COVID-19 Clinical Trial
Official title:
Therapeutic Plasmapheresis in Critically Ill Adult Patients With COVID-19 Confirmed Diagnosis / Plasmaféresis terapéutica en Pacientes Adultos críticamente Enfermos Con diagnóstico Confirmado de COVID-19
Introduction: The SARS-CoV-2 outbreak has left more than two million infected worldwide in
the first four months of COVID-19 epidemic. To date, there is no specific treatment for the
disease and in critically ill patients there is an additional challenge in controlling the
systemic inflammatory response, which is characterized by cytokine storm, alteration in
coagulation and endothelial activation in addition to infection. Strategies used in previous
viral epidemics, such as convalescent plasma, are therapeutic options to rescue, especially
in individuals with a critical presentation of the disease.
Aim: To establish clinical response of critically ill patients with COVID-19 who received
convalescent plasma from subjects recovered from SARS-CoV-2 during their stay in Intensive
Care Unit at Fundación Cardiovascular de Colombia (Hospital Internacional de Colombia).
Methodology: Quasi-experimental study (no randomization will be performed). Adult patients
who meet selection criteria will receive 500 ml of ABO compatible convalescent plasma,
obtained by apheresis from patients recovered from SARS-CoV-2 infection. The main outcome
will be in-hospital mortality at 30 days, while indication for ventilatory support
(intubation) and adverse events at thirty days will be evaluated as secondary outcomes,
compared to subjects receiving usual treatment for clinical sign and symptoms given the
absence of ABO compatible plasma units. A survival analysis will be performed using
Kaplan-Meier method and association strength will be reported using HR and 95% CI crude and
adjusted for confounding variables.
Expected results: It is expected to know the clinical and paraclinical response of patients
receiving convalescent plasma in our institution, as well as to establish their probability
of survival and its associated factors.
n/a
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