DEVICES, SYSTEMS AND METHODS FOR ENDOVASCULAR TEMPERATURE CONTROL
Devices, systems and methods for controlling a patient's body temperature by endovascular heat exchange and/or surface heat exchange.
This is a continuation in part of copending U.S. patent application Ser. No. 15/594,541 entitled Devices, Systems and Methods for Endovascular Temperature Control filed May 12, 2017, which is a continuation in part of U.S. patent application Ser. No. 15/423,581 entitled Devices, Systems and Methods or Endovascular Temperature Control filed Feb. 2, 2017. Additionally, this application is a continuation in part of copending PCT International Patent Application No. PCT/US18/16754 entitled Devices, Systems and Methods for Endovascular Temperature Control filed Feb. 2, 1018. The entire disclosure of each such prior application is hereby expressly incorporated herein by reference.
FIELD OF THE INVENTIONThe present disclosure relates generally to the fields of medicine and engineering and more particularly to devices, systems and methods for controlling a patient's body temperature by endovascular heat exchange.
BACKGROUNDPursuant to 37 CFR 1.71(e), this patent document contains material which is subject to copyright protection and the owner of this patent document reserves all copyright rights whatsoever.
In various clinical situations, it is desirable to warm, cool or otherwise control the body temperature of a subject. For example, hypothermia can be induced in humans and some animals for the purpose of protecting various organs and tissues (e.g., heart, brain, kidneys) against the effects of ischemic, anoxic or toxic insult. For example, animal studies and/or clinical trials suggest that mild hypothermia can have neuroprotective and/or cardioprotective effects in animals or humans who suffer from ischemic cardiac events (e.g., myocardial infract, acute coronary syndromes, etc.), postanoxic coma after cardiopulmonary resuscitation, traumatic brain injury, stroke, subarachnoid hemorrhage, fever and neurological injury. Also, studies have shown that whole body hypothermia can ameliorate the toxic effects of radiographic contrast media on the kidneys (e.g., radiocontrast nephropathy) of patients with pre-existing renal impairment who undergo angiography procedures.
One method for inducing hypothermia is by endovascular temperature management (ETM) wherein a heat exchange catheter is inserted into a blood vessel and a thermal exchange fluid is circulated through a heat exchanger positioned on the portion of the catheter that is inserted in the blood vessel. As the thermal exchange fluid circulates through the catheter's heat exchanger, it exchanges heat with blood flowing past the heat exchange in the blood vessel. Such technique can be used to cool the subject's flowing blood thereby resulting in a lowering of the subject's core body temperature to some desired target temperature. ETM is also capable of warming the body and/or of controlling body temperature to maintain a monitored body temperature at some selected temperature. If a controlled rate of re-warming or re-cooling from the selected target temperature is desired, that too can be accomplished by carefully controlling the amount of heat added or removed from the body and thereby controlling the temperature change of the patient.
SUMMARYIn accordance with the present disclosure, there are provided heat exchange devices, systems and methods which facilitate efficient endovascular and/or body surface heat exchange.
In accordance with one embodiment, there is provided a system for circulating a warmed or cooled thermal exchange fluid through an endovascular heat exchanger (e.g., an endovascular heat exchange catheter), wherein a) the system produces a pulsatile flow of thermal exchange fluid and b) the system is connected to the endovascular heat exchanger by way of one or more conduits which comprise a pulse damping conduit that functions not only as a conduit through which the thermal exchange fluid flows but also a pulse damper for damping pulses or pressure in the thermal exchange fluid as it flows therethrough. The pulse damping conduit may comprise, for example, tubing that has sufficient elastic or flexural properties to dampen or reduce the amplitude of pulses in the thermal exchange fluid as it flows therethrough.
In accordance with another embodiment, there is provided a system for warming or cooling the body of a human or animal subject, such system comprising an extracorporeal control system that is connectable to one or more changeable component(s) (e.g., an endovascular heat exchange catheter, a body surface heat exchange pad, tubing, a cassette through which thermal exchange fluid circulates, other disposable components, etc.). When the changeable component(s) is/are connected to the extracorporeal control system, the system is useable to effect heat exchange with the subject's body. The changeable component(s) may include machine readable encoded information. The extracorporeal control system includes a reader or processor that receives and reads the encoded information. The extracorporeal control system uses such encoded information to identify, qualify, confirm or control the operation of the changeable component(s). The encoded information may be stored in any suitable electronic storage medium and may be embedded in a chip or microchip mounted on or in the changeable component(s). Examples of the types of encoded information that may be stored include but are not limited to; unique identifier(s) for the changeable components (e.g., manufacturer identification, part number, lot number, etc.), indications of whether the changeable component(s) have previously been used (e.g., an encoded indication of first use), indications of whether the changeable component(s) is/are expired (e.g., encoded expiration date), operational characteristic(s) and or operational variables (e.g., minimum and/or maximum pressure, minimum and or maximum flow rate, control algorithm to be used, etc.) of the changeable component(s) (e.g., encoded indications of the size, type, volume, etc. of the changeable component(s). Examples of the types of information storage that may be utilized include but are not necessarily limited to: non-volatile random access memory (RAM), non-volatile flash memory, electrically erasable programmable read-only memory (EEPROM) or ferroelectric random access memory (FRAM). The extracorporeal control system may comprises a controller (e.g., a processor) programmed to take one or more actions in response to the encoded information. For example, the controller may be programmed to determine whether the encoded information meets a prerequisite requirement and to proceed with warming or cooling of the subject's body only if said prerequisite requirement is met.
In accordance with another embodiment, there is provided a thermal exchange engine for warming or cooling a thermal exchange fluid. Such thermal exchange engine comprises thermal exchange plates or evaporators which are alternately coolable by circulation of refrigerant through the plates and warmable by heaters positioned on or in the plates. A cassette receiving space is located between the temperature controlled plates and is configured for receiving a cassette or heat exchanger. The cassette comprises a frame and an expandable vessel (e.g., a bag or other expandable fluid containing vessel). The expandable vessel is finable with thermal exchange fluid, e.g., after the cassette has been inserted into the cassette receiving space. Heat is thereby transferred between the refrigerant and the thermal exchange fluid or the heater(s) and the thermal exchange fluid. In some embodiments, outer surface(s) of the expandable vessel may be coated with a release material, covered with a layer of releasable material or otherwise treated or modified to deter sticking of the expandable vessel to the adjacent thermal exchange plates. In some embodiments, surface(s) of the thermal exchange plates and/or surfaces of the expandable vessel or a layer on a surface of the expandable vessel may be textured or provided with holes, groves or other surface features to deter sticking of the expandable vessel to the adjacent thermal exchange plates. In some embodiments, the cassette may comprise a housing attached to an insertable portion (e.g., the frame and expandable vessel) by a hinged attachment such that the cassette may be disposed in a folded or closed configuration prior to use and converted to an unfolded or open configuration at the time of use. Such hinged connection between the housing and the insertable portion may be constructed so that, once unfolded or opened, the cassette locks in the unfolded or open configuration. In some embodiments, a plurality of hooks located in the console or system may be initially positioned in retracted positions allowing insertion of the insertable portion into the cassette receiving space between the thermal exchange plates and, thereafter, may be moved to advanced positions wherein they hold the insertable portion of the cassette within the cassette receiving space.
In accordance with another embodiment, there is provided a system configured to circulate warmed or cooled thermal exchange fluid through a body heat exchanger to warm or cool the body or a human or animal subject, wherein the system comprises a first display device which receives signals from one or more temperature sensors and displays temperature data based on signals received from said one or more temperature sensors. The first display device is connectable, by wired or wireless connectivity, to a second display device (e.g., a bedside monitor, central unit monitor, remote monitor, etc.), so as to transmit said signals received from said one or more temperature sensors from the first display device to the second display device. The system further comprises circuitry for minimizing or eliminating any effect of ambient temperature on such signals as they are transmitted from the first display device to the second display device. In some embodiments, the signals transmitted from the first display device to the second display device may comprise signals representative of sensed temperatures, such as patient body temperature, temperature of thermal exchange fluid flowing to the body heat exchanger, temperature of thermal exchange fluid flowing from the body heat exchanger, etc.
Disclosed herein is a system comprising: a heat exchange catheter which comprises (i) a catheter body having a distal end, (ii) a elongate member attached to the catheter body and extending beyond its distal end, and (iii) at least one helically coiled tube disposed on the elongate member and connected to delivery and return lumen in the catheter body; and fluid cooling apparatus comprising a refrigeration apparatus, cooling plates, and a cassette connected to the delivery and return lumens of the catheter body and operative to circulate a cooled thermal exchange fluid through the cassette, into the catheter, through said at least one helically coiled tube, out of the catheter and back into the cassette, wherein the heat exchange catheter and fluid cooling apparatus and said at least one helically coiled tube are sized, configured and constructed to render the system capable of delivering at least about 600 watts of cooling power. The fluid cooling apparatus may be configured to deliver to the heat exchange catheter a flow of heat exchange fluid that is cooled to a temperature at or below 4° C. at a rate of at least 600 mL/min at steady state, when up to 700 W of heat is being added to the flowing saline as a result of heat exchange through the catheter's heat exchanger. The fluid cooling apparatus may be configured to deliver to the heat exchange catheter a flow of heat exchange fluid that is cooled to a temperature at or below 4° C. at a rate of from 200 mL/min to 240 mL/min at steady state, when up to 70 W of heat is being added to the flowing saline as a result of heat exchange through the catheter's heat exchanger. The fluid cooling apparatus may be configured to deliver to the heat exchange catheter a flow of heat exchange fluid that is warmed to a temperature at or above 42° C. at a rate of at least 400 mL/min at steady state, when up to 200 W of heat is being removed from the flowing saline as a result of heat exchange through the catheter's heat exchanger. The system may be configured to deliver greater than or equal to 600 W of cooling power by circulating heat exchange fluid that is cooled to a temperature at or below 4° C. through the heat exchange catheter at a catheter pressure of about 60 PSI. The system may further comprise heating apparatus useable for warming rather than cooling the heat exchange fluid. Such heating apparatus may deliver greater than or equal to 50 W of warming power by circulating heat exchange fluid that is warmed to a temperature above 37° C. through the heat exchange catheter at a catheter pressure of about 40 PSI.
In another aspect, disclosed herein is a system comprising: at least one set of thermal exchange plates which warm or cool a heat exchange fluid for delivery to a body surface or endovascular heat exchanger; a refrigeration unit for circulating cold refrigerant through said at least one thermal exchange plate; at least one heater for heating the thermal exchange plate; a programmable controller; wherein the system further comprises a bypass circuit for alternately circulating hot refrigerant from the refrigeration unit through said at least one thermal exchange plate; and wherein the controller is programmed to monitor the power output of said at least one heater and, if said power output exceeds a limit, to cause hot refrigerant to flow through the bypass circuit and through said at least one thermal exchange plate, thereby assisting said at least one heater in warming said at least one thermal exchange plate. The controller may be further programmed to incrementally or progressively reduce the amount of hot refrigerant being circulated through said at least one thermal exchange plate in the event that the power output of said at least one heater falls below the limit until a target temperature has been reached.
In another aspect, disclosed herein is a body heat exchange system comprising: heater/cooler apparatus for alternately warming or cooling a heat exchange fluid for delivery to a body heat exchange device for surface or endovascular heat exchange in or on the body of a subject; a pump for circulating the heat exchange fluid through the body heat exchange device; a controller which is programmed to selectively vary both the temperature and flow rate of the heat exchange fluid to maintain the subject's body temperature at or within a permissible range of a target body temperature. The controller may be programmed such that, after a body temperature of the subject has been warmed or cooled to a target temperature, the controller will cause the system to maintain said body temperature at or within a permissible variance range of the target temperature by: holding the temperature of the heat exchange fluid constant and varying the operation of the pump to adjust the flow rate of heat exchange fluid through the catheter as needed to maintain said body temperature at or within a permissible variance range of the target temperature so long as the speed of the pump does not exceed a maximum pump speed; and if the pump exceeds the predetermined maximum pump speed, adjusting the temperature of the heat exchange fluid such that said body temperature at or within a permissible variance range of the target temperature without exceeding the maximum pump speed. If it is necessary to switch between cooling mode and warming mode in order to maintain said body temperature at or within a permissible variance range of the target temperature, the controller may, upon making such switch, adjust the temperature of the heat exchange fluid irrespective of whether the maximum pump speed has been exceeded. The system may be combined with a body heat exchange device. The body heat exchange device may comprise an endovascular heat exchange catheter. The body heat exchange device comprises a body surface heat exchange member.
In another aspect, disclosed herein is a body heat exchange system comprising: heater/cooler apparatus for alternately warming or cooling a heat exchange fluid for delivery to a body heat exchange device for surface or endovascular heat exchange in or on the body of a subject; a pump for circulating the heat exchange fluid through the body heat exchange device; a temperature sensor for sensing the temperature of the heat exchange fluid; a pressure sensor for sensing the pressure of the heat exchange fluid and a controller which receives a maximum pump speed set point and signals from the temperature sensor and pressure sensor, said controller being programmed to: a) establish current cold/warm status of the heat exchange fluid based on the sensed temperature of the heat exchange fluid; b) determining whether operation of the pump at the maximum pump speed set point will cause over-pressurization of the heat exchange fluid or under-pressurization of the heat exchange fluid; and c) if it is determined that operation of the pump at the maximum pump speed set point will cause over-pressurization of the heat exchange fluid, causing the maximum pump speed set point to change to an adjusted maximum pump speed set point at which the pump may operate without causing over-pressurization of the heat exchange fluid; or d) if it is determined that operation of the pump at the maximum pump speed set point will cause an under-pressurization of the heat exchange fluid, causing the maximum pump speed set point to change to an adjusted maximum pump speed set point at which the pump may operate without causing under-pressurization of the heat exchange fluid. The controller may be programmed to perform steps a through c repeatedly. The controller may be programmed to repeat Steps a through c at least once every 3 seconds. The controller may be programmed to repeat Steps a through c every three seconds. The controller may be programmed to cause the maximum pump speed set point to change by applying a maximum pump speed set point adjustment integrator. The application of the maximum pump speed adjustment integrator may cause the maximum pump speed set point to change slowly. The controller may be programmed to determine that operation of the pump at the maximum pump speed set point will cause over-pressurization of the heat exchange fluid based on different maximum pressure limits for cold status and warm status. The maximum pressure limit when operating with cold status heat exchange fluid may, for example, be 40 psi and the maximum pressure limit when operating with warm status heat exchange fluid may, for example, be 60 psi. The controller may be programmed to establish warm status in Step a if the sensed temperature of the heat exchange fluid is above 19.5 degree C. and to establish cold status in Step a if the sensed temperature of the heat exchange fluid is not above 19.5 degrees C. The controller may be further programmed to store the most recent prior maximum pump speed set point for warm status and cold status. The controller may be further programmed such that, if performance of Step a results in a change from warm status to cold status, the controller will reset the maximum pump speed set point to the most recent stored maximum pump speed set point for cold status heat exchange fluid. The controller may be further programmed such that, if performance of Step a results in a change from cold status to warm status, the controller will reset the maximum pump speed set point to the most recent stored maximum pump speed set point for warm status heat.
In another aspect, disclosed herein is a method for deterring reperfusion injury in a human or animal subject who is suffering from ischemia and who undergoes reperfusion to relieve the ischemia, said method comprising the steps of: cooling a body temperature of the subject to a target temperature of 35 degrees C. or below; and performing the reperfusion after the body temperature of the subject has been cooled to the target temperature; and maintaining the target temperature for a period of time after reperfusion. The target temperature may be between 32 degrees C. and 34 degrees C. The step of cooling a body temperature of the subject to a target temperature of 35 degrees C. or below may be performed in less than 30 minutes. The target temperature may be maintained for a period of 1-5 hours after reperfusion. The step of cooling a body temperature of the subject to a target temperature of 35 degrees C. or below in less than 30 minutes may comprise: inserting a heat exchange catheter into the subject's vasculature; circulating heat exchange fluid through the heat exchange catheter at a temperature and flow rate sufficient to cold said body temperature to said target temperature in less than 30 minutes. The heat exchange catheter may comprise (i) a catheter body having a distal end, (ii) a elongate member attached to the catheter body and extending beyond its distal end, and (iii) at least one helically coiled tube disposed on the elongate member and connected to delivery and return lumen in the catheter body; and the heat exchange fluid may be circulated through the delivery lumen, at least one helically coiled tube and return lumen of the catheter by a cooling apparatus that comprises a refrigeration apparatus, cooling plates, and a cassette which is connected to the delivery and return lumens of the catheter body and may be operative to circulate the cooled heat exchange fluid through the cassette, into the catheter, through the delivery lumen, through said at least one helically coiled tube, out of the return lumen and back into the cassette; wherein the heat exchange catheter and fluid cooling apparatus and said at least one helically coiled tube are sized, configured and constructed to render the system capable of delivering at least about 600 watts of cooling power. The fluid cooling apparatus may be configured to deliver to the heat exchange catheter a flow of heat exchange fluid that is cooled to a temperature at or below 4° C. at a rate of at least 600 mL/min at steady state, when up to 700 W of heat is being added to the flowing saline as a result of heat exchange through the catheter's heat exchanger. The fluid cooling apparatus may be configured to deliver to the heat exchange catheter a flow of heat exchange fluid that is cooled to a temperature at or below 4° C. at a rate of from 200 mL/min to 240 mL/min at steady state, when up to 70 W of heat is being added to the flowing saline as a result of heat exchange through the catheter's heat exchanger. The fluid cooling apparatus may be configured to deliver to the heat exchange catheter a flow of heat exchange fluid that is warmed to a temperature at or above 42° C. at a rate of at least 400 mL/min at steady state, when up to 200 W of heat of heat is being removed from the flowing saline as a result of heat exchange through the catheter's heat exchanger. s added to the saline loop. The fluid cooling apparatus may be configured to deliver to greater than or equal to 600 W of cooling power by circulating heat exchange fluid that is cooled to a temperature at or below 4° C. through the heat exchange catheter at a catheter pressure of about 60 PSI.
In another aspect, disclosed herein is a system comprising: a heat exchange catheter which comprises (i) a catheter body having a distal end, (ii) a elongate member attached to the catheter body and extending beyond its distal end, and (iii) at least one helically coiled tube disposed on the elongate member and connected to delivery and return lumen in the catheter body; and fluid cooling apparatus comprising a refrigeration apparatus, thermal exchange plates through which refrigerant circulates having a cassette receiving space between the thermal exchange plates, a cassette connected to the delivery and return lumens of the catheter body and operative to circulate a cooled thermal exchange fluid through the cassette, into the catheter, through said at least one helically coiled tube, out of the catheter and back into the cassette; wherein the heat exchange catheter and fluid cooling apparatus are configured to render the system capable of delivering at least about 600 watts of cooling power.
A system according to claim 38 wherein the fluid cooling apparatus are configured to deliver to the heat exchange catheter a flow of heat exchange fluid that is cooled to a temperature at or below 4° C. at a rate of at least 600 mL/min at steady state, when up to 700 W of heat is being added to the flowing saline as a result of heat exchange through the catheter's heat exchanger. The fluid cooling apparatus may be configured to deliver to the heat exchange catheter a flow of heat exchange fluid that is cooled to a temperature at or below 4′C at a rate of from 200 mL/min to 240 mL/min at steady state, when up to 70 W of heat is being added to the flowing saline as a result of heat exchange through the catheter's heat exchanger. The fluid cooling apparatus may be configured to deliver to the heat exchange catheter a flow of heat exchange fluid that is warmed to a temperature at or above 42° C. at a rate of at least 400 mL/min at steady state, when up to 200 W of heat is being removed from the flowing saline as a result of heat exchange through the catheter's heat exchanger. s added to the saline loop. The fluid cooling apparatus are configured to deliver greater than or equal to 600 W of cooling power by circulating heat exchange fluid that is cooled to a temperature at or below 4° C. through the heat exchange catheter at a catheter pressure of about 60 PSI. The system may further comprise apparatus useable for warming rather than cooling the heat exchange fluid. The system may be configured to deliver greater than or equal to 50 W of warming power by circulating heat exchange fluid that is warmed to a temperature above 37° C. through the heat exchange catheter at a catheter pressure of about 40 PSI. The system may further comprise at least one heater for warming the thermal exchange plates and a controller programmed to monitor the power output of said at least one heater and, if said power output exceeds a limit, to cause hot refrigerant to flow through the bypass circuit and through said at least one thermal exchange plate, thereby assisting said at least one heater in warming said at least one thermal exchange plate. The controller may be further programmed to incrementally or progressively reduce the amount of hot refrigerant being circulated through said at least one thermal exchange plate in the event that the power output of said at least one heater falls below the limit until a target temperature has been reached. The system may further comprise at least one heater for warming the thermal exchange plates, a pump for pumping the heat exchange fluid at varied flow rates, and a controller programmed to selectively vary both the temperature and flow rate of the heat exchange fluid to maintain the subject's body temperature at or within a permissible range of a target body temperature. The controller may be programmed such that, after a body temperature of the subject has been warmed or cooled to a target temperature, the controller will cause the system to maintain said body temperature at or within a permissible variance range of the target temperature by: holding the temperature of the heat exchange fluid constant and varying the operation of the pump to adjust the flow rate of heat exchange fluid through the catheter as needed to maintain said body temperature at or within a permissible variance range of the target temperature so long as the speed of the pump does not exceed a maximum pump speed; and if the pump exceeds the predetermined maximum pump speed, adjusting the temperature of the heat exchange fluid such that said body temperature at or within a permissible variance range of the target temperature without exceeding the maximum pump speed. If it is necessary to switch between cooling mode and warming mode in order to maintain said body temperature at or within a permissible variance range of the target temperature, the controller may, upon making such switch, adjust the temperature of the heat exchange fluid irrespective of whether the maximum pump speed has been exceeded. The system may further comprise at least one heater for warming the thermal exchange plates, a pump for pumping the heat exchange fluid at varied flow rates, a temperature sensor for sensing the temperature of the heat exchange fluid, a pressure sensor for sensing the pressure of the heat exchange fluid, and a controller which receives a maximum pump speed set point and signals from the temperature sensor and pressure sensor, said controller being programmed to: a) establish current cold/warm status of the heat exchange fluid based on the sensed temperature of the heat exchange fluid; b) determine whether operation of the pump at the maximum pump speed set point will cause over-pressurization of the heat exchange fluid or under-pressurization of the heat exchange fluid; and c) if it is determined that operation of the pump at the maximum pump speed set point will cause over-pressurization of the heat exchange fluid, causing the maximum pump speed set point to change to an adjusted maximum pump speed set point at which the pump may operate without causing over-pressurization of the heat exchange fluid; or d) if it is determined that operation of the pump at the maximum pump speed set point will cause an under-pressurization of the heat exchange fluid, causing the maximum pump speed set point to change to an adjusted maximum pump speed set point at which the pump may operate without causing under-pressurization of the heat exchange fluid. The controller may be programmed to perform steps a through c repeatedly. The controller may be programmed to repeat Steps a through c at least once every 3 seconds. The controller may be programmed to repeat Steps a through c every three seconds. The controller may be programmed to cause the maximum pump speed set point to change bay applying a maximum pump speed set point adjustment integrator. The application of the maximum pump speed adjustment integrator may cause the maximum pump speed set point to change slowly. The controller may be programmed to determine that operation of the pump at the maximum pump speed set point will cause over-pressurization of the heat exchange fluid based on different maximum pressure limits for cold status and warm status. The maximum pressure limit when operating with cold status heat exchange fluid may be, for example, 40 psi and the maximum pressure limit when operating with warm status heat exchange fluid may be, for example, 60 psi. The controller may be programmed to establish warm status in Step a if the sensed temperature of the heat exchange fluid is above 19.5 degree C. and to establish cold status in Step a if the sensed temperature of the heat exchange fluid is not above 19.5 degrees C. The controller may be further programmed to store the most recent prior maximum pump speed set point for warm status and cold status. The controller may be further programmed such that, if performance of Step a results in a change from warm status to cold status, the controller will reset the maximum pump speed set point to the most recent stored maximum pump speed set point for cold status heat exchange fluid. The controller may be further programmed such that, if performance of Step a results in a change from cold status to warm status, the controller will reset the maximum pump speed set point to the most recent stored maximum pump speed set point for warm status heat. The system may be configured to deliver greater than or equal to 700 W of cooling power.
In another aspect; disclosed herein is a system usable for circulating warmed or cooled thermal exchange fluid through a plurality of different changeable heat exchange components which are available and alternately connectable to the system, said system comprising: thermal exchange fluid warming/cooling apparatus for warming, cooling or alternately warming and cooling the thermal exchange fluid; a pump for pumping the thermal exchange fluid; a controller; and apparatus for communicating, to the controller, identifying data which is associated with a selected one of said plurality of changeable heat exchange components; wherein the controller is programmed to assign, on the basis of the identifying data, operational variables for use in connection with the selected one of said plurality of different changeable heat exchange components and to thereafter control the operation of at least one of said thermal exchange fluid warming/cooling apparatus and said pump in accordance with the assigned operational variables. The thermal exchange fluid warming/cooling apparatus may comprise an extracorporeal heat exchange system through which the thermal exchange circulates. The apparatus for communicating to the controller may comprise apparatus for communicating to the controller machine readable identifying data that is encoded on or in the selected one of said plurality of different changeable heat exchange components. The plurality of different changeable heat exchange components may be selected from: endovascular heat exchange catheters, body surface heat exchangers, tubings or tubing sets and cassettes through which the thermal exchange fluid circulates. The plurality of different changeable heat exchange components may comprise a plurality of different types of heat exchange catheters or a plurality of different cassettes each of which is used in connection with a different type of heat exchange catheter and the operational variables may comprise at least one of: minimum fluid pressure, maximum fluid pressure, minimum fluid flow rate, maximum fluid flow rate, number of temperature sensors, location(s) of temperature sensor(s), maximum temperature, minimum temperature and control algorithm to be used.
In another aspect, disclosed herein is a system for warming or cooling the body of a human or animal subject, such system comprising: an extracorporeal control console having a warming and/or cooling apparatus, a pump and a controller and a cassette having a fluid flow path that is connectable to a body heat exchanger positionable on or in a subject's body, such cassette being positionable at an operating position on or in the extracorporeal unit while connected to a body heat exchanger, such that a) the pump will circulate heat exchange fluid through the cassette's heat exchange fluid flow path, through the connected body heat exchanger and back into the cassette's heat exchange fluid flow path and b) the warming and/or cooling apparatus will warm and/or cool the circulating heat exchange fluid. Such cassette may further comprise an electronic storage medium containing machine readable encoded information. The extracorporeal control console may further comprise a reader which receives and reads the cassette's encoded information and the controller may use the cassette's encoded information, as read by the reader, to control operation of one or more components of the system. In some embodiments, the cassette is useable or approved for use with only a single body heat exchanger type and the encoded information either includes, or causes the controller to select and use, a control algorithm, operational setting or parameter that is suitable for that single body heat exchanger type. In some embodiments the cassette may be useable or approved for use with a plurality of different body heat exchanger types and the encoded information includes, or causes the controller to select and use, a control algorithm, operational setting or parameter that is suitable for any of the body heat exchanger types useable or approved for use with the cassette. In some embodiments the extracorporeal control console may be alternately useable with a first cassette that is useable or approved for use with only a single body heat exchanger type and has encoded information that either includes, or causes the controller to select and use, a control algorithm, operational setting or parameter that is suitable for that single body heat exchanger or a second cassette having a fluid flow path that is connectable to a body heat exchanger, such second cassette being alternately positionable, instead of said cassette, in said operating position such that a) the pump will circulate heat exchange fluid through the second cassette's heat exchange fluid flow path, through the connected body heat exchanger and back into the second cassette's heat exchange fluid flow path and b) the warming and/or cooling apparatus will warm and/or cool the circulating heat exchange fluid; the second cassette further comprising an electronic storage medium containing machine readable encoded information; wherein the reader receives and reads the second cassette's encoded information; and wherein the controller uses the second cassette's encoded information, as read by the reader, to control operation of one or more components of the system. Such second cassette may be useable or approved for use with a plurality of different body heat exchanger types and the encoded information includes, or causes the controller to select and use, a control algorithm, operational setting or parameter that is suitable for any of the body heat exchanger types useable or approved for use with the second cassette. Such plurality of approved body heat exchangers may have a recommended pressure limit and the second cassette's encoded information may include, or cause the controller to select and use, a control algorithm, operational setting or parameter that limits the speed of the pump such that heat exchange fluid pressure within the body heat exchanger connected to the second cassette will not exceed a maximum pressure limit for that body heat exchanger, irrespective of which of the plurality of body heat exchanger types is connected to the second cassette. In some embodiments, the second cassette's encoded information may distinguish the second cassette from the cassette and wherein the controller is pre-programmed to select and use, in the basis of that encoded information, a control algorithm, operational setting or parameters suitable for the body heat exchanger(s) that are useable or approved for use of either the cassette or the second cassette, depending on which is presently inserted in the operating position. The electronic storage medium may comprise a medium type selected from: non-volatile random access memory (RAM); non-volatile flash memory; electrically erasable programmable read-only memory (EEPROM); ferroelectric random access memory (FRAM); a chip-embedded storage medium and a microchip-embedded storage medium. The cassette's encoded information may include an indication that the cassette meets a prerequisite requirement and the extracorporeal unit will proceed with warming or cooling of the heat exchange fluid only if the reader has determined that the encoded information includes said indication that the cassette meets a prerequisite requirement. An indication that the cassette meets a prerequisite requirement may comprise at least one of: an expiration date and the absence of an indication that the cassette has been previously used. The body heat exchanger(s) may comprise heat exchange catheters or body surface heat exchangers.
In another aspect, disclosed herein is a body temperature management system comprising: a body heat exchanger positionable on or in a subject's body,
a heat exchange fluid warmer and/or cooler; a heat exchange fluid pump which circulates heat exchange fluid through the heat exchange fluid warmer and/or cooler and through the body heat exchanger; a sensor for sensing the subject's actual body temperature; a user interface configured to receive a user-input patient temperature set point; and a controller which receives signals indicating the user-input patient temperature and the currently-sensed actual body temperature; wherein the controller is programmed to control the heat exchange fluid warmer or cooler and/or the heat exchange fluid pump to initially cause the system to perform a first phase of warming or cooling, during which the heat exchange fluid circulates through the body heat exchanger at temperature and flow rate to cause the sensed actual body temperature to increase or decrease until the sensed actual body temperature reaches a predetermined interim temperature, said interim body temperature being less than the user-input patient temperature set point if the subject is being warmed or greater than the patient temperature set point if the subject is being cooled; and, thereafter, cause the system to perform a second phase of warming or cooling to increase or decrease from the interim temperature to the user input temperature set point at one or more rates which are slower than said initial rate, until the sensed actual body temperature becomes equal to the user-input patient temperature set point without substantially overshooting the user input patient temperature set point; and, thereafter, cause the system to perform a third phase of warming or cooling during which the temperature and/or flow rate of the heat exchange fluid is/are periodically adjusted as needed to maintain the sensed actual body temperature substantially equal to the user-input patient temperature set point. The user interface may allow a user to select a rate of warming or cooling and the controller will cause the system to perform said first, second and third phases only when the selected rate of warming or cooling is greater than a triggering rate. Such triggering rate may be greater than 0.1 degrees C. per hour. The user interface may allow the user to select a maximum rate of warming or cooling and the controller will cause the system to perform said first, second and third phases when the maximum rate is selected. During the first phase, the temperature and/or flow rate of the heat exchange fluid or pump speed may be periodically adjusted as needed to cause the sensed actual body temperature to increase or decrease until the sensed actual body temperature reaches a predetermined interim temperature. During the second phase the temperature and/or flow rate of the heat exchange fluid or pump speed may be periodically adjusted as needed to cause the sensed actual body temperature to increase or decrease to the user input temperature set point. During the first phase the temperature and flow rate of the heat exchange fluid may be substantially constant and not varied based on sensed changes in the actual patient temperature. During the second phase, the actual patient body temperature may warm or cool at a rate of 0.05 degrees C. per hour to 0.1 degrees C. per hour. The user interface may allow the user to select a patient temperature set point and the controller will cause the system to perform said first, second and third phases only when the patient temperature set point is greater than a triggering patient temperature set point. Such triggering patient temperature set point may be greater than 37.8 degrees C.
Still further aspects and details of the present invention will be understood upon reading of the detailed description and examples set forth herebelow.
The following detailed description and examples are provided for the purpose of non-exhaustively describing some, but not necessarily all, examples or embodiments of the invention, and shall not limit the scope of the invention in any way.
The following detailed description and the accompanying drawings to which it refers are intended to describe some, but not necessarily all, examples or embodiments of the invention. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The contents of this detailed description and the accompanying drawings do not limit the scope of the invention in any way.
In the embodiment shown, the endovascular heat exchange catheter 12 comprises an elongate catheter body 16 and a heat exchanger 18 positioned on a distal portion of the catheter body 16. Inflow and outflow lumens (not shown) are present within the catheter body 16 to facilitate circulation of a thermal exchange fluid (e.g., sterile 0.9% sodium chloride solution or other suitable thermal exchange fluid) through the heat exchanger 18. Optionally, the catheter shaft 16 may also include a working lumen (not shown) which extends through the catheter body 16 and terminates distally at an opening in the distal end of the catheter body 16. Such working lumen may serve as a guidewire lumen to facilitate insertion and position of the catheter 12 and/or may be used after insertion of the catheter 12 for delivery of fluids, medicaments or other devices. For example, as shown in
With reference to
A hub 1700 is mounted on the proximal end PE of the proximal catheter body 1300. The hub 1700 has an inflow connector 30000 that is connected to the inflow lumen 1500a of the catheter body 1300 and an outflow connector 32000 that is connected to the outflow lumen 1500b of the proximal catheter body 1300. A through lumen port 2200 on the hub 1700 is connected to the through lumen 1500c.
The heat exchanger 1304 of this catheter embodiment comprises at least first and second coiled heat exchange tube segments 1307a, 1307b. In some embodiments, additional (e.g., third, fourth) heat exchange tube segments may be used. The heat exchange tube segments 1307a, 1307b may be formed of any suitable material. In the particular example shown, the heat exchange tube segments 1307a, 1307b may be advantageously formed of a noncompliant polymeric material, such as polyethylene terephthalate (PET), Pebax, Polyolefin, Polyurethane and/or Nylon, or other suitable compliant or noncompliant material and may be formed of a single tube or one or more tubes. In some embodiments the heat exchange tube segments 1307a, 1307b may expand and collapse depending on whether or not they are filled with fluid and, in such embodiments, the heat exchange tube segments 1307a, 1307b may be referred to a “balloons.” For some applications, the heat exchange tube segments 130fa, 1307b may have outer diameters in the range of 2 mm-19 mm and wall thicknesses in the range of 0.0127 mm-0.1 mm.
In this example, the proximal end of the first tube segment 1307a is connected to the inflow lumen 1500a and the proximal end of the second tube 1307b segment is connected to the outflow lumen 1500b. The distal ends of the first and second tube segment 1307a, 1307b are directly or indirectly in fluidic connection with each other such that heat exchanger fluid that has flowed in the distal direction through the first tube segment 1307a will then return in the proximal direction through the second tube segment 1307b. The distal ends of the heat exchange tube segment 1307a, 1307b are connected to the inflow and outflow connectors 30000, 32000 of the catheter 12
As seen in detail in
The term “elongate member,” may mean, in at least some embodiments, a member, e.g., a spine or similar structure, which extends from a catheter body and upon which at least one heat exchange member is disposed. In at least some embodiments, the elongate member 4000 is distinguishable from the proximal body 1302 on the basis of one or more differences in structure or physical property. In the particular embodiment shown, the elongate member 4000 comprises an elongate, generally C-shaped member having receiving features 4600 which comprise spaced-apart transverse notches, recesses or grooves formed along the open side of the generally C-shaped member. The heat exchange member(s) 1307 may be inserted in these recessed, groove, or notch-type receiving features 4600 such that the helical loops extend around the closed side of the generally C-shaped elongate member 4000. The heat exchange member(s) 1307 may be secured to the receiving features 4600 by adhesive or other suitable means.
Non-limiting examples of other heat exchange catheters and related apparatus that may be used are described in U.S. Pat. No. 9,492,633, and United States Patent Application Publications Nos. 2013/0090708, 2013/0178923, 2013/0079855, 2013/0079856, 2014/0094880, 2014/0094882, 2014/0094883, and unpublished, copending U.S. patent application Ser. Nos. 15/395,858, 15/395,923 and 15/412,390, the entire disclosure of each such patent and application being expressly incorporated herein by reference. Other examples of catheters that may be used in this invention include those commercially available from ZOLL Circulation, Inc., San Jose, Calif., such as the Cool Line® Catheter, Icy® Catheter, Quattro® Catheter: Solex 7® Catheter, InnerCool® RTx Accutrol Catheter and the InnerCool RTx Standard Catheter. Additionally incorporated herein by reference is the entire disclosure of U.S. patent application Ser. No. 15/594,539 entitled Advanced Systems and Methods for Patent Body Temperature Control, filed on May 12, 2017.
The extracorporeal control console 14 generally comprises a main housing 20 and a console head 24. As described in detail herebelow, the main housing 20 contains various apparatus and circuitry for warming/cooling thermal exchange fluid to controlled temperature(s) and for pumping such warmed or cooled thermal exchange fluid through the catheter 18 to effectively modify and/or control the subject's body temperature. The console head 24 comprises a display device or user interface, such as a touch screen system, whereby certain information may be input by, and certain information may be displayed to, users of the system 10. On the housing 20 there are provided a first connection port 40 for connection of a temperature sensor TS that is inserted through the heat exchange catheter 12 as shown in
The tubing/cassette/sensor module assembly 60 or cassette assembly, which is seen in further detail in
As seen in
When operating in a cooling mode, the thermal exchange engine 108 emits heat. Fans 96 and 104 circulate air through air plenums or spaces adjacent to the thermal exchange engine 108 and over surfaces of the compressor and compressor heat sink 100 to exhaust emitted heat and maintain the thermal exchange engine 108 at a suitable operating temperature. Specifically, in the embodiment shown, air enters air intake 84 through filter 90, circulates through the device as indicated by arrows on
The structure and function of the thermal exchange plates may be appreciated in further detail in
Optionally, as shown in the views of
A schematic diagram of an embodiment of a thermal exchange engine or refrigeration loop useable in the systems described herein is shown in
Priming of the system, when the cassette 64 is positioned in the cassette receiving space 66 between thermal exchange plates 80, may be performed quickly by using one or more pump direction changes. The pump 70 may be switched back and forth between running in reverse and running in a forward direction for various durations of time, at various speeds. The first pump reversal creates a vacuum and the subsequent reversals help remove bubbles from the system/line.
To purge the thermal exchange fluid from the system the pump 70 may be run in reverse. In one example, the pump 70 may be run in reverse at 60% of max pump speed for about 20 seconds, during which the return line or vessel outlet line is closed to prevent the cassette vessel/bag from refilling with thermal exchange fluid or saline when the pump is reversed or opened. A check valve may be utilized, which may be positioned in the cassette housing, e.g., in the vessel outlet tubing, between the tubing and the reservoir, to prevent the vessel/bag from refilling with thermal exchange fluid or saline when the pump is reversed or open. For example, in some embodiments, the check valve may be integrated into the inflow connector 206 seen in
To minimize the force required to insert or remove the Heat Exchange (Hx) Bag or vessel from the Cold Plates, several methods are described below.
The frictional force between the Cold Plates and the Hx Bag may be reduced by adding coating to the surface of the Cold Plates that lowers its coefficient of friction. Possible coatings include Teflon or similar. The surface of the Cold Plates may be polished. A coating may be added to the surface of the Hx Bag that lowers its coefficient of friction, e.g., materials that may be used include silicone, or similar (these can be brushed, sprayed, dipped, etc.)
In some embodiments, a layer (release layer or antifriction layer) of material may be placed over the outside surface of the Hx Bag which lowers its coefficient of friction. Possible materials include paralyene, HDPE (Triton), ePTFE, PTFE, FEP or similar. A low friction sheet made of these materials may be used. In certain embodiments, a fluoropolymer may be placed on the cold plates and use a urethane HX bag with HDPE release layer on the bag. The HX bag may include an HDPE release layer on each side of the bag with each layer and the urethane bag affixed to the cassette frame h pegs or clamps. Alternatively, a single longer piece of HDPE release layer may be folded around the HX bag and then the hag and release layers are affixed to the cassette frame with pegs or clamps
The pulse-damping outflow conduit 30 functions not only as a conduit through which the thermal exchange fluid flows but also a pulse damper for damping pulses in the thermal exchange fluid as it flows through the outflow conduit, to a catheter. Pulses may arise due to the nature of the pump used for the thermal exchange fluid. For example, in the case of a peristaltic pump with two drive rollers, at certain times both drive rollers are in contact with the pump tubing, and at other times only one drive rollers is in contact with the pump tubing, depending on the angular position of the pump rotor within the raceway. The thermal exchange fluid system volume suddenly increases when a roller from the peristaltic pump loses contact with the pump tubing as a normal part of the pump's rotation. This happens because a section of the pump tubing that had been flattened, and had zero cross-sectional area, suddenly becomes round and contains a non-zero cross-sectional area. The increase in system volume is approximately the cross-sectional area of the tubing in its round state multiplied by the length of tubing flattened by the roller. The pulse dampener should have enough flexibility to contract suddenly and decrease its volume by approximately this amount in order to dampen the pulse. For example, the volume gained by the pump tubing when a roller leaves contact with it may be 2 to 3 mL. Therefore it is desirable for a pulse dampener to be able to decrease its volume by this amount with a minimal change in system pressure. The pulse damping conduit may comprise, for example, tubing that has sufficient elastic or flexural properties to dampen, attenuate or reduce the amplitude of pulses in the thermal exchange fluid as it flows therethrough. For example, if the conduit is able to expand by a volume of 20 to 30 mL under 60 psi of pressure, then it will be able to contract by 2 to 3 mL when the pressure drops by approximately 6 psi. The more compliant the conduit is, the smaller the pressure drop that occurs when the tubing contracts, and therefore the better the conduit performs its damping function. While a highly compliant tubing is desirable, at the same time, the conduit should have sufficient mechanical strength to expand and contract by this amount repeatedly without rupture. For example if a peristaltic pump has two driving rollers, turns at 40 RPM, and a procedure lasts for 12 hours, the conduit must withstand 57,600 pulsation cycles. To balance these conflicting requirements, for example, in certain embodiments, the length of the pulse damping conduit may be about 90″ and could range between 20″ and 100″. The conduit may be made of a low durometer polyurethane (Prothane II 65-70A) and have a large ID at 0.25″ and could range between 0.15″ and 0.40″. The wall thickness of the conduit is about 0.094″ and could range between 0.06″ and 0.25″.
As seen in
Details of the sensor module 34 are shown in
Power (Watts)=(HE Fluid Temp OUT−HE Fluid Temp IN)·Flow Rate·CP
-
- wherein:
- HE Fluid Temp IN is the current measured temperature of heat exchange fluid flowing into the heat exchanger 18;
- HE Fluid Temp OUT is the current measured temperature of heat exchange fluid flowing out of the heat exchanger;
- Flow Rate is the measured or calculated flow rate of heat exchange fluid through the heat exchanger; and
- CP is the specific heat capacity of the heat exchange fluid.
Also, the controller may be programmed to check and accept the encoded information from the electronic storage medium 310 before allowing the system 10 to be used for warming or cooling the body of the subject and/or to adjust operating variable or parameters to suit operative characteristics (e.g., size, operating volume, type) of the catheter 14, cassette 64, temperature probe, tubing or other components. This pre-check of the encoded information may occur in various sequences or processes. One example of a process by which this pre-check may occur is by the following steps:
-
- 1. User connects tubing/cassette/sensor module assembly 60 to control console 14.
- 2. Console controller detects this connection. Such detection of the connection may occur by the controller scanning the temperature sensor channels, which will open channels when no tubing/cassette/sensor module assembly 60 is connected but will become non-open when a tubing/cassette/sensor module assembly 60 is connected. Alternatively, this could be done by the controller polling the pressure sensor in the cassette 64 or the EEPROM in the sensing module 34 for a response.
- 3. Controller establishes a secure communication session with the EEPROM and reads its content. The EEPROM's content may be encrypted such that it is readable only by a processor having a secret key. In some embodiments, the EEPROM itself may be encoded with a secret key such that the controller may establish a secure session in connection with the sensing module 34.
- 4. In some embodiments, the EEPROM content may comprise the following information, some or all of which must be checked and verified/accepted by the controller before priming and operation of the system 10 may occur:
- a. Manufacturer ID (factory written)
- b. Cassette part #(factory written)
- c. Shelf-life Expiration date (factory written)
- d. Lot #(factory written)
- e. Expiration duration since first use (factory written)
- f. First-Use date (written when the cassette is first plugged into the console)
Referring to
In some embodiments, a particular tubing/cassette/sensor module assembly 60 (a “first” cassette assembly) may be useable or approved for use with only one type of body heat exchanger. In such embodiments, the sensing module 34 may be encoded with information that is specific not only to the first cassette but which also includes or causes the system controller to use algorithms and/or operational settings/variables that are specific to the particular body heat exchanger type, e.g., catheter type or body surface heat exchanger (e.g., pad or garment) type that is useable or approved for use with that first cassette assembly 60. In other embodiments, an example of which is shown in
In other embodiments, the body heat exchanger, e.g., catheter or body surface heat exchanger such as pad or garment, may contain encoded information which includes, or which causes the system controller to select and use, algorithms and/or operational settings/parameters suitable for the particular body heat exchanger. Specifically, the encoded information in the body heat exchanger may include the particular algorithms and/or operational settings/parameters to be used, or alternatively the system controller may be pre-programmed with a number of different algorithms and/or operational settings/parameters and may be further programmed to select and implement, on the basis of the encoded body heat exchanger information, the algorithm and/or operational settings/parameters suitable for the particular body heat exchanger. Encoded information that is specific to a cassette or body heat exchanger may also cause a change in the user display of the console or system, which corresponds to the algorithms or operational settings/parameters for the cassette or body heat exchanger.
To set up the system 10 a new tubing/cassette/sensor module assembly 60 or cassette assembly is obtained and removed from its packaging and the cassette 64 is unfolded to the opened and locked configuration seen in
After the system has been primed, the catheter 12 is connected and inserted into the subject's body and the system 10 is operated to warm or cool the subject's body as desired.
Additionally, this system 10a includes a body surface heat exchange fluid circuit 400 such that the system can provide body surface heat exchange by circulating warmed or cooled heat exchange fluid through at least one body surface heat exchanger 402 (e.g., a heat exchange pad, blanket, garment, etc.) Such operation of the body surface heat exchange fluid circuit 400 and body surface heat exchanger 402 may be performed in addition to or instead of endovascular heat exchange. The body surface heat exchange fluid circuit includes a fluid reservoir, a pump, a bypass valve, a vent valve, thermal exchange plates and a body surface heat exchange device, e.g., a pad. A fluid, e.g., water, is added to the fluid reservoir. When the bypass valve is closed to the vent valve and open to the bypass line, fluid circulates from the pump, through the body surface fluid chambers in the thermal exchange plates, the reservoir, the bypass valve, and back into the pump. This allows the volume of fluid within the system to come to thermal equilibrium with the thermal exchange plates, which may be useful in preparing the device to deliver temperature management treatment to the patient. In normal operation, the bypass valve is open to the vent valve and the vent valve is closed, and fluid circulates from the pump, through the body surface fluid chambers in the thermal exchange plates, through the reservoir, bypass valve, and vent valve, to the body surface heat exchange device and then back through the pump. To drain the body surface heat exchange device, the vent valve is opened which allows air into the circuit and prevents fluid from flowing from the bypass valve. This forces fluid out of the body surface heat exchange device to the pump. The pump is a positive displacement pump capable of pumping air or liquid through the body surface fluid chambers in the thermal exchange plates, to the reservoir. The reservoir is open to ambient air (to allow excess air to escape the system if introduced by the draining process or normal operation, or to accommodate changes in fluid volume due to thermal expansion) and includes a fill port or drain. The circuit also includes body surface heat exchange fluid temperature sensors to provide feedback to the controller, and fluid temperature sensors and fluid flow sensors for use in power calculations.
In certain embodiments, one or more of the systems described herein may also include one or more physiological alarms and/or technical alarms. The physiological alarms may appear next to the patient's temp on the display screen, and may occur when the patient temperature exceeds the high or low patient temperature alarm value. Technical alarms may appear elsewhere on the display screen and may be triggered by console errors or other events, e.g., probe or catheter disconnection, saline loop overpressure, pump malfunction or open lid, and may be displayed by priority. Any of the alarms may be audible. The system may also transmit data, including patient and/or treatment data wirelessly, e.g., via Wifi, Bluetooth or other wireless connection. Data may also be transmitted via USB, Ethernet or wired connection. The system may be electrically powered or battery powered.
The endovascular temperature management system 10 described in various embodiments herein is a high powered system, capable of rapidly cooling a patient.
In certain embodiments, the cassette/console is designed and configured such that it is capable of delivering ≤4° C. working fluid or saline at a rate of ≥600 mL/min, at steady state, when up to 700 W of heat is added to the working fluid or saline loop (e.g., heat added by the subject's body).
In certain embodiments, the cassette/console is designed and configured such that it is capable of delivering ≤4° C. working fluid or saline at a rate of 220+−20 mL/min, at steady state, when ≤70 W of heat is added to the working fluid or saline loop (e.g., heat added by the subject's body).
In certain embodiments, the cassette/console is designed and configured such that it is capable of delivering ≥42° C. working fluid or saline at a rate of >400 mL/min, at steady state, when up to 200 W of heat is removed from the working fluid or saline loop.
In certain embodiments, the system (cassette, console, and catheter) is designed and configured such that it is capable of delivering greater than 400 Watts, or greater than or equal to 500 Watts, or greater than or equal to 600 Watts of cooling power, e.g., with ≤4° C. working fluid or saline at a catheter pressure of about 60 PSI. In certain embodiments, the system may deliver from 500 to 700 W or 600 to 700 W of cooling power or about 675 W of cooling power or greater than 700 W of cooling power.
In certain embodiments, the system (cassette, console, and catheter) is designed and configured such that it is capable of delivering > or equal to 50 W of warming power e.g., with >37° C. working fluid or saline at a catheter pressure of about 40 PSI.
In certain embodiments, the system performance parameters were verified during a bench test. The bench test included placing a catheter (which is connected to a console/cassette assembly) in a rigid 22 mm ID tube, which simulates the average IVC (inferior vena cava) diameter, through which water at a temperature of 37 degrees C. is flowing at a rate of 2.5 liters per minute (simulating blood flow) over the catheter in a direction from the proximal end of the catheter to the distal end of the catheter.
In certain embodiments, in maintenance and controlled rate warming, the system may control a stable patient's temperature, as measured by console, within about 0.3° C. of target when using a temperature sensor or probe on or in the catheter. During normal use and in the case of a sudden saline loop blockage, the system shall regulate and limit working fluid or saline pressure for catheters as follows: <20 C: 60 psi nominal, 90 psi limit; >=20 C: 40 psi nominal, 70 psi limit; or 40 psi nominal, 70 psi limit. The console working fluid pump and cassette shall be capable of an output up to 600 mL/min at 70 psi. Saline or working fluid pressure at the outlet of the saline pump may be measured, e.g., over a range of 0-100 psi with an accuracy of ±5 psi over the range 10-70 psi. The system may be used concurrently with a defibrillator, electro surgical unit or other device or during an MRI. The console and cassette together may be capable of delivering <8° C. saline, at a rate of 600 mL/min, within 5 minutes of turning on the console, when starting with the system equilibrated to ambient temperature. The console and cassette together may be capable of changing the temperature from 4° C. to 40° C. within 10 minutes.
Supplemental Warming by Hot Gas BypassWith reference to
To provide incremental or continuous change of the amount of supplemental heating provided by the hot gas bypass, the controller in some embodiments of the system 10 may be programed to vary duty cycle of the hot gas bypass as the monitored power output of the heater(s) 82 changes. For example, if the maximum heating power output of the heater(s) 82 occurs at a heater duty cycle (HDC) of 30%, the predetermined limit may be set at an HDC of 15% (i.e., one half of the maximum possible heater output). The hot gas bypass circuit may be operative to deliver hot refrigerant to the thermal exchange plates 80 on a hot gas bypass valve duty cycle (BVDC). For example, at a BVDC of 50%, a bypass valve would open for a period of 50 seconds to allow a 50 second flow of hot refrigerant to the thermal exchange plates 80 and would then close for a period of 50 seconds to halt the flow of hot refrigerant to the thermal exchange plates 80 for a subsequent period of 50 seconds, etc. Once the monitored heater power has exceeded the 15% HDC predetermined limit, the controller will trigger the bypass circuit to begin delivering hot refrigerant to the thermal exchange plates 80. Once the flow of hot refrigerant to the thermal exchange plates 80 has commenced, the controller will cause the BVDC to increase as the HDC increases above the 15% HDC predetermined limit and will cause the BVDC to decrease as the HDC decreases below the 15% HDC predetermined limit. There may be a maximum and minimum limit of the BVDC, and the BVDC cannot exceed those limits (e.g., max of 90% and min of 0%).
Combined Variation of Heat Exchange Fluid Flow Rate and Temperature for Precision Maintenance of Target Body TemperatureIn some embodiments of the system 10, the controller/processor(s) may be programmed to vary not only the temperature of the heat exchange fluid being circulated through the heat exchange catheter 12, but also the rate and/or frequency of such flow. One non-limiting example of this is shown in the flow diagram of
For example, after the system 10 has cooled a subject to a target body temperature of 32 degrees C., the subject's body may tend to rewarm. Thus, the system will operate in cooling mode to maintain the target body temperature against the body's inherent tendency to rewarm. In doing so, the system will maintain a constant temperature of heat exchange fluid and will vary the speed of the pump 70 as needed to maintain the target body temperature. However, if it becomes necessary for the pump 70 to run at a speed that exceeds a predetermined limit, the controller will cause the cooling engine 108 to reduce the temperature of the heat exchange fluid by an amount which will allow the pump to slow to a predetermined limit while still maintaining the target body temperature.
Pressure FeedbackAs described, the heat exchange catheter system 10 may incorporate pressure sensor(s) for sensing the pressure of the circulating heat exchange fluid. During a given treatment session, over-pressurization events can occur. This is when the saline pressure is above the saline pressure predetermined limit. Such over-pressurization events are typically of a transient nature and result from temporary compression or bending of the catheter 12 or associated tubing, or other causes. During a given treatment session, under-pressurization events can also occur. Such under-pressurization events occur when the Saline Pump Maximum Set Point (SPM_set) is reached, meaning the saline pump is not allowed to move any faster, but the saline pressure is below the saline pressure predetermined limit. When an over-pressurization or under-pressurization event of significant magnitude occurs, it may be desirable to adjust SPM_set. However, it is preferable not to abruptly change or overly reduce/increase the pump speed. Additionally, after a transient over-pressurization or under-pressurization event has past, it is desirable to return the speed of the pump 70 to optimal operating speeds to maintain normal pressurization of the circulating heat exchange fluid.
Optionally, the controller/processor(s) may also be programmed to store the most recent SPM_set for “cold” and “hot” heat exchange fluids. Thus, when the saline temperature threshold is crossed, the system 10 will switch from “cold” mode to “hot” mode, or vice versa, and upon doing so may recall and apply the recently calculated SPM_set setting for that temperature. In this example, the SPM_set adjustment protocol repeats every three seconds, however other intervals could alternatively be used.
Control of Body Cooling or Warming to Prevent OvershootIn some situations, when warming or cooling a subject's body to a target temperature, it may be desirable to control such cooling or warming in a manner that substantially prevents or avoids overshooting the target patient temperature. For example, in embodiments of the system 10 which allow a user to select a “maximum” rate of warming or cooling, the system controller may be programed to follow a multi-phase warming or cooling protocol, examples of which are shown in
Phase 1—In phase 1 the system controller initially causes the system 10 to circulate heat exchange fluid through a body heat exchanger, such as a heat exchange catheter 12 or body surface heat exchanger (pad or garment), using a maximum pump speed and maximum heat exchange fluid temperature (e.g., the maximum safe temperature and flow rate for warming). The actual patient temperature is received by the controller. During phase 1, the heat exchange fluid temperature and/or pump speed may be periodically recalculated and adjusted based on feedback of the sensed patient temperature, as needed, to cause the sensed actual body or patient temperature to increase from the current temperature to a predetermined interim temperature. During phase 1, the controller may incrementally adjust the control patient temperature set point over time, e.g., from 32 degrees C. to 37.8 degrees C., at the user defined rate, e.g., at 0.5 degrees C. per hour. The pump speed and heat exchange fluid temperature used during phase 1 causes the sensed actual body or patient temperature to increase until it reaches a predetermined interim temperature, which is lower than the user-input patient temperature set point or user-input target patient temperature. In this non-limiting example the interim temperature is 37.8 degrees C. If the rate is chosen to be max, the rate at which the actual patient temperature changes during phase 1 may not necessarily be linear or constant as seen in the graph of
Phase 2—as shown in
Phase 3—As shown in
In cases where the system 10 is being used to warm a subject's body, an overall warming rate of 0.01 degrees C. per hour to 0.2 degrees C. per hour may be used during phase 2. For example, a warming rate of 0.05 degrees C. per hour to 0.1 degrees C. per hour may be used during phase 2. In cases where the system 10 is being used to cool a subject's body, an overall cooling rate of 0.05 degrees C. per hour to 1.0 degrees C. per hour may be used during phase 2.
In some embodiments, during warming, if the user-input patient temperature set point is greater than 37.8 the controller may be programmed to actually cause the heat exchange fluid to stop flowing through the body heat exchanger when the sensed actual body or patient temperature reaches 37.8 degrees C., irrespective of the user-input patient temperature set point.
In certain embodiments, an additional feature to ensure the patient temperature does not exceed 38.0 degrees C. may be provided. If the actual patient temperature is higher than 38.0 degrees C. and the saline temperature is determined to be higher than 38.0 degrees C., the saline pump will turn off. This prevents warming of the patient when the actual patient temperature is above 38.0 degrees C.
Hypothermic Treatment to Deter Reperfusion InjuryAs explained herein, the above-described heat exchange catheter system 10 has the unique ability to cool an adult human subject's body to a hypothermic temperature below 34 degrees C., and preferably between 32 degrees C. and 34 degrees C., in approximately 20 minutes. This rapid induction of hypothermia allows caregivers to select an appropriate time to perform the reperfusion procedure after the subjects body temperature has been lowered to the target temperature. Prior studies have indicated that if hypothermia below 35 degrees C. is effected prior to reperfusion, the severity of reperfusion injury, and hence the size or severity of any permanent tissue infarction, is reduced. Applicant has performed a pilot study using the above-described protocol for deterrence of reperfusion injury in human subjects presenting at hospital emergency departments suffering from acute ST elevation myocardial infarction (STEW). In this pilot study, subjects were randomized into hypothermia and non-hypothermia (control) groups. Subjects in the hypothermia group received standard anti-shivering medication and a heat exchange catheter was placed in the inferior vena cava (IVC). A high power heat exchange catheter system was then used to rapidly cool the body of each subject in the hypothermia group to a temperature below 34 degrees C. within <90 minutes of the subject's arrival in the emergency department. Each subject then underwent percutaneous coronary Intervention (PCI) resulting in reperfusion of the ischemic myocardium. The subjects in the hypothermia group had a body temperatures at the time of reperfusion (i.e., measured at PCI wire crossing) of 33.6+1.0 degrees C.
Following completion of the reperfusion procedure, hypothermia was maintained in each hypothermia group subject for a period of three hours at a target temperature setting of 32 degrees C. Thereafter, the hypothermia group subjects were gradually rewarmed to a body temperature of 36 degrees C.
Four to six days after the event, each subject underwent cardiac magnetic resonance imaging (cMR) and infarct size divided by left ventricular mass (IS/LVM) was determined. On average, subjects in the hypothermia group had a 7.1% absolute change in IS/LVM and approximately a 30% relative reduction compared to the non-hypothermia controls. A 5% absolute change in IS/LVM is generally viewed as a good clinical outcome.
The results of this pilot study, when compared with previously reported data, suggests that 1) cooling of the subject's body temperature at a faster rate (i.e., made possible by using a high cooling power system) results in reduced infarct size measured as IS/LVM, 2) There appears to be a dose-response relationship whereby lower body temperature at the time of reperfusion correlates with greater protection against reperfusion injury and, thus, smaller infarct size.
Accordingly, a method for reducing reperfusion injury in a human or animal subject who undergoes a reperfusion procedure following an ischemic event (e.g., myocardial infarction, acute coronary syndrome, stroke, infarction or ischemia of any metabolic tissue or organ including but not limited to heart, lung, kidney, liver and brain) is provided. In this method, the heat exchange catheter 12 is inserted into the subject's vasculature and the system 10 is used to lower a body temperature of the subject to a temperature below 34 degrees C. and preferably between 32 degrees C. and 34 degrees C. prior to reperfusion. The above described techniques for estimating body temperature at a target location may be utilized in this method and the target location may be in or near the organ or tissue where the ischemia is occurring. For example, in a subject suffering from an evolving myocardial infarction of myocardial ischemia, the system 10 may operate to lower the estimated cardiac temperature (LV Temperature) to the hypothermic temperature. Thereafter, caregivers may perform a reperfusion procedure at a selected time after the body temperature has been cooled to the target hypothermic temperature, thereby deterring reperfusion injury and/or reducing the amount of tissue that ultimately becomes infarcted or necrotic.
Although the invention has been described hereabove with reference to certain examples or embodiments of the invention, various additions, deletions, alterations and modifications may be made to those described examples and embodiments without departing from the intended spirit and scope of the invention. For example, any elements, steps, members, components, compositions, reactants, parts or portions of one embodiment or example may be incorporated into or used with another embodiment or example, unless otherwise specified or unless doing so would render that embodiment or example unsuitable for its intended use. Also, where the steps of a method or process have been described or listed in a particular order, the order of such steps may be changed unless otherwise specified or unless doing so would render the method or process unsuitable for its intended purpose. Additionally, the elements, steps, members, components, compositions, reactants, parts or portions of any invention or example described herein may optionally exist or be utilized in the absence or substantial absence of any other element, step, member, component, composition, reactant, part or portion unless otherwise noted. All reasonable additions, deletions, modifications and alterations are to be considered equivalents of the described examples and embodiments and are to be included within the scope of the following claims.
Claims
1-14. (canceled)
15. A body temperature management system comprising:
- a body heat exchanger positionable on or in a subject's body,
- a heat exchange fluid warmer and/or cooler;
- a heat exchange fluid pump which circulates heat exchange fluid through the heat exchange fluid warmer and/or cooler and through the body heat exchanger;
- a sensor for sensing the subject's actual body temperature;
- a user interface configured to receive a user-input patient temperature set point; and
- a controller which receives signals indicating the user-input patient temperature and the currently-sensed actual body temperature;
- wherein the controller is programmed to control the heat exchange fluid warmer or cooler and/or the heat exchange fluid pump to:
- i) initially cause the system to perform a first phase of warming or cooling, during which the heat exchange fluid circulates through the body heat exchanger at temperature and flow rate to cause the sensed actual body temperature to increase or decrease until the sensed actual body temperature reaches a predetermined interim temperature, said interim body temperature being less than the user-input patient temperature set point if the subject is being warmed or greater than the patient temperature set point if the subject is being cooled; and, thereafter,
- ii) cause the system to perform a second phase of warming or cooling to increase or decrease from the interim temperature to the user input temperature set point at one or more rates which are slower than said initial rate, until the sensed actual body temperature becomes equal to the user-input patient temperature set point without substantially overshooting the user input patient temperature set point; and, thereafter,
- iii) cause the system to perform a third phase of warming or cooling during which the temperature and/or flow rate of the heat exchange fluid is/are periodically adjusted as needed to maintain the sensed actual body temperature substantially equal to the user-input patient temperature set point.
16. A system according to claim 15 wherein the user interface allows the user to select a rate of warming or cooling and the controller will cause the system to perform said first, second and third phases only when the selected rate of warming or cooling is greater than a triggering rate.
17. A system according to claim 16 wherein the triggering rate is greater than 0.1 degrees C. per hour.
18. A system according to claim 15 wherein the user interface allows the user to select a maximum rate of warming or cooling and the controller will cause the system to perform said first, second and third phases when the maximum rate is selected.
19. A system according to claim 15 wherein during the first phase the temperature and/or flow rate of the heat exchange fluid or pump speed is/are periodically adjusted as needed to cause the sensed actual body temperature to increase or decrease until the sensed actual body temperature reaches a predetermined interim temperature.
20. A system according to claim 15 wherein during the second phase the temperature and/or flow rate of the heat exchange fluid or pump speed is/are periodically adjusted as needed to cause the sensed actual body temperature to increase or decrease to the user input temperature set point.
21. A system according to claim 15 wherein during the first phase the temperature and flow rate of the heat exchange fluid are substantially constant and are not varied based on sensed changes in the actual patient temperature.
22. A system according to claim 15 wherein, during phase 2, the actual patient body temperature warms or cools at a rate of 0.05 degrees C. per hour to 0.1 degrees C. per hour.
23. A system according to claim 15 wherein the user interface allows the user to select a patient temperature set point and the controller will cause the system to perform said first, second and third phases only when the patient temperature set point is greater than a triggering patient temperature set point.
24. A system according to claim 21, wherein the triggering patient temperature set point is greater than 37.8 degrees C.
Type: Application
Filed: Feb 18, 2022
Publication Date: Aug 4, 2022
Inventors: John William Jacobsen (San Jose, CA), Ayan Majumdar (San Jose, CA), Sean W. Yip (Mountain View, CA), Jeremy Thomas Dabrowiak (Santa Clara, CA)
Application Number: 17/651,609
