Arterial blood pressure sensor fixing box and pipeline combing method thereof
By designing an arterial blood pressure sensor mounting box that integrates a limiting mechanism and a rotating pin mechanism, the problems of tubing entanglement and unstable syringe fixation in existing technologies have been solved. This has enabled orderly management of the tubing and stable operation of the equipment, improving monitoring accuracy and operational standardization.
Patent Information
- Application Number
- CN202511452576.6
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-10-12
- Publication Date
- 2026-02-13
AI Technical Summary
Existing arterial blood pressure sensors, due to the lack of a dedicated classification and constraint structure in clinical applications, suffer from issues such as tubing entanglement, inaccurate monitoring data, and high operational difficulty. Furthermore, the syringes are not securely fixed and are prone to falling off, increasing the risk of delays in diagnosis and treatment.
Design an arterial blood pressure sensor fixing box that integrates a limiting mechanism and a rotating pin mechanism. Through the classification holes and elastic limiting components on the transparent hexagonal box body, it can achieve orderly management of the tubing and prevent the syringe from falling off. The polycarbonate material is used to ensure high strength and transparency, making it easy to observe.
This enabled the orderly management of pipelines, reduced operational risks, improved the accuracy of monitoring data and the stability of equipment, and reduced equipment wear and tear and medical costs.
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Figure CN121512486A_ABST
Abstract
Description
TECHNICAL FIELD
[0001] The present application relates to the field of medical devices, in particular to an arterial blood pressure sensor fixing box and a pipeline arrangement method thereof. BACKGROUND
[0002] In the critical care scene such as ICU and CCU, arterial blood pressure monitoring is the core operation for evaluating the patient's circulation function, guiding fluid resuscitation and drug use. As the key equipment of the monitoring system, the stable operation and standard management of the arterial blood pressure sensor directly affect the accuracy of clinical diagnosis and treatment decision. However, the existing arterial blood pressure sensor is long-term limited by the defects of the fixing and pipeline management system in clinical application, which derives a series of problems such as high operation risk, large equipment loss and rising medical cost. Among them, the arterial blood pressure monitoring system needs to be connected with multiple functional pipelines simultaneously, including a pressure catheter for real-time pressure monitoring, a signal line for transmitting monitoring data, a special pipeline for assisting central venous pressure (CVP) measurement, and a flushing pipeline for preventing pipeline blockage.
[0003] In the existing clinical scene, these pipelines lack special classification constraint structure and are in a disordered stacking state. The pressure catheter and the signal line are prone to be tangled and bent due to pulling, which not only may block the pressure catheter and affect the accuracy of monitoring data, such as abnormal blood pressure fluctuation, but also increases the operation difficulty of medical staff. In the case of emergency adjustment, such as patient turning over and equipment shifting, the tangled pipeline is easy to be pulled by mistake, which may cause monitoring interruption or pipeline damage, and indirectly increase the risk of diagnosis and treatment delay. Clinical operation statistics show that about 35% of arterial blood pressure monitoring data abnormal events are directly related to pipeline blockage or signal interference caused by pipeline tangling, which seriously affects the evaluation of the circulation state of critically ill patients.
[0004] In addition, in order to maintain the smoothness of the arterial blood pressure monitoring pipeline, a syringe is needed for regular pipeline flushing, such as saline flushing. The existing syringes are mostly fixed beside the sensor by simple buckles or adhesive tapes. Such fixing method has poor stability. For example, in the ICU environment, the vibration of the equipment, such as the operation of the breathing machine and the adjustment of the bed, may cause the syringe to fall off. The fallen syringe not only may contaminate the pipeline interface, but also may interrupt the flushing operation, increase the risk of pipeline thrombosis, and increase the burden of medical resources. SUMMARY
[0005] The present application aims to provide an arterial blood pressure sensor fixing box and a pipeline arrangement method thereof to solve the problems raised in the background.
[0006] In order to achieve the above-mentioned purpose, the present application provides the following technical scheme:
[0007] An arterial blood pressure sensor fixing box, comprising a limiting mechanism arranged on a box body.
[0008] As a preferred embodiment, the limiting mechanism comprises a pipeline hole at one end of the box body for pressure monitoring and a signal hole at the other end of the box body for pipeline flushing, and the top surface of the box body is further provided with a pipeline hole for CVP measurement and a fixing hole for fixing a syringe.
[0009] As a preferred embodiment, the diameter of the pipeline hole is 0.4-0.6cm; preferably 0.5cm.
[0010] As a preferred embodiment, the diameter of the signal hole is 0.8-1.2cm; preferably 1cm.
[0011] As a preferred embodiment, the diameter of the pipeline hole is 0.4-0.6cm; preferably 0.5cm.
[0012] As a preferred embodiment, the diameter of the fixing hole is 1.3-1.7cm; preferably 1.5cm.
[0013] As a preferred embodiment, the center distance between the pipeline hole and the fixing hole is 3.2-3.8cm; preferably 3.5cm.
[0014] As a preferred embodiment, the inner wall of the fixing hole is nested with an elastic limiting piece.
[0015] As a preferred embodiment, the elastic limiting piece is a ring-shaped silica gel gasket.
[0016] As a preferred embodiment, the cross section of the ring-shaped silica gel gasket is a trapezoidal structure, the inner diameter is 1.2cm±0.1cm; and the axial compression deformation is 0.3-0.5mm.
[0017] As a preferred embodiment, the box body is integrated with a rotating pin mechanism.
[0018] As a preferred embodiment, the rotating pin mechanism comprises a base injection molded with the box body, and a U-shaped pin is hinged on the base, and a locking buckle is arranged at the free end of the U-shaped pin.
[0019] As a preferred embodiment, the box body is made of polycarbonate material and is transparent hexagonal, and the wall thickness is 1.2mm+0.2mm.
[0020] As a preferred embodiment, the visible light transmittance of the box body is >90%.
[0021] Preferably, the size of the box body ranges from 14-18cm in length, 8-12cm in width, and 1.5-2.5cm in height.
[0022] As a preferred embodiment, the inner cavity of the box body is provided with an arterial blood pressure sensor.
[0023] An arterial blood pressure sensor fixing box pipeline arrangement method, comprising:
[0024] The arterial blood pressure sensor body is placed in the inner cavity of the box body, the pressure catheter is led out through the main line pipeline hole, the signal line is led out through the signal line hole signal hole, the pipeline hole measures CVP, and the neck of the syringe is clamped in the syringe fixing hole; wherein the arterial blood pressure sensor body is stably placed in the inner cavity of the box body, and pipeline pulling caused by shaking is avoided.
[0025] The pressure catheter of the arterial blood pressure sensor is extended along the corresponding path in the inner cavity of the box body, and is led out from the main line pipeline hole at one end of the box body; the length of the catheter led out is appropriate to meet the connection requirement of the pressure monitoring equipment, and the catheter is ensured to be free of bending and twisting. The signal line of the sensor is led out from the signal hole at the other end of the box body, the line arrangement is arranged, the signal line is separated from the pressure catheter, and cross winding is avoided. The pipeline for CVP, central venous pressure measurement is led out from the pipeline hole on the top surface of the box body, the hole position is kept at a center distance of 3.5 cm from the fixing hole, the CVP pipeline is ensured to be free of interference with the syringe operation area. The neck of the syringe used in cooperation is clamped in the fixing hole on the top surface of the box body, elastic fixing is realized through the annular silica gel gasket nested in the hole wall, and the syringe is prevented from falling off; after the syringe is connected with the flushing pipeline, it is ensured that the flushing path is unobstructed and free of winding with other pipelines.
[0026] Compared with the prior art, the beneficial effects of the present application are that:
[0027] 1. The transparent hexagonal box body of the present application integrates pipeline classification leading holes, signal line holes, main line holes, elastic limiting syringe fixing holes and rotating pin mechanisms, realizes orderly management of the pipelines, prevents the syringe from falling off and facilitates convenient fixing of the sensor, and solves the problems of traditional management confusion and unreliable fixing.
[0028] 2. The polycarbonate material is used in the present application, the wall thickness is accurately controlled, the visible light transmittance is greater than 90%, high strength is ensured, and the sensor is protected, and the pipeline state is convenient for clinical observation, and the functions and observation requirements are considered.
[0029] 3. The present application constructs a complete arterial blood pressure monitoring system, the sensor, the pipeline and the syringe are cooperatively adapted through the fixing box, a standardized and modular management scheme is formed, the blank of a special fixing device is filled, and the operation standardization of critical care is improved. BRIEF DESCRIPTION OF DRAWINGS
[0030] In order to more clearly illustrate the technical solutions in the embodiments of the present application or the prior art, the following will briefly introduce the drawings needed to be used in the embodiments or prior art description. Obviously, the drawings in the following description only show some embodiments of the present application, and all the other drawings can be obtained by those skilled in the art without any creative effort based on these drawings. In the drawings:
[0031] The drawings described herein are for illustrative purposes only, and are not intended to limit the scope of the present application in any way. In addition, the shapes and scale sizes of the components in the drawings are only illustrative, and are used to help understand the present application, and are not specifically limited to the shapes and scale sizes of the components. Those skilled in the art can select various possible shapes and scale sizes to implement the present application according to specific circumstances under the teaching of the present application.
[0032] Fig. 1 A three-dimensional structure schematic diagram of an arterial blood pressure sensor fixing box according to the present application is shown in the figure.
[0033] Fig. 2 A three-dimensional structure schematic diagram of an arterial blood pressure sensor fixing box according to the present application is shown in the figure.
[0034] Fig. 3 A front elevation structure schematic diagram of an arterial blood pressure sensor fixing box according to the present application is shown in the figure.
[0035] Figs. 1-3 In the figure, the reference signs include:
[0036] 1, box body; 111, pipeline hole;
[0037] 121, signal hole;
[0038] 131, pipeline hole; 132, fixing hole;
[0039] 14, rotating pin mechanism. DETAILED DESCRIPTION
[0040] In order to make the purpose, features and advantages of the present application more obvious and easy to understand, the technical solutions in the embodiments of the present application will be described clearly and completely in combination with the drawings of the embodiments of the present application. Obviously, the following described embodiments are only some of the embodiments of the present application, but not all the embodiments. Based on the embodiments in the present application, all the other embodiments obtained by those skilled in the art without any creative effort are within the scope of the present application.
[0041] In the description of the present application, it needs to be understood that when one component is considered to be connected to another component, it can be directly connected to another component or there can be a component arranged in the middle. When one component is considered to be arranged on another component, it can be directly arranged on another component or there can be a component arranged in the middle.
[0042] In addition, the terms such as long, short, inside, outside, etc. indicating the orientation or positional relationship are based on the orientation or positional relationship shown in the drawings, which is only for the convenience of describing the present application, and does not indicate or imply that the device or element referred to must have this particular orientation, be constructed in a particular orientation, and cannot be understood as a limitation of the present application.
[0043] The present application will be described in detail below in conjunction with the specific embodiments shown in the drawings. However, these embodiments do not limit the present application, and the changes made by those of ordinary skill in the art in structure, method, or function based on these embodiments are all included within the scope of protection of the present application.
[0044] Referring to Figs. 1-3 The arterial blood pressure sensor fixing box provided in the embodiment includes a limiting mechanism arranged on the box body 1.
[0045] The limiting mechanism includes a pipeline hole 111 arranged at one end of the box body 1 for pressure monitoring and a signal hole 121 arranged at the other end of the box body 1 for pipeline flushing. The top surface of the box body 1 is further provided with a pipeline hole 131 for CVP measurement and a fixing hole 132 for fixing a syringe.
[0046] The diameter of the pipeline hole 111 is 0.4-0.6 cm; preferably 0.5 cm.
[0047] The diameter of the signal hole 121 is 0.8-1.2 cm; preferably 1 cm.
[0048] The diameter of the pipeline hole 131 is 0.4-0.6 cm; preferably 0.5 cm.
[0049] The diameter of the fixing hole 132 is 1.3-1.7 cm; preferably 1.5 cm.
[0050] The center distance between the pipeline hole 131 and the fixing hole 132 is 3.2-3.8 cm; preferably 3.5 cm.
[0051] Specifically, before operation, first check the appearance state of the box body 1 polycarbonate transparent hexagonal, confirm that the box body has no cracks, the wall thickness is uniform; the standard 1.2 mm ± 0.2 mm, the visible light transmittance is normal > 90%, which can be judged by observing whether the box is clear, to avoid affecting the subsequent fixing stability due to the damage of the box body.
[0052] Specifically, the key components and the hole positions are checked. The hole wall of the pipeline hole 111 with a diameter of 0.5 cm, the signal hole 121 with a diameter of 1 cm, the pipeline hole 131 with a diameter of 0.5 cm, and the fixing hole 132 with a diameter of 1.5 cm are free of burrs. The annular silica gel gasket nested in the inner wall of the fixing hole 132 has a trapezoidal cross section, an inner diameter of 1.2 cm ± 0.1 cm, and no shedding or deformation, so as to ensure that it can be normally compressed axially with a compression amount of 0.3-0.5 mm. The rotating pin mechanism 14 is checked. The base and the box body are injection molded without looseness. The U-shaped pin is hingedly flexible. The locking buckle at the free end can be normally buckled to avoid falling off during use of the fixing box. The rotating pin mechanism 14, the base and the box body are injection molded without looseness. The U-shaped pin is hingedly flexible. The locking buckle at the free end all adopts the U-shaped pin of the prior art. This embodiment does not describe too much, and the drawings also do not show too much.
[0053] Specifically, according to the type of the arterial blood pressure sensor, it is confirmed that the pressure catheter diameter is adapted to the pipeline hole 111 (0.4-0.6 cm), and the signal line diameter is adapted to the signal hole 121 (0.8-1.2 cm). It is confirmed that the CVP measuring pipeline diameter is adapted to the pipeline hole 131 (0.4-0.6 cm), and the syringe neck diameter is adapted to the fixing hole 132 (1.3-1.7 cm). If the syringe neck is slightly thick, the elastic compression of the silica gel gasket can achieve tight clamping without forcibly extruding and damaging the components.
[0054] The inner wall of the fixing hole 132 is nested with an elastic limiting piece.
[0055] The elastic limiting piece is an annular silica gel gasket.
[0056] The cross section of the annular silica gel gasket is a trapezoidal structure, and the inner diameter is 1.2 cm ± 0.1 cm. It can be axially compressed and deformed by 0.3-0.5 mm.
[0057] Specifically, the installation operation of the arterial blood pressure sensor and the pipeline is as follows:
[0058] Hold the box body 1 at the bottom with one hand, and take out the arterial blood pressure sensor body with the other hand. Place it stably into the inner cavity of the box body 1 (the inner cavity size is adapted to the sensor to avoid shaking of the sensor in the box): Ensure that the pressure catheter interface and the signal interface of the sensor are directed towards the corresponding hole positions of the box (the pressure catheter is directed towards the pipeline hole 111, and the signal line is directed towards the signal hole 121) to facilitate subsequent pipeline connection and reduce pipeline bending.
[0059] Hold the pressure catheter end of the arterial blood pressure sensor (away from the sensor body end), align it with the pipe hole 111 (diameter 0.5 cm) at one end of the box body 1, slowly pass through the hole, and the length of the pipe hole is usually 10-15 cm, which can meet the subsequent pressure monitoring connection requirements (usually 10-15 cm, to avoid pulling the sensor too short), and avoid excessive bending of the catheter (to prevent catheter blockage or damage). Hold the signal line connector of the sensor (if the connector is connected, confirm that the connector size is suitable for the signal hole 121, and remove the connector sheath first), align the signal hole 121 (diameter 1 cm) at the other end of the box body 1, and smoothly pass through the hole, and then arrange the signal line to naturally hang down to avoid winding on the pressure catheter.
[0060] Take out the CVP measurement pipeline, align one end of the pipeline with the pipeline hole 131 (diameter 0.5 cm) on the top surface of the box body 1, slowly pass through the hole, and the other end is connected to the CVP monitoring device (such as a pressure monitor), and ensure that the pipeline is not twisted after passing through the hole, and there is no obvious gap between the hole and the pipeline (to avoid pipeline shaking).
[0061] Specifically, take out the matching syringe (usually a syringe for flushing or sampling), hold the syringe barrel, and align the neck of the syringe (near the needle seat) with the fixing hole 132 (diameter 1.5 cm) on the top surface of the box body 1. Gently press the neck into the annular silicone gasket on the hole wall: the silicone gasket tightly wraps the neck of the syringe through axial compression (0.3-0.5 mm) to achieve fixation, ensuring that the syringe does not fall off when placed vertically or slightly inclined, and checking whether the syringe can be slightly removed after fixation (to facilitate subsequent replacement and avoid damaging the gasket due to excessive tightness).
[0062] The box body 1 is integrated with a rotating pin mechanism 14.
[0063] The rotating pin mechanism 14 includes a base that is injection molded with the box body 1, and a U-shaped pin is hinged on the base, and a locking buckle is provided on the free end of the U-shaped pin.
[0064] Specifically, the box body 1 is made of transparent polycarbonate material in the shape of a hexagon, and the wall thickness is 1.2 mm+0.2 mm.
[0065] The visible light transmittance of the box body 1 is >90%.
[0066] Preferably, the size of the box body 1 ranges from 14-18 cm in length, 8-12 cm in width, and 1.5-2.5 cm in height.
[0067] The inner cavity of the box body 1 is provided with an arterial blood pressure sensor.
[0068] Specifically, the rotating pin mechanism uses:
[0069] According to the clinical operation scene (such as bedside, beside the monitor), adjust the angle of the rotating pin mechanism 14: pinch the middle part of the U-shaped pin, rotate around the base hinge point to the appropriate angle (usually 90° or 120° with the box 1, convenient for fixing), align the free end of the U-shaped pin with the fixed carrier (such as the bed rail, monitor support, medical staff uniform pocket edge), gently buckle, make the locking buckle tightly clamp the carrier, complete the position fixing of the fixed box. After fixing, pull the box 1 gently, confirm that the pin is not loose and the locking buckle is not fallen off, to avoid the fixed box falling during use; if you need to adjust the position, press the locking buckle to open the pin, adjust the angle again and fix it.
[0070] Specifically, when selecting a fixed position, the following requirements need to be met:
[0071] ① The box 1 remains horizontal to avoid pressure monitoring errors caused by the inclination of the sensor body;
[0072] ② No excessive pulling of each pipeline (pressure conduit, signal line, CVP pipeline), leaving a certain activity allowance (avoiding pulling the pipeline when the patient turns over or the equipment moves);
[0073] ③ The box 1 is away from the liquid source (such as below the infusion bottle, beside the sink), to prevent liquid from splashing into the box and damaging the sensor;
[0074] ④ The transparent box 1 needs to be directed towards the direction convenient for the medical staff to observe (such as directly opposite the side of the monitor screen), to facilitate real-time viewing of the sensor status.
[0075] Specifically, after all the pipelines are installed, the pipelines are combed:
[0076] ① Respectively arrange the pressure conduit, signal line, and CVP pipeline to ensure that each pipeline extends in the fixed direction without crossing and winding (the direction can be combed according to the pipeline hole 111 pipeline to the left, signal hole 121 line to the right, and pipeline hole 131 pipeline to the front);
[0077] ② Check the contact between each pipeline and the hole position. If there is a risk of pipeline wear (such as slightly rough edges of the hole wall), a circle of medical tape can be wrapped around the contact point (to avoid covering the pipeline scale or affecting the flow of liquid);
[0078] ③ After fixing the syringe, ensure that the plunger is directed towards the direction convenient for operation (such as upwards or sideways), to facilitate subsequent pipeline flushing or sampling operation.
[0079] Specifically, check the fixed box status every 1-2 hours:
[0080] ① Observe whether the sensor in the box is normal (no alarm indicator light, no liquid leakage);
[0081] ② Check whether each pipeline is unobstructed (no bending, blockage), whether the syringe in the fixing hole 132 is stable (no looseness, falling);
[0082] ③ Confirm the fixing state of the rotating pin mechanism 14, and re-engage in time if there is looseness.
[0083] Specifically, if the surface of the box body 1 is contaminated with dust or liquid, use clean medical gauze to dip a small amount of normal saline or 75% medical alcohol and gently wipe (avoiding alcohol penetration into the box). After wiping, dry and keep the box transparent and clear, which is convenient for observing the internal sensor state.
[0084] Specifically, if the annular silicone gasket is aged or deformed (such as unable to rebound after compression), or the hole position is damaged, the fixing box or the corresponding accessories (such as replacing the silicone gasket alone) need to be replaced in time to avoid affecting the fixing effect of the pipeline; if the locking buckle of the rotatable pin is damaged, the pin mechanism needs to be replaced to ensure the stability of the fixing box position.
[0085] Specifically, when the fixing box needs to be removed, operate in the order of outside first and then inside:
[0086] ① First, pull out the syringe in the fixing hole 132, then disconnect the CVP pipeline from the monitoring equipment, and pull out the CVP pipeline from the pipeline hole 131;
[0087] ② Disconnect the signal line from the monitor, and pull out the signal line from the signal hole 121;
[0088] ③ Disconnect the pressure conduit from the pressure monitoring equipment, and pull out the pressure conduit from the pipeline hole 111;
[0089] ④ Finally, take out the arterial blood pressure sensor body in the box to avoid damaging the sensor by pulling the pipeline.
[0090] Specifically, after disassembly is completed, clean the fixing box:
[0091] ① Wipe the inside and outside of the box body with dry gauze to ensure that there is no liquid residue;
[0092] ② Check whether the annular silicone gasket and the rotating pin mechanism 14 are intact, and clean thoroughly if there are stains;
[0093] ③ Put the fixing box into a special storage bag or sterilization box (avoid mixing with sharp instruments to prevent the box from being scratched), and store it in a dry and ventilated environment for easy next use.
[0094] An arterial blood pressure sensor fixing box pipeline arrangement method, comprising:
[0095] The arterial blood pressure sensor body is placed in the inner cavity of the box body 1, the pressure conduit thereof is led out through the main line conduit hole 111, the signal line thereof is led out through the signal hole 121, the tube hole 131 is used for measuring CVP, and the neck of the syringe is clamped in the syringe fixing hole 132; wherein the arterial blood pressure sensor body is stably placed in the inner cavity of the box body 1, and the tube is prevented from being pulled due to shaking.
[0096] The pressure conduit of the arterial blood pressure sensor is extended along the corresponding path in the inner cavity of the box body 1, is led out from the main line conduit hole 111 (0.4-0.6 cm in diameter, preferably 0.5 cm) at one end of the box body 1, the length of the conduit led out is appropriate to meet the connection requirement of the pressure monitoring equipment, and the conduit is prevented from being bent and twisted. The signal line of the sensor is led out from the signal hole 121 (0.8-1.2 cm in diameter, preferably 1 cm) at the other end of the box body 1, the line is arranged in a manner that the signal line is separated from the pressure conduit and is prevented from being crossed and wound. The tube for measuring CVP (central venous pressure) is led out from the tube hole 131 (0.4-0.6 cm in diameter, preferably 0.5 cm) at the top surface of the box body 1, the hole is kept at a center distance of 3.2-3.8 cm (preferably 3.5 cm) from the fixing hole 132, and the CVP tube is prevented from interfering with the operation area of the syringe. The neck of the syringe used in cooperation is clamped in the fixing hole 132 (1.3-1.7 cm in diameter, preferably 1.5 cm) at the top surface of the box body 1, the syringe is elastically fixed by the annular silica gel gasket (trapezoidal section, 1.2 cm±0.1 cm in inner diameter, and 0.3-0.5 mm in axial compression) nested in the hole wall, and the syringe is prevented from falling off; after the syringe is connected with the flushing tube, the flushing path is ensured to be smooth and free from winding with other tubes. Through the above, the pressure monitoring tube, the signal line, the CVP measuring tube and the syringe flushing tube are physically separated and arranged in order through the special hole, and a tube management system with clear classification and convenient operation is formed.
[0097] It should be understood that although the present specification is described in terms of embodiments, not every embodiment contains only one independent technical solution, and the specification is described in this way only for the sake of clarity, and those skilled in the art should consider the specification as a whole, and the technical solutions in each embodiment can also be appropriately combined to form other embodiments that those skilled in the art can understand.
[0098] The series of detailed descriptions listed above are only specific descriptions of the feasible embodiments of the present application, and are not used to limit the protection scope of the present application, and equivalent embodiments or changes made without departing from the spirit of the present application should be included in the protection scope of the present application.
Claims
1. An arterial blood pressure sensor fixation case characterized by, The limiting mechanism is arranged on the box body (1).
2. The arterial blood pressure sensor fixation case according to claim 1, wherein The limiting mechanism comprises a pipeline hole (111) arranged at one end of the box body (1) for pressure monitoring and a signal hole (121) arranged at the other end of the box body (1) for pipeline flushing, and the top surface of the box body (1) is further provided with a pipeline hole (131) for CVP measurement and a fixing hole (132) for fixing a syringe. The diameter of the pipeline hole (111) is 0.4-0.6 cm; the diameter of the signal hole (121) is 0.8-1.2 cm; the diameter of the pipeline hole (131) is 0.4-0.6 cm; and the diameter of the fixing hole (132) is 1.3-1.7 cm.
3. The arterial blood pressure sensor fixation case according to claim 2, characterized in that, The center distance between the pipeline hole (131) and the fixing hole (132) is 3.2-3.8 cm.
4. An arterial blood pressure sensor fixation case according to claim 2 or 3, characterized in that The inner wall of the fixing hole (132) is nested with an elastic limiting piece, and the elastic limiting piece is a ring-shaped silica gel gasket.
5. The arterial blood pressure sensor fixation case according to claim 4, characterized in that, The cross section of the ring-shaped silica gel gasket is a trapezoidal structure, the inner diameter of which is 1.2 cm±0.1 cm; and the axial compression deformation is 0.3-0.5 mm.
6. The arterial blood pressure sensor fixation case according to claim 1, wherein, The box body (1) is provided with a rotating safety pin mechanism (14).
7. The arterial blood pressure sensor fixation case according to claim 6, characterized in that, The rotating safety pin mechanism (14) comprises a base which is injection molded with the box body (1), and a U-shaped safety pin is hinged on the base, and the free end of the U-shaped safety pin is provided with a locking buckle.
8. The arterial blood pressure sensor fixation case according to claim 1, wherein, The box body (1) is made of polycarbonate material and is transparent hexagonal, and the wall thickness is 1.2 mm+0.2 mm.
9. The arterial blood pressure sensor fixation case according to claim 1, wherein, The inner cavity of the box body (1) is provided with an arterial blood pressure sensor.
10. An arterial blood pressure sensor fixation case tubing grooming method, characterized by, The box body (1) is provided with a rotating safety pin mechanism (14). Firstly, the arterial blood pressure sensor body is placed in the inner cavity of the box body (1), the pressure catheter is led out through the main line pipeline hole (111), the signal line is led out through the signal line hole signal hole (121), the pipeline hole (131) measures CVP, and the neck of the syringe is clamped in the syringe fixing hole (132); wherein the arterial blood pressure sensor body is stably placed in the inner cavity of the box body (1), so as to avoid pipeline pulling caused by shaking.