There are various types of surgical robotic systems on the market or under development. Some surgical robotic systems use a plurality of robotic arms. Each arm carries a surgical instrument, or the camera used to capture images from within the body for display on a monitor. See U.S. Pat. No. 9,358,682. Other surgical robotic systems use a single arm that carries a plurality of instruments and a camera that extend into the body via a single incision. See WO 2016/057989. Each of these types of robotic systems uses motors to position and/or orient the camera and instruments and to, where applicable, actuate the instruments. Typical configurations allow two or three instruments and the camera to be supported and manipulated by the system. Input to the system is generated based on input from a surgeon positioned at a master console, typically using input devices such as input handles and a foot pedal. Motion and actuation of the surgical instruments and the camera is controlled based on the user input. The image captured by the camera is shown on a display at the surgeon console. The console may be located patient-side, within the sterile field, or outside of the sterile field.
US Patent Publication US 2010/0094312 (the '312 application) describes a surgical robotic system in which sensors are used to determine the forces that are being applied to the patient by the robotic surgical tools during use. This application describes the use of a 6 DOF force/torque sensor attached to a surgical robotic manipulator as a method for determining the haptic information needed to provide force feedback to the surgeon at the user interface. It describes a method of force estimation and a minimally invasive medical system, in particular a laparoscopic system, adapted to perform this method. As described, a robotic manipulator has an effector unit equipped with a six degrees-of-freedom (6-DOF or 6-axes) force/torque sensor. The effector unit is configured for holding a minimally invasive instrument mounted thereto. In normal use, a first end of the instrument is mounted to the effector unit of the robotic arm and the opposite, second end of the instrument (e.g. the instrument tip) is located beyond an external fulcrum (pivot point kinematic constraint) that limits the instrument in motion. In general, the fulcrum is located within an access port (e.g. the trocar) installed at an incision in the body of a patient, e.g. in the abdominal wall. A position of the instrument relative to the fulcrum is determined. This step includes continuously updating the insertion depth of the instrument or the distance between the (reference frame of the) sensor and the fulcrum. Using the 6 DOF force/torque sensor, a force and a torque exerted onto the effector unit by the first end of the instrument are measured. Using the principle of superposition, an estimate of a force exerted onto the second end of the instrument based on the determined position is calculated. The forces are communicated to the surgeon in the form of tactile haptic feedback at the hand controllers of the surgeon console.
During the course of surgical procedures, it is necessary for the surgeon to place tissues under tension so that s/he can then dissect, cut, or perform some other step involving that tissue. During dissection or other such surgical procedures, it is often advantageous to use three instruments, one for traction, one for dissection (scissors/ultrasonic/electrosurgical, etc.), and one for counter-traction. The tension resulting from the two opposing traction forces on the tissue being dissected improves the cut quality and speed of the dissection.
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This application describes aspects of a surgical robotic system that allow tissue retraction forces to be automatically modulated where, as above, the surgeon is unable to actively control forces applied by both the retraction instruments.
The present application describes a system and method for maintaining optimal tissue tension between instruments of a surgical robotic system.
The surgical system may be of a type described in the Background, or any other type of robotic system used to maneuver surgical instruments at an operative site within the body. The surgical system is one configured to determine or estimate the forces and/or torque each robotically manipulated surgical instrument applies to tissue. It thus may include one or more sensors positioned to estimate or determine the. The system might employ one or more single-axis sensors, multi-axis sensors, or a combination of single- and multi-axis sensors. Exemplary positions for the sensor(s) include the instrument tip, instrument shaft, the robotic arm or some combination of these positions. Types of sensor arrangements that can be used include, without limitation, those described in US Patent Publication US 2010/0094312 or PCT/US2017/015691, as well as other configurations. Other embodiments might derive force information by reading the motor currents at the joints of the robotic manipulator arm, a configuration that also will be referred to as a “sensor” for the purposes of this description. It should be understood that the scope of the invention is not limited to any particular type of sensor type or location, as the invention may be practiced using any sensor type or sensor location that will allow the system to determine the force or torque apply by a surgical instrument to tissue.
A simple embodiment incorporating principles of the present invention is depicted in the flow chart of
This initial step may be performed by a user who manipulates a control handle at the surgeon console to command the robotic arm to navigate the first instrument to the tissue and to apply the force having the desired magnitude and direction to the tissue (“surgeon control.”). An instruction is given to the system to “set” this force magnitude and direction for use in force maintenance mode, described below.
This initial step need not be performed under surgeon control. Instead, a user standing adjacent to the patient may manually guide the robotic arm and first instrument into a desired position, and to move the instrument into contact with the tissue to apply the force/torque. Depending on the instrument and the capabilities of the robotic system, this might involve using a manual actuator to close the jaws of a grasping instrument onto tissue and then moving the arm to apply the force, or by manually moving the arm to push a retractor against the tissue. The direction of the force might then be set by aligning the shaft of the instrument along the desired axis of force (e.g. if traction is to be applied by the instrument), or an input device can be used to instruct the system as to the desired direction of force with respect to the endoscopic image of the instrument on the endoscopic display. For example, an eye tracking device positioned to receive input based on movement of the user's eyes across the endoscopic image display might be activated to record eye motion as the user traces the intended direction of force with his/her eyes along the display. Alternatively, the user might move a cursor across the display or employ a touch input or/overlaying the display to set the direction.
Next, the user places the system in a force maintenance mode, under which the magnitude and direction of the force or torque set by the user or imparted on the tissue by the first instrument is dynamically maintained under robotic control. The force is maintained through autonomous movement of the first instrument using the robotic arm. While the system is in force maintenance mode, the user causes other surgical instruments (manual instruments or those manipulated using robotic arms) to act on the tissue in ways that might cause variation in the magnitude of the force/torque applied by the first instrument had it not been placed in force maintenance mode.
This embodiment might be modified so that a sudden decrease in the magnitude of the force (i.e. a decrease in the force by more than a pre-determined amount within a predetermined period of time) might cause the system to hold the position of the first instrument rather than attempting to maintain the force. This feature is discussed in further detail in connection with the embodiment of
The system can be configured to receive input defining the boundaries in a number of different ways. For example, the user might trace the boundaries using a touch interface on or over the endoscopic image display, or using input from an eye tracker generated during movement of the user's eyes over the endoscopic display to define the boundaries. In these examples, the depth of the bound space might be defined using a variety of means, such as by placing the tip of an instrument such as the endoscopic camera at the maximum depth to be input to the system. In other examples, the keep-out boundaries might be defined by the user prior to the procedure using models generated using pre-operative images or scans, or the system might be configured to recognize delicate tissue structures using computer vision and to register the areas containing such structures as keep-out zones. Another pre-set or user settable limit might include maximum force limits.
If the movement needed to maintain the magnitude of the force is determined to be safe, the robotic arm autonomously moves the instrument. If the system determines that the movement would not be safe, the system alerts the user (e.g. using auditory, visual or tactile feedback) and does not move the instrument beyond the safe limits.
In a multi-arm robotic system making use of the configuration described with reference to
A second embodiment will next be described with reference
In this embodiment, first and second instruments 1, 2 (such as retractors) are positioned in a surgical workspace and used to engage or contact to tissue. The steps of positioning the instruments in the workspace and engaging the tissue are preferably performed by the surgical robotic system based on active surgeon input (“surgeon control”, although manual positioning might instead be used as discussed above. For example, the surgeon might use a first input device (e.g. a first input handle 17,
After the instruments are positioned and used to contact or engage tissue, the system is operated in a force or torque modulation mode (which in this embodiment is a traction modulation mode). In this mode, the system is operated so that one instrument may be actively telemanipulated by the surgeon using an input device (which will be referred to here as “surgeon-controlled” to mean that the robotic surgical system controls motion of the traction instrument to move it based on input from the surgeon). The other instrument is not actively telemanipulated by a surgeon but applies a force or torque to tissue under control of the robotic system. This type of control will be referred to here as “autonomously controlled” to mean that the robotic surgical system is not directly responding to surgeon input from an input device paired with the traction instrument to control the position of the second instrument. It instead automatically controls force/torque (in this specific example countertraction forces) applied by the second instrument based on other parameters. In preferred embodiments, the direction and magnitude of the applied force of the autonomously-controlled instrument is determined by the robotic system based on the direction and magnitude of the force of the surgeon-controlled instrument as it is actively telemanipulated by the surgeon.
As countertraction is applied to tissue by the first and second traction instruments 1, 2, a third, preferably surgeon-controlled, instrument 3 is used to perform a procedure on the tissue. The third instrument may be a treatment instrument such as a dissection instrument that separates tissue using blades, energy, forces, or some other modality, or it might be some other type of instrument such as a stapler, ligation instrument, suturing instrument, sealing instrument, etc.
One embodiment of the described system might make use of components of a system of the type shown in
Using the measured or derived direction and magnitude of the force/torque applied to tissue by the first instrument, the system determines a complementary force/torque magnitude and direction to be applied to tissue by the second instrument. As an example of this embodiment, when this mode of operation is triggered, the second arm 16 will cause the second traction instrument 2 to pull the tissue using a force that is of substantially equal magnitude and that has a direction that is mirrored relative to the direction of movement of the first instrument relative to a defined plane. The plane may be defined relative to the camera vector or a tissue plane, or it may be at a location defined by the user using input techniques described elsewhere in this application. In some cases the force/torque applied to the second instrument might be of substantially equal force and/or in an equal and opposite direction from the first traction instrument 1 on the first arm. Determining the complementary magnitude and direction might take into account other parameters such as the type or properties of the tissue receiving force/torque from the first or second instruments and other factors.
The autonomous modulation may be limited by a not-to-exceed force value as described with respect to the first embodiment. The not-to-exceed force value may be statically set, be dynamically determined, or selectively set by the user.
The travel of the robotically-controlled traction instrument may also be limited by certain travel limits. This may take the form of a maximum-allowable deviation from the instrument's current position, the avoidance of static or dynamically-set “keep-out” zones (into which the instrument will not be permitted to pass), or any combination thereof. See the description of the first embodiment.
In one implementation, the second arm causes the second instrument 2 to apply the same force to the tissue that the first instrument held by the surgeon-controlled first arm applies. In another implementation, the instrument held by the second arm maintains a set tension, with a not-to-exceed limit. This value may be set once prior to the procedure, may be adjusted by the surgeon during the procedure, or may be dynamically set during the procedure and calculated by the surgical robot.
With traction and counter-traction applied, the surgeon carries out the dissection procedure using instrument 3, which is manipulated by arm 17, in accordance with user input using input device 18, while the system in traction modulation mode provides continuous, optimal tension adjustments through the robotically-controlled movement of instrument 2.
In preferred implementations, a hybrid of force control and position control is used to prevent overshoot of the robotically-controlled traction instrument 2 upon a sudden decrease of tension resulting from a release of tissue or the cutting of a specimen, such as during dissection or cutting using instrument 3. In the embodiment depicted in
In other implementations, the system is configured so that the forces/torque (in this embodiment traction and counter-traction) applied by the instruments 1, 2 may be automatically applied by robotically-controlled arms modulated to a safe value.
Another application for the principles described herein is one in which a robotically-controlled arm may be used to provide tissue tension during suturing, provide optimal apposition of tissue at the suture line, etc. In this example, a first instrument is surgeon controlled to manipulate a first tissue, and a second instrument is autonomously manipulated using force/torque having a magnitude and direction determined based on the magnitude and direction of the force/torque applied by the first instrument, with the effect of maintaining the first and second tissues in apposition during tissue suturing or other forms of fastening or attachment.
In another embodiment, autonomously modulated force/torque is used in some procedure-specific contexts. For example, the system might be programmed to move an instrument that is applying force to tissue along a path or according to a sequence that is based on the surgical procedure being performed. For example, in a cholecystectomy procedure, a first instrument is used to grasp and elevate the gallbladder. A second instrument is used to dissect the gallbladder from the liver bed. As the dissection progresses, it can be beneficial to change the magnitude and direction of the load applied to the gallbladder according to a sequence that is pre-defined or dynamically defined based on keep-out zones and other parameters. A sequence of this type might include changing the nature of the force from a lifting force to a rotational force during the course of the sequence (e.g. as the gallbladder is being rotated off the liver bed).
Although the above embodiments describe surgical instruments on separate robotic arms, systems such as those in WO 2016/057989, which use of a plurality of surgical devices disposed on a single arm, can also be used with the present invention. For example, the first and second traction instruments may be retractors that bend or articulate using robotically driven actuators. In use, a first, surgeon-controlled, traction force is applied to tissue by bending/articulation of one of the retractors engaged with tissue, based on surgeon input using a user input device. A second, robotically-controlled, retraction force is applied to the tissue by the other one of the retractors which is caused to bend/articulate so as to apply the second force having direction and magnitude determined by the system using principles described above. A third, surgeon-controlled, instrument is used to perform the dissection.
The disclosed inventions provide several advantages over systems and methods of the prior art, including automation of the maintenance of force on tissue (of tension on tissue while dissecting), use of the force sensors in the robotic arms to aid in the maintenance of tension between two instruments, and the combined use of force control and position control to maintain safe positions of the robot, especially when tissue tearing, dissection, or detachment from tissue occurs.
This application claims the benefit of U.S. Provisional Application No. 62/503,062, filed May 9, 2017.