Continuous Real Time CSF Shunt Flow Monitor ShuntCheck

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$993,751.00
Award Year:
2013
Program:
SBIR
Phase:
Phase II
Contract:
2R44NS074486-02
Award Id:
n/a
Agency Tracking Number:
R44NS074486
Solicitation Year:
2013
Solicitation Topic Code:
NINDS
Solicitation Number:
PA12-189
Small Business Information
3333 Street Road, SUITE 210, Bensalem, PA, -
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
828682240
Principal Investigator:
MAREK SWOBODA
(215) 645-1280
dr.marekswoboda@gmail.com
Business Contact:
FREDERICK FRITX
(609) 865-4426
ffritz@neurodx.com
Research Institute:
Stub




Abstract
DESCRIPTION (provided by applicant): This Phase II SBIR will develop Continuous Real Time (CRT) ShuntCheck, the first portable, non- invasive device for real time, continuous monitoring of changes in flow in CSF shunts. This device will result in improvedclinical management of hydrocephalus by providing a non-invasive method for monitoring and researching shunt function. Hydrocephalus, a common condition in which CSF accumulates in the brain ventricles, is corrected by placing a VP shunt that drains excessCSF to the abdomen. Shunts frequently malfunction, usually by obstruction, but the symptoms of shunt failure are unspecific - headache, nausea. Diagnosis of shunt malfunction is expensive and presents risks (exposure to radiation from CT Scans, risk of infection from radionuclide testing). Additionally, ongoing clinical management of shunted patients is complex (due to a lack of tools for investigating CSF over drainage, for assessing the performance of specific shunt valves and siphon control devices andfor streamlining the adjustment of programmable shunt valves). NeuroDx's existing device, ShuntCheck-Micro-Pumper, is a shunt obstruction detector and addresses the need for a non-invasive test for shunt malfunction. While this makes it a valuable tool forthe Emergency Dept, the short duration of the test limits its utility for shunt valve adjustment, investigating suspected shunt over drainage, etc. A non-invasive, non-radiologic device which can track changes in CSF flow rate would address many ongoing clinical management needs and become a valuable tool for the neurosurgery clinic. In our Phase I studies, we developed a laboratory prototype CRT based upon a breakthrough innovation in our thermal dilution technology and validated its safety and accuracy in bench and animal studies. CRT can reliably differentiate between no, low and robust shunt flow and can track changes in shunt flow rates over extended time periods. The goal of this Phase II project is to refine CRT ShuntCheck from a laboratory prototypeto a production-ready device, validate its safety and accuracy in bench and animal testing, and complete a 510k submission for FDA clearance. Post-Phase II clinical studies will demonstrate the clinical utility and cost effectiveness of CRT ShuntCheck forstreamlining valve adjustment in pediatric and in adult NPH patients. NeuroDx's business model for this product involves the generation of revenue primarily from the ongoing sale of single-use, disposable sensors for these tests. Shunt management testingconstitutes approximately 105,000 shunt flow tests annually in the United States alone. The need for new diagnostic tools for managing hydrocephalus patients is highlighted by the NIH announcement Advanced Tools and Technologies for Cerebrospinal Fluid Shunts (PA-09-206), to which this application is responding. Our application directly responds to the request for Diagnostic tools for use in a hospital or outpatient setting that work in real-time to quantitatively determine shun function. PUBLICHEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: This application addresses the need for diagnostic tools for use in a hospital or outpatient setting that work in real-time to quantitatively determine shunt function by providing the first portable, non-invasivedevice for continuous real time monitoring of changes in flow in CSF shunts. Ongoing clinical management of shunted patients is complex due to a lack of tools for investigating CSF over drainage, for assessing the performance of specific shunt valves andsiphon control devices and for streamlining the adjustment of programmable shunt valves. This new device will address many ongoing clinical management needs and become a valuable tool for the neurosurgery clinic.

* information listed above is at the time of submission.

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