Incidence of COVID-19 Test Conversion in Post-surgical Patients
Sars-CoV2

About this trial
This is an interventional diagnostic trial for Sars-CoV2 focused on measuring Sars-CoV2, surgery, infection, transmission, Covid-19, safety, nosocomial, virus, corona, COVID, incidence
Eligibility Criteria
Inclusion Criteria:
- Patients of any ethnic background undergoing an elective surgical procedure with a minimum of 24-hour hospital admission.
- Age ≥18.
- Written Voluntary Informed Consent.
Exclusion Criteria:
- Patients age < 18 years.
- Prior documented COVID-19 Infection.
- Current hospital inpatient prior to procedure.
- Person Under Investigation for COVID-19 infection.
- Current use of antiviral medications.
- Severe or uncontrolled, concurrent medical disease (e.g. uncontrolled diabetes, unstable angina, myocardial infarction within 6 months, congestive heart failure, etc.) .
- Documented immunodeficiency.
- Patients with dementia or altered mental status that would prohibit the giving and understanding of informed consent at the time of study entry.
- Outpatient procedures with planned same-day discharge.
Sites / Locations
- North Shore University Hospital
- Long Island Jewish Medical Center
Arms of the Study
Arm 1
Experimental
Study Group
Patients will be recruited as an outpatient prior to their surgical procedure or during their hospital admission. If they consent, they will provide signed informed consent and will receive testing with serology and PCR for COVID-19 infection at pre-surgical testing 24-48 hours prior to their scheduled procedure. If they consent while inpatient postoperatively, signed informed consent will be procured after they have completed their pre-operative COVID-19 testing. PCR for COVID entails obtaining a nasopharyngeal swab to determine whether there is active viral replication and viral shedding. They will then have a second test with serology and PCR for COVID-19 infection 12-16 days after discharge from the hospital.