OpGen's QuickFISH Rapid Pathogen ID Test Demonstrates Clinical Utility and Cost Effectiveness in Community Hospital’s Antimicrobial Stewardship Program
than $760,000 from use of the OpGen test, which resulted in a 30% reduction in
patient length of stay and a 65% reduction in vancomycin use
The study, entitled “The Impact of Implementation of Rapid QuickFISH Testing for Detection of Coagulase-Negative Staphylococci at a
The study was published online on
“True infections with Staphylococcus aureus present considerable clinical challenges to hospitals, such as increased mortality rates, prolonged hospital stays and additional costs,” says
According to the study, the
- A 90% reduction in time to report pathogen identity (mean of 17.16 hours reduced to a mean of 1.35 hours).
- A 30% reduction in length of stay (mean of 4.89 days reduced to mean of 3.44 days).
- A 65% decrease in days on vancomycin (mean of 2.52 days to mean of 0.89 days).
- Savings from the use of QuickFISH with an antimicrobial stewardship program calculated to be
$764,316 using the mean costs per day at a not-for-profit hospital in the state ofFlorida . - QuickFISH was shown to be fast and easy to perform in a busy microbiology laboratory, requiring only 5 minutes of hands-on time.
“We believe QuickFISH is a significant breakthrough for community hospitals looking to launch effective antimicrobial stewardship programs,” says
About QuickFISH
QuickFISH provides rapid and accurate identification of critical bloodstream infections 1-3 days earlier than conventional identification methods. Conventional methods employ sub-culturing, overnight incubation and phenotypic identification that can take days and could result in use of empiric therapy coverage with broad-spectrum antibiotics until results become available. With QuickFISH, results are available within 30 minutes from the positive blood culture, enabling clinicians to optimize antibiotic therapy sooner. QuickFISH enables de-escalation of broad spectrum antimicrobials (e.g. vancomycin) for patients with contaminated blood cultures (Forrest et al. J Antimicrob Chemo 2006; 58(1):154-158.)
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OpGen Forward-Looking Statements
This press release includes statements relating to the company's products and services. These statements and other statements regarding our future plans and goals constitute "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, and are intended to qualify for the safe harbor from liability established by the Private Securities Litigation Reform Act of 1995. Such statements are subject to risks and uncertainties that are often difficult to predict, are beyond our control, and which may cause results to differ materially from expectations. Factors that could cause our results to differ materially from those described include, but are not limited to, the rate of adoption of our products and services by hospitals, the success of our commercialization efforts, the effect on our business of existing and new regulatory requirements, and other economic and competitive factors. For a discussion of the most significant risks and uncertainties associated with
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