Resource: FDA Issues Authorization for Quidel QuickVue At-Home COVID-19 Test
Source: U.S. Food and Drug Administration
Synopsis: The agency issued an Emergency Use Authorization (EUA) to Quidel for

Resource: FDA Authorizes Adaptive Biotechnologies T-Detect COVID Test
Source: U.S. Food and Drug Administration
Synopsis: The U.S. Food and Drug Administration issued an emergency use authorization

Resource: FDA Permits Marketing of First SARS-CoV-2 Diagnostic Test Using Traditional Premarket Review Process
Source: U.S. Food and Drug Administration
Synopsis: The U.S. Food and Drug Administration

Resource: The Safe Resumption of Elective Plastic Surgery in Accredited Ambulatory Surgery Facilities During the COVID-19 Pandemic
Source: Aesthetic Surgery Journal
Synopsis: This is a prospective

Resource: Evaluating Postoperative Outcomes of Patients Undergoing Elective Procedures in an Ambulatory Surgery Center During the COVID-19 Pandemic
Source: Aesthetic Surgery Journal
Synopsis: A total

Resource: Timing of surgery following SARS‐CoV‐2 infection: an international prospective cohort study
Source: Anesthesia
Summary:  Although it is known that preoperative COVID-19 infection increases

Resource: SBI Recommendations for the Management of Axillary Adenopathy in Patients with Recent COVID-19 Vaccination
Source: Society of Breast Imaging
Synopsis: SBI considerations for the management

Resource: FDA Issues Emergency Use Authorization for Third COVID-19 Vaccine
Source: U.S. Food and Drug Administration
Synopsis: The U.S. Food and Drug Administration issued an emergency use

Resource: Utility of D-dimer in predicting venous thromboembolism in non-mechanically ventilated COVID survivors
Source: Thrombosis Research
Synopsis: Although D-dimer has been found to be a

Resource: IDSA Guidelines on the Treatment and Management of Patients with COVID-19
Source: Infectious Disease Society of America
Synopsis: Among hospitalized adults with progressive severe* or