Abstract

PurposeInspiring high partial pressure of oxygen (FiO2 > 0.6) for a prolonged duration can lead to lung damage termed pulmonary oxygen toxicity (PO2T). While current practice is to limit oxygen exposure, there are clinical and military scenarios where higher FiO2 levels and partial pressures of oxygen are required. The purpose of this study is to develop a non-invasive breath-based biomarker to detect PO2T prior to the onset of clinical symptoms.MethodsMale Yorkshire swine (20–30 kg) were placed into custom airtight runs and randomized to air (0.209 FiO2, n = 12) or oxygen (>0.95 FiO2, n = 10) for 72 h. Breath samples, arterial blood gases, and vital signs were assessed every 12 h. After 72 h of exposure, animals were euthanized and the lungs processed for histology and wet-dry ratios.ResultsSwine exposed to hyperoxia developed pulmonary injury consistent with PO2T. Histology of oxygen-exposed swine showed pulmonary lymphatic congestion, epithelial sloughing, and neutrophil transmigration. Pulmonary injury was also evidenced by increased interstitial edema and a decreased PaO2/FiO2 ratio in the oxygen group when compared to the air control group. Breath volatile organic compound (VOC) sample analysis identified six VOCs that were combined into an algorithm which generated a breath score predicting PO2T with a ROC/AUC curve of 0.72 defined as a of PaO2/FiO2 ratio less than 350 mmHg.ConclusionExposing swine to 72 h of hyperoxia induced a pulmonary injury consistent with human clinical endpoints of PO2T. VOC analysis identified six VOCs in exhaled breath that preceded PO2T. Results show promise that a simple, non-invasive breath test could potentially predict the risk of pulmonary injury in humans exposed to high partial pressures of oxygen.

Highlights

  • Inhaled oxygen administration is common in both healthcare settings and certain military operations for numerous indications

  • Lung injury known as pulmonary oxygen toxicity (PO2T) may develop

  • Pulmonary oxygen toxicity is a progressive disease heralded by acute tracheobronchitis, which manifests as cough and burning sensation with respiration

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Summary

Introduction

Inhaled oxygen administration is common in both healthcare settings and certain military operations for numerous indications. To minimize oxygen toxicity in clinical settings, the fractional inspired oxygen (FiO2) is typically titrated to maintain a hemoglobin saturation of >90% (Beers, 2008; Mikkelsen et al, 2014); there are clinical scenarios such as acute respiratory distress syndrome (ARDS) and refractory hypoxemia, in which a FiO2 > 0.6 may be required to prevent end-organ damage It is not uncommon for pilots, divers, and astronauts to inhale high concentrations of oxygen prior to operations in order to reduce the risk of decompression sickness (Webb and Pilmanis, 1993, 1998; United States Navy, 2011). By the time current diagnostic modalities in pulmonary function testing detect injury, significant pulmonary damage has already occurred

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