Exposure to ambient air pollutants and acute respiratory distress syndrome risk in sepsis

Intensive Care Medicine - Tập 49 - Trang 957-965 - 2023
John P. Reilly1,2, Zhiguo Zhao3, Michael G. S. Shashaty1,2, Tatsuki Koyama3, Tiffanie K. Jones1,2,4, Brian J. Anderson1,2, Caroline A. Ittner1,2, Thomas Dunn1,2, Todd A. Miano4, Oluwatosin Oniyide1,2, John R. Balmes5,6, Michael A. Matthay6,7, Carolyn S. Calfee6,7, Jason D. Christie1,2,4, Nuala J. Meyer1,2, Lorraine B. Ware8,9
1Division of Pulmonary, Allergy, and Critical Care, University of Pennsylvania, Perelman School of Medicine, Philadelphia, USA
2Center for Translational Lung Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, USA
3Department of Biostatistics, Vanderbilt University School of Medicine, Nashville, USA
4Center for Clinical Epidemiology and Biostatics, University of Pennsylvania, Perelman School of Medicine, Philadelphia, USA
5Division of Environmental Health Sciences, School of Public Health, University of California, Berkeley, USA
6Department of Medicine, University of California, San Francisco, USA
7Department of Anesthesia and Cardiovascular Research Institute, University of California, San Francisco, USA
8Department of Medicine, Vanderbilt University School of Medicine, Nashville, USA
9Department of Pathology, Microbiology, and Immunology, Vanderbilt University School of Medicine, Nashville, USA

Tóm tắt

Exposures to ambient air pollutants may prime the lung enhancing risk of acute respiratory distress syndrome (ARDS) in sepsis. Our objective was to determine the association of short-, medium-, and long-term pollutant exposures and ARDS risk in critically ill sepsis patients. We analyzed a prospective cohort of 1858 critically ill patients with sepsis, and estimated short- (3 days), medium- (6 weeks), and long- (5 years) term exposures to ozone, nitrogen dioxide (NO2), sulfur dioxide (SO2), carbon monoxide (CO), particulate matter < 2.5 μm (PM2.5), and PM < 10 μm (PM10) using weighted averages of daily levels from monitors within 50 km of subjects’ residences. Subjects were followed for 6 days for ARDS by the Berlin Criteria. The association between each pollutant and ARDS was determined using multivariable logistic regression adjusting for preselected confounders. In 764 subjects, we measured plasma concentrations of inflammatory proteins at presentation and tested for an association between pollutant exposure and protein concentration via linear regression. ARDS developed in 754 (41%) subjects. Short- and long-term exposures to SO2, NO2, and PM2.5 were associated with ARDS risk (SO2: odds ratio (OR) for the comparison of the 75–25th long-term exposure percentile 1.43 (95% confidence interval (CI) 1.16, 1.77); p < 0.01; NO2: 1.36 (1.06, 1.74); p = 0.04, PM2.5: 1.21 (1.04, 1.41); p = 0.03). Long-term exposures to these three pollutants were also associated with plasma interleukin-1 receptor antagonist and soluble tumor necrosis factor receptor-1 concentrations. Short and long-term exposures to ambient SO2, PM2.5, and NO2 are associated with increased ARDS risk in sepsis, representing potentially modifiable environmental risk factors for sepsis-associated ARDS.

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