Science Brief

epidemiology-public-health-implementation, science-brief

Supporting Long-term Care Home Residents during Omicron

epidemiology-public-health-implementation, science-brief

Use of Rapid Antigen Tests during the Omicron Wave

The emergence of the now provincially and globally dominant SARS-CoV-2 Omicron variant demands a reassessment of the diagnostic performance of rapid antigen tests. Rapid antigen tests are less sensitive for the Omicron variant compared to the Delta variant in nasal samples, especially in the first 1-2 days after infection. However, rapid antigen tests can more reliably detect infectious cases of the Omicron variant in combined oral-nasal samples. Individuals can collect these samples by initially swabbing both cheeks, followed by the back of the tongue or throat, and then both nostrils. In light of currently very high SARS-CoV-2 transmission rates in Ontario and the limited sensitivity of rapid antigen tests for the Omicron variant, a single negative rapid antigen test result cannot reliably rule out infection; a single negative test result is not conclusive and should not be used as a green light for abandoning or reducing precautions. Conversely, in this context, an individual with a positive rapid test result should be considered and managed as a case of COVID-19 and should immediately isolate; additional confirmation by polymerase chain reaction (PCR) is not necessary in most settings. If asymptomatic testing strategies are considered, rapid antigen tests need to be performed frequently to be effective. When using ‘Test-to-Stay’ strategies as an alternative to large-scale isolation, asymptomatic close contacts of a positive case need to do rapid antigen testing daily. When using ‘Voluntary Asymptomatic Screen Testing’ strategies, asymptomatic individuals should do rapid antigen testing 3-5 times per week.
epidemiology-public-health-implementation, science-brief

Update on COVID-19 Projections: Additional Modelling on Booster Doses

epidemiology-public-health-implementation, science-brief

Update on COVID-19 Projections

infectious-diseases-clinical-care, science-brief

Nirmatrelvir/Ritonavir (Paxlovid): What Prescribers and Pharmacists Need to Know

infectious-diseases-clinical-care, science-brief

Clinical Practice Guideline Summary: Recommended Drugs and Biologics in Adult Patients with COVID-19

infectious-diseases-clinical-care, science-brief

Clinical Practice Guideline Summary: Recommended Drugs and Biologics in Adult Patients with COVID-19

epidemiology-public-health-implementation, science-brief

Ontario Returns to School: An Overview of the Science

infectious-diseases-clinical-care, science-brief

Fluvoxamine: What Prescribers and Pharmacists Need to Know

infectious-diseases-clinical-care, science-brief

Baricitinib for Hospitalized Patients with COVID-19

Baricitinib, a Janus-associated kinase (JAK) inhibitor, reduces mortality and may reduce progression to mechanical ventilation in COVID-19 patients, with no increase in serious adverse events. Baricitinib should be used in moderately ill patients (i.e., requiring supplemental oxygen via nasal prongs) and critically ill hospitalized patients (i.e., requiring oxygen via high-flow nasal cannula, non-invasive ventilation (NIV), invasive mechanical ventilation (IMV) or extracorporeal membrane oxygenation (ECMO)) with COVID-19 who are on recommended doses of dexamethasone (or another dose-equivalent corticosteroid) or who have a contraindication to corticosteroids. Combined use of baricitinib and interleukin-6 (IL-6) inhibitors is not recommended due to a lack of efficacy and safety data. Decisions regarding the use of baricitinib versus an IL-6 inhibitor should be made based on clinical judgement and patient preference regarding availability, side effects and contraindications. The baricitinib dose should be 4 mg PO or NG (2 x 2 mg tablets) daily for 14 days or until discharge. This should be reduced to 2 mg daily in patients with an eGFR 30-60 mL/min/1.73m2. It should not be used in patients with eGFR <30 mL/min/1.73m2.
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