Characteristics of outpatient nirmatrelvir/ritonavir recipients during the 2022/2023 era in Alberta, Canada: A

Khanh Vu1, Jason Randall1, Karen Martins1

  • 1Real World Evidence Unit, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB.

Abstract

Insights

Nirmatrelvir/ritonavir (NMV-r) was prescribed to adults in Alberta, Canada, primarily those at high risk for severe COVID-19. Findings highlight demographic patterns and inform strategies for equitable access to this vital antiviral therapy.

Area of Science:

  • Infectious Diseases
  • Pharmacology
  • Public Health

Background:

  • Real-world data on nirmatrelvir/ritonavir (NMV-r; Paxlovid™) use in Canada is crucial for optimizing therapy access and utilization.
  • Understanding patient profiles receiving NMV-r informs public health strategies for managing COVID-19.

Purpose of the Study:

  • To characterize adults who received outpatient nirmatrelvir/ritonavir (NMV-r) in Alberta, Canada.
  • To identify demographic and clinical factors associated with NMV-r prescription.

Main Methods:

  • Population-level administrative data from Alberta, Canada, was analyzed for outpatient NMV-r dispensations between January 2022 and March 2023.
  • The study included 11,793 adults aged 18 years and older, during a period dominated by Omicron variants.

Main Results:

  • The cohort (n=11,793) had a mean age of 65 years, with 60.4% being female. 83.9% had health conditions increasing risk for severe COVID-19.
  • Recipients were more likely to reside in urban areas (89.8%) and be socioeconomically well-off compared to the general population.
  • 81.6% received three or more vaccine doses, and prescriptions were predominantly from physicians (83.6%).

Conclusions:

  • Adults receiving NMV-r in Alberta exhibited characteristics of high risk for severe COVID-19 and proactive healthcare engagement.
  • Observed patterns in urban/rural and socioeconomic distribution suggest potential access disparities.
  • Findings support the development of strategies to overcome barriers and ensure equitable access to NMV-r for at-risk populations.

Related Concept Videos

Antiviral Nucleoside Inhibitors01:22

Antiviral Nucleoside Inhibitors

Antiviral Nucleoside InhibitorsAntiviral nucleoside inhibitors are structural analogs of natural nucleosides that interfere with viral DNA or RNA synthesis. These compounds selectively target viral polymerases due to their resemblance to host nucleosides, thereby disrupting viral genome replication.Mechanism of Acyclovir ActionAcyclovir is a guanosine analog with a three-carbon acyclic side chain. It selectively targets herpes simplex virus type 1 (HSV-1), herpes simplex virus type 2 (HSV-2),...
Respiratory Syncytial Virus Disease01:29

Respiratory Syncytial Virus Disease

Human respiratory syncytial virus (RSV) is a widespread pathogen that primarily targets infants and young children but also poses a serious health risk to elderly and immunocompromised individuals. Belonging to the Pneumoviridae family, RSV is a negative-sense, single-stranded RNA virus within the Pneumovirus genus. Its global health burden is significant, with millions of cases annually resulting in hospitalizations and mortality, particularly in resource-limited settings. Although most...
Bioavailability Study Design: Healthy Subjects Versus Patients01:15

Bioavailability Study Design: Healthy Subjects Versus Patients

Bioavailability studies are essential for evaluating a drug's therapeutic efficacy and understanding its absorption patterns under various physiological conditions. Conducting such studies on target patient populations provides more relevant data by simulating real-world disease states. However, practical challenges often necessitate the use of young, healthy adult volunteers as study subjects.Patients may exhibit altered drug absorption patterns due to the effects of the disease itself,...
Therapeutic Drug Monitoring: Affecting Factors01:29

Therapeutic Drug Monitoring: Affecting Factors

Therapeutic Drug Monitoring (TDM) is the clinical practice of measuring specific drug levels in a patient's blood or body tissues to manage and optimize therapy. TDM is crucial for drugs with narrow therapeutic windows, like warfarin and phenytoin, where incorrect doses can lead to treatment failure or severe side effects. This monitoring ensures the dosage administered is within a safe and effective range. The factors affecting therapeutic drug monitoring include:Patient-Specific Factors:a.