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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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Acute respiratory distress syndrome. Potential pharmacologic interventions.

TL;DR: Clinical studies in ARDS, as well as sepsis, the leading cause of AR DS, have increased in number, size, and quality over this same period, and each has laid the groundwork for more efficient and more elegant studies of the problem.
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Steroid treatment for persistent ARDS: a word of caution.

TL;DR: These results provide reasons for concern for a harmful effect of MPS on mortality later in the course of ARDS, and were reported by us as significant for prediction of mortality in ARDS/acute lung injury.
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Perilla ketone: a model of increased pulmonary microvascular permeability pulmonary edema in sheep.

TL;DR: It is concluded that perilla ketone causes increased lung microvascular permeability pulmonary edema without acute changes in pulmonary hemodynamics and this model permits study of the pathophysiologic aspects of increased lungmicrov vascular permeability without the concomitant functional alterations that complicate most other experimental models of diffuse lung injury.
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Early exposure to hyperoxia and mortality in critically ill patients with severe traumatic injuries.

TL;DR: In mechanically ventilated patients with severe traumatic injuries, hyperoxia in the first 24 hours of admission was not associated with increased risk of death or worsened neurological outcomes in a setting without brain tissue oxygenation monitoring.
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Therapeutic Targets in Sepsis: Past, Present, and Future

TL;DR: The evolution of sepsis therapy is examined and theorizes about why so many well-reasoned therapies have not worked in human trials and trial designs that might lead to successful treatments for sepsi are examined.