ABSTRACT
Disturbed alveolar fibrin turnover is intrinsic to acute lung injury/acute respiratory
distress syndrome (ALI/ARDS) and pneumonia and is important to its pathogenesis. Recent
studies also suggest disturbed alveolar fibrin turnover to be a feature of ventilator-induced
lung injury (VILI). The mechanisms that contribute to alveolar coagulopathy are localized
tissue factor–mediated thrombin generation, impaired activity of natural coagulation
inhibitors, and depression of bronchoalveolar urokinase plasminogen activator–mediated
fibrinolysis, caused by the increase of plasminogen activator inhibitors. Administration
of anticoagulant agents (including activated protein C, antithrombin, tissue factor–factor
VIIa pathway inhibitors, and heparin) and profibrinolytic agents (including plasminogen
activators) attenuate pulmonary coagulopathy. Several preclinical studies show additional
anti-inflammatory effects of these therapies in ALI/ARDS and pneumonia. In this article,
we review the involvement of coagulation and fibrinolysis in the pathogenesis of ALI/ARDS
pneumonia and VILI and the potential of anticoagulant and profibrinolytic strategies
to reverse pulmonary coagulopathy and pulmonary inflammatory responses.
KEYWORDS
Acute lung injury - acute respiratory distress syndrome - coagulation - fibrinolysis
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Jorrit–Jan H HofstraM.D.
Department of Intensive Care Medicine, Academic Medical Center
University of Amsterdam, 1105 AZ Amsterdam, The Netherlands
eMail: j.j.hofstra@amc.uva.nl