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About:
Emerging pharmacological therapies for ARDS: COVID-19 and beyond
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
associated with source
document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
Attributes
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Emerging pharmacological therapies for ARDS: COVID-19 and beyond
Creator
Bellani, Giacomo
Nichol, Alistair
Laffey, John
Mcauley, Danny
Mcnicholas, Bairbre
Pham, Tài
Rocco, Patricia
O'kane, Cecilia
Curley, Ger
Horie, Shahd
Rezoagli, Emanuele
Santos, Claudia Dos
Source
Medline; PMC
abstract
ARDS, first described in 1967, is the commonest form of acute severe hypoxemic respiratory failure. Despite considerable advances in our knowledge regarding the pathophysiology of ARDS, insights into the biologic mechanisms of lung injury and repair, and advances in supportive care, particularly ventilatory management, there remains no effective pharmacological therapy for this syndrome. Hospital mortality at 40% remains unacceptably high underlining the need to continue to develop and test therapies for this devastating clinical condition. The purpose of the review is to critically appraise the current status of promising emerging pharmacological therapies for patients with ARDS and potential impact of these and other emerging therapies for COVID-19-induced ARDS. We focus on drugs that: (1) modulate the immune response, both via pleiotropic mechanisms and via specific pathway blockade effects, (2) modify epithelial and channel function, (3) target endothelial and vascular dysfunction, (4) have anticoagulant effects, and (5) enhance ARDS resolution. We also critically assess drugs that demonstrate potential in emerging reports from clinical studies in patients with COVID-19-induced ARDS. Several therapies show promise in earlier and later phase clinical testing, while a growing pipeline of therapies is in preclinical testing. The history of unsuccessful clinical trials of promising therapies underlines the challenges to successful translation. Given this, attention has been focused on the potential to identify biologically homogenous subtypes within ARDS, to enable us to target more specific therapies ‘precision medicines.’ It is hoped that the substantial number of studies globally investigating potential therapies for COVID-19 will lead to the rapid identification of effective therapies to reduce the mortality and morbidity of this devastating form of ARDS.
has issue date
2020-07-11
(
xsd:dateTime
)
bibo:doi
10.1007/s00134-020-06141-z
bibo:pmid
32654006
has license
no-cc
sha1sum (hex)
5b1584d718cb6789a528719033005842b97a39a3
schema:url
https://doi.org/10.1007/s00134-020-06141-z
resource representing a document's title
Emerging pharmacological therapies for ARDS: COVID-19 and beyond
has PubMed Central identifier
PMC7352097
has PubMed identifier
32654006
schema:publication
Intensive Care Med
resource representing a document's body
covid:5b1584d718cb6789a528719033005842b97a39a3#body_text
is
schema:about
of
named entity 'severe'
named entity 'insights'
named entity 'number'
named entity 'effects'
named entity 'hypoxemic'
named entity 'develop'
named entity 'patients'
named entity 'ARDS'
named entity 'ARDS'
named entity '1967'
named entity 'pleiotropic'
named entity 'therapies'
named entity 'PHASE'
named entity 'SPECIFIC'
named entity 'REMAINS'
named entity 'INDUCED'
named entity 'TEST'
named entity 'LEAD'
named entity 'SUCCESSFUL'
named entity 'NEED'
named entity 'ASSESS'
named entity 'ACUTE'
named entity 'management'
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named entity 'induced'
named entity 'COVID-19'
named entity 'potential'
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named entity 'advances'
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named entity 'pharmacological'
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named entity 'preclinical models'
named entity 'elafin'
named entity 'MAPK'
named entity 'LPS'
named entity 'protease inhibitors'
named entity 'Type I interferon'
named entity 'tetracycline'
named entity 'community-acquired pneumonia'
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named entity 'receptor'
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named entity 'open-label'
named entity 'Ulinastatin'
named entity 'ARDS'
named entity 'imatinib'
named entity 'remdesivir'
named entity 'steroids'
named entity 'immunomodulatory drug'
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