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Michelle Ng Gong

Researcher at Albert Einstein College of Medicine

Publications -  17
Citations -  3641

Michelle Ng Gong is an academic researcher from Albert Einstein College of Medicine. The author has contributed to research in topics: ARDS & Lung injury. The author has an hindex of 15, co-authored 17 publications receiving 2907 citations. Previous affiliations of Michelle Ng Gong include Montefiore Medical Center & Harvard University.

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Surviving Sepsis Campaign: guidelines on the management of critically ill adults with Coronavirus Disease 2019 (COVID-19)

Waleed Alhazzani, +41 more
TL;DR: The Surviving Sepsis Campaign CO VID-19 panel issued several recommendations to help support healthcare workers caring for critically ill ICU patients with COVID-19, and will provide new recommendations in further releases of these guidelines.
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Surviving Sepsis Campaign: Guidelines on the Management of Critically Ill Adults with Coronavirus Disease 2019 (COVID-19).

TL;DR: A panel of 36 experts from 12 countries issued several recommendations to help support healthcare workers caring for critically ill ICU patients with COVID-19, and assessed the certainty in the evidence using the Grading of Recommendations, Assessment, Development and Evaluation approach.
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Clinical Characteristics and Outcomes of Sepsis-Related vs Non-Sepsis-Related ARDS

TL;DR: Sepsis-related ARDS has a higher overall disease severity, poorer recovery from lung injury, lower successful extubation rate, and higher mortality than non-sepsis- related ARDS, which appears to be driven by disease severity and comorbidities.
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Polymorphism in the surfactant protein-B gene, gender, and the risk of direct pulmonary injury and ARDS.

TL;DR: The variant polymorphism of the SP-B gene is associated with ARDS and with direct pulmonary injury in women, but not in men, and further study is needed to confirm the association between the variant SP- B gene, and gender, ARDS, and direct pulmonary Injury.
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Pre-B-cell colony-enhancing factor gene polymorphisms and risk of acute respiratory distress syndrome.

TL;DR: The PBEFT-1001G variant allele and related haplotype are associated with increased odds of developing ARDS and increased hazard of intensive care unit mortality among at-risk patients, whereas the C-1543T variant allele or haplotype is associated with decreased odds of ARDS among patients with septic shock and better outcomes among patientswith ARDS.