Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
  • A61F7/12—Devices for heating or cooling internal body cavities
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
  • A61F2007/0001—Body part
  • A61F2007/0002—Head or parts thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
  • A61F2007/0059—Heating or cooling appliances for medical or therapeutic treatment of the human body with an open fluid circuit
  • A61F2007/0063—Heating or cooling appliances for medical or therapeutic treatment of the human body with an open fluid circuit for cooling
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
  • A61F2007/0086—Heating or cooling appliances for medical or therapeutic treatment of the human body with a thermostat
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
  • A61F2007/0093—Heating or cooling appliances for medical or therapeutic treatment of the human body programmed
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
  • A61F2007/0095—Heating or cooling appliances for medical or therapeutic treatment of the human body with a temperature indicator
  • A61F2007/0096—Heating or cooling appliances for medical or therapeutic treatment of the human body with a temperature indicator with a thermometer
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F7/00—Heating or cooling appliances for medical or therapeutic treatment of the human body
  • A61F7/12—Devices for heating or cooling internal body cavities
  • A61F2007/126—Devices for heating or cooling internal body cavities for invasive application, e.g. for introducing into blood vessels

Definitions

• the invention relates to a medical device used to reduce tissue injury resulting from ischemia, occurring naturally, through trauma, or from surgery.
• the invention also allows the application of adjunctive therapies such as angioplasty, stent placement, and intracranial thrombectomy.
• Tissue in the human body is regulated at a constant temperature of
• hypothermia decreases tissue metabolism, concentrations of toxic metabolic byproducts, and suppresses the inflammatory response in the aftermath of ischemic tissue injury.
• hypothermia can be intra-ischemic, post-ischemic, or both.
• Hypothermic ischemic protection is preventive if tissue metabolism can be slowed down, and may enhance recovery by ameliorating secondary tissue injury or decreasing ischemic edema formation. Since the metabolic reduction is less than 10% per degree Celsius, only deep hypothermia targeting 20-25 degrees Celsius, conceivably provides adequate tissue protection via metabolic slowdown. Secondary tissue injury, thought to be mainly caused by enzymatic activity, is greatly diminished by mild to moderate hypothermia targeting 32-35 degrees Celsius. As early as 24 hours after onset of ischemia, secondary tissue injury can set off a mass effect with detrimental effects on viable surrounding tissues. Late post-ischemic hypothermia decreases edema formation and may therefore salvage tissue at risk.
• enhancement approaches that do not add mixing energy to the fluid system of interest. They are particularly effective when fluid pumping power is not limited or prohibitive in cost.
• the approach involves adding surface area and / or inducing turbulence adjacent to the effective exchange surface area. These approaches are used throughout the heating and air conditioning industry where fluid pumping power or hydraulic energy can easily be adjusted. This differs, however, from the human body where physiological constraints naturally limit the hydraulic energy or fluid pumping power.
• aggressive passive enhancement techniques particularly in small vessels, vessels that lead to individual organs like the brain, spinal cord, or kidney, are likely to lead to substantial blood side flow resistance that will likely affect cardiac output and or organ perfusion.
• adjunctive therapies are less likely or common. As a result, these designs do not integrate well with existing endovascular tools for organ arteries nor do they offer pathways for adjunctive therapies.
• the present invention provides several embodiments of insulative Knudsen- Effect catheter with minimized eccentricity.
• Each embodiment comprises a rear external hub used to connect the device to an outside control console, a hub strain relief, an insulative shaft, and a distal section that is flexible, atraumatic, and radiopaque.
• the inner lumen is sized for passage of microcatheters, guidewires, and similar interventional tools as well as therapeutic agents.
• the outer lumen is sized to either act as a guide catheter for other interventional tools or sized to pass within existing guide catheters.
• Two specific interventions are of interest: emergency angioplasty and intracranial thrombectomy. Additionally, any procedure that requires deep penetration into the body and may be enhanced with temperature control is amenable to the present invention. All of the embodiments have a concentric pathway configuration with an insulative or heat transfer minimizing annular space.
• the invention provides rapid, localized, deep cooling to ischemic organs without significant reductions in blood perfusion or vessel wall damage.
• "Deep cooling” is considered below 32°C, a temperature at which whole body cooling is normally deemed unsafe.
• the present invention provides a catheter that has a lumen body having a distal end and a proximal end.
• a hub is connected to the proximal end.
• the hub includes a luer connection and a vacuum port assembly.
• FIG. 1 shows a lateral view of the carotid artery and cranial blood vessels.
• FIG. 2 shows an enlarged view of the carotid artery and cranial blood vessels taken from FIG. 1.
• FIG. 3 shows an anterior view of a heart and the coronary arteries on the heart.
• FIG. 4 shows a perspective view of an insulating catheter according to an exemplary embodiment of the present invention.
• FIG. 5 is a side elevational view of a proximal end of the catheter of FIG. 4.
• FIG. 6 is a sectional view of a distal end of the catheter of FIG. 4 taken along lines 6—6 of FIG. 4.
• FIG. 7 is a perspective view of a first exemplary embodiment of an inner lumen for insertion within the outer lumen.
• FIG. 8 is a distal elevational view of the catheter of FIG. 4, showing the inner lumen of FIG. 7 centrally located within an outer lumen.
• FIG. 9 is a distal elevational view of the catheter of FIG. 4, showing the inner lumen of FIG. 7 in a first eccentric position within the outer lumen.
• FIG. 10 is a distal elevational view of the catheter of FIG. 4, showing the inner lumen of FIG. 7 in a second eccentric position within the outer lumen.
• FIG. 11 is a perspective view of a second exemplary embodiment of an inner lumen for insertion within the outer lumen.
• FIG. 12 is a side elevational view of the inner lumen of FIG. 11.
• FIG. 13 is a perspective view of the distal end of the catheter of FIG. 4, with a third exemplary embodiment of an inner lumen inserted within the outer lumen.
• FIG. 14 is a distal elevational view of the catheter of FIG. 13, showing the inner lumen of FIG. 13 centrally located within the outer lumen.
• FIG. 15 is a perspective view of a fourth exemplary embodiment of an inner lumen for insertion within the outer lumen.
• FIG. 16 is a distal elevational view of the inner lumen of FIG. 15.
• FIG. 17 is a perspective view of a fifth exemplary embodiment of an inner lumen for insertion within the outer lumen.
• FIG. 18 is a distal elevational view of the inner lumen of FIG. 17.
• FIG. 19 is a distal elevational view of a sixth exemplary embodiment of an inner lumen inserted into the outer lumen.
• FIG. 20 is a side elevational view, in section, of the inner lumen of FIG. 19.
• FIG. 21 is a graph of Insulative Quality v. Pressure for the inventive catheter assembly.
• FIG. 22 is a plot of saline delivery temperature vs flow rate and insulation.
• FIG. 23 is a plot of saline delivery temperature vs flow rate and catheter type.
• FIG. 24 is a plot of tissue temperature vs time for the inventive Knudsen Effect catheter.
• proximal is intended to mean a direction closer to a user of the inventive catheter and the term “distal” is intended to mean a direction farther from the user of the inventive catheter.
• exemplary is used herein to mean serving as an example, instance, or illustration. Any aspect or design described herein as "exemplary” is not necessarily to be construed as preferred or advantageous over other aspects or designs. Rather, use of the word exemplary is intended to present concepts in a concrete fashion.
• the present invention is an insulative catheter that is used to provide infusate, such as a cooling fluid, to small arteries, such as cranial or cardiac arteries.
• infusate such as a cooling fluid
• small arteries such as cranial or cardiac arteries.
• the infusate is used to cool the cells in an area where an aneurysm, a stroke, a myocardial infarction, or other traumatic event, has occurred, thereby slowing the body's metabolism in and around the affected area, and providing additional time for medical personnel to treat the affected area before irreparable damage occurs.
• FIGS. 1-3 show the physiological landscape where a catheter according to the present invention can be used.
• FIG. 1 shows the aorta 50, with blood flow (shown by the arrow) into the external carotid artery 52 and subsequently to cranial arteries 54.
• the inner diameter of the common carotid artery 52 ranges from 6 to 8 mm and its length ranges from 8 to 12 cm.
• FIG. 2 is a close-up view of the neck and cranial arteries, including the internal carotid artery 53.
• the coronary arteries 56, shown in FIG. 3 are significantly smaller, with proximal inner diameters ranging from 2 to 3.5 mm and length ranging from 2 to 4 cm.
• the distal end of the inventive catheter is required to be able to be advanced through the larger of these arteries into the smaller of these arteries to deliver the infusate.
• Catheter assembly 100 extends along a longitudinal axis 102 and includes, from a proximal end to a distal end, a connection hub 110, an elongate body 140 extending distal ly from hub 110, and a distal tip 160 at the distal end of body 140.
• connection hub 110 connects the catheter assembly 100 to external systems such a cooling console (not shown) that is used to pump infusate into and out of the catheter assembly 100 and pre-existing interventional tools such as dilation catheters and stents (not shown).
• the connection hub 110 includes a hub base 112 having a though-passage 113 extending along the longitudinal axis 102.
• a proximal end 114 of the hub base 112 can include a luer connection 116 for removable connection to standard luer fittings.
• Body 140 is connected to a distal end of hub 110 and carries infusate from hub 110 to distal tip 160 for discharge into a blood vessel.
• a strain relief 141 provides a solid connection between hub 110 and body 140.
• body 140 can be between about 80 and 150 centimeters long although those skilled in the art will recognize that body 140 can be other lengths as well.
• Body 140 is insulated to reduce the amount of heat transfer between the exterior of catheter 100 and the infusate as the infusate flows through body 140.
• Body 140 includes an outer lumen or jacket 142 and an inner lumen 144.
• Outer lumen 142 is generally tubular in cross section, with a reinforcing coil or braid 146 molded therein and extending the length of body 140. Reinforcing coil 146 is used to reduce the kinking of body 140 as catheter 100 is advanced through blood vessels.
• An inner liner 147 defines an inner perimeter of outer lumen 142.
• outer lumen 142 is constructed from Polyether block amide or Pebax ® , although those skilled in the art will recognize that other materials can be used.
• the inner liner 147 can be constructed from Polytetrafluoroethylene or "PTFE".
• Inner lumen 144 is generally tubular in cross section, with an inner volume that is circular in cross section with smooth walls to enhance the flow of infusate through lumen 144.
• the inner volume is in fluid communication with the luer connection 116 so that fluid provided to catheter assembly 100 via luer connection 116 flows through the inner volume for discharge from distal tip 160.
• an insulator 150 is provided in the space 148 between outer lumen 142 and inner lumen 144.
• the insulator 150 acts as a thermal barrier between the outer lumen 142, which is in contact with the patient's bodily fluids, which can be at a temperature of about 37 degrees Celsius, and the infusate in the inner lumen 144, which can be at a temperature as cold as -2 degrees Celsius.
• An exemplary insulator 150 can be Enova® aerogel, manufactured by Cabot Corp., located in Billerica, Massachusetts. Aerogel can be provided in powder form and has a particle size range between about 1 micron and about 120 micron, with a pore size of around 20 nm, and with a thermal conductivity of about 0.012W/m°K at 25 degrees Celsius. To further enhance the insulative properties of the insulator 150, space 148 is in a vacuum, with a pressure of less than about 300 mbar absolute.
• Inner lumen 144 has a small enough outer diameter relative to the inner diameter of outer lumen 142 such that inner lumen 144 can "float" within outer lumen 142. Ideally, inner lumen 144 is centered within the space 148 to minimize heat transfer between body fluids or tissue and infusate. However, in reality, inner lumen 144 will likely engage the inner liner 147 of outer lumen 142, resulting in at least some conductive heat transfer between the lumens 142, 144. To minimize the amount of contact area, inner lumen 144 can include a plurality of raised ribs 152 extending radially outwardly from inner lumen 144. Ribs 152 have a generally rectangular cross section. As shown in FIG.
• ribs 152 can extend the entire length of inner lumen 144.
• ribs 152 can extend in smaller sections along the length of inner lumen 144, with distances along the length of inner lumen 144 that are free of any ribs 152.
• three ribs 152 are provided and are evenly spaced about 120 degrees such that, in the event that inner lumen 144 is eccentrically located within outer lumen 142 as shown in FIGS. 8 and 9, only corner edges of no more than two of the ribs 152 engage the inner wall of outer lumen 142 with linear contact, thereby minimizing the area of contact between inner lumen 144 and outer lumen 142, and minimizing heat transfer from outer lumen 142 to inner lumen 144.
• FIG. 10 shows an alternative eccentric configuration of inner lumen 144 within outer lumen 142 such that only a single rib 152 engages the inner wall of outer lumen 142, also providing a small area of contact between inner lumen 144 and outer lumen 142.
• FIGS. 11-20 show an inner lumen 244 having ribs 252 with triangular shaped cross sections. Similar to inner lumen 144, inner lumen 244 has a small enough outer diameter relative to the inner diameter of outer lumen 142 such that inner lumen 244 can "float" within outer lumen 142. When inner lumen 244 is eccentrically located within outer lumen 142, ribs 252 only engage the inner wall of the outer lumen 142 with linear contact.
• FIGS. 13 and 14 Another alternative embodiment of a catheter body 340 is shown in FIGS. 13 and 14. Catheter body 340 includes an outer lumen 342 with a reinforcing coil 346 and an inner liner 347. With this embodiment, inner lumen 344 is physically
• rib 352 is connected to outer lumen 342 via a single rib 352 that extends the length of inner lumen 344. While heat conduction from outer lumen 342 to inner lumen 344 is conceded via rib 352, rib 352 maintains a generally constant centered positioning of inner lumen 344 within the space 348, thereby eliminating any additional heat conduction pathways directly between the outer lumen 342 and the inner lumen 344.
• FIGS. 1-10 Still another alternative embodiment of an inner lumen 444 is shown in FIGS.
• Inner lumen 444 includes a pair of diametrically spaced arms assemblies 452 having a connection end 454 that extends obliquely away from inner lumen 444 and an arm 456 that radially extends from connection end 454 over an arc of about 90 degrees, leaving a void 458 between inner lumen 444 and arm 456.
• arms 456 bias inner lumen 444 away from the outer lumen, thereby maintaining a generally constant centered positioning of inner lumen 444 within outer lumen 142, and eliminating any other potential heat conduction pathways directly between the outer lumen 142 and the inner lumen 444.
• inner lumen 544 is provided in FIGS. 17 and 18. Similar to inner lumen 144, inner lumen 544 can have a small enough outer diameter relative to the inner diameter of outer lumen 142 (not shown in FIGS. 17 and 18) such that inner lumen 544 can "float" within outer lumen 142. Ideally, inner lumen 544 is centered inside outer lumen 142 to minimize heat transfer.
• inner lumen 544 will likely engage the inner wall of outer lumen 142, resulting in at least some conductive heat transfer between the lumens 142,
• inner lumen 544 can include a plurality of tangs 552 extending radially outwardly from inner lumen 544.
• Tangs 552 each have a connection end 554, shown in FIG. 18, that extends obliquely away from inner lumen 544 and an arm 556 that radially extends from connection end 554. Each arm 556 ends in a corner edge 558. As shown in FIG. 17, tangs 552 can extend the entire length of inner lumen 544. Alternatively, tangs 552 can extend in smaller sections along the length of inner lumen 544, with distances along the length of inner lumen 544 that are free of any tangs 552.
• three tangs 552 are provided and are evenly spaced about 120 degrees such that, in the event that inner lumen 544 is eccentrically located within outer lumen 142, at most, only corner edges 558 of two of the tangs 552 engage the inner wall of outer lumen 142, thereby minimize the area of contact between inner lumen 544 and outer lumen 142, and minimizing heat transfer from outer lumen 142 to inner lumen 544.
• FIGS. 19 and 20 show an inner lumen 644 having diametrically opposed ribs 652 with triangular shaped cross sections. Ribs 652 have a generally triangular cross section. Inner lumen 644 and ribs 652 are sized so that ribs 652 engage outer lumen 142, thereby generally centering inner lumen 644 within the space 148. As shown in FIG. 20, ribs 652 are segmented, with spaces 654 between adjacent ribs 652 on either side of inner lumen 644 to reduce contact area with outer lumen 142, thereby reducing conductive heat transfer between the outer lumen 142 and the inner lumen 644.
• the distal end of the inner lumen 144-644 is attached to the distal tip 160 such that the inside of the inner lumen 144-644 is in fluid communication with the tip 160.
• inner lumens 144-644 While ribs, arms, and other structures extending outwardly from inner lumens 144-644 are shown, those skilled in the art will recognize that other structures for centering the inner lumens within their respective outer lumens can be used.
• such structures can extend inwardly from the outer lumens 142 instead of or in addition to the structures extending outwardly from the inner lumens.
• a vacuum port assembly 120 is used to draw at least a partial vacuum on space 148 to further reduce the thermal transfer to inner lumens 144-644 and further enhance the Knudsen effect of the catheter assembly 100.
• Thermal conductivity of the gas inside an aerogel is inversely dependent on the Knudsen number, Kn. This number, Kn, is defined as the ratio of the mean free path to the average pore size. When vacuums are applied at virtually any level, the mean free path increases, Kn increase, and the thermal conductivity in the gas inside the aerogel particles and the air surrounding the particles decreases.
• Vacuum port assembly 120 includes a central longitudinal axis 122 with a passage 124 extending along axis 122 from a proximal end 121 and in fluid communication with space 148 in body 140. Passage 124 intersects with space 148 at a hub juncture 126.
• a filter 130 is located along axis 122 proximally of hub juncture 126.
• Filter 130 includes filter media fine enough to prevent the insulation, namely, aerogel, from being drawn out of space 148 during the vacuum process.
• a check valve 132 is located proximally of filter 130 to prevent air from flowing from atmosphere, through passage 124, and into space 148.
• a thin metallic coating can be applied to sections of the catheter that are exposed to air to reduce ability of air to permeate the polymer.
• MetaPolyTM the MetaPolyTM process, by ProPlate, wherein the bond between the polymer substrate and electroplated metal is comparable to a metal to metal atomically electroplated bond, which eliminates the adhesion issues experienced utilizing alternative methods.
• the medical device applications are limitless, the Meta-PolyTM process is especially exciting for catheter applications.
• ProPlate® can selectively add radiopaque markers and current conducting paths to polymers.
• Meta- PolyTM provides the same benefits as plating on metallic surfaces; eliminates risk of dislodgment, maintains a low profile, offers cost reduction, and provides endless possibilities for design customization.
• FIG. 21 shows how aerogel thermal conductivity changes with surrounding pressure; vacuum pressures ranging from 0.001 mbar to 1000 mbar or 1 atmosphere. Between about 0.001 mbar and about 10 mbar thermal conductivity is only between about 3 x 10 3 W/(m-K) and about 4 x 10 3 W/(m-K).
• the thermal insulation properties of aerogel are increased when the aerogel is a powder, which increases contact resistance; the aerogel is at low pressure (contact area drops and mean free path increases); and the aerogel has small pore sizes, leading to larger Knudsen numbers and small gas phase component.
• an infrared opacifier can be added to the aerogel, reducing radiative heat transfer. Opacified or doped aerogels reduce radiative heat transfer by limiting the mean free path of photons.
• FIG. 22 is a plot of saline delivery temperature vs flow rate and insulation.
• FIG. 23 is a plot of saline delivery temperature vs flow rate and catheter type. This plot shows that the cooling capacity of the inventive Knudsen Effect catheter outperforms a standard catheter at all flow rates.
• FIG. 24 is a plot of tissue temperature vs time for the inventive Knudsen Effect catheter. This plot shows the tissue temperature response as a function of time.
• Six brain probes are used to show how temperature varies within the brain. Cooling begins at 13:01 : 55 at a delivery flow rate that varies from 0 to 35 ml/min over a span of 5 minutes. At approximately 13:07:00, reperfusion occurs and the flow rate is reduced to 22 ml/min. Cooling is maintained at 22 ml/min for approximately 20 minutes and then followed by ramped reduction of cooling flow rate for 5 minutes (22 ml/min to 0 ml/min).
• the effective total thermal conductivity A eff can be expressed as the sum of the solid thermal conductivity of the solid backbone A s , the effective thermal conductivity of the gaseous phase A g , and finally, the radiative conductivity A r , as calculated in the equation :
• Ae ff (T, Pg) As(T) + Ag(T, Pg) + A r (T)
• the distal tip 160 of the catheter assembly 100 is where the infusate emerges, cooled and prepared to reduce organ tissue temperatures.
• the distal tip 160 can be a low durometer (super flexible) Pebax®, such as a 25D with 20% BaSC>4 (added for radiopacity).
• the distal tip 160 includes a passage 162 (shown in FIG. 4) through inner lumen 144 that allows the infusate or other device to exit the catheter assembly 100.
• Outer lumen 142 has a closed distal end to retain insulating material in the space 148 between inner lumen 144 and outer lumen 142.
• the tip 160 can be placed at the ostium of the heart or within the small coronary arteries 56. Tip 160 is radiopaque to allow visualization of the location of tip 160 via radiographic means. For brain cooling, the tip 160 can be placed in the carotid, inner carotid, or middle cerebral arteries.
• catheter assembly 100 is inserted into a patient's blood vessel according to known methods and advanced to an area where cooling is desired/required.
• the radiopaque tip 160 allows the interventionist to see where the tip 160 is located in the patient.
• the infusate supply is connected to the proximal end 114 of hub 110 and pumped through the catheter body 140 to the distal tip 160, out the distal tip 160, and to the desired location in the patient.
• the vacuum can be drawn on space 148 by connecting a syringe or vacuum pump (not shown) to the vacuum port assembly 120 at proximal end 121.

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• Health & Medical Sciences (AREA)
• Vascular Medicine (AREA)
• Thermal Sciences (AREA)
• Engineering & Computer Science (AREA)
• Biomedical Technology (AREA)
• Heart & Thoracic Surgery (AREA)
• Physics & Mathematics (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
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• Media Introduction/Drainage Providing Device (AREA)

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• 2019
  • 2019-06-05 WO PCT/US2019/035484 patent/WO2020149873A1/en active Application Filing
  • 2019-06-05 CN CN201980089189.7A patent/CN113382764A/zh not_active Withdrawn
  • 2019-06-05 JP JP2021541073A patent/JP2022517373A/ja active Pending

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