Abdominal pressure monitoring and alarming device for patient before aortic dissection operation

Abstract

The utility model discloses an aortic dissection preoperative patient abdominal cavity pressure monitoring alarm device, which relates to the technical field of monitoring and comprises a bandage body, a positioning buckle is fixedly mounted on the surface of the bandage body, and the inner side and the outer side of the bandage body are respectively connected with a guide buckle and a placing plate in a sliding manner. The opposite sides of the guide buckle and the placement plate abut against the surface of the bandage body, and limiting rods are fixedly installed on the opposite sides of the guide buckle and the placement plate. The device has the advantages that the navel, the left waist and the right waist can be conveniently adjusted and monitored at the same time, meanwhile, the device has a flexible adjusting effect, so that the high efficiency of monitoring and using patients with different body types is realized, and the defect of low operation efficiency when the patients are monitored before the traditional aortic dissection operation is overcome; meanwhile, the monitoring operation steps of the patient are simplified.

Description

TECHNICAL FIELD

[0001] The utility model relates to monitoring technical field especially relates to a kind of preoperative abdominal cavity pressure monitoring alarm device of aortic dissection. BACKGROUND

[0002] Abdominal circumference and bladder pressure are significantly positively correlated, and the bladder pressure of patient can be calculated by measuring abdominal circumference, and the intra-abdominal pressure is obtained, based on the non-invasive characteristics of measuring abdominal circumference, the pain of patient can be greatly reduced, so it has practical application significance.

[0003] For abdominal cavity pressure monitoring of preoperative aortic dissection patient, the patient is usually taken supine position, the bladder is emptied, the soft ruler is wound around the abdomen through navel, the ruler is taken as the starting and ending point of navel, the section is kept perpendicular to the long axis of trunk, and the reading is taken at the end of expiration of patient, this method has the non-invasive characteristics of measuring abdominal circumference, but the change of abdominal cavity pressure of patient can only be roughly understood, and there is great inconvenience when one person operates, so it causes the low efficiency of abdominal cavity pressure monitoring of preoperative aortic dissection patient. UTILITY MODEL CONTENT

[0004] The utility model aims at solving one of the problems in the prior art.

[0005] To achieve the above-mentioned purpose, the utility model provides the following technical scheme: a kind of preoperative abdominal cavity pressure monitoring alarm device of aortic dissection patient, including bandage body, the surface of the bandage body is fixedly installed with positioning buckle, the inner side and the outer side of bandage body are slidably connected with guide buckle and placement plate respectively, the opposite side of guide buckle and placement plate is abutted on the surface of bandage body, and the opposite side of guide buckle and placement plate is fixedly installed with limit rod.

[0006] Preferably, the inner side of the guide buckle is screw-mounted with a guide column, the inner side of the guide buckle is provided with an internal groove, the surface of the guide column is fixedly installed with an internal baffle, and the surface of the internal baffle is slidably installed in the inner side of the internal groove.

[0007] Preferably, the inner side of the guide column is provided with a groove, the surface of the groove is adhesively installed with a convex point block, and the shape of the convex point block is pointed.

[0008] Preferably, the inside of the placement plate is rotatably installed with an auxiliary ball, and the auxiliary ball and the guide column are in the same horizontal plane at the opposite side of guide buckle and placement plate.

[0009] Preferably, the surface of the placement plate is provided with a positioning groove, the inner wall of the positioning groove is adhesively installed with a glue column, and the side, away from the limit rod, of the placement plate is provided with an electrode piece groove.

[0010] Preferably, the surface of the limiting rod is rotatably installed with a rotating sleeve, and the rotating sleeve is located on the upper and lower sides of the bandage body.

[0011] Preferably, the number of the guide buckles is two groups, and the two groups of guide buckles are slidably installed on the surface of the bandage body, and the structures on the two groups of guide buckles are the same.

[0012] Compared with the prior art, the aortic dissection preoperative patient abdominal pressure monitoring alarm device has the following beneficial effects:

[0013] (1), the aortic dissection preoperative patient abdominal pressure monitoring alarm device, the guide column extrudes the bandage body gradually and is attached to the auxiliary ball, until the guide column is limited to rotate to the predetermined position in the built-in groove through the built-in baffle, at this time, the guide column is limited to form the positioning effect of the guide buckle after adjustment through the extrusion of the internal pointed convex block on the bandage body, which guarantees the convenience of adjusting and monitoring the navel and the left and right two waist at the same time when the aortic dissection preoperative patient abdominal pressure is monitored, and also has the flexible adjustment effect to realize the efficiency of monitoring different patients, reduces the low operation efficiency of the traditional aortic dissection preoperative patient monitoring, and simplifies the steps of the patient monitoring operation. BRIEF DESCRIPTION OF DRAWINGS

[0014] The utility model is further illustrated in connection with the drawings and examples as follows:

[0015] Figure 1 It is a structure schematic view of the aortic dissection preoperative patient abdominal pressure monitoring alarm device of the utility model;

[0016] Figure 2 It is a structure schematic view of the guide buckle of the utility model;

[0017] Figure 3 It is a structure schematic view of the placement plate of the utility model;

[0018] Figure 4 It is a structure schematic view of the guide column of the utility model;

[0019] Figure 5 It is a structure schematic view of the placement plate of the utility model.

[0020] The drawings are as follows: 1, bandage body; 2, positioning buckle; 3, guide buckle; 4, placement plate; 5, limiting rod; 6, positioning groove; 7, glue column; 8, electrode piece groove; 9, rotating sleeve; 10, guide column; 11, built-in groove; 12, built-in baffle; 13, recess; 14, convex block; 15, auxiliary ball. DETAILED DESCRIPTION

[0021] The detailed embodiments of the present application will be described in this part, and the preferred embodiments of the present application are shown in the drawings, the drawings are used to supplement the description of the text part, so that people can intuitively and visually understand each technical feature and the overall technical scheme of the present application, but it cannot be understood as a limitation on the protection scope of the present application.

[0022] In the description of the present application, it should be understood that the orientation description, such as the orientation or position relationship indicated by up, down, front, back, left, right and the like, is based on the orientation or position relationship shown in the drawings, which is only for the convenience of describing the present application and simplifying the description, and does not indicate or imply that the device or element must have a specific orientation, be constructed and operated in a specific orientation, therefore it cannot be understood as a limitation on the present application.

[0023] In the description of the present application, greater than, less than, more than and the like are understood as not including the number, and above, below and the like are understood as including the number. If the first and the second are described, it is only for the purpose of distinguishing technical features, and cannot be understood as indicating or implying relative importance or implicitly indicating the number of indicated technical features or the sequence of indicated technical features.

[0024] In the description of the present application, unless otherwise explicitly limited, the words such as setting, installing and connecting should be understood in a broad sense, and the person skilled in the art can reasonably determine the specific meaning of the above words in the present application in combination with the specific content of the technical scheme.

[0025] Please refer to Figures 1-5 The present application provides a technical scheme: an abdominal cavity pressure monitoring and alarming device for aortic dissection preoperative patient, comprising a binding belt body 1, a positioning buckle 2 is fixedly installed on the surface of the binding belt body 1, a guide buckle 3 and a placing plate 4 are slidably connected to the inner side and the outer side of the binding belt body 1 respectively, the opposite sides of the guide buckle 3 and the placing plate 4 abut on the surface of the binding belt body 1, the opposite sides of the guide buckle 3 and the placing plate 4 are fixedly installed with a limiting rod 5, and the guide buckle 3 and the placing plate 4 are limited on the surface of the binding belt body 1 by the limiting rod 5 for sliding adjustment and use.

[0026] Further, a positioning groove 6 is formed on the surface of the placing plate 4, a glue column 7 is adhesively installed on the inner wall of the positioning groove 6, an electrode piece groove 8 is formed on the side of the placing plate 4 away from the limiting rod 5, by forming the electrode piece groove 8 on the placing plate 4, a sensor device similar to an electrode piece can be placed on the inner side of the electrode piece groove 8, and then a sensing line is connected to an abdominal cavity pressure sensor instrument for use, and the glue column 7 at the positioning groove 6 limits and positions the external wire, so as to stabilize the sensor device placed at the electrode piece groove 8, and further realize the reliability of data when monitoring the abdominal cavity pressure of the aortic dissection preoperative patient.

[0027] Further, the surface of the limiting rod 5 is rotatably installed with a rotating sleeve 9, which is located on the upper and lower sides of the banding body 1. The rotating sleeve 9 on the limiting rod 5 ensures the smooth sliding adjustment of the guide buckle 3 and the placement plate 4 on the surface of the banding body 1.

[0028] Further, the inner side of the guide buckle 3 is threadedly installed with a guide column 10, the inner side of the guide buckle 3 is provided with an internal groove 11, the surface of the guide column 10 is fixedly installed with an internal baffle 12, the surface of the internal baffle 12 is slidably installed on the inner side of the internal groove 11, the inner side of the guide column 10 is provided with a groove 13, the surface of the groove 13 is adhesively installed with a protruding point block 14, the protruding point block 14 is in the shape of a sharp end, the inside of the placement plate 4 is rotatably installed with an auxiliary ball 15, the auxiliary ball 15 and the guide column 10 are at the same horizontal plane on the opposite sides of the guide buckle 3 and the placement plate 4, the number of the guide buckle 3 is two groups, and the two groups of guide buckles 3 are slidably installed on the surface of the banding body 1. The structures on the two groups of guide buckles 3 are the same.

[0029] Specifically, when the abdominal cavity pressure of the patient before the aortic dissection surgery needs to be monitored, the medical staff only needs to pre-bind the banding body 1 according to the body type of the patient, and then the medical staff can adjust and change the position of the two groups of guide buckles 3 according to the body type of the patient. Since the positioning buckle 2 on the banding body 1 is positioned at the navel of the patient's abdominal cavity, the two groups of guide buckles 3 can be slidably adjusted according to the patient's body state. When the guide buckle 3 is slidably adjusted to a predetermined position, the medical staff controls the guide column 10 to move in the inner side of the guide buckle 3, so that the guide column 10 extrudes the banding body 1 to gradually fit the auxiliary ball 15, until the guide column 10 is limited to rotate to a predetermined position in the internal groove 11 through the internal baffle 12. At this time, the guide column 10 extrudes and limits the banding body 1 through the internal sharp protruding point block 14 to form the positioning effect after the adjustment of the guide buckle 3. This way ensures the convenience of monitoring the navel and the left and right waist at the same time when the abdominal cavity of the patient before the aortic dissection surgery is monitored. At the same time, the device also has a flexible adjustment effect to realize the efficiency of monitoring different types of patients, and reduces the low operation efficiency of the traditional aortic dissection surgery. At the same time, it simplifies the steps of the patient's monitoring operation.

[0030] Working principle: a kind of abdominal cavity pressure monitoring alarm device for patient before aortic dissection surgery, when the abdominal cavity pressure of the patient before the aortic dissection surgery needs to be monitored, the medical staff only needs to pre-bind the banding body 1 according to the body type of the patient, and then the medical staff can adjust and change the position of the two groups of guide buckles 3 according to the body type of the patient. At this time, the two groups of guide buckles 3 can be slidably adjusted according to the patient's body state.

[0031] The utility model embodiment makes the detailed explanation in combination with the drawing, but the utility model is not limited to the above -mentioned embodiment, still can make various changes in the knowledge range of ordinary skill in the art person who has possessed under the premise of not departing from the utility model tenet.

Claims

1. A preoperative abdominal pressure monitoring and alarm device for patients undergoing aortic dissection surgery, comprising a strap (1), characterized in that: A positioning buckle (2) is fixedly installed on the surface of the strap body (1). A guide buckle (3) and a placement plate (4) are slidably connected to the inner and outer sides of the strap body (1), respectively. The opposite sides of the guide buckle (3) and the placement plate (4) abut against the surface of the strap body (1). A limit rod (5) is fixedly installed on the opposite sides of the guide buckle (3) and the placement plate (4).

2. The intra-abdominal pressure monitoring and alarm device for patients undergoing aortic dissection surgery according to claim 1, characterized in that: The guide buckle (3) has a guide post (10) threaded on its inner side. The guide buckle (3) has an inner groove (11). An inner baffle (12) is fixedly installed on the surface of the guide post (10). The inner baffle (12) is slidably installed on the inner side of the inner groove (11).

3. The intra-abdominal pressure monitoring and alarm device for patients undergoing aortic dissection surgery according to claim 2, characterized in that: The guide post (10) has a groove (13) on its inner side, and a protrusion block (14) is bonded to the surface of the groove (13). The protrusion block (14) is pointed in shape.

4. The intra-abdominal pressure monitoring and alarm device for patients undergoing aortic dissection surgery according to claim 3, characterized in that: An auxiliary ball (15) is rotatably mounted inside the placement plate (4). The auxiliary ball (15) and the guide post (10) are on the same horizontal plane on opposite sides of the guide buckle (3) and the placement plate (4).

5. The intra-abdominal pressure monitoring and alarm device for patients undergoing aortic dissection surgery according to claim 4, characterized in that: The surface of the placement plate (4) is provided with a positioning groove (6), and the inner wall of the positioning groove (6) is bonded with a glue column (7). An electrode plate groove (8) is provided on the side of the placement plate (4) away from the limiting rod (5).

6. The intra-abdominal pressure monitoring and alarm device for patients undergoing aortic dissection surgery according to claim 5, characterized in that: The surface of the limiting rod (5) is rotatably mounted with a rotating sleeve (9), which is located on the upper and lower sides of the strap body (1).

7. The intra-abdominal pressure monitoring and alarm device for patients undergoing aortic dissection surgery according to claim 6, characterized in that: The guide buckle (3) is in two sets. Both sets of guide buckles (3) are slidably installed on the surface of the strap body (1). The structures on both sets of guide buckles (3) are the same.

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