Investigational pharmacological agents for the treatment of ARDS

被引:8
作者
Aribindi, Katyayini [1 ,2 ]
Lim, Michelle [3 ]
Lakshminrusimha, Satyan [4 ]
Albertson, Timothy [1 ]
机构
[1] Univ Calif Davis, Dept Internal Med, Div Pulm Crit Care & Sleep Med, Sch Med, Sacramento, CA 95817 USA
[2] Vet Affairs North Calif Hlth Care Syst, Dept Med, Mather, CA USA
[3] Univ Calif Davis, Dept Pediat, Div Pediat Crit Care Med, Sch Med, Sacramento, CA USA
[4] Univ Calif Davis, Dept Pediat, Div Neonatal Perinatal Med, Sch Med, Sacramento, CA USA
关键词
ARDS; acute lung injury; corticosteroids; tocilizumab; interferon beta 1a; neuromuscular blocking agents; mesenchymal stem cells; JAK inhibitors; ACUTE RESPIRATORY-DISTRESS; ACUTE LUNG INJURY; NEUTROPHIL ELASTASE INHIBITOR; MESENCHYMAL STEM-CELLS; RANDOMIZED CLINICAL-TRIAL; CRITICALLY-ILL PATIENTS; INHALED NITRIC-OXIDE; GAMMA-LINOLENIC ACID; STROMAL CELLS; INFLAMMATORY RESPONSE;
D O I
10.1080/13543784.2024.2315128
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionAcute Respiratory Distress Syndrome (ARDS) is a heterogeneous form of lung injury with severe hypoxemia and bilateral infiltrates after an inciting event that results in diffuse lung inflammation with a high mortality rate. While research in COVID-related ARDS has resulted in several pharmacotherapeutic agents that have undergone successful investigation, non-COVID ARDS studies have not resulted in many widely accepted pharmacotherapeutic agents despite exhaustive research.Areas coveredThe aim of this review is to discuss adjuvant pharmacotherapies targeting non-COVID Acute Lung Injury (ALI)/ARDS and novel therapeutics in COVID associated ALI/ARDS. In ARDS, variable data may support selective use of neuromuscular blocking agents, corticosteroids and neutrophil elastase inhibitors, but are not yet universally used. COVID-ALI/ARDS has data supporting the use of IL-6 monoclonal antibodies, corticosteroids, and JAK inhibitor therapy.Expert opinionAlthough ALI/ARDS modifying pharmacological agents have been identified in COVID-related disease, the data in non-COVID ALI/ARDS has been less compelling. The increased use of more specific molecular phenotyping based on physiologic parameters and biomarkers, will ensure equipoise between groups, and will likely allow more precision in confirming pharmacological agent efficacy in future studies.
引用
收藏
页码:243 / 277
页数:35
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