New Research Demonstrates Clinical Utility of Daxor Corporation Blood Volume (BVA-100®) Diagnostic in Neurocritical Care
09 Novembre 2021 - 2:00PM
Daxor Corporation (NYSE
MKT: DXR), the global leader in blood volume measurement
technology, today announces new data demonstrating the clinical
utility of the BVA-100 blood test in patients with non-traumatic
subarachnoid hemorrhage (nSAH) presented at the virtual
NeuroCritical Care Society (NCS) 19th Annual Meeting.
The study titled, “The Influence of Blood Volume
Analysis on the Clinical Management of Non-Traumatic Subarachnoid
Hemorrhage,” surveyed whether intravascular volume assessments
would influence clinical decision making in nSAH. The data showed
69% responded with different management strategies after being
provided with BVA results. Lindsey Carvalho M.D., lead investigator
concluded, “All participants indicated a preference for BVA over
invasive hemodynamic monitoring if given an option of either
modality to monitor volume status in nSAH due to the former’s less
invasive nature.”
Prior research presented at NCS in 2020 titled
the “Blood Volume Analysis in the Management of Volume Status in
Non-Traumatic Subarachnoid Hemorrhage,” studied whether BVA would
change clinical practice guidelines for management of nSAH to
prevent Delayed Cerebral Ischemia (DCI) during the high-risk
periods. Of the BVA tests completed, 54% resulted in a change of
treatment management after interpretation of the BVA test
results.
“Non-traumatic subarachnoid hemorrhage can cause
complicated, irreversible neurological injury and achieving optimal
intravascular volume plays an important role in improving patient
outcomes,” said Michael Feldschuh, CEO and President of Daxor
Corporation. “These new data further demonstrate that Daxor’s
unique blood volume measurement helps guide physicians to
effectively determine treatment options to manage fluid
derangements for these critically-ill patients and is the driver of
this test for standard clinical practice.”
Prior data in the area of Surgical ICU
Management showed a similarly high level of BVA-100 tests resulting
in a change of treatment strategy. In a randomized control trial
(RCT) published in the journal Shock, the BVA-100 test has shown to
reduce ICU mortality by 66% (P=0.03) and reduce ventilator days in
patients suffering predominantly from acute respiratory distress
syndrome and septic shock. Additionally, the analysis showed 44% of
BVA test results led to a change in treatment strategy (P=0.004)
that care teams would not have performed absent the data from the
BVA volume status measure.
About Daxor
Corporation
Daxor Corporation (NYSE: DXR) is the global
leader in blood volume measurement technology focused on blood
volume testing innovation (organized as an investment company with
fully-owned innovative medical instrumentation and biotechnology
operations). We developed and market the BVA-100® (Blood Volume
Analyzer), the first diagnostic blood test cleared by the FDA to
provide safe, accurate, objective quantification of blood volume
status and composition compared to patient-specific norms. The BVA
technology enhances hospital performance metrics in a broad range
of surgical and medical conditions, including heart failure and
critical care, by informing treatment strategies, resulting in
significantly improved multiple measures of patient outcomes.
Daxor's mission is to advance healthcare by enabling optimal fluid
management with blood volume analysis. Daxor’s vision is optimal
blood volume for all. For more information, please visit our
website at Daxor.com.
Forward-Looking Statements
Certain statements in this release may include
forward-looking statements within the meaning of the Private
Securities Litigation Reform Act of 1995, including without
limitation, statements regarding the impact of hiring sales staff
and expansion of our distribution channels. Forward-looking
statements are predictions, projections and other statements about
future events that are based on current expectations and
assumptions and, as a result, are subject to risks and
uncertainties. Many factors could cause actual future events to
differ materially from the forward-looking statements in this
release, including, without limitation, those risk associated with
our post-market clinical data collection activities, benefits of
our products to patients, our expectations with respect to product
development and commercialization efforts, our ability to increase
market and physician acceptance of our products, potentially
competitive product offerings, intellectual property protection,
FDA regulatory actions, our ability to integrate acquired
businesses, our expectations regarding anticipated synergies with
and benefits from acquired businesses, and additional other risks
and uncertainties described in our filings with the SEC.
Forward-looking statements speak only as of the date when made.
Daxor does not assume any obligation to publicly update or revise
any forward-looking statements, whether as a result of new
information, future events or otherwise.
Investor Relations Contact:Bret
ShapiroSr. Managing Partner, CORE
IR516-222-2560brets@coreir.com
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