Evidence map›Paper›PMID 36051937›Full record

ArticleWorld journal of critical care medicine2022

Immunomodulatory therapy for the management of critically ill patients with COVID-19: A narrative review.

David Andaluz-Ojeda, Pablo Vidal-Cortes, Álvaro Aparisi Sanz, Borja Suberviola, Lorena Del Río Carbajo, Leonor Nogales Martín, Estefanía Prol Silva, Jorge Nieto Del Olmo, José Barberán, Ivan Cusacovich

Open access · diamondAbstract read
In one paragraph

Article in World journal of critical care medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
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  5. Review
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

10 authors at 6 institutions in 1 country.

David Andaluz-OjedaDepartment of Critical Care, Hospital Universitario HM Sanchinarro, Hospitales Madrid, Madrid 28050, Spain. davidandaluz78@yahoo.es.
Pablo Vidal-CortesDepartment of Intensive Care, Complejo Hospitalario Universitario de Ourense, Ourense 32005, Spain.
Álvaro Aparisi SanzDepartment of Cardiology, Hospital del Mar, Barcelona 08003, Spain.
Borja SuberviolaDepartment of Intensive Care, Hospital Universitario Marqués de Valdecilla, Santander 39008, Spain.
Lorena Del Río CarbajoDepartment of Intensive Care, Complejo Hospitalario Universitario de Ourense, Ourense 32005, Spain.
Leonor Nogales MartínDepartment of Intensive Care, Hospital Clínico Universitario de Valladolid, Valladolid 47005, Spain.
Estefanía Prol SilvaDepartment of Intensive Care, Complejo Hospitalario Universitario de Ourense, Ourense 32005, Spain.
Jorge Nieto Del OlmoDepartment of Intensive Care, Complejo Hospitalario Universitario de Ourense, Ourense 32005, Spain.
José BarberánDepartment of Internal Medicine, Hospital Universitario HM Montepríncipe, Hospitales Madrid, Boadilla del Monte 28860, Madrid, Spain.
Ivan CusacovichDepartment of Internal Medicine, Hospital Clínico Universitario de Valladolid, Valladolid 47005, Spain.
Hospital Universitario HM Sanchinarro · ESHospital Clínico Universitario de Valladolid · ESMarqués de Valdecilla University Hospital · ESComplejo Hospitalario de Ourense · ESHospital Del Mar · ESHospital Universitario HM Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the ongoing coronavirus disease 2019 (COVID-19) pandemic. Understanding the physiological and immunological processes underlying the clinical manifestations of COVID-19 is vital for the identification and rational design of effective therapies.

aimTo describe the interaction of SARS-CoV-2 with the immune system and the subsequent contribution of hyperinflammation and abnormal immune responses to disease progression together with a complete narrative review of the different immunoadjuvant treatments used so far in COVID-19 and their indication in severe and life-threatening subsets.

methodsA comprehensive literature search was developed. Authors reviewed the selected manuscripts following the PRISMA recommendations for systematic review and meta-analysis documents and selected the most appropriate. Finally, a recommendation of the use of each treatment was established based on the level of evidence of the articles and documents reviewed. This recommendation was made based on the consensus of all the authors.

resultsA brief rationale on the SARS-CoV-2 pathogenesis, immune response, and inflammation was developed. The usefulness of 10 different families of treatments related to inflammation and immunopathogenesis of COVID-19 was reviewed and discussed. Finally, based on the level of scientific evidence, a recommendation was established for each of them.

conclusionAlthough several promising therapies exist, only the use of corticosteroids and tocilizumab (or sarilumab in absence of this) have demonstrated evidence enough to recommend its use in critically ill patients with COVID-19. Endotypes including both, clinical and biological characteristics can constitute specific targets for better select certain therapies based on an individualized approach to treatment.

Indexed as

COVID-19Critically ill patientsImmunomodulary drugsImmunosupressionPhenotypeTreatment

Identifiers

PMID36051937
PMCPMC9305685
OpenAlexW4284893049

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.