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Research Article Free access | 10.1172/JCI114733

Elevated von Willebrand factor antigen is an early plasma predictor of acute lung injury in nonpulmonary sepsis syndrome.

D B Rubin, J P Wiener-Kronish, J F Murray, D R Green, J Turner, J M Luce, A B Montgomery, J D Marks, and M A Matthay

Department of Medicine, University of California Medical Center, San Francisco General Hospital Medical Center 94143.

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Department of Medicine, University of California Medical Center, San Francisco General Hospital Medical Center 94143.

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Department of Medicine, University of California Medical Center, San Francisco General Hospital Medical Center 94143.

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Department of Medicine, University of California Medical Center, San Francisco General Hospital Medical Center 94143.

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Department of Medicine, University of California Medical Center, San Francisco General Hospital Medical Center 94143.

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Department of Medicine, University of California Medical Center, San Francisco General Hospital Medical Center 94143.

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Department of Medicine, University of California Medical Center, San Francisco General Hospital Medical Center 94143.

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Department of Medicine, University of California Medical Center, San Francisco General Hospital Medical Center 94143.

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Department of Medicine, University of California Medical Center, San Francisco General Hospital Medical Center 94143.

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Published August 1, 1990 - More info

Published in Volume 86, Issue 2 on August 1, 1990
J Clin Invest. 1990;86(2):474–480. https://doi.org/10.1172/JCI114733.
© 1990 The American Society for Clinical Investigation
Published August 1, 1990 - Version history
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Abstract

In this prospective study of 45 patients, we tested the hypothesis that markedly elevated levels of plasma von Willebrand antigen (vWf-Ag) a marker of endothelial cell injury, might predict the development of acute lung injury in patients with nonpulmonary sepsis syndrome. Acute lung injury was quantified on a four-point scoring system. At the time of entry into the study, none of the 45 patients had evidence of lung injury. Subsequently, 15 patients developed lung injury and 30 patients did not develop lung injury. The mean plasma vWf-Ag level was markedly elevated in the 15 patients who developed lung injury compared with the 30 patients who did not develop lung injury (588 +/- 204 vs. 338 +/- 196, percentage of control, P less than 0.01). Furthermore, a plasma vWf-Ag level greater than or equal to 450 was 87% sensitive and 77% specific for predicting the development of acute lung injury in the setting of nonpulmonary sepsis. In addition, the combination of a plasma vWf-Ag greater than 450 and nonpulmonary organ failure at the time of entry into the study had a positive predictive value of 80% for acute lung injury. Also, a plasma vWf-Ag level greater than 450 had a positive predictive value of 80% for identifying nonsurvivors. Thus, in patients with nonpulmonary sepsis, an elevated level of plasma vWf-Ag is a useful, early biochemical marker of endothelial injury and it has both predictive and prognostic value.

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