# US 10,499,816 B2 · CSF shunt flow evaluation apparatus and method using a conformable expanded dynamic range thermosensor > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 10,499,816 B2 - Document ID: US10499816B2 - Status: Granted - Kind: B2 - Application number: 14/648,358 - Filed: 2013-11-26 - Published: 2015-10-29 - Granted: 2019-12-10 - Earliest claimed: 2012-12-06 - Assignees: ShuntCheck, Inc. - Applicants: Shuntcheck, Inc.; Frederick J. Fritz; Marek Swoboda; Mark E. Mattiucci; Matias G. Hochman - Inventors: Frederick J. Fritz; Marek Swoboda; Mark E. Mattiucci; Matias G. Hochman - Web page: https://patentgrep.com/patent/US10499816B2 ## CPC - A61B 5/01: Measuring temperature of body parts {; Diagnostic temperature sensing, e.g. for malignant or inflamed tissue} (clinical contact thermometers G01K13/20) - A61B 5/015: {By temperature mapping of body part} - A61B 5/14507: {specially adapted for measuring characteristics of body fluids other than blood (devices for taking samples of body liquids A61B10/0045)} - A61B 5/6833: {Adhesive patches} - A61B 5/684: {Indicating the position of the sensor on the body} - A61M 27/006: {Cerebrospinal drainage; Accessories therefor, e.g. valves} - A61B 5/031: {Intracranial pressure} - A61B 5/032: {Spinal fluid pressure} - A61B 2562/0271: Thermal or temperature sensors - A61B 2562/043: in a linear array - A61B: DIAGNOSIS; SURGERY; IDENTIFICATION (usefulness limited to only animals A61D) - A61M: DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY (introducing media into or onto the bodies of animals A61D7/00; means for inserting tampons A61F13/26; devices for administering food or medicines orally A61J; containers for collecting, storing or administering blood or medical fluids A61J1/05); DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY (surgery A61B; chemical aspects of surgical articles A61L); DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR {(Electrotherapy, e.g. producing anaesthesia by the use of alternating or intermittent currents A61N1/36021)} ## Abstract An apparatus and method that utilizes thermal dilution to detect a wide range of flow rates and/or flow status in cerebrospinal fluid (CSF) shunt systems. The use of a large cold source in combination with thermosensor pad of a particular construction provide a fluid flow analyzer with the ability to detect very low levels of CSF flow. In addition, a method for adjusting thermal dilution readings to compensate for varying shunt catheter depth is shown and for determining a steady state of the thermal dilution readings. The thermosensor pad is conformable to a patient's skin contour thereby making the apparatus and method less sensitive to ambient temperature errors and, as a result, more accurate in assessing CSF flow. Furthermore, a software error check is provided for identifying poor sensor-to-skin contact for alerting an operator to re-apply the thermosensor pad to correct, as well as a post-test check to determine if temperature data is reasonable before determining flow status or flow rate. ## Claims ### Claim 1 An apparatus for evaluating cerebrospinal fluid (CSF) flow rate or flow status in a CSF shunt positioned under the skin of a patient, said apparatus comprising: a sensor pad comprising a flexible material configured for conforming to a patient's skin contour and having a body comprising a plurality of temperature sensors that are positioned transversely across said body at predetermined positions, said plurality of temperature sensors being aligned such that when said sensor pad is applied to the skin over the CSF shunt, one of said plurality of temperature sensors is positioned over the CSF shunt while the remaining plurality of temperature sensors are equally positioned on opposite sides of the CSF shunt; each of said temperature sensors configured to generate respective temperature data related to movement of a temperature pulse introduced into the CSF shunt from a cold source applied to the skin for a predetermined period, said body further comprising an alignment member that protrudes from an outside edge of said body, said alignment member acting as a guide for a user in positioning said cold source at a predetermined position upstream of said sensor pad; said sensor pad being disposable; and a sensor processing device that is electrically coupled to said sensor pad for receiving temperature data from each of said temperature sensors, said sensor processing device using said temperature data to determine a flow rate or flow status of said CSF through said shunt when said cold source is applied at said predetermined upstream position. ### Claim 2 (depends on 1) The apparatus of claim 1 wherein said sensor processing device determines said flow rate or flow status by taking a difference between said temperature data of said one of said plurality of temperature sensors that is positioned over the CSF shunt and an average of said temperature data of said remaining plurality of temperature sensors positioned on opposite sides of the CSF shunt, said difference being subsequently referred to as “temperature difference”. ### Claim 3 (depends on 2) The apparatus of claim 2 wherein said sensor processing device adjusts said temperature difference based on the location of the CSF shunt below the skin surface by multiplying said temperature difference by a ratio of actual skin thickness over the CSF shunt to average skin thickness over the CSF shunt. ### Claim 4 (depends on 3) The apparatus of claim 3 wherein said sensor processing device determines a lowest point in said difference for determining a steady state of said temperature difference data. ### Claim 5 (depends on 2) The apparatus of claim 2 wherein said sensor processing device instructs an operator to conduct a test procedure for the determination of the CSF flow status or CSF flow rate by: applying the cold source against the patient's skin over the subcutaneously positioned CSF shunt for a first time period at predetermined upstream position, away from said pad, to transfer an initial cold pulse into said the CSF in said CSF shunt; displacing said cold source away from against the patient's skin over the subcutaneously positioned CSF shunt at said predetermined upstream position for a second time period so as not to cause discomfort to the patient by the application of the cold source for a prolonged period while said device receives temperature data from said plurality of temperature sensors based on said first cold pulse; re-applying said cold source a second time against the patient's skin over the subcutaneously positioned CSF shunt for a third time period at said predetermined upstream position; and removing said cold source from against the patient's skin over the subcutaneously positioned CSF shunt while said device again receives temperature data from said plurality of temperature sensors to determine the CSF flow status or CSF flow rate and thereby complete the test procedure. ### Claim 6 (depends on 5) The apparatus of claim 5 wherein the subcutaneously positioned CSF shunt comprises a valve positioned closely adjacent an outer skin surface of the patient and wherein said step of removing said cold source comprises externally applying a vibrating member to be in contact with said valve via the outer skin surface and activating said vibrating member to apply mechanical vibratory motion to said valve, for a fourth time period of time, such that physical reciprocation of said vibrating member causes said valve to reciprocate. ### Claim 7 (depends on 1) The apparatus of claim 1 wherein said sensor processing device alerts an operator, prior to running an evaluation of said CSF flow rate or CSF flow status, that said sensor pad comprising at least one of said plurality of temperature sensors is in partial or complete loss of contact with the skin of the patient, said alert being generated based on signal noise being detected in an output of at least one of said plurality of temperature sensors that exceeds a predetermined signal noise threshold during a pretest operation of said apparatus and if so to readjust positioning of said sensor pad against the patient's skin until outputs of said plurality of temperature sensors are below said predetermined signal noise threshold before running said evaluation of said CSF flow rate or CSF flow status, said pretest operation comprising the steps of: measuring each rise and fall in temperature detected by each one of said plurality of sensors; converting each fall in temperature, comprising a negative number, into a positive number for each one of said plurality of sensors; totaling all temperature changes for each one of plurality of sensors to form a total error for each sensor; and comparing said total error of each sensor to said predetermined signal noise threshold to determine if said total error exceeds said predetermined threshold or not and instructing an operator to re-apply said sensor pad to the skin and obtaining a new set of temperature data for all of said plurality of temperature sensors with said cold source applied if said predetermined threshold is exceeded. ### Claim 8 (depends on 7) The apparatus of claim 7 wherein said sensor processing device comprises a post-test setting mode in which said device alerts the operator that temperature data collected by at least one of said plurality of temperature sensors during said evaluation of CSF flow rate or CSF status exceeds a predetermined threshold for signal noise standard deviation and that said evaluation of CSF flow rate or CSF status should be repeated, said post-test setting mode comprising the steps of: separating temperature data collected from each one of said plurality of temperature sensors into time increments of multiple seconds; establishing a straight line for each one of said temperature data within each time increment; computing a standard deviation of an actual temperature signal with said straight line; averaging all of said standard deviations to form an average standard deviation; comparing said average standard deviation to an experimentally-established threshold; and activating a warning to the operator whenever said average standard deviation exceeds said experimentally-established threshold in order to have the operator re-collect temperature data from said plurality of temperature sensors by running said evaluation of said CSF flow rate or CSF flow status again. ### Claim 9 (depends on 1) The apparatus of claim 1 wherein said plurality of temperature sensors are coupled to a flex circuit secured to a first side of said body, said flex circuit configured to be in contact with the skin and configured to be applied to the skin, said flex circuit being conformable to the clavicle of the patient when said sensor pad is applied to the skin. ### Claim 10 (depends on 9) The apparatus of claim 9 wherein said plurality of temperature sensors comprises three temperature sensors and wherein said flex circuit comprises a long side segment from which projects three prongs, each comprising a respective one of said three temperature sensors and wherein said long side segment is transversely positioned across said body, said long side segment with said three prongs forming a configuration that minimizes a bulk of said flex circuit near said temperature sensors for reducing thermal conductivity and thermal crosstalk between said temperature sensors, thereby providing higher quality temperature signals. ### Claim 11 (depends on 10) The apparatus of claim 10 wherein said three temperature sensors are positioned 15 mm from each other. ### Claim 12 (depends on 10) The apparatus of claim 10 wherein said flex circuit comprises electric leads and wherein said electric leads are 4 mil wide, said 4 mil wide electrical leads reducing thermal conductivity while improving conformability. ### Claim 13 (depends on 9) The apparatus of claim 9 wherein said flex circuit is coupled to the body using a first adhesive layer applied to said first side. ### Claim 14 (depends on 13) The apparatus of claim 13 wherein a second adhesive layer is applied over said flex circuit, and wherein said second adhesive layer is in direct contact with said first adhesive layer, on said first side and wherein a release liner is applied over said second adhesive layer, said second adhesive layer forming a continuous adhesive layer configured for preventing each one of said plurality of temperature sensors from making contact with the skin of the patient. ### Claim 15 (depends on 9) The apparatus of claim 9 wherein said body comprises a second side, opposite said first side, and upon which alignment indicia is printed for directing the user to position said sensor pad correctly over the CSF shunt. ### Claim 16 (depends on 1) The apparatus of claim 1 wherein said pad comprises an outside edge and wherein a distance (SD) between said outside edge and said plurality of temperature sensors is defined as 16 mm