Noninvasive continuous blood pressure detector for preeclampsia risk prediction of pregnant women in perinatal period

Abstract

The invention relates to a noninvasive continuous blood pressure detector for preeclampsia risk prediction of a perinatal pregnant woman, which comprises a fixing frame main body, a blood pressure detection device, a detection buffer protection mechanism, an electronic detector and a visualization mechanism, the detection buffer protection mechanism is connected to the position between the blood pressure detection device and the fixing frame body, the electronic detector is electrically connected with the blood pressure detection device, the visualization mechanism is connected with the electronic detector, a bottom supporting rod is installed at the bottom of the damping bottom plate, and a movable positioning mechanism is installed at the bottom of the bottom supporting rod. Multiple sets of sensors are installed in the blood pressure detection device, an operation table is fixedly connected to one end of the bottom of the fixing frame body, a limiting base is installed at the top of the operation table, the electronic detector is located on one side of the limiting base, and the blood pressure detection device is installed in the limiting base; the method has the advantages that the detection precision is high, the detection stability is high, and results support clinical decisions.

Description

Technical Field

[0001] This invention belongs to the technical field of blood pressure monitoring equipment, specifically relating to a non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in perinatal pregnant women. Background Technology

[0002] Preeclampsia is a serious pregnancy complication that is often accompanied by abnormal fluctuations in blood pressure. If it is not identified and intervened in the early stages, it can seriously threaten the lives of both the pregnant woman and the fetus. Therefore, in the perinatal management process, early, continuous, and dynamic monitoring of the pregnant woman's blood pressure by medical institutions is of great significance for risk assessment and clinical decision-making regarding preeclampsia. Currently, in clinical prenatal examinations, a single blood pressure measurement is usually performed on the pregnant woman using a manual or electronic blood pressure monitor. However, this method only reflects the blood pressure status at a specific moment and is difficult to obtain the trend of blood pressure changes over a longer period of time, especially at night or at rest. Abnormal circadian rhythms of blood pressure (such as non-dipper blood pressure) are clinically recognized as an important early risk signal of preeclampsia. In practical clinical applications, single-measurement methods can easily lead to delayed or missed risk identification. Chinese Patent Publication No. CN221105818U discloses a blood pressure monitor that achieves blood pressure detection through a main unit, connecting tube, and wrist-arm cuff structure, and includes a storage mechanism for easy retraction and protection of the wrist-arm cuff. While this design represents an improvement in structural storage, its blood pressure detection method remains based on the traditional cuff inflation principle, primarily suitable for routine blood pressure monitoring scenarios. Furthermore, in clinical perinatal monitoring, the intermittent blood pressure monitoring method using a periodically inflated cuff still has limitations. Firstly, repeated inflation and pressurization can easily cause discomfort to pregnant women, affecting their cooperation during the examination, especially when observing blood pressure trends over extended periods, increasing the subject's tension and fatigue. Secondly, existing monitoring equipment is highly sensitive to changes in body position and limb movement during continuous monitoring, easily introducing motion artifacts that affect the stability and reliability of blood pressure data, thus limiting its clinical application in continuous perinatal risk assessment. In summary, there is a need for a non-invasive continuous blood pressure monitor for predicting the risk of preeclampsia in perinatal pregnant women, in order to solve the problems of existing technologies, such as the difficulty in non-invasive continuous and stable monitoring, the inability to accurately reflect the trend of blood pressure changes, and the difficulty for doctors to dynamically assess the risk of preeclampsia. Summary of the Invention

[0003] The purpose of this invention is to address the shortcomings of existing technologies, such as the difficulty in non-invasive continuous and stable monitoring, the inability to accurately reflect blood pressure change trends, and the difficulty for doctors to dynamically assess the risk of preeclampsia. This invention provides a specialized device that can combine non-invasiveness, comfort, long-term continuous monitoring with high precision, strong anti-interference capabilities, and integrated intelligent analysis and visualization early warning functions, so as to achieve closed-loop management of the blood pressure status of pregnant women in the perinatal period and early and dynamic prediction of the risk of preeclampsia. To achieve the above-mentioned technical objectives, the specific technical solution adopted by the present invention is as follows: A non-invasive continuous blood pressure monitor for predicting the risk of preeclampsia in perinatal pregnant women includes a fixed frame body, a blood pressure monitoring device, a detection buffer and protection mechanism, an electronic monitor, and a visualization mechanism. The blood pressure monitoring device is mounted on the fixed frame body. The detection buffer and protection mechanism is connected between the blood pressure monitoring device and the fixed frame body. The electronic monitor is electrically connected to the blood pressure monitoring device. The visualization mechanism is connected to the electronic monitor. A bottom support rod is installed at the bottom of the shock-absorbing base plate. A movable positioning mechanism is installed at the bottom of the bottom support rod. The movable positioning mechanism is used to switch between supporting and moving the overall device. Multiple sensors are installed inside the blood pressure monitoring device. An operating table is fixedly connected to one end of the bottom of the fixed frame body. A limit seat is installed on the top of the operating table. The electronic monitor is located on one side of the limit seat, and the blood pressure monitoring device is installed inside the limit seat. Furthermore, the mobile positioning mechanism includes side positioning blocks, a bottom fixing plate is fixedly connected to one bottom end of the bottom support rod, side positioning blocks are fixedly connected to the outside of the bottom fixing plate at equal intervals, a bottom mounting frame is fixedly connected to the bottom of each side positioning block, a universal wheel is installed inside each bottom mounting frame, and a support foot is installed at the bottom of the bottom mounting frame and on one side of the universal wheel. Furthermore, a shock-absorbing base plate is installed at the bottom of the operating table. The detection buffer protection mechanism is located between the operating table and the shock-absorbing base plate and is equidistant and symmetrically distributed. The detection buffer protection mechanism includes springs. Equidistant and symmetrically distributed springs are installed between the operating table and the shock-absorbing base plate. Damping shock absorbers are installed inside each spring. A skin-friendly pad is installed on the inner wall of the blood pressure detection device. A side fixing rod is installed between the visualization mechanism and the main body of the fixed frame. Furthermore, a spring bottom connecting plate is fixedly connected to one bottom end of each spring, and the bottom of the spring bottom connecting plate is fixedly connected to the shock-absorbing base plate. A spring top connecting plate is fixedly connected to one top end of each spring, and a shock-absorbing seat is installed on the top of each spring top connecting plate. A second positioning bolt that penetrates the spring top connecting plate is threaded into the inside of each shock-absorbing seat, and the top of each shock-absorbing seat is fixedly connected to the bottom of the operating table. Furthermore, a fourth positioning bolt is installed between the bottom mounting frame and the side positioning block to cooperate with the support foot seat for limiting, and positioning pins for use with the casters are installed on the outer side of the bottom mounting frame. Furthermore, reinforcing inclined plates are fixedly connected to the top of the bottom fixing plate and around the bottom support rod, and one side of each of the multiple reinforcing inclined plates is fixedly connected to the bottom support rod. Furthermore, a connecting circuit is installed between the electronic detector and the limit seat, and the top of the limit seat is threaded with symmetrically distributed first positioning bolts that extend into the inside of the operating table. Furthermore, a worm gear reducer is installed on the top of the bottom support rod, and a drive motor is installed on the outside of the worm gear reducer. The output end of the drive motor is connected to the worm gear reducer, and the top output end of the worm gear reducer is fixedly connected to the bottom of the shock-absorbing base plate. Furthermore, the visualization mechanism is a control panel, and a display screen is fixedly connected to the side of the control panel away from the control panel mounting frame. The display screen, blood pressure detection device, electronic detector, connecting circuit and worm gear reducer are all electrically connected to the control panel. Furthermore, a fixing sleeve is installed on the outer side of the fixing frame body and above the operating table. The outer side of the fixing sleeve is threaded with a third positioning bolt extending to the inner wall of the fixing frame body. Side fixing rods are fixedly connected to both sides of the fixing sleeve. One side of each of the two side fixing rods is fixedly connected to the control panel mounting frame. The fixing sleeve has mounting holes inside to match the fixing frame body. By adopting the above technical solution, the present invention can also bring the following beneficial effects: 1. This invention discloses a non-invasive continuous blood pressure monitor for predicting the risk of preeclampsia in perinatal pregnant women. By setting up a fixed frame body and a blood pressure monitoring device, the blood pressure monitoring device can be stably installed on the upper limb of perinatal pregnant women and maintain continuous contact with the skin under the guidance of a doctor. At the same time, the blood pressure monitoring device is equipped with multiple sets of sensors for continuously collecting raw physiological signals such as pulse waves. With the addition of a detection buffer protection mechanism, when the pregnant woman's limbs are slightly moved or subjected to external vibrations, interference energy is absorbed and buffered, thereby reducing the impact of physical disturbances on the sensor's acquisition state, ensuring the relative stability of the sensor-skin contact interface, effectively suppressing motion artifacts, and improving the stability of continuous blood pressure monitoring data. It has the advantages of high monitoring stability and strong anti-interference ability. 2. This invention discloses a non-invasive continuous blood pressure monitor for predicting the risk of preeclampsia in perinatal pregnant women. It continuously collects pulse wave signals under relatively constant force and contact conditions using a photoplethysmography (PPG) sensor. The electronic monitor processes parameters such as pulse wave waveform characteristics and propagation time, and calculates continuous blood pressure values ​​using a pre-established calibration model. Damping shock absorbers and springs buffer and protect the overall device during use, reducing the impact of external mechanical interference on detection accuracy. This helps improve the accuracy and repeatability of continuous blood pressure measurements, offering advantages such as high detection accuracy and good measurement consistency. 3. This invention mentions a non-invasive continuous blood pressure monitor for predicting the risk of preeclampsia in perinatal pregnant women. It achieves continuous dynamic acquisition of blood pressure of perinatal pregnant women through multi-institutional collaboration, and combines risk prediction algorithms to analyze and warn of abnormal blood pressure fluctuations. This enables doctors to dynamically assess the risk of preeclampsia in pregnant women based on continuous blood pressure change trends. At the same time, the device structure supports standardized installation and height adjustment in medical institution environments, which is convenient for medical staff to operate and observe. Thus, it provides an effective auxiliary technical means for the screening, follow-up and intervention of preeclampsia, and has the advantages of timely risk assessment and high clinical auxiliary value. Attached Figure Description To more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings used in the embodiments will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the present invention. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort. Figure 1 This invention provides a schematic diagram of the structure of a non-invasive continuous blood pressure monitor for predicting the risk of preeclampsia in perinatal pregnant women; Figure 2 This is a schematic diagram of the connection structure between the operating table and the shock-absorbing base plate in this embodiment; Figure 3 This is a schematic diagram of the connection structure between the electronic detector and the connection circuit in this embodiment; Figure 4 This is an enlarged schematic diagram of the top structure of the control panel in this embodiment; Figure 5 This is an enlarged schematic diagram of the bottom structure of the bottom fixing plate in this embodiment; Figure 6 For this embodiment Figure 4 An enlarged schematic diagram of the structure at point A in the diagram; Figure 7 This is an enlarged schematic diagram of the mobile positioning mechanism in this embodiment; The components include: 1. Fixing frame main body; 2. Blood pressure monitoring equipment; 21. Skin-friendly pad; 22. Limiting seat; 23. First positioning bolt; 24. Electronic detector; 25. Connecting circuit; 26. Operating table; 27. Vibration-damping base plate; 3. Detection buffer protection mechanism; 31. Spring; 32. Damping shock absorber; 33. Spring top connecting plate; 34. Vibration-damping seat; 35. Second positioning bolt; 36. Spring bottom connecting plate; 4. Visualization mechanism; 41. Side fixing rod; 42. Control panel mounting frame; 43. Fixing sleeve; 44. Third positioning bolt; 5. Moving positioning mechanism; 51. Bottom fixing plate; 52. Bottom support rod; 53. Reinforcing inclined plate; 54. Side positioning block; 55. Bottom mounting frame; 56. Universal wheel; 57. Support foot; 58. Fourth positioning bolt; 59. Worm gear reducer. Detailed Implementation The embodiments of the present invention will now be described in detail with reference to the accompanying drawings. The following specific examples illustrate the implementation of the present invention. Those skilled in the art can easily understand other advantages and effects of the present invention from the content disclosed in this specification. Obviously, the described embodiments are only a part of the embodiments of the present invention, and not all of them. The present invention can also be implemented or applied through other different specific embodiments, and the details in this specification can also be modified or changed based on different viewpoints and applications without departing from the spirit of the present invention. It should be noted that, in the absence of conflict, the following embodiments and features in the embodiments can be combined with each other. All other embodiments obtained by those skilled in the art based on the embodiments of the present invention without creative effort are within the scope of protection of the present invention. It should be noted that various aspects of embodiments within the scope of the appended claims are described below. It will be apparent that the aspects described herein can be embodied in a wide variety of forms, and any particular structure and / or function described herein is merely illustrative. Based on this invention, those skilled in the art will understand that one aspect described herein can be implemented independently of any other aspect, and two or more of these aspects can be combined in various ways. For example, any number of aspects set forth herein can be used to implement the device and / or practice the method. Additionally, this device and / or method can be implemented using other structures and / or functionalities besides one or more of the aspects set forth herein. It should also be noted that the illustrations provided in the following embodiments are only schematic representations of the basic concept of the present invention. The drawings only show the components related to the present invention and are not drawn according to the actual number, shape and size of the components in the actual implementation. In the actual implementation, the form, quantity and proportion of each component can be arbitrarily changed, and the layout of the components may also be more complex. Furthermore, specific details are provided in the following description to facilitate a thorough understanding of the examples. However, those skilled in the art will understand that the described aspects can be practiced without these specific details. Example 1 like Figures 1 to 7 As shown, this embodiment provides a technical solution: a non-invasive continuous blood pressure monitor for predicting the risk of preeclampsia in perinatal pregnant women, including a fixed frame body 1, a visualization mechanism 4 installed on the outer side of the fixed frame body 1, an operating table 26 fixedly connected to one bottom end of the fixed frame body 1, an electronic detector 24 and a limiting seat 22 installed on the top of the operating table 26, the electronic detector 24 being located on one side of the limiting seat 22, and a blood pressure monitoring device 2 installed inside the limiting seat 22; a shock-absorbing base plate 27 is installed at the bottom of the operating table 26, and equidistant and symmetrically distributed [missing information] are installed between the operating table 26 and the shock-absorbing base plate 27. The detection buffer protection mechanism 3; the bottom of the shock-absorbing base plate 27 is equipped with a bottom support rod 52, and the bottom of the bottom support rod 52 is equipped with a moving positioning mechanism 5. The moving positioning mechanism 5 includes side positioning blocks 54. One end of the bottom of the bottom support rod 52 is fixedly connected to a bottom fixing plate 51. The outer side of the bottom fixing plate 51 is fixedly connected to equidistant side positioning blocks 54. The bottom of each side positioning block 54 is fixedly connected to a bottom mounting frame 55. The bottom of each bottom mounting frame 55 is equipped with a caster wheel 56. The bottom of the bottom mounting frame 55 and the side of the caster wheel 56 are each equipped with a support foot 57. The detection buffer protection mechanism 3 includes springs 31. Equally spaced and symmetrically distributed springs 31 are installed between the operating table 26 and the shock-absorbing base plate 27. Each spring 31 has a damping shock absorber 32 installed inside. A skin-friendly pad 21 is installed on the inner wall of the blood pressure detection device 2. A side fixing rod 41 is installed between the visualization mechanism 4 and the main frame 1. A spring bottom connecting plate 36 is fixedly connected to the bottom of each spring 31, and the bottom of each spring bottom connecting plate 36 is fixedly connected to the shock-absorbing base plate 27. A spring top connecting plate 33 is fixedly connected to the top of each spring top connecting plate 33. A shock-absorbing seat 34 is installed on the top of each shock-absorbing seat 34, and a second positioning bolt 35 is threaded through the shock-absorbing seat 34. The top of each shock-absorbing seat 34 is fixedly connected to the bottom of the operating table 26. The damping shock absorbers 32 and springs 31 provide a certain degree of buffer protection for the entire device during use, extending the device's service life and improving the accuracy of subsequent blood pressure detection. A fourth positioning bolt 58 is installed between the bottom mounting frame 55 and the side positioning block 54 to limit the position of the support foot 57. Positioning pins for use with the casters 56 are installed on the outer side of the bottom mounting frame 55. The corresponding casters 56 are locked by the positioning pins. The support height of the corresponding support foot 57 is adjusted by tightening the fourth positioning bolt 58 until the casters 56 and support feet 57 simultaneously support the entire equipment, facilitating flexible switching between movement and support operation modes. Reinforcing inclined plates 53 are fixedly connected to the top of the bottom fixing plate 51 and around the bottom support rod 52. One side of each reinforcing inclined plate 53 is fixedly connected to the bottom support rod 52, reinforcing the connection between the bottom fixing plate 51 and the bottom support rod 52 and improving the stability of the equipment. A connecting circuit 25 is installed between the electronic detector 24 and the limiting seat 22. The top of the limiting seat 22 is threaded with symmetrically distributed first positioning bolts 23 extending into the operating table 26. The first positioning bolts 23 reinforce the connection between the limiting seat 22 and the operating table 26, facilitating adjustment of the working position and improving the stability of the equipment during actual testing. A worm gear reducer 59 is installed on the top of the bottom support rod 52. A drive motor is installed on the outside of the worm gear reducer 59, and the output end of the drive motor is connected to the worm gear reducer 59. The top output end of the worm gear reducer 59 is fixedly connected to the bottom of the shock-absorbing base plate 27. When both the drive motor and the worm gear reducer 59 are running, the top shock-absorbing base plate 27 rotates, adjusting the overall detection position of the equipment and improving the flexibility of the equipment. The visualization mechanism 4 is a control panel. A display screen is fixedly connected to the side of the control panel away from the control panel mounting frame 42. The display screen, blood pressure detection device 2, electronic detector 24, connecting circuit 25 and worm gear reducer 59 are all electrically connected to the control panel. The control panel is used to control the operation of the display screen, blood pressure detection device 2, electronic detector 24, connecting circuit 25 and worm gear reducer 59. The whole system does not use a large amount of electrical equipment to assist in operation, saving the overall use and installation costs. A fixing sleeve 43 is installed on the outer side of the fixing frame body 1 and above the operating table 26. A third positioning bolt 44 extending to the inner wall of the fixing frame body 1 is threaded onto the outer side of the fixing sleeve 43. Side fixing rods 41 are fixedly connected to both sides of the fixing sleeve 43. One side of each of the two side fixing rods 41 is fixedly connected to the control panel mounting frame 42. The fixing sleeve 43 facilitates the connection of the visualization mechanism 4. The fixing sleeve 43 has mounting holes inside that are designed to fit the fixing frame body 1. The installation height of the visualization mechanism 4 can be adjusted by the cooperation of the third positioning bolt 44 and the mounting holes to meet the operating needs of staff of different heights. In use, medical personnel adjust the main body 1 of the fixation frame to a suitable position and stably fix the blood pressure monitoring device 2 to the upper limb of the perinatal pregnant woman, ensuring that the blood pressure monitoring device 2 remains in continuous contact with the skin. Then, the visualization mechanism 4 is activated and the device is started. Multiple sensors installed within the blood pressure monitoring device 2 continuously collect raw physiological signals such as the pregnant woman's pulse wave while in a stable contact state. During monitoring, when the pregnant woman's upper limb experiences slight movement or external vibration, the detection buffer protection mechanism 3 absorbs and buffers the corresponding interference, reducing the impact of limb movement on signal acquisition. This maintains the relative stability of the sensor-skin contact interface, ensuring the continuity and reliability of pulse wave signal acquisition. The collected raw physiological signals are transmitted via the connecting circuit 25. The electronic detector 24 performs preprocessing such as filtering and amplification on the signal, and calculates continuous blood pressure values ​​based on pulse wave waveform characteristics and related parameters. The continuous blood pressure values ​​include indicators such as systolic blood pressure, diastolic blood pressure, mean arterial pressure, and heart rate. At the same time, the continuous blood pressure data and the diurnal variation characteristics of blood pressure are input into a preset risk prediction model to analyze and assess the risk of preeclampsia in perinatal pregnant women. The analysis results are displayed in real time through the visualization mechanism 4 in the form of blood pressure change trends, diurnal rhythm types, and risk levels, so that medical staff can dynamically observe the blood pressure status of pregnant women and use it as a reference for preeclampsia screening, follow-up, and intervention. In summary, this invention has the advantages of high detection accuracy, strong detection stability, and results that support clinical decision-making. The above description is merely a specific embodiment of the present invention, but the scope of protection of the present invention is not limited thereto. Any variations or substitutions that can be easily conceived by those skilled in the art within the technical scope disclosed in the present invention should be included within the scope of protection of the present invention. Therefore, the scope of protection of the present invention should be determined by the scope of the claims.

Claims

1. A non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in pregnant women during the perinatal period, characterized in that: The system includes a fixed frame body (1), a blood pressure detection device (2), a detection buffer protection mechanism (3), an electronic detector (24), and a visualization mechanism (4). The blood pressure detection device (2) is mounted on the fixed frame body (1). The detection buffer protection mechanism (3) is connected between the blood pressure detection device (2) and the fixed frame body (1). The electronic detector (24) is electrically connected to the blood pressure detection device (2). The visualization mechanism (4) is connected to the electronic detector (24). A bottom support rod (52) is installed at the bottom of the shock-absorbing base plate (27). A moving positioning mechanism (5) is installed at the bottom of the bottom support rod (52). The shock-absorbing base plate (27) is equipped with a bottom support rod (52) at the bottom, and a moving positioning mechanism (5) is installed at the bottom of the bottom support rod (52). The moving positioning mechanism (5) is used to switch between supporting and moving the overall equipment. The blood pressure detection device (2) is equipped with multiple sets of sensors. The bottom end of the fixed frame body (1) is fixedly connected to an operating table (26). The top of the operating table (26) is equipped with a limit seat (22). The electronic detector (24) is located on one side of the limit seat (22). The blood pressure detection device (2) is installed inside the limit seat (22).

2. The non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in perinatal pregnant women according to claim 1, characterized in that: The mobile positioning mechanism (5) includes a side positioning block (54). A bottom fixing plate (51) is fixedly connected to one end of the bottom support rod (52). The side positioning blocks (54) are fixedly connected to the outside of the bottom fixing plate (51) at equal intervals. A bottom mounting frame (55) is fixedly connected to the bottom of each side positioning block (54). A universal wheel (56) is installed inside each bottom mounting frame (55). A support foot (57) is installed at the bottom of the bottom mounting frame (55) and on one side of the universal wheel (56).

3. The non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in perinatal pregnant women according to claim 2, characterized in that: The bottom of the operating table (26) is equipped with a shock-absorbing base plate (27). The detection buffer protection mechanism (3) is located between the operating table (26) and the shock-absorbing base plate (27) and is equidistant and symmetrically distributed. The detection buffer protection mechanism (3) includes a spring (31). The operating table (26) and the shock-absorbing base plate (27) are equipped with equidistant and symmetrically distributed springs (31). The inside of each spring (31) is equipped with a damping shock absorber (32). The inner wall of the blood pressure detection device (2) is equipped with a skin-friendly pad (21). The visualization mechanism (4) and the main body of the fixing frame (1) are equipped with a side fixing rod (41).

4. The non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in perinatal pregnant women according to claim 3, characterized in that: The bottom end of each spring (31) is fixedly connected to a bottom connecting plate (36), the bottom of which is fixedly connected to a damping base plate (27). The top end of each spring (31) is fixedly connected to a top connecting plate (33), and a damping seat (34) is installed on the top of each top connecting plate (33). The inside of each damping seat (34) is threaded with a second positioning bolt (35) that penetrates the top connecting plate (33). The top of each damping seat (34) is fixedly connected to the bottom of the operating table (26).

5. The non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in perinatal pregnant women according to claim 1, characterized in that: The bottom mounting frame (55) and the side positioning block (54) are each equipped with a fourth positioning bolt (58) that is used to limit the position of the support foot (57). The outer side of the bottom mounting frame (55) is equipped with a positioning pin that is used to cooperate with the caster wheel (56).

6. The non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in perinatal pregnant women according to claim 4, characterized in that: The bottom fixing plate (51) is fixedly connected to the top and around the bottom support rod (52) with reinforcing inclined plates (53), and one side of each of the reinforcing inclined plates (53) is fixedly connected to the bottom support rod (52).

7. The non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in perinatal pregnant women according to claim 3, characterized in that: A connection circuit (25) is installed between the electronic detector (24) and the limiting seat (22), and the top of the limiting seat (22) is threaded with first positioning bolts (23) that are symmetrically distributed and extend into the inside of the operating table (26).

8. The non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in perinatal pregnant women according to claim 7, characterized in that: A worm gear reducer (59) is installed on the top of the bottom support rod (52). A drive motor is installed on the outside of the worm gear reducer (59). The output end of the drive motor is connected to the worm gear reducer (59). The top output end of the worm gear reducer (59) is fixedly connected to the bottom of the shock-absorbing base plate (27).

9. The non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in perinatal pregnant women according to claim 8, characterized in that: The visualization mechanism (4) is a control panel. A display screen is fixedly connected to the side of the control panel away from the control panel mounting frame (42). The display screen, blood pressure detection device (2), electronic detector (24), connection circuit (25) and worm gear reducer (59) are all electrically connected to the control panel.

10. The non-invasive continuous blood pressure monitoring device for predicting the risk of preeclampsia in perinatal pregnant women according to claim 8, characterized in that: A fixing sleeve (43) is installed on the outside of the fixing frame body (1) and above the operating table (26). The fixing sleeve (43) is threaded with a third positioning bolt (44) extending to the inner wall of the fixing frame body (1). Side fixing rods (41) are fixedly connected to both sides of the fixing sleeve (43). One side of each of the two side fixing rods (41) is fixedly connected to the control panel mounting frame (42). The fixing sleeve (43) has mounting holes inside to cooperate with the fixing frame body (1).

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