A clinical obstetric membrane rupture device

By designing a clinical obstetric membrane rupturizer, including instrument rod body, diversion tube, mobile rod, membrane ruptured head and probe head, the problems of difficulty in controlling membrane ruptured process and patient safety risks in the prior art are solved, and smooth amniotic fluid drainage and patient safety protection are achieved.

CN222693496UActive Publication Date: 2025-04-01HAINAN MODERN WOMENS XINGGUANG HOSPITAL CO LTD
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Patent Information

Application Number
CN202421210492.2
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2024-05-30
Publication Date
2025-04-01
Estimated Expiration
2034-05-30

AI Technical Summary

Technical Problem

In obstetrics, the prior art is difficult to effectively control the membrane rupture process, which makes it difficult for doctors to control the intensity manually, which may cause harm to the patient. Moreover, the vascular forceps penetrate deep into the body and are inconvenient to observe, which increases the process of membrane rupture and may cause secondary damage.

Method used

A clinical obstetric membrane rupturizer is designed, including an instrument rod body, a flow tube, a moving rod, a ruptured head and a probe head. There is a hollow cavity and a flow guide tube in the body of the instrument rod to drain amniotic fluid; there is a rupture head and a probe head on the mobile rod. The probe head can help the doctor observe the rupture process and avoid excessive force.

Benefits of technology

Through this rupturizer, amniotic fluid can be drained smoothly to avoid accumulation and discomfort; the use of the probe head reduces the risk of excessive force from the doctor, protects the patient's safety, and can observe the movement of the moving rod at all times to prevent misalignment and other injuries.

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Abstract

The utility model relates to the technical field of obstetric membrane rupture devices, and in particular to a clinical obstetric membrane rupture device, comprising an instrument rod body, wherein a hollow cavity for amniotic fluid drainage is provided inside the instrument rod body, and a drainage tube communicating with the hollow cavity is installed on the instrument rod body; a moving rod passing through the hollow cavity is also arranged inside the instrument rod body, and a membrane rupture head is arranged on the side of the moving rod which is not in the hollow cavity, and a detection head is arranged on the moving rod. With the help of the detection head, the doctor can check the situation that the membrane rupture head contacts the fetal membrane. Once the fetal membrane is punctured, the doctor can stop the rotation of the adjustment screw, thereby avoiding the doctor's excessive force operation and effectively protecting the patient. At the same time, the existence of the detection head allows the doctor to observe the movement of the moving rod at all times, avoiding the phenomenon of movement dislocation of the moving rod and preventing the patient from other injuries.
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Description

Technical Field

[0001] The utility model relates to the technical field of obstetric membrane rupture devices, in particular to a clinical obstetric membrane rupture device. Background Art

[0002] In the clinical practice of obstetrics and gynecology, for parturients with weak and difficult uterine contractions during the active period, it is generally necessary to artificially puncture the amniotic membrane to help them give birth. Artificial rupture of membranes is to artificially intervene to tear the amniotic membrane at the cervical os in order to observe the color of amniotic fluid, strengthen uterine contractions and accelerate the progress of labor. Then doctors usually use vascular clamps to tear the fetal membrane, but vascular clamps are not sharp enough;

[0003] Therefore, in the actual process of rupturing the membrane, it is difficult for the doctor to control the strength during manual operation. Excessive force will cause harm to the patient and increase the difficulty of medical work. In addition, the vascular clamp needs to go deep into the patient's body. This situation is not convenient for the doctor to observe the position of the vascular clamp to perform the work, which will greatly increase the progress of the membrane rupture work. At the same time, during the penetration process, the vascular clamp will contact other parts of the patient, causing epidermal damage to the patient and causing secondary harm to the patient. Utility Model Content

[0004] In view of the above-mentioned problems that the membrane breaking operation is difficult and it is inconvenient to observe the membrane breaking situation, the present utility model is proposed.

[0005] In order to solve the above technical problems, the utility model provides the following technical solutions: a clinical obstetric membrane rupture device, comprising a device rod body, wherein a hollow cavity for amniotic fluid drainage is provided inside the device rod body, and a drainage tube communicating with the hollow cavity is installed on the device rod body;

[0006] A moving rod passing through the hollow cavity is also arranged in the rod body of the device, and a membrane breaking head is arranged on the side of the moving rod not in the hollow cavity, and a detection head is arranged on the moving rod.

[0007] As a preferred solution of the clinical obstetric membrane rupture device of the utility model, the membrane rupture head is symmetrically arranged above and below the detection head, wherein the membrane rupture head is arranged in a sharp shape on the side away from the moving rod.

[0008] As a preferred solution of the clinical obstetric membrane rupture device of the utility model, wherein: the device rod body is provided with a rubber plug, wherein an airway is installed on the rubber plug.

[0009] As a preferred solution of the clinical obstetric membrane rupture device of the utility model, the side of the airway tube away from the rubber stopper is connected to an inflation bag, wherein the airway tube passes through the rod body of the device.

[0010] As a preferred solution of the clinical obstetric membrane rupture device of the utility model, a collar fixedly connected to the rod body of the device is arranged in the hollow cavity, wherein a threaded adjustment screw is penetrated through the collar.

[0011] As a preferred solution of the clinical obstetric membrane rupture device of the utility model, the adjusting screw and the moving rod are movably connected, and a guide frame fixedly connected to the rod body of the device is arranged in the hollow cavity.

[0012] As a preferred solution of the clinical obstetric membrane rupture device of the utility model, a pull rod is arranged in the guide frame, wherein the pull rod is fixedly connected to the moving rod.

[0013] As a preferred solution of the clinical obstetric membrane rupture device of the utility model, an electric wire is provided through the middle of the adjusting screw, wherein the electric wire passes through the moving rod to be connected with the detection head.

[0014] Beneficial effects of the utility model:

[0015] 1. After the membrane ruptures, the amniotic fluid can enter the hollow cavity, and the drainage tube can be used to discharge the amniotic fluid inside the hollow cavity, which can prevent the amniotic fluid from accumulating in the patient's body and prevent the patient from feeling uncomfortable;

[0016] 2. With the help of the detection head, the doctor can check the contact between the rupture head and the fetal membrane. Once the fetal membrane is punctured, the doctor can stop the rotation of the adjustment screw to avoid the doctor's excessive force and effectively protect the patient. At the same time, the presence of the detection head allows the doctor to always observe the movement of the moving rod to avoid the movement of the moving rod and prevent the patient from other injuries. BRIEF DESCRIPTION OF THE DRAWINGS

[0017] In order to more clearly illustrate the technical solutions of the embodiments of the present utility model, the following briefly introduces the drawings required for the description of the embodiments. Obviously, the drawings described below are only some embodiments of the present utility model. For ordinary technicians in this field, other drawings can be obtained based on these drawings without creative labor. Among them:

[0018] Figure 1 It is a schematic diagram of the three-dimensional structure of the utility model.

[0019] Figure 2 It is a half-section stereoscopic schematic diagram of the rod body of the utility model.

[0020] Figure 3 It is a three-dimensional schematic diagram of the mobile rod of the utility model.

[0021] Figure 4It is a three-dimensional schematic diagram of the adjusting screw of the utility model.

[0022] Explanation of the reference numerals: 1. Instrument rod body; 101. Rubber plug; 102. Air guide tube; 103. Inflatable bag; 11. Hollow cavity; 1101. Ring; 1102. Adjustment screw; 1103. Guide frame; 1104. Pull rod; 1105. Electric wire; 12. Flow guide tube; 13. Moving rod; 14. Film breaking head; 15. Detection head. DETAILED DESCRIPTION

[0023] In order to make the above-mentioned purposes, features and advantages of the present invention more obvious and easy to understand, the specific implementation methods of the present invention are described in detail below in conjunction with the accompanying drawings.

[0024] Example 1

[0025] Reference Figure 1-2 , which is the first embodiment of the utility model, provides a clinical obstetric membrane rupture device, including an instrument rod body 1, the interior of the instrument rod body 1 is provided with a hollow cavity 11 for amniotic fluid drainage, and the instrument rod body 1 is installed with a drainage tube 12 which is interconnected with the hollow cavity 11; after the membrane is ruptured, the amniotic fluid can enter the interior of the hollow cavity 11, and the drainage tube 12 can be used to discharge the amniotic fluid inside the hollow cavity 11, so that the amniotic fluid can be prevented from accumulating in the patient's body and preventing the patient from feeling uncomfortable.

[0026] A moving rod 13 passing through the hollow cavity 11 is also provided in the instrument body 1 . The moving rod 13 is arranged in a T-shape, and a membrane breaking head 14 is provided on the side of the moving rod 13 which is not in the hollow cavity 11 . A detection head 15 is provided on the moving rod 13 .

[0027] The membrane-breaking heads 14 are symmetrically arranged above and below the detection head 15 , wherein the side of the membrane-breaking head 14 away from the moving rod 13 is arranged in a sharp shape.

[0028] The tool rod body 1 is provided with a rubber plug 101 , which is fixed to the tool rod body 1 by glue, wherein an air guide tube 102 is installed on the rubber plug 101 .

[0029] The side of the airway tube 102 away from the rubber plug 101 is connected to the inflation bag 103, wherein the airway tube 102 is arranged through the device rod 1. A one-way valve is arranged on the airway tube 102, and the gas inside the inflation bag 103 can be filled into the rubber plug 101 through the airway tube 102 to expand the rubber plug 101. The expanded rubber plug 101 can seal the patient's genitals to prevent the sudden outflow of amniotic fluid and affect the doctor's work.

[0030] Example 2

[0031] Reference Figure 1-4, which is the second embodiment of the utility model, and this embodiment is different from the first embodiment in that: a collar 1101 fixedly connected to the tool rod 1 is arranged in the hollow cavity 11, and the collar 1101 is welded to the tool rod 1, wherein a threaded adjustment screw 1102 is arranged through the collar 1101. The adjustment screw 1102 is arranged in a T shape.

[0032] The adjusting screw 1102 is movably connected to the moving rod 13 , and the adjusting screw 1102 and the moving rod 13 are connected via a rotating shaft, wherein a guide frame 1103 fixedly connected to the device rod body 1 is arranged in the hollow cavity 11 .

[0033] A tension rod 1104 is provided in the guide frame 1103 , wherein the tension rod 1104 is fixedly connected to the moving rod 13 .

[0034] A wire 1105 is provided through the middle of the adjustment screw 1102, wherein the wire 1105 passes through the moving rod 13 and is connected to the detection head 15. The wire 1105 is electrically connected to the detection head 15, and the side of the wire 1105 away from the detection head 15 is connected to the display screen.

[0035] After the rubber stopper 101 seals the patient's genitals, the adjusting screw 1102 is rotated to push the moving rod 13. Under the guidance of the guide frame 1103 on the tension rod 1104, the moving rod 13 moves. Through the movement of the moving rod 13, the membrane rupture head 14 is controlled to gradually approach the fetal membrane. At the same time, the doctor can use the detection head 15 to check the contact between the membrane rupture head 14 and the fetal membrane. Once the fetal membrane is punctured, the doctor can stop the rotation of the adjusting screw 1102, which can avoid the doctor's excessive force and effectively protect the patient. At the same time, the existence of the detection head 15 allows the doctor to observe the movement of the moving rod 13 at all times to avoid the movement dislocation of the moving rod 13 and prevent the patient from other injuries.

[0036] The remaining structures are the same as those of Example 1.

[0037] It should be noted that the above embodiments are only used to illustrate the technical solution of the utility model rather than to limit it. Although the utility model has been described in detail with reference to the preferred embodiments, ordinary technicians in the field should understand that the technical solution of the utility model can be modified or replaced by equivalents without departing from the spirit and scope of the technical solution of the utility model, which should be included in the scope of the claims of the utility model.

Claims

1. A clinical obstetric membrane rupture device, comprising a device rod (1), characterized in that: The device rod body (1) is provided with a hollow cavity (11) for amniotic fluid drainage, and a drainage tube (12) communicating with the hollow cavity (11) is installed on the device rod body (1); A moving rod (13) passing through the hollow cavity (11) is also provided in the tool rod body (1), and a membrane breaking head (14) is provided on the side of the moving rod (13) not in the hollow cavity (11), and a detection head (15) is provided on the moving rod (13).

2. A clinical obstetric membrane rupture device according to claim 1, characterized in that: The membrane-breaking head (14) is symmetrically arranged above and below the detection head (15), wherein the side of the membrane-breaking head (14) away from the moving rod (13) is arranged in a sharp shape.

3. A clinical obstetric membrane rupture device according to claim 1, characterized in that: The device rod body (1) is provided with a rubber stopper (101), wherein an air guide tube (102) is installed on the rubber stopper (101).

4. A clinical obstetric membrane rupture device according to claim 3, characterized in that: The side of the air guide tube (102) away from the rubber stopper (101) is connected to an inflation bag (103), wherein the air guide tube (102) is arranged through the device rod body (1).

5. The clinical obstetric membrane rupture device according to claim 2, characterized in that: A sleeve (1101) fixedly connected to the tool rod body (1) is arranged in the hollow cavity (11), wherein a threaded adjustment screw (1102) is provided through the sleeve (1101).

6. A clinical obstetric membrane rupture device according to claim 5, characterized in that: The adjusting screw rod (1102) is movably connected to the moving rod (13), wherein a guide frame (1103) fixedly connected to the tool rod body (1) is arranged in the hollow cavity (11).

7. A clinical obstetric membrane rupture device according to claim 6, characterized in that: A tension rod (1104) is arranged in the guide frame (1103), wherein the tension rod (1104) is fixedly connected to the moving rod (13).

8. A clinical obstetric membrane rupture device according to claim 7, characterized in that: An electric wire (1105) is provided through the middle of the adjusting screw rod (1102), wherein the electric wire (1105) passes through the moving rod (13) and is connected to the detection head (15).