TRAINING SYSTEM FOR SIMULATED SURGICAL PROCEDURES ON A MECHANICAL MODEL OBJECT AND METHOD FOR ITS OPERATION

Description

[0001] The invention relates to a training system for performing surgical interventions on a mechanical model object with an anatomical specimen or a simulation unit for representing parts of the human body, comprising at least a first functional section that depicts a region of the human bone system, as well as a second functional section that simulates a region of the human soft tissue system, and with a detection device for measuring selected, time-varying parameters of the specimen or the simulation unit during a surgical training intervention, wherein the detection device comprises at least one self-contained cavity incorporated into the anatomical specimen or the simulation unit, which is filled with a fluid during a surgical training intervention, wherein the fluid in the cavities is a gas or gas mixture, wherein a pumping device is provided,which, during operation of the training system, maintains the gas or gas mixture in the cavities permanently at an overpressure p Ü that is higher than the ambient pressure p U through gas supply lines leading into the cavities, wherein the detection device contains a separate pressure sensor for each of the cavities, which is assigned to one of the cavities and permanently measures the respective current internal pressure p I in this cavity, and wherein the training system comprises a feedback module that records the current pressure data of the cavities measured by the pressure sensors, permanently determines whether the condition p Ü > p U is met for each of the cavities, and in the event of any measurement of a pressure drop in a cavity, in particular caused by a mechanical injury to the same, passes this information on to the surgeon training on the training system in a manner that is recognizable to him.

[0002] Such a training system with the above features is known from US 2014 / 0051050 A1 (= reference

[00] ), where a pneumothorax simulator is described.

[0003] DE 11 2006 003 722 B4 (= reference [0]) also describes a simulation system for surgical interventions in human and veterinary medicine.

[0004] A similar training system, but without the cavity, is described in DE 10 2018 118 918 B3 (= reference [1]). Background of the invention

[0005] In many countries, there is a significantly growing need for realistic training opportunities for both prospective and practicing surgeons to learn and perfect their surgical skills without training on physical human bodies, such as cadavers in pathology or even living patients. Surgical training opportunities using human cadavers or body parts are relatively rare, expensive to operate, and in some countries, even inaccessible due to ethical considerations or corresponding legislation.

[0006] Therefore, there is a high demand for training systems of the type defined above, with which special surgical interventions can be rehearsed and practiced under conditions that are as realistic as possible, without having to resort to human bodies, but with realistically modelled working conditions as in in-vivo situations.

[0007] The aim is always to provide a training system that allows surgeons to practice as many of the typical steps of a real operation as possible in the model and thereby improve their corresponding skills.

[0008] This applies generally to all areas of surgical art. In the specialized field of otology, in particular, the reconstruction of the ossicular chain requires considerable sensitivity and practice from the surgeon. Typically, a beginner in otorhinolaryngology has very little experience with microscopic work using delicate instruments in very confined spaces. Freedom of movement is further restricted in the bony ear canal, which is why middle ear surgery is often referred to as "keyhole surgery." Learning these skills requires precise instruction and intensive support from instructors. Ideally, a hospital would have its own temporal bone laboratory with the opportunity to work on its own specimens. However, only a few hospitals offer this facility.It is therefore important to establish and further develop training systems of the type described above as patient simulators for prospective and practicing surgeons. Special suggestions from otology

[0009] DE 10 2005 041 942 A1 (= reference [2]) describes a training system similar to that in reference [1], with a simulation unit for representing parts of the human body. However, this system does not have a second functional section simulating a region of the human soft tissue system. Only tympanoplasties are provided, but no stapesplasties, no cartilage tissue, and no soft tissue. A visual representation of the transfer function after manipulation of the training system is not provided, nor is the recorded data processed to improve teaching or monitor learning success. Furthermore, the simulation unit does not contain an accurate anatomical representation or depictions of risk structures.

[0010] A similar training system to that in reference [1], but here using an anatomical specimen, is known from the publication by G. Strauß et al., "Evaluation of a training system for temporal bone surgery with opto-electronic detection," HNO 2009 · 57:999-1009, Springer Medizin Verlag, August 20, 2009 (= reference [3]). Here, too, no imaging of human cartilage or soft tissue is performed. No manipulation via an implant is planned, nor is there a visual representation of the transfer function after manipulation of the training system. Furthermore, the recorded data is not processed, for example, for the purposes of improving teaching or monitoring learning success.

[0011] In the publication by Shawn B. Mathews et al., "Incus and Stapes Footplate Simulator," Laryngoscope 107: December 1997, 1614-1616 (= reference [4]), a simulator for the incus and stapes footplate is described, which is intended to provide a training opportunity to improve otological-surgical skills. However, the simulator does not correspond to the anatomical conditions. Furthermore, the visual parameters are not accurately reproduced, a reproduction of the transfer function is not provided, and no representation of risk structures is provided.

[0012] The same applies to the publication by AO Owa et al., "A middle-ear simulator for practicing prosthesies placement for otosclerosis surgery using ward-based materials", The Journal of Laryngology & Otology, June 2003, Vol. 117, pp. 490-492 (=Reference [5]), which describes a middle ear simulator for training the implantation of middle ear prostheses.

[0013] The same applies to the publication by Robert Mills et al., "Surgical skills training in middle-ear surgery," The Journal of Laryngology & Otology, March 2003, Vol. 117, pp. 159-163 (=reference [6]), which provides an overview of otological-surgical training options in 2002. The described setups are simulators for anatomical teaching purposes only. A reproduction of the transfer function is not intended here, nor is a depiction of risk structures.

[0014] In the article "3D Printed Pediatric Temporal Bone: A Novel Training Model", Otology & Neurotology, 2015, 36:793-795 (=reference [7]), Evan A. Longfield et al. describe a 3D-printed pediatric training model with a child's temporal bone. However, this model only includes an image of the bony part of the temporal bone. Any manipulation using an implant is not planned, nor is there a visual representation of the transfer function after manipulation. The recorded data is not processed, for example, for the purposes of improving teaching or monitoring learning outcomes. Also, there is no image of the cartilage or soft tissue, and no feedback system is available in case of injury to structures at risk.

[0015] In their publication "A new physical temporal bone and middle ear model with complete ossicular chain for simulating surgical procedures", Proceedings of the 2015 IEEE Conference of Robotics and Biomimetics, Zhuhai, China, pp. 1654-1659 (=reference [8]), the authors Konrad Entsfellner et al. describe a model for the temporal bone and the complete ossicular chain for simulating surgical procedures. Here, too, no manipulation via an implant is planned, nor is there a visual representation of the transfer function after a manipulation. The recorded data is not processed, for example, for the purposes of improving teaching or monitoring learning success. Furthermore, no imaging of the cartilage or soft tissue is planned, and no feedback system is available in case of injury to risk structures.

[0016] In their article "Development and Validation of a Modular Endoscopic Ear Surgery Skills Trainer", Otology & Neurotology, 2017, 38:1193-1197 (=reference [9]), Matthew M. Dedmon et al. describe a training system for modular endoscopic ear surgery, which, however, does not demonstrate a particularly close correspondence to the actual anatomical conditions. Furthermore, no manipulation via an implant is planned, nor is there a visual representation of the transfer function after a manipulation. No processing of the recorded data takes place, for example, for the purposes of improving teaching or monitoring learning success. Furthermore, no imaging of the cartilage or soft tissue is provided, and no feedback system is available in case of injury to structures at risk.

[0017] In their article "Modifications to a 3D-printed temporal bone model for augmented stapes fixation surgery teaching," Eur Arch Otorhinolaryngol, 2017, 274:2733-2739 (=reference

[10] ), Yann Nguyen et al. describe learning opportunities for improving stapes fixation based on modifications to a 3D-printed temporal bone model. In particular, a force sensor on the stapes is included.

[0018] In the publication "From Reconstruction to Function; Tympanoplasty Training with Real-Time Feedback", HNO 7, 2021, 69:556-561 (=Reference

[11] ), T. Beleites et al. provide an overview of risk-free tympanoplasty training with real-time feedback.

[0019] In their textbook article "Surgical anatomy and pathology of the middle ear", J. Anat. (2016) 228, pp. 338-353 (=reference

[12] ), Jan Christoffer Luers et al. generally describe the state of middle ear surgery in 2015.

[0020] Although the training system described in the reference [1] already mentioned at the beginning describes some of the feature complexes of the generic simulation unit, it cannot in principle represent an implantation and, in particular, does not provide the training surgeon with any specific information about concrete injuries to risk structures during a training procedure.

[0021] The reference [0], also mentioned above, describes a training system with many of the feature complexes defined above. In particular, the detection device comprises self-contained cavities incorporated into the anatomical specimen or the simulation unit. These cavities are filled with a fluid during a surgical training procedure and are designed to leak in a manner visible to the training surgeon if a cavity is injured.

[0022] Finally, the reference

[00] , also cited at the beginning, describes a training system with all the features defined at the beginning, namely for a surgical training of a lung treatment. Object of the invention

[0023] The present invention, in contrast, is based on the object of improving a generic surgical training system of the type described above using the simplest technical means possible, in a simple and cost-effective manner, so that the above-described disadvantages and deficiencies of known devices are at least largely avoided. The invention aims to present a training simulator that, on the one hand, offers the training surgeon visible feedback in the event of surgical errors, especially at critical points in the risk structure, and, on the other hand, is nevertheless inexpensive, compact, and easily transportable.Furthermore, if a cavity in the simulation unit is damaged, no fluid should be able to leak out and possibly cause short circuits or other damage to components of the system, but the training surgeon should still be given recognizable feedback in the event of surgical errors.

[0024] In particular, the invention is intended to present a training system with which the training of a surgical procedure on the human ear can be better monitored. Brief description of the invention

[0025] This object is achieved according to the invention, based on the features stated at the outset and in the preamble of claim 1, in a manner that is as surprisingly simple as it is effective and cost-effective to implement in that the detection device has further sensors, in particular pressure sensors, which monitor the current force input to simulated middle ear structures as well as the success of the supply with active or passive middle ear implants in the form of transfer functions and the correct installation of a hearing supply unit, for example, by the training surgeon in real time during a surgical training procedure with the training system and transmit corresponding electrical signals to the feedback module, which converts these into optical or acoustic information and passes it on to the training surgeon.

[0026] The injury to one of the cavities and the resulting pressure drop in the injured cavity is equivalent to a simulated injury to a "real" living patient during a real operation. Therefore, these cavities, filled with an overpressure p U higher than the ambient pressure p U , are essential for the anatomical learning model in the training system according to the invention and enable immediate feedback for the training surgeon.

[0027] A pumping device generates excess pressure (e.g., by drawing in ambient air) in the cavities. If the risk structures (simulated by the gas-filled cavities) are damaged during manipulation of the simulator, for example, by drilling or milling, a pressure drop occurs in the damaged cavity. This pressure drop is detected by a pressure sensor, and a corresponding message regarding the currently damaged cavity is forwarded by the feedback module via a suitable output unit to the training surgeon as feedback.

[0028] As soon as a cavity subjected to overpressure p Ü is injured during training, the pressure sensor sounds an alarm.

[0029] The pumps used will generally be selected so that they operate very quietly and with little vibration in order not to unnecessarily irritate the user of the device according to the invention.

[0030] One of the decisive advantages of the solution according to the invention is that no liquids are provided in the simulator and therefore leakage of these liquids cannot lead to electrical short circuits or damage to components.

[0031] The pressure loss Δp Ü measured during a cavity injury may be higher or lower depending on the actual extent of the injury. Therefore, the measured pressure loss Δp Ü allows a direct conclusion to be drawn about the degree of injury to the injured risk structure without the use of complex and error-prone additional light-conducting and / or electrical structures. This is a major advantage, particularly compared to the state of the art according to reference [0], in contrast to monitoring by means of electrically conductive, leaking fluid, which per seand without any further complex tools it can only indicate THAT there is an injury to a cavity, but not to what extent.

[0032] A further advantage of the positive pressure principle applied in the invention is that the pumping device does not require an additional filter unit, since water or particles cannot enter the pumping device. If a cavity is damaged, the pump simply continues pumping, thus maintaining an—albeit somewhat lower—positive pressure in the damaged cavity. Any contamination, as with the use of liquid, need not be feared or prevented.

[0033] This innovative design with gas-filled, pressurized cavities and the resulting functionality of the training system according to the invention ensures that the surgical technique being practiced is anatomically correct and realistic, at least with regard to the risk structures. Any technical errors made by the training surgeon can be immediately highlighted to the trainee if a risk structure is injured during the training procedure. This allows the training surgeon to learn the practical skills required for surgery in a realistic manner, and the risk of serious injury during a subsequent real operation on a living patient can be significantly reduced.

[0034] The patient simulator according to the invention precisely replicates the anatomical requirements of bone tissue, soft tissue, and tendons. Simulation modules for vessels and nerve fibers, filled with pressurized gas, give the surgeon a real-life feel and help reduce errors in later practice, thus improving patient comfort. The simulator offers a very good and, above all, risk-free training option, especially for inexperienced physicians.

[0035] Further particular advantages of the device according to the invention compared to the prior art include: Ease of use :

[0036] The training system according to the invention also has a feedback module which indicates any surgical errors that may occur during the training procedure by the surgeon. Precision:

[0037] The production of the training system, for example, using 3D printing processes based on CT data for 3D printing, enables a very precise and anatomically correct replication of the actual conditions in "real" surgeries. Models with sensors can be specifically manufactured for the surgical treatment of specific physiological and anatomical disorders to be trained, for example, special right / left models or pediatric temporal bone models.

[0038] All model structures in the training system according to the invention are also realistically represented with regard to their surfaces: 1. moist 2. dry 3. adhesive (e.g. implants) 4. correct Shore hardness 5. realistic color(s)

[0039] This allows qualitative and reproducible scenarios of real surgical situations and applied surgical techniques to be recreated quite precisely and quantitatively true to the original on living (or even dead) patients. Security:

[0040] With the training system according to the invention, training is always conducted outside of a "real" surgery on a living or dead patient. In particular, this reliably avoids the risk of contamination or the transmission of pathogens, for example, from human specimens to the surgeon.

[0041] The scale between the real patient anatomy and the training simulator according to the invention will generally be 1:1. Preferred embodiments of the invention

[0042] Embodiments of the training system according to the invention are advantageous in which the gas in the cavities is dry and non-corrosive, in particular air, which can preferably be taken from the environment of the training system with the aid of the pumping device.

[0043] This effectively prevents corrosive attack on parts of the simulation unit. The simplest and most cost-effective method is to extract plain ambient air. However, this air can also be dried before use, for example, by passing it through a suitable filter or desiccator.

[0044] In any case, the gas or gas mixture used should contain only physiologically safe, especially non-toxic substances. This minimizes the risk of injury and / or even poisoning to the surgeon undergoing surgery.

[0045] Very particularly preferred embodiments of the invention are characterized in that the pumping device is designed such that it keeps the overpressure p Ü in the cavities constant during operation, at least as long as there is no mechanical damage to a cavity.

[0046] In this way, consistent operating conditions are ensured, especially in connection with the detection of cavity injuries.

[0047] Preferably, the overpressure p Ü in the cavities (13) will be between 100 hPa and 500 hPa, in particular at about 300 hPa, above the ambient pressure p U.

[0048] On the one hand, the pumping device used to generate an overpressure p Ü in this range does not need to be particularly strong, so that even cost-effective, smaller, and above all, more compact pumps can be selected for this purpose. On the other hand, this "relatively light" overpressure is usually sufficient for safe operation of the training system with reliable indication of cavity injuries.

[0049] Embodiments of the training system according to the invention are particularly preferred in which the pumping device comprises one or more pumps with a variably adjustable flow rate. This provides an important parameter for setting the optimal operating conditions of the device. In particular, the variably adjustable flow rate facilitates the detection of leaks in the event of a cavity injury, or even makes it possible in the first place.

[0050] Also advantageous is a class of embodiments of the invention which are characterized in that the pumping device comprises one or more low-vibration micropumps, in particular miniaturized double diaphragm pumps.

[0051] The micropumps ensure the overpressure p Ü in the cavities and set a defined pressure in the cavities. The micropumps are typically designed as miniaturized double-diaphragm pumps.

[0052] In preferred developments of this class of embodiments, the double diaphragm pumps can be operated with two piezo actuators each.

[0053] These piezo actuators are particularly space- and energy-saving.

[0054] In advantageous embodiments of the training system according to the invention, the pressure sensors are temperature-compensated.

[0055] This ensures consistent operation of the device even under fluctuating environmental conditions.

[0056] Preferably, the sensors are calibrated over a temperature range of 0 °C to 50 °C.

[0057] According to the invention, these sensors measure the overpressure p Ü in the cavities and cover a range of up to 15 psi with a total error band of ±1.5 %FSS.

[0058] Also preferred is a class of embodiments of the invention in which the pressure sensors used comprise one or more piezo-resistive sensors, preferably miniaturized silicon pressure sensors.

[0059] The performance of the simulation unit and the pump system can be enhanced by using integrated microsensors. These are preferably piezoresistive silicon pressure sensors. With a typical size of only 8 mm x 7 mm, these microsensors are relatively small and compact, which also has a positive effect on the overall size of the device according to the invention.

[0060] In particularly preferred developments of this class of embodiments, the pressure sensors contain an application-specific integrated circuit (="ASIC") which preferably calibrates the pressure sensors for sensor offset, sensitivity, accuracy and / or temperature influences.

[0061] The ASIC allows pressure sensors to be calibrated and temperature compensated for sensor offset, sensitivity, temperature effects, and accuracy. Calibrated pressure output values ​​are typically updated at approximately 1 kHz for analog and 2 kHz for digital applications. An ASIC can be safely used in contact with dry and non-corrosive gases.

[0062] Further advantageous embodiments of the invention are characterized in that the gas supply lines comprise one or more, preferably optically transparent, silicone tubes, in particular Tygon tubes with wall thicknesses and inner diameters in the order of 1 mm each.

[0063] This means that the gas supply lines fit perfectly with the micro pumps described above.

[0064] The preferred tubing material is suitable for use in medical-technical applications, as well as in the food and drinking water industries. It can be used for both liquids and gases. The tubing material offers a special property: permanent temperature resistance up to +200°C. Furthermore, silicone tubing is highly resistant to weather influences (e.g., ozone or UV light) and insensitive to moisture or the associated oxidation. Finally, it has a tensile strength of 11 N / mm².

[0065] The second functional section of the anatomical specimen or the simulation unit may additionally have a sub-functional section that simulates a region of the human nervous system and / or the human tendon system and / or the human vascular system and / or typical pathological diseases, which form the basis for the patient-free training for performing surgical procedures possible with the training system.

[0066] Of particular practical advantage are variants in which at least some of the cavities form part of the sub-functional section which simulates an area of ​​the human soft tissue system, wherein the sub-functional section is incorporated into the first functional section which depicts an area of ​​the human bone system, and wherein these cavities are geometrically designed in such a way that they realistically simulate certain risk structures of the human soft tissue system, in particular the sigmoid sinus (venous blood vessel in the brain) and / or the facial nerve (facial nerve) and / or the internal carotid artery (part of the blood supply to the brain) and / or the dura (outermost meninges) and / or the labyrinth block and / or the ossicles (chain of auditory ossicles).

[0067] Special developments of these variants are characterized in that one of the cavities in the sub-functional section simulates the sigmoid sinus in the form of an S-shaped, self-contained tube, which has an inner diameter between 1 mm and 5 mm, preferably about 3 mm, and an outer diameter between 2 mm and 8 mm, preferably about 6 mm, and is arranged along a region in the first functional section which simulates the posterior edge of the human petrous bone pyramid.

[0068] Alternative or supplementary variants are characterized in that one of the cavities in the sub-functional section simulates the facial nerve in the form of a curved, self-contained tube, which has an inner diameter between 1 mm and 3 mm, preferably about 1.5 mm, and an outer diameter between 3 mm and 7 mm, preferably about 5 mm, and is arranged along a region in the first functional section, which porus acusticus internus of the human temporal bone.

[0069] In a further variant, one of the cavities in the sub-functional section simulates the dura in the form of a curved, flat, self-contained cavity which has a surface area between 7 mm and 13 mm, preferably about 10 mm, and an outer diameter between 3 mm and 7 mm, preferably about 5 mm, and is arranged around an area in the first functional section which simulates the human middle ear and the inner ear.

[0070] Particularly preferred embodiments of the training system according to the invention are also those characterized in that the anatomical preparation or the simulation unit has a third functional section that simulates a region of the human cartilage system, in particular a part of the human ear.

[0071] To date, no simulator system has been described that simulates both bone and soft tissue, as well as cartilage. This is particularly important for applications in otology, where both bone and cartilage, as well as vessels, nerves, and other soft tissues, must be treated during a real operation.

[0072] The ossicular chain is mobile and various middle ear surgeries and implantations can be performed: Implantation of active middle ear hearing aids Tympanoplasty (according to Wullstein type 1 - 5) Stapesplasty Eardrum reconstructions Insertion of tympanic tubes

[0073] All of these and many other surgical procedures can be ideally planned and performed using the training system according to the invention. Thanks to the real-time feedback it provides during the training procedure, the training surgeon's treatment success (or failure) can be easily visualized, recorded, and even presented for teaching purposes afterward.

[0074] An embodiment of the invention is particularly ergonomically advantageous in which the materials used in the functional sections and, if applicable, in a sub-functional section have essentially the same haptic properties as the human models, in particular when milling bones or when cutting and suturing soft tissue.

[0075] For example, parts of bone models, such as the auditory ossicles, can be coated with silicone, preferably silicone rubber with a Shore hardness of 40 A. A model of the stapedius tendon (musculus stapedius) can be made of silicone. A model of an eardrum, for example, can be made of silicone rubber with a Shore hardness of 20 A and a thickness of approximately 0.1 mm, while the oval window can be made with a Shore hardness of 10 A and also approximately 0.1 mm thick.

[0076] The medial wall of the middle ear and the auditory ossicles are coated with a transparent, sticky, and hydrophilic layer. This replicates the natural adhesion forces prevalent in the human temporal bone.

[0077] In principle, it is possible to depict various and completely different clinical pictures and age groups.

[0078] Particularly preferred is also a class of embodiments of the training system according to the invention which are characterized in that the training system comprises a feedback module which can record further parameter data measured by the detection device and evaluate it by means of an expert system and / or artificial intelligence and can transmit to the surgeon during a surgical training procedure information based on the measured parameter data for improving the current procedure.

[0079] The feedback module thus detects mechanical damage to the cavities caused by pressure loss at the respective valves and signals to the training physician which risk structure is affected. The magnitude of the measured pressure loss indicates the extent of damage to risk structures. The classification distinguishes between minor injury, moderate damage, and total destruction of the risk structure.

[0080] Individual successes and failures of the training surgeon during the practice procedure can thus be recorded and immediately communicated via a processing and display unit, but in particular can also be stored and lead to targeted recommendations for improvement for future operations.

[0081] The present invention also includes a method for producing a training system of the type according to the invention described above, which is characterized in that the cavities of the detection device are produced by means of a 3D printing process in a hollow and tubular manner, preferably on the basis of high-resolution CT data sets of originals of the regions of the human body to be simulated, wherein the cavities are printed in one operation with the first functional section, which depicts a region of the human bone system.

[0082] The simulators according to the invention should be able to produce CT-compatible images (even after manipulation) to ensure objective control of the results. Various materials with the same reference (e.g., an implant or another object visible in the CT image) are tested in the CT scan.

[0083] The simulators should require little or no manual labor during production and be able to be separated and assembled into individual, easily assembled modules. Since the components must be easily separable, they are best not joined with glue or even welded.

[0084] Models for auditory ossicles, for example, are printed 20% smaller and then covered with a layer of silicone and connected together.

[0085] Finally, the present invention also includes a method for operating a training system of the type according to the invention described above during a surgical training procedure on the training system, which is characterized by the following steps: A training surgeon performs a surgical training procedure on the mechanical model object of the training system with the simulation unit for representing parts of the human body using an invasive surgical instrument, in particular using a scalpel, a drill, or a milling cutter. If a cavity (in particular one incorporated into the second functional section simulating an area of ​​the human soft tissue system) is injured by the training surgeon during the surgical training procedure, the pressure sensor assigned to this cavity measures a resulting pressure drop in this cavity and reports it to the feedback module. The feedback module informs the surgeon that the condition p Ü > p U is no longer met for each of the cavities and, in particular, which cavity is affected.

[0086] In special variants of the invention, the surgical training procedure is used to train a specific surgical procedure in otology by means of the invasive surgical instrument used, in particular an endaural or retroauricular opening, the insertion of active middle ear implants as well as passive implants, such as a tympanoplasty, a myringoplasty, a stapesplasty, a stapedectomy, a stapedotomy and / or a correction of pathological diseases, for example cholesteatoma removal.

[0087] The surgical training procedure can be trained or validated by specialist personnel using robot assistance.

[0088] In further special variants of the invention, the surgical training procedure uses sensors to visualize the hearing transmission being treated. The measured signal amplitudes and frequency responses allow implantation successes and implantation errors to be displayed in real time.

[0089] Further features and advantages of the invention will become apparent from the following detailed description of exemplary embodiments of the invention with reference to the figures of the drawing, which illustrate details essential to the invention, as well as from the claims. The individual features can be implemented individually or in combinations in variants of the invention. The embodiments shown and described are not to be understood as an exhaustive list, but rather are exemplary in nature for describing the invention. Detailed description of the invention and drawing

[0090] The schematic drawing shows embodiments of the invention, which are explained in more detail in the following description.

[0091] In detail: Fig. 1 shows a functional representation of an embodiment of the training system according to the invention with a simulation unit in a spatial sectional view, a schematic cavity with a pressure sensor, a schematic pumping device with a gas supply line to the cavity, a schematic feedback module, and a schematic processing and display unit; Fig. 2a shows an embodiment of the simulation unit according to the invention in a plan view from the side in the direction of the auricle; Fig. 2b shows a schematic sectional view of the embodiment of Fig. 2a rotated by approximately 70° to the right; Fig. 2c the sectional view of Fig. 2b, but without a large part of the first functional section, which depicts an area of ​​the human bone system, so that the view is clear to the second functional section, which depicts an area of ​​the human soft tissue system; Fig. 2dwie Fig. 2a , but rotated approximately 120° to the right; Fig. 3 an enlarged detail from Fig. 2b with a schematic replica of the human middle ear; and Fig. 4 shows a possible embodiment of the cavities according to the invention in the open state (thus initially without compressed gas filling).

[0092] The embodiments of the invention shown schematically but partly in detail in the figures of the drawing Training system 10 are used to carry out surgical interventions on a mechanical model object with an anatomical specimen or a Simulation Unit 11 for displaying parts of the human body. The simulation unit 11 comprises at least one first functional section 12',which depicts an area of ​​the human bone system, as well as a second functional section 12", which simulates a region of the human soft tissue system. Furthermore, a detection device is provided for measuring selected, time-varying parameters of the specimen or the simulation unit 11 during a surgical training procedure. The detection device comprises at least one self-contained sensor incorporated into the anatomical specimen or the simulation unit 11. Cavity 13 which is filled with a fluid during a surgical training procedure.

[0093] The training system 10 according to the invention is characterized in that the fluid in the cavities 13 is a gas or gas mixture; that a Pumping device 21 which, during operation of the training system 10, can be removed by means of cavities 13 Gas supply lines 22the gas or gas mixture in the cavities 13 is permanently maintained at an overpressure p Ü higher than the ambient pressure p U ; that the detection device has a separate pressure gauge for each of the cavities 13 Pressure sensor 23 which is assigned to one of the cavities 13 and permanently measures the respective current internal pressure p I in this cavity 13; and that the training system 10 is a Feedback module 15 which records the current pressure data of the cavities 13 measured by the pressure sensors 23, permanently determines whether the condition p Ü > p U is met for each of the cavities 13 and, in the event of a pressure drop being measured in a cavity 13, in particular caused by a mechanical injury thereto, passes this information on to the surgeon training on the training system 10 in a manner that is recognizable to him.

[0094] The pumping device 21 can be configured to maintain the overpressure p Ü in the cavities 13 constant during operation, at least as long as there is no mechanical damage to a cavity 13. The overpressure p Ü in the cavities 13 is between 100 hPa and 500 hPa, preferably approximately 300 hPa, above the ambient pressure p U . The pumping device 21 can comprise one or more pumps with variably adjustable flow rates. The pumps can be designed as low-vibration micropumps, in particular miniaturized double-diaphragm pumps, and are preferably operable with piezo actuators.

[0095] The pressure sensors 23 are preferably temperature-compensated and can comprise one or more piezoresistive sensors, preferably miniaturized silicon pressure sensors. Not specifically shown in the drawing are embodiments in which the pressure sensors 23 contain an application-specific integrated circuit (ASIC), which preferably calibrates the pressure sensors 23 for sensor offset, sensitivity, accuracy, and / or temperature influences.

[0096] The gas supply lines 22 may comprise one or more, preferably optically transparent, silicone tubes, in particular Tygon tubes with wall thicknesses and inner diameters in the order of 1 mm each.

[0097] The anatomical preparation or the simulation unit 11 preferably has a third functional section 12‴ that replicates an area of ​​the human cartilage system, specifically a part of the human ear.

[0098] The materials used in the functional sections 12'; 12"; 12‴ and, if applicable, in a sub-functional section have essentially the same haptic properties as the human models, in particular when milling bones or cutting and suturing soft tissue.

[0099] Furthermore, the design of Fig. 1 the detection device of the training system 10 a additional sensor 14 which, during a surgical training procedure with the training system 10, monitors the current force input to simulated middle ear structures 17; 17a; 17b; 17c; 17d, as well as the success of the provision of active or passive middle ear implants by the training surgeon in real time and transmits corresponding electrical signals to the feedback module 15, which converts these into optical or acoustic information and forwards them to the training surgeon.

[0100] As in Fig. 1Schematically illustrated, the training system 10 comprises a feedback module 15, which evaluates parameter data measured by the detection device and transmits information based on the measured parameter data to the surgeon during a surgical training procedure, particularly by means of an expert system and / or artificial intelligence, for improving the current procedure. The feedback module 15 serves to receive and transmit analog, possibly also digital, electrical signals from the detection device, particularly from the pressure sensors 23, but also from the additional sensors 14, as well as to filter and digitize them. These signals are converted into optical or acoustic information and transmitted to the training surgeon.

[0101] There is also a Processing and display unit 16This handles the processing of analog and / or digital information and, if necessary, draws on an expert system and / or artificial intelligence. This enables error diagnosis and simultaneous visualization of current work results during surgical training. A storage unit is also preferably provided to further improve learning success monitoring through comparison options.

[0102] Fig. 2a shows an embodiment of the simulation unit 11 according to the invention in a plan view from the side in the direction of an auricle as a component of the third functional section 12‴ for simulating a region of the human cartilage system.

[0103] In Fig. 2b is a sectional view AA of the embodiment of Fig. 2awith a right rotation of approximately 70°. The simulation unit 11 shown corresponds to the left section of the functional diagram of the training system according to the invention according to Fig. 1 The simulated bone structures in the first functional section 12', the simulated soft tissue structures of the second functional section 12" as well as the simulated cartilage structures of the third functional section 12" with a model of the human auricle are clearly visible. Also clearly visible is one of the closed cavities 13 according to the invention with a gas filling (not visible in the drawing).

[0104] To allow a clear view of the second functional section 12", which simulates a part of the human soft tissue system, Fig. 2c the sectional view of Fig. 2b without a large part of the first functional section 12', which depicts a region of the human bone system.

[0105] In this embodiment, the second functional section 12" of the simulation unit 11 has a sub-functional section that simulates a region of the human nervous system and the human vascular system. It is precisely such a special sub-functional section that forms the basis for the patientless training for performing surgical procedures possible with the training system 10.

[0106] This sub-functional section is incorporated into the first functional section 12', which represents a region of the human bone system. At least some of the sub-functional sections are realized as closed cavities 13 according to the invention, filled with compressed gas. These cavities are geometrically designed to realistically simulate certain risk structures of the human soft tissue system, in the present embodiment in particular the facial nerve 12a" as well as the internal carotid artery 12b". The facial nerve12a" is in the form of a curved, self-contained tube, which has an inner diameter between 1 mm and 3 mm, preferably about 1.5 mm, and an outer diameter between 3 mm and 7 mm, preferably about 5 mm, and is arranged along a region in the first functional section 12', which porus acusticus internus of the human petrous bone.

[0107] Fig. 2d illustrates the same embodiment as Fig. 2a , but rotated by approximately 120° to the right, so that the simulation unit 11 - in a non-sectioned representation - can be seen looking frontally at the simulated human ear approximately parallel to the plane of the auricle.

[0108] In Fig. 3 is an enlarged detail from Fig. 2b with a schematic Replica of the human middle ear 17 In particular, this model contains realistically modelled components of the human ossicular chain, the Stapes 17a, the Incus 17b, the Malleus 17c as well as the Eardrum 17d.

[0109] As a result, the simulation unit 11 modified according to the invention can be trained in a specific surgical procedure of otology during a surgical training procedure using a typical invasive surgical instrument, in particular an endaural or retroauricular opening, the insertion of a tympanoplasty, a myringoplasty, a stapesplasty, a stapedectomy, a stapedotomy and / or a cholesteatoma removal.

[0110] Fig. 4 Finally, in enlarged detail, shows a possible embodiment of the cavities 13 according to the invention in the open state without gas filling. Two Openings 13'; 13".At least one of these serves to fill the cavity 13 with gas or gas mixture. After the gas has been introduced, all openings 13'; 13" except for the one connected to the pumping device 21 are sealed fluid-tight, for example, thermally, preferably by exposure to UV radiation. However, the use of sealing plugs—not shown in the drawing—is also possible.

[0111] The cavities 13 of the detection device are first produced hollow and tubular using a 3D printing process, preferably based on high-resolution CT data sets of originals of the human body regions to be simulated. The cavities 13 are preferably printed in a single operation with the first functional section 12', which depicts a region of the human skeletal system.

[0112] A typical surgical training procedure using the training system 10 according to the invention is characterized in that a training surgeon practices the textbook procedure of such an operation on the simulation unit 11 modified according to the invention by means of an invasive surgical instrument, in particular by means of a scalpel, a drill or a milling cutter.

[0113] If a cavity 13 incorporated into a second functional section 12" simulating one area of ​​the human soft tissue system is injured by the training surgeon during the surgical training procedure, compressed gas escapes from the injured cavity 13 and the associated pressure sensor 23 detects an overpressure in the cavity 13 that is lower than the specified operating pressure and reports this to the feedback module 15. The feedback module then informs the surgeon that the condition p Ü > p U is no longer met for each of the cavities 13 and, in particular, which specific cavity 13 is affected. The training surgeon can then attribute this to an injury to the section of the soft tissue anatomy modeled with the corresponding cavity 13, in particular a vein, tendon, muscle, or nerve, caused by the invasive surgical instrument used. List of reference symbols:

[0114] 10Training system 11Simulation unit 12'First functional section (bone system) 12"Second functional section (soft tissue system) 12a"Facial nerve 12b"Internal carotid artery 12‴Third functional section (cartilage system) 13Cavity(ies) 13'; 13"Opening(s) 14Further sensor(s) 15Feedback module 16Processing and display unit 17Middle ear simulation 17aStapes 17bIncus 17cMalleus 17dEardrum 21Pump device 22Gas supply line(s) 23Pressure sensor(s) Reference list

[0115] Publications considered for the assessment of patentability:

[00] US 2014 / 0051050 A1 [0] DE 11 2006 003 722 B4 [1] DE 10 2018 118 918 B3 [2] DE 10 2005 041 942 A1 [3] G. Strauß et al., "Evaluation of eines Trainingssystems für die Felsenbeinchirurgie mit opto-elektronischer Detektion", HNO 2009 · 57:999-1009, Springer Medizin Verlag, 20. August 2009 [4] Shawn B. Mathews et al., "Incus and Stapes Footplate Simulator", Laryngoscope 107: December 1997, 1614-1616 [5] A. O. Owa et al., "A middle-ear simulator for practicing prosthesies placement for otosclerosis surgery using ward-based materials", The Journal of Laryngology & Otology, June 2003, Vol. 117, pp. 490-492 [6] Robert Mills et al., "Surgical skills training in middle-ear surgery", The Journal of Laryngology & Otology, March 2003, Vol. 117, pp. 159-163 [7] Evan A. Longfield et al., "3D Printed Pediatric Temporal Bone: A Novel Training Model", Otology & Neurotology, 2015, 36:793-795 [8] Konrad Entsfellner et al., "A new physical temporal bone and middle ear model with complete ossicular chain for simulating surgical procedures", Proceedings of the 2015 IEEE Conference of Robotics and Biomimetics, Zhuhai, China, pp. 1654-1659 [9] Matthew M. Dedmon et al., "Development and Validaton of a Modular Endoscopic Ear Surgery Skills Trainer", Otology & Neurotology, 2017, 38:1193-1197

[10] Yann Nguyen et al., "Modifications to a 3D-printed temporal bone model for augmented stapes fixation surgery teaching", Eur Arch Otorhinolaryngol, 2017, 274:2733-2739

[11] T. Beleites et al., "Von der Rekonstruktion zur Funktion; Tympanoplastik-Training mit Real-Time Feedback", HNO 7, 2021, 69:556-561

[12] Jan Christoffer Luers et al., "Surgical anatomy and pathology of the middle ear", J. Anat. (2016) 228, pp338-353.

Claims

1. Training system (10) for carrying out surgical procedures on a mechanical model object, which training system has an anatomical specimen or a simulation unit (11) for depicting parts of the human body, comprising at least a first functional portion (12') which represents a region of the human bone system, and a second functional portion (12") which simulates a region of the human soft tissue system, and which training system also has a detection device for measuring selected, time-varying parameters of the specimen or of the simulation unit (11) during a surgical training procedure, the detection device comprising at least one self-contained cavity (13) incorporated into the anatomical specimen or into the simulation unit (11), which self-contained cavity is filled with a fluid during a surgical training procedure, the fluid in the cavities (13) being a gas or gas mixture; a pump apparatus (21) being present which, during operation of the training system (10), through gas supply lines (22) which feed into the cavities (13), constantly maintains the gas or gas mixture in the cavities (13) at a higher overpressure pÜ than the ambient pressure pu, the detection device containing a separate pressure sensor (23) for each of the cavities (13), each pressure sensor being assigned to one of the cavities (13) and constantly measuring the relevant current internal pressure pI in this cavity (13); and the training system (10) comprising a feedback module (15) which receives the current pressure data, measured by the pressure sensors (23) of the cavities (13), constantly determines whether the condition pÜ > pu is fulfilled for each of the cavities (13) and, in the event of a pressure drop in a cavity (13) being measured, in particular caused by mechanical damage to the cavity, passes this information on to the surgeon training on the training system (10) in a manner that is recognizable to the surgeon, characterized in that the detection device has additional sensors (14) which, during a surgical training procedure using the training system (10), monitor the current force input to simulated middle ear structures (17; 17a; 17b; 17c; 17d) as well as the success of fitting active or passive middle ear implants by the training surgeon in real time and transmit corresponding electrical signals to the feedback module (15), which converts these into optical or acoustic information and passes them on to the training surgeon.

2. Training system according to claim 1, characterized in that the gas in the cavities (13) is dry and non-corrosive, in particular air which can preferably be taken from the surroundings of the training system (10) by means of the pumping apparatus (21).

3. Training system according to either claim 1 or claim 2, characterized in that the pumping apparatus (21) is designed to constantly maintain the overpressure pÜ in the cavities (13) during operation, at least as long as there is no mechanical damage to a cavity (13).

4. Training system according to any of the preceding claims, characterized in that the overpressure pÜ in the cavities (13) is between 100 hPa and 500 hPa, preferably about 300 hPa, above the ambient pressure pU.

5. Training system according to any of the preceding claims, characterized in that the pumping apparatus (21) comprises one or more pumps, which have a variably adjustable discharge rate.

6. Training system according to any of the preceding claims, characterized in that the pumping apparatus (21) comprises one or more low-vibration micropumps, in particular miniaturized double diaphragm pumps.

7. Training system according to claim 6, characterized in that the double diaphragm pumps can be operated with two piezo actuators each.

8. Training system according to any of the preceding claims, characterized in that the pressure sensors (23) are temperature-compensated.

9. Training system according to any of the preceding claims, characterized in that the pressure sensors (23) comprise one or more piezo-resistive sensors, preferably miniaturized silicon pressure sensors.

10. Training system according to claim 8 or claim 9, characterized in that the pressure sensors (23) contain an application-specific integrated circuit (="ASIC") which calibrates the pressure sensors (23) preferably for sensor offset, sensitivity, accuracy and / or temperature influences.

11. Training system according to any of the preceding claims, characterized in that the gas supply lines (22) comprise one or more, preferably optically transparent, silicone tubes, in particular Tygon tubes which have wall thicknesses and inner diameters in the order of 1mm each.

12. Training system according to any of the preceding claims, characterized in that the feedback module (15) can receive additional parameter data measured by the detection device and evaluate the data in particular by means of an expert system and / or artificial intelligence, and can transmit information based on the measured parameter data to the surgeon during a surgical training procedure in order to improve the current procedure.

13. Method for producing a training system (10) according to any of claims 1 to 12, characterized in that the cavities (13) of the detection device are produced such that they are hollow and tubular by means of a 3D printing process, preferably on the basis of high-resolution CT datasets of originals of the regions of the human body to be reproduced, the cavities (13) being printed in one action with the first functional portion (12'), which represents a region of the human bone system.

14. Method for operating a training system (10) according to any of claims 1 to 12 during a surgical training procedure on the training system (10), characterized in that a training surgeon performs, by means of an invasive surgical instrument, in particular by means of a scalpel, a drill or a fraise, a surgical training procedure on the mechanical model object of the training system (10) comprising the simulation unit (11) for depicting parts of the human body; in that in the event of mechanical damage to a cavity (13) by the training surgeon during the surgical training procedure, the pressure sensor (23) assigned to this cavity (13) measures a resulting pressure drop in this cavity (13) and reports the pressure drop to the feedback module (15); and in that the feedback module (15) informs the surgeon that the condition pÜ > pu is no longer fulfilled for each of the cavities (13), and in particular informs the surgeon which cavity (13) is affected.