The invention relates to a surgical robotic system for microsurgery.
An increasing number of surgeries is performed by means of surgical robots. These surgical robots may comprise so-called manipulators which generally have an end effector which handles a surgical instrument acting upon the patient.
In microsurgical procedures, such instruments include needle holders, forceps, vessel dilators and scissors, while the precision, stability and dexterity of the handling of such instruments are critical aspects in the outcome of the procedure. Various microsurgical robotic platforms are developed to enhance these aspects.
For example, it is known to provide slender wristed instrumentation to enable instrument articulation close to an operation site and therefore provide enhanced dexterity. Such wristed instrumentation is typically comprised of a wrist and a surgical instrument attached to or integrated into the wrist, which may together also be referred to as a ‘wristed instrument’. The wrist may be connected to a distal part of an elongated shaft, whereas the actuation of the instrument wrist may be performed proximally by means of, e.g., a cable and pulley mechanism. For example, this allows the orientation of jaws of the instrument to be changed with respect to the operation site, while the orientation of the elongated shaft stays the same or moves around a fixed remote center of motion. This is especially useful for minimally invasive surgery, where the elongated shaft may be inserted through a small incision in the skin of the patient to access a deeper lying operation site inside the body. The remote center of motion may prevent excessive strain on the skin incision during the procedure.
However, most microsurgery procedures do not have any accessibility constraints such as in minimally invasive surgery. These so-called open microsurgery procedures are performed close to the skin surface of the patient and do not involve any deeper lying operation sites. While enhanced dexterity may not be needed for open microsurgery, the use of wristed instrumentation in open surgery may still have various advantages, such as providing a less cluttered operation site.
For example, WO2014/055979A1 describes an articulating device which may be articulated and/or translated about five axes, as also shown in
A disadvantage of WO2014/055979A1 is that the articulating device held by the proximal support has relatively poor stability and allows insufficient precision when positioning the articulating device, e.g., at a desired position in the operating site.
An object of the invention is to obtain a surgical robotic system which comprises a wrist for holding a surgical instrument and which allows the surgical instrument held by the wrist to be positioned in an operation workspace with sufficient dexterity, stability and precision for be suitable for microsurgical procedures.
A first aspect of the invention provides a surgical robotic system, comprising:
The above measures relate to a manipulator of a surgical robotic system, e.g., of a surgical robot, which may be used for microsurgery, e.g., for surgery involving microsurgical procedures. Examples of surgery which involve microsurgical procedures are reconstruction of breasts after tumor removal, e.g., the so-called DIEP-method, reconstruction of fingers and hands to restore function after trauma and facial reconstruction after trauma. Typical steps during these procedures are (re-)connection of nerves and mutual connection of vessels using sutures, known as anastomosis. Anastomosis is one of the most difficult procedures, which is often a cause of complications occurring 5 to 10% of the time. A typical size of vessels in microsurgery is 0.8 to 2.0 mm and the vessel wall thickness may be 0.1 x the vessel diameter, while achievable human precision is considered to be 0.1 mm. A more extreme case is lymphovenous anastomosis (LVA), which is used for the treatment of lymphoedema. During this procedures, lymphatic vessels are connected to blood vessels. A typical size of lymphatic vessels is 0.2 to 0.8 mm. Due to the small size of such lymphatic vessels, such LVA procedures may also be categorized as super microsurgery.
The above measures provide a manipulator for a surgical robotic system which may be well-suited for such microsurgical procedures. Namely, the strut assembly may provide three translational degrees of freedom (DOF) in a parallel kinematic setup by each strut being independently actuatable in longitudinal direction and by the struts together forming a pyramidal structure at which distal portion the wrist may be attached. For translational DOF, a relatively small but accurate range of motion may be desired. The strut assembly as a parallel kinematic structure may satisfy such translational DOF requirements. Accordingly, the surgical instrument held by the wrist may be positioned in the operation workspace with sufficient dexterity, stability and precision for be suitable for microsurgical procedures.
To actuate the wrist, and in some examples the instrument held by the wrist, e.g., to open and close the instrument, at least one strut may comprise an actuation transmission mechanism which may transmit actuation forces to the wrist, for example from one or more actuators which may be attached to a proximate end of said strut. This may avoid the wrist from having to comprise the actuator(s) themselves, which may otherwise increase the weight and size of the wrist and which may hinder the dexterous, stable and precise positioning of the surgical instrument held by the wrist.
The strut assembly may form a pyramid-like shape which may not only provide an advantageous kinematic parallel setup, but which may be open and sparse since the struts may themselves occupy relatively little space due to their inherently elongated shape. This may avoid or reduce blocking the view of the microsurgical workspace for either a microscope or the direct view of the (assistant) surgeon. In particular, near the base of the pyramid, the struts may be spaced apart so as to allow the microscope to fit in between the struts. This may allow the microscope to relatively closely approach the microsurgical workspace and thereby obtain a good view thereof.
In a specific example, the strut assembly may consist of three struts, thereby forming a 3-sided pyramid, or of four struts, thereby forming a 4-sided pyramid. However, the strut assembly may also have any other suitable pyramidal shape.
In some examples, the manipulator may form a hybrid kinematic structure which combines favorable properties of both serial and parallel kinematics structures. More specifically, in addition to the strut assembly providing a parallel kinematic setup, the wrist may provide three rotational DOF in a serial kinematic setup. For rotational DOF, a relatively large range of motion may be desired but which may be relatively inaccurate, while it is recalled that for translational DOF, a relative accurate range of motion may be desired but which may be relatively small. Such requirements may be jointly met by using serial kinematics for rotational DOF and parallel kinematics for translational DOF. It is noted that in other examples, the wrist may not need to provide the three rotational DOF in a serial kinematic setup but rather in another manner.
Optionally, the surgical robotic system further comprises a driving mechanism for actuating the wrist via the actuation transmission mechanism, wherein the driving mechanism is attached to a proximate end of the elongated shaft. For example, one or more electric motors may be provided and controlled to actuate the wrist via the transmission of actuation forces through the elongated shaft as strut.
Optionally, the elongated shaft is attached to the base structure at an intermediate section before the proximate end so that the driving mechanism acts as a counterweight for the elongated shaft. The driving mechanism typically has a substantial mass, which may be used as a counterweight for the elongated shaft when the elongated shaft is held by the base structure at an intermediate position before the driving mechanism. This may reduce motor power consumption by gravitational force, and/or prevent or reduce the impact of the manipulator collapsing onto a patient in the case of power down or power failure associated with the surgical robotic system.
Optionally, one or more of the at least three struts are actuated by respective cranks or respective linear actuators.
Optionally, the strut assembly has an envelope which is geometrically represented by a pyramidal solid angle extending from the distal strut sections towards the base structure, wherein a crank is mounted on the base structure within the envelope of the strut assembly. Such mounting of the crank within the pyramidically shaped envelope may contribute to the compactness of the strut assembly. Accordingly, the strut assembly may be less of an obstacle in the operating workspace.
Optionally, one or more of the at least three struts are connected to the base structure with respective one or more ball-joints or respective one or more flexible hinges. Optionally, at least one of the one or more ball-joints is preloaded by a spring, wherein said preloaded spring is arranged substantially parallel to a respective strut.
The spring may in some examples be made out of thermoplastic polyurethane (TPU). TPU may be supplied as sterile material and at a relative low cost, which may enable the preloaded spring to be disposable.
Optionally, the wrist is attached to a distal end of the elongated shaft.
Optionally, one or more other struts are connected with their respective distal strut sections to the distal strut section of the elongated shaft with respective one or more ball-joints or respective one or more flexible hinges.
Optionally, the base structure is rotatable around a rotation point, and the strut assembly is mass-moment balanced to provide a center of mass at the rotation point. This may reduce motor power consumption by gravitational force, and/or prevent or reduce the impact of the manipulator collapsing onto a patient in the case of power down or power failure associated with the surgical robotic system.
Optionally, the base structure comprises a stereoscopic camera. Such a stereoscopic camera may enable the (assistant) surgeon to obtain a view of the operating workspace even if he/she is unable to obtain a direct view thereof, e.g., by being not present in the operating room or only at a distance of the patient. Due to the open and sparse shape of the strut assembly, a stereoscopic camera attached to the base structure may still have a good view of the operating workspace.
Optionally, the strut assembly and the wrist form a manipulator, wherein the surgical robotic system comprises two or more manipulators which are mutually arrangeable to assume different orientations with respect to a common surgical workspace. Such an arrangement may for example be well-suited for LVA surgery.
Optionally, the surgical robotic system is a master-slave robotic system, wherein the strut assembly and the wrist form a slave manipulator of the master-slave robotic system.
Optionally, the strut assembly is removably attachable to the base structure to allow a drape to be applied between the base structure and the strut assembly, wherein the strut assembly is attachable to the base structure via said applied drape.
In a further aspect of the invention, a kit of parts is provided comprising the surgical robotic system and the drape. It is noted that such a drape may be separately manufactured and sold.
It will be appreciated by those skilled in the art that two or more of the above-mentioned embodiments, implementations, aspects and/or optional aspects of the invention may be combined in any way deemed useful.
These and other aspects of the invention are apparent from and will be elucidated with reference to the embodiments described hereinafter. In the drawings,
It should be noted that items which have the same reference numbers in different figures, have the same structural features and the same functions, or are the same signals. Where the function and/or structure of such an item has been explained, there is no necessity for repeated explanation thereof in the detailed description.
It is noted that
The manipulator which is illustrated in
The hybrid kinematic structure which is conceptually shown in
Various components of the robotic surgical system which achieve and/or contribute to realizing the above-mentioned advantages are described in the following in more detail. It is noted that such components may also be used independently from each other. For example, the strut assembly as described in the specification may be used with another type of wrist, and/or the spherical wrist as described in this specification may be mounted to another type of assembly to provide the translational DOF, and/or the wrist may be configured to actuate a different type of instrument.
The neutral lines of the struts 150 and tube assembly 200 may intersect in the wrist’s center of rotation. The spherical wrist may be driven by a drive-box 500 via tubes, with the drive-box 500 being arranged on the proximate side of the tube assembly 200. The drive-box 500 may further contain one or more sensors which may measure (directly or indirectly, via a transmission) rotations of the spherical wrist. The opening and closing of the instrument 700 may be actuated by the drive-box via a string through the tubes of the tube assembly 200. The struts 150 and tube assembly 200 may be constrained and driven by cranks 300. The struts 150 may be constrained to be axially loaded. The tube assembly 200 may be constrained to be loaded both axially as well as in torsion along its centerline. The cranks 300 may be supported, actuated and measured at a frame 400 which may form a base structure of the manipulator. The frame 400 may be connected to a (further) support structure, which is not shown in
As described with reference to
Dimensions of the strut, crank and the angular stroke may be chosen to comply with the required range of motion and possible ball-joint angles.
The struts and ball-joints may be part of the sterilized component set, e.g., belonging to those components of the surgical robotic system which are sterilized between uses, since draping of these components may otherwise require a drape in the form of a tent, which may block the view and act as a sail, thereby introducing disturbances during movements. Therefore, in some examples, the struts and ball-joint components may be produced from stainless steel. The strut may be selected to be strain hardened austenitic stainless steel. Such type of steel may obtain a yield stress of ≥ 1200 MPa, which may reduce risk of component failure. Risk for failure is regarded most likely during sterilization. Equation (1) and (2) indicate the expected maximum buckling and bending force required for a 3 mm strut thickness.
where E is elastic module, L is length, d is diameter, and
A preload spring may be used to preload the ball-joints of the struts. In a specific example, the preload force may be set to be ≥ 7 N to handle forces at the instrument tip. Here, maximum forces by stall torque may be taken as a reference to keep the struts engaged, despite overloading. The preload spring may be placed almost parallel to the strut to minimize length perturbations during movement, since perturbations in spring length may indicate a variation in stored elastic energy. A change in stored elastic energy may impose a preferred position for the mechanism as it naturally searches for its minimum energy state. This searching for its minimum energy state may introduce parasitic forces on the actuators, which may be undesired.
Using a low stiffness spring instead of a high stiffness spring may help in minimizing this effect, as length variation for a lower stiffness has a smaller change in stored energy. However, a standard low stiffness steel spring typically has a lower eigenfrequency, which may be another source of disturbance. Additionally, a standard steel coil spring may be hard to clean. Accordingly, in some examples, a thermoplastic polyurethane (TPU) may be chosen as preload element. TPU is an elastomer, which is known for having large strain properties (sometimes ≥ 500%), excellent resistance to rupture, and good damping properties. Consequently, a large deformation of a relatively low stiffness TPU preload element may be used to obtain the required preload, while vibrations may be decreased by structural damping of the material. It will be appreciated, however, that the preloaded spring may also be of other materials, including the aforementioned steel if the aforementioned drawbacks are accepted.
As seen in
As may be seen in
Removal of the pitch axis may allow the wrist assembly to be disassembled for cleaning and sterilization. These pitch axis parts may be considered disposable and may be mass produced with suitable tolerances, e.g., by tube drawing companies.
The yaw part 622 may be constrained radially (2 DOF) by a plain bearing inside the outer tube part. The yaw tube may provide two plain bearings for the roll- and pitch gears tubes to constrain 2 radial DOF. As a result, the structural loop for the roll drive train may be stiffer with respect to a bearing between the roll and pitch tube. Furthermore, a less disturbed pitch tube may be convenient, since its rotational accuracy may be most sensitive to provide translational errors to the instrument tip. Additionally, from a manufacturing perspective, a single part providing bearings and axis may be also preferred, since a single part may allow for single fixation turning and or milling, which may enable high quality tolerances for bearings and the pitch axis to locate the bevel gear apexes; multiple bearing parts may require more well-defined and higher quality tolerated features. For example, each tube providing a bearing for a consequent tube requires at least two well defined and tolerated features. Longitudinal DOF for the yaw, pitch and roll tubes may be constrained at the drive-box to minimize additional friction in the wrist, despite tolerance disadvantages. However, a way of obtaining the desired tolerances is described under ‘concentric tubes assembly’.
As shown in
As seen in
The coupling parts may contain axial labyrinth seals for sealing between respective tubes. In the labyrinth, a sterile lipid/grease may be applied. The greased-filled axial labyrinth seals may create a sterile barrier to prevent non-sterile contamination by the drive-box during surgery. This may allow a coupling between sterile and non-sterile components, without contaminating the sterile zone, see also under the heading ‘sterile barrier’. As can be seen in
Tube swaging may enable larger diameter tubes to transmit torque to the wrist, instead of smaller straight tubes with a direct fit to the wrist. Swaging is a (cold) forming process for reducing a tube diameter, which may be applied locally. Therefore, a larger diameter tube may be locally swaged, see the swaged tube portion 212 in
An asymmetric design may be chosen over a symmetric design, as it may reduce components, provide a stationary reference point, and may provide more space for an actuation mechanism. As can be seen in
The instrument gripping force may in a specific example be ≈5N and may be provided by an ultra-high-molecular-weight polyethylene string 250 over a sliding pulley 730. The sliding pulley 730 may compensate for the lever ratio of the jaw to reduce the required actuation force. The gripping force may be limited by a mechanical stop 710 to prevent damaging the instrument tip in case of over-actuation. Another mechanical stop 712 may limit opening of the jaws, which may happen via a spring. This spring may keep the jaw ‘normally open’ and hold the string under tension. In a specific example, the pretension in the actuator string may obtain ≈0.2 - 0.6 N of force for spring volume 722. This force may be enough to keep the string preloaded.
The preload string may for example be made out of ultra-high-molecular-weight polyethylene (UHMWPE, UHMW) or high-modulus polyethylene (HMPE) fibers, for example out of so-called Dyneema fibers. The string may be fixated at either or both sides by turning over an end-part, thereby causing a thickening. Glue may be applied to keep the string formed at and near the thickened part, such that the thickened part is maintained during assembly of the string. The thickened part may fixate the string by hooking into a slot at the wrist, while the other end may be fixated and tensioned at the drive-box. For example, at the wrist, such fixating may comprise fixating the string to the center of a pulley at the string fixation point 720, while winding the string multiple revolutions around this pulley such that the string clamps itself onto the pulley. The fixation to the center of the pulley may prevent the complete winding from slipping over the pulley. Such fixation may for example be obtained as follows: firstly, the string may be wrapped several times into slots on the pulley. Secondly, a setscrew may clamp the string to the center of the pulley. Thirdly, the string may be wound-up a number of times over the pulley. Lastly, the string may be tensioned and held by a non-back drivable worm gear, similar to a guitar string. It will be appreciated that this way of fixation is merely an example, and that any other suitable fixation may be used as well.
In general, various other methods may be used for weight compensation. In general, the manipulator structure may be designed to have mass concentrated close to the intended COM, given inertia J oc r2, while balancing moment Mbalance ∝ r. It is further noted that the degree of motion compensation may be kept to a minimum or at least reduced by using a short instrument, in that a shorter instrument length may require less translation to compensate for the instrument rotations.
The design of the manipulator may facilitate sterilization. For example, the spherical wrist and tube assembly may each be sterilizable components which may be coupled to the drive-box 500 prior to surgery, and which may be designed for assembly and disassembly for such sterilization, similar to conventional surgical instrumentation. Additionally, the tube assembly may be designed to be coupled to the drive-box, while providing a sterile barrier to prevent non-sterile contamination by the drive-box.
In general, sterilization issues may be avoided if instrumentation enables easy cleaning. This may be achieved if the wrist can be disassembled, while individual parts of the wrist may be designed to avoid hard to reach geometrical cavities, such as blind holes. As previously described with reference to
A mechanical connection run between sterile and non-sterile components to transmit forces and torques to the instrument, which may be designed to avoid contamination of the sterile zone. The connection of the struts to the base structure, e.g., the frame, may be made by running the drape in between the fixation feature to the crank. The connection of tubes may be done inside the shielded zone, which may in principle contaminate the couplings of the tubes. However, the sterile zone inside the tube assembly may be maintained by axial labyrinth seals, while the drape may be attached to the tube assembly, as also previously illustrated in
Assembly of the sterile components may be done prior to surgery. As a first step, the drape 900 may be attached to the tube assembly, which may then be coupled to the drive-box. Thereafter, the drape 900 may be positioned and fixated around the manipulator. Positioning of the drape 900 may be done according to markings on the drape, which may help with aligning the drape to the manipulator. The drape may be fixated by sterile rubber bands and tape to minimize the volume taken by the drape so as to maintain a clear view of the surgical workspace. Some drape surface may not be fixated to facilitate movement of the cranks. The corresponding excess drape surface may be limited to allow local flexing and folding at drape positions close to the crank’s rotation axis. The fixation points of the drape may be part of the frame and associated frame panels (not shown in any Figures). Such frame panels of the frame may function as a form of shielding for protecting the drape from the gears and vice versa.
The following clauses define optional embodiments, which may be combined with the embodiments defined by the claims to form yet further embodiments to jointly improve the strut assembly, the spherical wrist and/or the surgical instrument.
Clause 1. A surgical robotic system (100), comprising:
2. The surgical robotic system (100) according to clause 1, wherein the elongated shaft is a tube assembly (200) comprising a concentric arrangement of at least three tubes (232, 234, 236), wherein each respective tube is configured to transmit a respective actuation force from the drive assembly (500) to the spherical wrist (600) to effect a rotation about a respective axis, wherein said preloading of the string (250) applies an axial tension on the tube assembly.
3. The surgical robotic system (100) according to clause 1 or 2, wherein the string (250) is elastically attached to or in the surgical instrument via a resilient fixation element (720).
4. The surgical robotic system (100) according to clause 3, wherein the resilient fixation element is a pulley (720), and wherein the string is attached to the pulley by being wound multiple revolutions around the pulley.
5. The surgical robotic system (100) according to any one of clauses 1 to 4, wherein the string (250) comprises or is made out of ultra-high-molecular-weight polyethylene, UHMWPE, or high-modulus polyethylene, HMPE, fibers.
6. The surgical robotic system (100) according to any one of clauses 1 to 5, wherein the spherical wrist (600) is actuatable by the tube assembly (200) to rotate about the roll axis (641) via a roll bevel gear (684) and about the pitch axis (631) via a pitch bevel gear (682).
7. The surgical robotic system (100) according to clause 6, wherein the string (250) runs over a pitch bevel gear shaft so as to apply a lateral force on said shaft to preload the pitch bevel gear (682) onto a yaw bevel gear (680) and the roll bevel gear (684).
8. The surgical robotic system (100) according to any one of clauses 1 to 7, wherein the spherical wrist (600) is directly actuatable by the tube assembly (200) to rotate about the yaw axis via a respective tube (232) of the tube assembly.
9. The surgical robotic system (100) according to any one of clauses 1 to 8, wherein the yaw axis (621), the pitch axis (631) and the roll axis (641) of the spherical wrist (600) form a serial kinematic chain, wherein the roll axis is placed last in the serial kinematic chain.
10. The surgical robotic system (100) according to any one of clauses 1 to 9, wherein the at least three tubes (232, 234, 236) of the tube assembly are swaged at the distal end of the tube assembly (200).
11. The surgical robotic system (100) according to any one of clauses 1 to 10, wherein the tube assembly (200) is coupled to the drive assembly (500) and/or to the spherical wrist (600) with a respective coupling part, wherein the respective coupling part comprises a lipid- or greased-filled axial labyrinth seal (754) for sealing between the respective tubes.
12. The surgical robotic system (100) according to any one of clauses 1 to 11, wherein the hinged surgical instrument (700) comprises a stationary jaw and a clamping jaw, wherein the clamping jaw is actuatable by the string (250).
13. The surgical robotic system (100) according to any one of clauses 1 to 12, wherein the roll axis (641) of the spherical wrist (600) is aligned with a longitudinal axis of the stationary jaw of the surgical instrument.
14. The surgical robotic system (100) according to any one of clauses 1 to 13, wherein the surgical instrument (600) comprises a sliding pulley (730), and wherein the string (250) runs over the sliding pulley to reduce a friction influencing the actuation force of the surgical instrument.
15. The surgical robotic system (100) according to any one of clauses 1 to 14, wherein the surgical instrument (700) comprises at least one of:
The above clauses involve a surgical robotic system, which may be a so-called master-slave system, which may comprise a manipulator holding a surgical instrument. The manipulator may comprise a spherical wrist arranged at a distal end of an elongated shaft. Here, the term ‘distal’ may refer to an end which is facing the patient and away from a base structure of the surgical robotic system. The surgical instrument may be held by the spherical wrist, and may be removable, for example to exchange and/or separately sterilize the surgical instrument. The spherical wrist may comprise at least three axes of rotation, namely a yaw axis, a pitch axis and a roll axis. The wrist may be spherical in that the three axes of rotation may jointly intersect each other. Thereby, the spherical wrist may provide the surgical instrument with at least three rotational degrees of freedom (DOF), enabling the surgical instrument to be suitably oriented in a surgical workspace. The roll axis of the spherical wrist may be aligned with a longitudinal axis of the surgical instrument. Thereby, the surgical instrument may perform a roll movement around the chosen longitudinal axis of the surgical instrument, which may allow controlled passage of a surgical needle, which may be held by the surgical instrument during surgery, into tissue that is to be sutured.
Attached to the proximate end of the elongated shaft may be a drive assembly, which may generate actuation forces and which may be transmitted by the elongated shaft to the spherical wrist to actuate any rotation of the spherical wrist. Here, the term ‘proximate’ may refer to an end which is facing away from the patient and towards a base structure of the surgical robotic system. To generate the actuation forces, the drive assembly, which may also be referred to as ‘drive-box’ or actuation mechanism’ elsewhere, may comprise one or more electric motors or other type of actuators. The elongated shaft may thus function as a slender supporting structure for the spherical wrist, e.g., to enable the spherical wrist and its surgical instrument to be positioned close to the patient without unnecessarily obstructing the workspace. In addition, the elongated shaft may function as a transmission mechanism for the actuation forces generated by the drive assembly. Thereby, it may not be needed for the spherical wrist itself to comprise all required actuators, such as electric motors. This may reduce the size and weight of the spherical wrist, which in turn may improve the handling and controllability of the instrument and reduce cluttering at the operation site.
The surgical instruments may be a hinged surgical instrument comprising jaws. Hinged surgical instruments are known per se, and may include different types of hinged surgical instruments, e.g., with different lengths, means of manipulation, hinging points or mechanisms. In general, such hinged surgical instruments may comprise two jaws, which may by themselves also be referred to as ‘beaks’ or ‘arms’ and as a pair form a grasper, cutter, dilator or coagulator, with the surgical tool being typically hinged at the front or at the rear end of the instrument. The surgical instrument held by the surgical robotic system may be a normally-open type of surgical instrument, which may mean that in a passive, e.g., non-actuated state, the surgical instrument’s jaws may be open or even fully opened, while in an actuated state, the surgical instrument’s jaws may be closed. It is known to establish such a normally-open passive state in various ways, which in general may involve a resilient biasing element, such as a spring or an elastic hinge or a nitinol element, which may bias the jaws into the open position when no or only insufficient actuation force is applied to the surgical instrument.
The surgical instrument may be actuated towards the closed position by the drive assembly. In accordance with the above measures, this may be established by a string which may run from the drive assembly via the elongated shaft to the surgical instrument. For example, the drive assembly may ‘pull’ the string to effect a closing of the surgical instrument. The string may be preloaded, which may mean that the string may be tensioned such that a preload force is exerted on the surgical instrument even in the passive state. However, the preload force may be chosen such that it may not fully compensate for the opening force exerted by the resilient biasing element. The preload force may therefore in itself not cause actuation of the surgical instrument. In other words, the force exerted on the jaws by the resilient biasing element may be larger than the string preload force. As the tension force in the string is increased by the drive assembly, the total string force, which may equal a constant preload force and a variable actuation force, may become larger than the force of the resilient biasing element, thus resulting in a closing movement of the jaws. This may be achieved during design or setup of the surgical robotic system by suitably selecting or configuring the resilient biasing element so that the passive jaw opening force has a suitable value in relation to the preload force, and/or by suitably tensioning the preload string such that its preload force has a suitable value in relation to the preload force. Thereby, the surgical instrument may remain normally-open in the passive state.
The above clauses may use a string for actuation which also serves as a preloading element for at least the actuation of the surgical instrument. Thereby, the constant (baseline) preload force may add up to the actuation force on the jaws when the surgical instrument is actuated, or specifically, when the instrument’s jaws are closed. This may remove or at least significantly reduce play in the actuation of the surgical instrument while increasing the stiffness of the surgical instrument and thereby improving their positioning accuracy when needed, e.g., while the instrument is holding and manipulating a needle. The string may also preload the transmission mechanism contained in the elongated shaft, which may also remove or at least significantly reduce play in the actuation of the spherical wrist, in addition to reducing the play in the actuation of the surgical instrument. Effectively, the preload string may reduce play in the overall kinematic structure by which the surgical instrument is positioned and actuated. Conversely, when the actuation force and thus tension on the jaws is released, the total force exerted by the string on the overall kinematic structure may be diminished since only the constant (baseline) preload force may remain, thereby reducing friction (resistance) in the mechanisms and allowing faster movements. Furthermore, also in the passive state of the surgical instrument, e.g., when the jaws are opened, the preload force may remove or at least significantly reduce play in the overall kinematic structure so as to establish a certain baseline precision.
In accordance with clause 2, to transmit the actuation forces generated by the drive assembly, the elongated shaft may comprise a concentric arrangement of tubes, in which a respective tube may, by its rotation about its longitudinal axis, transmit an actuation force to the spherical wrist to effect a rotation about a respective axis of rotation. Effectively, each tube may function as a driveshaft for a respective rotational DOF. Such a concentric arrangement of tubes may be an advantageous transmission mechanism, but which may also exhibit a certain amount of play. Since the string runs through the tube assembly to the surgical instrument, the preloading of the string may also cause an axial tension to be applied to the tube assembly, which in turn may remove or at least significantly reduce play in the tube assembly. This may result in improved measurability and, consequently, positioning accuracy when actuating any rotation of the spherical wrist. As such, the rotational positioning of the surgical instrument may be carried out more accurately.
It should be noted that the above-mentioned embodiments illustrate rather than limit the invention, and that those skilled in the art will be able to design many alternative embodiments without departing from the scope of the appended claims.
In the claims or clauses, any reference signs placed between parentheses shall not be construed as limiting the claim or clause. Use of the verb “comprise” and its conjugations does not exclude the presence of elements or stages other than those stated in a claim or clause. The article “a” or “an” preceding an element does not exclude the presence of a plurality of such elements. Expressions such as “at least one of″ when preceding a list or group of elements represent a selection of all or of any subset of elements from the list or group. For example, the expression, “at least one of A, B, and C” should be understood as including only A, only B, only C, both A and B, both A and C, both B and C, or all of A, B, and C. The invention may be implemented by means of hardware comprising several distinct elements, and by means of a suitably programmed computer. In the device enumerating several means, several of these means may be embodied by one and the same item of hardware. The mere fact that certain measures are recited in mutually different dependent claims or clauses does not indicate that a combination of these measures cannot be used to advantage.
The following list of references and abbreviations is provided for facilitating the interpretation of the drawings and shall not be construed as limiting the claims.
Number | Date | Country | Kind |
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20171159.5 | Apr 2020 | EP | regional |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2021/057318 | 3/22/2021 | WO |