Acute skin failure monitoring device and system

Abstract

The invention belongs to the technical field of critical care, and particularly relates to an acute skin failure monitoring device and system.The acute skin failure monitoring device comprises a skin failure monitoring device body, and a protective shell is fixedly connected to the end of the skin failure monitoring device body; the top of the protective shell is fixedly connected with a monitoring display screen; a monitoring station is mounted at the top of the protective shell; a connecting line is mounted at the end part of the skin failure monitoring device body; a detection head is mounted at the end part of the connecting line; then the detection head is attached to the sacrococcyx, the scapula, the occipital part, the heel, the lateral malleolus and other parts for monitoring, in the monitoring process, the electric push rod is opened to drive the partition plate to move towards the end part, so that the partition plate drives the partition ceramic holes to slide forwards so as to support and protect the end part of the connecting wire, and then the plurality of partition ceramic holes are formed, so that the connecting wire is prevented from being damaged. The connecting lines are separated, and the problem that the connecting lines are intertwined when the detection head drives the connecting lines to move is solved.

Description

Technical Field

[0001] The present invention belongs to the technical field of intensive care, and particularly relates to an acute skin failure monitoring device and system. Background Art

[0002] The concept of acute skin failure was proposed by LAPUMA in 1991; as the largest human organ with a mass accounting for 10% - 15% of the human body mass and a blood supply accounting for 25% - 33% of the cardiac output, like other organs such as the heart, lungs, liver, brain, and kidneys, acute failure can also occur during low perfusion. In 2015, DELMORE et al. believed that ASF is PI combined with critical and severe diseases.

[0003] In 2017, LEVINE proposed to define ASF as "an event in which skin tissue is damaged due to hypoxia, insufficient nutrient supply, posterior mechanical pressure, and accumulation of toxic metabolic by-products"; there is still no unified definition and diagnostic criteria for ASF so far. Currently, most scholars believe that ASF refers to an event in which the skin and underlying tissues suffer inevitable damage due to insufficient perfusion and are accompanied by severe diseases; the means that can be used to evaluate ASF include laser Doppler technology, ultrasonic detection technology, perfusion index monitoring technology, and skin mottling score; ASF is mainly identified by evaluating skin perfusion insufficiency; some studies have shown that arterial blood lactate is positively correlated with ASF. By designing a multifunctional monitoring device, it is possible to obtain the pressure condition of the skin tissue at the evaluation site, temperature value, humidity value, optically induced monitoring of blood perfusion, and transcutaneous oxygen saturation, and at the same time, a minimally invasive probe is used to obtain local tissue fluid to monitor the lactate value. The above-mentioned monitored values are comprehensively calculated and judged to indicate the risk degree of acute skin failure at this site.

[0004] Currently, in the prior art, when detecting the skin through an acute skin failure monitoring device, the probe is attached to the surface of the skin for monitoring. During the monitoring process, due to the large number of connecting wires of the probe, the detection connecting wires will be entangled with each other during the detection process, resulting in problems such as insufficient distance and reduced detection accuracy when placing the detection head due to the entanglement of the connecting wires when moving the detection head later; therefore, an acute skin failure monitoring device and system are proposed for the above problems. Summary of the Invention

[0005] In order to make up for the deficiencies of the prior art and solve at least one technical problem proposed in the background art, the present invention proposes an acute skin failure monitoring device and system.

[0006] The technical solution adopted by the present invention to solve its technical problems is as follows: An acute skin failure monitoring device and system according to the present invention includes a main body of the skin failure monitoring device, and a protective shell is fixedly connected to the end of the main body of the skin failure monitoring device; a monitoring display screen is fixedly connected to the top of the protective shell; a monitoring platform is installed on the top of the protective shell; a connecting wire is installed at the end of the main body of the skin failure monitoring device; a detection head is installed at the end of the connecting wire; an electric push rod is fixedly connected to the end of the main body of the skin failure monitoring device; a partition plate is fixedly connected to the end of the electric push rod; a plurality of partition ceramic holes are formed inside the partition plate; and the connecting wire is arranged inside the partition ceramic hole.

[0007] Preferably, an extrusion rubber strip is hinged to the end of the partition plate through a torsion spring, and is arranged in a circumferential array.

[0008] Preferably, a protective pad is fixedly connected to the end of the extrusion rubber strip, and the protective pad layer is semi-circular.

[0009] Preferably, the extrusion rubber strips are symmetrically arranged on both sides of the partition plate and are located at the ends of the partition ceramic holes; a plurality of suction cups are fixedly connected to the bottom of the protective shell.

[0010] Preferably, an air pipe is fixedly connected to the bottom of the protective shell; a pull rod is slidably connected in the rodless cavity of the air pipe, and the other end of the pull rod is fixedly connected to the bottom of the partition plate; a conduit is fixedly connected to the end of the suction cup, and the other end of the conduit is fixedly connected to the end of the air pipe.

[0011] An acute skin failure monitoring system, which is applicable to the acute skin failure monitoring device described in any of the above rights, is characterized in that: it includes a data terminal monitoring module; an ultrasonic detection module, a detection head module, a laser Doppler technology and a perfusion index monitoring module; the data terminal monitoring module is signal-connected to the ultrasonic detection module; the ultrasonic monitoring module is signal-connected to the detection head module; the data terminal monitoring die is signal-connected to the laser Doppler technology module; the data terminal monitoring module is signal-connected to the perfusion index monitoring die.

[0012] Preferably, the specific operation method of the detection head module includes the following methods; the detection head module is relatively soft in material and has a good fit with the skin, and is in the shape of an electrode sheet in appearance.

[0013] Preferably, the ultrasonic detection module is uploaded to the data acquisition terminal module through wired or wireless transmission for calculation to judge the risk level; when performing monitoring and judgment, multi-point monitoring is required, mainly concentrated on the monitoring of these pressure-bearing parts such as the sacrococcygeal region, scapula, occipital region, heel, and outer ankle.

[0014] The beneficial effects of the present invention:

[0015] The present invention provides an acute skin failure monitoring device and system. During the monitoring process, the detection head is mainly attached to the local skin, and then the detection head is attached to the sacrococcygeal, scapular, occipital, heel, and lateral malleolus parts for monitoring. During the monitoring process, by turning on the electric push rod to drive the partition plate to move towards the end, the partition plate drives the partition ceramic holes to slide forward, so as to support and protect the end of the connecting wire. Then, by providing a plurality of partition ceramic holes, the connecting wires are separated to reduce the problem of mutual entanglement when the detection head drives the connecting wires to move.

[0016] The present invention provides an acute skin failure monitoring device and system. When the partition ceramic holes limit and support the connecting wires, by installing a plurality of extrusion rubber strips at the ends of the partition ceramic holes, when the connecting wires slide, the connecting wires are clamped at the ends by the extrusion rubber strips, so as to support and protect the ends of the connecting wires. BRIEF DESCRIPTION OF THE DRAWINGS

[0017] The drawings described herein are used to provide a further understanding of the present invention, form a part of this application, and the schematic embodiments of the present invention and their descriptions are used to explain the present invention and do not constitute an improper limitation to the present invention.

[0018] In the drawings:

[0019] Figure 1 is the system flow schematic diagram of the present invention;

[0020] Figure 2 is the three-dimensional view of the present invention;

[0021] Figure 3 is the bottom view of the present invention;

[0022] Figure 4 is the structural schematic diagram of the extrusion rubber strip in the present invention;

[0023] Figure 5 is Figure 4 the enlarged view at A in

[0024] LEGEND DESCRIPTION:

[0025] 1. Acute skin failure monitoring device body; 11. Protective shell; 12. Monitoring platform; 21. Monitoring display screen; 22. Connecting wire; 23. Detection head; 24. Electric push rod; 25. Partition plate; 26. Partition ceramic hole; 31. Extrusion rubber strip; 32. Protective pad; 4. Suction cup; 51. Air pipe; 52. Conduit; 53. Pull rod. DETAILED DESCRIPTION OF THE INVENTION

[0026] The following will clearly and completely describe the technical solutions in the embodiments of the present invention with reference to the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only a part of the embodiments of the present invention, rather than all the embodiments. All other embodiments obtained by those of ordinary skill in the art based on the embodiments of the present invention without creative efforts shall fall within the protection scope of the present invention.

[0027] The following gives specific embodiments.

[0028] Please refer to Figures 1-5 , the present invention provides an acute skin failure monitoring device and system, including the main body 1 of the skin failure monitoring device. A protective shell 11 is fixedly connected to the end of the main body 1 of the skin failure monitoring device; a monitoring display screen 21 is fixedly connected to the top of the protective shell 11; a monitoring platform 12 is installed on the top of the protective shell 11; a connecting line 22 is installed at the end of the main body 1 of the skin failure monitoring device; a detection head 23 is installed at the end of the connecting line 22; an electric push rod 24 is fixedly connected to the end of the main body 1 of the skin failure monitoring device; a partition plate 25 is fixedly connected to the end of the electric push rod 24; a plurality of partition ceramic holes 26 are formed inside the partition plate 25; the connecting line 22 is arranged inside the partition ceramic holes 26; during operation, when monitoring acute skin, it is necessary to attach the detection head 23 to the surface of the skin for monitoring. During the monitoring process, the detection head 23 is mainly attached to the local skin, and then the detection head 23 is attached to the sacrococcygeal, scapular, occipital, heel, and outer ankle and other parts for monitoring. During the monitoring process, by turning on the electric push rod 24 to drive the partition plate 25 to move towards the end, the partition plate 25 drives the partition ceramic holes 26 to slide forward, so as to support and protect the end of the connecting line 22. Then, by providing a plurality of partition ceramic holes 26, the connecting lines 22 are separated from each other, reducing the problem of mutual entanglement when the detection head 23 drives the connecting line 22 to move.

[0029] Furthermore, as Figures 2-5 shown, an extrusion rubber strip 31 is hinged to the end of the partition plate 25 through a torsion spring, and is arranged in a circumferential array; during operation, when the partition ceramic holes 26 limit and support the connecting line 22, by installing a plurality of extrusion rubber strips 31 at the end of the partition ceramic holes 26, when the connecting line 22 slides, the connecting line 22 is clamped at the end by the extrusion rubber strips 31, so as to support and protect the end of the connecting line 22.

[0030] Furthermore, as Figures 2-5As shown in the figure, a protective pad 32 is fixedly connected to the end of the extrusion rubber strip 31, and the protective pad 32 is semi-circular; during operation, by fixedly connecting the protective pad 32 to the end of the extrusion rubber strip 31, the extrusion rubber strip 31 drives the protective pad 32 to clamp and fit on the surface of the connecting wire 22, and the connecting wire 22 is protected by the protective pad 32.

[0031] Furthermore, as Figures 2-5 shown in the figure, the extrusion rubber strips 31 are symmetrically arranged on both sides of the partition plate 25 and are located at the end of the partition ceramic hole 26; a plurality of suckers 4 are fixedly connected to the bottom of the protective shell 11; during operation, by installing the suckers 4 at the bottom of the protective shell 11, the skin failure monitoring device body 1 can be supported and limited during operation.

[0032] Furthermore, as Figures 2-5 shown in the figure, an air pipe 51 is fixedly connected to the bottom of the protective shell 11; a pull rod 53 is slidably connected in the rodless cavity of the air pipe 51, and the other end of the pull rod 53 is fixedly connected to the bottom of the partition plate 25; a conduit 52 is fixedly connected to the end of the sucker 4, and the other end of the conduit 52 is fixedly connected to the end of the air pipe 51; during operation, when the electric push rod 24 pushes the partition plate 25 to move towards the end, by driving the pull rod 53 to move towards the side end, the pull rod 53 slides inside the rodless cavity of the air pipe 51, and then air is pumped, and the gas inside the sucker 4 is pumped out through the conduit 52 to improve the adsorption effect of the sucker 4.

[0033] Furthermore, as Figure 1 shown in the figure, an acute skin failure monitoring system, which is applicable to any of the acute skin failure monitoring devices described in the above rights, is characterized in that: it includes a data terminal monitoring module; an ultrasonic detection module, a detection head module, a laser Doppler technology and a perfusion index monitoring module; the data terminal monitoring module is signal-connected to the ultrasonic detection module; the ultrasonic monitoring module is signal-connected to the detection head module; the data terminal monitoring die is signal-connected to the laser Doppler technology module; the data terminal monitoring module is signal-connected to the perfusion index monitoring die.

[0034] Furthermore, as Figure 1 shown in the figure, the specific operation method of the detection head module includes the following methods; the detection head module is relatively soft in material and has a good fit with the skin, and is in the shape of an electrode sheet in appearance.

[0035] Furthermore, as Figure 1As shown, the ultrasonic detection module is uploaded to the data acquisition terminal module through wired or wireless transmission for calculation to determine the risk level; when performing monitoring and judgment, multi-point monitoring is required, mainly focusing on the monitoring of pressure-bearing parts such as the sacrococcyx, scapula, occiput, heel, and outer ankle.

[0036] Working principle: When monitoring acute skin, the detection head 23 needs to be attached to the surface of the skin for monitoring. During the monitoring process, the detection head 23 is mainly attached to the local skin, and then the detection head 23 is attached to parts such as the sacrococcyx, scapula, occiput, heel, and outer ankle for monitoring. During the monitoring process, by turning on the electric push rod 24 to drive the partition plate 25 to move towards the end, the partition plate 25 drives the partition ceramic hole 26 to slide forward, so as to support and protect the end of the connecting wire 22. Then, by providing a number of partition ceramic holes 26, the connecting wire 22 is separated, reducing the problem of mutual entanglement when the detection head 23 drives the connecting wire 22 to move; when the partition ceramic hole 26 limits and supports the connecting wire 22, by installing a number of extrusion rubber strips 31 at the end of the partition ceramic hole 26, when the connecting wire 22 slides, the connecting wire 22 is clamped at the end by the extrusion rubber strips 31, so as to support and protect the end of the connecting wire 22; by fixedly connecting a protective pad 32 at the end of the extrusion rubber strip 31, the extrusion rubber strip 31 drives the protective pad 32 to clamp and fit on the surface of the connecting wire 22, and the connecting wire 22 is protected by the protective pad 32; by installing a suction cup 4 at the bottom of the protective shell 11, when the skin failure monitoring device body 1 works, it can support and limit the skin failure monitoring device body 1; when the electric push rod 24 pushes the partition plate 25 to move towards the end, by driving the pull rod 53 to move towards the side end, the pull rod 53 slides inside the rodless cavity of the air pipe 51, and then air is pumped, and the gas inside the suction cup 4 is pumped out through the catheter 52 to improve the adsorption effect of the suction cup 4.

[0037] The above shows and describes the basic principles, main features, and advantages of the present invention. Those skilled in the art should understand that the present invention is not limited by the above embodiments. What is described in the above embodiments and the specification only illustrates the principles of the present invention. Without departing from the spirit and scope of the present invention, the present invention will have various changes and improvements, and these changes and improvements all fall within the scope of the present invention claimed.

Claims

1. An acute skin failure monitoring device, comprising a skin failure monitoring device body (1), characterized in that: The end of the skin failure monitoring device body (1) is fixedly connected to a protective shell (11); the top of the protective shell (11) is fixedly connected to a monitoring display screen (21); the top of the protective shell (11) is installed with a monitoring platform (12); the end of the skin failure monitoring device body (1) is installed with a connecting line (22); the end of the connecting line (22) is installed with a detection head (23); the end of the skin failure monitoring device body (1) is fixedly connected to an electric push rod (24); the end of the electric push rod (24) is fixedly connected to a partition plate (25); a plurality of partition ceramic holes (26) are provided inside the partition plate (25); a connecting line (22) is provided inside the partition ceramic hole (26).

2. An acute skin failure monitoring device as claimed in claim 1, characterized in that: The ends of the partition plates (25) are hingedly connected with extruded rubber strips (31) via torsion springs and are arranged in a circumferential array.

3. An acute skin failure monitoring device as claimed in claim 2, characterized in that: A protective pad (32) is fixedly connected to the end of the extruded rubber strip (31), and the protective pad (32) is semi-arc-shaped.

4. An acute skin failure monitoring device as claimed in claim 2, characterized in that: The extruded rubber strips (31) are symmetrically arranged on both sides of the partition plate (25) and are located at the ends of the partitioning ceramic holes (26).

5. An acute skin failure monitoring device as claimed in claim 1, characterized in that: A plurality of suction cups (4) are fixedly connected to the bottom of the protective shell (11).

6. An acute skin failure monitoring device as claimed in claim 1, characterized in that: The bottom of the protective shell (11) is fixedly connected to an air pipe (51); a pull rod (53) is slidably connected in the rodless cavity inside the air pipe (51), and the other end of the pull rod (53) is fixedly connected to the bottom of the partition plate (25); the end of the suction cup (4) is fixedly connected to a conduit (52), and the other end of the conduit (52) is fixedly connected to the end of the air pipe (51).

7. An acute skin failure monitoring system, which is applicable to the acute skin failure monitoring device according to any one of claims 1 to 6, characterized in that: It includes a data terminal monitoring module; an ultrasonic detection module, a detection head module, a laser Doppler technology module and a perfusion index monitoring module; the data terminal monitoring module is connected to the ultrasonic detection module through signals; the ultrasonic monitoring module is connected to the detection head module through signals; the data terminal monitoring mold is connected to the laser Doppler technology module through signals; the data terminal monitoring module is connected to the perfusion index monitoring mold through signals.

8. An acute skin failure monitoring system as claimed in claim 7, characterized in that: The specific operation method of the detection head module includes the following method; the detection head module is relatively soft in material, has a good fit with the skin, and has an appearance in the shape of an electrode sheet.

9. An acute skin failure monitoring system as claimed in claim 7, characterized in that: The ultrasonic detection module is uploaded to the data acquisition terminal module through wired or wireless transmission for calculation to determine the degree of risk; when conducting monitoring and judgment, multi-point monitoring is required, mainly focusing on the monitoring of pressure-bearing areas such as the sacrum, scapula, occipital region, heel, and lateral malleolus.

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