The invention relates to neuroprotection apparatus.
Induced hypothermia is an established therapeutic treatment for treating medical conditions and an established therapeutic procedure during surgical procedures. Induced hypothermia can be classified as either induced systemic hypothermia for controlled reduction of a patient's core body temperature below 37 ° C. or induced local hypothermia for controlled reduction of the temperature of a particular organ or body part below 37° C. Induced hypothermia classification delineates induced mild hypothermia at 34-36.9° C., induced moderate hypothermia at 32-33.9° C., inducted moderate/deep hypothermia at 30-31.9° C. and deep induced hypothermia at <30° C. Conventional techniques for achieving induced systemic hypothermia include inter alia entire body immersion in ice water to reduce core body temperatures, a heart-lung machine to cool a patient's blood during open heart surgery, and the like. Heart-lung machines are typically capable of cooling a patient's blood supply from a normal 37° C. core body temperature to a chilled 33° C. Conventional techniques for inducing local brain hypothermia include inter alia helmets for external cooling of a stroke patient's head, IntraArterial Cold Infusion (IACI) regimes, and the like.
A human brain weighs only a small fraction typically in the range of 2-3% of human body weight but human cerebral blood flow is typically about 15% of human cardiac output. Accordingly, the temperature of a human brain changes considerably faster than core body temperature and IACI regimes have been shown to induce highly selective brain temperature decrease within minutes and reach targeted local hypothermia 10 to 30 times faster than conventional induced systemic hypothermia. IACI regimes typically chill a human brain from core body temperature to between 32° C. to 34° C. within 10 minutes.
Terminating induced systemic or local brain hypothermia can lead to neurodamage because of brain tissue heating up too rapidly from its induced hypothermic state. The preferred warming rate of a human brain from a hypothermic state to normal core body temperature is 30 about 0.5° C. per hour. After administration of cold infusion to induce a human brain into a hypothermic state and termination of the cold infusion, a hypothermic human brain naturally warms at a rate of about 2° C. per hour from its hypothermic state to its normal core body temperature due to incoming blood flow at normal 37° C. body core temperature and its ongoing cerebral activity which is a much higher than the preferred 0.5° C. per hour warming rate. Terminating induced systemic hypothermia results in a hypothermic human brain naturally warming at a slower rate than 2° C. per hour but still higher than the preferred 0.5° C. per hour warming rate.
Ischemic strokes lead to the formation of an ischemic infarct as a result of an obstruction by embolism or thrombosis, a hyperemic borderzone upstream of the infarct due to accumulation of vasoactive metabolites and acidosis, and a collaterally perfused ischemic penumbra region downstream of the infarct in the direction of flow of the blood stream. Such obstructions can be from about 70% occlusion and greater. A penumbra region is typically defined when blood perfusion drops below about 20 ml/100 g/min as opposed to normal perfusion of about 50 to 60 ml/100 g/min. The ischemic infarct is irreversibly injured brain tissue whilst the penumbra region is at risk but is salvageable if reperfusion occurs within a reasonably short period of several hours. Salvation of a penumbra region can be assisted by induced either systemic or local brain cooling which attributes to a reduction in oxygen demand: a 1° C. decrease in brain temperature lowers cerebral oxygen consumption by about 5% thus increasing tolerance to ischemic conditions.
IACIs are typically 3° C. to 4° C. saline solutions at a proximal indwelling catheter end 20 before infusion. IACIs are possibly mediated by suitable drugs including inter alia TPA, and the like. Typical IACI regimes involve the infusion of 5 to 30 cc/min over the period of several hours leading to a total saline infusion of from about 2 liter to 3 liter. Clinical practitioners intending on administering an IACI regime to a stroke patient for neuroprotection from ischemic brain damage are required to determine the most suitable cerebral target location of an indwelling catheter. Conventional brain scan technologies including inter alia MRI, CT, and the like, detect the three dimensional boundaries of an ischemic infarct and its associated penumbra for the purpose of accurate placement of an indwelling catheter upstream of an ischemic infarct. The brain scans also include information regarding degrees of occlusions of arteries and/or veins, blood flow in vessels, and perfusion in neurons. Clinical practitioners using conventional fluoroscopy units are capable of relatively accurate placing an indwelling catheter at a desired location. However, an arterial obstruction can cause the diversion of a considerable proportion of infusion flow from its intended artery to an adjoining artery thereby not cooling a penumbra downstream of an occlusion. Moreover, an indwelling catheter also may cause a considerable change to a flow regime of incoming saline due its relative large size compared to a brain artery in which it is placed. Accordingly, it is difficult to predict to what degree a penumbra is being cooled by a chilled infusion flow.
ThermopeutiX, Inc., San Diego, USA is developing systems and methods for selective cooling of a target site including a catheter having a supply lumen and a delivery lumen with inlet and outlet ports. Blood is withdrawn from the supply lumen and cooled or heated in a control unit. The treated blood is sent to a targeted area via delivery lumen. ThermopeutiX, Inc. is assignee of inter alia U.S. Pat. No. 8,192,392 entitled Methods for Selective Thermal Treatment to Solar et al.
“Brain temperature changes during selective cooling with endovascular Intracarotid Cold Saline Infusion (ICSI): simulation using human data fitted with an integrated mathematical model”, published in Journal of NeuroIntervention Surgery 2013; 5:165-171 by Matthew Aaron Harold Neimark et al. discloses a 3D thermal model for determining a temperature at spherical sections in a 3D space. The article discloses the use of dominant superior internal Jugular Venous Bulb blood Temperature (JVBT) as a surrogate for ipsilateral brain temperature. The article discloses the 3D thermal model is applied in two modes: (1) a forward model mode runs the 3D thermal model using initial conditions particular to each patient; and (2) an inverse model mode fits measured JVBT data to the model. The output of the forward mode provides expected jugular venous temperatures which may be used as a rough means of validating model fidelity. The output of the inverse mode provides estimates of intracranial brain temperatures which may be used as a means to better evaluate the feasibility of ICSI to obtain therapeutic brain temperatures. The article discusses that jugular venous blood contains a mixture of blood draining superficial and deep brain tissue from both cerebral hemispheres, infratentorial brain and extracranial tissues such that more accurate determination of the actual brain or Ipsilateral Anterior Circulation Territory (IACT) temperature during Intracarotid Cold Saline Infusion (ICSI) would be beneficial.
U.S. Pat. No. 8,343,097 entitled Systems and Methods for Intravascular Cooling to Pile-Spellman et al. discloses an indwelling catheter with a multitude of sensors therealong and a feedback system utilized to control the volume, temperature and/or infusate rate of an infusate to achieve a predetermined temperature at a target location based on sensed temperatures. US '097
There is a need for neuroprotection apparatus for assisting clinical practitioners to monitor brain temperatures during three phases of induced either systemic or local brain hypothermia as follows: Phase 1 for cooling of a human brain from normal 37° C. body core temperature to steady state hypothermia. Phase 2 for maintaining a human brain at steady state hypothermia. And Phase 3 for warming a human brain from steady state hypothermia to normal 37° C. body core temperature. There is yet a further need for improved administration of Intra-Arterial Cold Infusion (IACI) regimes for inducing local brain hypothermia.
The present invention is directed towards neuroprotection apparatus including a scalp temperature measurement acquisition device for acquiring scalp temperature measurements at a plurality of locations on a patient's scalp during an induced hypothermia and a neuroprotection processor for processing the scalp temperature measurements for determining real time patient temperature information for display on a human head image on a display device during the induced hypothermia.
Cerebral temperature changes take at least several minutes on infusion of a chilled infusion liquid to consecutively chill a brain, a cranium and a scalp to induce detectable temperature changes on a patient's scalp such that neuroprotection apparatus of the present invention affords near real-time clinical feedback. Moreover, cerebral temperature changes are also a function of the locations of one or more cold infusion sources in a patient's head. Accordingly, in the case of a single cold infusion source deployed in a patient's right middle cerebral artery (MCA), it will take longer for a detectable temperature change to appear on the left side of the patient's head as opposed to his right side. Also, after reaching hypothermic steady state, the right side of the patient's head will be colder than his left side.
The neuroprotection processor can process acquired scalp temperature measurements for determining a so-called patient scalp isotherm map. The scalp temperature measurements can be the result of induced either systemic or local brain hypothermia. Patient scalp isotherm maps typically include at least two scalp isotherms, namely, an innermost scalp isotherm which is the coldest scalp isotherm and an outermost scalp isotherm which is the warmest scalp isotherm corresponding to a normal scalp skin temperature typically in the range of from 34° C. to 35° C. depending on ambient temperatures. The human head image can preferably be an image of a patient's head.
The neuroprotection processor can process thermodynamic information in a 3D thermal model of an upper generally hemispherical section of a human head including its brain, cranium and scalp, for determining a so-called patient 3D temperature estimation mapping. The patient 3D temperature estimation mapping includes temperature estimations of 3D finite elements within the upper generally hemispherical section of a human head as bounded by the 3D thermal model. A suitable 3D thermal model is described in hitherto mentioned “Brain temperature changes during selective cooling with endovascular intracarotid cold saline infusion: simulation using human data fitted with an integrated mathematical model”, Neimark et al., published in J NeuroIntervent Surg 2013:5:1651-71 doi:10.1136/neurintsurg-2011-010150.
The 3D thermal model can be applied with induced either systemic or local hypothermia. In induced systemic hypothermia, the 3D thermal model models four cold infusion sources delivering chilled blood to a human brain, namely, a right pair of a carotid artery and a vertebral artery and a left pair of a carotid artery and a vertebral artery. In induced local brain hypothermia, the 3D thermal model typically models a single indwelling catheter tip as a cold 25 infusion source delivering infusion liquid to a human brain. The infusion liquid delivered by the single indwelling catheter may be saline, blood, a combined blood saline infusion, and the like. The 3D thermal model processes flow parameters associated with a cold infusion source including inter alia infusion temperature, infusion flow rate, and the like. The flow parameters can be obtained from a suitable indwelling catheter fitted with required sensors at its catheter tip. Also, the neuroprotection processor processes the location of the catheter tip of an indwelling catheter. The neuroprotection processor can display the temperature estimations of the 3D finite elements on one or more of the standard sagittal planes, transverse planes and coronal planes, and also cross sections selected by a clinical practitioner. The neuroprotection processor preferably displays the 3D temperature estimation mapping of the 3D finite elements on a MRI/CT scan image of a patient's head.
One preferred embodiment of a scalp temperature measurement acquisition device in accordance with the present invention includes one or more thermal imaging cameras for acquiring scalp temperature measurements. Another preferred embodiment of a scalp temperature measurement acquisition device in accordance with the present invention includes a temperature measurement sensor array in skin contact with a patient's scalp for acquiring scalp 10 temperature measurements. The scalp temperature measurement acquisition device can include a scalp cooling arrangement for external cooling a patient's scalp for assisting induced local hypothermia of stroke brains. The scalp temperature measurement acquisition devices can be designed as a disposable medical grade item intended for single patient use. Alternatively, scalp temperature measurement acquisition devices can be intended for multiple patient use. Single patient use scalp temperature measurement acquisition devices with a temperature measurement sensor array in skin contact with a patient's scalp can resemble stretch fit swim caps.
The neuroprotection apparatus can include a computer database having a benchmark stroke brain clinical image collection of benchmark stroke brain clinical images. The benchmark stroke brain clinical images each include an occlusion, an ischemic infarct and a downstream penumbra region. The benchmark stroke brain clinical images differ in terms of the location of an ischemic infarct, an occlusion percentage and size of its associated penumbra region. The benchmark stroke brain clinical images preferably also include clinical instructions including at least one of a placement of an indwelling catheter, infusion liquid flow rate, infusion liquid temperature and infusion liquid duration for administrating infusion liquid. A clinical practitioner can refer to the benchmark stroke brain clinical image collection to assist him to decide the most suitable IACI regime for a particular stroke patient.
The computer database can also include benchmark temperature information for assisting a clinical practitioner to monitor an induced either systemic or local brain hypothermia. The benchmark temperature information can assist a clinical practitioner to decide whether he needs to adjust one or more of the location of an indwelling catheter, an infusion liquid temperature and an infusion liquid flow rate during administration of an IACI regime thereby improving their neuroprotection efficacy. The benchmark temperature information can assist a clinical practitioner during the three phases of an induced either systemic or local brain hypothermia. The benchmark temperature information can include a benchmark scalp isotherm map collection of benchmark scalp isotherm maps and/or a benchmark 3D temperature estimation mapping collection of benchmark 3D temperature estimation mappings. The benchmark scalp isotherm map collection of benchmark scalp isotherm maps are cross referenced to the benchmark stroke brain clinical image collection of benchmark stroke brain clinical images. Similarly, the benchmark 3D temperature estimation mapping collection of benchmark 3D temperature estimation mappings are cross referenced to the benchmark stroke brain clinical image collection of benchmark stroke brain clinical images.
The neuroprotection processor can be programmed to compare acquired patient scalp temperature measurements to corresponding benchmark temperature information during an ongoing induced systemic or local brain hypothermia to determine a benchmark error index. Benchmark index errors can be useful for indicating a range of clinical occurrences requiring corrective action. Exemplary clinical occurrences include inter alia an incorrect region of a human brain is being cooled, a human brain is being chilled to too low a hypothermic temperature, a human brain is warming at a higher rate than the preferred 0.5° C. warming rate, and the like. The neuroprotection processor can compare the benchmark error index to a benchmark error threshold to automatically issue an alert for alerting a clinical practitioner.
In order to understand the invention and to see how it can be carried out in practice, preferred embodiments will now be described, by way of non-limiting examples only, with reference to the accompanying drawings in which similar parts are likewise numbered, and in which:
The patient is a stroke victim with a stroke brain having an occlusion 21 located, for example, along a Middle Cerebral Artery (MCA). The occlusion 21 can typically occupy from about 70% to about 90% of a cross sectional diameter of a cerebral artery. The occlusion 21 leads to an ischemic infarct 22 and a downstream penumbra region 23.
The neuroprotection apparatus 100 includes an operator interface 107 for entering patient information and induced hypothermia procedure details. Patient details include inter alia name, age, weight, and the like. Induced hypothermia procedure details include inter alia date, time, clinical practitioner, and the like. The operator interface 107 also enables a clinical practitioner to write notes in a free text box.
The benchmark stroke brain clinical images 113 preferably include preferred cerebral target locations for placement of indwelling catheters. The benchmark stroke brain clinical images 113 preferably include instructions regarding a preferred infusion liquid temperature, a preferred infusion liquid flow rate and a preferred infusion administration time for administrating an infusion. The benchmark stroke brain clinical images 113 also preferably include instructions regarding the use of micro-catheters for traversing through nearly 100% occlusions for directly delivering cold infusion liquid to a downstream penumbra region.
The computer database 111 also preferably includes benchmark temperature information in the form of a benchmark scalp isotherm map collection 114 of benchmark scalp isotherm 15 maps 116. A clinical practitioner can use the benchmark scalp isotherm map collection 114 during induced either systemic or local brain hypothermia to assist him to decide whether the patient's brain is being cooled according to a predetermined clinical protocol. Similarly, a clinical practitioner can use the benchmark scalp isotherm map collection 114 during restoration of a patient's brain from an induced hypothermic state to a normal core body temperature to assist him to decide whether the patient's brain is being warmed according to a predetermined clinical protocol to avoid too rapid warming which can inadvertently lead to neurodamage.
The benchmark scalp isotherm map collection 114 can include benchmark scalp isotherm maps 116 at different time intervals during the three phases of induced systemic or local brain hypothermia, namely, from normal core body temperature to steady state hypothermia, maintaining steady state hypothermia and warming from steady state hypothermia to normal core body temperature. Steady state in induced local brain hypothermia is usually reached within 10 to 20 minutes. Steady state in induced systemic hypothermia usually takes considerably longer. Suitable time intervals between consecutive benchmark scalp isotherm maps 116 are, say, between 3 to 5 minutes. The benchmark scalp isotherm map collection 114 can include benchmark scalp isotherm maps 116 acquired during infusions at different infusion liquid temperatures and/or different infusion liquid flow rates. The benchmark scalp isotherm map collection 114 can include benchmark scalp isotherm maps 116 acquired during induced systemic hypothermia at different blood temperatures and/or different blood rates and/or different body weights.
Exemplary uses of the benchmark scalp isotherm maps 116 are as follows: A clinical practitioner notices that a cold spot is developing on a stroke scalp in a location that does not match the location in which it should be developing in order to best treat a stroke patient. The clinical practitioner decides to reposition the catheter tip of an indwelling catheter to correspondingly modify the location of the developing cold spot.
A clinical practitioner notices that a cold spot is developing on a stroke scalp in a location that does match the location in which it should be developing but is developing too slowly. The clinical practitioner decides to not to reposition the indwelling catheter's catheter tip but rather decrease the infusion liquid temperature being administered at the same infusion liquid flow rate. Alternatively, the clinical practitioner could decide to increase the infusion liquid flow rate at the same infusion liquid temperature. Alternatively, again the clinical practitioner could decide to modify both the infusion liquid flow rate and the infusion liquid temperature.
A clinical practitioner regards that a patient's brain is being warmed too quickly on restoration from steady state hypothermia back to normal body core temperature. The clinical practitioner decides he decreased the infusion liquid flow rate too much and decides to increase same to slow down the warming. Alternatively, the clinical practitioner decides he increased the infusion liquid temperature too much and decides to decrease same to slow down the warming.
The neuroprotection processor 102A can be programmed to superimpose a patient scalp isotherm map on a benchmark scalp isotherm map to assist a clinical practitioner to discriminate the difference therebetween. The neuroprotection processor 102A can be programmed to compare acquired scalp temperature measurements to corresponding benchmark scalp temperature measurements during an ongoing induced systemic or local brain hypothermia to determine a benchmark error index. The benchmark error index can be determined using well known statistical techniques for comparing two sets of actual values and benchmark values. The benchmark error index can possibly include weighting factors for different isotherms, for example, the coldest isotherm can be weighted higher than the warmest isotherm. The neuroprotection processor 102A can compare the benchmark error index to a benchmark error threshold to automatically issue an alert for alerting a clinical practitioner. Suitable alerts include inter alia a visual alert, an audible alert, a SMS, and the like.
The neuroprotection processor 102B runs a 3D thermal model of an upper generally hemispherical section of a human head including its brain, cranium and scalp, for determining the patient 3D temperature estimation mapping 123. A suitable 3D thermal model can be based on a mathematical model described in hitherto described “Brain temperature changes during selective cooling with endovascular intracarotid cold saline infusion: simulation using human data fitted with an integrated mathematical model”, Neimark et al., published in J NeuroIntervent Surg 2013:5:1651-71 doi:10.1136/neurintsurg-2011-010150. The patient 3D temperature estimation mapping 123 includes temperature estimations of 3D finite elements of the 3D thermal model. The 3D finite elements of the 3D thermal model can be color coded in a similar manner to the scalp isotherm map 103.
Human brains have similar but not identical structures such that a 3D thermal model can only model an exemplary human brain and not a particular patient brain. The location of a placement of an indwelling catheter's catheter tip can only be estimated to within a few millimeters but such few millimeters can lead to considerable changes in cerebral blood flow. Also, the presence of an indwelling catheter and an infarct within an artery can considerably modify cerebral blood flow and/or cold infusion liquid flow within a stroke brain. Accordingly, the neuroprotection processor 102B runs the 3D thermal model in two modes as follows: a 3D thermal model configuration mode and a configured 3D thermal model ongoing procedure mode. The 3D thermal model configuration mode is intended to configure certain parameters of the 3D thermal model to a particular induced systemic or local brain hypothermia at hand including determining the location of an indwelling catheter's catheter tip within the 3D thermal model. The configured 3D thermal model ongoing procedure mode runs the configured 3D thermal model for the remainder of a patient induced hypothermia procedure.
The neuroprotection processor 102B processes flow parameters associated with an infusion source including inter alia infusion temperature, infusion flow rate, infusion duration, and the like, and acquired scalp temperature measurements. The flow parameters can be obtained from a suitable indwelling catheter fitted with required sensors at its catheter tip. The neuroprotection processor 102B also processes the location of a catheter tip of an indwelling catheter within a human brain. The flow parameters can be input manually at the operator interface 107. Alternatively, the flow parameters can be input to the neuroprotection processor 102B automatically. For example, the location of a catheter tip can be determined by a magnetic sensor.
The neuroprotection processor 102B can run the 3D thermal model in a forward model mode only in an iterative closed loop manner as follows: The neuroprotection processor 102B processes flow parameters of an induced hypothermia including the placement of an indwelling catheter, the infusion liquid flow rate and the infusion liquid temperature for determining a patient 3D temperature estimation mapping of a upper generally hemispherical section of a patient's head. The neuroprotection processor 102B compares the 3D temperature estimations at particular locations on the patient's scalp to the acquired scalp temperature measurements thereat to determine the deviations therebetween. The neuroprotection processor 102B can calculate a deviation between the 3D temperature estimation at a particular scalp location and the acquired scalp temperature measurement thereat from at least tens of scalp locations up to thousands of scalp locations depending on the scalp temperature measurement acquisition device 101. The greater the number of scalp locations taken into account improves the accuracy of the neuroprotection processor 102B but with the downside that each run of the 3D thermal model takes longer.
The neuroprotection processor 102B determines a deviation index based on the calculated deviations. The deviation index can be determined using well known statistical techniques for comparing two sets of actual values and estimated values. The deviation index can possibly include weighting factors for different isotherms, for example, the coldest isotherm can be weighted higher than the warmest isotherm. The neuroprotection processor 102B compares the calculated deviation index to a deviation threshold for determining whether to re-position the placement of the indwelling catheter in the 3D thermal model. For example, a deviation index can be the average temperature difference at all the scalp locations at which actual scalp temperature measurements have been acquired and a deviation threshold can be ±0.5° C. temperature difference. The deviation threshold can be optionally set by a clinical practitioner by means of the operator interface 107.
The neuroprotection processor 102B configures the 3D thermal model in the case a deviation index is less than a deviation threshold. If, however, a deviation index is greater than a deviation threshold, the neuroprotection processor 102B modifies the location of the placement of the indwelling parameter within the 3D thermal model and re-runs the 3D thermal model. The location of the placement of the indwelling catheter is selected from the three flow parameters for remodeling purposes because the infusion liquid flow rate and the infusion liquid temperature can be measured to a much higher degree of accuracy than the location of the placement of the indwelling catheter can be estimated based on a fluoroscopy image.
The direction of modification of the location of the placement of an indwelling catheter within an artery depends on whether the scalp temperature estimations are at higher temperatures than the actual scalp measurement temperatures or at lower temperatures than the actual scalp measurement temperatures. In the case of a particular scalp location, if the scalp temperature estimation thereat is colder than the acquired scalp temperature measurement thereat, then the 3D thermal model assumed the placement of an indwelling catheter is further downstream along an artery than it actually is on running the 3D thermal model. Therefore, the 3D thermal model needs to be re-run with the indwelling catheter placed further upstream. If, however, the scalp temperature estimation is warmer than the acquired scalp temperature measurement thereat, then the 3D thermal model assumed a placement of an indwelling catheter is more upstream along an artery than it actually is on running the 3D thermal model. Therefore, the 3D thermal model needs to be re-run with the indwelling catheter placed further downstream.
Alternatively, the neuroprotection processor 102B can run the 3D thermal model in the same two model modes as the hitherto described Neimark article, namely, in a forward model mode and an inverse model mode. In the forward model mode, the neuroprotection processor 102B processes flow parameters associated with an infusion source including inter alia infusion temperature, infusion flow rate, and its location. In the inverse model mode, the neuroprotection processor 102B processes the acquired scalp temperature measurements.
After configuration, the neuroprotection processor 102B proceeds to periodically run the configured 3D thermal model to display the patient scalp isotherm map 122 and/or a patient 3D temperature estimation mapping 123 on a human head image on a display device during an ongoing hypothermia. The neuroprotection apparatus 100 continues to acquire scalp temperature measurements from a patient scalp during ongoing procedure mode as a back-up safety measure in view of occurrences which can take occur during induced systemic or local brain hypothermia. Exemplary occurrences can include inter alia movement of an indwelling catheter, change in cerebral blood flow, formation of a blockage along an indwelling catheter, and the like. Thus, in the case of a drift between patient 3D temperature estimations and acquired scalp temperature measurements greater than an acceptable drift, then a clinical practitioner is required to investigate the source of the drift.
The computer database 111 storing the benchmark temperature information can further include a benchmark 3D temperature estimation mapping collection 124 of benchmark 3D temperature estimation mappings 126. The benchmark 3D temperature estimation mappings 126 can be determined at different times of the three phases of an induced systemic or local brain hypothermia from cooling from normal core body temperature through to steady state hypothermia, maintaining steady state hypothermia and warming from steady state hypothermia to normal core body temperature. A clinical practitioner can use the benchmark 3D temperature estimation mappings as a clinical reference during an ongoing induced hypothermia and restoring a patient's brain to normal core body temperature.
The temperature measurement sensor array 161 includes four temperature measurement sensor strips 162 aligned co-directional with the XZ sagittal plane on opposite sides of the patient's head. The preferred separation angle between adjacent temperature measurement sensor strips 162 is about α=15-20°. Each temperature measurement sensor strip 162 includes a 20 foremost sensor 163A above the patient's forehead frontal bone and a rearmost sensor 163B located slightly above the patient's parietal bone. The distance between adjacent sensors 163 along a temperature measurement sensor strip 162 is between about 5 mm and 15 mm such that each temperature measurement strip includes about 25 sensors. Accordingly, the scalp temperature measurement acquisition device 101C includes about 25×8=200 sensors 163. The sensors 163 preferably project between about 0.5 mm and 1.5 mm from the internal surface of the scalp temperature measurement acquisition device 101C for facilitating intimate contact with an outermost scalp skin surface 13. Suitable sensors 163 include, for example, NCP Series thermistors commercially available from Murata Ltd, Japan. Biocompatible thermal conductive gel or adhesive material is preferably employed for facilitating thermal measurements of the outermost scalp skin surface 14.
The clinical set up 200 includes a scan unit 201 for scanning a stroke patient's head 10 for displaying brain scans 202 on a display screen 203. The brain scans 202 can be along XY transverse planes, XZ sagittal planes, YZ coronal planes, and additional planes selected by a clinical practitioner. Suitable scan units 201 include MRI scan units and CT scan units. MRI employs lack of diffusion for determining the three dimensional boundary of an ischemic infarct 10 and perfusion for determining the three dimensional boundary of its associated upstream penumbra region. CT employs perfusion and angiography for determining the three dimensional boundaries of an ischemic infarct and its associated upstream penumbra region. The scan unit 201 is capable of providing brain scans for clearly visualizing a cerebral circulatory structure.
Brain scans 202 provide initial clinical stroke information including inter alia the location of an occlusion and its occlusion percentage, the boundary of its resulting ischemic infarct, the boundary of its associated upstream penumbra region, and the like. A clinical practitioner determines a preferred cerebral target location of an indwelling catheter 204 based on the brain scans 202 to best induce therapeutic hypothermia in the penumbra region 23 in order to prevent further infarction.
Suitable indwelling catheters 204 include inter alia a cerebral angiography diagnostic catheter with a size of 3 to 5 French. An indwelling catheter 204 is typically introduced via a sheath introducer (not shown). Suitable angiography diagnostic catheters include inter alia the Performa series Simmons 2 catheter available from Merit Medical Systems, Inc., Utah, USA www.meritoem.com. Such indwelling catheters 204 include a proximal end 204A for remaining 25 external to a patient and a distal end 204B for placement at a cerebral target location. The distal end 204B includes an opaque marking 204C for X ray imaging purposes. Such indwelling catheters 204 include steerage means for enabling its navigation to a preferred cerebral target location. Such indwelling catheters 204 preferably include insulation to avoid heating of cold saline from its proximal end external to the stroke patient to its distal end at a preferred cerebral target location. The indwelling catheters 204 can optionally be an open irrigation cryocatheter as disclosed in PCT International Application Number PCT/IL2013/050363 entitled Cryocatheter with Coolant Fluid Cooled Thermoelectric Module published under WIPO International Publication Number WO 2013/164820.
The clinical set-up 200 includes a fluoroscopy unit 207 for assisting clinical practitioners to place indwelling catheters 204 at preferred cerebral target locations. The fluoroscopy unit 207 displays a brain image 208 of a stroke brain 12 and the distal end 204B with the opaque marking 204C on a display screen 209. The clinical set-up 200 includes a saline source 211 of cold saline and control apparatus 212 for controlling the administration of an IACI regime to a stroke patient. The control apparatus 212 includes a peristaltic pump 213 for administering cold saline to a stroke patient.
Comparison between the
Comparison between
Step 1: Clinical practitioner acquires a brain scan of a stroke brain.
Step 2: Clinical practitioner compares the acquired brain scan to the benchmark stroke brain clinical image collection to select the benchmark stroke brain clinical image mostly closely matching the acquired brain scan.
Step 3: Clinical practitioner inserts an indwelling catheter at a preferred cerebral target for administering an IACI regime to the stroke brain in accordance with the selected benchmark stroke brain clinical image.
Step 4: Clinical practitioner sets the clinical set up to deliver the infusion liquid at a predetermined temperature of the infusion liquid and a predetermined flow rate.
Step 5: Clinical practitioner sets up the neuroprotection apparatus to acquire patient scalp temperature measurements.
Step 6: Clinical practitioner employs the neuroprotection apparatus to monitor the three phases of IACI regime and take corrective if required:
Phase 1: Cooling patient scalp from normal scalp skin temperature Ts to steady state hypothermia.
Phase 2: Maintaining patient scalp at steady state hypothermia
Phase 3: Warming patient scalp from steady state hypothermia to normal scalp skin temperature Ts.
In the case of the neuroprotection processor 102A and the benchmark scalp isotherm map collection 114, a clinical practitioner compares acquired patient scalp isotherm maps to benchmark scalp isotherm maps corresponding to the benchmark stroke brain clinical image to determine whether the acquired patient scalp isotherm map is within an acceptable tolerance. In the affirmative, the clinical practitioner is not required to take any corrective action. In the negative, the clinical practitioner should take corrective action with the intention of reducing the difference between acquired patient scalp isotherm map and the benchmark scalp isotherm map. Such corrective change can include one or more of moving the indwelling catheter, changing the infusion liquid temperature, and changing the infusion liquid flow rate.
For example, if an acquired brain scan is similar to
Clinical practitioners can employ the neuroprotection processor 102B and the benchmark 3D temperature estimation mapping collection 124 of benchmark 3D temperature estimation mappings 126 in a similar manner.
While the invention has been described with respect to a limited number of embodiments, it will be appreciated that many variations, modifications, and other applications of the invention can be made within the scope of the appended claims.
Number | Date | Country | Kind |
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238716 | May 2015 | IL | national |
Filing Document | Filing Date | Country | Kind |
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PCT/IL2016/050488 | 5/9/2016 | WO | 00 |