US20140051049A1 - Anatomical model and method for surgical training - Google Patents

Abstract

Implementations relate to anatomical models and surgical training. In some implementations, an anatomical training model includes a base portion and a top portion that form a hollow space between the base portion and top portion. A plurality of holes are positioned in the top portion. The model includes a plurality of cannula supports, where each cannula support is aligned with one or more corresponding holes in the top portion.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
• This application claims priority to U.S. Provisional Application No. 61/684,376, filed Aug. 17, 2012, and which is incorporated herein by reference in its entirety.
COPYRIGHT NOTICE
• A portion of the disclosure of this patent document contains material which is subject to copyright protection. The copyright owner has no objection to the facsimile reproduction by anyone of the patent document or the patent disclosure, as it appears in the Patent and Trademark Office patent file or records, but otherwise reserves all copyright rights whatsoever.
BACKGROUND
• Disclosed features concern medical training equipment and methods, and more particularly medical training equipment and methods used for training in minimally invasive surgical procedures and techniques.
• Minimally invasive surgical instrument port placement in a patient's anatomy, setup positioning of a minimally invasive surgical robotic system, and coupling the robotic system to cannulas positioned in the ports (“docking” the robot to the cannulas) are important tasks for surgeons and medical personnel to learn. Physical anatomic models dedicated for use in training these tasks or that provide standardized ways to evaluate these tasks do not exist. Current anatomical simulation models (e.g., from the Chamberlain Group, Limbs & Things LTD, Pacific Research Laboratories, Inc. (Sawbones®), ProMIS™ Simulator from CAE Healthcare of CAE, Inc., SimSurgery® SEP products, and the like) may simulate a portion of an abdomen, but such models do not provide features associated with these tasks or the necessary standardization required to measure performance parameters over time and populations. In some cases, for example, port locations on traditional laparoscopic models may not be appropriate for robotic surgery. Furthermore, many of the existing models have instrument handles (such as laparoscopic tool handles) rigidly attached to port locations so that robotic trocars or other components cannot be attached to the ports.
• The solutions developed thus far have not been specifically targeted to robotic surgery and instead have tried to encompass general surgery, laparoscopic surgery, and to a limited extent robotic surgery. This lack of dedicated robotic surgical training equipment has led to training exercises that are not ideally suited for the unique considerations of robotic surgery. For example, most other systems use a “skin” to lay over large openings in an abdomen model, and port locations must be placed through this large piece of skin. This situation often leads to only a single set of holes and lack of instruction through different choices, setups, etc. Students are not provided the opportunity to try various port placement patterns and to learn the benefits and disadvantages of specific patterns vis-à-vis a particular surgical task to be performed.
• During training to use a minimally invasive surgical system, many surgeons and medical personnel initially have difficulty with port placement, robot setup, and cannula docking tasks, and such difficulty may needlessly extend operating times and may even affect a surgeon's willingness to adopt such technology. In addition, personnel associated with training these tasks have identified a lack of proficiency in port placement and cannula docking as the major limiter for useful training outside of a dedicated training facility, such as at a hospital location. What is needed is dedicated training equipment and associated procedures to help surgeons and other medical personnel become proficient in these and related tasks.
SUMMARY
• Implementations of the present application relate to anatomical models and surgical training using such a model. In some implementations, an anatomical training model includes a base portion and a top portion that form a hollow space between the base portion and top portion. A plurality of holes are positioned in the top portion. The model includes a plurality of cannula supports, where each cannula support is aligned with one or more corresponding holes in the top portion. For example, each cannula support can be configured to hold a cannula that is positioned through the hole, in simulation of the various locations in a patient's body wall at which cannulas may be placed.
• Various implementations of the model are described. In some examples, the plurality of holes are greater in number than required by surgical procedures using the model. At least one of the plurality of holes can have one size to accommodate one size of instrument cannulas, and at least one of the plurality of holes can have a different size to accommodate a different size of instrument cannulas. In some implementations, the cannula supports include at least one cannula support piece positioned below one or more of the corresponding holes and above the bottom portion to simulate a patient body wall for one or more instruments inserted through at least one of the holes in the top portion. In other implementations, each of the cannula supports is positioned in a corresponding one of the plurality of holes in the top portion. For example, each of the cannula supports can include a flexible piece including an annular membrane for holding a cannula inserted through the cannula support and the corresponding hole. Some implementations can include a membrane positioned over the top portion and the plurality of holes.
• The base portion of the anatomical model can include a platform providing at least one surgical site to receive one or more instruments inserted in one or more corresponding holes in the top portion. The platform can be removable from the base portion in some implementations. The surgical site can be provided at a known position and orientation on the platform with respect to the plurality of holes to act as a fixed registration location for placement of one or more cannulas in one or more of the plurality of holes. For example, the platform can include structures at different locations of the platform to which the surgical site is operative to be attached, allowing varied positional placement of the at least one surgical site with respect to the plurality of holes in the top portion. The at least one surgical site can include, for example, a component having a soft material simulating tissue for surgical manipulating tasks, and/or a component having a curved pathway and one or more pieces moveable along the curved pathway.
• In some implementations, an anatomical training model includes a base portion including a removable platform providing at least one surgical site, and a top portion coupled to the base portion to form a hollow space between the base portion and the top portion. The top portion includes a plurality of holes each sized to receive one or more cannulas directed toward the surgical site. In various implementations, the surgical site can be provided at a known position and orientation on the platform with respect to the plurality of holes to act as a fixed registration location for placement of one or more cannulas in one or more of the plurality of holes. The platform can include structures at different locations of the platform to which the at least one surgical site is operative to be attached, allowing varied positional placement of the surgical site with respect to the plurality of holes in the top portion.
• In some implementations, a surgical training method includes measuring one or more parameters associated with one or more tasks, where the one or more tasks are performed with reference to an anatomical model and include at least one of: surgical instrument port placement, surgical robot arm setup, and cannula docking. An automatic comparison is performed between the measured one or more parameters and corresponding one or more stored parameters associated with the one or more tasks, and an evaluation is output that is based on the automatic comparison. In various implementations, the corresponding stored parameters are measured at a first time, and the measuring of the parameters is performed at a second time later than the first time. The parameters measured at the first time can be associated with a first person performing the tasks, and the parameters measured at the second time can be associated with a second person performing the one or more tasks. Alternatively, the parameters measured at the first time and the second time can be associated with a particular person performing the tasks. Outputting an evaluation can include outputting a score that is based on the time needed to perform the one or more tasks, and/or positioning or movement of surgical procedure components during the tasks.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a perspective view of an anatomical model;
• FIGS. 2A and 2B are a diagrammatic perspective views that illustrates surgical ports and associated cannula supports in an anatomical model;
• FIG. 3A is a perspective view of a cannula support;
• FIGS. 3B and 3C are perspective views of a cannula support and single site port;
• FIG. 4 is top perspective view of an anatomical model;
• FIG. 5 is a diagrammatic top view of port placement grids;
• FIG. 6 is a perspective view of a surgical robot with an anatomical model;
• FIG. 7 is a perspective view of one example of a surgical exercise task platform;
• FIG. 8 is a perspective view of another example of a surgical exercise task platform;
• FIG. 9 is a perspective view of one example of an anatomical model base portion and a surgical exercise task platform;
• FIG. 10 is a perspective view of another example of the anatomical model and a platform similar to the platform ofFIG. 8;
• FIG. 11 is a perspective view of an interior of one embodiment of an anatomical model;
• FIG. 12 is a perspective view of one example of an illustrative task exercise component for a platform similar to the platform ofFIG. 8;
• FIGS. 13A to 13H show example illustrative task exercise components which can be used for the platform in the anatomical model;
• FIG. 14 is a flow chart that illustrates an example method for evaluating patient-side surgical task exercises;
• FIG. 15 is a flow chart that illustrates an example method for evaluating surgical task operations; and
• FIG. 16 is a diagrammatic view of an example system for performing surgical exercise tasks and evaluation.
DETAILED DESCRIPTION
• The present application discloses features relating to anatomical models used in surgical procedure training exercises, and relating to methods evaluating performances of surgical procedures using an anatomical model. Various disclosed implementations of anatomical models provide and teach realistic positioning, placement, and use of cannula ports and surgical sites for particular surgical procedures. The anatomical model provides a known configuration to be used for surgical training, including positioning cannula ports and surgical sites at known, consistent locations. Implementations provide consistent and repeatable surgical task exercises to allow standardized and consistent measurement, evaluation, and comparison of performances of surgical techniques by many different trainees. Disclosed training methods include measurement and evaluation of surgical exercise tasks such as port placement, robot setup, cannula docking tasks, and surgical task operations, allowing trainees' performances to be evaluated and enabling trainees to improve their skills more efficiently.
• Some implementations are described using a robotic surgery system such as a da Vinci® Surgical System (e.g., a Model IS3000, marketed as the da Vinci® Si™ HD™ Surgical System), commercialized by Intuitive Surgical, Inc. of Sunnyvale, Calif. Knowledgeable persons will understand, however, that features disclosed herein may be embodied and implemented in various ways, including robotic and, if applicable, non-robotic embodiments and implementations. Implementations on da Vinci® Surgical Systems (e.g., the Model IS3000; the Model IS2000, commercialized as the da Vinci® S™ HD™ Surgical System) are merely exemplary and are not to be considered as limiting the scope of the inventive aspects disclosed herein.
• FIG. 1 is a perspective view of ananatomical model101 in accordance with some implementations disclosed herein. As shown, the model resembles an insufflated human abdomen and pelvic region. For example, the size and shape of themodel101 can be determined from values in medical literature and cadaver measurements. Various embodiments ofmodel101 may be sized differently to simulate various body sizes (e.g., pediatric, small female, average, large male, obese, etc.).
• The model includes atop portion102aand abase portion102b,which fit together and form an outer shell of the model. The model has a hollow interior betweentop portion102aandbase portion102b.Alternatively, the outer shell of the model is formed from a single piece, or from three or more pieces.
• Several port placement openings are formed in thetop portion102aof the model, and these openings allow one or more cannulas to be positioned in the model at various port locations. As shown in the example embodiment ofFIG. 1, the openings can include one or more sets of holes intop portion102ato allow operating instrument cannulas to pass therethrough and directed instruments toward a surgical site inside theanatomical model101. In this example, one set ofholes103 is positioned intop portion102ato accommodate cannulas for surgical instruments that are operating instruments, e.g., instruments used to contact and manipulate a simulated surgical site within the model. For example, operating instruments can include conventional laproscoping instruments and/or instruments having manipulable needle driver, stapler, scalpel, vessel sealer, scissors, forceps, grasping implements, cauterizing tools, irrigation tools, suction tools, etc. A second set ofholes104 are also positioned intop portion102ato accommodate cannulas for surgical instruments that are endoscopes or other camera instruments, e.g., instruments providing a camera and/or illumination to provide images of the surgical site to the surgeon or trainee. In some implementations, smaller camera instruments can be positioned through thesmaller holes103.
• In this example, holes104 can be positioned along a longitudinal centerline of thetop portion102a,in accordance with an aspect of a camera port placement technique that similarly positions the camera instrument port generally at a patient's abdominal centerline. In other embodiments, holes104 may be at other locations in the model. As shown, holes103 are positioned intop portion102alaterally of the model's longitudinal centerline.Holes103 simulate the various locations at which operating instrument cannulas can be placed.
• The various holes are placed to allow a trainee to place surgical instrument ports in the model in accordance with recommended surgical instrument port placement for various robotic surgery procedures, such as radical prostatectomy, radical hysterectomy, partial nephrectomy, multi- or single-port cholecystectomy, etc. In some embodiments, one ormore holes103 and/or104 are placed inbase portion102bto simulate access to a surgical site from a direction that originates atbase portion102b.Theholes103,104 can be placed at various locations in various embodiments to accommodate the learning objective or objectives to be supported by the use of the particular model embodiment. In various implementations, the density and/or number of holes intop portion102acan vary to allow for more or fewer port location options.
• In some implementations such as the embodiment shown, there can be a greater number ofholes103,104 provided in thetop portion102athan are required for a surgical procedure (or any surgical procedures intended to be practiced using the model), so that a trainee is required to select the proper subset of holes to use in order to reach a surgical site inside the simulated patient. Thus, various port placements can be explored for a certain surgical task. In this way a surgeon can more fully understand the relative advantages and disadvantages of one port placement strategy versus another port placement strategy for a certain surgical task.
• Furthermore, theanatomical model101 provides an array ofholes103 and104 which can be specifically-tailored in their positions to surgical instruments of a particular robotic surgical system, allowing training to be provided for a robotic system using an array of port locations.
• A simulatedsurgical site platform106 can be positioned inside the model's hollow interior. As explained in more detail below,platform106, or objects placed onplatform106, may have various configurations to simulate various surgical procedures at various positions inside the model. In this way, thesingle model101 can be used for surgical port training for various different surgical procedures.
• Theanatomical model101 can also be useful for a range of other surgical task exercises. For example, the model can be used for remote center alignment of instruments with the abdomen body wall, instrument exchange, camera and instrument insertion under direct vision, other training activities related to patient side skills (suture exchange using a laparoscopic tool, retraction using a laparoscopic tool by an assistant, etc.), understanding and illustration of workspace limits by the surgical instruments, setup conditions to avoid collisions of external robot arms, etc.
• FIG. 2A is a diagrammatic perspective view that illustrates surgical ports in the model and associated cannula supports. In this example, a cannula support piece201 is placed below and aligned with a set of theholes103,104 to simulate the patient's body wall. When a cannula is inserted through ahole103 or104 and the associated piece201, the piece201 acts as a support for the cannula and holds the cannula in a manner similar to the way a patient's body wall supports a cannula (e.g., a little floppy). By simulating the way a cannula is supported by a patient's body wall, medical personnel may be trained in a realistic situation to position, align, and dock a surgical robot manipulator to an associated cannula.
• In some examples, piece201 may be made of various materials such as foam or rubber (e.g., polyurethane). Different materials having different properties (e.g., stiffness) may be used to simulate different body wall characteristics at corresponding locations on the model. For example, one material may be used to simulate the umbilicus, and a second material may be used to simulate the anterior abdominal muscles. In some implementations, piece201 is sized to have thickness to simulate the patient's body wall thickness. A relatively thicker piece201 may be used in a relativelylarger model101 to simulate a relatively larger patient, whereas a relatively thinner piece201 may be used in a relativelysmaller model101 to simulate a relatively smaller patient. In a single anatomical model, cannula support thicknesses may be varied for one or more associatedholes103 to simulate different body wall characteristics (e.g., umbilicus vis-à-vis abdominal muscle).
• Piece201 may be supplied without any perforations, so that piece201 must be pierced to insert a cannula. Alternatively, the piece201 may be supplied with one or morepreformed openings202 through which the cannulas can be placed. The preformedopenings202 allow piece201 to be reusable. As shown inFIG. 2A, in some embodiments the preformedopenings202 may be single slit or cross slit implementations. Alternatively, other openings such as circular shapes of one or more diameters may be used. In some implementations, such as implementations in foam, a thin protective plastic layer may be placed ontop surface203 of piece201 in order to increase its service life during training.
• As illustrated inFIG. 2A, in some embodiments the anatomical model is configured to allow cannula support piece201 to be removable from the top portion of the model. As shown, a piece201 can be inserted into asupport bracket204 that underlies, for example, holes103 or104. A piece201 can be cut to the shape of asupport bracket204, for example. In some implementations, a piece201 can be disposable after one or more uses. Thesupport brackets204 underlying particular sets of holes may be identically sized, so that a piece201 may be inserted into one of two ormore brackets204. Alternatively, two ormore brackets204 may be differently sized, so that a different cannula support piece201 is required for different corresponding sets of holes. In other embodiments, a support piece201 may be permanently attached under a set of holes. In some embodiments one ormore support brackets204 may have one ormore openings205 that allow a cannula or an instrument to extend through the support piece201 and into the interior space within the model. In other embodiments, one ormore support brackets204 are solid, so that a cannula or instrument cannot extend beyond the support bracket.
• In somemodel101 embodiments, different cannula support types are used for different sets of holes. For example, one cannula support type is used for a set of holes used for endoscope insertion, and a second cannula support type is used for a set of holes used for tissue instrument insertion. In one example implementation, a foam type cannula support is used in association withholes104, and a different cannula support type is used in association withholes103.
• FIG. 2B illustrates a second embodiment of the anatomical model and associated cannula supports. As shown inFIG. 2B,top portion102ais configured with a plurality ofwindow openings206 that are relatively larger thanholes103 or104. Each cannula support piece can be inserted in acorresponding support bracket204 below the surface oftop portion102aand underneathholes103 and104, similarly as described above forFIG. 2A. A benefit of such relativelylarger window openings206 is that they allow a relatively more free port placement than embodiments in which port placement is constrained by the specific locations of theholes103 or104. In some embodiments, a thin membrane207 (shown above thetop portion102ain an exploded view) is placed over the openings to simulate skin on the model. A pattern ofport locations208 may be marked onmembrane207, each location being over anopening206. Variousdifferent membranes207 may have various different port location patterns208 (e.g., one pattern per membrane, or two or more patterns per membrane) to act as port placement guides for various different surgical procedures.Such membranes207 may also include anatomical landmarks along with the port placement guides to illustrate spatial relationships between the ports and the landmarks. In some embodiments, amembrane207 is used together with an anatomical model having the relatively smaller cannula port placement holes, such asholes103 and104.
• FIG. 3A is a perspective view of another example embodiment of a cannula support that may be used in the anatomical model. In one implementation of the anatomical model, acannula support301 is aligned with and placed in eachhole103.
• In the depicted implementation,cannula support301 is a flexible piece (e.g., rubber) sized to fit intoholes103 in the model.Support301 includesgrips302 around the outer perimeter to prevent or reduce dislodgement of the support from its associatedhole103. Thesupport301 includes an annularinner membrane303 that covers a portion of ahole103, and ahole304 in the center of themembrane303. A cannula is inserted throughhole304, and a friction fit between the inserted cannula and the membrane supports the cannula. As described above, a cannula inserted throughsupport301 is a little floppy, which provides realistic simulation and associated training benefits.Support301's dimensions (e.g., thickness) and material characteristics (e.g., stiffness) may be varied to produce a simulation of different cannula support characteristics at various anatomical positions as described above.
• To assist in training, similar cannula supports301 may be distinguished from one another by various characteristics, such as markings (e.g., letters, numbers, and the like) or colors.Supports301 having a particular identifying characteristic are placed in certain holes to aid instruction in proper port locations for particular scenarios. For example, in an array of blackcolored supports301 inholes103, redcolored supports301 may be placed in a first pattern ofholes103 that correspond to proper port placement for a prostatectomy, or the redcolored supports301 may be placed in a second pattern ofholes103 that correspond to proper port placement for a partial nephrectomy.
• FIG. 3B is a perspective view of another embodiment including acannula support301 andsingle site piece310 that may be used with the anatomical model.Cannula support301 can be similarly implemented as described above forFIG. 3A, which can be designed to accommodate asingle site piece310.Single site piece310 can be a supplemental piece used for guiding multiple cannulas or instruments through asingle hole103 or104. For example,single site piece310 can be a flexible (e.g., rubber or similar material) cup-shaped piece as shown inFIG. 3B includingmultiple holes312, each hole for guiding a cannula or instrument, such as acurved cannula314 inserted inhole316. In some implementations, thesingle site piece310 can also include an interior cup portion320 for securing thesingle site piece310 to the anatomical model and/or further guiding the cannulas or instruments.FIG. 3C is a perspective view of an example of three cannulas322 (disconnected from instruments and manipulators in this example) inserted through a single hole of theanatomical model101 using asingle site piece310.
• It should be noted that althoughanatomical model101 is generally described as a shell having a hollow interior, with one or more cannula supports being positioned in relation to the shell so as to support one or more cannulas inserted through the shell, in some embodiments an anatomical model may be made without a hollow interior so that the model provides the cannula support function but not the surgical site simulation function. For example, foam or other material may fill the anatomical model's interior. Or, the model may be made of a single, solid piece, such as molded plastic or wood. In such embodiments, a support piece201 may be inserted into a corresponding opening in the anatomical model, which acts as asupport bracket204, or other cannula supports such assupports301 may be positioned on an outer surface of the model with sufficient underlying space to allow a cannula to be inserted into and held by the cannula support.
• FIG. 4. is a top perspective view of an embodiment of theanatomical model101. As shown,top portion102aincludesseveral holes103, and eachhole103 has asupport301 inserted in it.Top portion102aalso includesseveral holes104, and a portion of a foam piece is placed under and cover eachhole104. In the depicted embodiment, one or more foam pieces401 similar to piece201 described above are permanently mounted under each hole104 (e.g., with screws, as shown), and a protective plastic covering is used with preformed cross slits visible over each foam piece401. Thus, the embodiment shown inFIG. 4 is reusable. Three illustrativeoperating instrument cannulas402 are shown placed in associatedsupports301 inholes103. Although not shown, a camera instrument cannula may be similarly placed in the foam support at ahole104. A relatively larger hole104 (not shown) can in some implementations be placed intop portion102a(e.g., at a location simulating the umbilicus) to allow training for single port access to a surgical site. In some examples, the introduction of curved cannulas and the required mounting to an associated robotic manipulator can be tasks that may require training as provided byanatomical model101 and methods described herein.
• In some implementations of theanatomical model101, atop surface403 oftop portion102acan include one or more marked target locations which can act as simulated anatomy locations of a patient. In some implementations,top surface403 oftop portion102ais formed to allow such markings to be erasably made (e.g., using grease pencil, white board marker, etc.). Such markings allow a training person to draw on or mark thetop portion102ato assist training and to help medical personnel understand port placement philosophy, such as to mark port relationship relative to one another (e.g., operating instrument port spacing from camera instrument port) for various different surgical procedures. An overlying membrane, such a membrane207 (FIG. 2B) may be similarly made to allow such erasable marking. In other implementations, the marked locations are fixedly made to the top surface for standard surgical procedures that are commonly trained using themodel101.
• In training exercises, the marked locations can be used to determine which holes103 and104 should be used with reference to the marked target locations. In some example implementations of trainee selection of proper port holes, a location can be marked to simulate a location of a standard pelvic anatomy feature of a patient, and the trainee then can be required to determine which of theholes103 and104 are to be used for cannulas in a particular surgical procedure on that pelvic location. In one example of particular port placements, proper placement of a camera instrument port should be 10-20 cm away from the target location, operating instrument ports should be 8-10 cm from the camera port and other operating instrument ports, and an accessory port should be at least 5 cm away from other ports. Similarly, another location ontop portion102acan be marked for an enlarged pelvic anatomy, another location can be marked for a lateral quadrant anatomy, etc. A trainee's performance in properly selecting and placing the cannula ports can be measured, as in the training procedures described below.
• In some implementations, at least a portion of the outer shell ofanatomical model101 is made transparent to allow a person being trained to view a target surgical site within the model's hollow interior and the relation between the target surgical site the cannula port placements and robot manipulator positions that are required to properly reach the target surgical site. For example,top portion102amay be made of a clear plastic material. Likewise, an overlying membrane such as membrane207 (FIG. 2) may be made transparent for a similar purpose.
• FIG. 5 is a diagrammatic top view of possibleport placement grids501 for an overlying membrane. In some implementations, one ormore grids501 are placed on athin membrane207 that coverstop portion102aof the model. Themembrane207 covers theholes103,104 (alternatively, window openings206), and so allows a person being trained to identify proper port placement in an appropriate hole (or one or more holes) of the one ormore grids501. In some embodiments, the membrane includes one or more anatomical features, such as the umbilicus, costal margins, or the xyphoid process, and these anatomical features provide anatomical references that help medical persons understand port placement. Similar anatomical feature markings may be placed directly on thetop surface403 of the anatomical model. Such features allow a more realistic simulation of a patient.Membrane207 may be marked as a surgeon would mark a patient when determining port placement during actual surgery. When port locations are selected onmembrane207, the membrane can be pierced and cannulas inserted though the nearestunderlying holes103,104 or throughwindows206.
• Once cannulas are in place in a patient body wall, a surgical robotic manipulator can be coupled (“docked”) to each cannula, so that the manipulator controls both the cannula and an instrument that extends through the cannula and into the patient to reach the surgical site.FIG. 6 is a perspective view of an exemplarysurgical robot601 with each manipulator (one for a camera instrument and three for operation instruments, as shown) coupled to an associated cannula in the anatomical model. Acamera instrument602 can be positioned through a cannula in acenterline hole104, and theoperation instruments603 are positioned through cannulas inholes103, one on one side of the model and two on the other side of the model (one is partially hidden). To enhance the simulation of working on a patient in a surgical operating room environment,model101 is placed on an operating table604 at a location corresponding to a patient's position on the table. Different surgical procedures require various different port placements, and so a person being trained may have to position therobot601 in one location for one procedure (e.g., at the foot of the operating table as shown, simulating a location between the patient's legs) and in a second location for another procedure (e.g., beside the operating table). In some implementations,anatomical model101 may include additional anatomical features, such as appendages or portions thereof (e.g., legs, arms), other anatomical areas (e.g., head and neck, upper torso), and natural orifices (e.g., mouth, anus, vagina) to help a person being trained understand how patient position and orientation, table position and orientation, cannula placement requirements, target surgical site location(s), and robotic manipulator position and orientation are interrelated in order to provide the most effective access to a desired surgical site.
• In some examples of surgical robotic systems, a trainee surgeon can teleoperate thesurgical instruments602 and603 from a separate console (not shown) that includes various controls providing signals to thesurgical robot601 to allow manipulation of the instruments in various ways. For example, various actuators inrobot601 and controlled by the console signals can drive movement of the instruments to perform surgical tasks. Other control systems can be used in various implementations.
• FIG. 7 is a perspective view that showsplatform106 in more detail, and howplatform106 is positioned within the hollow interior space ofanatomical model101. In one aspect,various platform106 embodiments are made, each embodiment corresponding to one or more different surgical procedures at different simulated surgical site locations. For example, oneplatform106 embodiment may have a simulated surgical site located relatively more cranially than anotherplatform106 embodiment having a simulated surgical site located relatively more caudally. Two or more simulated surgical sites may be located on asingle platform106 to simulate situations in which cannulas must be positioned to provide effective endoscopic camera and tissue instrument access to the two or more sites, or to demonstrate that in certain circumstances one set of cannula positions is required to effectively access one surgical site, and a second set of cannula positions is required to effectively access a second surgical site. In some circumstances, physical limitations of the instruments and/or associated robot manipulators may indicate that one set of cannula positions required to access one surgical site at a first anatomical location (e.g., lymph nodes in the lower abdomen), and a second set of cannula positions is required to access a second surgical site at a second anatomical location (e.g., lymph nodes in the upper abdomen). Consequently, in such circumstances the robot manipulators must be decoupled (“undocked”) from cannulas in the first setoff positions, cannulas are then inserted in the second set of positioned, and the robot manipulators are then docked to the cannulas in the second set of positions.
• Platform106 embodiments may also be configured to place a simulated surgical site at various depths within the model so as to simulate working relatively near the body wall through which the cannulas are inserted (e.g., anterior access to anteriorly located tissue) or relatively far away from the body wall through which the cannulas are inserted (e.g., anterior access to posteriorly located tissue).
• Aplatform106 can be removably placed within a fixture (not shown inFIG. 7) inbase102b,and the fixture acts as a fixed registration location for the associated required port placement. Thus when a platform is selected and positioned in the model, the platform is located at a constant position. Thus the model positions surgical task exercises in the same location inside the abdomen model across surgeons or between training sessions to enable consistent and repeatable comparison of trainee performance, and persons being trained can be evaluated to ensure that port placements they select are effective for the type of surgical procedure being simulated by the selected platform.
• As shown inFIGS. 7 and 8,various platform106 embodiments can each be configured to simulate a surgical site. As shown inFIG. 7, for example,platform106 may be configured with one or more structures at various locations, such as pegs701.FIG. 8 is a perspective view of aplatform106 embodiment that is configured withseveral openings801 that can accommodate surgical task training components at various positions and/or orientations on aplatform106. A simulated surgical task can be carried out by placing one or more objects (e.g., small rings) in relation to the structures or openings, such that the structures or openings can act as templates for exercises. In another aspect, acommon platform106 is configured to accommodate various removable components that simulate a surgical site. In these aspects, one or more structures or openings (e.g., pegs701,openings801, or holder902 (FIG. 9)) are used to consistently position removable surgical site simulation components onplatform106 and thus consistently position the components inmodel101.
• FIG. 9 is a perspective view ofbase portion102bwithplatform106 mounted.Platform106 is aligned inbase portion102bby positioning it inside alignment guides901. A surgical task exercise holder902 is fixed toplatform106 or may be an integrated part ofplatform106. Various surgical task exercise holder902 embodiments exist, such as guide rails (as shown), releasable fasteners (e.g., hook and loop (Velcro®) fasteners, 3M Company's Dual Lock™ fasteners), magnets, re-adherable adhesives, and the like). Various surgical task exercise components903 may be inserted into and held by holder902 at a known, constant position and orientation, so that exercises are consistently registered by location within the anatomical model.
• Embodiments of surgical task exercise holders may include two or more components, such as one component coupled toplatform106 and a second component coupled to the first component.FIG. 10 is a perspective view and shows a second surgical task exercise holder component902a,which slides between and is held in place by the rails of the first component which is the exercise holder902 ofFIG. 9. A surgical task exercise holder902 can hold one or more various surgical task exercise components such as component902a.Such surgical task exercise components may be permanently coupled to an associated exercise holder, or they may be removably coupled to an associated exercise holder in a manner similar to the way an exercise holder may be removably coupled toplatform106.
• FIG. 10 is a perspective view of another example embodiment of theanatomical model101 and aplatform106 similar to the embodiment shown inFIG. 8.Platform106 includes asurgical site component1002 positioned at one end. Theplatform106 can be inserted into an open end of theanatomical model101 as shown. For example, theplatform106 can be slid until secured in a known position within theanatomical model101.
• FIG. 11 is a perspective view of an example interior of one embodiment of ananatomical model101. Aplatform106 similar to the one shown inFIG. 10 has been inserted and has been secured in a known position with the interior, thus placing the platform in a known position relative to theholes103 and104 in the top portion of themodel101. In some implementations, theplatform106 can be secured in the known position by aplate1102 that slides into a locking position and is secured in that position by a fastener, such asknob1103 which can be screwed in placed by a trainee. A simulated surgicalsite including component1104 is provided on one end of theplatform106 and is referenced relative to threeoperating instruments1105 that have been inserted throughholes103 and acamera instrument1106 that has been inserted through ahole104. A trainee can controloperating instruments1105 to manipulate thesurgical site component1104 similarly to a real surgical site in a patient.
• FIG. 12 is a perspective view of one example of an illustrative task exercise component for aplatform106 similar to theplatform106 ofFIG. 8.Platform106 ofFIG. 12 includesmultiple openings801 which are spaced apart by a predetermined distance in multiple directions. Anexercise component1201 can include acomponent base1202 that holds thesurgical site component1203 on a top side, and also includes a number ofpegs1204 on a bottom side of thebase1202. Thepegs1204 are spaced to fit in theopenings801 of theplatform106. In this way, theexercise component1201 can be positioned in any of a variety of known locations on theplatform106. Each of these locations is a known location with respect to theholes103 and104. The selected position on theplatform106 for thecomponent1201 can be input to the robotic surgery system, for example. Theexercise component1201 can be any of a variety of types of components as described below.
• FIGS. 13A to 13H show several illustrative task exercise components which can be used forplatform106, e.g., as exercise component903 ofFIG. 9 or any of the surgical site exercise components ofFIGS. 10-12. For example, each task exercise component can be removably mounted on holder902 ofFIG. 9 by, for example, sliding under mountingrails1001 of thecomponent1310 as shown inFIG. 13E. Alternatively, each task exercise component can be provided on acomponent base1202 and inserted inopenings801 ofplatform106 as shown inFIG. 12.
• Exercise component1301 ofFIG. 13A,component1302 ofFIG. 13B,component1303 ofFIG. 13C, andcomponent1304 ofFIG. 13D involve moving small pieces such as rings orbeads1305 along a curved pathway, such as acurved wire1306. Thesecurved pathways1306 can be oriented vertically (as incomponents1301 and1302), primarily horizontally (as in component1303), or a combination of these orientations (as in component1304). For example, forceps or claws on the tips of operating instruments can be used to grasp thepieces1305 and move them. In some implementations, features such as the loops incomponent1302 can require hand-off by a trainee between two instruments, such as left hand and right hand instruments.
• Exercise component1310 ofFIG. 13E can be a portion of soft material (e.g., foam) to simulate tissue for manipulation tasks. For example,component1310 can be apiece1311 of foam havingmultiple holes1312. In some surgical tasks, the trainee can be required to insert a curved needle in the holes to perform sutures.FIG. 13F shows a closeup view of a portion ofcomponent1310 used for a suturing task, where aclaw1313 attached to an operating instrument manipulated by a trainee is routing asuture thread1314 throughholes1312.
• Exercise component1320 ofFIG. 13G can include a tubular or ring-shaped portion of soft material (e.g., foam) to simulate a structure often treated by surgeons.Tube piece1321 can be held to theplatform106 by asupport1322. Anopening1323 of thepiece1321 can be exposed to allow a trainee to close the opening with sutures.FIG. 13H shows a closeup view of thetube piece1321 in which a trainee has closed theopening1322 withsuture thread1323.
• Various exercise components903 may be used to simulate various surgical tasks; components ofFIGS. 13A-13H are merely illustrative. The abilities to easily and quickly remove and insert a platform in the anatomical model and change exercise components using platform systems such as shown inFIGS. 7-12 allows theanatomical model101 to be easy to use, offering a large amount of surgical exercises for training while maintaining standardized port locations and robot setup across all exercises performed by the trainee.
• In some implementations, while a surgical robot is coupled to cannulas inserted in the anatomical model, aplatform106 embodiment may be removed from the model (e.g., without undocking the robot manipulators from the associated cannulas or removing the endoscopic camera and tissue instruments from their associated cannulas). Then, either the removedplatform106 is reconfigured with another exercise component903 or the removedfirst platform106 is replaced by asecond platform106 with a second exercise component903, so that a trainee must evaluate port placement in view of a task associated with the reconfigured ornew platform106. For example, oneplatform106 embodiment may represent prostate location, which requires one set of port placements, and anotherplatform106 embodiment may represent upper abdomen lymph node location, which may require a second set of port placements. Since theplatform106 positions are the same with reference tobase102b(i.e., within the anatomical model), the surgical site locations are in their correct relative anatomical locations with reference to the anatomical model. If a trainee chooses an incorrect port placement pattern and is then required to complete the associated exercise task, the problems associated with the incorrect port placement (e.g., robotic manipulator collisions, instruments interfering with one another, inability to reach certain locations at the surgical site, proper camera position for viewing the surgical site during the operation, etc.) are highlighted and evaluated.
• The features of the anatomical model allow a trainee to be scored during the training process, so that performance and improvement can be measured. In addition, a trainee can be scored in relation to other trainees or in relation to historic data in order to determine how well the trainee can perform the required task. Also, aggregate historical scoring may reveal that trainees have difficulty performing a certain task, and so training can be modified to improve a training program for that task.
• In some examples, there can be two main categories of the training process. One skill category can be associated with actions physically near the patient's location (e.g., robot manipulator position and orientation setup, cannula port placement, docking, and the like)—so called “patient side” activities. The second skill category can be associated with performing the surgical task (e.g., telerobotically or manually positioning an endoscopic camera and moving tissue instruments at the surgical site). Parameters associated with these two categories may be evaluated to measure trainee improvement or to compare one trainee's performance parameters to corresponding parameters demonstrated by other trainees (concurrent or historic) or by persons considered to have expert skill levels. Thus a trainee's skill level in a particular parameter may be evaluated relative to peers (e.g., to determine the trainee's progress with reference to anticipated improvement) or relative to experts (e.g., to identify deviations from a high skill level). For patient side skills training, a trainee may be scored, for example, on how well port placement is selected for a selected surgical procedure, or how long it takes to determine the correct port placement. Or, a trainee may be scored on how the surgical robot is coupled to the placed cannulas (concerning, for example, manipulator arm collision avoidance) or how long it takes a trainee to couple the manipulators to the cannulas.
• In one aspect, a trainee skill level associated with a specified parameter is automatically scored by using information obtained from a surgical robotic system. In a typical surgical robotic system, various sensors (e.g., joint position sensors, servo motor position encoders, fiber Bragg grating shape sensors, etc.) are used to determine kinematic information (position and/or orientation) associated with the robot manipulators. Consequently, a surgical task exercise scoring system may use the robot kinematic information to determine positions and orientations of instruments directed during an exercise, and thereby determine if a trainee has properly selected ports for a specific surgical task exercise. As an example of such a scoring system, a kinematic setup template is created that defines a specific effective robot manipulator position and orientation for a specific surgical task. Data associated with a trainee's surgical task exercise performance is compared against the template to create a performance score. For example, a task exercise time parameter may be measured by starting a timer at the beginning of a cannula docking exercise and stopping the timer when the surgical robotic system senses that all manipulators have been properly docked to an associated cannula. As another example, a task exercise robot manipulator collision avoidance parameter may be measured by comparing kinematic information from each docked robot manipulator against template kinematic information to determine how close a trainee has come to placing the manipulators in prescribed ideal positions and orientations or within prescribed position and orientation envelopes. Similarly, kinematic information from the robot manipulators, in conjunction with known physical dimensions of an anatomical model101 (which may be various sizes, as described above) can be used to determine if a trainee has properly positioned the cannulas in a correct port placement pattern, or if the remote center of motion for each cannula (the location on each cannula that stays stationary in space as the manipulator moves) is correctly positioned so as to minimize tissue trauma at a patient's body wall. For any evaluation, metrics may be sampled during the exercise to indicate a trainee's performance as he or she completes the exercise, and these intermediate evaluations may be plotted against a template to obtain a score. For example, historic data may indicate that specific acts should be completed in a certain order in order to most effectively complete a task, kinematic data may be used to show the actual order in which a trainee performed the acts, and differences between the recommended versus actual order of acts completed is used to determine a trainee's score.
• FIG. 14 is a flow chart illustrating an example method for evaluating surgical task exercises. The example surgical exercise depicted inFIG. 14 is associated with the first category of training categories, patient side (e.g., setup) operations.
• Inblock1401, ananatomical model101 is selected, a desired surgical task is selected, and aplatform106 associated with the selected surgical task is inserted inside the anatomical model. Theplatform106 is provided with a simulating training exercise site selected to be appropriate for the surgical task and which is positioned on the platform for port placement appropriate for the surgical task through theholes103 and104 relative to the site. Inblock1402, the anatomical model is positioned on an operating room table.Blocks1401 and1402 may be performed in any order.
• Blocks1403,1404, and1405 are example exercise actions generally for setting up a robotic surgical task, which are performed by a trainee and measured by an evaluation component. Inblock1403, a trainee selects one or more ports for surgery for a specific target anatomy represented by the model. For example, camera cannulas and operating instrument cannulas can be placed so that the desired surgical site portions are in view of a camera instrument and are in operating range of operating instruments to be placed in the cannulas. One or more cannulas can be placed in one or more of the various holes in anatomical model embodiments described above, for example. Inblock1404, the trainee positions surgical robot manipulators for docking in view of parameters such as mutual manipulator collision avoidance and required instrument range of motion. Inblock1405, the trainee docks the robot manipulators to the associated cannulas. Duringblocks1403,1404, and1405, an evaluation component of the exercise, e.g., implemented by one or more processors of the surgical robot, can measure parameters associated with the tasks performed by the trainee, such as the overall completion time of all tasks inblocks1403 to1405, completion time of particular tasks, the position and orientation of manipulators, as well as other parameters of the actions taken by the trainee. Performance parameters (and metrics determined from the parameters) can be measured at multiple times during the performance of blocks1403-1405.
• Inblock1406 an automatic evaluation of the surgical task is completed. For example, the automatic evaluation can use kinematic information from the robotic surgical system obtained during the performance ofblocks1403,1404, and1405. Such kinematic information can use remote center positions of the surgical instruments and setup joint values. The kinematic information can be compared to a template of desired or ideal kinematic information to determine if robot manipulator setup joints and other structures are properly configured to place the associated robot manipulators at a proper position and orientation, and if cannula ports are properly positioned and spaced to allow effective surgical site access with minimized manipulator collision avoidance. The ideal template information can be, for example, clustered or averaged positions, movements, and/or placements from prior performances of trainees and/or experts, or known optimal positions for instruments, robot components, etc.
• As described above, in some implementations, the trainee's performance metrics for various skill parameters are based on measurements made at multiple times during the exercise. In some implementations, the individual trainee's performance can be compared to previous or historic performance data for that trainee and/or compared to historic performance data from other trainees and/or from experts to evaluate the trainee's relative learning speed and effectiveness and/or determined the trainee's skill level.
• Inblock1407, the results of the evaluation are output. In some examples, the results can be one or more scores that indicate a performance level or skill of the trainee based on the performance in blocks1403-1405. Some implementations can provide graphical feedback indicating the level or skill. For example, graphical diagrams can be displayed on a display device indicating how close the robot manipulators are positioned to ideal or correct positions for the surgical task. Furthermore, some implementations can output real-time feedback during the performance of blocks1403-1405, such as indicators of correct or incorrect placements and positions of surgical instruments, hints to the trainee, graphical indications of correct positioning and orientation and the acceptable range of motions and placements for particular instruments, etc. Some real-time feedback can be instructional, indicating where instruments should be placed or positioned. The robotic system, anatomical model, and trainee evaluation features can also be used to provide tutorials to persons, demonstrating how to select ports, position the robot, and dock robot arms.
• Inblock1408, various further actions may be taken to continue training, such as removing oneplatform106 and replacing with asecond platform106 or second surgical task exercise, as described above, either with or without undocking the robot manipulators from the cannulas, and then the process may return to1102 or other earlier block as appropriate.
• Other patient-side tasks can also or alternatively be included in the exercise actions of blocks1403-1405. For example, static registration techniques can be trained, which are used to determine the location of the abdomen model in space relative to surgical robot system components such as one or more instruments of thesurgical robot601. In some examples, static registration can include touching theanatomical model101 in three or more known locations of the model with one of the robotic arms while recording the kinematic information sensed by sensors of the arms. This kinematic data can be used to determine the 3D location and orientation of the anatomical model relative to the robot system. For example, this allows the system to more easily determine the ports and model locations which a trainee is using and to provide directed feedback, evaluation, and scoring on such ports and how to move to the correct ports, if necessary.
• FIG. 15 is a flow chart illustrating another example method for evaluating surgical tasks. The example surgical exercises depicted inFIG. 15 are associated with the second category of training categories, surgical task operations performed at the surgical site in the anatomical model.
• Inblock1501, ananatomical model101 is selected, a desired surgical task is selected, and aplatform106 associated with the selected surgical task is inserted inside the anatomical model. The platform has a training surgical site selected and positioned as appropriate for the selected surgical task. Inblock1502, the anatomical model is positioned on an operating room table.Blocks1501 and1502 may be performed in any order.
• Inblock1503, a trainee selects ports for surgery associated with specific target anatomy, inserts the appropriate cannulas into theanatomical model101, positions the robot manipulators, and docks the robotic manipulators to the associated cannulas. In some implementations, such patient-side actions can be measured inblock1503, as described above with reference toFIG. 14.
• Inblock1504, the trainee performs the simulated training exercise at the simulated surgical site inside the anatomical training model by teleoperating the robotic surgical instruments inserted through the cannulas. An example training exercise may be ones illustrated by components ofFIGS. 13A-13H described above (e.g., suturing, manipulating objects, etc.), or one or more other simulated tasks. In some implementations, parameters are measured during the performance ofblock1504, such as completion time of one or more tasks of the exercise, and robot kinematics for computing metrics (e.g., movement volume, errors in the exercise, economy of motion of the instruments, etc.). Performance parameters (and metrics determined from parameters) can be measured at multiple times during the performance ofblock1504.
• In one example, if using a component such as shown inFIGS. 13A-13D at the surgical site, a training procedure can require that the trainee pick up aring1305 with an operating instrument, move the ring along thepathway1306 to a finish position (transferring the ring to another instrument controlled by a different hand as needed) without dropping thering1305, while moving the camera to keep the ring and instrument tips in the center of view at all times, and while repositioning controllers to keep the trainee's hands in central controlling positions. In another example, if using a suturing exercise component such as components ofFIGS. 13E-13H, the trainee can be required to drive a needle in a predetermined pathway of suture holes in the component while keeping the site in view of the camera, or suture an opening closed with spatial requirements as to the locations of the sutures.
• Inblock1505, an automatic evaluation of the surgical task is completed. For example, parameters such as overall completion time and robot manipulator movements (e.g., within a particular range of motion envelope) can be scored against template values considered to be the correct parameters. Parameters that may be evaluated may include overall completion time, time to complete a particular training exercise and/or one or more stages within an exercise, errors made (e.g., dropping an item, breaking a suture, etc.) while completing the exercise, the volume covered by control inputs during the exercise, economy of control input motion, and frequency of moving the endoscope instrument during the task.
• Inblock1506, the results of the evaluation are output indicating an estimated level or skill of the trainee for the evaluated surgical exercise. Similarly as described above forFIG. 14, some implementations can provide graphical feedback, e.g., indicating how close the operating instrument end effectors are to ideal or correct positions for the surgical task, and/or ideal locations for sutures, cuts of tissue, etc. Furthermore, some implementations can output real-time feedback during the performance ofblocks1504, such as indicators of correct or incorrect sutures, instrument positions, hints to the trainee, etc. Some real-time feedback can be instructional, indicating how instruments should be placed, moved, or positioned.
• Inblock1507, various further actions may be taken to continue training, such as removing oneplatform106 and replacing with asecond platform106 or second surgical task exercise, as described above, either with without undocking the robot manipulators from the cannulas. The process may return to a previous block, e.g.,block1502,1503, or1504, as appropriate.
• Upon completion of an exercise, the metrics may be displayed to the trainee in theoutput block1506 so that the trainee can monitor his or her progress, or can compare his or her performance against other persons from a novice to expert range. Theanatomical model101 facilitates such automated performance tracking because it allows repeatable and standardized placement of simulated training exercises regardless of instructor or trainee. Current anatomical models are inadequate for such standardized evaluation, and aspects described herein facilitate the required standardization to ensure that the exercises are identically configured for each use, thus ensuring standardized training evaluation against peers and experts. In some implementations, parameters and metrics can be displayed in real-time to the trainee during the performance of an exercise inblock1504.
• Although the above methods inFIGS. 14 and 15 refer to measuring and evaluating performances from a single trainee, these methods can also be used to measure and evaluate performances of multiple trainees at once and in various roles during a training exercise. For example, the anatomical model and surgical robot system can provide training for teams of persons, such as one or more surgeons, assistants, nurses, etc. In some examples, one or more assistant trainees can perform patient-side surgical tasks for the method ofFIG. 14 and a surgeon trainee can perform surgical operations in the method ofFIG. 15 while operating a console. Trainees other than the surgeon can use the abdomen model to practice patient-side skills (e.g. port placement, docking, system setup, camera and instrument insertion) since they will often perform these activities in the operating room. The team can also train their communication to perform and coordinate various tasks such as exchange instruments, adjust ports, pass sutures using a conventional laparoscopic tool, coordinate a uterine manipulator to assist the console surgeon, etc.
• In some implementations providing training for such teams of trainees, the evaluation and scoring methodology described above can be extended to evaluate the performance of operating room teams in addition to individual trainees. For example, various scores can be output indicating the performance level or skill for coordinated team tasks. Such evaluation can be assisted by automated metrics to track progress and compare to historical data similarly as described above. These features can help provide proficiency standards for teams to understand their efficiency and how they can improve.
• The accurate tracking and comparison of a person's skill level as described above in the described training methods can provide important metrics useful in a variety of contexts. For example, certifying bodies, such as hospital credentialing committees, may use trainee evaluations and metrics to decide if a person is qualified for various medical practice areas or programs, such as performing robotic or manual minimally invasive surgery or qualifying for medical residency programs. Industry and academic researchers may also use such metrics to determine the relative effectiveness of various training programs or personnel actions associated with the anatomical model's capabilities, so that improved training methods and improved robotic platform configurations may be developed. Standardized port placement and exercise positioning as trained using disclosed features allows for comparison between subjects and quantification of results that can be included in summary documentation submitted to the Food and Drug Administration (FDA) or other governmental or controlling organizations. The standardization also allow consistent trainee setups and scenarios to be experienced by different users, enabling understanding of how they use the system and how certain features of the system can be improved, which in turn can be important for required testing of surgical systems as well as designing improvements to the systems. In a manufacturing context, such techniques also allow consistent and repeatable tests for systems coming off of an assembly line and ensure that all such systems are tested the same way. Such techniques also enable certain exercises to be directly replicated in a computer-simulated environment (e.g., ring manipulation) and used for side-by-side comparisons of computer simulation (dry-lab) and the physical simulation used in the training exercises. This can be important for computer simulation development to ensure a computer-simulated environment represents real world dynamics appropriately and teaches the trainee the proper skills (e.g., no negative learning). Direct side-by-side comparisons of this kind have been difficult in the past because a standardized setup for the physical exercises was difficult to achieve.
• Furthermore, the anatomical model with multiple port locations enables clinical development engineers and surgeons to explore and develop new and advanced port placement options for various surgical procedures without requiring a porcine model or actual patient. This enables more thorough exploration and understanding of how new and improved port placements can be discovered. It also can help define procedure-recommended port locations for new surgical instruments, new robotic systems, etc.
• FIG. 16 is a diagrammatic view that illustrates aspects of anexample system1600 which can be used for surgical exercise tasks and automated evaluation and scoring of surgical task exercises. As shown inFIG. 16, amedical device1601 is used, which can be a robotic surgical system or other system that is capable of providing data concerning the position and/or orientation of one or more medical devices, such as a system includingsurgical robot601. Themedical device601 provideskinematic information1602 to be stored in amemory1603 that is included in ascoring system1604.Kinematic information1602 can include performance parameters for a trainee's performance, as described above.Information1602 may be provided, for example, via an application program interface (API) interface in a surgical robotic system. Thekinematic information1602 can be provided from a patient-side cart component (e.g., including cannulas, arms, and other features as shown inFIG. 6), and or theinformation1602 can be provided from other components of the surgical robotic system, such as kinematic information describing position and/or orientation of controls for a operator (such as a surgeon or trainee) on a surgeon console used to manipulate surgical instruments provided on the patient-side cart. For example, such controls can include levers, joysticks, knobs, or other manipulandums moveable by the operator in one or more degrees of freedom.
• In some embodiments, anatomical model information1605 (e.g., physical dimensions, locations of possible cannula ports, location of surgical manipulators or instruments, etc.) associated with ananatomical model101 is also input to thememory1603. And,template information1606 is input intomemory1603, indicating baseline, desired, and/or correct parameters and data for comparison to trainee performance parameters. Other parameter information can also be stored inmemory1603, such as data processed fromkinematic information1602 and event data, e.g., recorded times related to trainee tasks and task completions, etc., and which can be collected and/or determined by other components ofsystem1600 such asprocessor1607, sensors of the system, etc. Thus,memory1603 as depicted is symbolic of one or more physical memory locations that can store information thatscoring system1604 uses to carry out an evaluation of a trainee's performance. Such an evaluation is executed byprocessor1607, which is likewise symbolic of one or more information processing devices (e.g., microprocessor(s) or other processing circuitry) that can be used to carry out the evaluation.
• The evaluation results, such as one or more scores and/or other information, can be output via anoutput device1608, such as a visible display on a display screen or other display device, a physical printout from a printer, or other output. The individual exercise results may be added to historic data1610 (e.g., depending on an input at operator selection input1609), which in turn may be used to modifytemplate information1606. In some embodiments, anoperator input device1609 enables a training system operator to input various selections related to training exercises, such as identifying a particular surgical exercise task to be carried out, and/or identifying a particular anatomical model that is being used. The scoring system can automatically select the appropriate information (e.g., proper template information1606) to use to carry out the evaluation.
• Embodiments of ascoring system1604 may be implemented, for example, on a small computer system, such as a laptop computer or other electronic device, or they may be embedded in surgical robot systems (e.g., with outputs displayed via the robot system's displays). Such scoring systems may also be networked to a central database to facilitate data collection from a number of medical devices and from a population of medical personnel (e.g., surgeons) and to facilitate data and/or scoring comparison within the trainee or surgeon population.
• In addition to use for robotic surgical system training, various features disclosed herein may be used for manual minimally invasive surgery. Scoring aspects for training can be adapted for training in such manual procedures, such as ability to reach locations at the surgical site, instrument interference, camera position, surgeon comfort, etc. Automated scoring aspects can be based on sensing a position of one or more components, such as cannulas, surgical instruments, etc. by various technologies such as machine vision, three dimensional tracking, fiber Bragg grating tether, electromagnetic position sensing, etc.
• Features of anatomical models and surgical training methods are disclosed herein. In various implementations, a standardized anatomical model can provide a known configuration to be used for surgical training. Holes and cannula support pieces can be placed at known locations in the model. Various surgical task exercises can be placed inside the interior of the anatomic model at known, consistent locations. Standardized positioning allows training metrics to be determined for various tasks, such as tasks associated with setting up a surgical robotic system to perform a specific procedure on a patient and tasks associated with carrying out the procedure. Training methods associated with the use of the standardized model allow specific parameters to be consistently measured for a population of trainees or experts. A specific trainee's measured parameters can be compared against the measured parameters of peer or expert populations or other reference data, and an evaluation can be determined and output. Furthermore, many of the metrics that can be captured with the disclosed models and methods are far greater in type and scope than what is measureable in previous and traditional laparoscopic training exercises. This can be of great advantage for analyzing, improving, and innovating surgical procedures and equipment.
• In the disclosure herein, the term “flexible” in association with a part, such as a mechanical structure, component, or component assembly, should be broadly construed. In essence, the term means the part can be repeatedly bent and restored to an original shape without harm to the part. Many “rigid” objects have a slight inherent resilient “bendiness” due to material properties, although such objects are not considered “flexible” as the term is used herein. A flexible part may have infinite degrees of freedom (DOF's). Examples of such parts include closed, bendable tubes (made from, e.g., NITINOL, polymer, soft rubber, and the like), helical coil springs, etc. that can be bent into various simple or compound curves, often without significant cross-sectional deformation. Other flexible parts may approximate such an infinite-DOF part by using a series of closely spaced components that are similar to a snake-like arrangement of serial “vertebrae”. In such a vertebral arrangement, each component is a short link in a kinematic chain, and movable mechanical constraints (e.g., pin hinge, cup and ball, live hinge, and the like) between each link may allow one (e.g., pitch) or two (e.g., pitch and yaw) DOF's of relative movement between the links. A short, flexible part may serve as, and be modeled as, a single mechanical constraint (joint) that provides one or more DOF's between two links in a kinematic chain, even though the flexible part itself may be a kinematic chain made of several coupled links. Knowledgeable persons will understand that a part's flexibility may be expressed in terms of its stiffness.
• Unless otherwise stated in this description, a flexible part, such as a mechanical structure, component, or component assembly, may be either actively or passively flexible. An actively flexible part may be bent by using forces inherently associated with the part itself. For example, one or more tendons may be routed lengthwise along the part and offset from the part's longitudinal axis, so that tension on the one or more tendons causes the part or a portion of the part to bend. Other ways of actively bending an actively flexible part include, without limitation, the use of pneumatic or hydraulic power, gears, electroactive polymer (more generally, “artificial muscle”), and the like. A passively flexible part is bent by using a force external to the part (e.g., an applied mechanical or electromagnetic force). A passively flexible part may remain in its bent shape until bent again, or it may have an inherent characteristic that tends to restore the part to an original shape. An example of a passively flexible part with inherent stiffness is a plastic rod or a resilient rubber tube. An actively flexible part, when not actuated by its inherently associated forces, may be passively flexible. A single part may be made of one or more actively and passively flexible parts in series.
• This description and the accompanying drawings that illustrate features and implementations should not be taken as limiting. Various mechanical, compositional, structural, electrical, and operational changes may be made without departing from the spirit and scope of this description and the claims. In some instances, well-known circuits, structures, or techniques have not been shown or described in detail in order not to obscure described features.
• Further, this description's terminology is not intended to limit the scope of the claims. For example, spatially relative terms—such as “beneath”, “below”, “lower”, “above”, “upper”, “proximal”, “distal”, and the like—may be used to describe one element's or feature's relationship to another element or feature as illustrated in the figures. These spatially relative terms are intended to encompass different positions (i.e., locations) and orientations (i.e., rotational placements) of a device in use or operation in addition to the position and orientation shown in the figures. For example, if a device in the figures is turned over, elements described as “below” or “beneath” other elements or features would then be “above” or “over” the other elements or features. Thus, the exemplary term “below” can encompass both positions and orientations of above and below. A device may be otherwise oriented (rotated90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted accordingly. Likewise, descriptions of movement along and around various axes includes various special device positions and orientations. In addition, the singular forms “a”, “an”, and “the” are intended to include the plural forms as well, unless the context indicates otherwise. Components described as coupled may be electrically or mechanically directly coupled, or they may be indirectly coupled via one or more intermediate components.
• Elements described in detail with reference to one implementation may, whenever practical, be included in other implementations in which they are not specifically shown or described unless the one or more elements would make an implementation non-functional or provide conflicting functions. For example, if an element is described in detail with reference to one embodiment and is not described with reference to a second embodiment, the element may nevertheless be included in the second embodiment.
• The functional methods, blocks, features, devices, and systems described in the present disclosure may be integrated or divided into different combinations as would be known to those skilled in the art. Disclosed methods and operations may be presented in a specific order, but the order may be changed in different particular implementations. In some implementations, multiple steps or blocks shown as sequential in this disclosure may be performed at least partially at the same time.

Claims (20)

We claim:

1. An anatomical training model comprising:

a base portion;

a top portion coupled to the base portion to form a hollow space between the base portion and the top portion, the top portion including a plurality of holes; and

a plurality of cannula supports, each cannula support being aligned with one or more corresponding holes of the plurality of holes in the top portion.

2. The anatomical training model ofclaim 1 wherein the plurality of holes are greater in number than required by surgical procedures using the anatomical training model.

3. The anatomical training model ofclaim 1 wherein at least one of the plurality of holes has one size to accommodate one size of instrument cannula, and at least one of the plurality of holes has a different size to accommodate a different size of instrument cannula.

4. The anatomical training model ofclaim 1 wherein the plurality of cannula supports include at least one cannula support piece positioned below one or more of the corresponding holes and above the bottom portion to simulate a patient body wall for one or more instruments inserted through at least one of the holes in the top portion.

5. The anatomical training model ofclaim 1 wherein each of the plurality of cannula supports is positioned in a corresponding one of the plurality of holes in the top portion.

6. The anatomical training model ofclaim 5 wherein each of the cannula supports includes a flexible piece including an annular membrane for holding at least one cannula inserted through the cannula support and the corresponding hole.

7. The anatomical training model ofclaim 1 further comprising a membrane positioned over the top portion and the plurality of holes.

8. The anatomical training model ofclaim 1 wherein the base portion includes a platform providing at least one surgical site to receive one or more instruments inserted in one or more corresponding holes in the top portion.

9. The anatomical training model ofclaim 8 wherein the at least one surgical site is provided at a known position and orientation on the platform with respect to the plurality of holes to act as a fixed registration location for placement of one or more cannulas in one or more of the plurality of holes.

10. The anatomical training model ofclaim 8 wherein the platform is removable from the base portion.

11. The anatomical training model ofclaim 8 wherein the platform includes a plurality of structures at different locations of the platform to which the at least one surgical site is operative to be attached, allowing varied positional placement of the at least one surgical site with respect to the plurality of holes in the top portion.

12. The anatomical training model ofclaim 1 wherein the at least one surgical site includes at least one of:

a component having a soft material simulating tissue for surgical manipulating tasks; and

a component having a curved pathway and one or more pieces moveable along the curved pathway.

13. An anatomical training model comprising:

a base portion including a removable platform providing at least one surgical site;

a top portion coupled to the base portion to form a hollow space between the base portion and the top portion, the top portion including a plurality of holes each sized to receive one or more cannulas directed toward the surgical site.

14. The anatomical training model ofclaim 13 wherein the at least one surgical site is provided at a known position and orientation on the platform with respect to the plurality of holes to act as a fixed registration location for placement of one or more cannulas in one or more of the plurality of holes.

15. The anatomical training model ofclaim 13 wherein the platform includes a plurality of structures at different locations of the platform to which the at least one surgical site is operative to be attached, allowing varied positional placement of the at least one surgical site with respect to the plurality of holes in the top portion.

16. A surgical training method comprising:

measuring one or more parameters associated with one or more tasks, wherein the one or more tasks are performed with reference to an anatomical model and include at least one of: surgical instrument port placement, surgical robot arm setup, and cannula docking;

performing an automatic comparison between the measured one or more parameters and corresponding one or more stored parameters associated with the one or more tasks; and

outputting an evaluation that is based on the automatic comparison.

17. The surgical training method ofclaim 16 wherein the corresponding one or more stored parameters are measured at a first time, and the measuring of the one or more parameters is performed at a second time later than the first time.

18. The surgical training method ofclaim 17 wherein the one or more parameters measured at the first time are associated with a first person performing the one or more tasks, and wherein the one or more parameters measured at the second time are associated with a second person performing the one or more tasks.

19. The surgical training method ofclaim 17 wherein the one or more parameters measured at the first time and the second time are associated with a particular person performing the one or more tasks the first time and the second time.

20. The surgical training method ofclaim 16 wherein outputting an evaluation includes outputting a score is based on one or more of:

the time needed to perform the one or more tasks, and

positioning or movement of surgical procedure components during the one or more tasks.

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