, MSc; Wei Shen Lim, BMedSci, BMBS, DM; Flávia R. Machado, MD, PhD; Colin McArthur, MBChB; Ferhat Meziani, MD, PhD; Morten Hylander Møller, MD, PhD; Anders Perner, MD, PhD; Marie Warrer Petersen, MD; Jelena Savović, BPharm, MSc, PhD; Bruno Tomazini, MD; Viviane C. Veiga, MD, PhD; Steve Webb, MBBS, MPH, PhD; John C. Marshall, MD.
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.