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ARDS Subphenotypes as a Guide to Therapy and Enrollment into Therapeutic Trials: Not So Fast
Jesús Villar1,2,3,4, Tamas Szakmany5, Ognjen Gajic6
1Ciber de Enfermedades Respiratorias, Instituto de Salud Carlos III, 28029 Madrid, Spain.
Identifying specific patient subgroups in acute respiratory distress syndrome (ARDS) is challenging due to dynamic heterogeneity. Current subphenotype definitions lack biological plausibility and proven treatment benefits for clinical use.
Area of Science:
- Critical Care Medicine
- Pulmonology
- Translational Research
Background:
- Acute respiratory distress syndrome (ARDS) is a complex critical illness with significant heterogeneity.
- Understanding ARDS subphenotypes is crucial for personalized treatment strategies and clinical trial design.
- Biomarkers are needed to guide precise ARDS management and improve patient outcomes.
Purpose of the Study:
- To examine the complexities in identifying distinct ARDS subphenotypes.
- To evaluate the biological plausibility and clinical utility of current subphenotype definitions.
- To discuss factors influencing ARDS heterogeneity and the search for treatable traits.
Main Methods:
- Review of current literature on ARDS subphenotyping.
- Analysis of factors contributing to clinical heterogeneity in ARDS.
- Evaluation of the evidence supporting targeted treatments for ARDS subphenotypes.
Main Results:
- ARDS heterogeneity is dynamic and influenced by multiple factors beyond lung pathophysiology.
- Current subphenotype definitions lack strong biological grounding.
- There is insufficient evidence to support the clinical use of current ARDS subphenotypes.
Conclusions:
- The search for reliable ARDS subphenotypes and treatable traits is complicated by dynamic heterogeneity.
- Current subphenotype definitions are not yet clinically warranted due to lack of biological plausibility and proven treatment efficacy.
- Further research is needed to develop biologically plausible and clinically useful ARDS subphenotypes.
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