Cardiac arrhythmias, such as atrial fibrillation, occur when regions of cardiac tissue abnormally conduct electric signals. Procedures for treating arrhythmia include surgically disrupting the conducting pathway for such signals. By selectively ablating cardiac tissue by application of energy (e.g., radiofrequency (RF) energy), it may be possible to cease or modify the propagation of unwanted electrical signals from one portion of the heart to another. The ablation process may provide a barrier to unwanted electrical pathways by creating electrically insulative lesions or scar tissue that effectively block communication of aberrant electrical signals across the tissue.
In some procedures, a catheter with one or more RF electrodes may be used to provide ablation within the cardiovascular system. The catheter may be inserted into a major vein or artery (e.g., the femoral artery) and then advanced to position the electrodes within the heart or in a cardiovascular structure adjacent to the heart (e.g., the pulmonary vein). The one or more electrodes may be placed in contact with cardiac tissue or other vascular tissue and then activated with RF energy to thereby ablate the contacted tissue. In some cases, the electrodes may be bipolar. In some other cases, a monopolar electrode may be used in conjunction with a ground pad or other reference electrode that is in contact with the patient. Irrigation may be used to draw heat from ablating components of an ablation catheter; and to prevent the formation of blood clots near the ablation site.
Examples of ablation catheters are described in U.S. Pub. No. 2013/0030426, entitled “Integrated Ablation System using Catheter with Multiple Irrigation Lumens,” published Jan. 31, 2013, the disclosure of which is incorporated by reference herein, in its entirety; U.S. Pub. No. 2017/0312022, entitled “Irrigated Balloon Catheter with Flexible Circuit Electrode Assembly,” published Nov. 2, 2017, the disclosure of which is incorporated by reference herein, in its entirety; U.S. Pub. No. 2018/0056038, entitled “Catheter with Bipole Electrode Spacer and Related Methods,” published Mar. 1, 2018, the disclosure of which is incorporated by reference herein, in its entirety; U.S. Pat. No. 10,130,422, entitled “Catheter with Soft Distal Tip for Mapping and Ablating Tubular Region,” issued Nov. 20, 2018, the disclosure of which is incorporated by reference herein, in its entirety; and U.S. Pat. No. 9,801,585, entitled “Electrocardiogram Noise Reduction,” issued Oct. 31, 2017, the disclosure of which is incorporated by reference herein, in its entirety.
Some catheter ablation procedures may be performed after using electrophysiology (EP) mapping to identify tissue regions that should be targeted for ablation. Such EP mapping may include the use of sensing electrodes on a catheter (e.g., the same catheter that is used to perform the ablation or a dedicated mapping catheter). Such sensing electrodes may monitor electrical signals emanating from conductive endocardial tissues to pinpoint the location of aberrant conductive tissue sites that are responsible for the arrhythmia. Examples of EP mapping systems and catheters are described in various references cited herein.
When using an ablation catheter, it may be desirable to ensure that the one or more electrodes of the ablation catheter are sufficiently contacting target tissue. For instance, it may be desirable to ensure that the one or more electrodes are contacting target tissue with enough force to effectively apply RF ablation energy to the tissue; while not applying a degree of force that might tend to undesirably damage the tissue. To that end, it may be desirable to include one or more force sensors or pressure sensors to detect sufficient contact between one or more electrodes of an ablation catheter and target tissue.
In addition to using force sensing or EP mapping, some catheter ablation procedures may be performed using an image guided surgery (IGS) system. The IGS system may enable the physician to visually track the location of the catheter within the patient, in relation to images of anatomical structures within the patient, in real time. Some systems may provide a combination of EP mapping and IGS functionalities, including the CARTO 3® system by Biosense Webster, Inc. of Irvine, Calif. Examples of catheters that are configured for use with an IGS system are disclosed in U.S. Pat. No. 9,480,416, entitled “Signal Transmission Using Catheter Braid Wires,” issued Nov. 1, 2016, the disclosure of which is incorporated by reference herein, in its entirety; and various other references that are cited herein.
While several catheter systems and methods have been made and used, it is believed that no one prior to the inventors has made or used the invention described, illustrated and claimed herein.
The drawings and detailed description that follow are intended to be merely illustrative and are not intended to limit the scope of the invention as contemplated by the inventors.
The following description of certain examples of the invention should not be used to limit the scope of the present invention. The drawings, which are not necessarily to scale, depict selected embodiments and are not intended to limit the scope of the invention. The detailed description illustrates by way of example, not by way of limitation, the principles of the invention. Other examples, features, aspects, embodiments, and advantages of the invention will become apparent to those skilled in the art from the following description, which is by way of illustration, one of the best modes contemplated for carrying out the invention. As will be realized, the invention is capable of other different or equivalent aspects, all without departing from the invention. Accordingly, the drawings and descriptions should be regarded as illustrative in nature and not restrictive.
Any one or more of the teachings, expressions, versions, examples, etc. described herein may be combined with any one or more of the other teachings, expressions, versions, examples, etc. that are described herein. The following-described teachings, expressions, versions, examples, etc. should therefore not be viewed in isolation relative to each other. Various suitable ways in which the teachings herein may be combined will be readily apparent to those skilled in the art in view of the teachings herein. Such modifications and variations are intended to be included within the scope of the claims.
As used herein, the terms “about” or “approximately” for any numerical values or ranges indicate a suitable dimensional tolerance that allows the part or collection of components to function for its intended purpose as described herein. More specifically, “about” or “approximately” may refer to the range of values±10% of the recited value, e.g. “about 90%” may refer to the range of values from 81% to 99%. In addition, as used herein, the terms “patient,” “host,” “user,” and “subject” refer to any human or animal subject and are not intended to limit the systems or methods to human use, although use of the subject invention in a human patient represents a preferred embodiment.
As will be described in greater detail below, end effector (140) includes various components configured to deliver RF energy to targeted tissue sites, provide EP mapping functionality, track external forces imparted on end effector (140), track the location of end effector (140), and disperse irrigation fluid. As will also be described in greater detail below, deflection drive assembly (200) is configured to deflect end effector (140) and a distal portion of catheter (120) away from a central longitudinal axis (L-L) (
As shown in
Guidance and drive system (10) of the present example include a console (12) and a display (18). Console (12) includes a first driver module (14) and a second driver module (16). First driver module (14) is coupled with catheter assembly (100) via cable (30). In some variations, first driver module (14) is operable to receive EP mapping signals obtained via microelectrodes (138) of end effector (140) as described in greater detail below. Console (12) includes a processor (not shown) that processes such EP mapping signals and thereby provides EP mapping as is known in the art.
First driver module (14) of the present example is further operable to provide RF power to a distal tip member (142) of end effector (140), as will be described in greater detail below, to thereby ablate tissue. Second driver module (16) is coupled with field generators (20) via cable (22). Second driver module (16) is operable to activate field generators (20) to generate an alternating magnetic field around the heart (H) of the patient (PA). For instance, field generators (20) may include coils that generate alternating magnetic fields in a predetermined working volume that contains the heart (H). First driver module (14) is also operable to receive position indicative signals from a navigation sensor assembly (150) in end effector (140). In such versions, the processor of console (12) is also operable to process the position indicative signals from navigation sensor assembly (150) to thereby determine the position of end effector (140) within the patient (PA).
Navigation sensor assembly (150) includes a pair of coils on respective panels (151) that are operable to generate signals that are indicative of the position and orientation of end effector (140) within the patient (PA). The coils are configured to generate electrical signals in response to the presence of an alternating electromagnetic field generated by field generators (20). Other components and techniques that may be used to generate real-time position data associated with end effector (140) may include wireless triangulation, acoustic tracking, optical tracking, inertial tracking, and the like. Alternatively, end effector (140) may lack a navigation sensor assembly (150).
Display (18) is coupled with the processor of console (12) and is operable to render images of patient anatomy. Such images may be based on a set of preoperatively or intraoperatively obtained images (e.g., a CT or MM scan, 3-D map, etc.). The views of patient anatomy provided through display (18) may also change dynamically based on signals from navigation sensor assembly (150) of end effector (140). For instance, as end effector (140) of catheter (120) moves within the patient (PA), the corresponding position data from navigation sensor assembly (150) may cause the processor of console (12) to update the patient anatomy views in display (18) in real time to depict the regions of patient anatomy around end effector (140) as end effector (140) moves within the patient (PA). Moreover, the processor of console (12) may drive display (18) to show locations of aberrant conductive tissue sites, as detected via electrophysiological (EP) mapping with end effector (140) or as otherwise detected (e.g., using a dedicated EP mapping catheter, etc.). By way of example only, the processor of console (12) may drive display (18) to superimpose the locations of aberrant conductive tissue sites on the images of the patient's anatomy, such as by superimposing an illuminated dot, a crosshair, or some other form of visual indication of aberrant conductive tissue sites.
The processor of console (12) may also drive display (18) to superimpose the current location of end effector (140) on the images of the patient's anatomy, such as by superimposing an illuminated dot, a crosshair, a graphical representation of end effector (140), or some other form of visual indication. Such a superimposed visual indication may also move within the images of the patient anatomy on display (18) in real time as the physician (PH) moves end effector (140) within the patient (PA), thereby providing real-time visual feedback to the operator about the position of end effector (140) within the patient (PA) as end effector (140) moves within the patient (PA). The images provided through display (18) may thus effectively provide a video tracking of the position of end effector (140) within a patient (PA), without necessarily having any optical instrumentation (i.e., cameras) viewing end effector (140). In the same view, display (18) may simultaneously visually indicate the locations of aberrant conductive tissue sites detected through EP mapping. The physician (PH) may thus view display (18) to observe the real time positioning of end effector (140) in relation to the mapped aberrant conductive tissue sites and in relation to images of the adjacent anatomical structures in the patient (PA).
Fluid source (42) of the present example includes a bag containing saline or some other suitable irrigation fluid. Conduit (40) includes a flexible tube that is further coupled with a pump (44), which is operable to selectively drive fluid from fluid source (42) to catheter assembly (100). As described in greater detail below, such irrigation fluid may be expelled through openings (158) of distal tip member (142) of end effector (140). Such irrigation may be provided in any suitable fashion as will be apparent to those skilled in the art in view of the teachings herein.
As shown in
As shown in
In versions where cylindraceous body (156) is formed of an electrically conductive material to provide RF electrical energy for tissue ablation, an electrically insulating material may be interposed between cylindraceous body (156) and EP mapping microelectrodes (138) to thereby electrically isolate EP mapping microelectrodes (138) from cylindraceous body (156). EP mapping microelectrodes (138) may be constructed and operable in accordance with the teachings of various patent references cited herein. While only one EP mapping microelectrode (138) is shown, distal tip member (142) may include two or more EP mapping microelectrodes (138). Alternatively, distal tip member (142) may lack EP mapping microelectrodes (138) altogether. Distal tip base (144) defines a central aperture configured to provide a path for communication of irrigation fluid to the hollow interior of distal tip member (142). Distal tip base (144) forms an annular shoulder that the proximal edge of distal tip member (142) may abut. Distal tip member (142) also defines a lateral notch that is configured to receive a proximally extending tab of distal tip member (142).
As shown in
In versions where coils are incorporated into distal circuit disk (146) and one or more other layers that are proximal to strain gauge assembly (148), such coils may thus enable wireless communication of electrical signals across strain gauge assembly (148) without requiring wires, vias, or other electrically conductive structures to pass longitudinally across strain gauge assembly (148). In some versions, distal circuit disk (146) includes at least one transmission coil (TX) that is paired with receiving coil (RX) of navigation sensor assembly (150) to detect strain being applied to strain gauge assembly (148) so as to determine the contact force applied to distal tip member (142). Some other versions of distal circuit disk (146) may simply omit a TX coil.
Strain gauge assembly (148) is positioned proximal to distal circuit disk (146) and is configured to sense external forces that impinge against distal tip member (142). When distal tip (142) encounters external forces (e.g., when distal tip (142) is pressed against tissue), those external forces are communicated from distal tip (142) to distal tip base (144), to distal circuit disk (146), and to strain gauge assembly (148) such that strain gauge may generate a suitable signal corresponding to the magnitude and direction of the external force. The signals from strain gauge assembly (148) may be communicated through vias or other structures in the layers that are proximal to strain gauge assembly (148), eventually reaching first driver module (14) of console (12) via cable (30). First driver module (14) may process the strain signals in accordance with any suitable fashion as would be apparent to one of ordinary skill in the art in view of the teachings herein. By way of example only, console (12) may provide audible feedback to alert the physician (PH) when strain gauge assembly (148) indicates that distal tip member (142) is encountering forces over a predetermined threshold, to thereby prevent the physician (PH) from unwittingly damaging a cardiovascular anatomical structure with distal tip member (142).
Navigation sensor assembly (150) may generate signals indicating the position and orientation of end effector (140) in three-dimensional space with substantial precision. Navigation sensor assembly (150) includes a plurality of panels (151), each including an RX coil that is operable to generate position-indicative electrical signals in response to the alternating magnetic fields generated by field generators (20). Each RX coil may be formed by electrical traces to define an electrical coil or antenna to receive radiofrequency signals emitted by external transmitters TX coils (e.g., three TX coils provided by field generators (20) positioned external of the patient (PA) body and emitting discrete radiofrequencies) such that the location and orientation of each RX coil can be determined with respect to the TX coils provided by field generators (20). The signals from navigation sensor assembly (150) may be communicated through vias or other structures in the layers that are proximal to strain navigation sensor assembly (150), eventually reaching first driver module (14) of console (12) via cable (30).
A central annular body of navigation sensor assembly (150) defines a central aperture configured to provide a path for communication of irrigation fluid to the hollow interior of distal tip member (142). In versions where central annular body of navigation sensor assembly includes wireless communication coils, such wireless communication coils may be further coupled with vias or other structures in the layers that are proximal to strain navigation sensor assembly (150), thereby providing a path for electrical communication with first driver module (14) of console (12) via cable (30).
In the present example, each distal spacer (153) is generally shaped like a disk, with a pair of chordal cutouts angularly offset from each other by 90 degrees. These cutouts are sized and configured to accommodate a respective panel (151) of navigation sensor assembly (150), thereby allowing panels (151) to be radially interposed between distal spacer stack (152) and outer sheath (122). Each distal spacer (153) also includes at least one cable notch, where two or more notches may be angularly offset from each other by 180 degrees. This cable notch is configured to receive distal end portion (164) of push-pull cable (160). Each distal spacer (153) further includes a central aperture configured to provide a path for communication of irrigation fluid to the hollow interior of distal tip member (142). Each proximal spacer (154) is shaped like a disk, with two or more apertures formed therethrough. A central aperture is configured to provide a path for communication of irrigation fluid to the hollow interior of distal tip member (142). The side aperture is sized and configured to receive proximal portion (162) of push-pull cable (160). A second side aperture may also be included.
As noted above and as shown in
As best shown in
In some instances, multiple production lines are used for construction of catheters. For example, a first production line may produce only uni-directional catheters, and a second production line may produce only bi-directional catheters. A uni-directional catheter is a catheter that deflects in only a single direction (e.g. up, down, left, or right) away from longitudinal axis (L-L). A bi-directional catheter is a catheter that deflects in two directions (e.g. up and down or left and right) away from longitudinal axis (L-L). Multiple production lines may be used because there are a few structural differences between a uni-directional catheter and a bi-directional catheter to achieve this difference in deflection. These differences may include the handle (110) and the deflection mechanism (e.g. the deflection drive assembly).
It may be beneficial to use some of the same components for both uni-directional and bi-directional catheters. This may be beneficial because the same production line may then be used to produce both the uni-directional catheter and the bi-directional catheter. Using the same production line may also save on the time necessary to train assembly operators, reduce the potential for mixing components on the production line, ensure cross-compatibility of assembly operators between uni-directional and bi-directional catheter lines, and generate larger volume discounts during the procurement of the components.
Using the same or similar handle (110) for uni-directional and bi-directional catheters may also provide a physician (PH) greater peace of mind, as the physician (PH) may be more comfortable with the user interface. Catheter assembly (100) captures modifying a bi-direction deflection mechanism to enable uni-directional usage. Conversely, a second exemplary catheter assembly (500) captures modifying a bi-direction deflection mechanism to enable uni-directional usage.
As will be described in greater detail below, exemplary deflection drive assemblies (300, 400, 508, 608) incorporate exemplary rack and pinion assemblies (304, 404, 518, 618) to either (1) transfer rotational motion of a pinion (308, 408) from a rocker arm (230, 501) into linear motion of a rack (306, 406), or (2) transfer linear motion of a rack (524, 624) from a linear slider (514, 614) into rotational motion of a pinion (526, 626). As shown, a single rack (306, 406, 524, 624) interacts with a pinion (308, 408, 526, 626). While the input member is shown as rocker arm (230, 501) in
Deflection drive assembly (300) is configured to deflect end effector (140) away from longitudinal axis (L-L) defined by a proximal portion of catheter (120). Deflection drive assembly (300) of the present example includes rocker arm (230) associated with handle (110), a translating assembly (302), and a rack and pinion assembly (304) coupled with rocker arm (230). Translating assembly (302) is indirectly or directly coupled with rack and pinion assembly (304) and end effector (140). As shown, translating assembly (302) includes push-pull cable (160). As will be described in greater detail below, the physician (PH) may actuate rocker arm (230) relative to handle (110), such that rack and pinion assembly (304) actuates push-pull cable (160) to selectively deflect end effector (140) laterally away from a longitudinal axis (L-L), thereby enabling the physician (PH) to actively steer end effector (140) within the patient (PA). Rocker arm (230) may drive translating assembly (302) to deflect end effector (140) away at an angle (A) relative to longitudinal axis (L-L) in two directions (up and down or left and right). Rocker arm (230) is configured to rotate relative to handle (110) about drive axis (D-D) without translating along longitudinal axis (L-L). As shown, drive axis (D-D) is perpendicular with longitudinal axis (L-L).
Rack and pinion assembly (304) has a rack (306) and a pinion (308). Only a single rack (306) is shown in
As shown, translating assembly (302) has a single push-pull cable (160) that is coupled with rack (306) and end effector (140). Particularly, push-pull cable (160) is coupled with rack (306) at a proximal attachment point (318) using any one of a variety of suitable attachment methods. Similarly, push-pull cable (160) is coupled with end effector (140) at a distal attachment point (321) using any one of a variety of suitable attachment methods. While push-pull cable (160) is generally coupled with rack (306) after rack (306) is engaged with pinion (308), it is also envisioned that push-pull cable (160) may be coupled with rack (306) before rack (306) is engaged with pinion (308). Deflection drive assembly (300) transfers linear motion of rack (306) to either push push-pull cable (160) in a distal direction (see
As shown in
Locking features (322, 324) are spaced at a distance from locking feature (320) in the unlocked configuration. As shown, locking features (320, 322, 324) are cylindraceous in shape. Particularly, locking feature (320) of pinion (308) is a cylindraceous pin (326), while locking features (322, 324) of rack (306) are cylindraceous detents (328, 330). Cylindraceous pin (326) of locking feature (320) of pinion (308) is configured to removably couple with (e.g. snap into) cylindraceous detents (328, 330) of locking features (322, 324) of rack (306) in the locked configuration. Cylindraceous pin (326) projects downwardly and unitarily from rocker arm (230); adjacent to pinion (308). Cylindraceous pin (326) may be positioned adjacent to the gear tooth tip. Cylindraceous detents (328, 330) may be formed into gear tooth troughs of rack (306).
With same or less amount of resistance using rocker arm (230), cylindraceous pin (326) of pinion (308) is removable from one of cylindraceous detents (328, 330) of rack (306) to unlock the deflection of end effector (140). Cylindraceous pin (326) and cylindraceous detents (328, 330) provide a coupling that is strong enough to resist unintended longitudinal movement of the rack (306) (e.g., in response to lateral forces exerted against the end effector by patient anatomy, etc.) when locking assembly (316) is in the state shown in
When the physician (PH) desires to deflect end effector (140) relative to central longitudinal axis (L-L) to the deflected position shown in
It may be desirable to modify deflection drive assembly (300) that is configured to provide bi-directional deflection to end effector (140) as shown in
Locking assembly (416) may include a biasing member (438) configured to bias rack (406) away from pinion (408) to convert locking assembly (416) from the locked configuration to the unlocked configuration. For example, rack (406) may be formed from a bendable material (e.g. a polymeric material). As shown, biasing member (438) projects outwardly from handle (411), such that biasing member (438) may be manually actuated by the physician (PH). It is envisioned that latching pin (436) or biasing member (438) may be used alone or in combination.
A catheter assembly including a translatable actuator (e.g. a linear slider) may be normally configured to only provide uni-directional deflection of end effector (140). It may be desirable to produce a catheter assembly including a linear slider that is capable of providing bi-directional deflection of end effector (140). Additionally, it may be desirable to use the same production line to produce both the uni-directional catheter including a linear slider and the bi-directional catheter including a linear slider. As previously described, using the same production line for uni-directional and bi-directional catheters may also save on the time necessary to train assembly operators, reduce the potential for mixing components on the production line, ensure cross-compatibility of assembly operators between uni-directional and bi-directional catheter production lines, and generate larger volume discounts during the procurement of the components. For at least these reasons, a second exemplary catheter assembly (500) includes an input member (shown as a linear slider (514)) that is capable of providing bi-directional deflection to an end effector (504). Bi-directional deflection provides a greater range of deflection angles to end effector (504) as compared to uni-directional deflection.
Translating assembly (516) includes a push-pull cable (520). Push-pull cable (520) and an irrigation tube (521), similar to irrigation tube (180), may extend along the length of catheter (120) to reach end effector (504). Cable (30) couples catheter assembly (500) with drive system (10) described above. Wires, similar to wires (32) of
Catheter assembly (500) is configured to enable irrigation fluid to be communicated from a fluid source, similar to fluid source (42) of
With continued reference to
As shown in 15A-15C, deflection drive assembly (300) may optionally include locking assembly (534) similar to locking assembly (316). Locking assembly (534) includes locking features (552, 554, 556) that define the locked configuration and the unlocked configuration. As shown in
Locking features (554, 556) are spaced at a distance from locking feature (552) in the unlocked configuration. In other words, in the unlocked position of
Alternatively, it is also envisioned that pulley wheel (542) may be substituted for a sprocket, and at least a portion of push-pull cable (520) (e.g., the portion that would directly engage the sprocket during operation) be substituted for a chain, such that the chain may be wrapped around the sprocket, with first and second push-pull cables being joined to each end of the chain. In such an alternative arrangement utilizing a chain and sprocket arrangement, first and second push pull cables move in opposite directions along longitudinal axis (L-L) in a manner similar to the bi-directional catheter shown and described in U.S. Prov. Pat. App. No. 62/866,109, entitled “Catheter Deflection System with Deflection Load Limiter,” filed on Jun. 25, 2019, the disclosure of which is incorporated by reference herein, in its entirety.
Linear slider (614) is configured to translate along longitudinal axis (L-L) relative to handle (606). Linear slider (614) is coupled with pinion (626) using a shaft (628). Shaft (628) rotatably couples pinion (626) and pulley wheel (642). Deflection drive assembly (608) includes pulley wheel (642) that is co-axial with pinion (626) of rack and pinion assembly (618). Pulley wheel (642) is rotatably coupled with pinion (626) using shaft (628). Pulley wheel (642) includes an interface surface (644) configured to contact push-pull cable (620). A distal portion of rack (524) may be coupled with a wire (546) at an attachment point (548). Push-pull cable (620) has portions (636, 638) similar to push-pull cable (520). Portion (636) of push-pull cable (620) is coupled at an attachment point, similar to attachment point (564) with distal tip member (523) of end effector (504). Portion (638) of push-pull cable (620) is coupled at an attachment point, similar to attachment point (566) with distal tip member (523) of end effector (504).
In lieu of or in addition to locking features (652, 654, 656), locking assembly (634) may include a locking feature (shown as a latching pin (668)), which selectively couples with teeth (670) of linear slider (614) to maintain the deflected angle of end effector (504) (see
Step (706a) of method (700) includes converting rotational motion of pinion (308, 408) into subsequent rotational motion of rack (306, 406) using rack and pinion assembly (304, 404). Step (706b) of method (700) includes transferring linear motion of rack (524, 624) into subsequent rotational motion of pinion (526, 626) using rack and pinion assembly (518, 618). Step (708a) of method (700) includes transferring subsequent linear motion of rack (306, 406) to translating assembly (302, 402). Step (708b) of method (700) includes transferring subsequent rotational motion of pinion (526, 626) to translating assembly (516, 616).
Step (710) of method (700) includes deflecting end effector (140) away at an angle relative to longitudinal axis (L-L) using translating assembly (302, 402) or deflecting end effector (504) away at an angle relative to longitudinal axis (L-L) using translating assembly (516, 616). Step (712) of method (700) includes locking end effector (140, 504, 604) at the desired angle away from longitudinal axis (L-L) in the locked configuration using locking assembly (316, 416, 534, 634).
The following examples relate to various non-exhaustive ways in which the teachings herein may be combined or applied. It should be understood that the following examples are not intended to restrict the coverage of any claims that may be presented at any time in this application or in subsequent filings of this application. No disclaimer is intended. The following examples are being provided for nothing more than merely illustrative purposes. It is contemplated that the various teachings herein may be arranged and applied in numerous other ways. It is also contemplated that some variations may omit certain features referred to in the below examples. Therefore, none of the aspects or features referred to below should be deemed critical unless otherwise explicitly indicated as such at a later date by the inventors or by a successor in interest to the inventors. If any claims are presented in this application or in subsequent filings related to this application that include additional features beyond those referred to below, those additional features shall not be presumed to have been added for any reason relating to patentability.
An apparatus, comprising: (a) a handle; (b) a catheter extending distally from the handle, a proximal portion of the catheter defining a longitudinal axis; (c) an end effector extending distally from the catheter, the end effector including at least one electrode; and (d) a deflection drive assembly configured to deflect the end effector away from the longitudinal axis, the deflection drive assembly comprising: (i) an input member associated with the handle, (ii) a translating assembly coupled to the end effector, and (iii) a rack and pinion assembly coupled with the input member and the translating assembly, the rack and pinion assembly being configured to drive the translating assembly to deflect the end effector away at an angle relative to the longitudinal axis, the rack and pinion assembly consisting of a rack and a pinion, the rack and pinion assembly being configured to either: (1) transfer rotational motion of the pinion from the input member into linear motion of the rack to push distally or pull proximally the translating member, or (2) transfer linear motion of the rack from the input member into rotational motion of the pinion to move a first end of the translating member proximally and a second end of the translating member distally.
The apparatus of Example 1, the input member comprising a rocker arm configured to rotate relative to the handle about a drive axis, the rack and pinion assembly configured to transfer the rotational motion of the pinion from the rocker arm into the linear motion of the rack to push distally or pull proximally the translating member.
The apparatus of Example 2, the translating assembly further comprising a push-pull cable coupled with the rack, the deflection drive assembly configured to transfer the linear motion of the rack to either push the push-pull cable in a distal direction or pull the push-pull cable in a proximal direction.
The apparatus of any one or more of Examples 2 through 3, the rocker arm and the pinion being co-axial about the drive axis.
The apparatus of Example 1, the input member comprising a linear slider configured to move longitudinally along the longitudinal axis, the rack and pinion assembly being configured to transfer the linear motion of the rack from the linear slider into the rotational motion of the pinion to move the first end of the translating member proximally and the second end of the translating member distally.
The apparatus of Example 1, the translating assembly further comprising a push-pull cable having first and second portions, the deflection drive assembly being configured to transfer the rotational motion of the pinion to push the first portion of the push-pull cable in a distal direction and pull the second portion of the push-pull cable in a proximal direction.
The apparatus of Example 6, the deflection drive assembly further comprising a pulley wheel that is co-axial with the pinion of the rack and pinion assembly, the pulley wheel including an interface surface configured to contact the push-pull cable.
The apparatus of any one or more of Examples 5 through 7, the linear slider being fixably coupled with the rack and the pulley wheel being rotatably coupled with the pinion.
The apparatus of any preceding Example, further comprising a locking assembly interposed between the input member and the translating assembly, the locking assembly being movable between locked and unlocked configurations, the locking assembly configured to lock the end effector at the angle relative to the longitudinal axis in the locked configuration.
The apparatus of Example 9, the locking assembly comprising first and second locking features configured to transition between a locked configuration and an unlocked configuration, the locking assembly being configured to prevent the translating assembly from translating along the longitudinal axis in the locked configuration.
The apparatus of Example 10, the first locking feature being disposed on the pinion, the second locking feature being disposed on the rack, the second locking feature being complementary to the first locking feature, the first and second locking features being configured to engage one another in the locked configuration, the first and second locking features being configured to be spaced at a distance from one another in the unlocked configuration.
The apparatus of any one or more of Examples 10 through 11, the first and second locking features being cylindraceous.
The apparatus of Example 12, the first locking feature including a cylindraceous pin, the second locking feature including a cylindraceous detent configured to receive the cylindraceous pin in the locked configuration.
The apparatus of Example 13, the cylindraceous pin projects unitarily from the input member, the cylindraceous detent being formed into a gear tooth trough of the rack.
The apparatus of any of Examples 9 through 14, the locking assembly further comprising a biasing member configured to bias the rack away from the pinion to switch to the unlocked configuration.
The apparatus of any one or more of Examples 1 through 8, further comprising a locking assembly, the locking assembly comprising first and second locking features configured to transition between a locked configuration and an unlocked configuration, the first locking feature being disposed on the translating assembly and the second locking feature being selectively positioned on the handle.
The apparatus of Example 10, the input member comprising a rocker arm configured to rotate relative to the handle about a drive axis, the first locking feature being disposed on the rocker arm and the second locking feature being movable on the handle.
The apparatus of Example 17, the drive axis being perpendicular with the longitudinal axis.
The apparatus of Example 10, the input member comprising a linear slider configured to translate relative to the handle along the longitudinal axis, the first locking feature being disposed on the linear slider and the second locking feature being movable on the handle.
The apparatus of Example 1, the translating assembly consisting of a single push-pull cable, the rack and pinion assembly being configured to drive the single push-pull cable in opposing directions.
The apparatus of Example 20, the single push-pull cable comprising a stainless-steel rod.
The apparatus of any one or more of Examples 1 through 21, the at least one electrode being configured to emit RF energy.
The apparatus of any one or more of Examples 1 through 22, the at least one electrode being configured to perform electrophysiology mapping.
The apparatus of any one or more of Examples 1 through 23, the end effector comprising a strain gauge assembly.
The apparatus of any one or more of Examples 1 through 24, the end effector being configured to emit irrigation fluid.
The apparatus of any one or more of Examples 1 through 25, the end effector comprising a position sensor.
An apparatus, comprising: (a) a handle; (b) a catheter extending distally from the handle, a proximal portion of the catheter defining a longitudinal axis; (c) an end effector extending distally from the catheter, the end effector including at least one electrode; (d) a deflection drive assembly configured to deflect the end effector away from the longitudinal axis, the deflection drive assembly comprising: (i) an input member associated with the handle, (ii) a translating assembly coupled to the end effector, the input member being configured to drive the translating assembly to deflect the end effector away at an angle from the longitudinal axis, and (iii) a rack and pinion assembly coupled with the input member and the translating assembly, the rack and pinion assembly consisting of a rack and a pinion, the rack and pinion assembly configured to either: (1) transfer rotational motion of the pinion from the input member into linear motion of the rack to push distally or pull proximally the translating member, or (2) transfer linear motion of the rack from the input member into rotational motion of the pinion to move a first end of the translating member proximally and a second end of the translating member distally; and (e) a locking assembly configured to transition between a locked configuration and an unlocked configuration, the locking assembly comprising first and second locking features, the first and second locking features configured to lock the end effector at the angle away from the longitudinal axis in the locked configuration, the first and second locking features configured to allow the end effector to move along a range of angles in the unlocked configuration.
The apparatus of Example 27, the locking assembly being interposed between the input member and the translating assembly, the locking assembly being configured to prevent the translating assembly from translating along the longitudinal axis in the locked configuration.
The apparatus of Example 28, the first locking feature being disposed on the pinion, the second locking feature being disposed on the rack, the second locking feature being complementary to the first locking feature, the first and second locking features are configured to engage one another in the locked configuration, the first and second locking features are configured to be spaced at a distance from one another in the unlocked configuration.
The apparatus of claim of any one or more of Examples 27 through 30, the first and second locking features being cylindraceous.
The apparatus of Example 30, the first locking feature being a cylindraceous pin, the second locking feature being a cylindraceous detent configured to receive the cylindraceous pin in the locked configuration.
A method of operating an apparatus, the apparatus comprising: (a) a handle; (b) a catheter extending distally from the handle, a proximal portion of the catheter defining a longitudinal axis; (c) an end effector extending distally from the catheter, the end effector including at least one electrode; and (d) a deflection drive assembly configured to deflect the end effector away from the longitudinal axis, the deflection drive assembly comprising: (i) an input member associated with the handle, (ii) a translating assembly coupled to the end effector, and (iii) a rack and pinion assembly coupled with the input member and the translating assembly, the rack and pinion assembly consisting of a rack and a pinion, the method comprising: (a) manually actuating the input member using rotational motion or linear motion; (b) transferring the rotational motion of the input member to the pinion or transferring the linear motion of the input member to the rack; (c) transferring the rotational motion of the pinion into subsequent linear motion of the rack or transferring the linear motion of the rack into subsequent rotational motion of the pinion using the rack and pinion assembly; (d) transferring the subsequent linear motion to the translating assembly or the subsequent rotational motion to the translating assembly; and (e) deflecting the end effector at an angle away from the longitudinal axis using the translating assembly.
The method of Example 32, further comprising locking the end effector at the angle away from the longitudinal axis in the locked configuration.
A method of manufacturing an apparatus, the apparatus comprising: (a) a handle; (b) a catheter extending distally from the handle, a proximal portion of the catheter defining a longitudinal axis; (c) an end effector extending distally from the catheter, the end effector including at least one electrode; and (d) a deflection drive assembly configured to deflect the end effector away from the longitudinal axis, the deflection drive assembly comprising: (i) an input member associated with the handle, (ii) a translating assembly coupled to the end effector, and (iii) a rack and pinion assembly coupled with the input member and the translating assembly, the rack and pinion assembly consisting of a rack and a pinion, the method comprising: (a) inserting the pinion to be engaged with the rack at a first position configured for uni-directional end effector deflection that is longitudinally spaced from than a second position along the rack for bi-directional end effector deflection or inserting the pinion to be engaged with the rack at a third position configured for bi-directional end effector deflection that is longitudinally spaced from a fourth position along the rack for uni-directional end effector deflection; and (b) attaching the translating assembly with the rack and pinion assembly.
Any of the instruments described herein may be cleaned and sterilized before and/or after a procedure. In one sterilization technique, the device is placed in a closed and sealed container, such as a plastic or TYVEK bag. The container and device may then be placed in a field of radiation that can penetrate the container, such as gamma radiation, x-rays, or high-energy electrons. The radiation may kill bacteria on the device and in the container. The sterilized device may then be stored in the sterile container for later use. A device may also be sterilized using any other technique known in the art, including but not limited to beta or gamma radiation, ethylene oxide, hydrogen peroxide, peracetic acid, and vapor phase sterilization, either with or without a gas plasma, or steam.
It should be understood that any of the examples described herein may include various other features in addition to or in lieu of those described above. By way of example only, any of the examples described herein may also include one or more of the various features disclosed in any of the various references that are incorporated by reference herein.
It should be understood that any one or more of the teachings, expressions, embodiments, examples, etc. described herein may be combined with any one or more of the other teachings, expressions, embodiments, examples, etc. that are described herein. The above-described teachings, expressions, embodiments, examples, etc. should therefore not be viewed in isolation relative to each other. Various suitable ways in which the teachings herein may be combined will be readily apparent to those skilled in the art in view of the teachings herein. Such modifications and variations are intended to be included within the scope of the claims.
It should be appreciated that any patent, publication, or other disclosure material, in whole or in part, that is said to be incorporated by reference herein is incorporated herein only to the extent that the incorporated material does not conflict with existing definitions, statements, or other disclosure material set forth in this disclosure. As such, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting material incorporated herein by reference. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material set forth herein will only be incorporated to the extent that no conflict arises between that incorporated material and the existing disclosure material.
Having shown and described various versions of the present invention, further adaptations of the methods and systems described herein may be accomplished by appropriate modifications by one skilled in the art without departing from the scope of the present invention. Several of such potential modifications have been mentioned, and others will be apparent to those skilled in the art. For instance, the examples, versions, geometrics, materials, dimensions, ratios, steps, and the like discussed above are illustrative and are not required. Accordingly, the scope of the present invention should be considered in terms of the following claims and is understood not to be limited to the details of structure and operation shown and described in the specification and drawings.
This application claims priority to U.S. Provisional Pat. App. No. 62/948,527, entitled “Catheter Deflection Control Assembly,” filed Dec. 16, 2019, the disclosure of which is incorporated by reference herein, in its entirety.
Number | Date | Country | |
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62948527 | Dec 2019 | US |