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  1. 3421
    “…RESULTS: A total of 121 ARDS patients and 100 healthy individuals were enrolled. …”
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    Serum sphingosine-1-phosphate levels and Sphingosine-1-Phosphate gene polymorphisms in acute respiratory distress syndrome: a multicenter prospective study
  2. 3422
    “…BACKGROUND: There is a dearth of drug therapies available for the treatment of acute respiratory distress syndrome (ARDS). Certain metabolites play a key role in ARDS and could serve as potential targets for developing therapies against this respiratory disorder. …”
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    Increased mortality of acute respiratory distress syndrome was associated with high levels of plasma phenylalanine
  3. 3423
    “…PURPOSE: Previous studies assessing impact of acute respiratory distress syndrome (ARDS) on mortality have shown conflicting results. …”
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    Acute respiratory distress syndrome-attributable mortality in critically ill patients with sepsis
  4. 3424
    “…BACKGROUND: Acute respiratory distress syndrome (ARDS) has different phenotypes and distinct short-term outcomes. …”
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    One-year patient outcomes based on lung morphology in acute respiratory distress syndrome: secondary analysis of LIVE trial
  5. 3425
    “…Finally, for in vivo experimental verification, we established an oleic acid-induced ARDS rat model, mainly through histological evaluation and the ELISA method to evaluate both the protective effect of CEP on ARDS and its effect on inflammation. …”
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    Network analysis-based strategy to investigate the protective effect of cepharanthine on rat acute respiratory distress syndrome
  6. 3426
    “…METHOD: In total, 195 patients without CPB-induced ARDS were included in the control group, and 85 patients with ARDS were included in the ARDS group. …”
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    Clinical Value and Mechanism of Long Non-Coding RNA UCA1 in Acute Respiratory Distress Syndrome Induced by Cardiopulmonary Bypass
  7. 3427
    “…BACKGROUND: The incidence of acute respiratory distress syndrome (ARDS) has decreased in the last decade by improvement in trauma and critical care. …”
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    Incidence of acute respiratory distress syndrome and associated mortality in a polytrauma population
  8. 3428
    “…METHODS: We studied critically ill patients with hematologic malignancies with the dual objectives of describing patients with ARDS during neutropenia recovery and identifying risk factors for ARDS during neutropenia recovery. …”
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    Risk factors for acute respiratory distress syndrome during neutropenia recovery in patients with hematologic malignancies
  9. 3429
    “…Apart from these pandemic viruses, respiratory viruses are rarely responsible for viral pneumonia and ARDS. Other than antiviral drug (mainly oseltamivir) administration and avoidance of corticosteroids, management of ARDS due to these viruses does not differ from that for ARDS caused by other diseases. …”
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    Virus-induced acute respiratory distress syndrome: Epidemiology, management and outcome
  10. 3430
    “…BACKGROUND: Few data exist on deep vein thrombosis (DVT) in patients with acute respiratory distress syndrome (ARDS), a group of heterogeneous diseases characterized by acute hypoxemia. …”
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    Prevalence, risk, and outcome of deep vein thrombosis in acute respiratory distress syndrome
  11. 3431
    “…The different stages of ARDS have distinctive biochemical and clinical profiles. …”
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    Phospholipases A2 as biomarkers in acute respiratory distress syndrome
  12. 3432
    “…The occurrence of ARDS was identified using a validated computerized search strategy. …”
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    Admission serum sodium and osmolarity are not associated with the occurrence or outcomes of acute respiratory distress syndrome in critically ill
  13. 3433
    “…Acute lung injury/acute respiratory distress syndrome (ALI/ARDS) is a devastating respiratory disorder with high rates of mortality and morbidity, but the detailed underlying mechanisms of ALI/ARDS remain largely unknown. …”
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    Emerging roles of mechanosensitive ion channels in acute lung injury/acute respiratory distress syndrome
  14. 3434
    “…Inositol can relieve lung injuries induced by ARDS. However, the mechanism of myo-inositol in the development of ARDS is unclear, which limits its use in the clinic. …”
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    Inositol Alleviates Pulmonary Fibrosis by Promoting Autophagy via Inhibiting the HIF-1α-SLUG Axis in Acute Respiratory Distress Syndrome
  15. 3435
    “…INTRODUCTION: Coagulation and fibrinolysis remain sparsely addressed with regards to acute respiratory distress syndrome (ARDS). We hypothesized that ARDS development might be associated with changes in plasma coagulation and fibrinolysis. …”
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    Activation of Coagulation and Fibrinolysis in Acute Respiratory Distress Syndrome: A Prospective Pilot Study
  16. 3436
    “…Diabetes mellitus may reduce the risk of acute respiratory distress syndrome (ARDS), but data from previous studies are conflicting. …”
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    Identifying associations between diabetes and acute respiratory distress syndrome in patients with acute hypoxemic respiratory failure: an analysis of the LUNG SAFE database
  17. 3437
    “…The role of early, serial measurements of protein biomarkers in sepsis-induced acute respiratory distress syndrome (ARDS) is not clear. OBJECTIVES: To determine the differences in soluble receptor for advanced glycation end-products (sRAGEs), angiopoietin-2, and surfactant protein-D (SP-D) levels and their changes over time between sepsis patients with and without ARDS. …”
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    Serial Measurements of Protein Biomarkers in Sepsis-Induced Acute Respiratory Distress Syndrome
  18. 3438
    “…The COVID-19 pandemic has seen a surge of patients with acute respiratory distress syndrome (ARDS) in intensive care units across the globe. As experience of managing patients with COVID-19-associated ARDS has grown, so too have efforts to classify patients according to respiratory system mechanics, with a view to optimising ventilatory management. …”
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    COVID-19-associated acute respiratory distress syndrome: is a different approach to management warranted?
  19. 3439
    “…Although the acute respiratory distress syndrome (ARDS) is well defined by the development of acute hypoxemia, bilateral infiltrates and non-cardiogenic pulmonary edema, ARDS is heterogeneous in terms of clinical risk factors, physiology of lung injury, microbiology, and biology, potentially explaining why pharmacologic therapies have been mostly unsuccessful in treating ARDS. …”
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    Phenotypes and personalized medicine in the acute respiratory distress syndrome
  20. 3440
    “…Acute respiratory distress syndrome (ARDS) is a devastating critical illness that can be triggered by a wide range of insults and remains associated with a high mortality of around 40%. …”
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    Precision medicine in acute respiratory distress syndrome: workshop report and recommendations for future research
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