IMAGE-GUIDED SURGICAL SYSTEMS WITH AUTOMATED TRAJECTORY GUIDE SYSTEMS AND RELATED DEVICES AND METHODS
20210282866 · 2021-09-16
Inventors
Cpc classification
A61B5/061
HUMAN NECESSITIES
G01R33/4818
PHYSICS
A61B2017/00911
HUMAN NECESSITIES
A61B2034/107
HUMAN NECESSITIES
A61B34/70
HUMAN NECESSITIES
A61B90/11
HUMAN NECESSITIES
A61B2034/102
HUMAN NECESSITIES
G01R33/285
PHYSICS
G01R33/543
PHYSICS
A61B5/055
HUMAN NECESSITIES
A61B34/20
HUMAN NECESSITIES
A61B90/37
HUMAN NECESSITIES
A61B90/10
HUMAN NECESSITIES
A61B2034/101
HUMAN NECESSITIES
International classification
A61B34/20
HUMAN NECESSITIES
G01R33/28
PHYSICS
G01R33/54
PHYSICS
Abstract
Surgical systems and methods for an MRI suite include a housing residing in an MRI scanner room of the MRI suite. The housing comprises a plurality of motors coupled to at least one motor driver (in the same or a different housing); and a plurality of elongate cables, one coupled to one of the plurality of motors residing in the same housing or a different housing. The elongate cables comprise MRI compatible material and having a length in a range of about 24 inches and 60 inches. One of the cables couples to one of the motors at a first end portion and a corresponding one actuator of the actuators of a trajectory guide at a second end portion.
Claims
1. An image-guided surgical method, comprising: providing an image guided surgical system comprising a computer system configured with a surgical procedure workflow; providing a trajectory guide adapted to be held adjacent to or affixed to a patient, the trajectory guide comprising a plurality of actuators for positionally adjusting an intrabody trajectory defined by the trajectory guide for placing at least one surgical device along a desired intrabody trajectory; providing a plurality of motors and coupling one of the plurality of motors to a corresponding one of the plurality of actuators; providing at least one housing, wherein the least one housing contains a controller that communicates with the plurality of motors; and transmitting instructions from the computer system of the image guided surgical system to the controller then to one or more of the plurality of motors to controllably activate one or more of the motors to turn a corresponding one or more of the plurality of actuators to adjust the intrabody trajectory defined by the trajectory guide.
2. The method of claim 1, wherein the image guided system is an MRI-image guided system coupled to an MRI scanner system, wherein the computer system resides at least partially in a control room of an MRI suite, wherein the motors are MRI-compatible motors, and wherein the at least one housing resides in a scanner room of the MRI suite.
3. The method of claim 2, wherein each MRI-compatible motor of the plurality of MRI-compatible motors is coupled to and/or comprises a control cable that extends to one or more of the at least one housing.
4. The method of claim 3, wherein the control cable has a length in a range of about 24 inches and 60 inches, and wherein the control cable and the at least one housing are formed of one or more MRI compatible materials.
5. The method of claim 1, wherein the plurality of motors are provided as a plurality of separate motor assemblies, wherein each of the motor assemblies comprise a motor assembly housing having an open channel under a sealed compartment, wherein the sealed compartment that holds a respective one of the plurality of motors, and wherein each of the motor assemblies also comprise an actuator connector held in the open channel, the method further comprising placing a respective actuator of the plurality of actuators into a corresponding open channel and attaching the actuator connector to the respective actuator.
6. The method of claim 1, further comprising matching colors of actuators and actuator connectors to identify actuator and actuator connector pairs, then attaching the matching color actuator and actuator connector pairs to couple the plurality of motors to the plurality of actuators.
7. The method of claim 1, wherein the at least one housing comprises a plurality of motor drivers that are coupled to the plurality of motors, the method further comprising controlling the plurality of motors using the motor drivers and transmitting status updates of motor operation of respective motors of the plurality of motors to the computer system of the image guided surgical system.
8. The method of claim 2, wherein the computer system of the image guided surgical system: transmits slice plane parameters to a computer system of the MRI scanner system; evaluates images obtained by the MRI scanner system using the slice plane parameters; identifies a first intrabody trajectory provided by the trajectory guide as a current defined intrabody trajectory; compares the first intrabody trajectory to the desired intrabody trajectory that intersects a target intrabody site; calculates directional adjustments of one or more of the plurality of actuators of the trajectory guide to achieve the desired intrabody trajectory; then transmits the instructions to a controller coupled to motor drivers that are coupled to the MRI-compatible motors; and then directs one or more of the plurality of MRI-compatible motors to turn a corresponding actuator to adjust the first intrabody trajectory to a new defined intrabody trajectory to thereby provide the desired intrabody trajectory.
9. The method of claim 8, wherein the computer system is configured to direct two or more of the MRI-compatible motors to serially turn corresponding actuators.
10. The method of claim 8, wherein the computer system is configured to direct at least two of the MRI-compatible motors to concurrently turn at least two of the cables and corresponding actuators.
11. The method of claim 2, further comprising transmitting status data from the one or more of the plurality of MRI-compatible motors to the computer system of the image guided surgical system, wherein the method further comprises triggering the computer system of the image guided surgical system based, at least in part, on the transmitted status data, to communicate with a computer system of the MRI scanner to initiate slice acquisitions to thereby obtain further image slices.
12. The method of claim 1, wherein the plurality of actuators comprises a roll actuator and a pitch actuator.
13. The method of claim 12, wherein the plurality of actuators further comprises an X direction actuator and a Y direction actuator.
14. The method of claim 1, wherein the plurality of motors are coupled to respective rotary encoders that have a resolution in a range of about 100-300 μrad.
15. The method of claim 2, wherein the computer system of the image guided surgical system (a) transmits slice plane parameters to a computer system of the MRI scanner system to obtain images of slices extending across only a top end portion of a targeting cannula, then (b) evaluates the obtained images and identifies whether a projected error of alignment relative to the desired intrabody trajectory is within a first defined value, wherein, if so, the computer system of the image guided surgical system then (c) transmits slice plane parameters to the computer system of the MRI scanner system to initiate acquisition of at least a first stack of images in a first plane with image slices that extend over at least a major length and/or width of the targeting cannula, and then (d) evaluates the first stack of images and identifies whether a current projected error of alignment relative to the desired intrabody trajectory is within a second defined value, wherein the second defined value is less than the first defined value.
16. The method of claim 2, wherein the MRI-compatible motors are MRI-compatible stepper motors coupled to respective encoders.
17. The method of claim 1, wherein the at least one housing further comprises a plurality of motor drivers held therein, and wherein the transmitting step comprises transmitting direction command instructions from the controller to one or more of the plurality of motor drivers that then directs an appropriate one or more of the plurality of motors to turn at a defined speed and time to carry out positional adjustments of one or more of the plurality of actuators.
18. A surgical system for an MRI suite, comprising: a housing configured to reside in an MRI scanner room of the MRI suite, the housing comprising a controller; and a plurality of motor assemblies including at least a first motor assembly housing and a second separate motor assembly housing, wherein the first motor assembly housing encloses a first motor and a first actuator connector, wherein the first actuator connector is coupled to the first motor, wherein the second motor assembly housing encloses a second motor and a second actuator connector, and wherein the second actuator connector is coupled to the second motor.
19. The system of claim 18, further comprising a trajectory guide comprising at least first and second spaced apart actuators, wherein the first actuator is connected to the first actuator connector of the first motor assembly and the second actuator is coupled to the second actuator connector of the second motor assembly.
20. The system of claim 19, wherein the first motor assembly housing comprises an enclosure cap coupled to an enclosure leg, wherein a motor shaft coupler and a secondary drive shaft as well as the first actuator connector and the first actuator reside in the enclosure leg of the first motor assembly housing, wherein the second motor assembly housing comprises an enclosure cap coupled to an enclosure leg, and wherein a motor shaft coupler and a secondary drive shaft as well as the second actuator connector and the second actuator reside in the enclosure leg of the second motor assembly housing.
21. The system of claim 20, wherein the first motor is sealably held in the enclosure cap above the enclosure leg of the first motor assembly housing, wherein the second motor is sealably held in the enclosure cap above the enclosure leg of the second motor assembly housing, and wherein the first motor assembly housing and the second motor assembly housing are adjacent to each other and each has a maximal longitudinal length of about 1.5 inches to about 3.5 inches.
22. The system of claim 18, wherein the first motor assembly housing comprises a first elongate cable extending outward thereof coupled at a first end portion to the first motor and coupled at a second end portion to the housing comprising the controller, wherein the second motor assembly housing comprises a second elongate cable extending outward thereof coupled at a first end portion to the second motor and coupled at an opposing second end portion to the housing comprising the controller.
23. The system of claim 22, wherein the first and second elongate cables comprise MRI compatible material or MRI compatible materials and have a length in a range of about 24 inches to about 60 inches, and wherein the first and second actuator connectors are configured to releasably couple to a respective thumbwheel of respective first and second actuators of a trajectory guide.
24. The system of claim 18, further comprising a scanner bed attachment assembly coupled to or coupleable to the housing comprising the controller.
25. The system of claim 22, wherein the housing comprising the controller, the first motor assembly housing and the second motor assembly housing are non-ferromagnetic, wherein the housing comprising the controller also contains at least one motor driver in communication with the controller and a power supply coupled to the controller and/or the at least one motor driver.
26. The system of claim 18, wherein the first and second motors are coupled to respective rotary encoders that have a resolution in a range of about 100-300 μrad.
27. The system of claim 18, wherein the housing comprising the controller comprises RF shielding.
28. The system of claim 18, wherein the housing comprising the controller is coupled to at least one fiber optic cable that has a length sufficient to extend through a wave guide of an MRI suite between a control room and a scanner room.
29. The system of claim 18, wherein the system is configured to transmit status data of the first and/or second motor to a computer system of the MR scanner system to initiate slice acquisitions to thereby obtain image slices.
30. An image-guided surgical system, comprising: a computer system configured with a surgical procedure workflow, wherein the computer system resides at least partially in a control room of a magnetic resonance imaging (MRI) suite of a magnetic resonance (MR) scanner system; a trajectory guide adapted to be held adjacent to or affixed to a patient, the trajectory guide comprising a plurality of actuators for positionally adjusting an intrabody trajectory defined by the trajectory guide for placing at least one surgical device along a desired intrabody trajectory; and a plurality of motors that reside in a scanner room of the MRI suite, one motor in communication with one of the plurality of actuators of the trajectory guide, wherein the motors are MRI compatible motors, wherein instructions from the computer system of the image guided surgical system controllably activates one or more of the motors to turn to adjust the intrabody trajectory defined by the trajectory guide.
31. The system of claim 30, further comprising a drive control enclosure comprising a controller and motor drivers, wherein the drive control enclosure resides in the scanner room, and wherein the computer system of the image guided surgical system is further configured to: transmit slice plane parameters to a computer system of the MR scanner system; evaluate images obtained by the MR scanner system using the slice plane parameters; identify a first intrabody trajectory provided by the trajectory guide as a current defined intrabody trajectory; compare the first intrabody trajectory to the desired intrabody trajectory that intersects a target intrabody site; calculate directional adjustments of one or more of the actuators of the trajectory guide to achieve the desired intrabody trajectory; and then transmit instructions to the controller in the drive control enclosure which then directs the motor drivers to communicate with one or more of the motors to turn a corresponding actuator to adjust the first intrabody trajectory to a new defined intrabody trajectory.
32-37. (canceled)
38. A surgical motor assembly for an image-guided surgical navigation system, comprising: a motor assembly housing: a motor held in the housing; and an actuator connector held in the housing below the motor, wherein the actuator connector is coupled to the motor.
39. The assembly of claim 38, wherein the motor assembly housing comprises an enclosure cap coupled to an enclosure leg, wherein the actuator connector resides in the enclosure leg, and wherein the leg has at least one wall that surround an open downwardly extending channel.
40-47. (canceled)
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION OF EMBODIMENTS OF THE INVENTION
[0127] The present invention now is described more fully hereinafter with reference to the accompanying drawings, in which some embodiments of the invention are shown. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art.
[0128] Like numbers refer to like elements throughout. In the figures, the thickness of certain lines, layers, components, elements or features may be exaggerated for clarity. The terms “FIG.” and “Fig.” are used interchangeably with the word “Figure” in the specification and/or figures.
[0129] The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, steps, operations, elements, components, and/or groups thereof. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items.
[0130] Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the specification and relevant art and should not be interpreted in an idealized or overly formal sense unless expressly so defined herein. Well-known functions or constructions may not be described in detail for brevity and/or clarity.
[0131] It will be understood that when an element is referred to as being “on”, “attached” to, “connected” to, “coupled” with, “contacting”, etc., another element, it can be directly on, attached to, connected to, coupled with or contacting the other element or intervening elements may also be present. In contrast, when an element is referred to as being, for example, “directly on”, “directly attached” to, “directly connected” to, “directly coupled” with or “directly contacting” another element, there are no intervening elements present. It will also be appreciated by those of skill in the art that references to a structure or feature that is disposed “adjacent” another feature may have portions that overlap or underlie the adjacent feature.
[0132] Spatially relative terms, such as “under”, “below”, “lower”, “over”, “upper” and the like, may be used herein for ease of description to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the figures. It will be understood that the spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if the device in the figures is inverted, elements described as “under” or “beneath” other elements or features would then be oriented “over” the other elements or features. Thus, the exemplary term “under” can encompass both an orientation of “over” and “under”. The device may be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted accordingly. Similarly, the terms “upwardly”, “downwardly”, “vertical”, “horizontal” and the like are used herein for the purpose of explanation only unless specifically indicated otherwise.
[0133] The term “lead” means an electrical path created by one or more wires. The wires are typically insulated wires, particularly where exposed. The term “cable” can refer to an electrical cable, a mechanical cable or a fiber optic cable.
[0134] The term “about” means that the noted parameter can vary somewhat from the stated number, typically by +/−20%.
[0135] The term “MRI suite” refers to an enclosure that includes at least two rooms or chambers separated by RF shielding and/or an RF shielded wall as is well known to those of skill in the art.
[0136] The term “computer system” refers to a device with at least one digital signal processor and/or data processing system. The computer system can be provided as a desktop, laptop, smartphone or other device. A respective computer system can comprise computer program code configured to provide defined operational functions and/or interfaces with other computer systems.
[0137] The term “MRI-compatible” means that a device is safe for use in an MRI environment and/or that a device that can operate as intended in an MRI environment and not introduce artifacts into MRI signal data. As such, if residing within the high-field strength region of the magnetic field of an MRI suite, the MRI-compatible device is typically made of a non-ferromagnetic MRI-compatible material(s) suitable to reside and/or operate in a high magnetic field environment. The term “RF safe” means that the lead or probe is configured to safely operate when exposed to RF signals, particularly RF signals associated with MRI systems, without inducing unplanned current that inadvertently unduly heats local tissue or interferes with the planned therapy or procedure. The term “shield” and derivatives thereof refer to an RF shield that can attenuate unwanted RF signal.
[0138] The term “high magnetic field” refers to magnetic fields above 0.5 T, typically between 1.5 T to 10 T, such as about 3.0 T and includes-high-field magnet closed bore and open bore MRI systems. MRI scanners are well known to those of skill in the art and include, for example, the SIGNA 1.5 T/3.0 T from GE Healthcare: the ACHEIVA 1.5 T/3.0 T and the INTEGRA 1.5 T from Philips Medical System; and the MAGNETOM Avanto, the MAGNETOM Espree, the MAGNETOM Symphony, and the MAGNETOM Trio, from Siemens Medical.
[0139] The term “fiducial marker” refers to a marker that can be electronically identified using image recognition and/or electronic interrogation, typically interrogation of CT or MRI image data. The fiducial marker can be provided in any suitable manner, such as, but not limited to, a geometric shape, a component on or in the device, optical or electrical tracking coils, a coating or fluid-filled component or feature (or combinations of different types of fiducial markers) that makes the fiducial marker(s) MRI-visible or CT visible with sufficient signal intensity (brightness) for identifying location and/or orientation information for the device and/or components thereof in space.
[0140] The term “grid” refers to a pattern of crossed lines or shapes used as a reference for locating points or small spaces, e.g., a series of rows and intersecting columns, such as horizontal rows and vertical columns (but orientations other than vertical and horizontal can also be used). The grid can include at least one fiducial marker. The grid can include associated visual indicia such as alphabetical markings (e.g., A-Z and the like) for rows and numbers for columns (e.g., 1-10) or the reverse. Other marking indicia may also be used. The grid can be provided as a flexible patch that can be releasably attached to the skin of a patient. For additional description of suitable grid devices, see co-assigned U.S. patent application Ser. No. 12/236,621 (U.S. Pat. No. 8,195,272), the contents of which are hereby incorporated by reference as if recited in full herein.
[0141] Embodiments of the present invention provide image-guided surgical systems 10 that can be configured to carry out or facilitate CT and/or MRI guided procedures, including, for example diagnostic and interventional procedures such as to guide and/or place interventional devices to any desired internal region of the body or object, including deep brain sites for neurosurgeries or other target intrabody locations for other procedures. The object can be any object and may be particularly suitable for animal and/or human subjects. For example, the system and/or devices thereof can be used for gene, e.g., antibody, and/or stem-cell based therapy delivery or other therapy delivery to intrabody targets in the brain, heart, lungs, liver, kidney, ovary, stomach, intestine, colon, spine or to other locations. In addition, embodiments of the systems can be used to treat cancer sites.
[0142] In some embodiments, the systems can be used to ablate tissue and/or deliver pharmacologic material in the brain, heart or other locations. In some embodiments, it is contemplated that the systems can be configured to treat AFIB, deliver stem cells or other cardio-rebuilding cells or products into cardiac tissue, such as a heart wall, via a minimally invasive MRI guided procedure while the heart is beating (i.e., not requiring a non-beating heart with the patient on a heart-lung machine).
[0143] Turning now to the figures,
[0144] A RF shielded wall 150 can reside between the control room 100A and the MRI scanner room 100B. A wave guide 175 (as discussed in the Background) can extend between the two rooms 100A, 100B through the RF shielded wall 150.
[0145] The image-guided surgical system 10 can include components in both the control room 100A and the MRI scanner room 100B. Certain components (e.g., motors 310 coupled to the actuators 200a) in the MRI scanner room 100B can be controlled by components (e.g., the computer system 31) in the control room 100A. Thus, the computer system 31 of a surgical procedure workstation 30 of the surgical navigation system 10 in the control room 100A can be in communication with a plurality of actuators 200a of a trajectory guide 200 in the MRI scanner room 100B.
[0146] Optionally, at least one fiber optic cable 75 can be routed through the wave guide 175 and couple the computer system 31 in the control room 100A to a housing 300 comprising a plurality of motors 310 in the MRI scanner room 100B. The computer system 31 can connect to a communications cable 32 which can couple to an input of a USB to fiber optic converter 33. The USB to fiber optic converter 33 can provide an output that is coupled to the fiber optic cable 75. The USB to fiber optic converter 33 can reside in the control room 100A.
[0147] It is contemplated that wireless communication systems, optionally BLUETOOTH, WiFi, LTE and/or infrared systems, may be used to couple the computer system 31 to the motors 310 in lieu of the at least one fiber optic cable 75 or with the at least one fiber optic cable 75.
[0148] The surgical procedure workstation 30 of the surgical system 10 can comprise a display 38 that provides images and information to a user during a surgical procedure. The computer system 31 of the surgical procedure workstation 30 can be configured to provide a defined workflow(s) of actions including identifying a desired trajectory to a target surgical site using a targeting cannula Tc (
[0149] The computer system 31 can be coupled to a computer system 25 of the MRI scanner console 25C, also in the control room 100A, via a communications cable 130. The computer system 25 of the MRI scanner console 25C controls operation of the MRI scanner 22, e.g., applies selected and/or defined pulse sequences, slice selection, scan planes, signal acquisition (transmit excitation pulses and/or receive MR data of the patient) and the like. The computer system 25 in the control room 100A can communicate with or be at least partially installed in a control cabinet 28 with RF amplifiers, gradient amplifiers and/or circuits associated therewith.
[0150] The image-guided surgical system 10 can include at least one housing 300 in the MRI scanner room 100B that holds a plurality of components that communicate with the computer system 25 in the control room 100A, optionally including motors 310 coupled to respective actuators 200a of the trajectory guide 200. In other embodiments, the motors 310 are held adjacent respective actuators 200a, spaced apart from and outside the at least one housing 300 with control cables 1225 connecting the components in the housing 300 and the respective motors 310 (see,
[0151] The at least one housing 300 can also hold a fiber optic to USB converter 133 and at least one microcontroller 140.
[0152] The at least one housing 300 can be a unit housing that holds the motors 310, the controller 140 and the converter 133 or that holds only the controller 140 and the converter 133.
[0153] The motors 310 can be coupled to the at least one microcontroller 140. The at least one microcontroller 140 is in communication with the computer system 31 of the surgical procedure workstation 30 in the control room 100A whereby the computer system 31 provides instructions to the at least one microcontroller 140, that then provides instructions to one or more of the motors 310 for controlled directional movement of the one or more motors 310 for accurate positional turns of one or more of the actuators 200a.
[0154] The surgical systems 10 can be configured to provide bi-directional communication between the microcontroller 140 in the MR scanner room 100B and the surgical procedure computer system 31 in the MR control room 100A using the computer system 31 and the microcontroller 140 and to provide status updates to the computer system 31 of when completion of directional movement of one or more motors 310 has occurred, with the motors 310 being provided directional commands (right, left) controlled by the computer system and microcontroller. When one or more of the motors 310 has completed its commanded directional movement, a status signal can be transmitted to the computer system 31 which can then trigger the MR computer system 25 to commence new image acquisitions to verify an adjusted trajectory of the trajectory guide 200. The status signals can facilitate a time-efficient trajectory alignment protocol.
[0155] Each motor 310 can be coupled to a respective actuator 200a of the trajectory guide 200, optionally via a corresponding cable 220 or via a relatively short motor shaft coupler 1220 provided by a motor drive assembly 1200 (
[0156] Referring to
[0157] Referring to
[0158] For additional discussion of suitable trajectory guides, see, U.S. application Ser. No. 12/134,412, and co-assigned U.S. patent application Ser. Nos. 12/236,950, and 14/515,105, the contents of which are hereby incorporated by reference as if recited in full herein.
[0159] Referring to
[0160] In some embodiments, the cables 220 can comprise torque transfer shafts 220s. The torque transfer shafts 220s can comprise a rigid or semi-rigid internal cable 226 and an outer shaft 227 enclosing the internal cable 226. The term “semi-rigid” means that the referred to object, e.g., in this case, the cable 220 has a self-supporting shape and but may flex side-to-side when assembled to the trajectory guide 200 and/or a corresponding motor 310, optionally via flex coupler 321 (
[0161] In some particular embodiments, the internal cable 226, where used, can have a spiral rib(s) on an outer surface that can provide increased surface area to bond with an adhesive or filler material and fixedly couple to the outer shaft 227. The internal cable 226 can have a maximal outer diameter that is in a range of about 0.01 inches to about 0.3 inches. The outer shaft 227 can have a maximal outer diameter that is in a range of about 0.02 inches to about 0.5 inches.
[0162] In some embodiments, in an assembled position, the shape of one or more of the cables 220 can be arcuate over at least a major portion of its length and extend in a curvilinear shape between opposing ends (
[0163] Where used, the internal cable 226 can comprise non-ferromagnetic material such as, for example, Nitinol steel. Where used, the outer shaft 227 can comprise a different non-ferromagnetic material than the internal cable 226. The internal cable 226 can have a solid core. The internal cable 226 can extend out of a distal end 227d of the outer shaft 227 and couple to a connector 229. The internal cable 226 can extend out of a proximal end 227p of the outer shaft 227 and couple to a connector 228. The extension lengths can be in a range of 0.1 inches to about 2 inches, in some embodiments. Thus, the internal cable 226 can have a continuous length that is longer than the length of the outer shaft 227. The outer shaft 227 can be fixedly coupled to the internal cable 226 via a non-ferromagnetic filler material to provide additional structural support over a length of the cable 220.
[0164] Referring to
[0165] The connector 228 at the proximal end portion 220p of the cable 220 can be directly or indirectly coupled to a motor 310, such as a piezo motor 310p. The motor 310 can comprise or couple to a motor shaft 310s that couples to the cable 220.
[0166] Referring to
[0167] Where used, the first shaft 309 can be rigid and non-ferromagnetic. The first length L.sub.1 can be less than the second length L.sub.2. The first length L.sub.1 can be in a range of 1-4 inches. The second length L.sub.2 can be in a range of 2-6 inches. The first shaft 309 can be metallic and non-ferromagnetic. Where used, the second shaft 308 can be rigid or semi-rigid and have a diameter that is greater than that of the first shaft 309. The second shaft 309 can comprise a polymer and/or fiberglass. The first and second shafts 309, 308 can each have an outer diameter that is greater than the cable 226 of the torque transfer shaft 220.
[0168] The control knob connector 328 can be configured to receive the connector 228 at the proximal end 220p of the cable 220, e.g., the first connector of the cable 220. The control knob connector 328 can have a channel 328c that receives the connector 228 and attaches thereto to be able to rotate as a unit. The connector 328 can be configured as a substantial duplicate of the thumbwheel or control knob 200k of a respective actuator 200a of the trajectory guide 200. That is, the control knob connector 328 can have substantially the same external body configuration, e.g., it can be formed of the same material and have the same outer diameter size and length as the corresponding knob 200k of the actuator 200a.
[0169] The first and second shafts 308, 309 and the coupler 321 can all be non-ferromagnetic.
[0170] The motors 310 can be non-ferromagnetic motors. The motors 310 can be piezo motors or pneumatic motors, for example. For further details of an example piezo motor, see, e.g., U.S. Pat. No. 9,136,778 to Discovery Technology International, Inc., the contents of which are hereby incorporated by reference as if recited in full herein. By way of example, a commercially available piezoelectric motor is the non-magnetic rotary piezo motor RBS Series from DTI, Inc., Sarasota, Fla. MRI compatible pneumatic stepper motors are described in U.S. Pat. No. 10,024,160 and PCT/NL2017/050552, the contents of which are hereby incorporated by reference as if recited in full herein.
[0171] Referring to
[0172] The pitch stepper motor 311 can be coupled to the pitch direction actuator 206. The roll stepper motor 312 can be coupled to the roll direction actuator 205. The X-direction stepper motor 313 can be coupled to the X-direction actuator 208. The Y-direction stepper motor 314 can be coupled to the Y-direction actuator 207.
[0173] Each motor 310 can be coupled to a dedicated respective motor driver 145 and/or dedicated microcontroller 140 (four microcontrollers for four motors 310, for example, not shown). All the motors 310 can be coupled to a common, single microcontroller 140 and a single motor driver 145 (
[0174] Two or more motors 310 can serially or concurrently rotate a respective torque transfer shaft 220 to position the tower 210 of the trajectory guide 200 at an adjusted trajectory based on commands from the computer system 31 of the workstation 30. Referring to
[0175] The housing 300, 300′ can be EMI and/or RF-shielded 333 such as with copper fingers flashing or casings and/or epoxy at apertures and seams and can use appropriate externally accessible RF-attenuated connector(s) to reduce or eliminate any RF emissions from internal components.
[0176] In some embodiments, the power supply 165 and a USB and serial communications unit or module 170 and driver 145 are located in a separate electrically shielded enclosure 1300 (“drive control enclosure”) that can be placed in the scanner room 100B but further away from the bore of the MRI magnet relative to the other housing 300 with the motors 310 (“motor enclosure”). A suitable multiconductor electrical cable carries signals from the at least one motor driver 145 to the motors 310 and the output of the encoder back to the at least one motor driver 145. This approach can reduce or minimize electrical interaction between the MR scanner 22 and the motor driver 145, microcontroller 140, power supply 165 and USB serial communication unit 170 electronics. Electrical interaction can create artifacts in the MRI images. During the process of creating an MRI image very strong electromagnetic pulses are generated in the MRI scanner bore by the RF coil and gradient coils. These pulses can potentially cause the at least one motor driver 145, microcontroller 140, power supply 165 and USB serial communication unit 170 electronics to malfunction if not properly positioned and/or electrically isolated.
[0177] Referring to
[0178] In some embodiments, as shown in
[0179] The motor enclosure/housing 300, the at least one fiber optic cable 310 and all internal components of the housing 300, including the motors 311-314, cables 220, connectors 228, 229, and flexible coupler 321 are made of non-ferromagnetic (MRI compatible) material and do not experience any significant magnetic force pull from the MRI superconducting magnet 22M. The housing 1300 and/or the motor driver 145, microcontroller 140 and power supply 165 may include minimally magnetic components.
[0180] Communication between the computer system 31 and the at least one motor driver 145 can be two-way. The at least one motor driver 145 can signal the computer system 31 once one or more of the motors 310 has finished turning the required angle.
[0181] Embodiments of the invention can provide the communication between the computer system 31 and the microcontroller 140 and the at least one motor driver 145 using one or a plurality of fiber optic cables 75
[0182]
[0183] Referring to
[0184] Referring to
[0185] Referring to
[0186] The at least one fiber optic cable 75 is electrically nonconductive and prevents or inhibits outside radio frequency signals from penetrating through the shield (Faraday Cage) of the MRI scanner room 100B. The MRI scanner 22 is enclosed in the shielded room/Faraday cage as external radio frequency signals will interfere with the functioning of the ultra-sensitive radio frequency receivers of the MRI scanner. This interference appears as artifacts in the MRI images.
[0187] The controller 140 can be configured to programmatically decode the motor turn instructions, send appropriate signals to (start and stop inputs) the motors 310, optionally by sending commands to the associated driver 145 or to a quad motor driver 145 (
[0188] The controller 140 can also be configured to provide status updates to the surgical procedure workstation 30 and/or computer system 31 thereof. The status updates can include one or more of: one or more driver still in motion for adjusting an actuator 200a, motor completed its commanded turn motion to turn a respective actuator for the current positional turn direction instructions.
[0189] In some embodiments, after executing all commands to turn the actuators 200a, the microprocessor 140 sends back a defined code (which indicates the completion of all commands), as well as the value of the number of counted pulses (4 bytes), when the last command is executed. A rotary encoder can have a resolution in a range of about 100-300 μrad, such as about 196 μrad (32,000 PPR) after interpolation and quadrature detection. Thus, for example, 32,000 pulses can correspond to one complete turn of the motor shaft 310s.
[0190] Referring to
[0191] After each positional adjustment or a set of adjustments of one or more actuators 200a by one or more motor 310, the workstation 30 and/or computer system 31 thereof can be configured to direct and/or trigger the computer system 25 of the MRI scanner console to acquire new sets of images.
[0192] Referring to
[0193] Referring to
[0194] In an example set-up, as shown in
[0195] For example, in block 610 of
[0196] The surgical procedure system 10 can define a set of actions (a workflow) for the image-guided surgical navigation system 10. See, for example, U.S. Pat. No. 8,315,689B2, entitled MRI Surgical Systems for Real-Time Visualizations Using MRI Image Data And Predefined Data Of Surgical Tools (which describes components of, inter alia, an image-guided system also known as the CLEARPOINT® image-guided surgical system from MRI Interventions, Inc., Irvine, Calif.), the contents of which are hereby incorporated by reference as if recited in full herein.
[0197] During an interventional surgical procedure, the trajectory guide 200 is adjusted to a desired trajectory based on directions from the computer system 31 which iteratively (1) acquires MRI images at certain imaging planes in 3D space, (2) uses the acquired images to locate a position in three dimensional image space of a Tc (
[0198] In embodiments of the present invention, the surgical procedure workflow can occur after the trajectory guide is mounted to or adjacent the patient head and the trajectory guide adjustment can be broken into two primary adjustment actions. That is, the trajectory guide 200 can be directly attached to a skull of a patient or held by a support assembly such as that described in U.S. patent applications number Ser. Nos. 14/619,847; 62/964,340 (Attorney Dkt. 9450-137PR) and 62/968,210 (Attorney Dkt. 9450-138PR), the contents of which are hereby incorporated by reference as if recited in full herein.
[0199] A rough or preliminary adjustment can be provided by an ‘Align’ action(s) in the surgical procedure workflow. This can be followed by a finer adjustment or an ‘Adjust’ action(s) in the surgical procedure workflow. The trajectory guide 200 can couple to a targeting cannula (Tc,
[0200]
[0201] If the projected error is less than the desired value (i.e., 2 mm), the orthogonal #1 and #2 image stack plane parameters are set on and/or to the MRI console (block 635). Next, acquisition of a first stack of contiguous orthogonal slices that cover the entire targeting cannula is initiated (block 640). The acquired images of the first stack of contiguous orthogonal slices are downloaded (block 645). Acquisition of a second stack of contiguous orthogonal slices that cover the entire targeting cannula is initiated (block 650). The acquired images of the second stack of contiguous orthogonal slices are downloaded (block 655). The projected error is again calculated to determine if the projected error is less than a desired value (typical 2D projected error is <1 mm) (block 665). If the projected error is not less than the desired value (i.e., about 1 mm or less), one or more of the pitch and roll motors and/or X and Y stage motors (where used) can be directionally turned via fiber optic interface (block 660). The steps of the operation are repeated starting with downloading the acquired images of the first stack of contiguous orthogonal slices (block 645). Typically, two-four (2-4) iterations are needed to achieve a sufficiently accurate defined intrabody trajectory. If the projected error is less than the desired value (i.e., about 1 mm or less), the trajectory alignment goal is met and the position adjustment can be ended.
[0202] As discussed above, MRI compatible stepper motors 310 can be used to make the required positional adjustments. The automated system can reduce the time taken to finalize the trajectory frame adjustment from 60 minutes to less than about 10 minutes. This savings in time can provide a procedure value to surgeons and facilitate an ease in performing the surgery with accuracy and overall reduction in cost.
[0203] The controller 140 can have embedded software that decodes motor turn instructions, sends appropriate signals to start and stop motors 310 by sending commands to the individual motor drivers 145 or to a quad motor driver that communicates with each motor 310. The controller 140 can also provide status updates to the surgical procedure workstation 30. After each adjustment, the computer system 31 of the surgical procedure workstation 30 can trigger the computer system 25 of the MRI scanner to acquire new sets of images. From these new images, the position of the targeting cannula Tc is segmented, a trajectory is re-calculated and new thumb wheel/knob adjustment values are generated by the surgical procedure workstation 30. The adjustment process can be repeated until projected error is below a certain defined value that can be a default value or a predetermined by the user or the adjustment knobs are maxed out.
[0204] The system 10 can be configured to render or generate real time visualizations of the target anatomical space using MRI image data and predefined data of the trajectory guide and at least one surgical tool to segment the image data and place the trajectory guide and/or tool in the rendered visualization in the correct orientation and position in 3D space. Embodiments of the present invention may include steps, features, aspects, components, procedures and/or systems as disclosed in U.S. patent application Ser. No. 12/236,854, published as U.S. Published Patent Application No. 2009/0171184, the disclosure of which is incorporated herein by reference. Embodiments of the present invention use the surgical support system 10 with an automated or semi-automated surgical procedure system comprising defined workflows and DICOM communication with the computer system 25 of the MR Scanner. See, e.g., U.S. Pat. No. 10,105,485, the contents of which are hereby incorporated by reference as if recited in full herein.
[0205] According to some embodiments, the systems are configured to provide a substantially automated or semi-automated and relatively easy-to-use MRI-guided system with defined workflow steps and interactive visualizations. In particular embodiments, the systems define and present workflow with discrete steps for guiding the alignment of the targeting cannula Tc held by the trajectory guide 200 to a planned trajectory, monitoring the insertion of a delivery cannula, and adjusting the (X-Y) position in cases where the placement needs to be corrected.
[0206] A relatively long multiple (e.g., four or more) conductor, fiberoptic or optical cables 75 can be used. The fiber optic cable 75 can be between about 5-50 meters long or longer, such as about 5 meters, about 6 meters, about 7 meters, about 8 meters, about 9 meters, and about 10 meters, about 20 meters, about 30 meters, about 40 meters, and about 50 meters, in some embodiments. The cable 75 can be obtained from any suitable supplier such as, for example, Lastar Cables 2 Go, Irvine, Calif. and Opticis, Sungnam City, Rep. of Korea. The interface at the housing 300 can include an EMI filter, RF shielding and a copper contact strip 333 from any suitable supplier such as Laird or Shaffner EMC referenced above.
[0207] As discussed above, other communications systems may be used that do not require fiber optic cables, such as BLUETOOTH and/or infrared systems.
[0208] Embodiments of the present invention can be configured to carry out diagnostic and interventional procedures such as to guide and/or place interventional devices to any desired internal region of the body or object but may be particularly suitable for neurosurgeries for ablation or fluid delivery or withdrawal. The object can be any object and may be particularly suitable for animal and/or human subjects. The system 10 can be used for gene and/or stem-cell based therapy delivery or other neural therapy delivery and allow user-defined custom targets in the brain or to other locations. In addition, embodiments of the systems can be used to ablate tissue in the brain or other locations. In some embodiments, it is contemplated that the systems can be configured to treat AFIB in cardiac tissue, and/or to deliver stem cells or other cardio-rebuilding cells or products into cardiac tissue, such as a heart wall, via a minimally invasive MRI guided procedure while the heart is beating (i.e., not requiring a non-beating heart with the patient on a heart-lung machine).
[0209] Examples of known treatments and/or target body regions are described in U.S. Pat. Nos. 6,708,064; 6,438,423; 6,356,786; 6,526,318; 6,405,079; 6,167,311; 6,539,263; 6,609,030 and 6,050,992, the contents of which are hereby incorporated by reference as if recited in full herein.
[0210] Embodiments of the present invention may take the form of an entirely software embodiment or an embodiment combining software and hardware aspects, all generally referred to herein as a “circuit” or “module.” In some embodiments, the circuits include both software and hardware and the software is configured to work with specific hardware with known physical attributes and/or configurations. Furthermore, the present invention may take the form of a computer program product on a computer-usable storage medium having computer-usable program code embodied in the medium. Any suitable computer readable medium may be utilized including hard disks, CD-ROMs, optical storage devices, a transmission media such as those supporting the Internet or an intranet, or other storage devices.
[0211] Computer program code for carrying out operations of the present invention may be written in an object-oriented programming language such as Java®, Smalltalk or C++. However, the computer program code for carrying out operations of the present invention may also be written in conventional procedural programming languages, such as the “C” programming language. The program code may execute entirely on the user's computer, partly on the user's computer, as a stand-alone software package, partly on the user's computer and partly on another computer, local and/or remote or entirely on the other local or remote computer. In the latter scenario, the other local or remote computer may be connected to the user's computer through a local area network (LAN) or a wide area network (WAN), or the connection may be made to an external computer (for example, through the Internet using an Internet Service Provider).
[0212] The present invention is described in part below with reference to flowchart illustrations and/or block diagrams of methods, apparatus (systems) and computer program products according to embodiments of the invention. It will be understood that each block of the flowchart illustrations and/or block diagrams, and combinations of blocks in the flowchart illustrations and/or block diagrams, can be implemented by computer program instructions. These computer program instructions may be provided to a processor of a general purpose computer, special purpose computer, or other programmable data processing apparatus to produce a machine, such that the instructions, which execute via the processor of the computer or other programmable data processing apparatus, create means for implementing the functions/acts specified in the flowchart and/or block diagram block or blocks.
[0213] These computer program instructions may also be stored in a computer-readable memory that can direct a computer or other programmable data processing apparatus to function in a particular manner, such that the instructions stored in the computer-readable memory produce an article of manufacture including instruction means which implement the function/act specified in the flowchart and/or block diagram block or blocks.
[0214] The computer program instructions may also be loaded onto a computer or other programmable data processing apparatus to cause a series of operational steps to be performed on the computer or other programmable apparatus to produce a computer implemented process such that the instructions which execute on the computer or other programmable apparatus provide steps for implementing the functions/acts specified in the flowchart and/or block diagram block or blocks.
[0215] The flowcharts and block diagrams of certain of the figures herein illustrate exemplary architecture, functionality, and operation of possible implementations of embodiments of the present invention. In this regard, each block in the flow charts or block diagrams represents a module, segment, or portion of code, which comprises one or more executable instructions for implementing the specified logical function(s). It should also be noted that in some alternative implementations, the functions noted in the blocks may occur out of the order noted in the figures. For example, two blocks shown in succession may in fact be executed substantially concurrently or the blocks may sometimes be executed in the reverse order or two or more blocks may be combined, depending upon the functionality involved.
[0216] As illustrated in
[0217] In particular, the processor 1110p can be commercially available or custom microprocessor, microcontroller, digital signal processor or the like. The memory 1136 may include any memory devices and/or storage media containing the software and data used to implement the functionality circuits or modules used in accordance with embodiments of the present invention. The memory 1136 can include, but is not limited to, the following types of devices: ROM, PROM, EPROM, EEPROM, flash memory, SRAM, DRAM and magnetic disk. In some embodiments of the present invention, the memory 1136 may be a content addressable memory (CAM).
[0218] As further illustrated in
[0219] The input/output device drivers 1158 typically include software routines accessed through the operating system 1152 by the application programs 1154 to communicate with devices such as the input/output circuits 1146 and certain memory 1136 components. The application programs 1154 are illustrative of the programs that implement the various features of the circuits and modules according to some embodiments of the present invention. Finally, the data 1156 represents the static and dynamic data used by the application programs 1154 the operating system 1152 the input/output device drivers 1158 and other software programs that may reside in the memory 1136.
[0220] The data 1156 may include MRI image data sets with metadata correlated to respective patients. As further illustrated in
[0221] While the present invention is illustrated with reference to the application programs 1154, and modules 1124, 1126 and 1127 in
[0222] The computer system 25 of the MRI scanner can include a console that has a “launch” application or portal for allowing communication to the circuit 31 of the surgical procedure workstation 30.
[0223] The scanner console can acquire volumetric T1-weighted (post-contrast scan) data or other image data (e.g., high resolution image data for a specific volume) of a patient's head or other anatomy. In some embodiments, the console can push DICOM images or other suitable image data to the workstation 30 and/or computer system 31. The workstation 30 and/or computer system 31 can be configured to passively wait for data to be sent from the computer system 25 of the MR scanner 22 and the workstation 30 does not query the Scanner or initiate a communication to the Scanner. In other embodiments, a dynamic or active communication protocol between the circuit computer system 31/workstation 30 and the computer system 25 of the Scanner may be used to acquire image data and initiate or request particular scans and/or scan volumes.
[0224] Also, in some embodiments, pre-DICOM, but reconstructed image data, can be sent to the circuit workstation 30 for processing or display. In other embodiments, pre-reconstruction image data (e.g., substantially “raw” image data) can be sent to the workstation 30 for Fourier Transform and reconstruction. Embodiments of the present invention use the surgical support system 10 with an automated or semi-automated surgical navigation system comprising defined workflows and DICOM communication with an MR Scanner. See, e.g., U.S. Pat. No. 10,105,485, the contents of which are hereby incorporated by reference as if recited in full herein.
[0225] Turning now to
[0226] The motor assembly 1200 can be light weight and size to avoid introducing torque forces onto the trajectory guide 200. The motor assembly 1200, absent the control cable 1225, can have a weight that is in a range of about 50 grams to about 100 grams. The housing 1200h can have a compact maximal height H or length dimension “L” and maximal width “W” dimension, with each in a range of about 1.5 inches to about 3.5 inches, such as each within a range of about 1.5 inches, about 1.75 inches about 2 inches, about 2.5 inches, about 3 inches and about 3.5 inches. The H, L and W dimensions can be different. The L dimension can be greater than the W dimension. The housing 1200h can be non-ferromagnetic and may optionally be molded from a PEEK or polycarbonate material. The housing 1200h can have at least a portion that is visually transmissive at least adjacent the drive wing receiving region to facilitate ease of installation. The housing 1200h or a lower portion thereof can be provided as a translucent and/or transparent non-ferromagnetic material such as a transparent or translucent polymer
[0227] The housing 1200h can have a chamber 1200c that receives the motor 310. The chamber 1200c can be provided by an enclosure cap 1202c. The motor assembly 1200 can include a seal 1204, such as an O-ring, that is held in a circumferential recess of the enclosure cap 1202c between an outer perimeter portion 310o of the bottom 310b of the motor 310 and the recess 1205. Other seal configurations and types may be used, such as, for example, a gasket or other seal.
[0228] The housing 1200h can comprise an enclosure leg 1212 that couples to the enclosure cap 1202. The enclosure leg 1212 can be surround an open channel 1212c that extends under the enclosure cap 1202. The enclosure leg 1212 can have a top 1212t that is circular and attaches to the enclosure cap 1201 to sandwich the seal 1204 therebetween. The top 1212t can have an open medial portion 1212m. The shaft 310s of the drive motor 310 can extend a distance into the leg enclosure 1212 through the open medial portion 1212m. A second seal 1214 can reside above the shaft on the bottom 310b of the motor 310, between the bottom of the motor 310 and a motor shaft coupler 1220. The second seal 1214 has a smaller outer diameter than the (first) seal 1204.
[0229] Attachment members 1216 can attach the enclosure cap 1202 to the enclosure leg 1212. The attachment members 1216 can extend through pairs of aligned ears 1203, 1213 to attach the enclosures 1202, 1212 and seal the motor 310. At least one other attachment member 1219 (shown as three) can extend through the top 1212t of the leg enclosure into a bottom portion of the motor 310 to help affix/stabilize the motor to the housing 1200h.
[0230] The motor shaft coupler 1220 can be relatively short in length, typically having a length in a range of 5 mm to 50 mm and may be rigid. The motor shaft coupler 1220 can be non-ferromagnetic. The motor shaft coupler 1220 can be attached to a secondary drive shaft 1222 of smaller diameter than the drive shaft 310s that is directly attached to and/or provided by the motor 310. The secondary shaft 1222 can have an outer diameter that is in a range of 10-50% of an outer diameter of the primary drive shaft 310s. The secondary drive shaft 1222 can be coupled to a connector 229, shown as a drive wing. The connector 229 is sized and configured to couple to the actuator 200a, shown as a thumbwheel 200k in
[0231] The secondary drive shaft 1222 can extend a distance into a channel 229c of the connector 229. The secondary drive shaft 1222 can be internal to the motor shaft coupler 1220 and internal to the connector 229 with little to no externally exposed segment. Stated differently, the distal end 1220d of the motor shaft coupler 1220 can reside flush with or closely spaced apart from a proximal end 229p of the connector 229. In some embodiments, a longitudinally extending gap space “g” of between 0.001 mm and 10 mm, more typically between 0.01 and 8 mm, can reside between the distal end of the motor shaft coupler 1220 and the proximal end of the connector 229 with both held inside the enclosure leg 1212. The drive shaft (e.g., cable) 1222 can be configured to be more flexible the more exposed it is. Our current Thumb Wheel Extension, which also uses a drive cable to manually operate the thumb wheels at a distance, has an exposed length of about 8 mm.
[0232] The housing 1200h can include an outwardly extending strain relief arm 1220a that provides a cable path for control cable 1225. As shown, the strain relief arm 1200a as provided by matably configured arm segments 1207, 1217 of respective enclosure cap 1202 and leg enclosure 1212. The control cable 1225 can be non-ferromagnetic.
[0233] In some embodiments, a length of one side 1212s of the enclosure leg 1212 can be shorter than other sides 1212s. As shown, the side 1212s that is spaced apart 90 degrees from the side 1212s with the strain relief 1200a can have a shorter length than the other sides forming an open window region that can allow the enclosure leg 1212 to extend down over a support segment 219 under the corresponding actuator 205 (
[0234] The enclosure leg 1212 can have four sides 1212s.sub.1-1212s.sub.4 corresponding to a rectangular shape (in cross-section) as shown, but other shapes may be used such as, for example, circles, particularly where the support segment 219 has other shapes such as, for example, a cylindrical shape (not shown).
[0235] The housing 1200h can be sized and configured to slidably receive one thumbwheel 200k of a respective actuator 200a mounted on the trajectory guide 200. The thumbwheel 200k is rotatable by the connector 229 while inside an end portion of the housing 1200h. At least some of the enclosure leg 1212 may be visually translucent for ease of visualizing the attachment for ease of installation/assembly. The distal end 229d of the connector 229 can be slidably received and frictionally coupled to a (diametrically extending) slot, recess or channel 200r in an outer surface of the thumbwheel or knob 200k.
[0236] The distal end 229d of the actuator connector 229 can reside a distance “d.sub.1” above an open distal end 1212d of the enclosure leg 1212. The distance d.sub.1 can be in a range of about 10 mm to about 50 mm. This allows at least part, typically the entire length and width, of the actuator 200a to be received into the channel 1212c. In some embodiments, the entire thumbwheel 200k resides above the open end of the channel 1212c so that at least part of a support feature or structure 219 can also be received into the channel 1212c and provide structural support for the assembly 1200.
[0237] Referring to
[0238]
[0239] As shown in
[0240] Each control cable 1225 (
[0241] Referring to
[0242] The foregoing is illustrative of the present invention and is not to be construed as limiting thereof. Although a few exemplary embodiments of this invention have been described, those skilled in the art will readily appreciate that many modifications are possible in the exemplary embodiments without materially departing from the teachings and advantages of this invention. Accordingly, all such modifications are intended to be included within the scope of this invention as defined in the claims. The invention is defined by the following claims, with equivalents of the claims to be included therein.