Disclosure of Invention
The invention aims to at least solve the problems that the prior hemostatic forceps and other devices for blood occlusion need manual intervention and have larger workload. The purpose is realized by the following technical scheme:
the first aspect of the present invention provides a blood occlusion device, which includes a spiral air bag unit, an air pressure control unit, and an intelligent control unit:
the spiral air bag unit comprises a spiral air bag, a metal wire and a pressure sensor, the metal wire is spirally arranged, the spiral air bag is sleeved outside the metal wire, and the pressure sensor is arranged on the spiral air bag;
the air pressure control unit comprises an air pump which is communicated with the spiral air bag;
the intelligent control unit comprises a central processing unit, and the central processing unit is used for processing the pressure value of the pressure sensor so as to control the air pump to be opened or closed.
According to the blood blocking device, the blood blocking condition can be judged by reading the pressure value of the spiral air bag, the blood vessel is intermittently blocked by the intelligent control system, the purpose of intelligently controlling blood blocking can be achieved, and the workload is low.
In addition, the blood occlusion device according to the present invention may have the following additional technical features:
in some embodiments of the present invention, the intelligent control unit further comprises a pressure signal control module, the pressure sensor sends the pressure value to the pressure signal control module, and the pressure signal control module judges whether the blood vessel is blocked or not according to the pressure value.
In some embodiments of the present invention, the pressure sensor is electrically connected to the pressure signal control module through a data transmission line or a wireless transmission unit, and the data transmission line is used for transmitting the pressure value.
In some embodiments of the invention, the pressure sensor is disposed near one end of the air pump.
In some embodiments of the present invention, the spiral air bag is communicated with the air pump through an air duct, and the data transmission line is located in the air duct.
In some embodiments of the present invention, the air pump is provided with a connection interface communicated with the air duct, and the connection interface is a luer, a threaded interface, a leko interface, an o-shaped rubber ring or a magnetic interface.
In some embodiments of the present invention, the intelligent control unit further includes an air pump control module, and the air pump control module controls the switch of the air pump to be turned on or off after receiving the signal from the central processing unit.
In some embodiments of the present invention, the wire may be made of memory metal, platinum-tungsten alloy, platinum-iridium alloy, stainless steel, or gold-plated tungsten.
In some embodiments of the invention, the helical bladder is made of silicone rubber, polyamide, polyether block amide, polyurethane, polytetrafluoroethylene, polyethylene, polypropylene, polyvinyl chloride, polymethyl methacrylate, polyethylene terephthalate, nylon, or polycarbonate.
DETAILED DESCRIPTION OF EMBODIMENT (S) OF INVENTION
Exemplary embodiments of the present disclosure will be described in more detail below with reference to the accompanying drawings. While exemplary embodiments of the present disclosure are shown in the drawings, it should be understood that the present disclosure may be embodied in various forms and should not be limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the disclosure to those skilled in the art.
It is to be understood that the terminology used herein is for the purpose of describing particular example embodiments only, and is not intended to be limiting. As used herein, the singular forms "a", "an" and "the" may be intended to include the plural forms as well, unless the context clearly indicates otherwise. The terms "comprises," "comprising," "including," and "having" are inclusive and therefore specify the presence of stated features, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, steps, operations, elements, components, and/or groups thereof. The method steps, processes, and operations described herein are not to be construed as necessarily requiring their performance in the particular order described or illustrated, unless specifically identified as an order of performance. It should also be understood that additional or alternative steps may be used.
Although the terms first, second, third, etc. may be used herein to describe various elements, components, regions, layers and/or sections, these elements, components, regions, layers and/or sections should not be limited by these terms. These terms may be only used to distinguish one element, component, region, layer or section from another region, layer or section. Terms such as "first," "second," and other numerical terms when used herein do not imply a sequence or order unless clearly indicated by the context. Thus, a first element, component, region, layer or section discussed below could be termed a second element, component, region, layer or section without departing from the teachings of the example embodiments.
For convenience of description, spatially relative terms, such as "inner", "outer", "lower", "below", "upper", "above", and the like, may be used herein to describe one element or feature's relationship to another element or feature as illustrated in the figures. Such spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if the device in the figures is turned over, elements described as "below" or "beneath" other elements or features would then be oriented "above" or "over" the other elements or features. Thus, the example term "below … …" can include both an orientation of above and below. The device may be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted accordingly.
A first aspect of the invention proposes a blood occlusion device for occluding blood during surgery.
As shown in fig. 1 to 5, the blood occluding device in the present embodiment includes: spiral gasbag unit 1, atmosphericpressure control unit 2 and intelligent control unit 3:
the spiral air bag unit 1 comprises aspiral air bag 11, ametal wire 12 and apressure sensor 13, wherein themetal wire 12 is spirally arranged, the metal wire is sleeved outside theblood vessel 4, thespiral air bag 11 is sleeved outside themetal wire 12, thepressure sensor 13 is arranged on thespiral air bag 11 and can be arranged on the inner side of thespiral air bag 11, close to theblood vessel 4 or on the outer side of thespiral air bag 11 and used for measuring the pressure in thespiral air bag 11;
the airpressure control unit 2 comprises anair pump 21, and theair pump 21 is communicated with thespiral air bag 11;
theintelligent control unit 3 comprises acentral processing unit 31, and thecentral processing unit 31 is used for processing the pressure value of thepressure sensor 13 so as to control theair pump 21 to be turned on or off.
As shown in fig. 6, thespiral balloon 11 may have a one-turn or multi-turn spiral structure, and the cross-sectional shape of thespiral balloon 11 is elliptical, circular or rectangular. Thewire 12 is wrapped in thespiral balloon 11. In the process of forming thespiral bladder 11, thewire 12 and thespiral bladder 11 are integrally formed. Or thespiral airbag 11 can be wrapped in thespiral airbag 11 at a later stage after thespiral airbag 11 is formed. Thepressure sensor 13 can be positioned on thespiral air bag 11 through a buckling mode or a sticking mode and the like, and is attached to theblood vessel 4 when being blocked, so that the pressure measurement is directly carried out, and the measured pressure value is more accurate. The helical balloon unit 1 acts on the outer wall of thevessel 4 to achieve an occlusion of the blood, preferably thehelical balloon 11 has an inner diameter slightly larger than the diameter of thevessel 4.
As shown in figure 7, the condition of blood flow blockage can be judged by reading the pressure value of thespiral air bag 11, intermittent blockage is adopted for blood in theblood vessel 4 through the intelligent control system, thespiral air bag 11 is inflated to flatten theblood vessel 4 to block the airway of theblood vessel 4, the purpose of intelligently controlling blood blockage can be achieved, the workload is low, and the damage to organ tissues can be greatly reduced by inflating and deflating thespiral air bag 11 compared with a hemostatic forceps.
In some embodiments of the present invention, theintelligent control unit 3 further includes a pressuresignal control module 32, thepressure sensor 13 sends the pressure value to the pressuresignal control module 32, and the pressuresignal control module 32 determines whether the blood in theblood vessel 4 is blocked or not blocked according to the pressure value.
In some embodiments of the present invention, thepressure sensor 13 is electrically connected to the pressuresignal control module 32 through adata transmission line 14 or a wireless transmission unit, and thedata transmission line 14 is used for transmitting the pressure value. The wireless transmission unit and thecentral processor 31 can be positioned in thespiral air bag 11 for convenient use.
In some embodiments of the present invention, thepressure sensor 13 is disposed near one end of theair pump 21. Thepressure sensor 13 of thespiral air bag 11 is arranged at the tail end of thespiral air bag 11, which is close to theair pump 21, so that thedata transmission line 14 is at least partially arranged in thespiral air bag 11, the bending of thedata transmission line 14 is reduced, and the reliability of the device is improved.
In some embodiments of the present invention, thespiral balloon 11 is in communication with theair pump 21 via anair tube 15, and thedata transmission line 14 is located in theair tube 15.
The gas-guidingtube 15 has a certain strength, and may be made of, but not limited to, silicone rubber, polyurethane, polytetrafluoroethylene, polyethylene, polypropylene, polyvinyl chloride, polymethyl methacrylate, polyethylene terephthalate, nylon, polycarbonate, etc. When theair pump 21 inflates the balloon through theair duct 15, the balloon starts to expand to squeeze theblood vessel 4, so that blood blocking can be achieved.
In some embodiments of the present invention, theair pump 21 is provided with aconnection interface 22 communicating with theair duct 15, and theconnection interface 22 is a luer, a screw interface, a lewy interface, an o-shaped rubber ring or a magnetic interface. The end of theair duct 15 is connected with anair pump 21 through a connectinginterface 22.
In some embodiments of the present invention, theintelligent control unit 3 further includes an airpump control module 33, and the airpump control module 33 controls the switch of theair pump 21 to be turned on or off after receiving the signal from thecentral processing unit 31.
In some embodiments of the present invention, thewire 12 may be formed of a memory metal, platinum-tungsten alloy, platinum-iridium alloy, stainless steel, or gold-plated tungsten.
Thewire 12 is used to maintain a helical shape so that thehelical balloon 11 is wrapped around theblood vessel 4, and thus has a certain stiffness and also requires a certain elasticity. Thus, shape memory metals, platinum-tungsten alloys, platinum-iridium alloys, stainless steel, gold-plated tungsten, and the like may be used, including but not limited to. The shape memory metal of (2) may be a nickel-titanium-based shape memory alloy, a copper-nickel-based alloy, a copper-aluminum-based alloy, a copper-zinc-based alloy, an iron-based alloy, or the like.
In some embodiments of the present invention, spiralbladder 11 is made of silicone rubber, polyamide, polyether block amide, polyurethane, polytetrafluoroethylene, polyethylene, polypropylene, polyvinyl chloride, polymethyl methacrylate, polyethylene terephthalate, nylon, or polycarbonate.
Thehelical bladder 11 may be made of one elastic material or a plurality of elastic/inelastic materials.
In another aspect of the present invention, a blood blocking method is provided, where the blood blocking method has any one of the blood blocking devices described above, and includes the following steps:
thespiral air bag 11 is sleeved outside theblood vessel 4, theintelligent control unit 3 starts theair pump 21 to inflate thespiral air bag 11, when the pressure value measured by thepressure sensor 13 reaches a preset pressure value, it is determined that the blood in theblood vessel 4 is blocked, and theintelligent control unit 3 closes theair pump 21;
after the time for the blood blockage to reach the preset pressure value reaches the preset time, theintelligent control unit 3 closes theair pump 21 to deflate thespiral air bag 11.
In some embodiments of the invention, when theair pump 21 inflates the balloon, the balloon begins to expand, compressing theblood vessel 4, and thus, the blood occlusion may be achieved.
As an implementation mode, theintelligent control unit 3 controls theair pump 21, and theair pump 21 inflates thespiral air bag 11 to block blood. Thepressure sensor 13 transmits the pressure value in real time, and when the pressure reaches a preset value, the blood is confirmed to be blocked, and theair pump 21 stops inflating. After the pressure is kept for a certain time (for example, 15 to 20 minutes), theintelligent control unit 3 controls theair pump 21 to deflate, and after the blood is kept not blocked for a certain time (for 5 to 10 minutes), the blood is blocked again. The above steps are repeated to achieve the effect of intermittent blood blocking until the operation is completely finished. Theintelligent control unit 3 carries out programmed setting, and carries out intermittent blocking on blood, thereby effectively reducing the necrosis of organs in the operation process.
According to the blood blocking device, theintelligent control unit 3 controls theair pump 21, theair pump 21 is started to inflate, the pressure value of blood is obtained in real time, and the blood flow condition is judged. Then, the operation of theair pump 21 is controlled to adjust the pressure of thespiral bladder 11 to a target value, and the blood is blocked. The pressure value is then maintained and the occlusion of the blood is performed for a period of time. Deflation then begins so that blood can circulate. The blood is then maintained for a period of time and the impedance of inflation is again performed. The above process is repeated until the operation is finished. The intelligent blood intermittent blocking method can ensure that the blood is completely blocked, prevent organs from being necrotic due to blood loss, reduce side effects and effectively ensure the success of the operation.
In summary, in the blood occlusion device of the present invention, the pressure value of thespiral balloon 11 is read to determine the blood occlusion condition, and the intelligent control system intermittently occludes the blood in the blood vessel, so as to achieve the purpose of intelligently controlling the blood occlusion, and reduce the workload.
The above description is only for the preferred embodiment of the present invention, but the scope of the present invention is not limited thereto, and any changes or substitutions that can be easily conceived by those skilled in the art within the technical scope of the present invention are included in the scope of the present invention. Therefore, the protection scope of the present invention shall be subject to the protection scope of the claims.