New Sepsis
Detector Shrinks the Diagnosis from Days to Hours
Sepsis affects more than a million people every year in the U.S. alone, and
diagnosis can take five days. A new tool cuts the time to five hours.
A new FDA-approved diagnostic test can detect
sepsis-causing pathogens directly from a blood sample.
Hospitals are beginning to use a new, more potent
weapon against sepsis, the devastating condition that kills more than 25
percent of its victims and costs hospitals billions of dollars annually. In the
U.S. alone, more than a million people become infected each year, and it
contributes to as many half of all deaths in hospitals.
Last fall, the U.S. Food and Drug Administration
approved the new technology, developed by T2 Biosystems, for
diagnosing sepsis caused by a fungus called Candida. Several
hospitals have begun deploying T2’s Candida-detection
system, which is based on the same physical principle behind magnetic resonance
imaging. By the end of this year the company aims to have 30 hospitals signed
on to purchase and use the technology.
Sepsis is a destructive reaction to an infection
marked by an overwhelming inflammatory response throughout the body. If left
untreated, sepsis can cause organ malfunction and death. Treating a septic
patient requires pinpointing the bacterial or fungal organism that is the root
cause. Today that process takes at least a day, and can take up to five days,
as the patient’s condition worsens. T2 Biosystems says its novel pathogen
detector, called T2 Magnetic Resonance (T2MR), can identify the bug within five
hours.
Doctors typically give a septic patient an immediate
dose of a so-called broad-spectrum antibiotic that kills a variety of different
bacteria, and then try to figure out the specific bug at fault by drawing blood
and performing a lab test called a blood culture. At that point it is a race
against the unidentified pathogen, and the blood culture step, which often doesn’t
work, simply takes too long, says T2 Biosystems CEO John McDonough. McDonough
cites clinical data that implies that if patients can get the right drug within
12 hours of first showing symptoms, the chance of death can be cut in half.
“Every hour of delayed therapy increases mortality by 7 to 8 percent,” he says.
Broad-spectrum antibiotics often don’t work, and are
useless against fungal sepsis, which is even more deadly than bacterial
sepsis. Candida infections in the bloodstream kill some 40
percent of patients.
“We have the only technology we’re aware of that can
go directly from a blood sample to a species-specific diagnostic test result,”
says McDonough. It’s also more accurate than a blood culture. In a recent head-to-head
comparison involving 55 patients known to have Candida infections, T2MR detected the pathogen in
96 percent of the patients, whereas blood culture detected it in only 60
percent.
The T2MR detector works by measuring changes in the
magnetic properties of the water molecules in the sample. After some processing
steps, magnetic nanoparticles, equipped on their surface with strands of DNA
complementary to strands in the target pathogen, are mixed with the
sample. If a given target is present, the particles will attach to it and
cluster, causing changes in the magnetic properties of the water molecules in
the sample.
Applying magnetic pulses elicits a response from those molecules,
called T2 relaxation, and by measuring the change in this signal, the device
automatically determines whether or not a given bug is present.
Six hospitals have begun using the Candida diagnostic
test, and 13 more have signed contracts to adopt the technology. Next in the
pipeline is a bacteria detector aimed at the bugs not covered by broad-spectrum
antibiotics. The company expects to begin testing the bacteria detector in
clinical trials by the end of this year. If it can get FDA-approval for this
test as quickly as it did for the Candida test, the bacteria diagnostic could
be in the market as early as 2017.
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