TSXV:SQD.H - Post by User
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FactFinder1994on Sep 28, 2022 9:04am
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Post# 34991671
RE:RE:RaliDx for Pneumonia
RE:RE:RaliDx for Pneumonia Here are a few paragraphs from recent paper on RALI-Dx
Take Home Message: The RALI-Dx assay is a biomarker-based approach to emergency department triage for patients with respiratory illness and is superior to conventional strategies. This diagnostic test will help to optimize the utilization of scarce healthcare resources.
Conclusions: The rapid diagnostic biomarker panel accurately identified the need for inpatient care in patients presenting with respiratory symptoms, including COVID-19. The RALI-Dx test is broadly and easily applicable across many jurisdictions and represents an important diagnostic adjunct to advance emergency department decision- making protocols.
Introduction
Symptoms of respiratory tract infection are a common cause of emergency department (ED) visits. From 2018-2019 in Canada, more than 200,000 ED visits were associated with respiratory illness.1 This demand is traditionally increased in the seasonal flu months and has been further complicated in the COVID-19 pandemic,1 where ED visits for respiratory illness have dramatically increased to the point of repeatedly overwhelming health care systems worldwide.
In conclusion, a predictive model using a rapid inflammation diagnostic immunoassay (RALI-Dx) represents a valuable tool to accurately assess the individual patient’s host inflammatory response in patients presenting to an ED with respiratory illness. This pragmatic assay will augment the precision of clinical decision-making: to admit patients who are likely to develop severe illness, and safely discharge those on a milder course to recover outside of the hospital, thereby better managing limited health care resources. RALI-Dx measures the host inflammatory response in patients with any respiratory illness and, therefore, will be broadly applicable for patients with COVID-19, its variants, as well as any future respiratory pandemic.
Funding Sources: This study was funded in part by the Canadian Institutes of Health Research (FRN #440205) and SQI Diagnostics. Neither funder played any role in study design, data collection, analysis, interpretation of the data, writing the report, or in the decision to submit the paper for publication. All authors confirm access to all data collected throughout the study term.