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Gordon R. Bernard

Researcher at Vanderbilt University Medical Center

Publications -  366
Citations -  82519

Gordon R. Bernard is an academic researcher from Vanderbilt University Medical Center. The author has contributed to research in topics: Lung injury & Sepsis. The author has an hindex of 103, co-authored 346 publications receiving 70417 citations. Previous affiliations of Gordon R. Bernard include Vanderbilt University & Louisiana State University.

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A randomized, controlled trial of furosemide with or without albumin in hypoproteinemic patients with acute lung injury*

TL;DR: The addition of albumin to furosemide therapy in hypoproteinemic patients with acute lung injury/acute respiratory distress syndrome significantly improves oxygenation, with greater net negative fluid balance and better maintenance of hemodynamic stability.
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Beyond Mortality: Future Clinical Research in Acute Lung Injury

TL;DR: The workshop assessed the current state of clinical research addressing ALI, identified research needs, and recommended: continued performance of trials evaluating treatments of patients with ALI; development of strategies to perform ALI prevention trials; and development of a standardized format for reporting methods, endpoints, and results of ALI trials.
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The american-european consensus conference on ARDS, Part 2. Ventilatory, pharmacologic, supportive therapy, study design strategies and issues related to recovery and remodeling

TL;DR: The American-European Consensus Committee on ARDS was formed to re-evaluate the standards for the ICU care of patients with acute lung injury (ALI), with regard to ventilatory strategies, the more promising pharmacologic agents, and the definition and quantification of pathological features of ALI that require resolution.
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Effects of drotrecogin alfa (activated) on organ dysfunction in the PROWESS trial.

TL;DR: Drotrecogin alfa (activated) demonstrated significant improvements in organ function compared with placebo in a large phase 3 clinical trial that has shown a mortality benefit in patients with severe sepsis.
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Drotrecogin alfa (activated) administration across clinically important subgroups of patients with severe sepsis.

TL;DR: The administration of drotrecogin alfa (activated) to patients with severe sepsis was associated with a significant survival benefit that tended to increase with higher baseline likelihood of death, and the increased absolute risk of experiencing a serious bleeding event with treatment did not seem to vary according to the baseline predicted risk of mortality.