Prostate suspension instrument

Abstract

The invention provides a prostate suspension instrument. The prostate suspension instrument comprises a conveying device and an anchor assembly. The delivery device is configured to deploy the anchor assembly on the prostate tissue; the anchor assembly comprises a first anchor component, an indicating component is arranged on the conveying device, and the indicating component is connected with the first anchor component through a middle component in the conveying device so as to achieve linkage with the first anchor component. And the indicating part is used for assisting in judging the fixing condition of the first anchor part on one side of the prostate capsule. According to the embodiment of the invention, the indicating part is arranged on the conveying device, so that the defect that a clinician cannot directly observe the fixing condition of the first anchor part on one side of the prostate capsule during an operation in the prior art is effectively overcome; the indicating component is arranged on the conveying device, and the indicating component is linked through the multiple middle components, so that a clinician can judge the fixing condition of the first anchor component on one side of the prostate capsule by observing the movement condition of the indicating component.

Description

Technical Field

[0001] The present invention relates to the technical field of medical devices, and in particular to a prostate suspension device. Background Art

[0002] Benign prostatic hyperplasia (BPH) is a common disease in middle-aged and elderly men, and the incidence is increasing with the aging of the global population. The incidence of BPH increases with age, but there may not be clinical symptoms when there are hyperplastic lesions. The incidence rate in urban areas is higher than in rural areas, and racial differences also affect the degree of hyperplasia.

[0003] The prostate gland is located below the bladder. The tube that carries urine from the bladder to the penis (urethra) passes through the center of the prostate gland. The prostate gland continues to grow throughout most men's lives. In some men, the prostate capsule surrounding the prostate gland may prevent the prostate gland from enlarging further, which can cause the inner area of ​​the prostate gland to press against the urethra. This pressure on the urethra increases the resistance to urine flowing through the area of ​​the urethra surrounded by the prostate gland. Therefore, the bladder must exert more pressure to force urine through the increased urethral resistance. Chronic overstraining can cause the muscle wall of the bladder to remodel and become stiffer. This increased urethral resistance and increased stiffness of the urine stream, as well as hypertrophy of the bladder wall, can lead to a variety of lower urinary tract symptoms that can significantly reduce a person's quality of life. These symptoms include a weak or intermittent urine stream when urinating, straining when urinating, hesitation before starting to urinate, a feeling that the bladder is not completely empty even after urinating, dribbling or leaking urine at the end of urination, especially increased frequency of urination at night, and urgency to urinate.

[0004] Prostatic urethral lift (PUL) is a new, nearly non-invasive implantable prostate hyperplasia treatment for the treatment of lower urinary tract symptoms caused by benign prostatic hyperplasia in men. This treatment uses an instrument to push back the prostate hyperplasia lobe through the urethra, and a tiny device (anchor component) is permanently implanted to fix the hyperplastic prostate lobe in the retracted position, thereby maintaining the integrity of the prostate and restoring the urethra. It effectively relieves urine flow and greatly improves frequent or difficult urination caused by prostate hyperplasia.

[0005] The prostate suspension device is a medical device based on the principle of PUL technology. The product consists of a delivery device and an anchor component. The anchor component is located inside the delivery device. The delivery device is equipped with a power source, and the deployment of the anchor component is achieved by mechanical transmission. The anchor component includes a first anchor component, a second anchor component and a suture, and the first anchor component and the second anchor component are connected by sutures. Specifically, the product is passed through the urethra to the prostate segment urethra under cystoscope visualization, and a suitable puncture point is selected in the prostate segment urethra to fully compress the prostate tissue, and the puncture needle is fired to the outside of the prostate capsule. While retrieving the puncture needle, the first anchor component is released on the outside of the prostate capsule, and the second anchor component is released in the prostate segment urethra. The first anchor component and the second anchor component are connected by sutures to form an "I"-shaped structure, which effectively suspends the hyperplastic prostate tissue. The anchor components need to be implanted in pairs, usually 4 to 6 sets of rivet systems are implanted, which can fully suspend the prostate segment urethra and relieve urethral obstruction. It has the advantages of minimally invasive, retaining sexual function, local anesthesia surgery, and fast recovery.

[0006] When the prostate suspension device in the prior art is used for surgical implantation, the clinician cannot directly observe the fixation of the first anchor component on one side of the prostate capsule, and the doctor cannot confirm the expected therapeutic effect of each implantation on site. Summary of the invention

[0007] The purpose of the present invention is to provide a prostate suspension device, by providing an indicator component on the prostate suspension device, so that clinicians can assist in judging the fixation of the first anchor component on one side of the prostate capsule by observing the indicator component during the prostate urethra lifting therapy operation.

[0008] To achieve the above-mentioned purpose, the present invention provides a prostate suspension device, including a conveying device and an anchor assembly; the conveying device is configured to deploy the anchor assembly on the prostate tissue; the anchor assembly includes a first anchor component, the first anchor component is configured to be fixed on the outside of the prostate capsule, and is used to suspend the prostate tissue; the conveying device is provided with an indicating component, and the indicating component is connected to the first anchor component through an intermediate component in the conveying device to achieve linkage with the first anchor component; the indicating component is used to assist in judging the fixation status of the first anchor component on one side of the prostate capsule.

[0009] Preferably, the intermediate component includes a wire driving component and a wire assembly; the wire driving component is slidably connected to the intermediate plate of the conveying device; the wire assembly is connected to the wire driving component and performs linear reciprocating motion under the drive of the wire driving component; the indicating component is fixedly connected to the wire driving component; and the first anchor component is connected to the distal end of the wire assembly.

[0010] Preferably, the thread assembly includes a suture slider, suture, and a suture support tube; the suture slider is connected to the wire driving member, the suture support tube is connected to the suture slider, the suture is passed through the interior of the suture support tube and is fixedly connected to the suture support tube, and the first anchor component is fixedly connected to the distal end of the suture.

[0011] Preferably, the conveying device includes a needle driving member and a needle assembly; the needle driving member is slidably connected to the middle plate of the conveying device and is connected to the needle assembly, and the needle driving member is used to drive the needle assembly to perform linear reciprocating motion; the needle driving member is connected to the wire driving member through a spring, and the spring is used to keep the tension of the suture constant.

[0012] Preferably, the spring is a constant force spring.

[0013] Preferably, the indicating part includes a connecting part and an indicating part; the indicating part is fixedly connected to the wire driving part through the connecting part, and the connecting part is a triangular structure; the indicating part is located at the top of the connecting part, and the bottom of the indicating part is slidably connected to the middle plate.

[0014] Preferably, the conveying device comprises a shell, the intermediate plate is arranged inside the shell, the intermediate plate cooperates with the shell to form a guide groove, and the lower end of the indicating part is provided with a sliding part which is slidably connected with the guide groove.

[0015] Preferably, the conveying device is further provided with a transparent protective shell, and the transparent protective shell cover is arranged on the outside of the indicating part to protect the indicating part.

[0016] Preferably, an indicative mark is provided on the transparent protective shell for cooperating with the indicating component to assist in determining the fixing status of the first anchor component.

[0017] Preferably, the conveying device is provided with a scale, and the scale is arranged on one side of the indicating component, and is used for cooperating with the indicating component to assist in judging the fixing condition of the first anchor component.

[0018] The beneficial effect of the present invention is that: this embodiment effectively compensates for the fact that in the prior art, clinicians cannot directly observe the fixation of the first anchor component on one side of the prostate capsule during surgery by setting an indicator component on the delivery device, so that the expected effect of each implantation cannot be confirmed on site. By setting an indicator component on the delivery device and making the indicator component linked through multiple intermediate components, clinicians can judge the fixation of the first anchor component on one side of the prostate capsule by observing the movement of the indicator component. BRIEF DESCRIPTION OF THE DRAWINGS

[0019] Figure 1 This is a schematic diagram of the overall structure of the prostate suspension device according to an embodiment of the present invention; Figure 2 This is a schematic diagram of the structure of the anchor assembly after deployment in an embodiment of the present invention; Figure 3 It is a schematic diagram of the separation of the handle and the replacement chamber of the prostate suspension device according to an embodiment of the present invention; Figure 4 It is a structural exploded view of the handle of the prostate suspension device according to an embodiment of the present invention; Figure 5 It is a structural exploded view of a replacement cabin of a prostate suspension device according to an embodiment of the present invention; Figure 6 Schematic diagram of the structure of the wire drive member and the wire assembly in an embodiment of the present invention; Figure 7 It is a schematic structural diagram of a needle driving member and a needle assembly in an embodiment of the present invention; Figure 8 A schematic diagram of the connection relationship between the indicator component and the line driver in an embodiment of the present invention; Fig. 9 This is a diagram of the internal structure of the prostate suspension device according to an embodiment of the present invention (the left housing has been removed); Fig.10 for Fig. 9 Enlarged view of point A in the middle; Fig.11 This is a schematic diagram of the structure of a transparent protective shell in an embodiment of the present invention; Fig.12 It is a partial structural schematic diagram of a handle in an embodiment of the present invention (right side view); Fig.13 It is a partial structural schematic diagram of a handle in an embodiment of the present invention (left side view); Fig.14 It is an exploded view of a part of the structure of the handle in an embodiment of the present invention (left side view); Fig.15 Schematic diagram of the structure of the replacement cabin in an embodiment of the present invention.

[0020] Reference numerals: 1- conveying device; 100-handle; 110-left housing; 111-middle plate; 112-right housing; 120-line driver; 121-first slot; 130-needle driving member; 131-second slot; 132-constant force spring; 140-indicating member; 141-connecting portion; 142-indicating portion; 143-sliding portion; 144-guide groove; 150-transparent protective shell; 152-first mark; 153-second mark; 160- trigger mechanism; 161- driving gear; 162- ratchet; 163- cam; 200 - replacement cabin; 210 - replacement cabin inner shell; 211 - guide plate; 212 - intervention rod; 213 - replacement cabin outer shell; 220-thread assembly; 221-suture; 222-suture support tube; 223-suture slider; 224-first protrusion; 230-needle assembly; 231-needle rod; 232-transport needle; 233-needle slider; 234-second protrusion; 240-push rod assembly; 250-tangent assembly; 260 - anchor assembly; 261 - first anchor member; 262 - second anchor member; 263 - suture portion; 270 - unlock switch; 271 - knob; 272 - operating handle; 273 - concave structure. DETAILED DESCRIPTION

[0021] In order to make the purpose, technical scheme and advantages of the present invention clearer, the technical scheme in the embodiment of the present invention will be clearly and completely described below in conjunction with the drawings of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without making creative work belong to the scope of protection of the present invention. Unless otherwise defined, the technical terms or scientific terms used herein should be the usual meanings understood by people with general skills in the field to which the present invention belongs. "Including" and similar words used in this article mean that the elements or objects appearing before the word include the elements or objects listed after the word and their equivalents, without excluding other elements or objects. Unless otherwise specified, the "connection" described in this article can be a direct connection or an indirect connection, that is, a connection through an intermediate.

[0022] See also Figure 1-Figure 2 The present invention provides a prostate suspension device, comprising a delivery device 1 and an anchor assembly 260; the delivery device 1 is configured to deploy the anchor assembly 260 on the prostate tissue to achieve lifting of the prostate urethra.

[0023] like Figure 2As shown, the anchor assembly 260 implanted in the prostate tissue includes a first anchor component 261, a second anchor component 262 and a suture portion 263. During the operation, the first anchor component 261 is configured to be fixed on the outside of the prostate capsule, the second anchor is deployed in the prostate urethra segment, and the suture portion 263 penetrates the prostate lateral lobe and is respectively connected to the first anchor component 261 and the second anchor component 262 at both ends. The three together form an "I"-shaped structure, which can effectively suspend the hyperplastic prostate tissue. In order to facilitate clinicians to judge the fixation of the first anchor component 261 on the outside of the prostate capsule during the operation, and then achieve the expected effect of implanting the anchor assembly 260, an indication component 140 is provided on the conveying device 1, and the indication component 140 is connected to the first anchor component 261 through the intermediate component in the conveying device 1 to achieve linkage with the first anchor component 261; the indication component 140 is used to assist in judging the fixation of the first anchor component 261 on one side of the prostate capsule.

[0024] See also Figure 3 and Figure 2 In one embodiment of the present invention, the conveying device 1 includes a handle 100 and a replacement capsule 200, and the replacement capsule 200 can be installed on the handle 100. The replacement capsule 200 is configured to be a component that carries the anchor assembly 260, and the handle 100 is configured to transfer mechanical energy to the replacement capsule 200 to convey the anchor assembly 260.

[0025] See also Figure 4 , Figure 5 and Figure 6 In this embodiment, the intermediate component includes a wire drive member 120 and a wire assembly 220 (such as Figure 6 ); wherein the wire drive member 120 is arranged in the handle 100, and the wire assembly 220 is arranged in the replacement cabin 200, and the wire drive member 120 and the wire assembly 220 are configured so that when the replacement cabin 200 and the handle 100 are positioned and fixedly combined, the wire drive member 120 and the wire assembly 220 are engaged, and the linkage between the wire drive member 120 and the wire assembly 220 is realized.

[0026] See also Figure 4The handle 100 includes a left shell 110, a middle plate 111 and a right shell 112, wherein the middle plate 111 is installed between the left shell 110 and the right shell 112, and the left shell 110, the middle plate 111 and the right shell 112 are configured to provide installation space for multiple components between the left shell 110 and the middle plate 111 or between the middle plate 111 and the right shell 112. The wire drive member 120 is slidably connected to the middle plate 111 of the conveying device 1, and performs linear reciprocating sliding under the constraints of the left shell 110 and the middle plate 111; the wire assembly 220 is connected to the wire drive member 120 (the connection method will be further explained below), and performs linear reciprocating motion under the drive of the wire drive member 120, and the first anchor component 261 is connected to the distal end of the wire assembly 220; the indicating component 140 is fixedly connected to the wire drive member 120, and the clinician can judge the fixation of the first anchor component 261 on the outside of the prostate capsule by the moving distance of the indicating component 140 combined with clinical experience.

[0027] See also Figure 5 The replacement capsule 200 includes a guide plate 211, a replacement capsule inner shell 210, and an intervention rod 212. The guide plate 211 and the replacement capsule 200 are connected by a plurality of fasteners, and the proximal end of the intervention rod 212 is connected to the replacement capsule inner shell 210. The guide plate 211 and the replacement capsule 200 are configured to provide installation space for a plurality of components between the guide plate 211 and the replacement capsule inner shell 210, and the wire assembly 220 is slidably connected between the replacement capsule inner shell 210 and the guide plate 211.

[0028] See also Figure 5-Figure 6 In some embodiments, the thread assembly 220 includes a suture slider 223, a suture 221, and a suture support tube 222; the suture support tube 222 is connected to the suture slider 223, the suture 221 is passed through the suture support tube 222 and is fixedly connected to the suture support tube 222, and the first anchor component 261 is fixedly connected to the distal end of the suture 221. The suture slider 223 is disposed between the guide plate 211 and the replacement chamber inner shell 210, and is slidably connected to the guide plate 211 and the replacement chamber inner shell 210.

[0029] Further, the suture slider 223 is connected to the wire driver 120. Specifically, the suture slider 223 has a first protrusion 224 on the side opposite to the wire driver 120. The wire driver 120 is provided with a first slot 121 corresponding to the first protrusion 224. The first protrusion 224 and the first slot 121 are configured such that when the replacement chamber 200 and the handle 100 are positioned and fixedly combined, the first protrusion 224 is inserted into the first slot 121. In this embodiment, the wire assembly 220 is connected by the suture slider 223 and the wire driver 120, so that the wire assembly 220 and the wire driver 120 are linked.

[0030] See also Figure 5-Figure 7 In some embodiments, the delivery device 1 includes a needle drive 130 and a needle assembly 230; in this embodiment, the needle drive 130 is arranged inside the handle 100, and the needle assembly 230 is arranged inside the replacement chamber 200; the needle drive 130 is slidably connected to the intermediate plate 111; the needle drive 130 is connected to the needle assembly 230, and the needle drive 130 is used to drive the needle assembly 230 to perform linear reciprocating motion; specifically, the needle assembly 230 includes a needle The needle rod 231 has a delivery needle 232 connected to its distal end, and a needle slider 233 connected to its proximal end; further, the needle slider 233 has a second protruding piece 234 on a side opposite to the needle driving member 130, and correspondingly, the needle driving member 130 has a second slot 131, and the second protruding piece 234 and the second slot 131 are configured such that when the replacement chamber 200 and the handle 100 are positioned and fixedly combined, the second protruding piece 234 is inserted into the second slot 131. The needle slider 233 is disposed between the guide plate 211 and the replacement chamber inner shell 210, and is slidably connected to the guide plate 211 and the replacement chamber inner shell 210.

[0031] It should be noted that before the prostate suspension instrument is activated, the first anchor component 261 and the suture portion 263 are engaged with each other and accommodated in the needle assembly 230, and the second anchor component 262 is disposed in the intervention rod 212. After the first anchor component 261 and the suture portion 263 have been placed in the prostate tissue, the second anchor component 262 is firmly engaged with the suture portion 263 to form a fully assembled anchor assembly 260.

[0032] Please still refer to Figure 5In some embodiments, the replacement capsule 200 further includes a push rod assembly 240 and a cutting assembly 250. The push rod assembly 240 is used to push the second anchor component 262 to move toward the distal end of the intervention rod 212 and finally connect with the suture 221, and to separate the second anchor component 262 from the intervention rod 212 and enter the prostatic urethra segment. The cutting assembly 250 is used to cut the suture 221 after the second anchor component 262 is deployed.

[0033] See also Figure 8 In this example, the needle drive 130 is connected to the wire drive 120 via a constant force spring 132, and the constant force spring 132 is used to keep the tension of the suture 221 constant. Specifically, after the anchor assembly 260 is implanted into the prostate tissue, the tension of the suture portion 263 between the first anchor component 261 and the second anchor component 262 will change with the size and hardness of the prostate, thereby causing the anchor assembly 260 to have different lifting effects on the prostate. In this embodiment, by setting the constant force spring 132, before the suture 221 is cut, the force of the constant force spring 132 in the handle 100 acts on the suture 221 through the intermediate component, ensuring that the tension of the suture portion 263 remains consistent after cutting.

[0034] Please still refer to Figure 8 In some embodiments, the indicating component 140 includes a connecting portion 141 and an indicating portion 142; the indicating component 140 is fixedly connected to the wire driving component 120 through the connecting portion 141, the connecting portion 141 is a triangular structure, the indicating portion 142 is located at the top of the connecting portion 141, and the bottom of the indicating portion 142 is slidably connected to the intermediate plate 111.

[0035] See also Figure 9-10 In some embodiments, the conveying device 1 includes a housing, the intermediate plate 111 is arranged inside the housing, the intermediate plate 111 cooperates with the housing to form a guide groove 144, and the lower end of the indicating part 142 is provided with a sliding part 143 that cooperates and slides with the guide groove 144. Specifically, the housing includes the left housing 110 and the right housing 112, and the intermediate plate 111 cooperates with the right housing 112 to form the guide groove 144. In this embodiment, the stability of the movement of the indicating part 140 is improved by the cooperation of the sliding part 143 and the guide groove 144.

[0036] The wire drive component 120 is located between the left shell body 110 and the middle plate 111. In order to make the indicating part 142 of the indicating component 140 be located on the central axis of the handle 100, a crank arm is formed between the connecting part 141 and the indicating part 142 of the indicating component 140. The crank arm is "L" shaped. The design of the crank arm makes the indicating part 142 exactly located on the central axis of the handle 100, thereby increasing the overall aesthetics of the conveying device 1.

[0037] See also Figure 8-Figure 9 In some embodiments, the conveying device 1 is further provided with a transparent protective shell 150, which is arranged on the outside of the indicating part 142 to protect the indicating part 140. Furthermore, the transparent protective shell 150 is fixedly mounted on the top of the shell, and the movement of the indicating part 142 can be clearly observed through the transparent shell.

[0038] See also Fig.11 In some embodiments, the transparent protective shell 150 is provided with an indicative mark for cooperating with the indicating component 140 to assist in determining the fixation of the first anchor component 261. Further, the indicative mark includes a first mark 152 and a second mark 153, wherein the first mark 152 is located on the side of the transparent protective shell 150 close to the proximal end of the intervention rod 212, and the second mark 153 is located on the side of the transparent protective shell 150 close to the distal end of the intervention rod 212.

[0039] In some embodiments, the conveying device 1 is provided with a scale (not shown in the drawings), which is arranged on one side of the indicating component 140, and is used to cooperate with the indicating component 140 to assist in determining the fixing status of the first anchor component 261. In this embodiment, the scale is arranged on the top of the transparent protective shell 150, and is located between the first mark 152 and the second mark 153.

[0040] In other embodiments, the scale is disposed on the left housing 110 or the right housing 112 .

[0041] After the replacement chamber 200 is installed on the handle 100 and before it is activated, the indicator 142 is located at the first mark 152 position.

[0042] The anchor assembly 260 is deployed through a series of steps. The needle assembly 230 is driven by the needle driver 130 to slide toward the distal end of the intervention rod 212. The delivery needle 232 extends from the outlet at the distal end of the intervention rod 212 to a fully extended position, so that at least a portion of the delivery needle 232 penetrates the patient's prostate capsule. The first anchor component 261 and the distal end of the suture 221 are contained in the delivery needle 232 and move together with the delivery needle 232 to penetrate the prostate tissue. During this process, the indicator portion 142 of the indicator component 140 moves from the first mark 152 to the second mark 153.

[0043] Next, while the first anchor member 261 and the distal end of the suture 221 remain in the proper position outside the prostate capsule, the needle assembly 230 moves toward the proximal end of the intervention rod 212, so that the delivery needle 232 moves to a partially retracted position, that is, the delivery needle 232 moves proximally relative to its fully extended position, but has not yet been fully retracted into the intervention rod 212. The wire support tube helps to maintain the distal position of the first anchor member 261 and the suture 221 while the needle assembly 230 moves toward the proximal end of the intervention rod 212. Therefore, the first anchor member 261 and the distal end of the suture 221 remain near the surface of the prostate tissue and are no longer in the delivery needle 232. Therefore, during this process, the indicator member 140 remains stationary. That is, the indicator portion 142 is still located at the second mark 153.

[0044] In the next step, the needle assembly 230 is further moved proximally to be retracted into the intervention rod 212, while the wire assembly 220 is also moved proximally. The first anchor component 261 is pulled against the tissue surface, which causes the first anchor component 261 to rotate around its connection with the suture 221, so that the first anchor component 261 is now transverse to the distal end of the suture 221. In this process, as the wire assembly 220 moves toward its proximal end, the indicator component 140 synchronously moves toward the direction close to the first mark 152. When the tension of the suture 221 reaches the calibration value of the constant force spring 132, the wire assembly 220 stops moving, and the indicator component 140 stops moving synchronously. The doctor can judge whether the deployment of the first anchor component 261 is in place based on the position where the indicator component 140 stops moving, combined with clinical experience, and further judge whether the operation can achieve the expected therapeutic effect.

[0045] In the next step, the push rod assembly 240 within the handle 100 will be actuated to cause the second anchor component 262 to engage the suture 221, which action defines a suture portion 263 that becomes part of the final anchor assembly 260 implanted in the patient. At this point, the anchor assembly 260 is now completely separated from the cartridge and handle 100 system. Please refer to Figure 4 , Fig.12 , Fig.13 , Fig.14It should be noted that the handle 100 is provided with a driving mechanism for driving a series of actions in the replacement capsule 200, and the driving mechanism includes a trigger member 160, a driving gear 161, a ratchet 162 and a cam 163. The trigger member 160 interacts with the cam 163 through the driving gear 161 and the ratchet 162. The cam 163 interacts with other mechanisms in the handle 100 (including the wire drive member 120 and the needle drive member 130) to promote the movement of various components in the replacement capsule 200 (such as the needle assembly 230, the wire assembly 220, the push rod assembly 240 and the cutting assembly).

[0046] Please refer to Fig.15 The replacement cabin also includes a replacement cabin shell 213 and an unlocking switch 270. The replacement cabin shell 213 is connected to the guide plate 211 and the replacement cabin inner shell 210 to form a replacement cabin body. The unlocking switch 270 is connected to the replacement cabin shell 213. The unlocking switch 270 includes a knob 271. The knob 271 is provided with an operating handle 272 for easy operation. The operating handle 272 has symmetrically arranged concave structures 273 on both sides. The concave structure 273 facilitates the removal of the replacement cabin from the handle after unlocking.

[0047] In summary, the prostate suspension device proposed by the present invention provides an indication component 140 on the handle 100, and the indication component 140 is linked through multiple intermediate components, so that the clinician can judge the fixation of the first anchor component 261 on one side of the prostate capsule by observing the movement of the indication component 140. Therefore, the present invention effectively overcomes the defects of the prior art and has a high industrial utilization value.

[0048] The above is only a specific implementation of the embodiment of the present application, but the protection scope of the embodiment of the present application is not limited thereto, and any changes or replacements within the technical scope disclosed in the embodiment of the present application should be included in the protection scope of the embodiment of the present application. Therefore, the protection scope of the embodiment of the present application should be based on the protection scope of the claims.

Claims

1. A prostate suspension device, characterized in that: including a delivery device and an anchor assembly; The delivery device is configured to deploy the anchor assembly on prostate tissue; The anchor assembly includes a first anchor component configured to be fixed outside the prostate capsule for suspending prostate tissue; The conveying device is provided with an indicating component, which is connected to the first anchor component through an intermediate component in the conveying device to realize linkage with the first anchor component; the indicating component is used to assist in judging the fixation status of the first anchor component on one side of the prostate capsule.

2. The prostate suspension device according to claim 1, characterized in that: The intermediate component includes a wire drive member and a wire assembly; The wire drive is slidably connected to the middle plate of the conveying device; the wire assembly is connected to the wire drive and performs linear reciprocating motion under the drive of the wire drive; The indicating component is fixedly connected to the wire driving component; and the first anchor component is connected to the distal end of the wire assembly.

3. The prostate suspension device according to claim 2, characterized in that: The thread assembly includes a suture slider, suture, and a suture support tube; The suture slider is connected to the wire driving member, the suture support tube is connected to the suture slider, the suture is passed through the inside of the suture support tube and is fixedly connected to the suture support tube, and the first anchor component is fixedly connected to the distal end of the suture.

4. The prostate suspension device according to claim 3, characterized in that: The delivery device includes a needle drive and a needle assembly; The needle driving member is slidably connected to the middle plate of the conveying device and is connected to the needle assembly, and the needle driving member is used to drive the needle assembly to perform linear reciprocating motion; The needle driving member is connected to the wire driving member via a spring, and the spring is used to keep the tension of the suture constant.

5. The prostate suspension device according to claim 4, characterized in that: The spring is a constant force spring.

6. The prostate suspension device according to claim 2, characterized in that: The indicating component comprises a connecting portion and an indicating portion; The indicating component is fixedly connected to the wire driving component through the connecting portion, and the connecting portion is a triangular structure; The indicating portion is located at the top end of the connecting portion, and the bottom end of the indicating portion is slidably connected to the middle plate.

7. The prostate suspension device according to claim 6, characterized in that: The conveying device comprises a shell, the intermediate plate is arranged inside the shell, the intermediate plate cooperates with the shell to form a guide groove, and the lower end of the indicating part is provided with a sliding part which cooperates with the guide groove for sliding connection.

8. The prostate suspension device according to claim 6, characterized in that: The conveying device is also provided with a transparent protective shell, and the transparent protective shell cover is arranged on the outside of the indicating part to protect the indicating part.

9. The prostate suspension device according to claim 8, characterized in that: The transparent protective shell is provided with an indicative mark for cooperating with the indicating component to assist in determining the fixing status of the first anchor component.

10. The prostate suspension device according to claim 1, characterized in that: The conveying device is provided with a scale, and the scale is arranged on one side of the indicating component, and is used to cooperate with the indicating component to assist in judging the fixing status of the first anchor component.

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