CN221691146U - A clinical rapid hemostasis device - Google Patents

Abstract

The utility model provides a rapid clinical hemostatic device, which belongs to the technical field of medical appliances; the hemostatic head comprises a main body belt and an elastic belt which are used for being worn on a wrist or an arm by a patient, and a hemostatic head, a screw rod and a screwing cover which are used for compressing wound hemostasis, wherein a positioning seat is fixed on the main body belt, a sliding groove is formed in the inner side of the positioning seat, a sliding edge is fixedly connected to the bottom end of the screwing cover, the screwing cover is rotatably arranged on the positioning seat through the sliding edge, and the screw rod and the screwing cover are screwed together by screw threads and further comprise sterilized cotton used for medicine feeding and sterilization. Through setting up logical groove, weeping hole and disinfection cotton, wear this hemostasis device on one's body the back when the patient, medical personnel can use the needle tubing to feed medicine from screw rod top logical notch department, and the medicine can flow to disinfection cotton along logical groove on, and then from weeping hole in to on the patient's wound, can in time disinfect or go up the medicine for patient's wound, and then accelerate wound hemostasis or healing, convenient operation, the practicality is higher.

Description

A clinical rapid hemostasis device

Technical Field

The utility model relates to the technical field of medical use, in particular to a clinical rapid hemostasis device.

Background Art

In outpatient medical treatment, for trauma, if the injury is severe, the tissue is particularly deep, and there are ruptures of large blood vessels, veins, or even arteries, a band should be used to tightly bind the wound above the wound to prevent the blood vessels in the distal bleeding area from bleeding.

Currently, the more common rapid hemostatic device is similar to a bracelet, which is provided with a hemostatic component that moves in a threaded manner. However, the existing device still has inconveniences. When a patient's arm is ruptured, a hemostatic device is needed to stop the bleeding in time, and the traditional hemostatic device squeezes the hemostatic component onto the bleeding part. Since the wound has been compacted, it is inconvenient to disinfect and apply medicine to the patient's wound. Therefore, the present application provides a clinical rapid hemostatic device to meet the demand.

Utility Model Content

The technical problem to be solved by the utility model is to provide a clinical rapid hemostasis device to solve the problem that the existing hemostasis device squeezes the hemostasis component on the bleeding part, which is inconvenient to disinfect and apply medicine to the patient's wound because the wound has been compacted.

In order to solve the above technical problems, the utility model provides the following technical solutions:

A clinical rapid hemostasis device comprises a main body band and an elastic band for patients to wear on their wrists or arms, and a hemostasis head, a screw and a screw cover for compressing wounds to stop bleeding. A positioning seat is fixed on the main body band, a sliding groove is provided on the inner side of the positioning seat, a sliding edge is fixedly connected to the bottom end of the screw cover, the screw cover is rotatably mounted on the positioning seat via the sliding edge, the screw and the screw cover are threadedly connected, and also comprises disinfectant cotton for applying medicine and disinfecting.

Preferably, a placement groove is provided inside the hemostatic head, a plurality of evenly distributed leakage holes are provided on the hemostatic head, the disinfecting cotton is placed in the placement groove, a through groove extending from the head end to the tail end is provided on the screw rod, a connecting plate is connected and fixed to the bottom end of the screw rod, the hemostatic head is mounted on the connecting plate, and a connecting port connected to the through groove is provided on the connecting plate.

Preferably, the disinfecting cotton is located directly below the connecting plate, the connecting plate is located below the main body belt, and the main body belt is provided with a through hole for the screw to pass through.

Preferably, an embedding opening is provided at the lower end of the connecting plate, and the hemostatic head is installed in the embedding opening.

Preferably, both elastic bands are provided with Velcro tapes that adhere to each other, and both elastic bands are made of cloth.

Preferably, two limit blocks are fixed on the main body belt, both of which are located at the bottom of the main body belt, and the limit blocks are made of silicone.

Preferably, the disinfectant cotton is a sponge.

Preferably, the screw rod and the connecting plate are both made of transparent plastic.

Compared with the prior art, the utility model has at least the following beneficial effects:

In the above scheme, by providing a through groove, a leakage hole and disinfectant cotton, when the patient wears the hemostatic device, medical staff can use a syringe to add medicine from the through groove at the top of the screw. The medicine will flow along the through groove to the disinfectant cotton, and then flow from the leakage hole to the patient's wound. The patient's wound can be disinfected or medicated in time, thereby accelerating the hemostasis or healing of the wound. The operation is convenient and the practicability is high.

By setting two limit blocks, which are clamped on the arms on both sides of the patient's wound, the hemostatic device can be installed more stably. By setting a connecting plate and an embedding opening, after the disinfection cotton is embedded in the hemostatic head, the hemostatic head can be bonded and fixed by brushing glue in the embedding opening, thereby facilitating the installation of the disinfection cotton and the processing and production of the hemostatic device.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated herein and constitute a part of the specification, illustrate embodiments of the present disclosure and, together with the description, further serve to explain the principles of the present disclosure and to enable those skilled in the relevant art to make and use the present disclosure.

FIG1 is a schematic diagram of the three-dimensional structure of a clinical rapid hemostasis device;

FIG2 is a schematic diagram showing a partial structural separation structure;

FIG3 is a schematic diagram of the axonometric structure of FIG2 ;

FIG4 is a schematic diagram of an exploded three-dimensional structure of some components;

FIG5 is a schematic diagram of the axonometric structure of FIG4 ;

[reference numerals]

1. Main body belt; 2. Elastic belt; 3. Velcro; 4. Hemostatic head; 5. Connecting plate; 6. Limiting block; 7. Screw; 8. Screw cover; 9. Positioning seat; 10. Through groove; 11. Sliding groove; 12. Through hole; 13. Sliding edge; 14. Leakage hole; 15. Embedding port; 16. Disinfection cotton; 17. Placement slot; 18. Connecting port.

As shown in the figure, in order to clearly implement the structure of the embodiment of the utility model, specific structures and devices are marked in the figure, but this is only for illustrative purposes and is not intended to limit the utility model to the specific structure, device and environment. According to specific needs, ordinary technicians in this field can adjust or modify these devices and environments, and the adjustments or modifications made are still included in the scope of the attached claims.

DETAILED DESCRIPTION

The following is a detailed description of a clinical rapid hemostasis device provided by the utility model in combination with the accompanying drawings and specific embodiments. At the same time, it is explained here that in order to make the embodiments more detailed, the following embodiments are the best and preferred embodiments, and those skilled in the art may also adopt other alternative methods to implement some known technologies; and the accompanying drawings are only for a more specific description of the embodiments, and are not intended to specifically limit the utility model.

It should be noted that the references to "one embodiment", "an embodiment", "an exemplary embodiment", "some embodiments" and the like in the specification indicate that the embodiments described may include specific features, structures or characteristics, but not every embodiment may include the specific features, structures or characteristics. In addition, when a specific feature, structure or characteristic is described in conjunction with an embodiment, it should be within the knowledge of a person skilled in the art to implement such feature, structure or characteristic in conjunction with other embodiments (whether or not explicitly described).

In general, a term can be understood, at least in part, from its use in context. For example, depending, at least in part, on the context, the term "one or more" as used herein can be used to describe any feature, structure, or characteristic in the singular sense, or can be used to describe a combination of features, structures, or characteristics in the plural sense. Additionally, the term "based on" can be understood as not necessarily intended to convey an exclusive set of factors, but can instead, depending, at least in part, on the context, allow for the presence of other factors that are not necessarily explicitly described.

It will be understood that the meaning of “on,” “over,” and “above” in this disclosure should be interpreted in the broadest manner, so that “on” not only means “directly on” something, but also includes the meaning of being “on” something with intervening features or layers therebetween, and “on” or “over” not only means “on” or “above” something, but also includes the meaning of being “on” or “above” something with no intervening features or layers therebetween.

Additionally, spatially relative terms such as "under," "beneath," "lower," "above," "upper," and the like may be used herein for descriptive convenience to describe the relationship of one element or feature to another element or features, as shown in the accompanying drawings. Spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the accompanying drawings. The device may be oriented in other ways, and the spatially relative descriptors used herein may be similarly interpreted accordingly.

As shown in Fig. 1 to Fig. 5, an embodiment of the utility model provides a clinical rapid hemostasis device, comprising a main body band 1 and an elastic band 2 for patients to wear on their wrists or arms, and a hemostasis head 4, a screw rod 7 and a screw cover 8 for compressing wounds to stop bleeding. A positioning seat 9 is fixed on the main body band 1, a sliding groove 11 is provided on the inner side of the positioning seat 9, a sliding edge 13 is fixedly connected to the bottom end of the screw cover 8, and the screw cover 8 is rotatably mounted on the positioning seat 9 through the sliding edge 13. The screw rod 7 and the screw cover 8 are threadedly connected, and a disinfectant for applying medicine and disinfecting is also included. Poisonous cotton 16, a placement groove 17 is provided inside the hemostatic head 4, a plurality of evenly distributed leakage holes 14 are provided on the hemostatic head 4, the disinfectant cotton 16 is placed in the groove 17, a through groove 10 extending from the head end to the tail end is provided on the screw 7, the bottom end of the screw 7 is connected and fixed with a connecting plate 5, the hemostatic head 4 is mounted on the connecting plate 5, the connecting plate 5 is provided with a connecting port 18 connected to the through groove 10, the disinfectant cotton 16 is located directly below the connecting plate 5, the connecting plate 5 is located below the main belt 1, and the main belt 1 is provided with a through hole 12 for the screw 7 to pass through. The thickness of one side of the leakage hole 14 opened by the hemostatic head 4 does not exceed 2 mm, and it is in close contact with the disinfection cotton 16. After the main body belt 1 is fixed on the patient's arm or forearm through the elastic belt 2, the hemostatic head 4 is aimed at the patient's wound, and then the screw cover 8 is turned clockwise to push the hemostatic head 4 downward, and then squeezed on the patient's wound to perform compression hemostasis. When applying medicine, a syringe is used to inject from the through groove 10 at the top of the screw 7. The medicine will flow along the through groove 10 to the disinfection cotton 16. The disinfection cotton 16 absorbs a part of it, and the other part will flow from the leakage hole 14 to the patient's wound, thereby performing disinfection or applying medicine. The setting of the disinfection cotton 16 can prevent more medicine from flushing the wound in an instant, causing discomfort to the patient, and the absorption function of the disinfection cotton 16 can also help to slow down the volatilization of the medicine, so as to keep the wound disinfected or medicated for a long time.

As shown in Figures 4 and 5, in this embodiment, the lower end of the connecting plate 5 is provided with an embedding opening 15, and the hemostatic head 4 is installed in the embedding opening 15. During processing and production, the sterilized cotton 16 is first placed in the hemostatic head 4, and then glue is brushed on the embedding opening 15, and then the hemostatic head 4 can be bonded and fixed, which is convenient for production and processing.

As shown in FIG. 1 , in this embodiment, the two elastic bands 2 are both provided with Velcro 3 that adhere to each other, and the two elastic bands 2 are both made of cloth, and the cloth material is highly soft, which can increase the comfort of the patient when wearing it.

As shown in FIG1 , in this embodiment, two limit blocks 6 are fixed on the main belt 1. Both limit blocks 6 are located at the bottom of the main belt 1. The limit blocks 6 are made of silicone. The limit blocks 6 are used to be clamped on both sides of the patient's arms to facilitate the installation of the hemostatic device to be more stable.

As shown in Figures 4 and 5, in this embodiment, the disinfection cotton 16 is a sponge. The sponge has the function of absorbing water, which can facilitate the patient's wound to be disinfected or applied with anti-inflammatory drugs for a long time, accelerate the healing of the wound, and avoid the nurse from frequently applying medicine to the patient.

As shown in FIG. 1 , FIG. 4 and FIG. 5 , in this embodiment, the screw rod 7 and the connecting plate 5 are both made of transparent plastic. This arrangement can facilitate medical personnel to observe the addition of drugs and stop adding or applying drugs in time.

The technical solution provided by the utility model, by setting a through groove, a leakage hole and a disinfectant cotton, when the patient wears the hemostatic device, the medical staff can use a needle to add medicine from the through groove at the top of the screw, and the medicine will flow along the through groove to the disinfectant cotton, and then flow from the leakage hole to the patient's wound, so that the patient's wound can be disinfected or medicated in time, thereby accelerating the hemostasis or healing of the wound, and the operation is convenient and practical. By setting two limit blocks, the two limit blocks are clamped on the arms on both sides of the patient's wound, so that the installation of the hemostatic device can be more stable, and by setting a connecting plate and an embedding port, after the disinfectant cotton is embedded in the hemostatic head, the hemostatic head can be bonded and fixed by brushing glue in the embedding port, thereby facilitating the installation of the disinfectant cotton and the processing and production of the hemostatic device.

The present invention covers any substitution, modification, equivalent method and scheme made on the essence and scope of the present invention. In order to make the public have a thorough understanding of the present invention, specific details are described in detail in the following preferred embodiments of the present invention, and those skilled in the art can fully understand the present invention without the description of these details. In addition, in order to avoid unnecessary confusion about the essence of the present invention, well-known methods, processes, procedures, components and circuits are not described in detail.

A person skilled in the art will appreciate that all or part of the steps in the above-mentioned embodiment method can be completed by instructing related hardware through a program, and the program can be stored in a computer-readable storage medium, such as ROM/RAM, a disk, an optical disk, etc.

The above is only a preferred embodiment of the present invention. It should be pointed out that for ordinary technicians in this technical field, several improvements and modifications can be made without departing from the principle of the present invention. These improvements and modifications should also be regarded as the protection scope of the present invention.

Claims (8)

1. A clinical rapid hemostasis device, characterized in that it comprises: a main body band and an elastic band for patients to wear on their wrists or arms, and a hemostasis head, a screw and a screw cover for compressing wounds to stop bleeding, a positioning seat being fixed on the main body band, a sliding groove being provided on the inner side of the positioning seat, a sliding edge being fixedly connected to the bottom end of the screw cover, the screw cover being rotatably mounted on the positioning seat via the sliding edge, the screw and the screw cover being threadedly connected, and also comprising a disinfecting cotton for applying medicine and disinfecting. 2. A clinical rapid hemostasis device according to claim 1, characterized in that a placement groove is provided inside the hemostasis head, a plurality of evenly distributed leakage holes are provided on the hemostasis head, the disinfectant cotton is placed in the placement groove, a through groove extending from the head end to the tail end is provided on the screw rod, a connecting plate is connected and fixed to the bottom end of the screw rod, the hemostasis head is mounted on the connecting plate, and a connecting port communicating with the through groove is provided on the connecting plate. 3. A clinical rapid hemostasis device according to claim 2, characterized in that the disinfection cotton is located directly below the connecting plate, the connecting plate is located below the main body belt, and the main body belt is provided with a through hole for the screw to pass through. 4. A clinical rapid hemostasis device according to claim 2, characterized in that an embedding opening is opened at the lower end of the connecting plate, and the hemostasis head is installed in the embedding opening. 5. A clinical rapid hemostasis device according to claim 1, characterized in that both of the two elastic bands are provided with Velcro tapes that adhere to each other, and both of the two elastic bands are made of cloth. 6. A clinical rapid hemostasis device according to claim 1, characterized in that two limit blocks are fixed on the main body belt, the two limit blocks are both located at the bottom of the main body belt, and the limit blocks are made of silicone. 7. A clinical rapid hemostasis device according to claim 1, characterized in that the sterile cotton is a sponge. 8. A clinical rapid hemostasis device according to claim 2, characterized in that the screw rod and the connecting plate are both made of transparent plastic.