Patent Application
20250018566
The systems and methods disclosed herein are directed to input devices, and more particularly to input devices for robotic surgical systems.
A robotically enabled medical system is capable of performing a variety of medical procedures, including both minimally invasive procedures, such as laparoscopy, and non-invasive procedures, such as endoscopy (e.g., bronchoscopy, ureteroscopy, gastroscopy, etc.).
Such robotic medical systems may include robotic arms configured to control the movement of medical tool(s) during a given medical procedure. The robotic medical system may also include an input device used to control the positioning and/or actuation of the medical tool(s) during the medical procedure.
The systems, methods and devices of this disclosure each have several innovative aspects, no single one of which is solely responsible for the desirable attributes disclosed herein.
In one aspect, an input device for controlling a robotic surgical tool is provided. The input device can include a first pair of opposing links and a second pair of opposing links. The first pair of opposing links and the second pair of opposing links can be arranged radially symmetrically. The input device can be configured to control operation of the robotic surgical tool.
In another aspect, a physician console can be provided. The physician console can include an input device including a first grasper and a second grasper. The input device can be configured to control a surgical tool. At least one of the first and second grasper can include a four-link radially symmetrical grasper for controlling operation of the surgical tool.
In another aspect, an input device for controlling operation of a robotic arm is provided. The input device can include a first finger pad that includes a first set of two or more electrodes for determining a user presence at the first finger pad. The input device can also include a processor for modifying operation of the robotic arm in response to information from the input device regarding user presence at the first finger pad.
In another aspect, a medical system with a user input device for controlling a medical instrument is provided. The user input device is operable in an unassisted mode with a first set of parameters for operation of the user input device, and an assisted mode with a second set of parameters, distinct from the first set, for operation of the user input device. The medical system further includes a sensor coupled to the user input device for generating information related to the user input device. The medical system also includes a processor and memory storing instructions for execution by the processor. The stored instructions include instructions for, while operating the user input device in the unassisted mode, identifying drift of the user input device based on the information from the sensor; and, in accordance with identifying the drift, switching operation of the user input device from the unassisted mode to the assisted mode.
In accordance with some embodiments, a method for operating a medical system that includes a user input device for controlling a medical instrument is performed by one or more processors executing instructions store in memory. The method includes, while operating in the unassisted mode, detecting drift of the user input device; and in accordance with detecting the drift, switching operation of the user input device to an assisted mode, including applying a second set of parameters that is distinct from the first set of parameters. The method also includes, while operating in the assisted mode, determining that the user input device is stable; and, in accordance with the determination, switching the operation of the user input device to the unassisted mode.
In accordance with some embodiments, a method for operating a medical system that includes a user input device for controlling a medical instrument is performed by one or more processors executing instructions store in memory. The method includes operating the user input device in an unassisted mode, including applying a first set of parameters to the user input device. The method further includes, while operating in the unassisted mode, identifying drift of the user input device; and, in accordance with detecting the drift, switching operation of the user input device to an assisted mode, including applying a second set of parameters that is distinct from the first set of parameters.
The disclosed aspects will hereinafter be described in conjunction with the appended drawings, provided to illustrate and not to limit the disclosed aspects, wherein like designations denote like elements.
Aspects of the present disclosure may be integrated into a robotically-enabled medical system capable of performing a variety of medical procedures, including both minimally invasive, such as laparoscopy, and non-invasive, such as endoscopy, procedures. Among endoscopic procedures, the system may be capable of performing bronchoscopy, ureteroscopy, gastroscopy, etc.
In addition to performing the breadth of procedures, the system may provide additional benefits, such as enhanced imaging and guidance to assist the physician. Additionally, the system may provide the physician with the ability to perform the procedure from an ergonomic position without the need for awkward arm motions and positions. Still further, the system may provide the physician with the ability to perform the procedure with improved case of use such that one or more of the instruments of the system can be controlled by a single user.
Various embodiments will be described below in conjunction with the drawings for purposes of illustration. It should be appreciated that many other implementations of the disclosed concepts are possible, and various advantages can be achieved with the disclosed implementations. Headings are included herein for reference and to aid in locating various sections. These headings are not intended to limit the scope of the concepts described with respect thereto. Such concepts may have applicability throughout the entire specification.
The robotically-enabled medical system may be configured in a variety of ways depending on the particular procedure.
With continued reference to
The endoscope 13 may be directed down the patient's trachea and lungs after insertion using precise commands from the robotic system until reaching the target destination or operative site. In order to enhance navigation through the patient's lung network and/or reach the desired target, the endoscope 13 may be manipulated to telescopically extend the inner leader portion from the outer sheath portion to obtain enhanced articulation and greater bend radius. The use of separate instrument drivers 28 also allows the leader portion and sheath portion to be driven independently of each other.
For example, the endoscope 13 may be directed to deliver a biopsy needle to a target, such as, for example, a lesion or nodule within the lungs of a patient. The needle may be deployed down a working channel that runs the length of the endoscope to obtain a tissue sample to be analyzed by a pathologist. Depending on the pathology results, additional tools may be deployed down the working channel of the endoscope for additional biopsies. After identifying a nodule to be malignant, the endoscope 13 may endoscopically deliver tools to resect the potentially cancerous tissue. In some instances, diagnostic and therapeutic treatments can be delivered in separate procedures. In those circumstances, the endoscope 13 may also be used to deliver a fiducial to “mark” the location of the target nodule as well. In other instances, diagnostic and therapeutic treatments may be delivered during the same procedure.
The system 10 may also include a movable tower 30, which may be connected via support cables to the cart 11 to provide support for controls, electronics, fluidics, optics, sensors, and/or power to the cart 11. Placing such functionality in the tower 30 allows for a smaller form factor cart 11 that may be more easily adjusted and/or re-positioned by an operating physician and his/her staff. Additionally, the division of functionality between the cart/table and the support tower 30 reduces operating room clutter and facilitates improving clinical workflow. While the cart 11 may be positioned close to the patient, the tower 30 may be stowed in a remote location to stay out of the way during a procedure.
In support of the robotic systems described above, the tower 30 may include component(s) of a computer-based control system that stores computer program instructions, for example, within a non-transitory computer-readable storage medium such as a persistent magnetic storage drive, solid state drive, etc. The execution of those instructions, whether the execution occurs in the tower 30 or the cart 11, may control the entire system or sub-system(s) thereof. For example, when executed by a processor of the computer system, the instructions may cause the components of the robotics system to actuate the relevant carriages and arm mounts, actuate the robotics arms, and control the medical instruments. For example, in response to receiving the control signal, the motors in the joints of the robotics arms may position the arms into a certain posture.
The tower 30 may also include a pump, flow meter, valve control, and/or fluid access in order to provide controlled irrigation and aspiration capabilities to the system that may be deployed through the endoscope 13. These components may also be controlled using the computer system of the tower 30. In some embodiments, irrigation and aspiration capabilities may be delivered directly to the endoscope 13 through separate cable(s).
The tower 30 may include a voltage and surge protector designed to provide filtered and protected electrical power to the cart 11, thereby avoiding placement of a power transformer and other auxiliary power components in the cart 11, resulting in a smaller, more moveable cart 11.
The tower 30 may also include support equipment for the sensors deployed throughout the robotic system 10. For example, the tower 30 may include optoelectronics equipment for detecting, receiving, and processing data received from the optical sensors or cameras throughout the robotic system 10. In combination with the control system, such optoelectronics equipment may be used to generate real-time images for display in any number of consoles deployed throughout the system, including in the tower 30. Similarly, the tower 30 may also include an electronic subsystem for receiving and processing signals received from deployed electromagnetic (EM) sensors. The tower 30 may also be used to house and position an EM field generator for detection by EM sensors in or on the medical instrument.
The tower 30 may also include a console 31 in addition to other consoles available in the rest of the system, e.g., console mounted on top of the cart. The console 31 may include a user interface and a display screen, such as a touchscreen, for the physician operator. Consoles in the system 10 are generally designed to provide both robotic controls as well as preoperative and real-time information of the procedure, such as navigational and localization information of the endoscope 13. When the console 31 is not the only console available to the physician, it may be used by a second operator, such as a nurse, to monitor the health or vitals of the patient and the operation of the system 10, as well as to provide procedure-specific data, such as navigational and localization information. In other embodiments, the console 31 is housed in a body that is separate from the tower 30.
The tower 30 may be coupled to the cart 11 and endoscope 13 through one or more cables or connections (not shown). In some embodiments, the support functionality from the tower 30 may be provided through a single cable to the cart 11, simplifying and de-cluttering the operating room. In other embodiments, specific functionality may be coupled in separate cabling and connections. For example, while power may be provided through a single power cable to the cart 11, the support for controls, optics, fluidics, and/or navigation may be provided through a separate cable.
The carriage interface 19 is connected to the column 14 through slots, such as slot 20, that are positioned on opposite sides of the column 14 to guide the vertical translation of the carriage 17. The slot 20 contains a vertical translation interface to position and hold the carriage 17 at various vertical heights relative to the cart base 15. Vertical translation of the carriage 17 allows the cart 11 to adjust the reach of the robotic arms 12 to meet a variety of table heights, patient sizes, and physician preferences. Similarly, the individually configurable arm mounts on the carriage 17 allow the robotic arm base 21 of the robotic arms 12 to be angled in a variety of configurations.
In some embodiments, the slot 20 may be supplemented with slot covers that are flush and parallel to the slot surface to prevent dirt and fluid ingress into the internal chambers of the column 14 and the vertical translation interface as the carriage 17 vertically translates. The slot covers may be deployed through pairs of spring spools positioned near the vertical top and bottom of the slot 20. The covers are coiled within the spools until deployed to extend and retract from their coiled state as the carriage 17 vertically translates up and down. The spring-loading of the spools provides force to retract the cover into a spool when the carriage 17 translates towards the spool, while also maintaining a tight seal when the carriage 17 translates away from the spool. The covers may be connected to the carriage 17 using, for example, brackets in the carriage interface 19 to ensure proper extension and retraction of the cover as the carriage 17 translates.
The column 14 may internally comprise mechanisms, such as gears and motors, that are designed to use a vertically aligned lead screw to translate the carriage 17 in a mechanized fashion in response to control signals generated in response to user inputs, e.g., inputs from the console 16.
The robotic arms 12 may generally comprise robotic arm bases 21 and end effectors 22, separated by a series of linkages 23 that are connected by a series of joints 24, each joint comprising an independent actuator, each actuator comprising an independently controllable motor. Each independently controllable joint represents an independent degree of freedom available to the robotic arm 12. Each of the robotic arms 12 may have seven joints, and thus provide seven degrees of freedom. A multitude of joints result in a multitude of degrees of freedom, allowing for “redundant” degrees of freedom. Having redundant degrees of freedom allows the robotic arms 12 to position their respective end effectors 22 at a specific position, orientation, and trajectory in space using different linkage positions and joint angles. This allows for the system to position and direct a medical instrument from a desired point in space while allowing the physician to move the arm joints into a clinically advantageous position away from the patient to create greater access, while avoiding arm collisions.
The cart base 15 balances the weight of the column 14, carriage 17, and robotic arms 12 over the floor. Accordingly, the cart base 15 houses heavier components, such as electronics, motors, power supply, as well as components that either enable movement and/or immobilize the cart 11. For example, the cart base 15 includes rollable wheel-shaped casters 25 that allow for the cart 11 to easily move around the room prior to a procedure. After reaching the appropriate position, the casters 25 may be immobilized using wheel locks to hold the cart 11 in place during the procedure.
Positioned at the vertical end of the column 14, the console 16 allows for both a user interface for receiving user input and a display screen (or a dual-purpose device such as, for example, a touchscreen 26) to provide the physician user with both preoperative and intraoperative data. Potential preoperative data on the touchscreen 26 may include preoperative plans, navigation and mapping data derived from preoperative computerized tomography (CT) scans, and/or notes from preoperative patient interviews. Intraoperative data on display may include optical information provided from the tool, sensor and coordinate information from sensors, as well as vital patient statistics, such as respiration, heart rate, and/or pulse. The console 16 may be positioned and tilted to allow a physician to access the console 16 from the side of the column 14 opposite the carriage 17. From this position, the physician may view the console 16, robotic arms 12, and patient while operating the console 16 from behind the cart 11. As shown, the console 16 also includes a handle 27 to assist with maneuvering and stabilizing the cart 11.
After insertion into the urethra, using similar control techniques as in bronchoscopy, the ureteroscope 32 may be navigated into the bladder, ureters, and/or kidneys for diagnostic and/or therapeutic applications. For example, the ureteroscope 32 may be directed into the ureter and kidneys to break up kidney stone build up using a laser or ultrasonic lithotripsy device deployed down the working channel of the ureteroscope 32. After lithotripsy is complete, the resulting stone fragments may be removed using baskets deployed down the ureteroscope 32.
Embodiments of the robotically-enabled medical system may also incorporate the patient's table. Incorporation of the table reduces the amount of capital equipment within the operating room by removing the cart, which allows greater access to the patient.
The robotic arms 39 may be mounted on the carriages 43 through a set of arm mounts 45 comprising a series of joints that may individually rotate and/or telescopically extend to provide additional configurability to the robotic arms 39. Additionally, the arm mounts 45 may be positioned on the carriages 43 such that, when the carriages 43 are appropriately rotated, the arm mounts 45 may be positioned on either the same side of the table 38 (as shown in
The column 37 structurally provides support for the table 38, and a path for vertical translation of the carriages 43. Internally, the column 37 may be equipped with lead screws for guiding vertical translation of the carriages, and motors to mechanize the translation of the carriages 43 based the lead screws. The column 37 may also convey power and control signals to the carriages 43 and the robotic arms 39 mounted thereon.
The table base 46 serves a similar function as the cart base 15 in the cart 11 shown in
With continued reference to
In some embodiments, a table base may stow and store the robotic arms when not in use.
In a laparoscopic procedure, through small incision(s) in the patient's abdominal wall, minimally invasive instruments may be inserted into the patient's anatomy. In some embodiments, the minimally invasive instruments comprise an elongated rigid member, such as a shaft, which is used to access anatomy within the patient. After inflation of the patient's abdominal cavity, the instruments may be directed to perform surgical or medical tasks, such as grasping, cutting, ablating, suturing, etc. In some embodiments, the instruments can comprise a scope, such as a laparoscope.
To accommodate laparoscopic procedures, the robotically-enabled table system may also tilt the platform to a desired angle.
For example, pitch adjustments are particularly useful when trying to position the table in a Trendelenburg position, i.e., position the patient's lower abdomen at a higher position from the floor than the patient's upper abdomen, for lower abdominal surgery. The Trendelenburg position causes the patient's internal organs to slide towards his/her upper abdomen through the force of gravity, clearing out the abdominal cavity for minimally invasive tools to enter and perform lower abdominal surgical or medical procedures, such as laparoscopic prostatectomy.
The adjustable arm support 105 can provide several degrees of freedom, including lift, lateral translation, tilt, etc. In the illustrated embodiment of
The surgical robotics system 100 in
The adjustable arm support 105 can be mounted to the column 102. In other embodiments, the arm support 105 can be mounted to the table 101 or base 103. The adjustable arm support 105 can include a carriage 109, a bar or rail connector 111 and a bar or rail 107. In some embodiments, one or more robotic arms mounted to the rail 107 can translate and move relative to one another.
The carriage 109 can be attached to the column 102 by a first joint 113, which allows the carriage 109 to move relative to the column 102 (e.g., such as up and down a first or vertical axis 123). The first joint 113 can provide the first degree of freedom (“Z-lift”) to the adjustable arm support 105. The adjustable arm support 105 can include a second joint 115, which provides the second degree of freedom (tilt) for the adjustable arm support 105. The adjustable arm support 105 can include a third joint 117, which can provide the third degree of freedom (“pivot up”) for the adjustable arm support 105. An additional joint 119 (shown in
In some embodiments, one or more of the robotic arms 142A, 142B comprises an arm with seven or more degrees of freedom. In some embodiments, one or more of the robotic arms 142A, 142B can include eight degrees of freedom, including an insertion axis (1-degree of freedom including insertion), a wrist (3-degrees of freedom including wrist pitch, yaw and roll), an elbow (1-degree of freedom including elbow pitch), a shoulder (2-degrees of freedom including shoulder pitch and yaw), and base 144A, 144B (1-degree of freedom including translation). In some embodiments, the insertion degree of freedom can be provided by the robotic arm 142A, 142B, while in other embodiments, the instrument itself provides insertion via an instrument-based insertion architecture.
The end effectors of the system's robotic arms may comprise (i) an instrument driver (alternatively referred to as “instrument drive mechanism” or “instrument device manipulator”) that incorporates electro-mechanical means for actuating the medical instrument and (ii) a removable or detachable medical instrument, which may be devoid of any electro-mechanical components, such as motors. This dichotomy may be driven by the need to sterilize medical instruments used in medical procedures, and the inability to adequately sterilize expensive capital equipment due to their intricate mechanical assemblies and sensitive electronics. Accordingly, the medical instruments may be designed to be detached, removed, and interchanged from the instrument driver (and thus the system) for individual sterilization or disposal by the physician or the physician's staff. In contrast, the instrument drivers need not be changed or sterilized, and may be draped for protection.
For procedures that require a sterile environment, the robotic system may incorporate a drive interface, such as a sterile adapter connected to a sterile drape, that sits between the instrument driver and the medical instrument. The chief purpose of the sterile adapter is to transfer angular motion from the drive shafts of the instrument driver to the drive inputs of the instrument while maintaining physical separation, and thus sterility, between the drive shafts and drive inputs. Accordingly, an example sterile adapter may comprise a series of rotational inputs and outputs intended to be mated with the drive shafts of the instrument driver and drive inputs on the instrument. Connected to the sterile adapter, the sterile drape, comprised of a thin, flexible material such as transparent or translucent plastic, is designed to cover the capital equipment, such as the instrument driver, robotic arm, and cart (in a cart-based system) or table (in a table-based system). Use of the drape would allow the capital equipment to be positioned proximate to the patient while still being located in an area not requiring sterilization (i.e., non-sterile field). On the other side of the sterile drape, the medical instrument may interface with the patient in an area requiring sterilization (i.e., sterile field).
The elongated shaft 71 is designed to be delivered through either an anatomical opening or lumen, e.g., as in endoscopy, or a minimally invasive incision, e.g., as in laparoscopy. The elongated shaft 71 may be either flexible (e.g., having properties similar to an endoscope) or rigid (e.g., having properties similar to a laparoscope) or contain a customized combination of both flexible and rigid portions. When designed for laparoscopy, the distal end of a rigid elongated shaft may be connected to an end effector extending from a jointed wrist formed from a clevis with at least one degree of freedom and a surgical tool or medical instrument, such as, for example, a grasper or scissors, that may be actuated based on force from the tendons as the drive inputs rotate in response to torque received from the drive outputs 74 of the instrument driver 75. When designed for endoscopy, the distal end of a flexible elongated shaft may include a steerable or controllable bending section that may be articulated and bent based on torque received from the drive outputs 74 of the instrument driver 75.
Torque from the instrument driver 75 is transmitted down the elongated shaft 71 using tendons along the elongated shaft 71. These individual tendons, such as pull wires, may be individually anchored to individual drive inputs 73 within the instrument handle 72. From the handle 72, the tendons are directed down one or more pull lumens along the elongated shaft 71 and anchored at the distal portion of the elongated shaft 71, or in the wrist at the distal portion of the elongated shaft. During a surgical procedure, such as a laparoscopic, endoscopic or hybrid procedure, these tendons may be coupled to a distally mounted end effector, such as a wrist, grasper, or scissor. Under such an arrangement, torque exerted on drive inputs 73 would transfer tension to the tendon, thereby causing the end effector to actuate in some way. In some embodiments, during a surgical procedure, the tendon may cause a joint to rotate about an axis, thereby causing the end effector to move in one direction or another. Alternatively, the tendon may be connected to one or more jaws of a grasper at the distal end of the elongated shaft 71, where tension from the tendon causes the grasper to close.
In endoscopy, the tendons may be coupled to a bending or articulating section positioned along the elongated shaft 71 (e.g., at the distal end) via adhesive, control ring, or other mechanical fixation. When fixedly attached to the distal end of a bending section, torque exerted on the drive inputs 73 would be transmitted down the tendons, causing the softer, bending section (sometimes referred to as the articulable section or region) to bend or articulate. Along the non-bending sections, it may be advantageous to spiral or helix the individual pull lumens that direct the individual tendons along (or inside) the walls of the endoscope shaft to balance the radial forces that result from tension in the pull wires. The angle of the spiraling and/or spacing therebetween may be altered or engineered for specific purposes, wherein tighter spiraling exhibits lesser shaft compression under load forces, while lower amounts of spiraling results in greater shaft compression under load forces, but limits bending. On the other end of the spectrum, the pull lumens may be directed parallel to the longitudinal axis of the elongated shaft 71 to allow for controlled articulation in the desired bending or articulable sections.
In endoscopy, the elongated shaft 71 houses a number of components to assist with the robotic procedure. The shaft 71 may comprise a working channel for deploying surgical tools (or medical instruments), irrigation, and/or aspiration to the operative region at the distal end of the shaft 71. The shaft 71 may also accommodate wires and/or optical fibers to transfer signals to/from an optical assembly at the distal tip, which may include an optical camera. The shaft 71 may also accommodate optical fibers to carry light from proximally-located light sources, such as light emitting diodes, to the distal end of the shaft 71.
At the distal end of the instrument 70, the distal tip may also comprise the opening of a working channel for delivering tools for diagnostic and/or therapy, irrigation, and aspiration to an operative site. The distal tip may also include a port for a camera, such as a fiberscope or a digital camera, to capture images of an internal anatomical space. Relatedly, the distal tip may also include ports for light sources for illuminating the anatomical space when using the camera.
In the example of
Like earlier disclosed embodiments, an instrument 86 may comprise an elongated shaft portion 88 and an instrument base 87 (shown with a transparent external skin for discussion purposes) comprising a plurality of drive inputs 89 (such as receptacles, pulleys, and spools) that are configured to receive the drive outputs 81 in the instrument driver 80. Unlike prior disclosed embodiments, the instrument shaft 88 extends from the center of the instrument base 87 with an axis substantially parallel to the axes of the drive inputs 89, rather than orthogonal as in the design of
When coupled to the rotational assembly 83 of the instrument driver 80, the medical instrument 86, comprising instrument base 87 and instrument shaft 88, rotates in combination with the rotational assembly 83 about the instrument driver axis 85. Since the instrument shaft 88 is positioned at the center of instrument base 87, the instrument shaft 88 is coaxial with instrument driver axis 85 when attached. Thus, rotation of the rotational assembly 83 causes the instrument shaft 88 to rotate about its own longitudinal axis. Moreover, as the instrument base 87 rotates with the instrument shaft 88, any tendons connected to the drive inputs 89 in the instrument base 87 are not tangled during rotation. Accordingly, the parallelism of the axes of the drive outputs 81, drive inputs 89, and instrument shaft 88 allows for the shaft rotation without tangling any control tendons.
The instrument handle 170, which may also be referred to as an instrument base, may generally comprise an attachment interface 172 having one or more mechanical inputs 174, e.g., receptacles, pulleys or spools, that are designed to be reciprocally mated with one or more torque couplers on an attachment surface of an instrument driver.
In some embodiments, the instrument 150 comprises a series of pulleys or cables that enable the elongated shaft 152 to translate relative to the handle 170. In other words, the instrument 150 itself comprises an instrument-based insertion architecture that accommodates insertion of the instrument, thereby minimizing the reliance on a robot arm to provide insertion of the instrument 150. In other embodiments, a robotic arm can be largely responsible for instrument insertion.
Any of the robotic systems described herein can include an input device or controller for manipulating an instrument attached to a robotic arm. In some embodiments, the controller can be coupled (e.g., communicatively, electronically, electrically, wirelessly and/or mechanically) with an instrument such that manipulation of the controller causes a corresponding manipulation of the instrument e.g., via master slave control.
In the illustrated embodiment, the controller 182 is configured to allow manipulation of two medical instruments, and includes two handles 184. Each of the handles 184 is connected to a gimbal 186. Each gimbal 186 is connected to a positioning platform 188.
As shown in
In some embodiments, one or more load cells are positioned in the controller. For example, in some embodiments, a load cell (not shown) is positioned in the body of each of the gimbals 186. By providing a load cell, portions of the controller 182 are capable of operating under admittance control, thereby advantageously reducing the perceived inertia of the controller while in use. In some embodiments, the positioning platform 188 is configured for admittance control, while the gimbal 186 is configured for impedance control. In other embodiments, the gimbal 186 is configured for admittance control, while the positioning platform 188 is configured for impedance control. Accordingly, for some embodiments, the translational or positional degrees of freedom of the positioning platform 188 can rely on admittance control, while the rotational degrees of freedom of the gimbal 186 rely on impedance control.
Traditional endoscopy may involve the use of fluoroscopy (e.g., as may be delivered through a C-arm) and other forms of radiation-based imaging modalities to provide endoluminal guidance to an operator physician. In contrast, the robotic systems contemplated by this disclosure can provide for non-radiation-based navigational and localization means to reduce physician exposure to radiation and reduce the amount of equipment within the operating room. As used herein, the term “localization” may refer to determining and/or monitoring the position of objects in a reference coordinate system. Technologies such as preoperative mapping, computer vision, real-time EM tracking, and robot command data may be used individually or in combination to achieve a radiation-free operating environment. In other cases, where radiation-based imaging modalities are still used, the preoperative mapping, computer vision, real-time EM tracking, and robot command data may be used individually or in combination to improve upon the information obtained solely through radiation-based imaging modalities.
As shown in
The various input data 91-94 are now described in greater detail. Preoperative mapping may be accomplished through the use of the collection of low dose CT scans. Preoperative CT scans are reconstructed into three-dimensional images, which are visualized, e.g., as “slices” of a cutaway view of the patient's internal anatomy. When analyzed in the aggregate, image-based models for anatomical cavities, spaces and structures of the patient's anatomy, such as a patient lung network, may be generated. Techniques such as center-line geometry may be determined and approximated from the CT images to develop a three-dimensional volume of the patient's anatomy, referred to as model data 91 (also referred to as “preoperative model data” when generated using only preoperative CT scans). The use of center-line geometry is discussed in U.S. patent application Ser. No. 14/523,760, the contents of which are herein incorporated in its entirety. Network topological models may also be derived from the CT-images, and are particularly appropriate for bronchoscopy.
In some embodiments, the instrument may be equipped with a camera to provide vision data (or image data) 92. The localization module 95 may process the vision data 92 to enable one or more vision-based (or image-based) location tracking modules or features. For example, the preoperative model data 91 may be used in conjunction with the vision data 92 to enable computer vision-based tracking of the medical instrument (e.g., an endoscope or an instrument advance through a working channel of the endoscope). For example, using the preoperative model data 91, the robotic system may generate a library of expected endoscopic images from the model based on the expected path of travel of the endoscope, each image linked to a location within the model. Intraoperatively, this library may be referenced by the robotic system in order to compare real-time images captured at the camera (e.g., a camera at a distal end of the endoscope) to those in the image library to assist localization.
Other computer vision-based tracking techniques use feature tracking to determine motion of the camera, and thus the endoscope. Some features of the localization module 95 may identify circular geometries in the preoperative model data 91 that correspond to anatomical lumens and track the change of those geometries to determine which anatomical lumen was selected, as well as the relative rotational and/or translational motion of the camera. Use of a topological map may further enhance vision-based algorithms or techniques.
Optical flow, another computer vision-based technique, may analyze the displacement and translation of image pixels in a video sequence in the vision data 92 to infer camera movement. Examples of optical flow techniques may include motion detection, object segmentation calculations, luminance, motion compensated encoding, stereo disparity measurement, etc. Through the comparison of multiple frames over multiple iterations, movement and location of the camera (and thus the endoscope) may be determined.
The localization module 95 may use real-time EM tracking to generate a real-time location of the endoscope in a global coordinate system that may be registered to the patient's anatomy, represented by the preoperative model. In EM tracking, an EM sensor (or tracker) comprising one or more sensor coils embedded in one or more locations and orientations in a medical instrument (e.g., an endoscopic tool) measures the variation in the EM field created by one or more static EM field generators positioned at a known location. The location information detected by the EM sensors is stored as EM data 93. The EM field generator (or transmitter) may be placed close to the patient to create a low intensity magnetic field that the embedded sensor may detect. The magnetic field induces small currents in the sensor coils of the EM sensor, which may be analyzed to determine the distance and angle between the EM sensor and the EM field generator. These distances and orientations may be intraoperatively “registered” to the patient anatomy (e.g., the preoperative model) in order to determine the geometric transformation that aligns a single location in the coordinate system with a position in the preoperative model of the patient's anatomy. Once registered, an embedded EM tracker in one or more positions of the medical instrument (e.g., the distal tip of an endoscope) may provide real-time indications of the progression of the medical instrument through the patient's anatomy.
Robotic command and kinematics data 94 may also be used by the localization module 95 to provide localization data 96 for the robotic system. Device pitch and yaw resulting from articulation commands may be determined during preoperative calibration. Intraoperatively, these calibration measurements may be used in combination with known insertion depth information to estimate the position of the instrument. Alternatively, these calculations may be analyzed in combination with EM, vision, and/or topological modeling to estimate the position of the medical instrument within the network.
As
The localization module 95 may use the input data 91-94 in combination(s). In some cases, such a combination may use a probabilistic approach where the localization module 95 assigns a confidence weight to the location determined from each of the input data 91-94. Thus, where the EM data may not be reliable (as may be the case where there is EM interference) the confidence of the location determined by the EM data 93 can be decrease and the localization module 95 may rely more heavily on the vision data 92 and/or the robotic command and kinematics data 94.
As discussed above, the robotic systems discussed herein may be designed to incorporate a combination of one or more of the technologies above. The robotic system's computer-based control system, based in the tower, bed and/or cart, may store computer program instructions, for example, within a non-transitory computer-readable storage medium such as a persistent magnetic storage drive, solid state drive, or the like, that, upon execution, cause the system to receive and analyze sensor data and user commands, generate control signals throughout the system, and display the navigational and localization data, such as the position of the instrument within the global coordinate system, anatomical map, etc.
Embodiments of the disclosure relate to systems and techniques for input devices for operating robotic medical systems and/or one or more medical instruments with such robotic medical systems.
Robotic medical systems, such as the systems described above, can include an input device that is configured to allow an operator (e.g., a physician performing a robotically-enabled medical procedure) to manipulate and control one or more instruments. In some embodiments, the robotic medical system can include an input device for operating one or more medical tools. In some examples, the input device can operate one or more medical tools remotely, such as via teleoperation or telesurgery.
One skilled in the art will appreciate that the input devices described herein can be applied in non-medical contexts as well. For example, the input devices can be useful for manipulating tools that involve hazardous substances. In addition, in some embodiments, the input devices described herein can be useful in grabbing objects in both physical and virtual environments. In some configurations, the input devices can be self-sufficient as service robots interacting with human operators. In some configurations, the input device can be coupled (e.g., communicatively, electronically, electrically, wirelessly and/or mechanically) with a medical instrument such that manipulation of the input device causes a corresponding manipulation of the medical instrument. In some configurations, the input device and the medical instrument are arranged in a master-slave pair. In some configurations, the input device can be configured to control operation of a robotic surgical tool. In some configurations, the input device can be referred to as a manipulator, emulator, master, controller, interface, etc.
The input device can serve as an input for an operator to control the actions of a medical instrument, such as in an endoscopic, endoluminal, laparoscopic, or open surgery. Movement of the input device by the operator can direct the movement of the medical instrument. For example, when an operator translates the input device in three-dimensional space (e.g., up, down, left, right, backwards, forwards), the system can cause a corresponding translation of the medical instrument. Similarly, if the operator rotates the input device (e.g., around any of three orthogonal axes), the system can cause a corresponding rotational movement of the medical instrument. The input device can also include one or more inputs that allow the operator to actuate the medical instrument. As one example, if the medical instrument includes a grasper instrument, the input device can include one or more inputs that allow the operator to open and close the grasper instrument.
In some embodiments, robotic medical systems include input devices with seven degrees of freedom that follow the operator's hand movement, with the seven degrees of freedom including three positional degrees of freedom (e.g., translational movement in x, y, z space), three rotational degrees of freedom (e.g., rotational movement around pitch, roll, and yaw axes), and one (or more) instrument actuation degree of freedom (e.g., an angular degree of freedom). In some embodiments, the instrument actuation degree of freedom can control the opening and closing of an end effector of the medical instrument, such as a gripper or grasper instrument to hold an object. In some embodiments, input devices can include greater or fewer numbers of degrees of freedom. For example, in some embodiments, the input device can include more than three positional degrees of freedom or more than three rotational degrees of freedom to provide one or more redundant degrees of freedom. In some embodiments, redundant degrees of freedom can provide additional mechanical flexibility for the input device, for example, to avoid singularities caused by the mechanical structure of the input device.
The grasper can be the portion of the input device that the operator (e.g., a physician, a user, etc.) touches and holds to allow the operator to control the components of the robotic system, such as the medical instruments. The grasper can be the operator's primary input into the system during surgery.
As illustrated in
The links 202, 204, 206, 208 can be arranged in pairs. For example, the grasper 200 can include a first pair of opposing links 202, 204 and a second pair of opposing links 206, 208. In the illustrated arrangement, the first pair of opposing links can include the first link 202 and the second link 204 spaced approximately 180 degrees from one another. In the illustrated arrangement, the second pair of opposing links can include the third link 206 and the fourth link 208 spaced approximately 180 degrees from one another. In modified arrangements, the links 202, 204 of the first pair of opposing links can be spaced less than 180 degrees from each the links 206, 208 of the second pair of opposing links.
With reference to
The central shaft 250 can support the plurality of links 202, 204, 206, 208. Each of the first pair of opposing links 202, 204 and each of the second pair of opposing links 206, 208 can be coupled to the central shaft 250. The first link 202 can have a proximal end 232 and a distal end 222. The second link 204 can have a proximal end 234 and a distal end 224. The third link 206 can have a proximal end 236 and a distal end 226. The fourth link 208 can have a proximal end 238 and a distal end 228. The plurality of links 202, 204, 206, 208 can be connected or operatively connected at their respective proximal ends 232, 234, 236, 238 and/or at their respective distal ends 222, 224, 226, 228.
The first pair of opposing links 202, 204 can each include a finger grip or pad 212, 214. The second pair of opposing links 206, 208 can each include a secondary input 216, 218. Each of the plurality of links 202, 204, 206, 208, can include a secondary link 242, 244, 246, 248 to attach the proximal ends 232, 234, 236, 238 of the links 202, 204, 206, 208 to the central shaft 250.
Each of the plurality of links can be configured to move from an open position where proximal ends 232, 234, 236, 238 of each of the plurality of links 202, 204, 206, 208 are positioned radially away from the central shaft 250 to a closed position where the proximal ends 232, 234, 236, 238 of each of the plurality of links 202, 204, 206, 208 are positioned radially close to the central shaft 250. With reference again to
With reference again to
Each of the plurality of links 202, 204, 206, 208 can be biased in an open position. In some configurations, each link can be spring-loaded in an open position. In some configurations, there are at least two springs (not shown) for each link with a first spring providing the majority of the force to bias the link in an open position. A second spring can provide a slight haptic feedback when the link reaches a certain degree of closure to indicates to the user when the grasper is closed and that further motion to close the grasper will result in an increase of clamping force of the surgical instrument.
For example, the first pair of opposing links 202, 204 and/or the second pair of opposing links 206, 208 can be maneuvered in a pinching motion, which can be translated to movement of the surgical instrument inside the body. For example, opening and closing the first pair of opposing links 202, 204 would correspond to opening and closing of a scissor tool or jaws of a medical instrument. The facilitated pinching motion can make grasper actuation natural and easy for the user.
The plurality of links 202, 204, 206, 208 on the grasper 200 can measure the input angle of the user's fingers. For example, the angle at which any one or more of the plurality of links 202, 204, 206, 208 are positioned relative to the central shaft 250 can be translated to the desired angle of a component of the instrument, such as one or more jaws of an end effector of the instrument.
The grasper 200 can have an increased number of links (such as four links as shown in
By having such a radially symmetric configuration of the grasper, a user can advantageously be capable of performing certain movements with ease (e.g., a roll maneuver) that would otherwise be challenging. If a user wants to do a roll-intensive task (e.g., suturing) with a grasper unlike those described herein, the user can only rotate the grasper approximately 180 degrees before their wrist runs out of range of motion without repositioning the user's hand. To continue rolling the grasper, they have to release their current position of the grasper, rotate their wrist and regrip the grasper to continue.
The radially symmetric grasper with the plurality of links spaced less than 180 degrees from each other allows the physician to roll the grasper between their fingertips while maintaining the desired orientation of the grasper (such as in the closed position or in maintaining the closure angle). This is possible since the user's fingers always contact at least two links because of the increased number of plurality of links and reduction of the dead zones that can exist between the plurality of links.
Some users may choose to work outside of the finger pads 212, 214, to hold the plurality of links 202, 204, 206, 208 closer to their distal ends 222, 224, 226, 228 of the plurality of links 202, 204, 206, 208. The grasper 200 advantageously is able to accommodate this and allow for comfortable use both in and out of the finger pads 212, 214. Additionally, when working outside of the finger pads 212, 214 (such as at the distal ends 222, 224, 226, 228 of one or more of the plurality of links 202, 204, 206, 208), the grasper 200 can have radial symmetry, such that the physician can close the grasper 200 (such as closing the first pair of opposing links 202, 204 and/or closing the second pair of opposing links 206, 208) and then roll the grasper 200 between their fingers. When executing this roll maneuver of the grasper 200, it can be desirable to have the grasper 200 remain in the closed position. The first pair of opposing links 202, 204 and/or the second pair of opposing links 206, 208 can be identical and symmetrical at their distal ends 222, 224, 226, 228, allowing the user to use any of the plurality of links 202, 204, 206, 208 to close the grasper 200.
The radial symmetry at the distal end can advantageously be more forgiving of misalignment of the user's hand when operating the grasper 200. Furthermore, the increased number of links being spaced closely together (such as, less than 180 degrees from one another) allows the user to more easily position their fingers to maintain contact with one or more of the plurality of links as they maneuver the grasper 200. For example, when working outside the finger pads 212, 214, the user can use any combination of the plurality of links to actuate the grasper 200. The plurality of links can increase the number of points of contacts for a user to actuate the grasper 200. This can allow the user to maintain contact with the actuators of the grasper more easily, to decrease difficultly of positioning and readjusting of the user's hand. The plurality of links and radial symmetry can give a user more freedom to manipulate the grasper 200.
The first pair of opposing links 202, 204 can be longer in length than the second pair of opposing links 206, 208. The plurality of links can be arranged such that the longer links 202, 204 oppose each other, with the shorter links 206, 208 located between the two. The two longer links 202, 204 can serve as the main grasping links. The longer links 202, 204 can have finger grips, pads, loops such as the finger pads 212, 214 of the illustrated arrangement.
In other examples, the first pair of opposing links 202, 204 and the second pair of opposing links 206, 208 can be of equal length. In other examples, the second pair of opposing links 206, 208 can be longer in length than the first pair of opposing links 202, 204.
As described above, as the user maneuvers the plurality of links of the grasper, the user's fingers can adjust the angle of the plurality of links. The plurality of links can be oriented or angled relative to the central axis or central shaft. The plurality of links on the grasper can that measure the input angle of the user's fingers. For example, the angle at which any one or more of the plurality of links are positioned relative to the central shaft can be translated to the desired angle of a component of the instrument, such as one or more jaws of an end effector of the instrument. The grasper 200 can include one or more sensors to measure the angle of the plurality of links and thus the input angle of the user's fingers. Also described above, the secondary input state can also be measured by one or more sensors.
The grasper can include one or more sensors in various locations. In some configurations, one or more sensors can be located in or coupled to one or more of the plurality of links. In some configurations, one or more sensors can be located in or coupled to the central shaft. The one or more sensors in the central shaft can be advantageous in that there is limited space on each of the plurality of links. The one or more sensors in the central shaft can also advantageously position the sensor away from motion of the links and from contact by the user, which can reduce risk of damaging the sensor.
In some configurations, the one or more sensors can include a hall effect sensor, such as a 3D hall effect sensor. The one or more sensors can include 3 different sensors in orthogonal orientations to each other. Using these sensor readings, an algorithm can be developed to determine both the angle of the plurality of links and detect a secondary input state. The position of the one or more sensors in the central shaft can also advantageously remove the need to run wires and package sensors on the links.
The one or more sensors can detect one or more magnets included in the plurality of link and/or one or more magnets in a secondary input. For example, each link can include one or more magnets in fixed locations. As the plurality of links changes angles, the one or more sensors can be used to detect the change in magnetic field due to the motion of these magnets.
Similarly, the secondary input can include or be operatively connected to one or more magnets, such that change or movement in the secondary input can change the position or orientation of the one or more magnets, which can be detected by the sensor. In some examples, the change of the magnetic field due to the secondary input can be coupled with the motion of the grasper or with one or more components of the grasper. In some examples, the angle of the plurality of links can be decoupled from the secondary input state.
In some configurations, the one or more sensors can be a 3 degrees-of-freedom sensor with physical electrical connections to the plurality of links and secondary inputs.
In some instances, the input device (e.g., the grasper) may not always be under the control of the operator. In addition, the input device may receive an input that is not intended by the user (e.g., unintended motion), which may be caused by the user or some other personnel in the operating room applying a disturbance to the input device or from gravity compensation errors (e.g., a user overcompensating for the gravity). In these instances, there may be a need to modify teleoperation and suppress or reduce movement of the robotic arms and its associated instruments. By detecting the unintended motion, the robotic system can respond to the user input to modify teleoperation and reduce, suppress, or stop movement of the robotic arms and associated instruments.
As shown in
In some embodiments, as shown in
In some embodiments, at least one sensor (e.g., sensor 310) of the one or more sensors 310 includes one electrode 311 (only), and the integrated circuit includes circuit 300 for measuring a self-capacitance of the electrode 311 (e.g., the capacitance between the electrode 311 and the earth), as shown in
In some embodiments, at least one sensor (e.g., sensor 310) of the one or more sensors 310 includes two or more electrodes 311-1 and 311-2, and the integrated circuit includes circuit 301 for measuring a mutual capacitance between the two electrodes 311-1 and 311-2, as illustrated in
In some embodiments, the signal 318 is processed (e.g., by the integrated circuit 328) before determining the user presence. For example, the signal 318 is filtered to remove or reduce the noise 320 (e.g., based on the rate of change by using, for example, a frequency domain filter, such as a Fourier filter or a derivative integral filter).
In some embodiments, each finger pad of the grasper 200 includes a sensor and the sensor of each finger pad is electrically coupled to the integrated circuit 328 through the flexible connector 330. For example, when the grasper 200 includes four finger pads (and hence at least four sensors), the integrated circuit 328 is electrically coupled to the four sensors via four flexible connectors 330 (e.g., one flexible connector 330 for each sensor).
In
In
Although
As described herein, the sensors (e.g., capacitance sensors, optical sensors, etc.) are used to determine the user presence, which can be used to reduce or eliminate unintended movements of the robotic arms or surgical tools. It is also helpful to determine the user control even when the user contact is not detected on the grasper 200. For example, when the user uses the finger loops or finger cups (shown in
In some embodiments, user control is determined by combining, information from the one or more sensors described above (e.g., capacitance sensors and/or optical sensors) with additional information (also called herein secondary information). In some embodiments, the movement of the robotic arms or surgical tools is controlled based on the information from the one or more sensors (e.g., capacitance sensors and/or optical sensors) and the secondary information, thereby enhancing operation of medical robotic systems.
In some embodiments, the additional information includes a grasper angle (e.g., an angle defined by the central axis of the grasper and a link, such as link 202). In some configurations, the grasper is at a fully open angle when no external force is applied (e.g., no user input). Thus, a grasper angle other than, or less than, a predefined grasper angle threshold (e.g., the fully open angle) indicates that the user is in control.
In some embodiments, the additional information includes a velocity or movement of one or more joints supporting the input device.
In some embodiments, the additional information includes a time period or duration from the most recent detection of user presence. By providing a time duration as an additional input, the system can advantageously account for when a user might be present, but temporarily withdraws his or her hand from the grasper for a short period (e.g., 0.01-0.04 seconds). In such a situation, the system may not want to halt movement of the robotic arms or surgical tools, as this may cause unnecessary interruptions, despite the presence of the user. Accordingly, in some embodiments, the system can incorporate different temporal thresholds to help refine the determination of user presence and control. For example, a first-time threshold can be provided (e.g., 0.05-1 second or greater) as a debounce, whereby if a user is not detected by the system within the first-time threshold, movement may be reduced or halted and/or monitored for unintended movement above a distance threshold. A second time threshold (e.g., 60 seconds, 90 seconds, 120 seconds, or greater) can be provided as a timeout, whereby if a user is not detected by the system within the second time threshold, movement may be automatically halted regardless of the distance of the unintended movement. Note that the time periods provided above for the first threshold and the second threshold are exemplary and not meant to be limiting.
In some embodiments, the additional information includes information indicating a change in the movement of robotic arms or surgical tools that is inconsistent with a user input. Such information can come from encoders (e.g., position sensors) and/or from derived information based on changes to velocity, acceleration, jerking, etc. For example, a bump or impulse in a motion profile of the robotic arms or surgical tools or information from mechatronic sensors, such as current, back electromotive force, torque, or force, could indicate movement of the robotic arms or surgical tools that are different from the movement of the robotic arms or surgical tools caused by the user input. In another example, gravity drift is detected based on the information from mechatronic sensors (e.g., an error in gravity compensation may result in a constant acceleration in a constant direction).
In some embodiments, the medical robotic system enters the unassisted teleoperation mode 381 as the result of a start-up procedure. In some embodiments, the medical robotic system enters the unassisted teleoperation mode 381 in response to detecting user control. In some embodiments, in accordance with a determination that user control is detected, the medical robotic system enters or remains in the unassisted teleoperation mode 381. In some embodiments, while the medical robotic system is in the unassisted teleoperation mode 381, the medical robotic system moves robotic arms and/or surgical instruments in accordance with a user input using a first set of parameters. In some embodiments, the first set of parameters includes forgoing any damping, or using a first damping that is less than a second damping provided while the medical robotic system is in the assisted teleoperation mode 382.
In some embodiments, in the event that drift (e.g., a lack of user control) is detected in conjunction with movement of the robotic arms or surgical tools, the medical robotic system transitions into the assisted teleoperation mode 382. In some embodiments, the medical robotic system modifies control algorithms while in the assisted teleoperation mode 382 to decrease the likelihood of hazardous unintended motion. In some embodiments, while in the assisted teleoperation mode 382, the medical robotic system does one or more of: (i) changing motion scaling so the input device motion results in smaller tool tip motion; (ii) adjusting damping on the input device to increase the load required to create input device motion; (iii) providing haptic feedback to maintain a current position of the input device; or (iv) saturating (e.g., capping) commanded velocity from the input device at a lower value than a value used for normal operation. In some embodiments, switching between the unassisted teleoperation mode 381 and the assisted teleoperation mode 382 includes temporarily pausing teleoperation command transmissions between the user input device and the robotic arm(s).
The advantage of operating in the assisted teleoperation mode 382 as opposed to disabling teleoperation includes that the teleoperation is not interrupted unnecessarily. For example, a situation may occur where, although a user presence/control might not be detected, it may not be warranted to enter into a safe mode whereby teleoperation is halted. In such a scenario, the system can, for example, dampen the motion of the input device, instead of immediately halting teleoperation of the system. In some circumstances, after disabling teleoperation (e.g., entering the safe mode 383), the medical robotic system must perform a set-up procedure to re-enter teleoperation. The set-up procedure requires a certain amount of time and this delay can be avoided by switching to the assisted teleoperation mode 382 rather than halting teleoperation.
In some embodiments, in the event that lack of user control is detected in conjunction with movement of the robotic arms or surgical tools, the medical robotic system transitions into the safe mode 383. In some embodiments, while operating in the assisted teleoperation mode 382, the medical robotic system detects an unsafe condition and transitions to the safe mode 383. While the medical robotic system is in the safe mode 383, teleoperation is halted or cut off between the input device and the robotic arm or surgical instrument. In some embodiments, to avoid unnecessary disruptions, the medical robotic system monitors the movement of the input device, and transition into the safe mode 383 if the position of the input device has changed by an unsafe distance in comparison to when the user was last detected to be in active control. In some embodiments, the medical robotic system transitions into the safe mode 383 if the motion (e.g., velocity, acceleration, etc.) of the input device is determined to be unsafe (e.g., the velocity of the input device exceeds a velocity threshold or the acceleration of the user acceleration exceeds an acceleration threshold) while the user is not detected to be in active control.
Thus, in accordance with detecting drift and/or an absence of user control, the medical robotic system may be configured to switch to the safe mode 383 (e.g., switch out of teleoperation modes on the master and/or slave side) until a user regains control. However, such halting of the teleoperation modes can be unnecessary and disruptive to smooth teleoperational control, particularly when the drift detection is a false positive. Therefore, it can be advantageous to switch to the assisted teleoperation mode 382 in accordance with detecting drift and/or an absence of user control rather than switching to the safe mode 383 in some circumstances.
Although the system diagram shown in
In some embodiments, the medical system transitions (374) from the “not driving” state 372 to the driving state 373 in accordance with a determination that a user input device (e.g., a gripper or grasper) is matched. In some embodiments, the medical system unlocks a haptic input device in conjunction with transitioning from the “not driving” state 372 to the driving state 373. In some embodiments, the medical system resets a timer (and/or restarts the timer) in conjunction with transitioning to the driving state 373, e.g., the timer is used to determine whether a user presence is not detected. In some embodiments, the medical system, while in the driving state 373, detects user presence (e.g., any sensor has detected user presence), and in response, remains in the driving state 373 and resets the timer, e.g., for determining whether the medical system should transition to the assisted state 371.
In some embodiments, the medical system transitions (375) from the driving state 373 to the assisted state 371 in accordance with a determination that a robotic arm or a surgical tool has drifted. For example, the robotic arm or surgical tool has drifted more than a distance threshold (e.g., 5, 10, 15, 20, 25, 30, 40, 50, or 60 mm or within an interval between any two of the aforementioned values). In some embodiments, the medical system identifies drift in accordance with detecting movement of the user input device without detecting user presence. In some embodiments, the medical system identifies drift in accordance with detecting unexpected and/or unsafe movement of the user input device. In some embodiments, detecting drift includes detecting unsafe movement, e.g., a grasper angle is greater than a first threshold angle (e.g., 30°, 40°, 45°, etc.) and the shoulder yaw axis 344 has a rotational speed above a first threshold speed (e.g., less than 0.1 rad/s, 0.2 rad/s, 0.3 rad/s, 0.4 rad/s, 0.5 rad/s, 0.6 rad/s, 0.7 rad/s, 0.8 rad/s, 0.9 rad/s, 1 rad/s, 2 rad/s, 3 rad/s, 4 rad/s, 5 rad/s, or 10 rad/s, etc.). In some embodiments, the medical system modifies one or more parameters used for operation of the input device in conjunction with transitioning to the assisted state.
In some embodiments, the medical system transitions (376) from the driving state 373 to the assisted state 371 in accordance with a determination that user presence is not detected, e.g., no sensor has detected user presence, or less than a certain number (e.g., two, three, or four) of sensors have detected user presence. In some embodiments, the medical system transitions from the driving state 373 to the assisted state 371 in accordance with a determination that the timer has elapsed a threshold duration (e.g., 5, 10, 15, 20, 25, 30, 40, 50, or 60 mm or within an interval between any two of the aforementioned values). In some embodiments, the medical system modifies one or more parameters for operation of the input device in conjunction with transitioning to the assisted state. For example, the medical system adjusts damping, stiffness, motion scaling, and/or break control in accordance with transitioning to the assisted state.
In some embodiments, the driving state 373 includes a “user detected” substate 380 and a “user not detected” substate 384. In some embodiments, in response to a lack of user presence being detected, the medical system transitions from the “user detected” substate 380 to the “user not detected” substate 384, e.g., prior to transitioning to the assisted state 371. In some embodiments, the medical system transitions from the “user not detected” substate 384 to the assisted state 371 in accordance with a preset amount of time elapsing (e.g., 1, 2, or 5 seconds) while in the “user not detected” substate. In some embodiments, the medical system transitions from the “user not detected” substate 384 to the “user detected” substate 380 in accordance with at least one sensor detecting user presence. In this way, a momentary lack of user presence may not trigger a transition to the assisted state 371 in some embodiments.
In some embodiments, secondary information (with or without the sensor information) is used to determine criteria for a state transition. In some embodiments, the timer serves as secondary information (e.g., in addition to sensing via capacitance) to help determine when the system can properly transition. For example, in some embodiments, when the system is in the “user not detected” substate 384 for longer than a pre-defined duration (e.g., 500 milliseconds), the system requires specific criteria based on the contact sensing and/or secondary information to transition back to the “user detected” substate 380. These criteria could be different than the criteria to re-establish “user detection” if the user has not been detected for less than that duration. For example, the system may require only one sensor to indicate presence if the system is in the “user not detected” substate 384 for less than 500 milliseconds, and require at least two sensors to indicate presence if the system is in the “user not detected” substate 384 for more than 500 milliseconds. As another example, the system may use secondary information such as G6 motion to indicate presence if the system is in the “user not detected” substate 384 for less than 500 milliseconds, but require contact sensors to indicate presence if the system is in “user not detected” state 384 for more than 500 milliseconds. Providing a timer as secondary information can advantageously help determine what criteria is sufficient to transition.
In some embodiments, the medical system resets a timer (and/or restarts the timer) in conjunction with transitioning to the assisted state 371. In some embodiments, the timer serves as secondary information (e.g., in addition to sensing via capacitance) to help determine when the system can properly transition back to the unassisted state 370 (e.g., the driving state 373). For example, in some embodiments, when the system is in the assisted state 371, it takes a certain amount of time before the system transitions back to the unassisted state 370 beyond an initial contact between the user and the user input device and the associated capacitance sensors. This is because the system may account for the initial touch by the user with the grasper pads prior to actual teleoperated driving. In this way, the system may not immediately transition to the driving state 373 upon the user's initial contact with the graspers. Providing a timer as secondary information in the assisted state 371 can advantageously help determine whether a user's contact has been made with the graspers long enough to represent actual driving. In some embodiments, the medical system resets the timer (and/or restarts the timer) in response to detecting the user presence, e.g., so that a certain period of time (e.g., 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, or 1 second) after the user presence has been detected can elapse before allowing the user to drive the robotic arm in the unassisted mode.
In some embodiments, when the system is in the assisted state 371 for longer than a pre-defined duration (e.g., 1 second), the system requires specific criteria based on the contact sensing and/or secondary information to transition back to the unassisted state 370 (e.g., the driving state 373). These criteria could be different than the criteria to re-establish “user detection” if the user has not been detected for less than the pre-defined duration. For example, the system may require only one sensor to indicate presence if the system was in the assisted state 371 for less than 1 second, and require at least two sensors to indicate presence if the system was in the assisted state 371 for more than 1 second. In some embodiments, the system uses secondary information such as a rotational movement (or a rotational velocity) of a rotational joint extending through the shoulder yaw axis 344 to indicate user presence if the system has been in the assisted state 371 for less than 1 second, but requires contact sensors to indicate user presence if the system has been in the assisted state 371 for more than 1 second. Providing a timer as secondary information in the assisted state 371 can advantageously help determine what criteria is sufficient to transition back to the unassisted state 370.
In some embodiments, the medical system transitions (377) from the assisted state 371 to the driving state 373 in accordance with a determination that a preset amount of time has elapsed while in the assisted state 371. In some embodiments, the preset amount of time corresponds to a settling time of the user input device (e.g., a time required for the user input device to go from uncontrolled motion to controlled motion). As used herein, settling time of the user input device is a time associated with the user input device transitioning from uncontrolled motion to controlled motion (e.g., from a non-steady state to a steady state). In some embodiments, the settling time is based on a configuration of the user input device (e.g., current position, velocity, angle, damping, etc.). In some embodiments, the settling time is stored in a lookup table in memory of the medical system. In some embodiments, the lookup table specifies a settling time for a corresponding user input device configuration. In some embodiments, the settling time corresponds to a worst-case scenario for the user input device (e.g., a time to recover from a maximum velocity drift). In some embodiments, the settling time is determined based on properties of detected drift (e.g., velocity, acceleration, and/or angle).
In some embodiments, the medical system transitions (378) from the assisted state 371 to the driving state 373 in accordance with a determination that a certain number of sensors (e.g., capacitance sensors or optical sensors), such as two or more sensors, have detected user presence. In some embodiments, the medical system transitions from the assisted state 371 to the driving state 373 in accordance with a determination that any sensor has detected user presence and/or the movement of the user input device is within an acceptable range. In some embodiments, the timer serves as secondary information (e.g., in addition to sensing via capacitance) to help determine when the system should properly transition back to a driver state 373. For example, in some embodiments, when the system is in the assisted state 371, it takes a certain amount of time before the system transitions back to the driving state 373, even beyond the initial contact between the user and the graspers and the associated capacitance sensors. In some embodiments, the medical system resets the timer (and/or restarts the timer) in conjunction with transitioning from the assisted state 371 to the driving state 373.
In some embodiments, the medical system transitions (379) from the assisted state 371 to the driving state 373 in accordance with position and movement of the user input device being in an acceptable range. In some embodiments, the position and movement of the user input device being in the acceptable range includes the user input device having a velocity below a preset velocity threshold and/or the user input device having an acceleration below a preset acceleration threshold. For example, a grasper angle being closed (e.g., less than a second threshold angle, such as 15°, 10°, 5°, etc.), or the shoulder yaw axis 344 having a rotational speed below a threshold speed (e.g., less than 0.1 rad/s, 0.2 rad/s, 0.3 rad/s, 0.4 rad/s, 0.5 rad/s, 0.6 rad/s, 0.7 rad/s, 0.8 rad/s, 0.9 rad/s, 1 rad/s, 2 rad/s, 3 rad/s, 4 rad/s, 5 rad/s, or 10 rad/s, etc.).
In some embodiments, the secondary information includes an end effector pose or information indicating a change in the end effector pose. For example, in some embodiments, the secondary information includes (i) the end effector pose or the information indicating a change in the end effector pose, and (ii) a rotational movement (or a rotational velocity) of a rotational joint extending through the shoulder yaw axis 344 so that the user control is determined based on the change in the end effector pose and the rotational movement, even when no user contact is detected (e.g., using a capacitance sensor). In some embodiments, the change in the end effector pose is used to select the criteria for the state transition. For example, in accordance with a determination that a movement of the end effector that is associated with user control (e.g., continuous or semi-continuous movement of the end effector, movement of the end effector at a speed below a threshold speed, movement of the end effector that includes a change in a direction of the end effector) is detected, first criteria (e.g., less stringent criteria, such as requiring detection of contact by a single sensor) are used for a state transition. In accordance with a determination that a movement, of the end effector, that is not associated with user control (e.g., gravity drift or bump), second criteria (e.g., more stringent criteria, such as requiring detection of contact by multiple sensors) are used for a state transition.
Additionally, although the system diagram shown in
The computing system operates (402) the user input device in an unassisted mode, including applying a first set of parameters to the user input device. For example, the computing system operates the user input device in the unassisted teleoperation mode 381 (e.g., the unassisted state 370). In some embodiments, the unassisted mode is a user-driven mode. For example, a user of the user input device manipulates the user input device to control movement of a robotic arm (e.g., a robotic arm 12) and/or medical instrument mounted on the robotic arm. In some embodiments, the first set of parameters include a damping parameter, a motion scaling parameter, a stiffness parameter, and a brake control parameter.
The computing system detects (404) drift of the user input device while operating in the unassisted mode. In some embodiments, the computing system includes, or is coupled with, various sensors (e.g., capacitance sensors, time-of-flight sensors, etc.) usable to detect drift of the user input device (e.g., a haptic input device). In some embodiments, detecting drift includes detecting unintended user-driven movement of the user input device. In some embodiments, detecting drift includes detecting a lack of user presence. In some embodiments, detecting drift includes detecting a lack of user presence while also detecting movement of the user input device. In some embodiments, the lack of user presence is detected (e.g., via the integrated circuit 328) based on a capacitance of the one or more electrodes (e.g., as illustrated in
In some embodiments, detecting drift of the user input device includes detecting a movement instability (e.g., inefficiency) in the user input device. In some embodiments, the movement instability represents an increase in total energy of the user input device.
In some embodiments, the electrodes include a second electrode that is interdigitated (e.g., coiled) with a first electrode. In some embodiments, the electrodes include a first electrode that is disposed adjacent to a second electrode. In some embodiments, the first electrode and the second electrode extend substantially in a same direction. In some embodiments, the user presence is determined based on the mutual capacitance (e.g., a mutual capacitance, above a threshold value, indicates the user presence). In some embodiments, the user input device includes an integrated circuit for measuring a mutual capacitance between the two or more electrodes and user presence is determined based on the mutual capacitance. In some embodiments, the user input device includes a plurality of finger pads (e.g., the finger pad 212) and user presence is determined based on finger presence at one or more of the plurality of finger pads.
In some embodiments, the computing system receives, from a sensor coupled to (e.g., embedded in) the user input device, sensor information related to a user presence at the user input device; and detects drift based on the sensor information. In some embodiments, the sensor is one of: a capacitance-based sensor, or a light-based sensor.
In some embodiments, detecting drift of the user input device includes tracking (406) movement of the user input device and determining that the tracked movement corresponds to an unintentional movement. In some embodiments, the computing system includes a sensor and (e.g., a motion sensor) and the sensor tracks movement of the user input device. In some embodiments, the determination that the tracked movement corresponds to an unintentional movement is based on historical data (e.g., historical movement data associated with the medical procedure being performed and/or the operator of the user input device). In some embodiments, the determination that the tracked movement corresponds to an unintentional movement is based on pattern recognition and/or machine learning.
In some embodiments, the computing system obtains secondary information associated with the user input device and the detection of drift is based on the secondary information. In some embodiments, the input device includes a joint and the secondary information includes a position and/or velocity of the joint. In some embodiments, the joint is a passively stationary joint of the input device. In some embodiments, the joint is a roll joint of the input device. In some embodiments, the secondary information includes a time threshold for comparison with a duration over which the sensor detects a lack of a user presence. In some embodiments, the secondary information includes a configuration of the user input device, such as an angle or velocity, motion of a passively stationary joint, and/or a time point of last movement or last-detected user presence. In some embodiments, the secondary information includes information indicating a change in a configuration (e.g., position and/or orientation) of the input device at a first time and a second time that is subsequent to the first time (e.g., current time).
In some embodiments, detecting drift includes comparing the change in the configuration of the input device and a configuration change threshold (e.g., a predefined distance and/or angle difference). In some embodiments, the information indicating the change in the configuration of the input device is obtained by determining a configuration (e.g., a position and/or orientation) of the input device at the first time, determining a configuration of the input device at the second time, and determining the change in the configuration of the input device based on the configuration of the input device at the first time and the configuration of the input device at the second time.
In some embodiments, the secondary information includes information indicating a change in a configuration (e.g., position and/or orientation) of the medical instrument at a first time and a second time that is subsequent to the first time. In some embodiments, the information indicating the change in the configuration of the medical instrument is obtained by determining a configuration (e.g., a position and/or orientation) of the medical instrument at the first time, determining a configuration of the medical instrument at the second time, and determining the change in the configuration of the medical instrument based on the configuration of the medical instrument at the first time and the configuration of the medical instrument at the second time.
The computing system switches (408) operation of the user input device to an assisted mode, including applying a second set of parameters that is distinct from the first set of parameters, in accordance with detecting the drift (e.g., transition 375 described above with respect to
In some embodiments, the second set of parameters includes (410) a modification to one or more parameters of the first set of parameters; and the modification to the one or more parameters includes adjustment of one or more of: a damping of the user input device, a stiffness of the user input device, a motion scaling between the user input device and the medical instrument, or a break control of a joint of the user input device. In some embodiments, adjusting motion scaling includes reducing the motion scaling between the input device and the robotic arm. For example, the robotic arm may move by a first distance in response to movement of an input device by a particular input distance before the adjustment and the robotic arm may move by a second distance, less than the first distance, in response to movement of the input device by the particular input distance after the adjustment. In some embodiments, adjusting motion scaling includes temporarily disabling motion updates from the user input device to the robotic arm. In some embodiments, modification of the one or more parameters includes providing haptic feedback to a user (e.g., via the user input device) to maintain a position of the user input device. In some embodiments, adjusting the damping and/or stiffness of the user input device includes increasing kinetic energy dissipation in the user input device. In some embodiments, adjusting the break control of the joint includes increasing friction within the joint.
In some embodiments, switching the operation of the user input device to the assisted mode includes (412) one or more of: performing a position control operation, or performing a velocity control operation. In some embodiments, performing a position control operation includes moving the user input device to a known good position (e.g., a last known good position). In some embodiments, moving the user input device to a known good position causes the robotic arm to move to a known good position as well. In some embodiments, performing the velocity control operation includes reducing a velocity of the robotic arm. In some embodiments, the velocity control operation includes setting the velocity of the user input device to zero. In some embodiments, setting the velocity of the user input device to zero cause the robotic arm velocity to be set to zero as well. In some embodiments, switching the operation of the user input device to the assisted mode includes temporarily pausing teleoperation command transmissions between the user input device and the robotic arm.
In some embodiments, the second set of parameters includes (414) a modification to one or more parameters of the first set of parameters, and the modification to the one or more parameters includes applying a weak feedback control. As used herein, weak feedback control is feedback control that can be overcome by the user (e.g., by applying more force to the user input device).
In some embodiments, the modification to the one or more parameters includes modifying (416) the one or more parameters of the first set of parameters within predefined limits. For example, setting a damping parameter to a maximum damping parameter of the predefined limits. In some configurations, the maximum damping parameter is selected so that the user can continue to move the user input device despite the damping applied to the user input device at the maximum damping parameter.
In some embodiments, the computing system continues (418) to operate the user input device in the assisted mode in accordance with a determination that the user input device is not stable. For example, after a preset amount of time, the computing system determines that the movement and/or position of the user input device is still not stable and continues to operate in the assisted mode. In some embodiments, in accordance with a determination that the user input device is not stable after a preset amount of the time, the computing system switches operation from the assisted mode to a safe mode (e.g., the safe mode 383).
The computing system determines (420) that the user input device is stable while operating in the assisted mode. In some embodiments, determining that the user input device is stable includes tracking an amount of time the user input device is in the assisted mode; and, in accordance with a determination that the amount of time meets a predetermined criterion, determining that the user input device is stable.
In some embodiments, determining that the user input device is stable includes determining (422) that the user input device has been operating in the assisted mode for a predetermined amount of time. In some embodiments, determining that the user input device is stable includes determining that the user input device has been operating in the assisted mode for a predetermined amount of time and user presence is detected at the user input device.
In some embodiments, the predetermined amount of time corresponds (424) to a settling time of the user input device. In some embodiments, the settling time depends on a configuration of the user input device (e.g., position, velocity, and acceleration). In some embodiments, the configuration of the user input device includes the configuration of the user input device while in the assisted mode (e.g., an amount of damping, stiffness, breaking, etc.). In some embodiments, the settling time is predetermined and stored in memory of the computing device. In some embodiments, the settling time is stored in a lookup table specifying a respective settling time for a corresponding user input device configuration. In some embodiments, the settling time corresponds to a worst-case scenario for the user input device (e.g., a scenario where the user input device is moving at a maximum velocity). In some embodiments, the settling time is based on one or more properties of the detected drift (e.g., a velocity or acceleration of the drift).
In some embodiments, determining that the user input device is stable includes determining (426) that a user presence at the user input device meets one or more predetermined criterion.
In some embodiments, determining that the user input device is stable includes determining (428) that movement of the user input device meets predetermined criteria.
The computing system switches (430) the operation of the user input device to the unassisted mode in accordance with the determination that the user input device is stable (e.g., transition 377, 378, or 379 described above with respect to
In some embodiments, while operating the user input device in the assisted mode, the computing system tracks movement of the user input device; and, in accordance with a determination that the movement of the user input device meets predetermined criteria, switches operation of the user input device from the assisted mode to the unassisted mode. In some embodiments, the predetermined criteria include a criterion that the speed of the user input device is below a predetermined threshold. In some embodiments, the predetermined criteria include both a time threshold and one or more motion criteria for the user input device.
In some embodiments, while operating the user input device in the assisted mode, the computing system monitors user presence at the user input device; and, in accordance with a determination that the user presence meets predetermined criteria, switches operation of the user input device from the assisted mode to the unassisted mode. In some embodiments, the predetermined criteria include a criterion that the user presence be detected for at least a threshold amount of time.
It should be noted that the terms “couple,” “coupling,” “coupled” or other variations of the word couple as used herein may indicate either an indirect connection or a direct connection. For example, if a first component is “coupled” to a second component, the first component may be either indirectly connected to the second component via another component or directly connected to the second component.
The term “computer-readable medium” refers to any available medium that can be accessed by a computer or processor. By way of example, and not limitation, such a medium may comprise random access memory (RAM), read-only memory (ROM), electrically erasable programmable read-only memory (EEPROM), flash memory, compact disc read-only memory (CD-ROM) or other optical disk storage, magnetic disk storage or other magnetic storage devices, or any other medium that can be used to store desired program code in the form of instructions or data structures and that can be accessed by a computer. It should be noted that a computer-readable medium may be tangible and non-transitory. As used herein, the term “code” may refer to software, instructions, code or data that is/are executable by a computing device or processor.
The methods disclosed herein comprise one or more steps or actions for achieving the described method. The method steps and/or actions may be interchanged with one another without departing from the scope of the claims. In other words, unless a specific order of steps or actions is required for proper operation of the method that is being described, the order and/or use of specific steps and/or actions may be modified without departing from the scope of the claims.
As used herein, the term “plurality” denotes two or more. For example, a plurality of components indicates two or more components. The term “determining” encompasses a wide variety of actions and, therefore, “determining” can include calculating, computing, processing, deriving, investigating, looking up (e.g., looking up in a table, a database or another data structure), ascertaining and the like. Also, “determining” can include receiving (e.g., receiving information), accessing (e.g., accessing data in a memory) and the like. Also, “determining” can include resolving, selecting, choosing, establishing and the like.
The phrase “based on” does not mean “based only on,” unless expressly specified otherwise. In other words, the phrase “based on” describes both “based only on” and “based at least on.”
The previous description of the disclosed implementations is provided to enable any person skilled in the art to make or use the present invention. Various modifications to these implementations will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other implementations without departing from the scope of the invention. For example, it will be appreciated that one of ordinary skill in the art will be able to employ a number corresponding alternative and equivalent structural details, such as equivalent ways of fastening, mounting, coupling, or engaging tool components, equivalent mechanisms for producing particular actuation motions, and equivalent mechanisms for delivering electrical energy. Thus, the present invention is not intended to be limited to the implementations shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.
Some embodiments or implementations are described with respect to the following clauses:
Clause 1. A medical system comprising:
Clause 2. The medical system of Clause 1, wherein the stored instructions further include instructions for, while operating the user input device in the assisted mode:
Clause 3. The medical system of Clause 2, wherein the predetermined criterion is a time threshold corresponding to a settling time of the user input device.
Clause 4. The medical system of any of Clauses 1-3, wherein the stored instructions further include instructions for, while operating the user input device in the assisted mode:
Clause 5. The medical system of any of Clauses 1-4, wherein the stored instructions further include instructions for, while operating the user input device in the assisted mode:
Clause 6. The medical system of any of Clauses 1-5, wherein the sensor includes a capacitance-based sensor or a light-based sensor.
Clause 7. The medical system of any of Clauses 1-6, wherein the sensor tracks movement of the user input device, and wherein identifying the drift of the user input device includes determining that the tracked movement corresponds to an unintentional movement.
Clause 8. The medical system of any of Clauses 1-7, wherein identifying the drift of the user input device comprises detecting a movement instability in the user input device.
Clause 9. The medical system of any of Clauses 1-8, wherein the second set of parameters includes a modification to one or more parameters of the first set of parameters, and the modification comprises one or more of:
Clause 10. The medical system of any of Clauses 1-9, wherein the second set of parameters includes a modification to one or more parameters of the first set of parameters, and the modification to the one or more parameters comprises applying a weak feedback control.
Clause 11. The medical system of Clause 10, wherein applying the weak feedback control includes modification of the one or more parameters of the first set of parameters within predefined limits.
Clause 12. The medical system of any of Clauses 1-11, further comprising a robotic arm coupled with the medical instrument for moving the medical instrument in accordance with one or more instructions from the processor.
Clause 13. A method for operating a medical system that includes a user input device for controlling a medical instrument, the method comprising:
Clause 14. The method of Clause 13, wherein determining that the user input device is stable comprises determining that the user input device has been operating in the assisted mode for a predetermined amount of time.
Clause 15. The method of Clause 14, wherein the predetermined amount of time corresponds to a settling time of the user input device.
Clause 16. The method of any of Clauses 13-15, wherein determining that the user input device is stable comprises determining that a user presence at the user input device meets one or more predetermined criterion.
Clause 17. The method of any of Clauses 13-16, wherein determining that the user input device is stable comprises determining that movement of the user input device meets predetermined criteria.
Clause 18. The method of any of Clauses 13-17, wherein detecting the drift of the user input device comprises:
Clause 19. The method of any of Clauses 13-18, wherein the second set of parameters includes a modification to one or more parameters of the first set of parameters, the modification to the one or more parameters comprises one or more of:
Clause 20. The method of any of Clauses 13-19, wherein switching the operation of the user input device to the assisted mode comprises one or more of:
Clause 21. The method of any of Clauses 13-20, wherein the second set of parameters includes a modification to one or more parameters of the first set of parameters, the modification to the one or more parameters comprises applying a weak feedback control.
Clause 22. The method of Clause 21, wherein applying the weak feedback control includes modification of the one or more parameters of the first set of parameters within predefined limits.
Clause 23. The method of any of Clauses 13-22, further comprising: in accordance with determining that the user input device is not stable while operating in the assisted mode, continuing to operate the user input device in the assisted mode.
Clause 24. A method for operating a medical system that includes a user input device for controlling a medical instrument, the method comprising:
This application is a continuation of International Patent Application No. PCT/IB2023/052510, filed Mar. 15, 2023, entitled “Continuous Teleoperation with Assistive Master Control,” which claims priority to U.S. Provisional Patent Application No. 63/321,041, entitled “Continuous Teleoperation with Assistive Master Control,” filed Mar. 17, 2022, the disclosures of each of which are incorporated by reference herein, in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 63321041 | Mar 2022 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/IB2023/052510 | Mar 2023 | WO |
| Child | 18886957 | US |
