|Videos|November 8, 2016

Influenza Antiviral Treatments: Prescribing Practices Across the US

Rebekah Stewart Schicker, MSN, MPH, APRN, Epidemic Intelligence Service (EIS) Officer at the Centers for Disease Control and Prevention, explains her recent research on influenza antiviral treatment prescribing practices in 60 outpatient settings across the United States.

Rebekah Stewart Schicker, MSN, MPH, APRN, Epidemic Intelligence Service (EIS) Officer at the Centers for Disease Control and Prevention, explains her recent research on influenza antiviral treatment prescribing practices in 60 outpatient settings across the United States.

Interview Transcript (slightly modified for readability)

“[For] the study that we did to look at influenza antiviral treatment in the outpatient setting, we used an existing study platform, called the US Influenza Vaccine Effectiveness Network, and this platform consists of five research sites across the US, which then consists of more than 60 outpatient practices. We used that platform because they test everyone for influenza as part of their research study. And so we would have information on their influenza status as well as their symptom onset and the treatment that was prescribed to them.

What we set out to study was to see if outpatient providers prescribed influenza antiviral medications for their [high risk] patients when they presented to the outpatient practice. We looked at any patient who came with an acute respiratory illness that was described as a cough within seven days of onset. We also looked at patients who arrived within two days of symptom onset, and then we also looked at patients who were influenza-positive. We wanted to [answer the questions]: did clinicians prescribe antivirals for those patients according to recommendations; and, did that change at all over the past five seasons? So we looked at the last five [influenza] seasons. The other [questions] we wanted to [answer were]: do patients actually present in a timely manner to an outpatient provider in order to benefit from these medications; and also, how much influenza is circulating among these patients who present with an acute respiratory illness during the influenza season?”


Related to this article

REMAP-CAP and the Tamiflu “Pre-Release”: A Set-Up for Disaster
Preliminary REMAP-CAP data suggesting oseltamivir may increase mortality in critically ill ICU influenza patients has sparked polarized reactions, but clinicians should await the full peer-reviewed manuscript before drawing broad conclusions, since the signal comes from a narrow, severely ill population and may reflect a therapeutic window effect rather than a blanket lack of efficacy.
GSK's mRNA Influenza Vaccine Moves to Phase 3 Trial
GSK will advance its investigational mRNA seasonal flu vaccine candidate, which targets both hemagglutinin and neuraminidase, into a phase 3 trial in September 2026 after the shot outperformed licensed flu vaccines in a phase 2 study.
How The Food Safety Surveillance Infrastructure Works in the US
In the first episode of our news series looking at the food safety network, Lynette Johnston, PhD, offers insights into how the federal government surveillance infrastructure operates, and how epidemiologists serve as food detectives in determining bacterial pathogens and potential foodborne outbreaks.
New Diagnositics for Legionella Pneumonia May Streamline Care Continuum
Reported cases of Legionnaires’ disease have been on the rise for the past decade, and identifying Legionella bacteria requires specialized testing in the microbiology lab. Here is a clinical overview of Legionella bacteria, including required testing, treatment, and reporting to public health officials.