This invention relates to deflectable medical catheters, namely steerable sheaths used in interventional vascular procedures to deliver tools into the human body. More particularly, the present invention is related to a slidable valve adaptor that solves the problems created by sheath lengthening when the sheath is subjected to elevated temperatures.
Deflectable medical catheters, namely steerable sheaths are used in interventional vascular procedures to deliver tools (e.g. electrophysiology catheters, guidewires, balloons catheters, stents, instruments, etc.) into the human body.
MRI has achieved prominence as a diagnostic imaging modality, and increasingly as an interventional imaging modality. The primary benefits of MRI over other imaging modalities, such as X-ray, include superior soft tissue imaging and avoiding patient exposure to ionizing radiation produced by X-rays. MRI's superior soft tissue imaging capabilities have offered great clinical benefit with respect to diagnostic imaging. Similarly, interventional procedures, which have traditionally used X-ray imaging for guidance, stand to benefit greatly from MRI's soft tissue imaging capabilities. In addition, the significant patient exposure to ionizing radiation associated with traditional X-ray guided interventional procedures is eliminated with MRI guidance.
A variety of MRI techniques are being developed as alternatives to X-ray imaging for guiding interventional procedures. For example, as a medical device is advanced through the patient's body during an interventional procedure, its progress may be tracked so that the device can be delivered properly to a target site. Once delivered to the target site, the device and patient tissue may be monitored to improve therapy delivery. Thus, tracking the position of medical devices is useful in interventional procedures. Exemplary interventional procedures include, for example, cardiac electrophysiology procedures including diagnostic procedures for diagnosing arrhythmias and ablation procedures such as atrial fibrillation ablation, ventricular tachycardia ablation, atrial flutter ablation, Wolfe Parkinson White Syndrome ablation, AV node ablation, SVT ablations and the like. Tracking the position of medical devices using MRI is also useful in oncological procedures such as breast, liver and prostate tumor ablations; and urological procedures such as uterine fibroid and enlarged prostate ablations.
MRI uses three fields to image patient anatomy: a large static magnetic field, a time-varying magnetic gradient field, and a radiofrequency (RF) electromagnetic field. The static magnetic field and time-varying magnetic gradient field work in concert to establish both proton alignment with the static magnetic field and also spatially dependent proton spin frequencies (resonant frequencies) within the patient. The RF field, applied at the resonance frequencies, disturbs the initial alignment, such that when the protons relax back to their initial alignment, the RF emitted from the relaxation event may be detected and processed to create an image.
Each of the three fields associated with MRI presents safety risks to patients when a medical device is in close proximity to or in contact either externally or internally with patient tissue. One important safety risk is the heating that may result from an interaction between the RF field of the MRI scanner and the medical device (RF-induced heating), especially medical devices that have elongated conductive structures, such as braiding and pull-wires in catheters and sheaths.
The RF-induced heating safety risk associated with elongated metallic structures in the MRI environment results from a coupling between the RF field and the metallic structure. In this case several heating related conditions exist. One condition exists because the metallic structure electrically contacts tissue. RF currents induced in the metallic structure may be delivered into the tissue, resulting in a high current density in the tissue and associated Joule or Ohmic tissue heating. Also, RF induced currents in the metallic structure may result in increased local specific absorption of RF energy in nearby tissue, thus increasing the tissue's temperature. The foregoing phenomenon is referred to as dielectric heating. Dielectric heating may occur even if the metallic structure does not electrically contact tissue, such metallic braiding used in a steerable sheath. In addition, RF induced currents in the metallic structure may cause Ohmic heating in the structure, itself, and the resultant heat may transfer to the patient. In such cases, it is important to attempt to both reduce the RF induced current present in the metallic structure and/or eliminate it all together by eliminating the use of metal braid and long metallic pull-wires.
The static field of the MRI will cause magnetically induced displacement torque on any device containing ferromagnetic materials and has the potential to cause unwanted device movement. It is important to construct the sheath and control handle from non-magnetic materials, to eliminate the risk of unwanted device movement.
When performing interventional procedures under MRI guidance, clinical grade image quality must be maintained. Conventional steerable sheaths are not designed for the MRI and may cause image artifacts and/or distortion that significantly reduce image quality. Constructing the sheath from non-magnetic materials and eliminating all potentially resonant conductive structures allows the sheath to be used during active MR imaging without impacting image quality. Similarly, it is as important to ensure that the control handle is also constructed from non-magnetic materials thereby eliminating potentially resonsant conductive structures that may prevent the control handle being used during active MR imaging.
MR compatible steerable sheaths utilize a fiber optic braid, a replacement for the stainless steel braid that has traditionally been used in sheath and catheter shafts. The advantage of the fiber optic braid is that it is entirely non-metallic, and therefore MR compatible. In addition, the fiber optic braid still imparts similar mechanical attributes to the sheath shaft as does a stainless steel braid. However, one significant disadvantage of the fiber optic braid is that when it is exposed to elevated temperatures, such as during a sterilization process, it expands in the linear direction and increases the overall length of the sheath shaft. Studies of sheath shaft designs have shown that the shaft may lengthen as much as 0.250″ during the elevated temperatures (65° C.). This effect has also occurs in shafts constructed with non-MR compatible sheaths such as stainless steel braid, but the lengthening is less, about 0.080″. When the shaft returns to room temperature, the length of the shaft returns to is original length. However, the expansion of the shaft creates an issue for the sheath in which the shaft is housed.
During the manufacture of the sheath, the shaft is assembled with taught pull wires. If the shaft is not assembled in this fashion, it creates a ‘dead zone’ in the sheath handle. The ‘dead zone’ is a moment in the sheath handle knob rotation in which movement of the knob causes no deflection in the sheath in either direction. Clinicians are accustomed to a slight ‘dead zone’ but more than half a knob turn is not desirable. Some clinicians, however, have expressed a desire for total elimination of the dead zone.
The sheath is subjected to elevated temperatures during the sterilization process prior to use. Additionally, the sheath assembly may also be exposed to elevated temperatures during transportation and storage as it makes its way to a hospital. When subjected to elevated temperatures the fiber optic braid expands, as noted above, and in turn causes the sheath shaft to expand. Because the pull wires are taught, as assembled, and made of non-expansionable Kevlar, the stress of the expansion has to be relieved somewhere in the shaft. The stress relief location is typically the softest section of the shaft, in which the steerable region is located. This results in permanent compression of the steerable region. When the shaft returns to normal temperature, the permanent deformation in the steerable section creates slack in the pull wires, which results in a significant ‘dead zone’ in the sheath handle.
Thus what is needed is a design MR compatible control handle that solves the foregoing dead-zone issues.
The foregoing need is addressed by the steerable sheath with slidable valve adaptor in accordance with the invention. Those of skill in the art will appreciate that the valve adaptor in accordance with the invention is disclosed as being utilized with the steerable sheath and control handle as described herein but may also be utilized with other steerable sheaths and control handles, all of which fall within the scope of the invention.
In one aspect of the invention a steerable sheath is provided that may be used in an MRI environment to deliver a variety of tools (catheters, guidewires, implantable devices, etc.) into the lumens of the body.
In a further aspect of the invention, the steerable sheath shaft comprises a reinforced polymer tube in which the reinforcing material is non-metallic based (Kevlar, PEEK, Nylon, fabric, polyimide, etc.) or a hybrid of metallic and non-metallic materials and the reinforcing geometry may comprise a braid, a coil, or a slit tube that mimics a coil and combinations of the foregoing. In yet another aspect of the invention, the reinforced polymer tube may also be segmented with varying flexibility along its length to provide the user with the ability to deflect the catheter in a region in which the segment is more flexible than other segments.
In yet another aspect of the invention the polymer tube may also include one or more passive visualization markers along the length of the tube and/or one or more active visualization markers along the length of the tube.
The steerable sheath in accordance with the invention also includes one or more pull-wires which are coupled with the reinforced tube and that allow the user to manipulate and deflect the polymer tube. In one aspect of the invention, the pull-wires are preferably made of a non-metallic material (Kevlar, PEEK, Nylon, fabric, etc.). One or more internal pull-wire lumens are positioned within the polymer tube construct and allow the user to manipulate the pull-wires to move smoothly during actuation. One or more anchor points connect the pull-wire in the distal portion of the polymer tube.
In another aspect of the invention a control handle on the proximal end of the reinforced tube operates longitudinal movement of the pull-wire(s). In one aspect of the invention, the handle includes paramagnetic or diamagnetic materials or combinations of paramagnetic and diamagnetic materials.
In another aspect of the invention, an MR compatible steerable sheath is provided. The MR compatible steerable sheath includes a steerable shaft including a proximal end and a deflectable distal tip, the steerable shaft configured to receive first and second longitudinal movement wires operably coupled to the deflectable distal tip, the proximal end slidably receivable within a lumen of a t-valve axel; a hemostasis valve assembly operably coupled to the proximal end of the steerable shaft; a slidable valve adaptor operably coupled to the hemostasis valve assembly and configured to be slidably receivable within the lumen of the t-valve axel; a control handle having a main body configured to receive the valve adaptor and hemostasis valve assembly and the first and second rack screws, the second rack screw including a threaded portion on an outer surface thereof, the steerable shaft extending axially through the control handle; the first longitudinal movement wire operably coupled to the first rack screw and the second longitudinal movement operably coupled to the second rack screw; and a rotatable adjustment knob operably engageable with the control handle, the rotatable adjustment knob having an internal threaded portion matingly engageable with the threaded portion of the second rack screw, the rotatable adjustment knob moveable between a first position in which the internal thread is configured to engage the thread on the outer surface of the second rack screw and cause the second rack screw to move proximally to cause proximal longitudinal movement of the second longitudinal movement wire and a second position in which the internal thread is configured to move the second rack screw in a distal direction to release tension on the second longitudinal movement wire, wherein the valve adaptor is configured to remove the slack from the first and second longitudinal movement wires when slidingly moved to a second position.
In another aspect of the invention, a valve adaptor is coupled to the sheath hemostasis valve assembly, the sheath hemostasis valve assembly being coupled to the sheath shaft. The valve adaptor is slidably moveable from a first position to a locked second position.
In another aspect of the invention, the slidable valve adaptor is configured to maintain the steerable shaft in a proximal position such that there is slack in said first and second longitudinal movement wires when said valve adaptor is in a first position, said slidable valve adaptor is configured to remove slack from said first and second longitudinal movement wires when said valve adaptor is slidably moved to said second position.
In another aspect of the invention the distance between the first and second positions is approximately 0.250″ or greater.
In another aspect of the invention a locking mechanism is provided to lock the valve adaptor in the second position.
In another aspect of the invention the valve adaptor moves to the first position by providing a mating relationship between the valve adaptor and a collar on the sheath.
In another aspect of the invention the valve adaptor moves to the first position by providing a spring mechanism that automatically moves the valve adaptor to the first position.
These and other aspects of the invention will now be described in detail with reference to the accompanying Figures.
For a better understanding of the invention, and to show how the same may be carried into effect, reference will now be made, by way of example, to the accompanying drawings, in which:
Numerous structural variations of an MR compatible steerable sheath and control handle in accordance with the invention are contemplated and within the intended scope of the invention. Those of skill in the art will appreciate that the exemplary control handle may be coupled to other types of steerable sheath shafts. In addition, those of skill in the art will appreciate that the exemplary steerable sheath shaft may be coupled with other control handles. Therefore, for purposes of discussion and not limitation, an exemplary embodiment of the MR compatible steerable sheath shaft and control handle with valve adaptor will be described in detail below.
Referring to the FIGS. like elements have been numbered with like reference numerals.
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Those of skill in the art will appreciate that the orientation of the first and second rack screws may be changed without departing from the scope of the invention. As may be seen in
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Rotatable adjustment knob 20′ of
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Distal end 14 includes transition section 180, deflectable tip portion 200, and magnetic marker 220. Pressure relief holes 240, 260 may be formed in the tubular shaft 120 at the distal end 140. Those of skill in the art will appreciate that while only two pressure relief holes 240, 260 are shown there may any number of pressure relief holes formed and still be within the scope of the invention. When retracting an item housed by the sheath shaft 100, such as a catheter or MR active tracking system, pressure may form at the end of the sheath thereby drawing or sucking in tissue. Pressure relief holes 240, 260 are designed to reduce this pressure thereby ameliorating the risk of tissue damage.
Transition section 180 is optionally included for purposes of manufacturability. The deflectable tip section 20 has a significantly lower durometer making it more malleable and flexible than the main body portion 170 of tubular shaft 120 which has a higher durometer or, in other words, quite stiff. As a consequence, these two sections do not bond to one another well. Transitional section 180 has a mid-range durometer allowing it to bond well to both the deflectable tip section 200 and the main body 170 of the tubular shaft 120. Those of skill in the art will appreciate that the transition section 180 may be of any length desired so as to provide an adequate transition between the distal tip portion 200 and the main body portion 170. In one exemplary embodiment transition section may range from about 0.25 to about 0.75 inches. In addition, those of skill in the art will appreciate that transition section may be eliminated and the deflectable tip section 200 may be coupled to the main body 170 of tubular shaft 120 by means known to those of skill in the art without departing from the spirit of the invention.
Steerable sheath shaft 100 includes central lumen 300 therewithin. In one aspect of the invention, the inner diameter 150 of the tubular shaft 120 is approximately 6 French or greater but those of skill in the art will appreciate that varying internal diameters may be used depending on the particular application without departing from the scope of the present invention. Central lumen 300 may include one or more liners (not shown) disposed therewithin to allow for easier movement of instruments therethrough. Liners may comprise materials made from polytetrafluoroethylene (PTFE), fluorinated ethylene propylene copolymer (FEP), nylons and combinations of the foregoing. Alternatively, the lumen 300 may be coated with any such polymers. The polymer tubular shaft 120 may also include one or more passive visualization markers, such as a ferrous or magnetic marker 220, disposed circumferentially about the tubular shaft 120 at one or more locations along the length thereof and/or one or more active visualization markers such as an active tracking coil along the length of the tube. An active tracking coil may comprise one or more small antennas integrated into the device and include traces on a circuit board, coiled wire, and/or a dipole. If an active visualization marker is used, one or more devices may be included in the conductors to mitigate RF field heating may be included. Such devices include chokes, transformers, impedances, and other such devices known to those of skill in the art. One or more fluoroscopy markers (not shown) may also be included along the length of the polymer tubular shaft 12.
One or more optional fluid ports (not shown) may be located on the proximal end 16 of the tubular shaft 12 to allow for homeostasis of the sheath with the patient body. The fluid port(s) allows access for the user or physician to aspirate blood from the steerable sheath lumen 30 and flush with saline. Aspirating and flushing of the sheath prevents air from entering the body before and during insertion of a tool and/or catheter.
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The material used in the reinforcement construct 320 may be non-metallic such as Kevlar, PEEK, Nylon, fabric, polyimide, fiber optic, silica glass and the like or may also be hybrid of metallic, such as stainless steel, and non-metallic materials. Those of skill in the art will appreciate that, the reinforced polymer tubular shaft 140 may be segmented and each segment may be constructed with varying flexibility along the segment to provide the user with the ability to deflect the sheath in a region in which the segment is more flexible than in other segments. Varying flexibility and thus deflectability may be accomplished by having braids or coils that have greater braiding or coils per sq. cm than in other segments where the braiding or coiling would be less per sq. cm. Flexibility and deflectability may also be accomplished by the varying durometers as herein described.
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One or more internal pull-wire lumens 360 are constructed of a flexible, non-metallic material such as PTFE. Internal pull-wire lumens 360 facilitate smooth manipulation of the pull-wires 320, 340 during actuation. Internal pull-wire lumens 360 have an outer diameter of approximately 0.12 inches and an inner diameter of approximately 0.010 inches. However, those of skill in the art will appreciate that the dimensions of the internal pull-wire lumens 360 may vary with the dimensions of both the pull-wires 320, 340 and the tubular shaft 120 so long as they are dimensioned to house the pull-wires and allow pull-wires to move smoothly during actuation.
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As rotatable adjustment knob 20, 20′ is rotated in the clockwise direction and engages rack screws which in turn engage pinion gears, second pull wire 340, 340′ is pulled toward the proximal direction as best seen in
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As rotatable adjustment knob 20, 20′ is rotated in the counter-clockwise direction first pull wire 320, 320′ is pulled toward the proximal direction as best seen in
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A critical element of this design is that the distance between the first and second valve adaptor positions must be greater than the largest amount of lengthening the shaft will undergo. In other words, there has to be so much slack that the pull wires never become taught during elevated temperatures and before the valve adaptor is slid into the distal position. Thus, if the shaft undergoes a maximum of 0.250″ of lengthening, then the distance between the first and second valve adaptor positions must be greater than 0.250″.
After the valve adaptor 600 is moved into the distal position, locking mechanism 614 locks it into place when snap hooks 616 engage locking barbs 618. Those of skill in the art will appreciate that many different locking mechanisms may be used including snap hooks, annular snap features, detents, magnets, living hinge hooks, and the like.
Those of skill in the art will appreciate that various manual means for slidably moving the valve adaptor to the distal position fall within the scope of the invention. For example, another manual mechanism may include providing a threaded collar between the valve adaptor and main handle components. In this aspect, the valve adaptor may include a thread on its outer surface that matingly engages a corresponding thread on the collar. When the collar is rotated from a first position to a second position, the threading is such that the valve adaptor moves from the proximal position to the distal position.
In another aspect of the invention, the valve adaptor may move automatically by automatic mechanisms such as a spring. In this aspect, the spring is compressed during packaging. When the sheath is removed from the tray or other packaging, the spring releases and the valve adaptor automatically moves distally. In another aspect, a temperature sensitive piece may be provided. The temperature sensitive piece may comprise Nitinol or other self-expanding materials known to those of skill in the art. The temperature sensitive piece pushes the valve adaptor into the proximal position when the temperature is elevated, but returns the valve adaptor into the distal position when the temperature returns to baseline. This design would be slightly different because the handle would be assembled and packaged such that the valve adaptor is in the distal position.
An optional aspect of the valve adaptor 600 in accordance with the invention includes a safety cap as best seen in
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Although the present invention has been described with reference to various aspects of the invention, those of ordinary skill in the art will recognize that changes may be made in form and detail without departing from the spirit and scope of the invention.
This application claims the benefit of priority to U.S. Provisional application Ser. No. 62/157,785, filed on May 6, 2015; and is a continuation-in-part of U.S. application Ser. No. 14/106,177, filed on Dec. 13, 2013; which is a continuation-in-part of U.S. application Ser. No. 13/819,981, filed on Feb. 28, 2013, (abandoned); which claims the benefit of PCT application Serial No.: PCT/US2012/069487, filed on Dec. 13, 2012; which claims the benefit of U.S. Provisional application Ser. No. 61/576,161, filed on Dec. 15, 2011; and U.S. application Ser. No. 14/106,177 is a continuation application of PCT application Serial No.: PCT/US2013/074331, filed on Dec. 11, 2013. The entireties of all of the foregoing are hereby incorporated by reference.
Number | Date | Country | |
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62157785 | May 2015 | US | |
61576161 | Dec 2011 | US |
Number | Date | Country | |
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Parent | PCT/US2013/074331 | Dec 2013 | US |
Child | 14106177 | US |
Number | Date | Country | |
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Parent | 14106177 | Dec 2013 | US |
Child | 14844739 | US | |
Parent | 13819981 | Jan 2014 | US |
Child | 14106177 | US |