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Silent hypoxia is not an identifiable characteristic in patients with COVID-19 infection.
Plummer, Nicholas Russell; Fogarty, Andrew; Shaw, Dominick; Card, Timothy; West, Joe; Crooks, Colin.
  • Plummer NR; Adult Critical Care, Nottingham University Hospitals NHS Trust, NG7 2UH, UK. Electronic address: nickplummer@nhs.net.
  • Fogarty A; NIHR Respiratory Biomedical Research Centre, University of Nottingham, NG7 2UH, UK.
  • Shaw D; NIHR Respiratory Biomedical Research Centre, University of Nottingham, NG7 2UH, UK.
  • Card T; Nottingham Digestive Diseases Centre, School of Medicine, University of Nottingham, NG7 2UH, UK; Population and Lifespan Sciences, School of Medicine, University of Nottingham, NG7 2UH, UK; NIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust, NG7 2UH, UK.
  • West J; Population and Lifespan Sciences, School of Medicine, University of Nottingham, NG7 2UH, UK; NIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust, NG7 2UH, UK.
  • Crooks C; Nottingham Digestive Diseases Centre, School of Medicine, University of Nottingham, NG7 2UH, UK; NIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust, NG7 2UH, UK.
Respir Med ; 197: 106858, 2022 06.
Article in English | MEDLINE | ID: covidwho-1805102
ABSTRACT

BACKGROUND:

We aimed to assess whether asymptomatic ("happy") hypoxia was an identifiable physiological phenotype of COVID-19 acute respiratory distress syndrome (ARDS), and associated with need for ICU admission.

METHODS:

We performed an observational cohort study of all adult patients admitted with hypoxaemic respiratory failure to a large acute hospital Trust serving the East Midlands, UK. Patients with confirmed COVID-19 were compared to those without. Physiological response to hypoxaemia was modelled using a linear mixed effects model.

RESULTS:

Of 1,586 patients included, 75% tested positive for SARS-CoV-2. The ROX index was 2.08 min-1 lower (1.56-2.61, p < 0.001) in the COVID-19 cohort when adjusted for age and ethnicity, suggesting an enhanced respiratory response to hypoxia compared to the non-Covid-19 patients. There was substantial residual inter- and intra-patient variability in the respiratory response to hypoxaemia. 33% of the infected cohort required ICU, and of these 31% died within 60 days. ICU admission and mortality were both associated with an enhanced respiratory response for all degrees of hypoxaemia.

CONCLUSIONS:

Patients with COVID-19 display a more symptomatic phenotype in response to hypoxaemia than those with other causes of hypoxaemic respiratory failure, however individual patients exhibit a wide range of responses. As such although asymptomatic hypoxaemia may be a phenomenon in any individual patient with hypoxaemic respiratory failure, it is no more frequently observed in those with SARS-CoV-2 infection than without.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Respiratory Insufficiency / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid Limits: Humans Language: English Journal: Respir Med Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Respiratory Insufficiency / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid Limits: Humans Language: English Journal: Respir Med Year: 2022 Document Type: Article