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The impact of rapid molecular diagnostic testing for respiratory viruses on outcomes for emergency department patients

Nasir Wabe
Med J Aust 2020; 212 (2): . || doi: 10.5694/mja2.50442
Published online: 3 February 2020

In reply: Katelaris and colleagues raise concerns that uncontrolled before‐and‐after studies are vulnerable to bias and that other factors (eg, the severity of influenza) may have confounded our findings.1 I agree that uncontrolled before‐and‐after studies, being observational studies, are generally prone to different types of bias and that other residual (unmeasured) factors may have confounded our study outcomes.2


  • Centre for Health Systems and Safety Research, Australian Institute of Health Innovation, Macquarie University, Sydney, NSW


Correspondence: nasir.wabe@mq.edu.au

Competing interests:

No relevant disclosures.

  • 1. Wabe N, Li L, Lindeman R, et al. The impact of rapid molecular diagnostic testing for respiratory viruses on outcomes for emergency department patients. Med J Aust 2019; 210: 316–320. https://www.mja.com.au/journal/2019/210/7/impact-rapid-molecular-diagnostic-testing-respiratory-viruses-outcomes-emergency
  • 2. Boyko EJ. Observational research — opportunities and limitations. J Diabetes Complications 2013; 27: 642–648.
  • 3. Rappo U, Schuetz AN, Jenkins SG, et al. Impact of early detection of respiratory viruses by multiplex pcr assay on clinical outcomes in adult patients. J Clin Microbiol 2016; 54: 2096–2103.
  • 4. Rogers BB, Shankar P, Jerris RC, et al. Impact of a rapid respiratory panel test on patient outcomes. Arch Pathol Lab Med 2015; 139: 636–641.

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