CN213940919U - Fetal sac resetting structure for emergent cervical cerclage operation of fetal sac protruding into vagina - Google Patents
Fetal sac resetting structure for emergent cervical cerclage operation of fetal sac protruding into vagina Download PDFInfo
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- CN213940919U CN213940919U CN202022612985.7U CN202022612985U CN213940919U CN 213940919 U CN213940919 U CN 213940919U CN 202022612985 U CN202022612985 U CN 202022612985U CN 213940919 U CN213940919 U CN 213940919U
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Abstract
The utility model discloses a fetal sac resetting structure used for emergent cervical cerclage operation in the protruding vagina of the fetal sac, which comprises an operating handle and a saccule structure used for pushing up the fetal sac, and is characterized in that the saccule structure is arranged at one end of the operating handle; the setting is used for assisting operating handle gets into the internal guide structure of patient, guide structure and operating handle sliding connection. Provide the guide effect for operating handle through guide structure, operating handle slides on guide structure, can guarantee that operating handle gets into the patient internal steadily. The technical scheme of the utility model the special apparatus of cervical around pushing up the fetal sac in the suture operation is provided, and the deflector provides the guide effect for operating handle, and under the common supporting role of slider and support, operating handle can keep at steady state, and the deflector is handed to the doctor, and the application of force can push into the patient with operating handle in promoting the handle internal, and the sacculus structure of operating handle front end then promotes the fetal sac and reply palace intracavity.
Description
Technical Field
The utility model belongs to the technical field of medical instrument, concretely relates to fetal sac reduction structure for when being used for the emergent cervical cerclage art in the protruding vagina of fetal sac.
Background
The cervical canal is characterized by a loose inner opening, also called cervical insufficiency, which means the state of the cervical canal with loose and weak tension. The relaxation of the internal opening of the cervical canal is one of the causes of habitual abortion and premature birth in the middle of pregnancy. When the internal opening of the cervical canal is relaxed, the function of the isthmus sphincter is reduced, so that the internal opening of the cervix is expanded in a pathological way. After the midgestation period, the fetal sac can protrude outwards from the inner opening of the cervical canal to induce uterine contraction and abortion. Generally, the symptoms are easy to relax from the 4 th to 5 th months of pregnancy, and if the symptoms occur, the symptoms are treated in time to avoid that the fetal cells fall into the vagina, so that water is broken to cause abortion.
The reasons for the relaxation of the internal os of the cervical canal can be divided into two categories: congenital and acquired. Congenital cervical canal internal orifice relaxation is caused by that the mother takes certain medicine or other reasons when pregnant to cause the female uterine hypoplasia; the acquired cervical canal internal orifice laxity is caused by birth injury, excessive uterine curettage or frequent perineal examination.
The cervical circumferential suture is an effective method for treating cervical canal internal opening looseness, namely, the cervical canal internal opening is annularly sutured by using nylon wires or 10-gauge silk threads, and the cervical canal is tightened and ligated. Is suitable for gestation period, and has simple method and easy stitches removal. Has no influence on pregnancy, does not risk cervical wound dehiscence, and does not need cesarean section during delivery.
The purpose of the surgical treatment is to repair the cervix and establish the formation and function of a normal cervical orifice, enabling pregnancy to be maintained to an advanced stage.
In the cervical encircling suture operation, a patient is ordered to have a head low and a hip high position, a simple sacculus similar to a ureter but made of softer material than the ureter is used, the sacculus is pushed upwards through the sacculus, so that the sacculus is restored to the uterine cavity as far as possible, and then cervical cerclage is performed. At present, no special tool for pushing the fetal sac up is clinically available, and a simple self-made balloon is generally adopted, so that the fetal sac is difficult to push up, the recovery effect is poor, and the operation time is prolonged.
The utility model aims at the above problem, provide a fetal sac reduction structure that is used for when emergent cervical cerclage art in the protruding vagina of fetal sac.
SUMMERY OF THE UTILITY MODEL
In order to overcome the problems in the background art, the utility model provides a fetal sac reduction structure used for emergent cervical cerclage operation in the protruding vagina of the fetal sac.
The fetal sac resetting structure used for emergent cervical cerclage operation with the fetal sac protruding out of the vagina comprises an operating handle and a saccule structure used for pushing up the fetal sac, and is characterized in that the saccule structure is arranged at one end of the operating handle; the setting is used for assisting operating handle gets into the internal guide structure of patient, guide structure and operating handle sliding connection. Provide the guide effect for operating handle through guide structure, operating handle slides on guide structure, can guarantee that operating handle gets into the patient internal steadily.
Further, operating handle's main part is the cylinder, and the sacculus structure sets up the one end that enters patient's internal at operating handle's front end promptly, sacculus structure and operating handle's lateral wall body coupling. The operating handle has smooth and non-angular appearance, and can avoid scratching the vagina and cervix of a patient.
Furthermore, the inside of operating handle includes the pipeline of a intercommunication sacculus structure, and operating handle passes through pipeline and sacculus structure intercommunication. This arrangement communicates the interior of the operating handle with the balloon structure.
Furthermore, an injection tube is arranged at the operation end of the operation handle, namely the end close to the doctor, the injection tube is communicated with the pipeline inside the operation handle, and liquid or gas is injected into the balloon structure through the injection tube. When the inflatable balloon is used, liquid or gas is input into the injection pipe through the injector, and the liquid or the gas enters the balloon structure after passing through the pipeline, so that the balloon structure is expanded to a proper size.
Further, the mouth of pipe of filling in the pipe sets up the rubber buffer, the edge of rubber buffer and the inner wall body coupling of filling in the pipe. When the rubber plug is used, the rubber plug is punctured through the injector so as to inject liquid or gas, and the arrangement of the rubber plug can avoid the overflow of the liquid or the gas.
Further, guide structure includes direction main part and bearing structure, and bearing structure sets up the front end at the direction main part, and bearing structure and direction main part body coupling. During the use, paste bearing structure on patient's health, for the direction main part provides the strong point, guarantee the steady of direction main part.
Further, the guide main body is a rectangular guide plate, a sliding groove is formed in the upper end of the guide plate, a sliding block is arranged in the sliding groove, and the upper end of the sliding block is fixedly connected with the operating end of the operating handle. When the puncture needle is used, a doctor pushes the operating end of the operating handle by hand, so that the sliding block can move in the sliding groove to enable the operating handle to move, and the balloon structure at the front end of the operating handle gradually enters the body of a patient, so that the fetal sac is pushed up.
Furthermore, the opening of the sliding groove is upward, and the sliding groove can accommodate the sliding block; the slider sets up to "protruding" font slider, and the spout is stretched out to the upper end of slider. This arrangement leaves operating space for pushing the operating handle.
Furthermore, a side wall at the upper end of the sliding block is provided with a handle which is convenient to push the sliding block to push, and the handle is integrally connected with the sliding block. When the handle is used, the sliding block and the operating handle can be pushed to move by applying force to the pushing handle by hands.
Furthermore, a support for supporting the front end of the operating handle is arranged at the front end of the guide plate, namely one end close to the patient, the support is arranged at the upper end of the guide plate, and the bottom of the support is integrally connected with the guide plate. The whole operating handle is kept in a stable state under the supporting action of the bracket, and when the operating handle is used, the operating handle is pushed to slide on the bracket.
Further, the support comprises a semicircular groove, the inner diameter of the groove is larger than the outer diameter of the operating handle, and the groove is used for supporting the operating handle.
Further, the supporting structure comprises a supporting plate and a contact pad, the supporting plate is integrally connected with the outer side wall of the front end of the guide plate, and the contact pad is integrally connected with the free end of the supporting plate. When the device is used, the contact pad is contacted with the buttocks of a patient, the supporting plate plays a main supporting role, and a supporting point is provided for the guide plate.
Further, the backup pad is the board of outwards expanding and main part for the rectangle, all sets up the backup pad at the left lateral wall and the right lateral wall of deflector. The supporting plate arranged in this way can not block the operation view of a doctor and can not block the movement of the operation handle.
Furthermore, the contact pad is made of soft medical nontoxic silica gel materials. The contact pad of this kind of setting has fine compliance and antiskid nature, can prevent that the backup pad from taking place to slide when guaranteeing patient's travelling comfort.
Furthermore, the upper end surface of the guide plate is provided with scale marks and scale values for measuring the depth of the operating handle entering the body of the patient. This arrangement provides a depth reference for the medical personnel to access the operating handle into the patient.
Furthermore, an anti-slip layer used for increasing friction force between the hand of the doctor and the guide plate is arranged at the rear end of the guide plate, namely one end close to the doctor, and the anti-slip layer is integrally connected with the outer side wall of the guide plate. The arrangement is convenient for a doctor to hold the guide plate for operation.
Further, the left outer side wall and the right outer side wall of the guide plate are both provided with anti-skid layers.
Furthermore, the balloon structure is made of medical nontoxic soft silica gel materials. The balloon structure has good flexibility and can not damage the fetal sac.
Compared with the prior art, the technical scheme of the utility model the special apparatus of cervical around the upward push foetal sac of suturing art is provided, and the deflector provides the guide effect for operating handle, and under the common supporting role of slider and support, operating handle can keep at steady state, and the deflector is handed to the doctor, and the application of force can push into the patient with operating handle in promoting the handle internal, and the sacculus structure of operating handle front end then promotes the foetal sac and reply palace intracavity.
The using method comprises the following steps: firstly, the contact pad is contacted with the proper position of the hip of a patient, the operation handle and the balloon structure on the guide plate are determined to be over against the vaginal orifice of the patient, then force is applied to the push handle so as to push the operation handle to enter the vaginal orifice of the patient, then gas or liquid is input through the injection tube to expand the balloon structure, the operation handle is continuously pushed to enter the body of the patient, and the expanded balloon structure pushes up the fetal sac to gradually push the fetal sac back to the uterine cavity.
Drawings
Fig. 1 is a schematic view of the overall structure of the present invention;
fig. 2 is a schematic view of the structure of the utility model;
FIG. 3 is a front view of the structure of the present invention;
fig. 4 is a schematic view of the overall cross-sectional structure of the present invention;
FIG. 5 is a schematic view of the enlarged partial structure of the present invention;
fig. 6 is a schematic structural view of the connection state of the operating handle, the balloon structure and the slider of the present invention;
fig. 7 is a schematic sectional structure view of the slide block and the chute of the present invention;
in the figure, 1, a guide plate; 11. a chute; 12. a slider; 121. pushing the handle; 13. an anti-slip layer; 14. scale lines; 15. a scale value; 16. a support; 17. a support plate; 171. a contact pad; 2. an operating handle; 21. an injection pipe; 211. a rubber plug; 3. a balloon structure.
Detailed Description
The technical solutions in the embodiments of the present invention will be described in detail below with reference to specific embodiments, and it should be understood that the described embodiments are only a part of the embodiments of the present invention, rather than all embodiments, and those skilled in the art can easily understand other advantages and effects of the present invention from the disclosure in the specification. The utility model discloses can also implement or use through other different concrete implementation manners, under the condition of conflict-free, the characteristics in following embodiment and the embodiment can make up each other, based on the embodiment in the utility model, all other embodiments that the ordinary skilled in the art obtained under the prerequisite of not making creative work all belong to the scope of protection of the utility model.
The utility model discloses in: the preceding lateral wall of deflector is the lateral wall that is close to patient's end, and the back lateral wall of deflector is the lateral wall that is close to doctor's end, and the up end of deflector is the face at spout opening place, and the bottom surface that is the deflector relative with the up end, and all the other two lateral walls are the left lateral wall and the right lateral wall of deflector respectively.
As shown in fig. 1-2, the fetal capsule repositioning structure for emergent cervical cerclage during the fetal capsule protruding intravaginal process in the embodiment comprises an operating handle 2 and a balloon structure 3 for pushing the fetal capsule upwards, and is characterized in that the balloon structure 3 is arranged at one end of the operating handle 2; the guiding structure is used for assisting the operating handle 2 to enter the body of a patient and is connected with the operating handle 2 in a sliding mode. Provide the guide effect for operating handle 2 through guide structure, operating handle 2 slides on guide structure, can guarantee that operating handle 2 gets into the patient internal steadily.
The inside of operating handle 2 includes a pipeline of intercommunication sacculus structure 3, and operating handle 2 passes through the pipeline and communicates with sacculus structure 3. This arrangement communicates the interior of the operating handle 2 with the balloon structure 3.
An injection tube 21 is provided at the operation end of the operation handle 2, i.e., the end close to the doctor, the injection tube 21 is communicated with the pipeline inside the operation handle 2, and liquid or gas is injected into the balloon structure 3 through the injection tube 21. When in use, liquid or gas is input into the injection tube 21 through the syringe, so that the balloon structure 3 is expanded to an appropriate size.
A rubber plug 211 is arranged at the nozzle of the injection tube 21, and the edge of the rubber plug 211 is integrally connected with the inner wall of the injection tube 21. When the rubber plug 211 is used, the syringe punctures the rubber plug 211 so as to inject liquid or gas, and the arrangement of the rubber plug 211 can avoid the overflow of the liquid or the gas.
The guide structure comprises a guide main body and a supporting structure, the supporting structure is arranged at the front end of the guide main body, and the supporting structure and the guide main body are integrally connected. During the use, paste bearing structure on patient's health, for the direction main part provides the strong point, guarantee the steady of direction main part.
The guide main body is a rectangular guide plate 1, a sliding groove 11 is formed in the upper end of the guide plate 1, a sliding block 12 is arranged in the sliding groove 11, and the upper end of the sliding block 12 is fixedly connected with the operating end of the operating handle 2. When the pneumatic puncture needle is used, a doctor pushes the operation end of the operation handle 2 by hand, so that the sliding block 12 can move in the sliding groove 11, the operation handle 2 moves, the balloon structure 3 at the front end of the operation handle 2 gradually enters the body of a patient, and a fetal sac is pushed upwards.
The support structure includes a support plate 17 and a contact pad 171, the support plate 17 is integrally connected to the outer side wall of the front end of the guide plate 1, and the contact pad 171 is integrally connected to the free end of the support plate 17. In use, the support plate 17 serves as the primary support by contacting the buttocks of the patient with the contact pad 171 and provides a point of support for the guide plate 1.
The balloon structure 3 is made of medical nontoxic soft silica gel material. The balloon structure 3 arranged in this way has good flexibility and does not damage the tyre bag.
The fetal sac resetting structure used for emergent cervical cerclage operation with the fetal sac protruding out of the vagina comprises an operating handle 2 and a balloon structure 3 used for pushing up the fetal sac, and is characterized in that the balloon structure 3 is arranged at one end of the operating handle 2; the guiding structure is used for assisting the operating handle 2 to enter the body of a patient and is connected with the operating handle 2 in a sliding mode. Provide the guide effect for operating handle 2 through guide structure, operating handle 2 slides on guide structure, can guarantee that operating handle 2 gets into the patient internal steadily.
As shown in fig. 3 and 6, the main body of the operating handle 2 is a cylinder, the balloon structure 3 is arranged at the front end of the operating handle 2, i.e. the end that enters the body of the patient at first, and the balloon structure 3 is integrally connected with the outer side wall of the operating handle 2. The operating handle 2 is smooth in appearance and free of edges and corners, and can avoid scratching the vagina and cervix of a patient.
The inside of operating handle 2 includes a pipeline of intercommunication sacculus structure 3, and operating handle 2 passes through the pipeline and communicates with sacculus structure 3. This arrangement communicates the interior of the operating handle 2 with the balloon structure 3.
An injection tube 21 is provided at the operation end of the operation handle 2, i.e., the end close to the doctor, the injection tube 21 is communicated with the pipeline inside the operation handle 2, and liquid or gas is injected into the balloon structure 3 through the injection tube 21. When in use, liquid or gas is input into the injection tube 21 through the syringe, so that the balloon structure 3 is expanded to an appropriate size.
A rubber plug 211 is arranged at the nozzle of the injection tube 21, and the edge of the rubber plug 211 is integrally connected with the inner wall of the injection tube 21. When the rubber plug 211 is used, the syringe punctures the rubber plug 211 so as to inject liquid or gas, and the arrangement of the rubber plug 211 can avoid the overflow of the liquid or the gas.
The guide structure comprises a guide main body and a supporting structure, the supporting structure is arranged at the front end of the guide main body, and the supporting structure and the guide main body are integrally connected. During the use, paste bearing structure on patient's health, for the direction main part provides the strong point, guarantee the steady of direction main part.
The guide main body is a rectangular guide plate 1, a sliding groove 11 is formed in the upper end of the guide plate 1, a sliding block 12 is arranged in the sliding groove 11, and the upper end of the sliding block 12 is fixedly connected with the operating end of the operating handle 2. When the pneumatic puncture needle is used, a doctor pushes the operation end of the operation handle 2 by hand, so that the sliding block 12 can move in the sliding groove 11, the operation handle 2 moves, the balloon structure 3 at the front end of the operation handle 2 gradually enters the body of a patient, and a fetal sac is pushed upwards.
The support structure includes a support plate 17 and a contact pad 171, the support plate 17 is integrally connected to the outer side wall of the front end of the guide plate 1, and the contact pad 171 is integrally connected to the free end of the support plate 17. In use, the support plate 17 serves as the primary support by contacting the buttocks of the patient with the contact pad 171 and provides a point of support for the guide plate 1.
As shown in fig. 3 to 4, the support plate 17 is a plate which is expanded outward and has a rectangular main body, and the support plate 17 is provided on both the left outer side wall and the right outer side wall of the guide plate 1. The supporting plate 17 thus arranged does not obstruct the view of the doctor's operation and does not obstruct the movement of the operating handle 2.
The contact pad 171 is made of a soft medical nontoxic silica gel material. The contact pad 171 has good flexibility and anti-slip property, so that the support plate 17 can be prevented from sliding while the comfort of the patient is ensured.
The balloon structure 3 is made of medical nontoxic soft silica gel material. The balloon structure 3 arranged in this way has good flexibility and does not damage the tyre bag.
The fetal sac resetting structure used for emergent cervical cerclage operation with the fetal sac protruding out of the vagina comprises an operating handle 2 and a balloon structure 3 used for pushing up the fetal sac, and is characterized in that the balloon structure 3 is arranged at one end of the operating handle 2; the guiding structure is used for assisting the operating handle 2 to enter the body of a patient and is connected with the operating handle 2 in a sliding mode. Provide the guide effect for operating handle 2 through guide structure, operating handle 2 slides on guide structure, can guarantee that operating handle 2 gets into the patient internal steadily.
The main part of operating handle 2 is the cylinder, and sacculus structure 3 sets up the one end that enters the patient at the front end of operating handle 2 promptly at first, sacculus structure 3 and operating handle 2's lateral wall body coupling. The operating handle 2 is smooth in appearance and free of edges and corners, and can avoid scratching the vagina and cervix of a patient.
The inside of operating handle 2 includes a pipeline of intercommunication sacculus structure 3, and operating handle 2 passes through the pipeline and communicates with sacculus structure 3. This arrangement communicates the interior of the operating handle 2 with the balloon structure 3.
An injection tube 21 is provided at the operation end of the operation handle 2, i.e., the end close to the doctor, the injection tube 21 is communicated with the pipeline inside the operation handle 2, and liquid or gas is injected into the balloon structure 3 through the injection tube 21. When in use, liquid or gas is input into the injection tube 21 through the syringe, so that the balloon structure 3 is expanded to an appropriate size.
A rubber plug 211 is arranged at the nozzle of the injection tube 21, and the edge of the rubber plug 211 is integrally connected with the inner wall of the injection tube 21. When the rubber plug 211 is used, the syringe punctures the rubber plug 211 so as to inject liquid or gas, and the arrangement of the rubber plug 211 can avoid the overflow of the liquid or the gas.
The guide structure comprises a guide main body and a supporting structure, the supporting structure is arranged at the front end of the guide main body, and the supporting structure and the guide main body are integrally connected. During the use, paste bearing structure on patient's health, for the direction main part provides the strong point, guarantee the steady of direction main part.
The guide main body is a rectangular guide plate 1, a sliding groove 11 is formed in the upper end of the guide plate 1, a sliding block 12 is arranged in the sliding groove 11, and the upper end of the sliding block 12 is fixedly connected with the operating end of the operating handle 2. When the pneumatic puncture needle is used, a doctor pushes the operation end of the operation handle 2 by hand, so that the sliding block 12 can move in the sliding groove 11, the operation handle 2 moves, the balloon structure 3 at the front end of the operation handle 2 gradually enters the body of a patient, and a fetal sac is pushed upwards.
As shown in fig. 4, the opening of the chute 11 is upward, and the chute 11 can accommodate the slider 12; the sliding block 12 is a convex sliding block 12, and the upper end of the sliding block 12 extends out of the sliding groove 11. This arrangement leaves an operation space for pushing the operation handle 2.
The support structure includes a support plate 17 and a contact pad 171, the support plate 17 is integrally connected to the outer side wall of the front end of the guide plate 1, and the contact pad 171 is integrally connected to the free end of the support plate 17. In use, the support plate 17 serves as the primary support by contacting the buttocks of the patient with the contact pad 171 and provides a point of support for the guide plate 1.
The support plate 17 is a plate which is expanded outwards and has a rectangular main body, and the support plate 17 is arranged on the left outer side wall and the right outer side wall of the guide plate 1. The supporting plate 17 thus arranged does not obstruct the view of the doctor's operation and does not obstruct the movement of the operating handle 2.
The contact pad 171 is made of a soft medical nontoxic silica gel material. The contact pad 171 has good flexibility and anti-slip property, so that the support plate 17 can be prevented from sliding while the comfort of the patient is ensured.
As shown in fig. 5, a scale line 14 and a scale value 15 for measuring the depth of the operation handle 2 into the patient are provided on the upper end surface of the guide plate 1. This arrangement provides a depth reference for the medical personnel to access the operating handle 2 into the patient.
An anti-slip layer 13 for increasing the friction force between the hand of the doctor and the guide plate 1 is arranged at the rear end of the guide plate 1, namely the end close to the doctor, and the anti-slip layer 13 is integrally connected with the outer side wall of the guide plate 1. This arrangement facilitates the operation of holding the guide plate 1 by a doctor.
And the left outer side wall and the right outer side wall of the guide plate 1 are both provided with an anti-skid layer 13.
The balloon structure 3 is made of medical nontoxic soft silica gel material. The balloon structure 3 arranged in this way has good flexibility and does not damage the tyre bag.
EXAMPLE 4 fetal sac replacement Structure for Emergency cervical cerclage with protruding fetal sac in vagina
The fetal sac resetting structure used for emergent cervical cerclage operation with the fetal sac protruding out of the vagina comprises an operating handle 2 and a balloon structure 3 used for pushing up the fetal sac, and is characterized in that the balloon structure 3 is arranged at one end of the operating handle 2; the guiding structure is used for assisting the operating handle 2 to enter the body of a patient and is connected with the operating handle 2 in a sliding mode. Provide the guide effect for operating handle 2 through guide structure, operating handle 2 slides on guide structure, can guarantee that operating handle 2 gets into the patient internal steadily.
The main part of operating handle 2 is the cylinder, and sacculus structure 3 sets up the one end that enters the patient at the front end of operating handle 2 promptly at first, sacculus structure 3 and operating handle 2's lateral wall body coupling. The operating handle 2 is smooth in appearance and free of edges and corners, and can avoid scratching the vagina and cervix of a patient.
The inside of operating handle 2 includes a pipeline of intercommunication sacculus structure 3, and operating handle 2 passes through the pipeline and communicates with sacculus structure 3. This arrangement communicates the interior of the operating handle 2 with the balloon structure 3.
An injection tube 21 is provided at the operation end of the operation handle 2, i.e., the end close to the doctor, the injection tube 21 is communicated with the pipeline inside the operation handle 2, and liquid or gas is injected into the balloon structure 3 through the injection tube 21. When in use, liquid or gas is input into the injection tube 21 through the syringe, so that the balloon structure 3 is expanded to an appropriate size.
A rubber plug 211 is arranged at the nozzle of the injection tube 21, and the edge of the rubber plug 211 is integrally connected with the inner wall of the injection tube 21. When the rubber plug 211 is used, the syringe punctures the rubber plug 211 so as to inject liquid or gas, and the arrangement of the rubber plug 211 can avoid the overflow of the liquid or the gas.
The guide structure comprises a guide main body and a supporting structure, the supporting structure is arranged at the front end of the guide main body, and the supporting structure and the guide main body are integrally connected. During the use, paste bearing structure on patient's health, for the direction main part provides the strong point, guarantee the steady of direction main part.
The guide main body is a rectangular guide plate 1, a sliding groove 11 is formed in the upper end of the guide plate 1, a sliding block 12 is arranged in the sliding groove 11, and the upper end of the sliding block 12 is fixedly connected with the operating end of the operating handle 2. When the pneumatic puncture needle is used, a doctor pushes the operation end of the operation handle 2 by hand, so that the sliding block 12 can move in the sliding groove 11, the operation handle 2 moves, the balloon structure 3 at the front end of the operation handle 2 gradually enters the body of a patient, and a fetal sac is pushed upwards.
The opening of the sliding chute 11 is upward, and the sliding chute 11 can accommodate a sliding block 12; the sliding block 12 is a convex sliding block 12, and the upper end of the sliding block 12 extends out of the sliding groove 11. This arrangement leaves an operation space for pushing the operation handle 2.
As shown in fig. 5, a push handle 121 for conveniently pushing the slider 12 is provided on one side wall of the upper end of the slider 12, and the push handle 121 is integrally connected with the slider 12. When the sliding block is used, the sliding block 12 and the operating handle 2 can be pushed to move by applying force to the push handle 121 by hands.
The support structure includes a support plate 17 and a contact pad 171, the support plate 17 is integrally connected to the outer side wall of the front end of the guide plate 1, and the contact pad 171 is integrally connected to the free end of the support plate 17. In use, the support plate 17 serves as the primary support by contacting the buttocks of the patient with the contact pad 171 and provides a point of support for the guide plate 1.
The support plate 17 is a plate which is expanded outwards and has a rectangular main body, and the support plate 17 is arranged on the left outer side wall and the right outer side wall of the guide plate 1. The supporting plate 17 thus arranged does not obstruct the view of the doctor's operation and does not obstruct the movement of the operating handle 2.
The contact pad 171 is made of a soft medical nontoxic silica gel material. The contact pad 171 has good flexibility and anti-slip property, so that the support plate 17 can be prevented from sliding while the comfort of the patient is ensured.
The upper end face of the guide plate 1 is provided with scale marks 14 and scale values 15 for measuring the depth of the operation handle 2 entering the body of a patient. This arrangement provides a depth reference for the medical personnel to access the operating handle 2 into the patient.
An anti-slip layer 13 for increasing the friction force between the hand of the doctor and the guide plate 1 is arranged at the rear end of the guide plate 1, namely the end close to the doctor, and the anti-slip layer 13 is integrally connected with the outer side wall of the guide plate 1. This arrangement facilitates the operation of holding the guide plate 1 by a doctor.
And the left outer side wall and the right outer side wall of the guide plate 1 are both provided with an anti-skid layer 13.
The balloon structure 3 is made of medical nontoxic soft silica gel material. The balloon structure 3 arranged in this way has good flexibility and does not damage the tyre bag.
EXAMPLE 5 fetal sac replacement Structure for Emergency cervical cerclage with protruding fetal sac in vagina
The fetal sac resetting structure used for emergent cervical cerclage operation with the fetal sac protruding out of the vagina comprises an operating handle 2 and a balloon structure 3 used for pushing up the fetal sac, and is characterized in that the balloon structure 3 is arranged at one end of the operating handle 2; the guiding structure is used for assisting the operating handle 2 to enter the body of a patient and is connected with the operating handle 2 in a sliding mode. Provide the guide effect for operating handle 2 through guide structure, operating handle 2 slides on guide structure, can guarantee that operating handle 2 gets into the patient internal steadily.
The main part of operating handle 2 is the cylinder, and sacculus structure 3 sets up the one end that enters the patient at the front end of operating handle 2 promptly at first, sacculus structure 3 and operating handle 2's lateral wall body coupling. The operating handle 2 is smooth in appearance and free of edges and corners, and can avoid scratching the vagina and cervix of a patient.
The inside of operating handle 2 includes a pipeline of intercommunication sacculus structure 3, and operating handle 2 passes through the pipeline and communicates with sacculus structure 3. This arrangement communicates the interior of the operating handle 2 with the balloon structure 3.
An injection tube 21 is provided at the operation end of the operation handle 2, i.e., the end close to the doctor, the injection tube 21 is communicated with the pipeline inside the operation handle 2, and liquid or gas is injected into the balloon structure 3 through the injection tube 21. When in use, liquid or gas is input into the injection tube 21 through the syringe, so that the balloon structure 3 is expanded to an appropriate size.
A rubber plug 211 is arranged at the nozzle of the injection tube 21, and the edge of the rubber plug 211 is integrally connected with the inner wall of the injection tube 21. When the rubber plug 211 is used, the syringe punctures the rubber plug 211 so as to inject liquid or gas, and the arrangement of the rubber plug 211 can avoid the overflow of the liquid or the gas.
The guide structure comprises a guide main body and a supporting structure, the supporting structure is arranged at the front end of the guide main body, and the supporting structure and the guide main body are integrally connected. During the use, paste bearing structure on patient's health, for the direction main part provides the strong point, guarantee the steady of direction main part.
The guide main body is a rectangular guide plate 1, a sliding groove 11 is formed in the upper end of the guide plate 1, a sliding block 12 is arranged in the sliding groove 11, and the upper end of the sliding block 12 is fixedly connected with the operating end of the operating handle 2. When the pneumatic puncture needle is used, a doctor pushes the operation end of the operation handle 2 by hand, so that the sliding block 12 can move in the sliding groove 11, the operation handle 2 moves, the balloon structure 3 at the front end of the operation handle 2 gradually enters the body of a patient, and a fetal sac is pushed upwards.
The opening of the sliding chute 11 is upward, and the sliding chute 11 can accommodate a sliding block 12; the sliding block 12 is a convex sliding block 12, and the upper end of the sliding block 12 extends out of the sliding groove 11. This arrangement leaves an operation space for pushing the operation handle 2.
A side wall at the upper end of the sliding block 12 is provided with a pushing handle 121 which is convenient for pushing the sliding block 12, and the pushing handle 121 is integrally connected with the sliding block 12. When the sliding block is used, the sliding block 12 and the operating handle 2 can be pushed to move by applying force to the push handle 121 by hands.
As shown in fig. 1, a bracket 16 for supporting the front end of the operation handle 2 is provided at the front end of the guide plate 1, i.e., the end close to the patient, the bracket 16 is provided at the upper end of the guide plate 1, and the bottom of the bracket 16 is integrally connected to the guide plate 1. The arrangement keeps the whole operating handle 2 in a stable state through the supporting function of the bracket 16, and when the operating handle 2 is pushed to use, the operating handle 2 slides over the bracket 16.
The bracket 16 includes a semicircular groove having an inner diameter larger than an outer diameter of the operating handle 2, the groove being used to support the operating handle 2.
The support structure includes a support plate 17 and a contact pad 171, the support plate 17 is integrally connected to the outer side wall of the front end of the guide plate 1, and the contact pad 171 is integrally connected to the free end of the support plate 17. In use, the support plate 17 serves as the primary support by contacting the buttocks of the patient with the contact pad 171 and provides a point of support for the guide plate 1.
The support plate 17 is a plate which is expanded outwards and has a rectangular main body, and the support plate 17 is arranged on the left outer side wall and the right outer side wall of the guide plate 1. The supporting plate 17 thus arranged does not obstruct the view of the doctor's operation and does not obstruct the movement of the operating handle 2.
The contact pad 171 is made of a soft medical nontoxic silica gel material. The contact pad 171 has good flexibility and anti-slip property, so that the support plate 17 can be prevented from sliding while the comfort of the patient is ensured.
The upper end face of the guide plate 1 is provided with scale marks 14 and scale values 15 for measuring the depth of the operation handle 2 entering the body of a patient. This arrangement provides a depth reference for the medical personnel to access the operating handle 2 into the patient.
An anti-slip layer 13 for increasing the friction force between the hand of the doctor and the guide plate 1 is arranged at the rear end of the guide plate 1, namely the end close to the doctor, and the anti-slip layer 13 is integrally connected with the outer side wall of the guide plate 1. This arrangement facilitates the operation of holding the guide plate 1 by a doctor.
And the left outer side wall and the right outer side wall of the guide plate 1 are both provided with an anti-skid layer 13.
The balloon structure 3 is made of medical nontoxic soft silica gel material. The balloon structure 3 arranged in this way has good flexibility and does not damage the tyre bag.
The above description of the embodiments is only intended to illustrate the present invention. It should be noted that, for those skilled in the art, without departing from the principle of the present invention, several modifications can be made to the present invention, and these modifications will fall within the protection scope of the claims of the present invention.
Claims (10)
1. The fetal sac resetting structure used for emergent cervical cerclage operation with the fetal sac protruding out of the vagina comprises an operating handle and a saccule structure used for pushing up the fetal sac, and is characterized in that the saccule structure is arranged at one end of the operating handle; the setting is used for assisting operating handle gets into the internal guide structure of patient, guide structure and operating handle sliding connection.
2. The fetal capsule repositioning structure for use in emergent intravaginal cervical cerclage of fetal capsule herniation according to claim 1, wherein the interior of the operating handle comprises a conduit communicating with the balloon structure, and the operating handle is communicated with the balloon structure through the conduit.
3. The structure of claim 2, wherein an injection tube is disposed at the operation end of the operation handle, i.e. the end close to the doctor, the injection tube is communicated with the pipeline inside the operation handle, and liquid or gas is injected into the balloon structure through the injection tube.
4. The structure of claim 3, wherein a rubber plug is arranged at the mouth of the injection tube, and the edge of the rubber plug is integrally connected with the inner wall of the injection tube.
5. The structure of claim 2, wherein the guide structure comprises a guide body and a support structure, the support structure is disposed at a front end of the guide body, and the support structure is integrally connected with the guide body.
6. The structure for the restoration of the fetal capsule during the emergent cervical cerclage operation with the protruding fetal capsule in the vagina as claimed in claim 5, wherein the guiding main body is a rectangular guiding plate, a sliding groove is arranged at the upper end of the guiding plate, a sliding block is arranged in the sliding groove, and the upper end of the sliding block is fixedly connected with the operating end of the operating handle.
7. The fetal capsule repositioning structure for the emergent intracervical cerclage with protruding fetal capsule in the vagina as claimed in claim 6, wherein a pushing handle is provided on one side wall of the upper end of the sliding block for pushing the sliding block conveniently, and the pushing handle is integrally connected with the sliding block.
8. The structure of claim 6, wherein a support for supporting the front end of the operation handle is provided at the front end of the guide plate, i.e. the end close to the patient, the support is provided at the upper end of the guide plate, and the bottom of the support is integrally connected with the guide plate.
9. The fetal capsule repositioning structure for use in emergent intravaginal cervical cerclage of a protruding fetal capsule according to claim 5, wherein the support structure comprises a support plate integrally connected to the outer sidewall of the front end of the guide plate and a contact pad integrally connected to the free end of the support plate.
10. The structure for the reduction of the fetal capsule during the emergent intravaginal cervical cerclage of the protruding fetal capsule according to any one of claims 6 to 9, wherein the guide plate is provided at the upper end surface thereof with graduation lines and graduation values for measuring the depth of the operating handle entering the body of the patient.
Priority Applications (1)
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CN202022612985.7U CN213940919U (en) | 2020-11-12 | 2020-11-12 | Fetal sac resetting structure for emergent cervical cerclage operation of fetal sac protruding into vagina |
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CN202022612985.7U CN213940919U (en) | 2020-11-12 | 2020-11-12 | Fetal sac resetting structure for emergent cervical cerclage operation of fetal sac protruding into vagina |
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CN202022612985.7U Active CN213940919U (en) | 2020-11-12 | 2020-11-12 | Fetal sac resetting structure for emergent cervical cerclage operation of fetal sac protruding into vagina |
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