Necrotizing Enterocolitis Clinical Trial
Official title:
Monitoring Necrotizing Enterocolitis in Premature Infants Using Depth-Resolved Broad Spectrum NIRS
The investigators are studying a disease called "necrotizing enterocolitis" (or "NEC" for short), which affects premature infants. It is the most common surgical emergency involving neonates admitted to Newborn Intensive Care Units. Currently, clinicians are unable to identify which infants will go on to develop NEC before they become ill. Clinical signs of illness occur relatively late in the course of the condition, making NEC more difficult to treat. The investigators will test a new probe that uses safe levels of visible and infrared light, with and without ultrasound imaging, to see if the investigators can identify infants before they get sick using a simple, noninvasive test, This test will be repeated through at least one feeding (which stresses the gut) each day. If successful, the health benefit will be large, as it is estimated that treating NEC alone (not including treating its later complications) adds $650 million to the annual health bill.
In this 5-year study, we extend our prior feasibility study to test the hypothesis that
very-low-birth-weight neonates (VLBW) who develop necrotizing enterocolitis (NEC) can be
reliably detected early in the process using broadband optical spectroscopy sensitive to
changes in perfusion of the gut. Such perfusion changes result in regional tissue hypoxemia,
which we have demonstrated to be detectable by combined broadband visible/near-infrared
tissue oximetry, a real-time method that can assess the adequacy of deep tissue oxygenation.
Initially this will be an optical-only device; then combining it with ultrasound will be
studied in years 2-5, first on the benchtop, and then in the intensive care unit.
Necrotizing enterocolitis (NEC) is the most common life-threatening surgical emergency
encountered in the neonatal intensive care unit [ ]. NEC is a multi-factorial (infectious,
inflammatory, and ischemic) disease of the gastrointestinal (GI) tract of newborns and
neonates. The end result is mucosal injury and/or transmural necrosis of the intestine.
Currently, there is no test to diagnose NEC in the early stages of the disease, before the
later and ominous clinical signs appear. The mortality of NEC ranges from 10% to 50%,
approaching 100% for neonates with severe forms of the disease characterized by
full-thickness necrosis of the intestine, followed by rupture and sepsis.
Ninety percent of NEC cases occur in infants born before 36 weeks' gestational age, occurring
in up to 10% of all very-low-birth-weight (VLBW, <1500g) neonates [ ]. A diagnosis of NEC
increases the NICU length of stay by 22−60 days, and increases the total hospital charges by
$76,000−$186,000 per case [ ]. Finally, Neonates recovering from NEC often incur additional
serious complications (malnutrition, liver dysfunction). NEC requiring surgery carries
increased risk of cerebral palsy, cognitive or psychomotor impairment, or both.
Repeated attempts to use clinical signs to reliably identify neonates most likely to progress
to severe NEC have been unsuccessful. Broadband oximetry appears to offer a solution.
Developed by the PI and others, broadband oximetry is sensitive to ischemia. It differs from
typical near-infrared spectroscopy (NIRS) methods that generally use only 2-4 wavelengths in
that broadband oximetry measures hundreds of wavelengths. Broadband approaches, have shown
significantly tighter normal ranges, lower noise, and better reproducibility in vivo.
Further, typical NIRS fails to account for shifts in water, fat, blood volume, and stool, any
of which can affect oxygenation measurements if not specifically accounted for, making NIRS
unreliable for quantitative studies of the gut. In contrast, in our just-completed 1-year
feasibility R43 trial, we demonstrated that NEC can be detected using broadband methods. The
question remains: how will this new device perform clinically in a multicenter study? By
incorporating broadband oximetry monitoring into the management of VLBW neonates, we may
detect NEC at its earliest stages and prevent the cascade that leads to bowel necrosis.
Success should lead quickly to clinical use, as this team has previously developed, received
FDA approval for, and commercialized two biomedical devices.
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