Corpus overview


Overview

MeSH Disease

Human Phenotype

Transmission

There are no transmission terms in the subcorpus


Seroprevalence

There are no seroprevalence terms in the subcorpus

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    Acute Pulmonary Embolism HP Pulmonary Embolism MESHD in Critically Ill Patients with COVID-19

    Authors: Madhura Manjunath; Julio Miranda; Liana Fraenkel; Paul Manje Johansen; Blessing Phinney; Georgianne Valli-Harwood; Cynthia Callahan; Hafez Alsmaan; David Oelberg

    doi:10.1101/2020.05.22.20110270 Date: 2020-05-24 Source: medRxiv

    Since the discovery of the novel coronavirus ( SARS-Co-V-2 MESHD) in December 2019, multiple characteristics have been reported, as our understanding of this new disease unfolds. One such association is its tendency to cause thromboembolic MESHD events, particularly venous thromboembolism MESHD thromboembolism HP (1,2). In a four-week period during the initial spread of COVID-19 at a 300 bed community hospital in western Massachusetts, 23 patients who were PCR positive for SARS-CoV-2 RNA required treatment in either the intensive care unit (ICU) or intermediate/step-down unit (SDU). All patients were treated with standard DVT prophylaxis from the time of admission, except for two patients who were on full anticoagulation for chronic atrial fibrillation HP atrial fibrillation MESHD. Of the 23 patients, 7 (30%) were diagnosed with acute, clinically significant, pulmonary embolism HP pulmonary embolism MESHD ( PE MESHD). Four of the 7 manifested evidence of acute cor pulmonale MESHD cor pulmonale HP, one of whom succumbed as a direct consequence of a massive PE MESHD. Other markers were reviewed in the 7 patients to identify trends that could allow for early suspicion of PE MESHD in COVID-19 patients. Although D-dimer tended to rise during the hospitalization relative to the control group, the results were inconsistent, and there were no other meaningful distinguishing features between the groups at the time of admission.

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MeSH Disease
Human Phenotype
Transmission
Seroprevalence


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