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. 2020 Jul 14;142(2):101-104.
doi: 10.1161/CIRCULATIONAHA.120.047915. Epub 2020 May 5.

Differentiating COVID-19 Pneumonia From Acute Respiratory Distress Syndrome and High Altitude Pulmonary Edema: Therapeutic Implications

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Differentiating COVID-19 Pneumonia From Acute Respiratory Distress Syndrome and High Altitude Pulmonary Edema: Therapeutic Implications

Stephen L Archer et al. Circulation. .
No abstract available

Keywords: acute lung injury; altitude; hypertension, pulmonary; hypoxia; mitochondria; pneumonia; pulmonary edema.

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Figures

Figure:
Figure:. Contrasting pulmonary hemodynamics in ARDS, COVID-19 pneumonia and HAPE
The figure is read from top left to bottom right in clockwise direction. The hallmarks of each syndrome are summarized in the green insert table. Top panel: HPV diverts blood away from an hypoxic alveolar segment, induced by a mucous plug in the bronchus. Blood from this segment is diverted toward a well-ventilated alveolar segment. There is no alveolar injury and segmental HPV does not elevate PA pressure or cause dyspnea. Second panel: In ARDS the primary insult is inflammatory alveolar injury with associated pulmonary hypertension. There is also impaired HPV which increases V/Q mismatch and worsens hypoxemia. The lungs become stiff and fibrotic (green fibrous tissue and fibroblasts in alveolar wall) and hyaline membranes in the alveoli (pink crescent) are a prominent feature. Dyspnea is profound. Third panel: In COVID-19 pneumonia the primary injury is airway inflammation due to SARS-CoV-2 infection. The resulting hypoxemia is exacerbated by an almost complete loss of HPV, resulting in a large V/Q mismatch. Unlike ARDS there is no fibrosis and hyaline membranes are less prominent. Dyspnea is variable and may be absent due to impaired oxygen sensing. Bottom left panel: In HAPE the primary pathology is vascular, namely increased, heterogenous HPV and pulmonary venoconstriction, resulting in capillary damage and leak. Dyspnea is profound.

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