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Initial standalone D-dimer testing followed by whole-leg compression ultrasonography in patients with positive D-dimer can safely rule out deep vein thrombosis

Negative D-Dimer Can Safely Rule Out DVT as Standalone Test

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Standalone D-dimer testing followed by whole-leg compression US in positive patients rules out DVT
Tranexamic acid given in the prehospital setting to injured patients at risk for hemorrhage does not lower 30-day mortality

ACS: Tranexamic Acid No Better Than Placebo After Severe Injury

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Antifibrinolytic agent may lower 30-day mortality when used within one hour of injury, for severe shock
Individuals with blood group O may have a reduced risk for severe acute respiratory syndrome coronavirus 2 infection

Individuals With Blood Group O Have Lower Risk for COVID-19

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And more COVID-19 patients with blood group A or AB require mechanical ventilation, CRRT
Antibodies decrease with time after COVID-19 symptom onset

Antibodies Decrease With Time After COVID-19 Symptom Onset

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For all donors of convalescent plasma, drop seen in anti-RBD antibody levels from first to last donation
For patients with COVID-19

Red Blood Cell Distribution Width, Mortality Tied in COVID-19

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Elevated RDW and increase in RDW during hospitalization linked to increased mortality risk
There is no evidence to support the use of convalescent plasma to treat COVID-19 patients

No Proof Convalescent Plasma Effective Against COVID-19

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NIH panel says data are insufficient to recommend either for or against the use of convalescent plasma
The use of blood plasma from COVID-19 survivors to treat patients hospitalized with the disease is still considered experimental

WHO: Plasma Therapy for COVID-19 Still Experimental

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FDA 'emergency use authorization' does not mean plasma therapy has been proven safe and effective
The U.S. Food and Drug Administration on Sunday cleared the way for more hospitalized COVID-19 patients to be treated with the blood plasma of COVID-19 survivors.

FDA Approves Wider Use of Plasma as COVID-19 Treatment

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President Donald Trump announced emergency approval as 'breakthrough' treatment during a news briefing Sunday
The U.S. Food and Drug Administration emergency approval of blood plasma as a COVID-19 treatment was put on hold last week after senior federal health officials said data supporting the therapy were too weak.

FDA Emergency Approval on Hold for Blood Plasma to Treat COVID-19

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More data are under review; the approval could still be issued in the near future
Transfusion of convalescent plasma is efficacious in patients with severe COVID-19

Convalescent Plasma Efficacious for Severe COVID-19

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Significant reduction seen in mortality, specifically among patients transfused with plasma within 72 hours