Fetal heart rate monitoring equipment for lateral position delivery

Abstract

The utility model discloses fetal heart monitoring equipment for lateral position delivery, which comprises at least two connecting seats, a placing cavity arranged on the connecting seats, a plurality of limiting components arranged in the placing cavity, and a detection probe positioned in the placing cavity and propped against the limiting components, the two belt bodies are symmetrically mounted on the connecting seat; the two belt bodies on one connecting base are connected with the other two belt bodies respectively, and the free ends of the other two belt bodies are connected through a buckle. The monitoring equipment in the device can monitor the fetal heart of a baby in the belly of a pregnant woman for lateral parturition, meanwhile, through the arranged belt body, the position of the detection probe can be fixed, the position of the detection probe is prevented from deviating, and therefore the accuracy of a detection result is guaranteed.

Description

Technical Field

[0001] The utility model belongs to the technical field of fetal heart monitoring, and in particular relates to a fetal heart monitoring device for lateral position delivery. Background Art

[0002] Based on the concept of healthy childbirth, promoting natural childbirth and reducing the cesarean section rate, various free-position delivery methods are being implemented in obstetrics and gynecology hospitals in my country. In clinical observations, it was found that side-lying delivery is beneficial to improving maternal and fetal blood supply and oxygen supply, correcting maternal and fetal problems such as fetal position and abnormal fetal heart sounds, and reducing the possibility of perineal laceration during vaginal delivery.

[0003] During the delivery process, in order to ensure the normal life activities of the baby, medical staff are required to hold the fetal heart rate monitor on the pregnant woman's belly. Since the delivery process is long, it will take a long time for medical staff to hold the monitor. Therefore, most of the existing side-lying delivery fetal heart rate monitors are provided with a belt with predetermined elasticity, which is put on the pregnant woman's belly through a buckle, and the position of the detection probe is adjusted by adjusting the position of the buckle to complete the monitoring of the baby's fetal heart rate. However, since the existing belt body and the detection probe are of an integrated structure, when the detection probe or the belt body is damaged, it needs to be replaced as a whole, which leads to a waste of resources.

[0004] Therefore, how to replace the corresponding damaged parts in the fetal heart monitoring device is a problem to be solved at present. Utility Model Content

[0005] The purpose of the utility model is to provide a fetal heart rate monitoring device for side-lying delivery to solve the above-mentioned problems existing in the prior art.

[0006] Technical solution: A fetal heart rate monitoring device for side-lying delivery, comprising:

[0007] At least two connecting seats, a placement cavity provided on the connecting seats, a plurality of limiter components provided in the placement cavity, a detection probe located in the placement cavity and abutting against the limiter components, and two belt bodies symmetrically installed on the connecting seats;

[0008] The two belt bodies on one of the connecting seats are respectively connected to the other two belt bodies, and the free ends of the other two belt bodies are connected by buckles.

[0009] In a further embodiment, the number of the limiting components is four and they are evenly arranged in the placement cavity.

[0010] In a further embodiment, the limiting assembly includes a mounting seat fixedly connected to the connecting seat, a rotating shaft rotatably connected to the mounting seat, an adjusting rod sleeved on the rotating shaft, and a limiting ball provided at one end of the adjusting rod;

[0011] The shell of the detection probe is provided with a limiting groove for accommodating a limiting ball and a limiting rod.

[0012] In a further embodiment, the limit assembly further includes a knob disposed on the rotating shaft;

[0013] The knob is located at one end of the rotation axis away from the patient. By rotating the knob, the position of the limit rod is adjusted so that the limit ball fixes the position of the detection probe.

[0014] In a further embodiment, the detection probes are respectively a uterine contraction probe and a fetal heart rate probe, and a transmission line for connecting the uterine contraction probe and the fetal heart rate probe;

[0015] During monitoring, the uterine contraction probe is located above the fetal heart rate probe.

[0016] In a further embodiment, the belt body has a predetermined elasticity.

[0017] In a further embodiment, a protection pad is provided at a position of the connecting seat close to the patient, and the protection pad has a predetermined elasticity.

[0018] Beneficial effect: The utility model relates to a fetal heart monitoring device for side-lying delivery. When the belt body or one of the detection probes is damaged, the medical staff manually rotates or rotates the knob through a tool, and the rotating knob can drive the rotating shaft to rotate, and the moving rotating shaft can drive the adjusting rod to rotate, and the moving adjusting rod can drive the limiting ball to move, so that the limiting ball can be away from the limiting groove on the detection probe, and the four knobs are rotated in sequence to make the limiting ball away from the detection probe. The medical staff then replaces the damaged belt body or detection probe, and then places the new detection probe in the placement cavity on the belt body, and rotates the knob in the opposite direction to make the limiting ball approach the detection probe and abut against the detection probe, thereby completing the replacement of the detection probe. The replaced monitoring device can monitor the fetal heart rate of the baby in the belly of a pregnant woman giving birth in the side-lying position. At the same time, the position of the detection probe can be fixed through the set belt body to avoid the position of the detection probe from being offset, thereby ensuring the accuracy of the detection result. BRIEF DESCRIPTION OF THE DRAWINGS

[0019] Figure 1 It is a schematic diagram of the utility model.

[0020] Figure 2 It is a schematic diagram of the limit assembly in the utility model.

[0021] Figure 3 It is a three-dimensional diagram of the position limiting component in the utility model.

[0022] The reference numerals in the figure are: connecting seat 1, belt body 2, buckle 3, transmission line 4, fetal heart rate probe 5, uterine contraction probe 6, limit assembly 7, mounting seat 71, knob 72, rotating shaft 73, adjusting rod 74, and limit ball 75. DETAILED DESCRIPTION

[0023] After the applicant's research and analysis, the reason for this problem (when the detection probe or belt body is damaged, it needs to be replaced as a whole, which leads to a waste of resources) is that most of the existing side-lying delivery fetal heart rate monitors are equipped with a belt with predetermined elasticity, which is put on the belly of the pregnant woman by a buckle, and the position of the detection probe is adjusted by adjusting the position of the buckle to complete the monitoring of the fetal heart rate of the baby. However, since the existing belt body and the detection probe are an integrated structure, when the detection probe or the belt body is damaged, it needs to be replaced as a whole. In the present invention, when the belt body or one of the detection probes is damaged, the medical staff manually turns the knob or uses a tool to turn the knob, and the rotating knob can drive the rotating shaft to rotate, and the rotation of the movement The shaft can drive the adjusting rod to rotate, and then the moving adjusting rod can drive the limiting ball to move, so that the limiting ball can be away from the limiting groove on the detection probe, and the four knobs are turned in sequence to make the limiting ball away from the detection probe. Then the medical staff replaces the damaged belt body or detection probe, and then places the new detection probe in the placement cavity on the belt body, and then turns the knob in the opposite direction to make the limiting ball approach the detection probe and abut against the detection probe, thereby completing the replacement of the detection probe. The replaced monitoring equipment can monitor the fetal heart rate of the baby in the belly of a pregnant woman giving birth in the side-lying position. At the same time, the position of the detection probe can be fixed through the set belt body to avoid the position of the detection probe from being offset, thereby ensuring the accuracy of the detection result.

[0024] A fetal heart rate monitoring device for side-lying delivery comprises: a connecting seat 1, a belt body 2, a buckle 3, a transmission line 4, a fetal heart rate probe 5, a uterine contraction probe 6, a limit assembly 7, a mounting seat 71, a knob 72, a rotating shaft 73, an adjusting rod 74, and a limit ball 75.

[0025] The device comprises at least two connecting seats 1, a placement cavity provided on the connecting seat 1, a plurality of limiting components 7 provided in the placement cavity, a detection probe located in the placement cavity and abutting against the limiting components 7, and two belt bodies 2 symmetrically mounted on the connecting seat 1; the two belt bodies 2 on one of the connecting seats 1 are respectively connected to the other two belt bodies 2, and the free ends of the other two belt bodies 2 are connected by buckles 3; the limiting component 7 comprises a mounting seat 71 fixedly connected to the connecting seat 1, a rotating shaft 73 rotatably connected to the mounting seat 71, an adjusting rod 74 sleeved on the rotating shaft 73, and a limiting ball 75 provided at one end of the adjusting rod 74; a limiting groove for placing the limiting ball 75 and the limiting rod is provided on the shell of the detection probe; the limiting component 7 also comprises a knob 72 provided on the rotating shaft 73; the knob 72 is located at one end of the rotating shaft 73 away from the patient, and the position of the limiting rod is adjusted by rotating the knob 72, so that the limiting ball 75 fixes the position of the detection probe; When the belt 2 or one of the detection probes is damaged, the medical staff manually rotates or rotates the knob 72 through a tool, and the rotating knob 72 can drive the rotating shaft 73 to rotate, and the moving rotating shaft 73 can drive the adjusting rod 74 to rotate, and the moving adjusting rod 74 can drive the limiting ball 75 to move, so that the limiting ball 75 can be away from the limiting groove on the detection probe, and the four knobs 72 are rotated in sequence to make the limiting ball 75 away from the detection probe. Then the medical staff replaces the damaged belt 2 or detection probe, and then places the new detection probe in the placement cavity on the belt 2, and then rotates the knob 72 in the opposite direction, so that the limiting ball 75 is close to the detection probe and abuts against the detection probe, thereby completing the replacement of the detection probe. The replaced monitoring device can monitor the fetal heart rate of the baby in the belly of a pregnant woman giving birth in the lateral position. At the same time, the detection probe position can be fixed through the set belt 2 to avoid the displacement of the detection probe position, thereby ensuring the accuracy of the detection result.

[0026] There are four limit components 7, which are evenly arranged in the placement cavity. Through the placement cavity, the initial limit work of the detection probe can be completed, thereby ensuring that the subsequent limit component 7 can complete the work of fixing the position of the detection probe.

[0027] The detection probes are respectively a uterine contraction probe 6 and a fetal heart rate probe 5, and a transmission line 4 for connecting the uterine contraction probe 6 and the fetal heart rate probe 5; during monitoring, the uterine contraction probe 6 is located above the fetal heart rate probe 5; through the set transmission line 4, the detection data in one of the probes can be transmitted to another probe, and the information is sent through the transmitter in the probe, and then can be received by the receiver, so that it can be displayed on the display, which makes it convenient for medical staff to record and monitor the fetal heart of the baby.

[0028] The belt body 2 has a predetermined elasticity; by providing the elastic belt body 2 and the buckle 3, the fetal heart monitoring device can be installed and the position can be adjusted, so that the detection probe can complete the fetal heart monitoring work of the baby.

[0029] The connection seat 1 is provided with a protective pad near the patient, and the protective pad has a predetermined elasticity to prevent the connection seat 1 from causing a huge squeeze on the belly of the pregnant woman and to prevent the baby from being injured.

[0030] The working principle is as follows: when the belt 2 or one of the detection probes is damaged, the medical staff manually rotates or uses a tool to rotate the knob 72, and the rotating knob 72 can drive the rotating shaft 73 to rotate, and the moving rotating shaft 73 can drive the adjusting rod 74 to rotate, and the moving adjusting rod 74 can drive the limiting ball 75 to move, so that the limiting ball 75 can be away from the limiting groove on the detection probe, and the four knobs 72 are rotated in sequence to make the limiting ball 75 away from the detection probe. Then the medical staff replaces the damaged belt 2 or detection probe, and then places the new detection probe in the placement cavity on the belt 2, and rotates the knob 72 in the opposite direction, so that the limiting ball 75 is close to the detection probe and abuts against the detection probe, thereby completing the replacement of the detection probe. The replaced monitoring device can monitor the fetal heart rate of the baby in the belly of a pregnant woman giving birth in the side-lying position.

[0031] As described above, although the present invention has been shown and described with reference to specific preferred embodiments, it should not be interpreted as limiting the present invention itself. Various changes can be made to it in form and detail without departing from the spirit and scope of the present invention defined in the appended claims.

Claims

1. A fetal heart rate monitoring device for side-lying delivery, characterized in that: include: At least two connecting seats, a placement cavity provided on the connecting seats, a plurality of limiter components provided in the placement cavity, a detection probe located in the placement cavity and abutting against the limiter components, and two belt bodies symmetrically installed on the connecting seats; The two belt bodies on one of the connecting seats are respectively connected to the other two belt bodies, and the free ends of the other two belt bodies are connected by buckles.

2. A fetal heart rate monitoring device for lateral delivery according to claim 1, characterized in that: The number of the limiting components is four, and they are evenly arranged in the placement cavity.

3. A fetal heart rate monitoring device for lateral delivery according to claim 2, characterized in that: The limiting assembly includes a mounting seat fixedly connected to the connecting seat, a rotating shaft rotatably connected to the mounting seat, an adjusting rod sleeved on the rotating shaft, and a limiting ball arranged at one end of the adjusting rod; The shell of the detection probe is provided with a limiting groove for accommodating a limiting ball and a limiting rod.

4. A fetal heart rate monitoring device for lateral delivery according to claim 3, characterized in that: The limiting assembly further includes a knob disposed on the rotating shaft; The knob is located at one end of the rotation axis away from the patient. By rotating the knob, the position of the limit rod is adjusted so that the limit ball fixes the position of the detection probe.

5. The fetal heart rate monitoring device for lateral delivery according to claim 1, characterized in that: The detection probes are respectively a uterine contraction probe and a fetal heart rate probe, and a transmission line for connecting the uterine contraction probe and the fetal heart rate probe; During monitoring, the uterine contraction probe is located above the fetal heart rate probe.

6. The fetal heart rate monitoring device for side-lying delivery according to claim 1, characterized in that: The belt body has predetermined elasticity.

7. The fetal heart rate monitoring device for lateral delivery according to claim 1, characterized in that: A protection pad is provided at a position of the connection seat close to the patient, and the protection pad has predetermined elasticity.

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