The Circulatory Devices Advisory Committee to the US Food and Drug Administration (FDA) on Monday recommended 510(k) clearance of PercuSurge’s GuardWire Plus […]
The aim of the present study was to investigate the factors that predicted the outcomes for patients who received mixed mode (veno-arterial [VA] and veno-venous {VV}) extracorporeal membrane oxygenation (ECMO) support in the ED.