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381
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ShareScore release 0.9.0
Dataset results
381 results for “acute respiratory distress syndrome”
Long-term Impact of COVID-19 Among COVID-19 Patients With Acute Respiratory Distress Syndrome in Brazil
ClinicalTrials.gov study NCT05225194. IPD Sharing: Not stated. Countries: 0. Publications: 0.
The Interaction Between Severe Acute Respiratory Distress Syndrome Viral Proteins and Monocytes
ClinicalTrials.gov study NCT00172263. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Standardized Application of High Frequency Oscillatory Ventilation in the Acute Respiratory Distress Syndrome (ARDS)
ClinicalTrials.gov study NCT01677130. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Immune Alveolar Alterations During Pneumonia-Associated Acute Respiratory Distress Syndrome
ClinicalTrials.gov study NCT03971006. IPD Sharing: NO. Countries: 0. Publications: 0.
The EVLW for Set the Positive End Expiratory Pressure (PEEP) in the Acute Respiratory Distress Syndrome (ARDS)
ClinicalTrials.gov study NCT00714987. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Driving Pressure-guided Tidal Volume Ventilation in the Acute Respiratory Distress Syndrome
ClinicalTrials.gov study NCT06322758. IPD Sharing: NO. Countries: 0. Publications: 0.
Effect of Mechanical Ventilation Strategy on Lung Injury in Patients With Less Severe Acute Respiratory Distress Syndrome: Targeted on RAGE
ClinicalTrials.gov study NCT01301872. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Evaluation of Von Willebrand Factor as a Marker For Early Diagnosis of Acute Respiratory Distress Syndrome (A.R.D.S) in Comparison to Interleukin 6 [IL-6]
ClinicalTrials.gov study NCT04317469. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Discovery of New Early Detection Biomarkers From Peripheral Blood of Acute Respiratory Distress Syndrome(ARDS)
ClinicalTrials.gov study NCT02967471. IPD Sharing: NO. Countries: 0. Publications: 0.
The ARCTIC Trial: Aerosolized Inhaled Adenosine Treatment in Patients With Acute Respiratory Distress Syndrome (ARDS) Caused by COVID-19
ClinicalTrials.gov study NCT04588441. IPD Sharing: NO. Countries: 0. Publications: 0.
Acute Respiratory Distress Syndrome in Taiwan
ClinicalTrials.gov study NCT03260348. IPD Sharing: NO. Countries: 0. Publications: 0.
Effect of Treatment With Stress-Doses Glucocorticoid in Patients With Acute Respiratory Distress Syndrome (ARDS)
ClinicalTrials.gov study NCT00773058. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Intermediate-size Expanded Access Program (EAP), Mesenchymal Stromal Cells (MSC) for Acute Respiratory Distress Syndrome (ARDS) Due to COVID-19 Infection
ClinicalTrials.gov study NCT04366830. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Temporal Changes in MicroRNA Expression in Blood Leukocytes from Patients with the Acute Respiratory Distress Syndrome
GEO Series GSE83630. Homo sapiens; synthetic construct. 16 samples. Type: Non-coding RNA profiling by array.
Evaluating the therapeutic potential of different sources of mesenchymal stem cells in acute respiratory distress syndrome
GEO Series GSE241186. Mus musculus. 20 samples. Type: Expression profiling by high throughput sequencing.
CircRNAs in BALF exosomes and plasma as diagnostic biomarkers in patients with acute respiratory distress syndrome caused by severe pneumonia
GEO Series GSE217763. Homo sapiens. 8 samples. Type: Non-coding RNA profiling by array.
Transcriptomic profiling of lung tissues from a rat model of acute respiratory distress syndrome and vagus nerve stimulation
GEO Series GSE311048. Rattus norvegicus. 20 samples. Type: Expression profiling by high throughput sequencing.
REcovery and SURvival of patients with moderate to severe acute REspiratory distress syndrome (ARDS) due to COVID-19: a multicentre, single-arm, Phase IV itolizumab Trial: RESURRECT
<p>Datasets pertaining to the manuscript, Original Research, entitled “<strong>RE</strong>covery and <strong>SUR</strong>vival of patients with moderate to severe acute <strong>RE</strong>spiratory distress syndrome (ARDS) due to <strong>C</strong>OVID-19: a multicentre, single-arm, Phase IV Itolizumab <strong>T</strong>rial: <strong>RESURRECT</strong>” are submitted here. </p>
Microcirculatory Alterations in Critically Ill Patients with COVID-19-Associated Acute Respiratory Distress Syndrome
<p>Di Dedda U, Ascari A, Fantinato A, Fina D, Baryshnikova E, Ranucci M. Microcirculatory Alterations in Critically Ill Patients with COVID-19-Associated Acute Respiratory Distress Syndrome. J Clin Med. 2022 Feb 16;11(4):1032. doi: 10.3390/jcm11041032. PMID: 35207303; PMCID: PMC8876221.</p> <p>Abstract</p> <p><strong>Background: </strong>Presently, a number of specific observations have been performed on microcirculatory function in a coronavirus disease-19 (COVID-19) setting. We hypothesized that, in the critically ill, endothelial dysfunction secondary to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the subsequent inflammation and coagulopathy may lead to microcirculatory alterations, further exacerbated by the hypoxemic state. A dysfunctional microcirculation may represent the hidden motor underlying the development of COVID-19's clinical manifestations.</p> <p><strong>Methods: </strong>A single center, prospective, observational study. We analyzed bedside sublingual microcirculation in twenty-four consecutive COVID-19-associated acute respiratory distress syndrome (ARDS) patients mechanically ventilated in an Intensive Care Unit (ICU), together with macro-hemodynamics, clinical parameters, echocardiography, and laboratory data at a single time-point after ICU admission. All participants were recruited between March and May 2020.</p> <p><strong>Results: </strong>The microcirculatory pattern was characterized by increased values of total vessel density and perfused vessel density, a reduced value of proportion of perfused vessels and microvascular flow index, and high values of heterogeneity index. The duration of mechanical ventilation before microcirculation assessment was inversely associated with the proportion of perfused vessels (<em>p</em> = 0.023). Within the macro-hemodynamic parameters, the right ventricle end-diastolic diameter was inversely associated with proportion of perfused vessels and microvascular flow index (<em>p</em> = 0.039 and 0.014, respectively) and directly associated with the heterogeneity index (<em>p</em> = 0.033).</p> <p><strong>Conclusions: </strong>In COVID-19-associated ARDS patients, the microcirculation showed impaired quality of flow parameters coupled with a high vessel density.</p> <p> </p>
Identification of Early and Intermediate Biomarkers for Acute respiratory distress syndrome (ARDS) Mortality by Multi-Omic Approaches
GEO Series GSE176529. Homo sapiens. 42 samples. Type: Methylation profiling by high throughput sequencing.
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OpenNeuro
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