Protective sleeve for intracranial pressure monitoring probe

Abstract

The intracranial pressure monitoring probe protective sleeve comprises an outer protective sleeve body and an inner protective sleeve body, the inner protective sleeve body is shorter than the outer protective sleeve body, the upper ends of the outer protective sleeve body and the inner protective sleeve body are of the same opening design and are provided with upper openings, and the lower ends of the outer protective sleeve body and the inner protective sleeve body are provided with a first lower opening and a second lower opening respectively. The periphery of the upper opening and the periphery of the first lower opening are each provided with a sealing reinforcing strip used for closing the sleeve opening. According to the utility model, the double-layer protective sleeve design is adopted, the structure is simple and clear, the probe joint is prevented from polluting other sterile articles or areas in the storage process, the monitoring precision of the probe joint can be prevented from being influenced by physical damage, and medical staff can operate the probe joint more conveniently and normatively, so that the working efficiency is improved. And the risk of adverse events caused by misoperation is reduced.

Description

Technical Field

[0001] This utility model relates to the field of medical device technology, specifically a protective cover for an intracranial pressure monitoring probe. Background Technology

[0002] An intracranial pressure monitoring probe is a medical device used to measure intracranial pressure. It can acquire intracranial pressure data in real time and accurately, providing crucial information for clinical diagnosis and treatment. Currently, the storage of intracranial pressure monitoring probes is usually done using sterile gloves and thread. During storage, the doctor wears an extra sterile glove on their left hand, holds the intracranial pressure monitoring probe connector in their right hand, and the circulating nurse holds the detector connector. After the doctor and circulating nurse connect the two connectors, they turn on the device and zero it. After zeroing, they turn off the device and separate the two connectors. The doctor holds the intracranial pressure monitoring probe connector with the glove on their left hand, turns the glove over to cover the intracranial pressure monitoring probe connector, and ties the opening of the glove tightly with thread, thus wrapping the connector inside their hand to complete the storage.

[0003] The above-mentioned glove storage method is not optimized for clinical use. Neurosurgical procedures have higher requirements for clinical infection control. In order to optimize the storage of intracranial pressure monitoring probe connectors after zeroing, and to better comply with aseptic principles and implement isolation techniques, this application was developed. Utility Model Content

[0004] To address the aforementioned technical issues, this utility model provides a protective sleeve for an intracranial pressure monitoring probe. The double-layer inner and outer design effectively houses and isolates the contaminated intracranial pressure monitoring probe connector, preventing contamination of the probe and surgical area.

[0005] To achieve its technical objectives, this utility model adopts the following technical solution:

[0006] A protective sleeve for an intracranial pressure monitoring probe includes an outer protective sleeve and an inner protective sleeve. The inner protective sleeve is shorter than the outer protective sleeve. The upper ends of the outer and inner protective sleeves are designed with the same opening and are provided with an upper opening. The lower ends are respectively provided with a first lower opening and a second lower opening. The outer periphery of the upper opening and the first lower opening are provided with a sealing and reinforcing strip for tightening the opening of the sleeve.

[0007] Preferably, the outer wall of the inner protective sleeve is provided with a semi-cut dotted line in the middle circumferential direction.

[0008] Preferably, the end of the sealing reinforcement strip is provided with double-sided adhesive with a protective sheet.

[0009] Preferably, the size of the first lower opening is equal to the size of the upper opening, and the size of the second lower opening is smaller than the size of the upper opening.

[0010] More preferably, the cross-section of the first lower opening is square, and the cross-section of the second lower opening is circular.

[0011] More preferably, both the first lower opening and the second lower opening can be folded upwards and returned to their original position downwards.

[0012] Preferably, both the outer protective sleeve and the inner protective sleeve are made of transparent material.

[0013] The beneficial effects of this utility model are as follows: The double-layer protective sleeve design has a simple and clear structure, which prevents the probe connector from contaminating other sterile items or areas during storage. It can also prevent the probe connector from being physically damaged and affecting its monitoring accuracy. At the same time, it makes the operation more convenient and standardized for medical staff, reducing the risk of adverse events caused by improper operation. Attached Figure Description

[0014] Figure 1 This is a three-dimensional structural schematic diagram of the present invention;

[0015] Figure 2 This is a three-dimensional structural diagram of the present invention in use.

[0016] Figure label:

[0017] 1. Top opening; 2. First bottom opening; 3. Second bottom opening; 4. Sealing and reinforcing strip; 5. Double-sided adhesive; 6. Semi-cut dotted line; 7. Inner protective sleeve; 8. Outer protective sleeve. Detailed Implementation

[0018] In the description of this utility model, it should be noted that the terms "middle", "upper / lower", "inner and outer", "top / bottom", etc., indicate the orientation or positional relationship based on the orientation or positional relationship shown in the accompanying drawings. They are only for the convenience of describing this utility model and simplifying the description, and do not indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation. Therefore, they should not be construed as limitations on this utility model.

[0019] In the description of this utility model, it should be noted that, unless otherwise explicitly specified and limited, the terms "installed," "equipped with," and "connected," etc., should be interpreted broadly. For example, "connected" can be a fixed connection, a detachable connection, or an integral connection; it can be a mechanical connection or an electrical connection; it can be a direct connection or an indirect connection through an intermediate medium; it can be a connection within the components of a compatible model. Those skilled in the art can understand the specific meaning of the above terms in this utility model based on the specific circumstances. Furthermore, unless otherwise specified, all components used in this application are commercially available components, and the connection between different components can be achieved through conventional technical means.

[0020] The present invention will now be described in further detail with reference to the accompanying drawings and specific embodiments.

[0021] This utility model provides a protective cover for an intracranial pressure monitoring probe, such as Figure 1 As shown, it includes an outer protective sleeve 8 and an inner protective sleeve 7. The inner protective sleeve 7 is shorter than the outer protective sleeve 8. The upper ends of the outer protective sleeve 8 and the inner protective sleeve 7 are designed with the same opening and are provided with an upper opening 1. The lower ends are respectively provided with a first lower opening 2 and a second lower opening 3. The outer periphery of the upper opening 1 and the first lower opening 2 are provided with a sealing and reinforcing strip 4 for tightening the sleeve opening.

[0022] Preferably, the inner protective sleeve 7 has a semi-cut dotted line 6 circumferentially arranged in the middle of the outer wall, and the inner protective sleeve 7 can be easily torn along the semi-cut dotted line 6.

[0023] Preferably, the end of the sealing reinforcement strip 4 is provided with double-sided adhesive 5 with a protective sheet, which can be used to stick and fix the sealing reinforcement strip 4 after the opening is closed.

[0024] Preferably, the size of the first lower opening 2 is equal to the size of the upper opening 1, and the size of the second lower opening 3 is smaller than the size of the upper opening 1.

[0025] Preferably, the cross-section of the first lower opening 2 is square, and the cross-section of the second lower opening 3 is circular.

[0026] As a preferred embodiment, the cross-section of the first lower opening 2 is rectangular.

[0027] As a preferred embodiment, both the first lower opening 2 and the second lower opening 3 can be folded upwards and returned to their original position downwards.

[0028] Preferably, both the outer protective sleeve 8 and the inner protective sleeve 7 are made of transparent material.

[0029] Preferably, the transparent material is a transparent polyethylene material.

[0030] The operation method of this utility model is as follows: In use, insert the intracranial pressure monitoring probe into the inner protective sleeve 7 of the double-layer protective sleeve through the upper opening 1. Tighten the sealing reinforcement strip 4 set around the outer periphery of the upper opening 1. Peel off the protective sheet on the surface of the double-sided adhesive 5 at the end of the sealing reinforcement strip 4, and stick the sealing reinforcement strip 4 in place. Then, fold upwards the first lower opening 2 and fold upwards along the semi-cut dotted line 6 of the second lower opening 3, exposing the intracranial pressure monitoring probe. Connect the connector of the intracranial pressure monitoring probe to the instrument connector and perform a cyclic zeroing adjustment. After the zeroing process is complete, disconnect the instrument connector, wrap the intracranial pressure monitoring probe around the upper part of the half-cut dotted line 6, pull down to reset the second lower opening 3, tear off the folded part of the inner protective sleeve 7 along the half-cut dotted line 6 to ensure that the inner protective sleeve 7 is clean and uncontaminated, finally pull down to reset the first lower opening 2, tighten the sealing reinforcement strip 4 set on the outer periphery of the first lower opening 2, peel off the protective sheet on the surface of the double-sided adhesive 5 at the end of the sealing reinforcement strip 4, and stick the sealing reinforcement strip 4 to fix it, thus completing the entire process of storing and protecting the intracranial pressure monitoring probe.

[0031] Although the embodiments of this utility model have been described in the specification, these embodiments are merely illustrative and should not limit the scope of protection of this utility model. Various omissions, substitutions, and modifications made without departing from the spirit of this utility model should be included within the scope of protection of this utility model.

Claims

1. A protective sleeve for an intracranial pressure monitoring probe, characterized in that, It includes an outer protective sleeve and an inner protective sleeve. The inner protective sleeve is shorter than the outer protective sleeve. The upper ends of the outer and inner protective sleeves are designed with the same opening and are provided with an upper opening. The lower ends are respectively provided with a first lower opening and a second lower opening. The outer periphery of the upper opening and the first lower opening are provided with a sealing and reinforcing strip for tightening the sleeve opening.

2. The protective sleeve for an intracranial pressure monitoring probe as described in claim 1, characterized in that, The outer wall of the inner protective sleeve is provided with a semi-cut dotted line in the middle circumferential direction.

3. The protective sleeve for an intracranial pressure monitoring probe as described in claim 1, characterized in that, The end of the sealing reinforcement strip is provided with double-sided adhesive with a protective sheet.

4. The protective sleeve for an intracranial pressure monitoring probe as described in claim 1, characterized in that, The size of the first lower opening is equal to the size of the upper opening, and the size of the second lower opening is smaller than the size of the upper opening.

5. A protective sleeve for an intracranial pressure monitoring probe as described in claim 4, characterized in that, The first lower opening has a square cross-section, and the second lower opening has a circular cross-section.

6. A protective sleeve for an intracranial pressure monitoring probe as described in claim 5, characterized in that, Both the first and second lower openings can be folded upwards and returned to their original position downwards.

7. A protective sleeve for an intracranial pressure monitoring probe as described in any one of claims 1 to 6, characterized in that, Both the outer protective sleeve and the inner protective sleeve are made of transparent material.

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