CA2382226C - Stretchable cryoprobe sheath - Google Patents
Stretchable cryoprobe sheath Download PDFInfo
- Publication number
- CA2382226C CA2382226C CA002382226A CA2382226A CA2382226C CA 2382226 C CA2382226 C CA 2382226C CA 002382226 A CA002382226 A CA 002382226A CA 2382226 A CA2382226 A CA 2382226A CA 2382226 C CA2382226 C CA 2382226C
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- probe
- catheter
- sheath
- cryosurgical
- catheter assembly
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/02—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by cooling, e.g. cryogenic techniques
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
- A61B1/00142—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with means for preventing contamination, e.g. by using a sanitary sheath
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/02—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by cooling, e.g. cryogenic techniques
- A61B18/0206—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by cooling, e.g. cryogenic techniques ultrasonic, e.g. for destroying tissue or enhancing freezing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/18—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves
- A61B18/20—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser
- A61B18/22—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser the beam being directed along or through a flexible conduit, e.g. an optical fibre; Couplings or hand-pieces therefor
- A61B18/24—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser the beam being directed along or through a flexible conduit, e.g. an optical fibre; Couplings or hand-pieces therefor with a catheter
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00017—Electrical control of surgical instruments
- A61B2017/00022—Sensing or detecting at the treatment site
- A61B2017/00084—Temperature
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/0023—Surgical instruments, devices or methods, e.g. tourniquets disposable
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/00234—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery
- A61B2017/00292—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery mounted on or guided by flexible, e.g. catheter-like, means
- A61B2017/00336—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery mounted on or guided by flexible, e.g. catheter-like, means with a protective sleeve, e.g. retractable or slidable
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00005—Cooling or heating of the probe or tissue immediately surrounding the probe
- A61B2018/00041—Heating, e.g. defrosting
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00053—Mechanical features of the instrument of device
- A61B2018/00059—Material properties
- A61B2018/00089—Thermal conductivity
- A61B2018/00095—Thermal conductivity high, i.e. heat conducting
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00053—Mechanical features of the instrument of device
- A61B2018/00059—Material properties
- A61B2018/00089—Thermal conductivity
- A61B2018/00101—Thermal conductivity low, i.e. thermally insulating
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00053—Mechanical features of the instrument of device
- A61B2018/00166—Multiple lumina
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/02—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by cooling, e.g. cryogenic techniques
- A61B2018/0212—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by cooling, e.g. cryogenic techniques using an instrument inserted into a body lumen, e.g. catheter
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/02—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by cooling, e.g. cryogenic techniques
- A61B2018/0231—Characteristics of handpieces or probes
- A61B2018/0262—Characteristics of handpieces or probes using a circulating cryogenic fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/30—Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure
- A61B2090/306—Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure using optical fibres
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B2218/00—Details of surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2218/001—Details of surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body having means for irrigation and/or aspiration of substances to and/or from the surgical site
- A61B2218/002—Irrigation
Abstract
A sheath (20) for use on a closed loop Joule-Thomson cryosurgical probe (10), and the combination of the sheath (20) and the closed loop probe (10). The sheath (20) is slipped over the probe (10), thereby separating the probe from the environment.
The sheath (20) has a grip (22) which fits over the handle (12) of the cryosurgical probe, and an extendible shroud (23) which can be longitudinally extended to cover tubing (18) and which are attached to the handle (12). The sheath (20) has a hollow multi-lumen catheter (24) shaped and sized to fit snugly over the cannula (14) of the cryosurgical probe (10). The catheter (24) is not thermally conductive, preventing transfer of heat from the ambient to the gas mixture, and preventing the freezing of tissues at undesired locations along the catheter. A thermally conductive cap or tip (26) is biased against the cold tip (16) on the probe (10) by a biasing element (28) in the sheath assembly.
The sheath (20) has a grip (22) which fits over the handle (12) of the cryosurgical probe, and an extendible shroud (23) which can be longitudinally extended to cover tubing (18) and which are attached to the handle (12). The sheath (20) has a hollow multi-lumen catheter (24) shaped and sized to fit snugly over the cannula (14) of the cryosurgical probe (10). The catheter (24) is not thermally conductive, preventing transfer of heat from the ambient to the gas mixture, and preventing the freezing of tissues at undesired locations along the catheter. A thermally conductive cap or tip (26) is biased against the cold tip (16) on the probe (10) by a biasing element (28) in the sheath assembly.
Description
TITLE OF THE INVENTION
Stretchable Cryoprobe Sheath BACKGROUND OF THE INVENTION
The present invention is in the field of cryosurgical probes used for freezing lo and thereby destroying biological tissues. More specifically, the present invelition is useful in the field of cryosurgical, probes which are cooled by a closed loop Joule-Thomson refrigeration system.
A Joule-Thomson refrigeration system operates by expanding a high pressure gas through an expansion element which incorporates some sort of a flow restriction.
The flow restriction might be a small orifice, a narrow capillary tube, or some other sort of restricted passageway. Typically, the refrigeration system includes a source of high pressure gas, a heat exchanger, an'expansion element, a heat transfer element, and various tubes or conduits to conduct the gas from one component to another. The high pressure gas passes through the heat exchanger to lower the gas temperature somewhat, then the gas temperature is further lowered in the expansion element, as isenthalpic expansion occurs. The expanded, cooled gas is exposed to the heat transfer element, where the gas absorbs heat which has been transferred from the environment. The operation of a Joule-Thomson refrigeration system can be severely affected by contaminants in the gas, such as water, oil, or particulates. Any such contaminant can easily block the flow restriction in the expansion element, because the flow restriction is typically very small.
Water and oil are particularly detrimental contaminants, because they will selectively collect at the flow restriction, where the majority of the cooling occurs. As the gas expands and cools, the temperature of entrained water and oil also lowers, resulting in the freezing or solidification of the water and oil. This solidification occurs exactly at the flow restriction, because that is where the cooling actually occurs. Water and oil, at least in trace amounts, are often found in ambient air, and they can consequently be introduced into the refrigeration system if any system joints are broken or any system parts are replaced.
Most Joule-Thomson systems are open loop, meaning that the gas is exhausted to the atmosphere after expansion and heat absorption. The source of the high pressure gas in such a system is usually a high pressure gas cylinder. As use proceeds, the amount of gas in the cylinder is depleted. An open loop system such as this can tolerate a certain amount of contamination, because the contaminants are exhausted from the system to the environment along with the gas, during use. If any contamination is introduced into the system during the replacement of parts, or when system joints are broken for other reasons, the contamination is largely flushed out as the gas is subsequently exhausted.
However, it is possible to operate a closed loop Joule-Thomson system, meaning that the gas is repressurized and circulated after expansion. After expansion in the expansion element, exposure to the heat transfer element, and absorption of t s heat_ the low pressure gas is returned to a compressor which can be used to repressurize the gas. The repressurized gas is then circulated back through the heat exchanger and the expansion element. None of the gas is exhausted from the system.
Therefore, any contaminants which enter the system are collected in the system, where they accumulate over a period of time. The level of contamination can eventually build up to a level where solidification of the water and oil will plug the expansion element. A method and apparatus have been developed for operating a micro-miniature mixed-gas Joulp-Thomson refrigeration system, as disclosed in U.S.
Patent Ser. No. 6,151,901, filed 10/12/95, and U.S. Patent Ser.
No. 5,787,715, filed 8/15/96. If such a mixed-gas is used, especially in a miniature or micro-miniature refrigeration system, the introduction of air into the system alters the gas mixture ratios, and it can significantly detract from the cooling performance of the gas mixture.
For these reasons, closed loop Joule-Thomson systems are often permanently sealed, to prevent the introduction of contaminants. Replacement of parts, or other breaking of system joints, is not possible in a permanently sealed system.
Some systems use self sealing couplings, which automatically close the system when they are broken apart. This automatic sealing limits the amount of leakage and contamination, but some contamination still occurs. Typically, the couplings used in a closed loop system are threaded fittings which are not designed for repetitive disconnection.
The contamination problem becomes more complicated in a closed loop mixed-gas Joule-Thomson refrigeration system which is used in a surgical device, such as a cryosurgical probe. Such a device will typically have a compressor hooked to the probe, with the probe consisting essentially of a handle, a cannula, and a cold tip. The heat exchanger is typically located in the handle, and the expansion element is typically located in the cold tip. The probe cannula or cold tip must be interchangeable with various shapes, such as flat, cylindrical, or sharp edged, to perform different functions. Further, the cold tip must be capable of being sterilized for use in a surgical application, to allow repeated use of the system on different patients.
Known cryosurgical probes are open loop systems for this reason. In an open loop system, the cannula or cold tip can be removed and sterilized or discarded.
Introduction of contaminants into the refrigeration system during removal and replacement of the cannula or cold tip is not a significant problem in an open loop system, since the contaminants can be flushed from the system during exhaust of the gas. Open loop systems are wasteful and expensive to operate, because of the necessity of continually replacing the gas. Also, exhaust of the gas to the enviromnent is not always environmentally safe. Closed loop systems are more economical and environmentally safe. If a known closed loop system were used in a surgical application, removal and replacement of the cannula or cold tip for sterilization purposes would introduce contaminants into the system, ultimately resulting in blockage of the expansion element. A closed loop surgical system could theoretically be provided with self sealing couplings, but contamination would still build up over a period of time. Further, self sealing couplings incorporate 0-rings and precision parts.
Sterilization of the cannula or cold tip would inevitably expose the 0-rings and precision parts to high temperatures and harsh chemicals, ultimately resulting in degradation of the sealing ability of the couplings.
Use of disposable replacement cannulas or cold tips would not solve this dilemma. First, even if the replaceable parts are discarded and replaced with new, sterile parts, repetitive disconnections are required, ultimately resulting in the buildup of contaminants. Second, most disposable parts are constructed of plastic, for reasons of economy. Plastics typically contain trace amounts of water. If a plastic part is exposed to the gas in a refrigeration system, the water can eventually leech out of the plastic and contaminate the gas in the system. Third, self sealing fittings typically add size, weight, and significant cost to a device, making them undesirable for use in a disposable device. Fourth, each time a disposable element, such as a cannula or cold tip, is discarded, the refrigerant gas contained within the disposable element is lost.
This requires replacement of the gas to avoid degradation of the cooling performance of the system. Evacuation of gas from the disposable component, or use of replacement components precharged with gas, would significantly add to the 1 o complexity and cost of the system.
Further, a typical cryosurgical probe will have one or more auxiliary instruments near the cold tip, for use in conjunction with the cold tip, such as temperature sensors, heaters, ultrasound transducers, optical elements, and fluid ports for irrigation and aspiration. If a reusable probe is employed, repetitive sterilization of these auxiliary instruments can degrade their performance. The ideal practice would be to incorporate these auxiliary instruments into a disposable element.
Finally, it is desirable to insulate the shaft of a cryosurgical probe, to prevent freezing of tissue at undesired sites along the probe when the probe is inserted into a body cavity or organ. One effective means of insulation would be to provide a vacuum space along the probe shaft. However, the level of the vacuum maintained in such a space can degrade over time, because of the outgassing of metals, plastics, and braze joints. This outgassing increases during sterilization procedures in which heat is applied to the probe. Therefore, it would be desirable to incorporate the vacuum insulation space into a disposable element. The disposable element would only be sterilized once, and the disposable element can then be economically discarded, minimizing the amount of vacuum degradation.
BRIEF SUMMARY OF THE INVENTION
The present invention is a sheath for use on a closed loop Joule-Thomson cryosurgical probe, and the combination of the sheath and the closed loop probe. The sheath is sufficiently flexible to be slipped over the probe, thereby separating the probe from the environment and allowing use of the probe in a surgical application.
The sheath has a grip which attaches to the handle of the cryosurgical probe, and an receiving a cannula portion of a cryosurgical probe; a thermally conductive segment on said catheter assembly, said conductive segment being in thermal contact with a heat transfer portion of a cryosurgical probe, when said catheter assembly is disposed over a cannula portion of a cryosurgical probe; and a biasing element on said catheter assembly, said biasing element being constructed to longitudinally bias said conductive segment of said catheter assembly against a heat transfer portion of a cryosurgical probe when said hollow grip is attached to a cryosurgical probe.
According to another aspect of the present invention, there is provided a cryosurgical instrument, comprising: a probe handle; a probe cannula attached to said probe handle; a heat transfer element on said probe cannula;
a cooling system providing a coolant at a desired temperature adjacent said heat transfer element; a hollow grip removably attachable to said probe handle; a catheter assembly attachable to said hollow grip, said catheter assembly having a tubular passageway for receiving said probe cannula; a thermally conductive segment on said catheter assembly, said conductive segment being in thermal contact with said heat transfer element, when said catheter assembly is disposed over said probe cannula; and a biasing element on said catheter assembly, said biasing element being constructed to longitudinally bias said conductive segment of said catheter assembly against a heat transfer portion of a cryosurgical probe when said hollow grip is attached to a cryosurgical probe.
According to still another aspect of the present invention, there is provided a sheath for use as a removable cover for a cryosurgical probe, said sheath comprising: a 5a hollow grip removably attachable to a cryosurgical probe; a connector body attachable to said hollow grip; a thermally resistive catheter attached to said connector body, said catheter having a tubular passageway for receiving a cannula portion of a cryosurgical probe; and a thermally conductive segment on said catheter, said conductive segment being in thermal contact with a heat transfer portion of a cryosurgical probe, when said catheter is disposed over a cannula portion of a cryosurgical probe; wherein said sheath is constructed to cause attachment of said hollow grip to a cryosurgical probe to result in a heat transfer portion of the probe pushing in a distal direction against said conductive segment of said catheter assembly, thereby stretching at least one of said catheter and said connector body, and thereby longitudinally biasing said conductive segment against the heat transfer portion of the cryosurgical probe.
The novel features of this invention, as well as the invention itself, will be best understood from the attached drawings, taken along with the following description, in which similar reference characters refer to similar parts, and in which:
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is an elevation view of a cryosurgical probe of the type which might be used in the present invention;
Figure 2A is an elevation view of a sheath according to the present invention;
Figure 2B is an elevation view of an alternative embodiment of the sheath according to the present invention;
5b Figure 2C is a distal end view of the alternative embodiment of the sheath shown in Figure 2B;
Figure 3 is an elevation view of a sheath in place over a cryosurgical probe, according to the present invention;
Sc Figure 4 is a schematic view of a cryosurgical probe as shown in Figure 1;
Figure 5 is a section view of the proximal portion of the sheath as shown in Figure 2A;
Figure 6 is a distal end view of the cryosurgical probe as shown in Figure 1;
Figure 7 is an elevation view of the proximal portion of the sheath of Figure 1, with the shroud furled;
Figure 8 is a section view of the proximal portion of the sheath of Figure 7, with the shroud furled;
Figure 9 is a longitudinal section view of the proximal portion of the connector body of the sheath;
Figure 10 is a longitudinal section view of the distal portion of the connector body of the sheath;
Figure 11 is a transverse section view of the distal portion of the connector body of the sheath;
Figure 12A is a transverse section view of the catheter of the sheath installed on the cannula of the cryosurgical probe;
Figure 12B is a transverse section view of an alternate embodiment of the catheter of the sheath, incorporating a vacuum jacket, installed on the cannula of the cryosurgical probe;
Figure 13 is an elevation view of the distal end of the catheter of the sheath;
Figure 14 is a longitudinal section view of the distal end of the catheter of the sheath;
Figure 15 is a longitudinal section view of another embodiment of the sheath according to the present invention; and Figure 16 is a partial longitudinal section view of a portion of the sheath shown in Figure 15.
DETAILED DESCRIPTION OF THE INVENTION
The present invention addresses the use of a sheath on a cryosurgical probe which operates on a closed loop mixed gas Joule-Thomson refrigeration system.
Such a cryosurgical probe 10 is shown in Figure 1. The probe 10 consists mainly of a handle 12, a hollow tubular cannula 14, and a cold tip 16. The handle 12 can be metallic, to facilitate effective sealing. The handle can have end caps vacuum brazed to the handle cylinder, to hold a vacuum inside the handle 12, thereby providing insulation. Alternatively, the handle 12 could be packed with insulating material, such as aerogel. Several components of the refrigeration system, such as a heat exchanger, can be housed within the handle 12, along with various auxiliary instrumentation to support items such as temperature sensors, heaters, illumination optics, viewing optics, laser optics, and ultrasonic transducers. An umbilical cord 18 extending from the proximal portion of the handle 12 can contain tubing for the refrigeration system, power cables for the electrical components, or fiber optical cables to support the illumination, viewing, and laser components.
Other components of the refrigeration system, such as a high pressure conduit to transport a high pressure gas mixture from the probe handle 12 to the cold tip 16, and a low pressure conduit to return the expanded gas mixture from the cold tip 16 to the probe handle 12, can be housed in the hollow cannula 14. Still other components of the refrigeration system, such as a Joule-Thomson expansion element, can be housed in the cold tip 16. The hollow cannula 14 is usually designed to minimize heat transfer from the surrounding tissues to the cryogenic gas mixture. It can be formed of a thermally resistive material, such as a rigid plastic, or it can be formed of a metal, with insulation applied internally or externally to inhibit heat transfer. The cannula 14 can be a rigid tube as shown, or it can be more flexible and shaped differently, depending upon the application. The cold tip 16 is a heat transfer element designed to maximize heat transfer from the target tissues to the expanded gas mixture. It can be formed of a thermally conductive material, such as a metal, preferably silver.
The cold tip 16 can be a cap shaped element on the distal end of the cannula 14 as shown, or it can have another shape and be placed elsewhere on the cannula 14, depending upon the application. A plurality of grooves 17 are formed in the cold tip 16 to allow the flow of thermal grease as the cold tip 16 is fitted inside the disposable sheath.
Since the cryosurgical probe 10 is used with a closed loop refrigeration system, it will necessarily be sealed to prevent contamination. It may have breakable joints which allow for replacement of parts, but any such joints will necessarily have sealing components which are not suitable for normal sterilization procedures.
Figure 2A shows a sheath 20 for disposition over the probe 10, to allow use of the probe 10 in a protected environment without degradation of the effectiveness of the probe 10. Optionally, the sheath 20 can be made of materials that are sterilized easily, and it can be constructed cheaply enough to be disposable. The sheath includes a grip 22 which fits over the probe handle 12, preferably with corrugations or other surface features to provide a secure feel for the surgeon. An extendible shroud 23 is attached to or formed on the proximal portion of the grip 22. The shroud 23 is shown in Figure 2A in the unfurled, or extended, condition, covering the umbilical cord 18 and the proximal portion of the probe handle 12. The grip 22 and the shroud 23 are constructed of a thermally non-conductive material, such as a plastic.
They should have some flexibility to allow them to fit over the probe handle 12 and the umbilical cord 18. The sheath 20 also includes a hollow tubular catheter 24 extending distally. The hollow catheter 24 is shaped and sized to cover the cannula portion 14 of the cryosurgical probe 10, preferably fitting tightly over the probe cannula 14 to avoid interference with use of the probe 10 in a surgical environment. The hollow catheter 24 is constructed of a thermally resistive material, such as a plastic, to further inhibit heat transfer from the surrounding tissues to the probe cannula 14.
Attached to the distal end of the hollow catheter 24 is a thermally conductive segment, such as a cap shaped tip 26. The sheath tip 26 is shaped and sized to fit snugly over the probe cold tip 16, to maximize the transfer of heat through the sheath tip 26 to the probe cold tip 16. The sheath tip 26 can be a cap shaped element on the distal end of the catheter 24 as shown, or it can be a thermally conductive segment shaped and located otherwise, to match the configuration and location of the probe cold tip 16. The thermally conductive segment of the sheath, such as sheath tip 26, must be constructed of a material which will readily transfer heat, such as a metal. All of the components of the sheath 20 are attached together in a sealing relationship, so that when the sheath 20 is sterile, it covers the probe 10 in a protective envelope, rendering the probe 10 suitable for use in a surgical environment. Various auxiliary instruments for use in conjunction with cryosurgery can be mounted in the hollow catheter 24 or the sheath tip 26, as will be explained below. These instruments can include temperature sensors, heaters, viewing optics, illumination optics, laser optics, and ultrasonic transducers. Controls for operating these instruments, or devices for displaying readings from these instruments, can be mounted in the probe handle 12 or elsewhere, for ease of observation and use by the surgeon. Connections between the instrumentation near the sheath tip 26 and the control devices in the probe handle 12 or proximal to the handle 12 can be carried by the hollow catheter 24 as will be explained.
The sheath 20 can also include a connector body 28, which performs several functions. The connector body 28 provides a means for connecting the hollow catheter 24 to the grip 22. It can also provide a means for latching the sheath 20 to the probe 10. Further, the connector body 28 can provide a mounting location for connectors, such as electrical contacts or optical elements, to connect auxiliary instrumentation near the sheath tip 26 to the probe handle 12.
Finally, the connector body 28 can provide a mounting location for a port or fitting 30, such as a luer fitting, which can be used to provide fluid flow to or from the area adjacent the sheath tip 26. Fluid flow to the area can be required in some applications where fluid such as a saline solution must be injected into a body cavity having a small opening. An example of such an application is insertion of the probe cannula 14 into the uterus for endometrial ablation. Fluid flow to the area around the tip 26, such as a saline solution or another fluid suitable for irrigation of the area, can be provided by a syringe attached to the fitting 30. Alternatively, as shown in Figures 2B and 2C, a pliable saline reservoir 25 can be mounted on the grip 22 and connected to the fitting 30 by a tube 27. Squeezing or depressing the saline reservoir 25 can inject saline solution into the fitting 30. The injected fluid can be retained in the body cavity by sliding a plug (not shown) over the cannula 14 and the catheter 24 to fit snugly between the catheter 24 and the opening of the body cavity. Similarly, a balloon (not shown) can be inflated around the catheter 24 to seal against the cavity opening. Fluid flow from the area around the tip 26 can be achieved by connecting a vacuum source to the fitting 30. Fluid flow can pass between the tip area and the fitting 30 via the hollow catheter 24, as will be explained below.
Figure 2A also shows the finger stop 32 formed on the distal portion of the sheath grip 22, and the finger slide 34 formed on the proximal portion of the connector body 28. As will be shown below, the finger slide 34 can be pulled toward the finger stop 32 to unlatch the connector body 28 from the probe handle 12.
Figure 3 shows the combined cryosurgical instrument 40 of the present invention, consisting of the sheath 20 disposed over the probe 10 as a protective cover, having a thermally conductive segment for effectively transferring heat from the target tissue to the cold tip 16 of the probe 10. It should be noted that the shroud 23 of the sheath 20 is sufficiently flexible to stretch over the proximal end of the probe handle 12 and the umbilical cord 18.
Figure 4 is a schematic drawing of the cryosurgical probe 10, in the style of a longitudinal section view, to illustrate the components and functions of the typical probe 10 which can be incorporated into the present invention. A high pressure gas tube 36 provides a warm high pressure gas mixture to the refrigeration components in the probe 10, and a low pressure gas tube 38 receives the cool low pressure gas mixture returning from the probe 10. The high pressure and low pressure gas tubing 36, 38 is connected to the outlet and inlet, respectively, of a gas compressor 42. The high pressure tube 36 is also connected to a high pressure passageway through a precooling heat exchanger 44, and the low pressure tube 38 is connected to a low pressure passageway through the heat exchanger 44. The heat exchanger 44 precools the warm high pressure gas mixture by heat exchange with the cool low pressure expanded gas mixture, before the high pressure gas is expanded at the cold tip 16.
A high pressure outlet 46 of the heat exchanger 44 is connected to a high pressure conduit 48 which passes through the hollow cannula 14 to the cold tip 16. At the distal end of the high pressure conduit 48 is a Joule-Thomson expansion element 50, located in, or immediately adjacent to, the cold tip 16. High pressure cryogenic gas mixture passing through the high pressure conduit 48 is isenthalpically expanded by the expansion element 50, to significantly lower the temperature of the gas mixture. The colder, low pressure gas mixture is then exposed to the cold tip 16, to cool the target tissue via the thermally conductive sheath tip 26. A separator plate 52 isolates the low pressure region of the cold tip 16 from the probe cannula 14.
Low pressure gas mixture passes back through openings in the separator plate 52 to return via the probe cannula 14 to the low pressure inlet 54 of the heat exchanger 44. The flow of the low pressure gas mixture back through the cannula 14 can actually be via a low pressure conduit not shown in Figure 4.
A female connector fitting 56 is provided in the distal portion of the probe handle 12, to provide for a mating location between the probe 10 and the sheath 20.
An inwardly projecting latching flange 58 can be provided around the outer perimeter of the female connector 56. One or more connector elements 60 can be provided within the female connector 56 for mating with auxiliary instrumentation carried by the sheath 20. The connector element 60 can be an electrical contact for use with auxiliary instrumentation such as a temperature sensor, a heater, or an ultrasonic transducer. Similarly, the connector element 60 can be an optical element for use with auxiliary instrumentation such as viewing optics, illumination optics, or laser optics.
The connector element 60 is connected by way of an instrumentation conductor 62 to a display or control device 64. The instrumentation conductor 62 can be an electrical conductor or an optical fiber bundle, as appropriate. Only one set of connector element 60, conductor 62 and display or control device 64 is shown, for the sake of simplicity, but it should be understood that a plurality of such systems could be used in any given cryosurgical instrument 40. Further, it should be understood that the display or control device 64 could be located remotely from the instrument 40, such as would be appropriate for a video optical viewing system. An alignment rib 66 can be formed on the perimeter of the probe handle 12, to assist in alignment of the probe handle 12 with the sheath grip 22.
Figure 5 shows that the connector body 28 has a longitudinal bore 68 therethrough, to allow the passage of the probe cannula 14. The fitting 30 is in fluid flow communication with the bore 68, to provide fluid flow to the exterior of the hollow catheter 24, which extends into the bore 68. A male connector fitting 70 is provided on the proximal portion of the connector body 28 to mate with the female connector fitting 56 in the distal portion of the probe handle 12. A
releasable latch 72 is provided on the male connector fitting 70, to engage the latching flange 58. One or more connector elements 74 are also provided on the male connector fitting 70 to engage the connector elements 60 within the female connector fitting 56 in the probe handle 12. Connection of the connector element 74 to the auxiliary instrumentation, and connection of the fluid flow path from the fitting 30 to the hollow catheter 24 are shown better in a later Figure. Figure 6 is an end view of the probe handle 12, showing the interior of the female connector fitting 56. A plurality of connector elements 60 are shown arranged in a circle within the female fitting 56.
Figure 7 shows the sheath 20 with the shroud 23 in the furled, or contracted, condition. The sheath would normally be shipped and stored in this condition until disposition over a cryosurgical probe 10. Tabs 78 are provided on the proximal end of the shroud 23 to assist in pulling the shroud 23 over the probe handle 12 and the umbilical cord 18. Figure 8 is a section view showing more detail of one embodiment of the sheath 20. An alignment groove 76 is shown in the inner bore of the sheath grip 22, to mate with the alignment rib 66 on the exterior of the probe handle 12.
It can be seen that the connector body 28 can be constructed as a multi-piece assembly.
Figure 9 shows more detail of one embodiment of the connector body 28 and its connection to the sheath grip 22. The connector body 28 comprises essentially a distal section 80, an intermediate section 82, and a proximal section 84. The distal section 80 includes the finger slide 34, and the distal portion of the distal section 80 is attached to the hollow catheter 24. The intermediate section 82 is mounted within the proximal portion of the distal section 80, and it provides a means of connecting the distal section 80 to the instrumentation connectors 74 and to the releasable latch 72.
The intermediate section 82 can consist of a barrel 92 as shown, threaded to the latch 72. A collet 86 is captured between the barrel 92 and the latch 72. The collet 86 is attached to a sleeve 90 which is in turn attached to a connector fixture 96.
Instrumentation conductors 94 are connected to the instrumentation connectors 74.
The instrumentation conductors 94 pass through or alongside the longitudinal bore 68 to the catheter 24.
Figure 10 shows more detail of one embodiment of the distal portion of the distal section 80 of the connector body 28. The distal end of the longitudinal bore 68 terminates in a fluid bore 100, which is in fluid flow communication with an internal bore 98 of the fitting 30. The proximal portion of the hollow catheter 24 extends into the fluid bore 100, with the diameter of the fluid bore 100 being larger than the outer diameter of the catheter 24. This leaves a fluid flow space surrounding the catheter 24 in the fluid bore 100. The proximal end 102 of the fluid bore 100 can be terminated by a shoulder in the longitudinal bore 68. Conversely, the proximal end 102 of the fluid bore 100 can be terminated by an epoxy seal. The probe cannula 14 can fit snugly within the longitudinal bore 68. The distal end of the connector body 28 can be fitted with a strain relief collar 106 to fasten the catheter 24 to the connector body 28. A space 108 within the collar 106 can be filled with epoxy to terminate the distal end of the fluid bore 100.
Figure 11 shows a section view of the distal portion of the connector body 28 and the proximal portion of the hollow catheter 24. In this view, it can be seen that the catheter 24 is a multi-lumen catheter. A plurality of lumens 110 pass longitudinally through the wall of the catheter 24. Some of the lumens I 10 are used to conduct fluid flow, as shown at 112, and other lumens are used to conduct auxiliary instrumentation signals, as shown at 114. Within the fluid bore 100 only, the fluid lumens 112 are open to the exterior of the catheter 24, while the fluid lumens along the remainder of the length of the catheter 24 are not open to the exterior. The instrumentation lumens 114 are closed to the exterior throughout the length of the catheter 24. Since the fluid lumens 112 are open to the exterior within the fluid bore 100, fluid can flow from the fitting 30 into the wall of the catheter 24, or out of the wall of the catheter 24 to the fitting 30. A central bore 116 passes through the catheter 24 to accommodate the probe cannula 14.
Figure 12A shows a transverse section view of the catheter 24 and the probe cannula 14, forward of the connector body 28. The cannula 14 incorporates a set of three coaxial stainless steel tubes 48,55,57, with the outer tube 57 fitting substantially snugly within the catheter 24. It can be seen that a vacuum or insulation space 118 is formed between the outer tube 57 and a low pressure conduit 55. The low pressure conduit 55 leads to the low pressure inlet 54 of the heat exchanger 44. The high pressure conduit 48 lies within the low pressure conduit 55.
Figure 12B shows a transverse section view of an alternate embodiment of the catheter 24 and the probe cannula 14, forward of the connector body 28. The cannula 14 incorporates a set of two coaxial stainless steel tubes 48, 55, with the outer tube 55 fitting substantially snugly within an inner tube 117 in the catheter 24. It can be seen that a vacuum jacket or insulation space 118 is formed within the catheter 24, between the inner tube 117 and the catheter 24. Here as before, the low pressure conduit 55 leads to the low pressure inlet 54 of the heat exchanger 44. The high pressure conduit 48 lies within the low pressure conduit 55.
Figure 13 shows an elevation view of the distal end of the hollow catheter 24 and the sheath tip 26. A plurality of ports 120 in the lumens I 10 are formed in the distal end of the catheter 24. Some of the ports 120 are for fluid flow to or from the area adjacent the sheath tip 26. Other ports 120 are for optical elements to support viewing, illumination, or laser systems. Still other ports 120 could be used as connection terminals for electrical connection to a temperature sensor, heater, or ultrasonic transducer in the sheath tip 26.
Figure 14 shows a longitudinal section of the distal portion of the catheter and the sheath tip 26. The auxiliary instrumentation conductor 94 passes through a lumen 114 to the distal end of the catheter 24, at which point it connects to an optical element in the port 120, or to an auxiliary instrument 126 in the sheath tip 26. The auxiliary instrument 126 could be a temperature sensor, a heater, a tissue impedance measuring component, or an integrated component for performing two or more of the temperature sensing, impedance measuring, and heating functions. For example, the instrument 126 could be a combination heater and resistance temperature detector (RTD) constructed of foil laminated between very thin (0.003 in.) sheets of polyimide film. Further, the auxiliary instrument could be an ultrasonic transducer.
Those auxiliary instruments 126 which are in the sheath tip 26 can be sandwiched between an inner thermally conductive layer 122 and an outer thermally conductive layer 124.
The inner conductive layer 122 can be made of copper, and the outer conductive layer 124 can be made of stainless steel. If desired, epoxy can be injected between the instrument 126 and the conductive layers 122, 124. An epoxy bleed hole 128 in the outer layer 124 is provided for this purpose. If insulating layers are placed between the instrument 126 and the inner and outer layers 122, 124, the insulating layers must be sufficiently thin to allow heat transfer therethrough. A thermally conducting grease 130 can be provided within the sheath tip 26 to maximize the thermal contact between the probe tip 16 and the sheath tip 26.
Figure 15 shows yet another embodiment of the sheath 220 of the present invention, in which one or more biasing elements in the catheter assembly 223 bias the conductive tip 226 of the catheter 224 against the cold tip 16 of the probe cannula 14. The sheath 220 includes a hollow grip 222, into which a catheter assembly 223 is attachable. The catheter assembly 223 includes a catheter 224 and a connector body 228. The sheath 220 can be attached to a cryosurgical probe handle represented in phantom, by means of one or more latches 225. The catheter 224 can be constructed of a pliable material, such as an elastomer, which can be stretched, and which will be biased toward its unstretched length. Similarly, the connector body 228 can be constructed of a pliable material, such as an elastomer, which can be deformed, and which will be biased toward its undeformed shape.
Figure 16 shows a larger scale longitudinal section view of the distal portion of the grip 222 and the proximal portion of the catheter assembly 223. Also shown is an elevation view of the proximal portion of the cannula 14 of the cryosurgical probe 10.
The connector body 228 has a substantially tubular distal portion 231 which fits snugly into a longitudinal bore in the distal end of the hollow grip 222. The distal portion 231 of the connector body 228 can be held in a desired longitudinal position by one or more annul.ar o-rings 227. The connector body 228 can also have a conical apron 233 on its proximal end, which bears against the distal wall of the cavity within the hollow grip 222. The proximal end 229 of the catheter 224 is attached within a longitudinal bore in the distal portion 231 of the connector body 228 by being glued or otherwise bonded thereto. The seal between the catheter 224 and the connector body 228, and the seal created by the o-rings 227, create a sterile barrier at the distal end of the hollow grip 222.
The catheter assembly 223, including its conductive tip 226, is formed with an undeformed length which is slightly less than the necessary length to accommodate the length of the cannula 14, including its cold tip 16. Therefore, when the cryoprobe 10 is inserted into the sheath 220, in order to latch the sheath 220 to the cryoprobe 10 handle, it is necessary to slightly stretch or otherwise deform one or more components of the catheter assembly 223. The stretching or deformation in the embodiment shown can occur in the connector body 228, or in the catheter 224, or in both.
When the catheter assembly 223 has been deformed to accommodate the length of the cannula 14, the elastic quality of the catheter assembly 223 causes it to bias the conductive tip 226 proximally against the cold tip 16 of the cryoprobe 10.
This insures a positive contact between the conductive tip 226 of the catheter assembly 223 and the cold tip 16 of the cryoprobe 10, thereby maximizing the heat transfer from the environment to the cryoprobe 10.
Rather than using elastic materials, a similar effect can be accomplished by using other types of biasing elements, such as one or more springs (not shown), to bias the catheter assembly proximally, without departing from the spirit of the present invention. Further, the conductive tip 226 or the cold tip 16, or both, can be slightly tapered to increase the positive contact area between the two tips.
While the particular invention as herein shown and disclosed in detail is fully capable of obtaining the objects and providing the advantages hereinbefore stated, it is to be understood that this disclosure is merely illustrative of the presently preferred embodiments of the invention and that no limitations are intended other than as described in the appended claims.
Stretchable Cryoprobe Sheath BACKGROUND OF THE INVENTION
The present invention is in the field of cryosurgical probes used for freezing lo and thereby destroying biological tissues. More specifically, the present invelition is useful in the field of cryosurgical, probes which are cooled by a closed loop Joule-Thomson refrigeration system.
A Joule-Thomson refrigeration system operates by expanding a high pressure gas through an expansion element which incorporates some sort of a flow restriction.
The flow restriction might be a small orifice, a narrow capillary tube, or some other sort of restricted passageway. Typically, the refrigeration system includes a source of high pressure gas, a heat exchanger, an'expansion element, a heat transfer element, and various tubes or conduits to conduct the gas from one component to another. The high pressure gas passes through the heat exchanger to lower the gas temperature somewhat, then the gas temperature is further lowered in the expansion element, as isenthalpic expansion occurs. The expanded, cooled gas is exposed to the heat transfer element, where the gas absorbs heat which has been transferred from the environment. The operation of a Joule-Thomson refrigeration system can be severely affected by contaminants in the gas, such as water, oil, or particulates. Any such contaminant can easily block the flow restriction in the expansion element, because the flow restriction is typically very small.
Water and oil are particularly detrimental contaminants, because they will selectively collect at the flow restriction, where the majority of the cooling occurs. As the gas expands and cools, the temperature of entrained water and oil also lowers, resulting in the freezing or solidification of the water and oil. This solidification occurs exactly at the flow restriction, because that is where the cooling actually occurs. Water and oil, at least in trace amounts, are often found in ambient air, and they can consequently be introduced into the refrigeration system if any system joints are broken or any system parts are replaced.
Most Joule-Thomson systems are open loop, meaning that the gas is exhausted to the atmosphere after expansion and heat absorption. The source of the high pressure gas in such a system is usually a high pressure gas cylinder. As use proceeds, the amount of gas in the cylinder is depleted. An open loop system such as this can tolerate a certain amount of contamination, because the contaminants are exhausted from the system to the environment along with the gas, during use. If any contamination is introduced into the system during the replacement of parts, or when system joints are broken for other reasons, the contamination is largely flushed out as the gas is subsequently exhausted.
However, it is possible to operate a closed loop Joule-Thomson system, meaning that the gas is repressurized and circulated after expansion. After expansion in the expansion element, exposure to the heat transfer element, and absorption of t s heat_ the low pressure gas is returned to a compressor which can be used to repressurize the gas. The repressurized gas is then circulated back through the heat exchanger and the expansion element. None of the gas is exhausted from the system.
Therefore, any contaminants which enter the system are collected in the system, where they accumulate over a period of time. The level of contamination can eventually build up to a level where solidification of the water and oil will plug the expansion element. A method and apparatus have been developed for operating a micro-miniature mixed-gas Joulp-Thomson refrigeration system, as disclosed in U.S.
Patent Ser. No. 6,151,901, filed 10/12/95, and U.S. Patent Ser.
No. 5,787,715, filed 8/15/96. If such a mixed-gas is used, especially in a miniature or micro-miniature refrigeration system, the introduction of air into the system alters the gas mixture ratios, and it can significantly detract from the cooling performance of the gas mixture.
For these reasons, closed loop Joule-Thomson systems are often permanently sealed, to prevent the introduction of contaminants. Replacement of parts, or other breaking of system joints, is not possible in a permanently sealed system.
Some systems use self sealing couplings, which automatically close the system when they are broken apart. This automatic sealing limits the amount of leakage and contamination, but some contamination still occurs. Typically, the couplings used in a closed loop system are threaded fittings which are not designed for repetitive disconnection.
The contamination problem becomes more complicated in a closed loop mixed-gas Joule-Thomson refrigeration system which is used in a surgical device, such as a cryosurgical probe. Such a device will typically have a compressor hooked to the probe, with the probe consisting essentially of a handle, a cannula, and a cold tip. The heat exchanger is typically located in the handle, and the expansion element is typically located in the cold tip. The probe cannula or cold tip must be interchangeable with various shapes, such as flat, cylindrical, or sharp edged, to perform different functions. Further, the cold tip must be capable of being sterilized for use in a surgical application, to allow repeated use of the system on different patients.
Known cryosurgical probes are open loop systems for this reason. In an open loop system, the cannula or cold tip can be removed and sterilized or discarded.
Introduction of contaminants into the refrigeration system during removal and replacement of the cannula or cold tip is not a significant problem in an open loop system, since the contaminants can be flushed from the system during exhaust of the gas. Open loop systems are wasteful and expensive to operate, because of the necessity of continually replacing the gas. Also, exhaust of the gas to the enviromnent is not always environmentally safe. Closed loop systems are more economical and environmentally safe. If a known closed loop system were used in a surgical application, removal and replacement of the cannula or cold tip for sterilization purposes would introduce contaminants into the system, ultimately resulting in blockage of the expansion element. A closed loop surgical system could theoretically be provided with self sealing couplings, but contamination would still build up over a period of time. Further, self sealing couplings incorporate 0-rings and precision parts.
Sterilization of the cannula or cold tip would inevitably expose the 0-rings and precision parts to high temperatures and harsh chemicals, ultimately resulting in degradation of the sealing ability of the couplings.
Use of disposable replacement cannulas or cold tips would not solve this dilemma. First, even if the replaceable parts are discarded and replaced with new, sterile parts, repetitive disconnections are required, ultimately resulting in the buildup of contaminants. Second, most disposable parts are constructed of plastic, for reasons of economy. Plastics typically contain trace amounts of water. If a plastic part is exposed to the gas in a refrigeration system, the water can eventually leech out of the plastic and contaminate the gas in the system. Third, self sealing fittings typically add size, weight, and significant cost to a device, making them undesirable for use in a disposable device. Fourth, each time a disposable element, such as a cannula or cold tip, is discarded, the refrigerant gas contained within the disposable element is lost.
This requires replacement of the gas to avoid degradation of the cooling performance of the system. Evacuation of gas from the disposable component, or use of replacement components precharged with gas, would significantly add to the 1 o complexity and cost of the system.
Further, a typical cryosurgical probe will have one or more auxiliary instruments near the cold tip, for use in conjunction with the cold tip, such as temperature sensors, heaters, ultrasound transducers, optical elements, and fluid ports for irrigation and aspiration. If a reusable probe is employed, repetitive sterilization of these auxiliary instruments can degrade their performance. The ideal practice would be to incorporate these auxiliary instruments into a disposable element.
Finally, it is desirable to insulate the shaft of a cryosurgical probe, to prevent freezing of tissue at undesired sites along the probe when the probe is inserted into a body cavity or organ. One effective means of insulation would be to provide a vacuum space along the probe shaft. However, the level of the vacuum maintained in such a space can degrade over time, because of the outgassing of metals, plastics, and braze joints. This outgassing increases during sterilization procedures in which heat is applied to the probe. Therefore, it would be desirable to incorporate the vacuum insulation space into a disposable element. The disposable element would only be sterilized once, and the disposable element can then be economically discarded, minimizing the amount of vacuum degradation.
BRIEF SUMMARY OF THE INVENTION
The present invention is a sheath for use on a closed loop Joule-Thomson cryosurgical probe, and the combination of the sheath and the closed loop probe. The sheath is sufficiently flexible to be slipped over the probe, thereby separating the probe from the environment and allowing use of the probe in a surgical application.
The sheath has a grip which attaches to the handle of the cryosurgical probe, and an receiving a cannula portion of a cryosurgical probe; a thermally conductive segment on said catheter assembly, said conductive segment being in thermal contact with a heat transfer portion of a cryosurgical probe, when said catheter assembly is disposed over a cannula portion of a cryosurgical probe; and a biasing element on said catheter assembly, said biasing element being constructed to longitudinally bias said conductive segment of said catheter assembly against a heat transfer portion of a cryosurgical probe when said hollow grip is attached to a cryosurgical probe.
According to another aspect of the present invention, there is provided a cryosurgical instrument, comprising: a probe handle; a probe cannula attached to said probe handle; a heat transfer element on said probe cannula;
a cooling system providing a coolant at a desired temperature adjacent said heat transfer element; a hollow grip removably attachable to said probe handle; a catheter assembly attachable to said hollow grip, said catheter assembly having a tubular passageway for receiving said probe cannula; a thermally conductive segment on said catheter assembly, said conductive segment being in thermal contact with said heat transfer element, when said catheter assembly is disposed over said probe cannula; and a biasing element on said catheter assembly, said biasing element being constructed to longitudinally bias said conductive segment of said catheter assembly against a heat transfer portion of a cryosurgical probe when said hollow grip is attached to a cryosurgical probe.
According to still another aspect of the present invention, there is provided a sheath for use as a removable cover for a cryosurgical probe, said sheath comprising: a 5a hollow grip removably attachable to a cryosurgical probe; a connector body attachable to said hollow grip; a thermally resistive catheter attached to said connector body, said catheter having a tubular passageway for receiving a cannula portion of a cryosurgical probe; and a thermally conductive segment on said catheter, said conductive segment being in thermal contact with a heat transfer portion of a cryosurgical probe, when said catheter is disposed over a cannula portion of a cryosurgical probe; wherein said sheath is constructed to cause attachment of said hollow grip to a cryosurgical probe to result in a heat transfer portion of the probe pushing in a distal direction against said conductive segment of said catheter assembly, thereby stretching at least one of said catheter and said connector body, and thereby longitudinally biasing said conductive segment against the heat transfer portion of the cryosurgical probe.
The novel features of this invention, as well as the invention itself, will be best understood from the attached drawings, taken along with the following description, in which similar reference characters refer to similar parts, and in which:
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is an elevation view of a cryosurgical probe of the type which might be used in the present invention;
Figure 2A is an elevation view of a sheath according to the present invention;
Figure 2B is an elevation view of an alternative embodiment of the sheath according to the present invention;
5b Figure 2C is a distal end view of the alternative embodiment of the sheath shown in Figure 2B;
Figure 3 is an elevation view of a sheath in place over a cryosurgical probe, according to the present invention;
Sc Figure 4 is a schematic view of a cryosurgical probe as shown in Figure 1;
Figure 5 is a section view of the proximal portion of the sheath as shown in Figure 2A;
Figure 6 is a distal end view of the cryosurgical probe as shown in Figure 1;
Figure 7 is an elevation view of the proximal portion of the sheath of Figure 1, with the shroud furled;
Figure 8 is a section view of the proximal portion of the sheath of Figure 7, with the shroud furled;
Figure 9 is a longitudinal section view of the proximal portion of the connector body of the sheath;
Figure 10 is a longitudinal section view of the distal portion of the connector body of the sheath;
Figure 11 is a transverse section view of the distal portion of the connector body of the sheath;
Figure 12A is a transverse section view of the catheter of the sheath installed on the cannula of the cryosurgical probe;
Figure 12B is a transverse section view of an alternate embodiment of the catheter of the sheath, incorporating a vacuum jacket, installed on the cannula of the cryosurgical probe;
Figure 13 is an elevation view of the distal end of the catheter of the sheath;
Figure 14 is a longitudinal section view of the distal end of the catheter of the sheath;
Figure 15 is a longitudinal section view of another embodiment of the sheath according to the present invention; and Figure 16 is a partial longitudinal section view of a portion of the sheath shown in Figure 15.
DETAILED DESCRIPTION OF THE INVENTION
The present invention addresses the use of a sheath on a cryosurgical probe which operates on a closed loop mixed gas Joule-Thomson refrigeration system.
Such a cryosurgical probe 10 is shown in Figure 1. The probe 10 consists mainly of a handle 12, a hollow tubular cannula 14, and a cold tip 16. The handle 12 can be metallic, to facilitate effective sealing. The handle can have end caps vacuum brazed to the handle cylinder, to hold a vacuum inside the handle 12, thereby providing insulation. Alternatively, the handle 12 could be packed with insulating material, such as aerogel. Several components of the refrigeration system, such as a heat exchanger, can be housed within the handle 12, along with various auxiliary instrumentation to support items such as temperature sensors, heaters, illumination optics, viewing optics, laser optics, and ultrasonic transducers. An umbilical cord 18 extending from the proximal portion of the handle 12 can contain tubing for the refrigeration system, power cables for the electrical components, or fiber optical cables to support the illumination, viewing, and laser components.
Other components of the refrigeration system, such as a high pressure conduit to transport a high pressure gas mixture from the probe handle 12 to the cold tip 16, and a low pressure conduit to return the expanded gas mixture from the cold tip 16 to the probe handle 12, can be housed in the hollow cannula 14. Still other components of the refrigeration system, such as a Joule-Thomson expansion element, can be housed in the cold tip 16. The hollow cannula 14 is usually designed to minimize heat transfer from the surrounding tissues to the cryogenic gas mixture. It can be formed of a thermally resistive material, such as a rigid plastic, or it can be formed of a metal, with insulation applied internally or externally to inhibit heat transfer. The cannula 14 can be a rigid tube as shown, or it can be more flexible and shaped differently, depending upon the application. The cold tip 16 is a heat transfer element designed to maximize heat transfer from the target tissues to the expanded gas mixture. It can be formed of a thermally conductive material, such as a metal, preferably silver.
The cold tip 16 can be a cap shaped element on the distal end of the cannula 14 as shown, or it can have another shape and be placed elsewhere on the cannula 14, depending upon the application. A plurality of grooves 17 are formed in the cold tip 16 to allow the flow of thermal grease as the cold tip 16 is fitted inside the disposable sheath.
Since the cryosurgical probe 10 is used with a closed loop refrigeration system, it will necessarily be sealed to prevent contamination. It may have breakable joints which allow for replacement of parts, but any such joints will necessarily have sealing components which are not suitable for normal sterilization procedures.
Figure 2A shows a sheath 20 for disposition over the probe 10, to allow use of the probe 10 in a protected environment without degradation of the effectiveness of the probe 10. Optionally, the sheath 20 can be made of materials that are sterilized easily, and it can be constructed cheaply enough to be disposable. The sheath includes a grip 22 which fits over the probe handle 12, preferably with corrugations or other surface features to provide a secure feel for the surgeon. An extendible shroud 23 is attached to or formed on the proximal portion of the grip 22. The shroud 23 is shown in Figure 2A in the unfurled, or extended, condition, covering the umbilical cord 18 and the proximal portion of the probe handle 12. The grip 22 and the shroud 23 are constructed of a thermally non-conductive material, such as a plastic.
They should have some flexibility to allow them to fit over the probe handle 12 and the umbilical cord 18. The sheath 20 also includes a hollow tubular catheter 24 extending distally. The hollow catheter 24 is shaped and sized to cover the cannula portion 14 of the cryosurgical probe 10, preferably fitting tightly over the probe cannula 14 to avoid interference with use of the probe 10 in a surgical environment. The hollow catheter 24 is constructed of a thermally resistive material, such as a plastic, to further inhibit heat transfer from the surrounding tissues to the probe cannula 14.
Attached to the distal end of the hollow catheter 24 is a thermally conductive segment, such as a cap shaped tip 26. The sheath tip 26 is shaped and sized to fit snugly over the probe cold tip 16, to maximize the transfer of heat through the sheath tip 26 to the probe cold tip 16. The sheath tip 26 can be a cap shaped element on the distal end of the catheter 24 as shown, or it can be a thermally conductive segment shaped and located otherwise, to match the configuration and location of the probe cold tip 16. The thermally conductive segment of the sheath, such as sheath tip 26, must be constructed of a material which will readily transfer heat, such as a metal. All of the components of the sheath 20 are attached together in a sealing relationship, so that when the sheath 20 is sterile, it covers the probe 10 in a protective envelope, rendering the probe 10 suitable for use in a surgical environment. Various auxiliary instruments for use in conjunction with cryosurgery can be mounted in the hollow catheter 24 or the sheath tip 26, as will be explained below. These instruments can include temperature sensors, heaters, viewing optics, illumination optics, laser optics, and ultrasonic transducers. Controls for operating these instruments, or devices for displaying readings from these instruments, can be mounted in the probe handle 12 or elsewhere, for ease of observation and use by the surgeon. Connections between the instrumentation near the sheath tip 26 and the control devices in the probe handle 12 or proximal to the handle 12 can be carried by the hollow catheter 24 as will be explained.
The sheath 20 can also include a connector body 28, which performs several functions. The connector body 28 provides a means for connecting the hollow catheter 24 to the grip 22. It can also provide a means for latching the sheath 20 to the probe 10. Further, the connector body 28 can provide a mounting location for connectors, such as electrical contacts or optical elements, to connect auxiliary instrumentation near the sheath tip 26 to the probe handle 12.
Finally, the connector body 28 can provide a mounting location for a port or fitting 30, such as a luer fitting, which can be used to provide fluid flow to or from the area adjacent the sheath tip 26. Fluid flow to the area can be required in some applications where fluid such as a saline solution must be injected into a body cavity having a small opening. An example of such an application is insertion of the probe cannula 14 into the uterus for endometrial ablation. Fluid flow to the area around the tip 26, such as a saline solution or another fluid suitable for irrigation of the area, can be provided by a syringe attached to the fitting 30. Alternatively, as shown in Figures 2B and 2C, a pliable saline reservoir 25 can be mounted on the grip 22 and connected to the fitting 30 by a tube 27. Squeezing or depressing the saline reservoir 25 can inject saline solution into the fitting 30. The injected fluid can be retained in the body cavity by sliding a plug (not shown) over the cannula 14 and the catheter 24 to fit snugly between the catheter 24 and the opening of the body cavity. Similarly, a balloon (not shown) can be inflated around the catheter 24 to seal against the cavity opening. Fluid flow from the area around the tip 26 can be achieved by connecting a vacuum source to the fitting 30. Fluid flow can pass between the tip area and the fitting 30 via the hollow catheter 24, as will be explained below.
Figure 2A also shows the finger stop 32 formed on the distal portion of the sheath grip 22, and the finger slide 34 formed on the proximal portion of the connector body 28. As will be shown below, the finger slide 34 can be pulled toward the finger stop 32 to unlatch the connector body 28 from the probe handle 12.
Figure 3 shows the combined cryosurgical instrument 40 of the present invention, consisting of the sheath 20 disposed over the probe 10 as a protective cover, having a thermally conductive segment for effectively transferring heat from the target tissue to the cold tip 16 of the probe 10. It should be noted that the shroud 23 of the sheath 20 is sufficiently flexible to stretch over the proximal end of the probe handle 12 and the umbilical cord 18.
Figure 4 is a schematic drawing of the cryosurgical probe 10, in the style of a longitudinal section view, to illustrate the components and functions of the typical probe 10 which can be incorporated into the present invention. A high pressure gas tube 36 provides a warm high pressure gas mixture to the refrigeration components in the probe 10, and a low pressure gas tube 38 receives the cool low pressure gas mixture returning from the probe 10. The high pressure and low pressure gas tubing 36, 38 is connected to the outlet and inlet, respectively, of a gas compressor 42. The high pressure tube 36 is also connected to a high pressure passageway through a precooling heat exchanger 44, and the low pressure tube 38 is connected to a low pressure passageway through the heat exchanger 44. The heat exchanger 44 precools the warm high pressure gas mixture by heat exchange with the cool low pressure expanded gas mixture, before the high pressure gas is expanded at the cold tip 16.
A high pressure outlet 46 of the heat exchanger 44 is connected to a high pressure conduit 48 which passes through the hollow cannula 14 to the cold tip 16. At the distal end of the high pressure conduit 48 is a Joule-Thomson expansion element 50, located in, or immediately adjacent to, the cold tip 16. High pressure cryogenic gas mixture passing through the high pressure conduit 48 is isenthalpically expanded by the expansion element 50, to significantly lower the temperature of the gas mixture. The colder, low pressure gas mixture is then exposed to the cold tip 16, to cool the target tissue via the thermally conductive sheath tip 26. A separator plate 52 isolates the low pressure region of the cold tip 16 from the probe cannula 14.
Low pressure gas mixture passes back through openings in the separator plate 52 to return via the probe cannula 14 to the low pressure inlet 54 of the heat exchanger 44. The flow of the low pressure gas mixture back through the cannula 14 can actually be via a low pressure conduit not shown in Figure 4.
A female connector fitting 56 is provided in the distal portion of the probe handle 12, to provide for a mating location between the probe 10 and the sheath 20.
An inwardly projecting latching flange 58 can be provided around the outer perimeter of the female connector 56. One or more connector elements 60 can be provided within the female connector 56 for mating with auxiliary instrumentation carried by the sheath 20. The connector element 60 can be an electrical contact for use with auxiliary instrumentation such as a temperature sensor, a heater, or an ultrasonic transducer. Similarly, the connector element 60 can be an optical element for use with auxiliary instrumentation such as viewing optics, illumination optics, or laser optics.
The connector element 60 is connected by way of an instrumentation conductor 62 to a display or control device 64. The instrumentation conductor 62 can be an electrical conductor or an optical fiber bundle, as appropriate. Only one set of connector element 60, conductor 62 and display or control device 64 is shown, for the sake of simplicity, but it should be understood that a plurality of such systems could be used in any given cryosurgical instrument 40. Further, it should be understood that the display or control device 64 could be located remotely from the instrument 40, such as would be appropriate for a video optical viewing system. An alignment rib 66 can be formed on the perimeter of the probe handle 12, to assist in alignment of the probe handle 12 with the sheath grip 22.
Figure 5 shows that the connector body 28 has a longitudinal bore 68 therethrough, to allow the passage of the probe cannula 14. The fitting 30 is in fluid flow communication with the bore 68, to provide fluid flow to the exterior of the hollow catheter 24, which extends into the bore 68. A male connector fitting 70 is provided on the proximal portion of the connector body 28 to mate with the female connector fitting 56 in the distal portion of the probe handle 12. A
releasable latch 72 is provided on the male connector fitting 70, to engage the latching flange 58. One or more connector elements 74 are also provided on the male connector fitting 70 to engage the connector elements 60 within the female connector fitting 56 in the probe handle 12. Connection of the connector element 74 to the auxiliary instrumentation, and connection of the fluid flow path from the fitting 30 to the hollow catheter 24 are shown better in a later Figure. Figure 6 is an end view of the probe handle 12, showing the interior of the female connector fitting 56. A plurality of connector elements 60 are shown arranged in a circle within the female fitting 56.
Figure 7 shows the sheath 20 with the shroud 23 in the furled, or contracted, condition. The sheath would normally be shipped and stored in this condition until disposition over a cryosurgical probe 10. Tabs 78 are provided on the proximal end of the shroud 23 to assist in pulling the shroud 23 over the probe handle 12 and the umbilical cord 18. Figure 8 is a section view showing more detail of one embodiment of the sheath 20. An alignment groove 76 is shown in the inner bore of the sheath grip 22, to mate with the alignment rib 66 on the exterior of the probe handle 12.
It can be seen that the connector body 28 can be constructed as a multi-piece assembly.
Figure 9 shows more detail of one embodiment of the connector body 28 and its connection to the sheath grip 22. The connector body 28 comprises essentially a distal section 80, an intermediate section 82, and a proximal section 84. The distal section 80 includes the finger slide 34, and the distal portion of the distal section 80 is attached to the hollow catheter 24. The intermediate section 82 is mounted within the proximal portion of the distal section 80, and it provides a means of connecting the distal section 80 to the instrumentation connectors 74 and to the releasable latch 72.
The intermediate section 82 can consist of a barrel 92 as shown, threaded to the latch 72. A collet 86 is captured between the barrel 92 and the latch 72. The collet 86 is attached to a sleeve 90 which is in turn attached to a connector fixture 96.
Instrumentation conductors 94 are connected to the instrumentation connectors 74.
The instrumentation conductors 94 pass through or alongside the longitudinal bore 68 to the catheter 24.
Figure 10 shows more detail of one embodiment of the distal portion of the distal section 80 of the connector body 28. The distal end of the longitudinal bore 68 terminates in a fluid bore 100, which is in fluid flow communication with an internal bore 98 of the fitting 30. The proximal portion of the hollow catheter 24 extends into the fluid bore 100, with the diameter of the fluid bore 100 being larger than the outer diameter of the catheter 24. This leaves a fluid flow space surrounding the catheter 24 in the fluid bore 100. The proximal end 102 of the fluid bore 100 can be terminated by a shoulder in the longitudinal bore 68. Conversely, the proximal end 102 of the fluid bore 100 can be terminated by an epoxy seal. The probe cannula 14 can fit snugly within the longitudinal bore 68. The distal end of the connector body 28 can be fitted with a strain relief collar 106 to fasten the catheter 24 to the connector body 28. A space 108 within the collar 106 can be filled with epoxy to terminate the distal end of the fluid bore 100.
Figure 11 shows a section view of the distal portion of the connector body 28 and the proximal portion of the hollow catheter 24. In this view, it can be seen that the catheter 24 is a multi-lumen catheter. A plurality of lumens 110 pass longitudinally through the wall of the catheter 24. Some of the lumens I 10 are used to conduct fluid flow, as shown at 112, and other lumens are used to conduct auxiliary instrumentation signals, as shown at 114. Within the fluid bore 100 only, the fluid lumens 112 are open to the exterior of the catheter 24, while the fluid lumens along the remainder of the length of the catheter 24 are not open to the exterior. The instrumentation lumens 114 are closed to the exterior throughout the length of the catheter 24. Since the fluid lumens 112 are open to the exterior within the fluid bore 100, fluid can flow from the fitting 30 into the wall of the catheter 24, or out of the wall of the catheter 24 to the fitting 30. A central bore 116 passes through the catheter 24 to accommodate the probe cannula 14.
Figure 12A shows a transverse section view of the catheter 24 and the probe cannula 14, forward of the connector body 28. The cannula 14 incorporates a set of three coaxial stainless steel tubes 48,55,57, with the outer tube 57 fitting substantially snugly within the catheter 24. It can be seen that a vacuum or insulation space 118 is formed between the outer tube 57 and a low pressure conduit 55. The low pressure conduit 55 leads to the low pressure inlet 54 of the heat exchanger 44. The high pressure conduit 48 lies within the low pressure conduit 55.
Figure 12B shows a transverse section view of an alternate embodiment of the catheter 24 and the probe cannula 14, forward of the connector body 28. The cannula 14 incorporates a set of two coaxial stainless steel tubes 48, 55, with the outer tube 55 fitting substantially snugly within an inner tube 117 in the catheter 24. It can be seen that a vacuum jacket or insulation space 118 is formed within the catheter 24, between the inner tube 117 and the catheter 24. Here as before, the low pressure conduit 55 leads to the low pressure inlet 54 of the heat exchanger 44. The high pressure conduit 48 lies within the low pressure conduit 55.
Figure 13 shows an elevation view of the distal end of the hollow catheter 24 and the sheath tip 26. A plurality of ports 120 in the lumens I 10 are formed in the distal end of the catheter 24. Some of the ports 120 are for fluid flow to or from the area adjacent the sheath tip 26. Other ports 120 are for optical elements to support viewing, illumination, or laser systems. Still other ports 120 could be used as connection terminals for electrical connection to a temperature sensor, heater, or ultrasonic transducer in the sheath tip 26.
Figure 14 shows a longitudinal section of the distal portion of the catheter and the sheath tip 26. The auxiliary instrumentation conductor 94 passes through a lumen 114 to the distal end of the catheter 24, at which point it connects to an optical element in the port 120, or to an auxiliary instrument 126 in the sheath tip 26. The auxiliary instrument 126 could be a temperature sensor, a heater, a tissue impedance measuring component, or an integrated component for performing two or more of the temperature sensing, impedance measuring, and heating functions. For example, the instrument 126 could be a combination heater and resistance temperature detector (RTD) constructed of foil laminated between very thin (0.003 in.) sheets of polyimide film. Further, the auxiliary instrument could be an ultrasonic transducer.
Those auxiliary instruments 126 which are in the sheath tip 26 can be sandwiched between an inner thermally conductive layer 122 and an outer thermally conductive layer 124.
The inner conductive layer 122 can be made of copper, and the outer conductive layer 124 can be made of stainless steel. If desired, epoxy can be injected between the instrument 126 and the conductive layers 122, 124. An epoxy bleed hole 128 in the outer layer 124 is provided for this purpose. If insulating layers are placed between the instrument 126 and the inner and outer layers 122, 124, the insulating layers must be sufficiently thin to allow heat transfer therethrough. A thermally conducting grease 130 can be provided within the sheath tip 26 to maximize the thermal contact between the probe tip 16 and the sheath tip 26.
Figure 15 shows yet another embodiment of the sheath 220 of the present invention, in which one or more biasing elements in the catheter assembly 223 bias the conductive tip 226 of the catheter 224 against the cold tip 16 of the probe cannula 14. The sheath 220 includes a hollow grip 222, into which a catheter assembly 223 is attachable. The catheter assembly 223 includes a catheter 224 and a connector body 228. The sheath 220 can be attached to a cryosurgical probe handle represented in phantom, by means of one or more latches 225. The catheter 224 can be constructed of a pliable material, such as an elastomer, which can be stretched, and which will be biased toward its unstretched length. Similarly, the connector body 228 can be constructed of a pliable material, such as an elastomer, which can be deformed, and which will be biased toward its undeformed shape.
Figure 16 shows a larger scale longitudinal section view of the distal portion of the grip 222 and the proximal portion of the catheter assembly 223. Also shown is an elevation view of the proximal portion of the cannula 14 of the cryosurgical probe 10.
The connector body 228 has a substantially tubular distal portion 231 which fits snugly into a longitudinal bore in the distal end of the hollow grip 222. The distal portion 231 of the connector body 228 can be held in a desired longitudinal position by one or more annul.ar o-rings 227. The connector body 228 can also have a conical apron 233 on its proximal end, which bears against the distal wall of the cavity within the hollow grip 222. The proximal end 229 of the catheter 224 is attached within a longitudinal bore in the distal portion 231 of the connector body 228 by being glued or otherwise bonded thereto. The seal between the catheter 224 and the connector body 228, and the seal created by the o-rings 227, create a sterile barrier at the distal end of the hollow grip 222.
The catheter assembly 223, including its conductive tip 226, is formed with an undeformed length which is slightly less than the necessary length to accommodate the length of the cannula 14, including its cold tip 16. Therefore, when the cryoprobe 10 is inserted into the sheath 220, in order to latch the sheath 220 to the cryoprobe 10 handle, it is necessary to slightly stretch or otherwise deform one or more components of the catheter assembly 223. The stretching or deformation in the embodiment shown can occur in the connector body 228, or in the catheter 224, or in both.
When the catheter assembly 223 has been deformed to accommodate the length of the cannula 14, the elastic quality of the catheter assembly 223 causes it to bias the conductive tip 226 proximally against the cold tip 16 of the cryoprobe 10.
This insures a positive contact between the conductive tip 226 of the catheter assembly 223 and the cold tip 16 of the cryoprobe 10, thereby maximizing the heat transfer from the environment to the cryoprobe 10.
Rather than using elastic materials, a similar effect can be accomplished by using other types of biasing elements, such as one or more springs (not shown), to bias the catheter assembly proximally, without departing from the spirit of the present invention. Further, the conductive tip 226 or the cold tip 16, or both, can be slightly tapered to increase the positive contact area between the two tips.
While the particular invention as herein shown and disclosed in detail is fully capable of obtaining the objects and providing the advantages hereinbefore stated, it is to be understood that this disclosure is merely illustrative of the presently preferred embodiments of the invention and that no limitations are intended other than as described in the appended claims.
Claims (19)
1. A sheath for use as a removable cover for a cryosurgical probe, said sheath comprising:
a hollow grip removably attachable to a cryosurgical probe;
a thermally resistive catheter assembly attachable to said hollow grip, said catheter assembly having a tubular passageway for receiving a cannula portion of a cryosurgical probe;
a thermally conductive segment on said catheter assembly, said conductive segment being in thermal contact with a heat transfer portion of a cryosurgical probe, when said catheter assembly is disposed over a cannula portion of a cryosurgical probe; and a biasing element on said catheter assembly, said biasing element being constructed to longitudinally bias said conductive segment of said catheter assembly against a heat transfer portion of a cryosurgical probe when said hollow grip is attached to a cryosurgical probe.
a hollow grip removably attachable to a cryosurgical probe;
a thermally resistive catheter assembly attachable to said hollow grip, said catheter assembly having a tubular passageway for receiving a cannula portion of a cryosurgical probe;
a thermally conductive segment on said catheter assembly, said conductive segment being in thermal contact with a heat transfer portion of a cryosurgical probe, when said catheter assembly is disposed over a cannula portion of a cryosurgical probe; and a biasing element on said catheter assembly, said biasing element being constructed to longitudinally bias said conductive segment of said catheter assembly against a heat transfer portion of a cryosurgical probe when said hollow grip is attached to a cryosurgical probe.
2. A sheath as recited in claim 1, wherein said biasing element comprises an elastic material.
3. A sheath as recited in claim 1, wherein said catheter assembly comprises:
a connector body attachable to said hollow grip; and a catheter attached to said connector body.
a connector body attachable to said hollow grip; and a catheter attached to said connector body.
4. A sheath as recited in claim 3, wherein said connector body comprises said biasing element.
5. A sheath as recited in claim 4, wherein said connector body comprises an elastic material.
6. A sheath as recited in claim 3, wherein said catheter comprises said biasing element.
7. A sheath as recited in claim 6, wherein said catheter comprises an elastic material.
8. A sheath as recited in claim 3, wherein said catheter and said connector body, in combination, comprise said biasing element.
9. A sheath as recited in claim 8, wherein said catheter and said connector body comprise elastic materials.
10. A cryosurgical instrument, comprising:
a probe handle;
a probe cannula attached to said probe handle;
a heat transfer element on said probe cannula;
a cooling system providing a coolant at a desired temperature adjacent said heat transfer element;
a hollow grip removably attachable to said probe handle;
a catheter assembly attachable to said hollow grip, said catheter assembly having a tubular passageway for receiving said probe cannula;
a thermally conductive segment on said catheter assembly, said conductive segment being in thermal contact with said heat transfer element, when said catheter assembly is disposed over said probe cannula; and a biasing element on said catheter assembly, said biasing element being constructed to longitudinally bias said conductive segment of said catheter assembly against a heat transfer portion of a cryosurgical probe when said hollow grip is attached to a cryosurgical probe.
a probe handle;
a probe cannula attached to said probe handle;
a heat transfer element on said probe cannula;
a cooling system providing a coolant at a desired temperature adjacent said heat transfer element;
a hollow grip removably attachable to said probe handle;
a catheter assembly attachable to said hollow grip, said catheter assembly having a tubular passageway for receiving said probe cannula;
a thermally conductive segment on said catheter assembly, said conductive segment being in thermal contact with said heat transfer element, when said catheter assembly is disposed over said probe cannula; and a biasing element on said catheter assembly, said biasing element being constructed to longitudinally bias said conductive segment of said catheter assembly against a heat transfer portion of a cryosurgical probe when said hollow grip is attached to a cryosurgical probe.
11. A cryosurgical instrument as recited in claim 10, wherein:
said probe cannula is inserted in a distal direction into said catheter assembly;
and said biasing element generates a proximally directed bias against said conductive segment of said catheter assembly.
said probe cannula is inserted in a distal direction into said catheter assembly;
and said biasing element generates a proximally directed bias against said conductive segment of said catheter assembly.
12. A cryosurgical instrument as recited in claim 11, wherein insertion of said probe cannula into said catheter assembly and attachment of said hollow grip to said probe handle axially stretches said biasing element to create said proximally directed bias.
13. A cryosurgical instrument as recited in claim 12, wherein said biasing element comprises a catheter in said catheter assembly.
14. A cryosurgical instrument as recited in claim 13, wherein said catheter comprises an elastic material.
15. A cryosurgical instrument as recited in claim 12, wherein said biasing element comprises a connector body in said catheter assembly.
16. A cryosurgical instrument as recited in claim 15, wherein said connector body comprises an elastic material.
17. A cryosurgical instrument as recited in claim 12, wherein said biasing element comprises a catheter and a connector body, in said catheter assembly.
18. A cryosurgical instrument as recited in claim 17, wherein said catheter and said connector body comprise elastic materials.
19. A sheath for use as a removable cover for a cryosurgical probe, said sheath comprising:
a hollow grip removably attachable to a cryosurgical probe;
a connector body attachable to said hollow grip;
a thermally resistive catheter attached to said connector body, said catheter having a tubular passageway for receiving a cannula portion of a cryosurgical probe; and a thermally conductive segment on said catheter, said conductive segment being in thermal contact with a heat transfer portion of a cryosurgical probe, when said catheter is disposed over a cannula portion of a cryosurgical probe;
wherein said sheath is constructed to cause attachment of said hollow grip to a cryosurgical probe to result in a heat transfer portion of the probe pushing in a distal direction against said conductive segment of said catheter assembly, thereby stretching at least one of said catheter and said connector body, and thereby longitudinally biasing said conductive segment against the heat transfer portion of the cryosurgical probe.
a hollow grip removably attachable to a cryosurgical probe;
a connector body attachable to said hollow grip;
a thermally resistive catheter attached to said connector body, said catheter having a tubular passageway for receiving a cannula portion of a cryosurgical probe; and a thermally conductive segment on said catheter, said conductive segment being in thermal contact with a heat transfer portion of a cryosurgical probe, when said catheter is disposed over a cannula portion of a cryosurgical probe;
wherein said sheath is constructed to cause attachment of said hollow grip to a cryosurgical probe to result in a heat transfer portion of the probe pushing in a distal direction against said conductive segment of said catheter assembly, thereby stretching at least one of said catheter and said connector body, and thereby longitudinally biasing said conductive segment against the heat transfer portion of the cryosurgical probe.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/382,533 | 1999-08-25 | ||
| US09/382,533 US6270494B1 (en) | 1996-12-26 | 1999-08-25 | Stretchable cryoprobe sheath |
| PCT/US2000/018788 WO2001013782A1 (en) | 1999-08-25 | 2000-08-24 | Stretchable cryoprobe sheath |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2382226A1 CA2382226A1 (en) | 2001-03-01 |
| CA2382226C true CA2382226C (en) | 2008-07-08 |
Family
ID=23509380
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002382226A Expired - Fee Related CA2382226C (en) | 1999-08-25 | 2000-08-24 | Stretchable cryoprobe sheath |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6270494B1 (en) |
| EP (1) | EP1210000B1 (en) |
| JP (1) | JP4275341B2 (en) |
| AT (1) | ATE317663T1 (en) |
| AU (1) | AU757135B2 (en) |
| CA (1) | CA2382226C (en) |
| DE (1) | DE60026041T2 (en) |
| ES (1) | ES2254214T3 (en) |
| WO (1) | WO2001013782A1 (en) |
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-
1999
- 1999-08-25 US US09/382,533 patent/US6270494B1/en not_active Expired - Lifetime
-
2000
- 2000-08-24 WO PCT/US2000/018788 patent/WO2001013782A1/en active IP Right Grant
- 2000-08-24 EP EP00959145A patent/EP1210000B1/en not_active Expired - Lifetime
- 2000-08-24 ES ES00959145T patent/ES2254214T3/en not_active Expired - Lifetime
- 2000-08-24 CA CA002382226A patent/CA2382226C/en not_active Expired - Fee Related
- 2000-08-24 DE DE60026041T patent/DE60026041T2/en not_active Expired - Fee Related
- 2000-08-24 AT AT00959145T patent/ATE317663T1/en not_active IP Right Cessation
- 2000-08-24 JP JP2001517928A patent/JP4275341B2/en not_active Expired - Fee Related
- 2000-08-24 AU AU70516/00A patent/AU757135B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| ATE317663T1 (en) | 2006-03-15 |
| EP1210000B1 (en) | 2006-02-15 |
| AU757135B2 (en) | 2003-02-06 |
| EP1210000A1 (en) | 2002-06-05 |
| CA2382226A1 (en) | 2001-03-01 |
| DE60026041T2 (en) | 2006-10-26 |
| US6270494B1 (en) | 2001-08-07 |
| JP2003507110A (en) | 2003-02-25 |
| JP4275341B2 (en) | 2009-06-10 |
| DE60026041D1 (en) | 2006-04-20 |
| AU7051600A (en) | 2001-03-19 |
| ES2254214T3 (en) | 2006-06-16 |
| EP1210000A4 (en) | 2004-08-04 |
| WO2001013782A1 (en) | 2001-03-01 |
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Legal Events
| Date | Code | Title | Description |
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| EEER | Examination request | ||
| MKLA | Lapsed |
Effective date: 20130826 |