key: cord-0959820-1xb5k0ix authors: Huang, Ching-Feng; Sun, Pei-Ting; Tay, Chee Kiang title: Bronchiolitis and Potential Pathophysiological Implications in Coronavirus Disease 2019 ARDS Patients With Near-Normal Respiratory Compliance date: 2020-06-23 journal: Crit Care Med DOI: 10.1097/ccm.0000000000004470 sha: f0c51b6f1b9e1bedc1ac38ca5a53e719ec274601 doc_id: 959820 cord_uid: 1xb5k0ix nan W e read with enthusiasm the study by Mauri et al (1) using electrical impedance tomography to assess recruitment potential in patients with acute respiratory distress syndrome (ARDS) from coronavirus disease 2019 . The authors reported large variability in recruitability, reiterating individualized mechanical ventilation (MV) treatment. The discrepancy between hypoxemia severity and radiology/ respiratory mechanics in COVID-19 ARDS patients has been attributed to loss of hypoxic pulmonary vasoconstriction. This "Type L/1 phenotype" is purported to have low recruitability (2) . Our experience supports what Mauri et al (1) reported. In addition, we opine in recruitment-response COVID-19 ARDS patients: 1) bronchiolitis, in a histologic context, is a plausible pathophysiological mechanism and 2) a simple bedside physiologic test could potentially determine recruitment potential in resource-limited settings. Chest CT scans are regulated due to infection control reasons at our center. Chest radiographs, we observed, often failed to reflect the degree of hypoxemia. Ground-glass opacities, especially milder ones are frequently radiolucent. Similarly, small airway disease cannot be readily appreciated on radiographs-which engendered our bronchiolitis postulation and bedside study. We define bronchiolitis as inflammation of noncartilaginous airways immediately proximal to the pulmonary acinus. In first half of April 2020, four among five severe COVID-19 ARDS patients had radiologic-physiologic mismatch and received protocolized MV below. Median preintubation Pao 2 /Fio 2 (PF) ratio was 125.4 (range 92.9-160.0) on venturi mask 50%/nonrebreather mask. Respiratory static compliance values were ≥ 40 mL/cmH 2 o. In all patients, Spo 2 ≥ 90% was achieved while lowering Fio 2 (range 0.3-0.5) and increasing PEEP (range 10-14 cmH 2 o). Twenty-four hours later, median PF ratio was 220 (range 176.5-265.0). None required paralysis/prone positioning. Alveolar pattern and bronchiolitis are well-accepted pathology in many acute viral bronchiolitis. In COVID-19, bronchiolitis as true viral-related pathology is gaining traction (3, 4) . Physiologic-wise, bronchiolitis remains compatible with our findings suggesting positive recruitment potential, and we elucidate this, aided by physiologic changes observed in our 61-year-old female patient. Bronchiolitis could be likened to age-related lung elasticity loss. Both lead to small airway closure, increased ventilation/ perfusion (VQ) mismatch, and hypoxemia, which PEEP counters by increasing end-expiratory lung volume past the elevated "diseased" closing capacity. Exploiting Enghoff modification of Bohr's equation's drawback in physiologic dead space (V D ) calculation, that is, V D disproportionately affected by VQ mismatch compared with shunt/diffusion limitation (5), expected physiologic effects on volume-control ventilation are: increased alveolar ventilation, and 3. reduced global VQ heterogeneity; improved oxygenation. Lung mechanics, arterial blood gas, and end-tidal Co 2 were repeated 10 minutes apart on unchanged MV settings/ min ventilation except PEEP (5 and 14 cmH 2 O). The resultsreduction in V D /V T (0.27-0.11) and alveolar-arterial gradient (165.3-147.5), improvement in V A (246.2-321.6 mL), and PF ratio (163.5-218.3)-lend strength to our postulation Potential for lung recruitment and ventilation-perfusion mismatch in patients with the acute respiratory distress syndrome from coronavirus disease 2019 COVID-19 pneumonia: Different respiratory treatments for different phenotypes? Intensive Care Med Infection and rapid transmission of SARS-CoV-2 in ferrets COVID-19 autopsies Dead space: the physiology of wasted ventilation Copyright © 2020 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved