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10.1186/s12931-020-01462-5

http://scihub22266oqcxt.onion/10.1186/s12931-020-01462-5
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32723327!7385717!32723327
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suck abstract from ncbi

pmid32723327      Respir+Res 2020 ; 21 (1): 198
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  • The pathophysiology of happy hypoxemia in COVID-19 #MMPMID32723327
  • Dhont S; Derom E; Van Braeckel E; Depuydt P; Lambrecht BN
  • Respir Res 2020[Jul]; 21 (1): 198 PMID32723327show ga
  • The novel coronavirus disease 2019 (COVID-19) pandemic is a global crisis, challenging healthcare systems worldwide. Many patients present with a remarkable disconnect in rest between profound hypoxemia yet without proportional signs of respiratory distress (i.e. happy hypoxemia) and rapid deterioration can occur. This particular clinical presentation in COVID-19 patients contrasts with the experience of physicians usually treating critically ill patients in respiratory failure and ensuring timely referral to the intensive care unit can, therefore, be challenging. A thorough understanding of the pathophysiological determinants of respiratory drive and hypoxemia may promote a more complete comprehension of a patient's clinical presentation and management. Preserved oxygen saturation despite low partial pressure of oxygen in arterial blood samples occur, due to leftward shift of the oxyhemoglobin dissociation curve induced by hypoxemia-driven hyperventilation as well as possible direct viral interactions with hemoglobin. Ventilation-perfusion mismatch, ranging from shunts to alveolar dead space ventilation, is the central hallmark and offers various therapeutic targets.
  • |*Betacoronavirus[MESH]
  • |*Pandemics[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*complications/epidemiology[MESH]
  • |Critical Illness[MESH]
  • |Humans[MESH]
  • |Hypoxia/*etiology/metabolism/physiopathology[MESH]
  • |Lung/*physiopathology[MESH]
  • |Oxygen Consumption/*physiology[MESH]
  • |Pneumonia, Viral/*complications/epidemiology[MESH]
  • |Respiratory Insufficiency/*complications/metabolism/physiopathology[MESH]


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