CN217592974U - Gynaecologist and obstetrician is with quick hemostasis device - Google Patents

Abstract

The utility model provides a quick hemostasis device for gynecologists. The compression assembly at least comprises a restraint band and a compression assembly, wherein the restraint band is provided with at least two compression assemblies which are arranged along the axial direction of the restraint band and can independently press a patient, and the compression assemblies are arranged in a mode that a specific part of the patient can be pressed under the condition that the restraint band restrains the patient. The utility model provides a obstetrical doctor is with quick hemostasis device need not the manual hemostasis of pressing of medical staff, can be to bleeding the position at present seamless hemostasis by compression, can carry out hemostasis by compression to specific position.

Description

Quick hemostasis device for gynecologists

Technical Field

The utility model relates to the field of medical equipment, especially, relate to a gynaecology and obstetrics doctor is with quick hemostasis device.

Background

Gynaecology and obstetrics is one of four main subjects of clinical medicine, and caesarean section operation is one of the main clinical operations of gynaecology and obstetrics. At present, a hospital generally adopts a mode of winding a bandage on the abdomen of a puerpera in caesarean section to stop bleeding, medicines are placed on the bandage to align to an incision to assist recovery, when the wound carelessly cracks and bleeds or when the wound of a patient needs to stop bleeding and change medicines, the bandage wound layer by layer needs to be unwound to apply medicines again, so that the working efficiency is reduced, and the labor intensity of medical workers is increased.

Patent publication No. CN210408525U provides a hemostatic device of gynaecology and obstetrics to when solving cesarean deliery lying-in woman's wound carelessly splits open the bleeding, need untie the bandage and medicine on again, the technical problem that wastes time and energy. This patent provides a hemostasis device of gynaecology and obstetrics, including the lumbar support area, hemostasis subassembly and two first connecting pieces, two first connecting pieces are the symmetry and set up the both ends at the lumbar support area, all be equipped with on every first connecting piece with first connecting piece grafting complex second connecting piece, through hemostasis subassembly fixed connection between two second connecting pieces, the hemostasis subassembly includes the gasbag package, the gasbag, the hose, gasbag ball and extrusion hemostasis part, gasbag package and two second connecting piece fixed connection, the gasbag sets up in the gasbag package, the gasbag ball sets up the below at the gasbag package, the both ends of hose are linked together with gasbag and gasbag ball respectively, extrusion hemostasis part and gasbag package fixed connection. This gynaecology and obstetrics's hemostasis device breaks away from two second connecting pieces and two first connecting pieces, then the lumbar support area is placed at the abdominal waist of caesarean section lying-in woman, extrude hemostasis part alignment caesarean section lying-in woman's abdominal edge of a knife afterwards, again with two second connecting pieces and two first connecting pieces interpolation, make extrusion hemostasis part inseparable with the abdominal edge of a knife laminating of caesarean section lying-in woman, extrude gasbag ball at last, the air in the gasbag ball enters into to the gasbag through the hose in, the increase is aerifyd to the gasbag, gasbag package increases thereupon, the extrusion hemostasis part with gasbag package fixed connection oppresses the abdominal edge of a knife of caesarean section lying-in woman thereupon, reach the mesh of stanching to the knife mouth.

In summary, the prior art at least has the following technical problems:

(1) Under the condition of adopting bandage to stop bleeding, the bandage wound layer by layer causes the working efficiency of medical personnel to be limited when the medical personnel apply medicine again, and also increases the labor intensity of the medical personnel;

(2) When hemostasis is performed in the obstetrics and gynecology department hemostasis device provided in the patent with publication number CN210408525U, the extrusion hemostasis part compresses the whole incision to achieve the purpose of hemostasis, and the incision length of cesarean section is long (generally about 10 cm), and for the condition that only part of bleeding points exist on the whole incision, the prior art cannot compress the bleeding part alone to stop bleeding, and the whole incision still needs to be compressed to stop bleeding.

The utility model discloses to above-mentioned technical problem, designed a gynecologist and obstetrics doctor with quick hemostasis device. The utility model is provided with a plurality of compression components which work independently on the restraint strap, wherein, the second surface of the restraint strap can be closely attached to the contact part, thereby realizing seamless compression hemostasis on the bleeding part; when the incision of the pregnant woman is healed, when only partial bleeding points exist on the whole incision, the medical staff inflate the compression assembly at the corresponding position of the bleeding points, so that the air bag in the compression assembly expands to apply pressure to the restraint strap, the bleeding part is further extruded, and the bleeding part of the incision is compressed to stop bleeding under the condition that the blood circulation of the bleeding part of the incision is not influenced. Furthermore, the utility model provides a hemostasis device still is applicable to the hemostasis by compression of rectangular form wound among other surgical operations, especially only has the condition of partial bleeding point on the rectangular form wound.

Furthermore, on the one hand, due to the differences in understanding to those skilled in the art; on the other hand, since the inventor studied a lot of documents and patents when making the present invention, but the space did not list all details and contents in detail, however, this is by no means the present invention does not possess these prior art features, but on the contrary the present invention has possessed all features of the prior art, and the applicant reserves the right to increase the related prior art in the background art.

SUMMERY OF THE UTILITY MODEL

Not enough to prior art, the utility model provides a gynaecology and obstetrical doctor is with quick hemostasis device includes about band and oppression subassembly at least, wherein, about band exists two at least edges about band axial sets up and can independently to the oppression subassembly that the patient applyed, the oppression subassembly is according to about band sets up the mode that can exert pressure to patient specific part under the condition that the patient retrained.

According to a preferred embodiment, the compression assembly comprises an air bag, an air passage and a fixing block, the first end face of the fixing block is connected with the air bag, the fixing block wraps the air passage, and the first end of the air passage is connected to the interior of the air bag.

According to a preferred embodiment, the pressing assembly is disposed on the restraining belt in an embedded manner, wherein a first end of the fixing block in the pressing assembly is nested in the restraining belt, and a second end of the fixing block protrudes from the first end face of the restraining belt to form a protrusion.

According to a preferred embodiment, the balloon is completely embedded in the restraining strip and is arranged to press the patient's area by inflating and pressing the second end face of the restraining strip in case pressure is required on the patient.

According to a preferred embodiment, the air passage is arranged in the middle of the fixed block and far away from the edge, the air passage penetrates through the fixed block, and the second end of the air passage protrudes out of the second end face of the fixed block.

According to a preferred embodiment, the compression assembly is connected to a control assembly by air tubes, the control assembly being connected to at least two air tubes simultaneously.

According to a preferred embodiment, the control assembly is connected to an air pump through a conduit, the control assembly can form an air flow channel with the trachea by controlling and communicating the conduit, and the air pump inflates/deflates the compression assembly through the air flow channel.

According to a preferred embodiment, the second end surface of the restraining strip is arranged to be able to fit closely to the patient, and the portion of the restraining strip that is in contact with the balloon is arranged to be able to deform.

According to a preferred embodiment, the restraining strip is provided with a recess for receiving the compression assembly, the shape of the recess provided by the restraining strip including at least one of a circle, an oval or a square, the shape of the recess corresponding to the shape of the compression assembly.

According to a preferred embodiment, the control assembly is provided with an air pressure monitoring module, the air pressure monitoring module is connected with the pressing assembly through the air pipe, and the air pressure monitoring module can monitor the air pressure of the air bag in the pressing assembly in real time.

The utility model provides a pair of gynecologist and obstetrics doctor is with quick hemostasis device has following one or more advantages at least:

(1) In the embodiment, the air pump is used for inflating the compression assembly in a manner that the air pump inflates the compression assembly so that the air bag in the compression assembly expands to compress the position of the patient needing to press hemostasis to achieve the effect of pressing hemostasis, and medical staff do not need to manually press hemostasis;

(2) The restraint strap of the embodiment can be encircled on the part of a patient needing to be pressed, so that the second surface of the restraint strap can be tightly attached to the contact part under the condition that medical staff use the hemostasis device of the embodiment, and seamless compression hemostasis is further realized on the bleeding part;

(3) In the embodiment, the compression assembly is arranged on the restraint strap, so that the compression assembly corresponding to the target part is inflated by medical staff under the condition that the specific part of the patient needs to be pressed, the air bag in the compression assembly expands to apply pressure to the restraint strap, the target part is further extruded, and the compression hemostasis is performed on the specific part.

Drawings

Fig. 1 is a schematic view of a preferred gynecologist-used rapid hemostasis device of the present invention;

fig. 2 is a schematic view of a preferred compression assembly of the present invention;

fig. 3 is a schematic view of a preferred compression assembly of the present invention;

fig. 4 is a three-dimensional schematic view of a preferred hemostatic device of the present invention;

FIG. 5 is a top view of a first surface of a preferred restraining strip in accordance with the invention;

figure 6 is a top view of a second surface of a preferred restraining strip in accordance with the invention.

List of reference numerals

100: the hemostatic device 110: the restraint band 120: air bag

130: air passage 140: fixing block 150: trachea

160: the control component 170: the conduit 180: air pump

190: compression assembly

Detailed Description

The following detailed description is made with reference to the accompanying drawings.

In the description of the present invention, it is to be understood that the terms "center", "longitudinal", "lateral", "length", "width", "thickness", "upper", "lower", "front", "rear", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", "clockwise", "counterclockwise", and the like indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings, and are only for convenience of description and to simplify the description, but do not indicate or imply that the device or element referred to must have a particular orientation, be constructed and operated in a particular orientation, and therefore should not be construed as limiting the present invention.

As shown in figure 1, the utility model provides a quick hemostasis device for gynecologists. The utility model provides a doctor of gynaecology and obstetrics uses quick hemostasis device includes about band 110 and oppression subassembly 190 at least. There are at least two compression assemblies 190 disposed axially along the restraining strip 110 and capable of independently applying pressure to the patient, of the restraining strip 110. The compression assembly 190 is configured to apply pressure to a particular portion of a patient while the restraining strap 110 restrains the patient.

Referring to fig. 2-3, the compression assembly 190 is comprised of the bladder 120, the air channel 130, and the mounting block 140. A first end surface of the fixing block 140 is connected to the airbag 120. The mounting block 140 wraps around the air passage 130. A first end of the air passage 130 is connected to the inside of the balloon 120. Preferably, the compression assembly 190 is disposed on the restraining strip 110 in an inset manner. Wherein the first end of the retention block 140 of the compression assembly 190 is nested within the restraining strip 110. A second end of the fixing block 140 protrudes from the first end surface of the restraint band 110 to form a protrusion. Preferably, the air passage 130 is provided at a position in the middle of the fixing block 140 away from the edge. The air passage 130 penetrates the fixing block 140. A second end of the air passage 130 protrudes beyond a second end surface of the fixing block 114. Preferably, the bladder 120 is completely embedded in the restraining strip 110. The balloon 120 is positioned to compress the patient site by inflating and compressing the second end of the restraining band 110 in the event that pressure is needed to be applied to the patient.

Preferably, compression assembly 190 is connected to control assembly 160 through air tube 150. The control module 160 is connected to at least two air tubes 150 simultaneously. Preferably, the control assembly 160 is connected to an air pump 180 via a conduit 170. The control assembly 160 can form an air flow passage with the air tube 150 by controlling the conducting catheter 170. The air pump 180 inflates/deflates the compression assembly 190 through the air flow path. Preferably, the second end of the restraining strip 110 is configured to closely conform to the patient. The portion of the second end surface of the restraining band 110 that contacts the bladder 120 is disposed so as to be deformable.

Preferably, the restraining strip 110 is provided with a recess to accommodate the compression assembly 190. The shape of the groove provided by the restraining strip 110 includes at least one of a circle, an ellipse, or a square. The shape of the groove corresponds to the shape of compression assembly 190. Preferably, the control assembly 160 is provided with a barometric pressure monitoring module. The air pressure monitoring module is connected to the compression assembly 190 through the air tube 150. The air pressure monitoring module can monitor the air pressure of the air bladder 120 in the compression assembly 190 in real time.

Preferably, the restraining strip 110 is provided with a plurality of equally spaced grooves for receiving the compression assemblies 190. The compression assemblies 190 are evenly distributed over the restraining strip 110. Preferably, the shape of the groove in which the restraining strip 110 is disposed may be square. Preferably, the shape of the fixing block 140 in the pressing assembly 190 is square. The shape of the fixing block 140 in the pressing assembly 190 is the same as the shape of the groove provided in the restraining strip 110. A portion of the anchor block 140 adjacent the first end surface of the anchor block 140 can be placed in a recess provided in the restraining strip 110. The portion of the fixing block 140 near the second end of the fixing block 140 is exposed outside the groove provided in the restraining band 110. The air bag 120 is disposed on a first end surface of the fixing block 140. The shape of the balloon 120 is at least one of square, circular and oval. Preferably, the shape of the balloon 120 may be square. Preferably, the size of the air bag 120 is smaller than that of the fixing block 140. The air passage 130 penetrates the fixing block 140. A first end of the air passage 130 passes through a first end surface of the fixing block 140. A second end of the air passage 130 passes through a second end surface of the fixing block 140. The cross-sectional shape of the air passage 130 may be at least one of square, circular, elliptical, triangular, and polygonal. Preferably, the cross-sectional shape of the air passage 130 may be circular. The first end of the air passage 130 penetrates into the inside of the balloon 120. The air passage 130 is disposed at the center of the fixing block 140.

Preferably, a plurality of compression assemblies 190 are uniformly distributed on the restraining strip 110 in an equally spaced manner. Each compression assembly 190 is independently coupled to a first end of one of the air tubes 150. Preferably, airway 130 in compression assembly 190 is connected to a first end of airway tube 150. Preferably, the second end of the air duct 130 passes through the second end surface of the fixing block 140, and then is connected to the first end of the air duct 150 at the center of the second end surface of the fixing block 140. The second ends of the plurality of air tubes 150 are simultaneously connected to the control assembly 160. Preferably, the control assembly 160 is connected to the air pump 180 via a conduit 170. The control assembly 160 enables the at least one airway tube 150 to form an airflow path with the conduit 170. Preferably, the control assembly 160 is capable of simultaneously channeling two, three or more airstreams 150 with the catheter 170. Preferably, the control assembly 160 is capable of simultaneously channeling all of the gas tubes 150 with the conduit 170.

Medical personnel can inflate compression device 190 through air flow path formed by air tube 150 and conduit 170 by controlling assembly 160 with air pump 180. Preferably, the gas passes through the gas flow path and then enters the airbag 120 through the gas passage 130. The bladder 120 is made of an elastic material. The air pressure inside the airbag 120 is increased due to the inflating operation of the air pump 180. The airbag 120 is inflated based on an increase in the internal air pressure. Preferably, the anchor block 140 is placed in a recess provided in the restraining strip 110 by means of gluing. Preferably, the first end surface of the fixing block 140 connected to the airbag 120 is not deformed in the case where the airbag 120 is inflated. The air bag 120 is expanded in a direction away from the first end surface of the fixing block 140 under the condition that the internal air pressure is increased. The balloon 120 compresses the portion of the second end of the restraining strip 110 that contacts the balloon 120 upon inflation, thereby compressing the portion of the hemostatic device 100 that contacts the patient. Preferably, the portion of the second end surface of the restraining strip 110 that contacts the bladder 120 is made of an elastic material. Preferably, the portion of the second end surface of the restraining strip 110 that contacts the bladder 120 is made of silicone.

In order to facilitate understanding, the working principle of the rapid hemostasis device for the gynecology and obstetrical doctors is explained.

The utility model provides a pair of doctor of gynaecology and obstetrics is with quick hemostasis device, under the condition that needs carry out hemostasis to the patient, medical staff will restrain the area around the position that the patient need be pressed. The second surface of the restraint strap can be tightly attached to the contact part, and then seamless compression hemostasis is realized on the bleeding part. Medical staff switches on the catheter and the trachea through the control assembly to form an airflow channel, and under the condition that the catheter and the trachea form the airflow channel, the air pump inflates the air bag in the outer air bag pressing assembly, so that the air bag in the pressing assembly expands to apply pressure to the second surface of the restraint belt, a target part is further extruded, and pressing of the specific part is achieved. The utility model provides a doctor of gynaecology and obstetrics is with device that stanchs fast need not that medical staff is manual to be pressed and stanchs, can realize seamless hemostasis by compression to the position of bleeding, can stanch by compression to the specific site.

It should be noted that the above-mentioned embodiments are exemplary, and that those skilled in the art, having benefit of the present disclosure, may devise various arrangements that are within the scope of the present disclosure and that fall within the scope of the invention. It should be understood by those skilled in the art that the present specification and figures are illustrative only and are not intended to be limiting on the claims. The scope of the invention is defined by the claims and their equivalents.

Claims (8)

1. A rapid hemostatic device for gynecologists, characterized in that, at least comprises a restraint band (110) and a compression component (190), wherein,

at least two compression assemblies (190) are arranged along the axial direction of the restraint strap (110) and can independently pressurize the patient,

the pressing component (190) is arranged in a mode that a specific part of a patient can be pressed under the condition that the restraint strap (110) restrains the patient; the pressing component (190) consists of an air bag (120), an air passage (130) and a fixing block (140),

the first end surface of the fixing block (140) is connected with the air bag (120), the fixing block (140) wraps the air passage (130), and the first end of the air passage (130) is connected to the inside of the air bag (120); the size of the air bag (120) is smaller than that of the fixing block (140);

the balloon (120) is completely embedded in the restraining strip (110), and the balloon (120) is arranged to press the patient part by expanding and pressing the second end face of the restraining strip (110) in case of pressing the patient.

2. Hemostatic device according to claim 1, wherein the compression assembly (190) is arranged in an embedded manner on the restraining strip (110), wherein,

the first end of the fixing block (140) in the pressing assembly (190) is nested in the restraint strap (110), and the second end of the fixing block (140) protrudes out of the first end face of the restraint strap (110) to form a protrusion.

3. The hemostatic device according to claim 2, wherein the air passage (130) is disposed in the middle of the fixing block (140) away from the edge, the air passage (130) penetrates the fixing block (140), and the second end of the air passage (130) protrudes from the second end face of the fixing block (140).

4. Hemostatic device according to claim 3, wherein the compression assembly (190) is connected to a control assembly (160) via a trachea (150), the control assembly (160) being connected to at least two of the tracheas (150) simultaneously.

5. Hemostatic device according to claim 4, wherein the control unit (160) is connected to an air pump (180) via a catheter (170), wherein the control unit (160) is capable of forming an air flow path with the trachea (150) by controlling the catheter (170), and wherein the air pump (180) inflates/deflates the compression unit (190) via the air flow path.

6. Hemostatic device according to claim 5, wherein the second end of the restraining strip (110) is arranged to be able to fit closely to the patient and wherein the part of the restraining strip (110) that is in contact with the balloon (120) is arranged to be able to deform.

7. The hemostatic device according to claim 6, wherein the restraining strip (110) is provided with a groove for receiving the compression assembly (190), the shape of the groove of the restraining strip (110) comprises at least one of a circle, an ellipse, or a square, the shape of the groove corresponding to the shape of the compression assembly (190).

8. Hemostatic device according to claim 7, wherein the control assembly (160) is provided with a gas pressure monitoring module connected to the compression assembly (190) via the gas tube (150), the gas pressure monitoring module being capable of monitoring the gas pressure of the balloon (120) in the compression assembly (190) in real time.

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