Postoperative hemostasis nursing device for thoracic surgery rehabilitation
The chest surgery post-operative care device stabilizes wound pressure and reduces pain and bleeding by adapting to respiratory movements, enhancing healing and infection prevention through a pliable pad with a pressure-adjusting mechanism and cooling system.
Patent Information
- Application Number
- CN202510735071.4
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-06-04
- Publication Date
- 2025-07-15
AI Technical Summary
The existing post-thoracic hemostasis care device for thoracic surgery caused by the pressure changes caused by the patient's thoracic cavity during breathing may aggravate the pain and increase the risk of bleeding, affecting the healing of the blade.
The combination of care box, plastic pad, pressure cylinder, tension detection mechanism, pressure regulating unit and liquid supply unit is adopted to automatically adjust the binding force and compression force, and cooperate with the disinfection unit and refrigeration components to achieve dynamic adjustment and continuous disinfection and bleeding.
Effectively reduces patients' pain, prevents postoperative bleeding, promotes knife healing, reduces the risk of infection, and improves the stability and efficiency of hemostasis care.
Smart Images

Figure CN120304905A_ABST
Abstract
Description
Technical Field
[0001] The invention belongs to the technical field of medical instruments, and in particular relates to a postoperative hemostasis nursing device for rehabilitation of thoracic surgery. Background Art
[0002] Thoracic surgery involves many vascular-rich organs and tissues in the chest cavity, such as the heart and lungs. The surgery is traumatic, vascular damage is difficult to avoid, and bleeding is easy to occur after the operation. Therefore, special hemostatic care is generally required after thoracic surgery to prevent bleeding from the wound, help the incision heal, and promote patient recovery.
[0003] At present, postoperative hemostasis care for thoracic surgery generally uses a bandage to tie a tourniquet, dressing, etc. to the surgical incision. The bandage can be used to apply a certain pressure to the incision with the tourniquet, etc., and the compression hemostasis method promotes the healing of the incision and reduces the possibility of bleeding from the incision. For example, a postoperative hemostasis care device for thoracic surgery rehabilitation is disclosed in patent announcement number CN211460369U;
[0004] The incision during thoracic surgery is close to the chest cavity. The rise and fall of the chest cavity during breathing will affect the incision. The chest cavity expands during inhalation, and the pressure between the wound and the binding increases accordingly. This will not only aggravate the patient's pain. If the pressure exceeds the tolerance range, it may also cause the wound that has just stopped bleeding to bleed again. This will undoubtedly hinder the healing of the incision, increase the risk of infection, and prolong the recovery period. Summary of the invention
[0005] The purpose of the present invention is to provide a postoperative hemostasis nursing device for thoracic surgery rehabilitation in view of the above problems.
[0006] To achieve the above object, the present invention adopts the following technical scheme: a postoperative hemostasis nursing device for thoracic surgery rehabilitation, comprising a nursing box and a plastic pad arranged on one side of the nursing box, a controller is installed on the side wall of the nursing box, a detachable gauze pad is installed on the bottom of the plastic pad, and further comprising:
[0007] A pressure cylinder is fixedly inserted into the side wall of one side of the plastic cushion block, a movable piston is slidably arranged inside the pressure cylinder, and a supporting spring is fixedly arranged between the movable piston and the inner wall of the pressure cylinder;
[0008] A connecting block is arranged on one side of the pressure cylinder, and a tension detection mechanism is installed together with the moving piston, a side wall of the plastic cushion away from the connecting block is fixedly connected with a binding strap, a locking assembly is installed on the connecting block, and the binding strap is connected to the connecting block through the locking assembly;
[0009] A pressure regulating unit is installed inside the nursing box and is connected to the inside of the pressure cylinder. The controller controls the pressure regulating unit to work according to the electrical signal fed back by the tension detection mechanism.
[0010] The pressing groove is opened at the bottom of the plastic cushion block, and an elastic sealing film is installed inside the pressing groove. The nursing box is equipped with a liquid supply unit, and the liquid supply unit is communicated with the inside of the pressing groove;
[0011] The disinfection unit is installed at the bottom of the plastic cushion block, and the disinfection unit is communicated with the liquid supply unit.
[0012] Preferably, the tensile force detection mechanism includes an installation groove opened on the side wall of the connecting block, and a tensile force detector is fixedly installed inside the installation groove. A fixed block is installed at the detection end of the tensile force detector. A group of pull ropes are fixedly arranged between the side wall of the fixed block and the moving piston, and each pull rope is slidably connected to the end of the pressure cylinder. The tensile force detector is electrically connected to the controller.
[0013] Preferably, the locking assembly includes an adjustment channel opened inside the connecting block. One end of the strap close to the connecting block passes through the adjustment channel. A pressing block is slidably connected to the side wall of the adjustment channel, and an adjustment bolt is rotatably connected to the side wall of the pressing block. The adjustment bolt is threadedly connected to the side wall of the connecting block.
[0014] Preferably, the pressure regulating unit includes a hollow column fixedly installed inside the nursing box, and an electromagnetic push rod is fixedly installed inside the hollow column. The telescopic end of the electromagnetic push rod is fixedly connected to a pressure regulating piston, and the pressure regulating piston is slidably arranged inside the hollow column. One end of the hollow column far from the electromagnetic push rod is fixedly communicated with a pressure regulating hose. One side of the top of the plastic cushion block is fixedly connected to a hollow block, and the pressure regulating hose is communicated with the hollow block. A liquid injection pipe is fixedly inserted at the bottom of the pressure regulating hose, and the liquid injection pipe is communicated with the inside of the pressure cylinder. Hydraulic oil is filled on the side of the pressure regulating piston far from the electromagnetic push rod inside the hollow column. Elastic sealing sleeves are sleeved on the outer sides of the pull ropes, and each elastic sealing sleeve is arranged between the pressure regulating piston and the pressure cylinder. The electromagnetic push rod is electrically connected to the controller.
[0015] Preferably, the liquid supply unit includes a liquid storage cavity and an installation cavity arranged inside the nursing box. The controller and the hollow column are both arranged inside the installation cavity. The inside of the liquid storage cavity is filled with disinfected alcohol. A peristaltic pump is fixedly installed on the side wall of the nursing box, and the suction end of the peristaltic pump is communicated with the inside of the liquid storage cavity. The liquid outlet end of the peristaltic pump is fixedly communicated with an infusion tube, and the liquid outlet end of the infusion tube is fixedly communicated with a liquid inlet hose. The liquid inlet hose is communicated with the inside of the pressing groove. A reflux hose is fixedly inserted into the bottom of the pressing groove on the side far away from the liquid inlet hose. A reflux hard tube is fixedly inserted into the wall of the liquid storage cavity, and the reflux hard tube is communicated with the reflux hose. A pressure regulating valve is installed inside the reflux hard tube. A hydraulic detection probe is inserted into the end face of the plastic cushion block, and the detection end of the hydraulic detection probe is arranged inside the pressing groove. The controller controls the operation of the pressure regulating valve according to the electrical signal fed back by the hydraulic detection probe. A refrigeration component is arranged inside the liquid storage cavity.
[0016] Preferably, the disinfection unit includes a plastic frame fixedly inserted at the bottom of the plastic cushion block, and a frame-shaped groove is opened at the bottom of the plastic frame. A plurality of shunt tubes are fixedly inserted into the wall of the frame-shaped groove, and an electric control valve is installed inside each shunt tube. Each shunt tube is communicated with the inside of the pressing groove. The plastic cushion block is provided with a detection and start component, and the controller controls the operation of each electric control valve according to the electrical signal fed back by the detection and start component.
[0017] Preferably, the refrigeration component includes a semiconductor refrigeration device fixedly inserted into the side wall of the liquid storage cavity, and the refrigeration end of the semiconductor refrigeration device is arranged inside the liquid storage cavity. A heat dissipation fan is fixedly inserted into the side wall of the installation cavity. A plurality of heat dissipation holes are opened at the top of the installation cavity. The semiconductor refrigeration device and the heat dissipation fan are both electrically connected to the controller.
[0018] Preferably, the detection and start component includes a detection tube fixedly inserted into the plastic cushion block, and the detection tube is communicated with the inside of the frame-shaped groove. A humidity-sensitive element is arranged inside the detection tube. An insulating bracket corresponding to the position of the detection tube is fixedly installed on the top of the plastic cushion block, and the humidity-sensitive element is installed at the bottom of the insulating bracket. The humidity-sensitive element is electrically connected to the controller. Each electric control valve is electrically connected to the controller.
[0019] Compared with the existing technology, the advantages of a postoperative hemostasis nursing device for thoracic surgery rehabilitation are as follows:
[0020] 1. Through the mutual cooperation of the provided nursing box, plastic cushion block, controller, gauze pad, pressure cylinder, moving piston, support spring, connecting block, tensile force detection mechanism, binding strap, locking assembly and pressure regulating unit, the surgical incision after thoracic surgery can be protected by binding, and the binding tension can be automatically adjusted based on the change of the binding tension, so as to avoid the increase of the pressure on the incision caused by the expansion of the chest cavity during breathing, improve the hemostasis protection effect on the postoperative incision, and relieve the pain of the patient.
[0021] 2. Through the mutual cooperation of the provided compression groove, elastic sealing film and liquid supply unit, the postoperative incision can be compressed, and the incision can be promoted to heal by compression. By cooperating with the way of cold compress, the possibility of postoperative incision bleeding can be further reduced.
[0022] 3. Through the provided disinfection unit, the gauze pad at the postoperative incision can be automatically supplemented with disinfection alcohol, so as to avoid the weakening of the disinfection and sterilization effect on the surrounding of the incision due to the reduction of the disinfection alcohol caused by volatilization, and further improve the protection effect on the postoperative incision. Description of the Drawings
[0023] Figure 1 is a schematic structural diagram of a postoperative hemostasis nursing device for thoracic surgery rehabilitation provided by the present invention;
[0024] Figure 2 is a schematic internal structure diagram of the nursing box of a postoperative hemostasis nursing device for thoracic surgery rehabilitation provided by the present invention;
[0025] Figure 3 is a schematic internal structure diagram of the plastic cushion block of a postoperative hemostasis nursing device for thoracic surgery rehabilitation provided by the present invention;
[0026] Figure 4 is a postoperative hemostasis nursing device for thoracic surgery rehabilitation provided by the present invention Figure 3 The enlarged structural view of part A in;
[0027] Figure 5 is a postoperative hemostasis nursing device for thoracic surgery rehabilitation provided by the present invention Figure 3 The enlarged structural view of part B in.
[0028] In the figure: 1 nursing box, 2 plastic cushion blocks, 3 controller, 4 gauze pad, 5 pressure cylinder, 6 moving piston, 7 support spring, 8 connecting block, 9 tension detection mechanism, 91 installation groove, 92 tension detector, 93 fixed block, 94 pull rope, 10 strap, 11 locking assembly, 111 adjustment channel, 112 pressing block, 113 adjustment bolt, 12 pressure regulating unit, 121 hollow column, 122 electromagnetic push rod, 123 pressure regulating piston, 124 pressure regulating hose, 125 hollow block, 126 liquid injection pipe, 127 hydraulic oil, 128 elastic sealing sleeve, 13 pressing groove, 14 elastic sealing film, 15 liquid supply unit, 151 liquid storage cavity, 152 installation cavity, 153 peristaltic pump, 154 infusion pipe, 155 liquid inlet hose, 156 return hose, 157 return rigid pipe, 158 pressure regulating valve, 159 hydraulic detection probe, 16 disinfection unit, 161 plastic frame, 162 frame-shaped groove, 163 shunt pipe, 164 electric control valve, 17 refrigeration assembly, 171 semiconductor refrigeration device, 172 cooling fan, 173 heat dissipation holes, 18 detection start assembly, 181 detection pipe, 182 humidity-sensitive element, 183 insulating bracket. Specific implementation mode
[0029] Next, the technical solutions in the embodiments of the present invention will be clearly and completely described in conjunction with the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only a part of the embodiments of the present invention, rather than all the embodiments.
[0030] As Figures 1 - 5 shown, a postoperative hemostasis nursing device for thoracic surgery rehabilitation includes a nursing box 1 and a plastic cushion block 2 arranged on one side of the nursing box 1. A controller 3 is installed on the side wall of the nursing box 1, and a detachable gauze pad 4 is installed at the bottom of the plastic cushion block 2. It further includes: a pressure cylinder 5, which is fixedly inserted into the side wall of one side of the plastic cushion block 2. A moving piston 6 is slidably arranged inside the pressure cylinder 5, and a support spring 7 is fixedly arranged between the moving piston 6 and the inner wall of the pressure cylinder 5. A connecting block 8 is arranged on one side of the pressure cylinder 5, and a tension detection mechanism 9 is jointly installed on the connecting block 8 and the moving piston 6. The tension detection mechanism 9 includes an installation groove 91 opened on the side wall of the connecting block 8, and a tension detector 92 is fixedly installed inside the installation groove 91. A fixed block 93 is installed at the detection end of the tension detector 92. A group of pull ropes 94 are fixedly arranged between the side wall of the fixed block 93 and the moving piston 6, and each pull rope 94 is slidably connected to the end of the pressure cylinder 5. The tension detector 92 is electrically connected to the controller 3. The tension detector 92 can convert the tension into an electrical signal and feedback the electrical signal to the controller 3 in time when the tension exceeds or is lower than the set threshold.
[0031] A side wall of the plastic spacer 2 away from the connecting block 8 is fixedly connected with a strap 10. The connecting block 8 is provided with a locking assembly 11, and the strap 10 is connected to the connecting block 8 through the locking assembly 11. The locking assembly 11 includes an adjustment channel 111 opened inside the connecting block 8. One end of the strap 10 close to the connecting block 8 passes through the adjustment channel 111. A pressing block 112 is slidably connected to the side wall of the adjustment channel 111, and an adjustment bolt 113 is rotatably connected to the side wall of the pressing block 112. The adjustment bolt 113 is threadedly connected to the side wall of the connecting block 8.
[0032] The pressure regulating unit 12 is installed inside the nursing box 1 and is communicated with the inside of the pressure cylinder 5. The controller 3 controls the operation of the pressure regulating unit 12 according to the electrical signal fed back by the tension detection mechanism 9. The pressure regulating unit 12 includes a hollow column 121 fixedly installed inside the nursing box 1, and an electromagnetic push rod 122 is fixedly installed inside the hollow column 121. The telescopic end of the electromagnetic push rod 122 is fixedly connected with a pressure regulating piston 123, and the pressure regulating piston 123 is slidably arranged inside the hollow column 121. One end of the hollow column 121 away from the electromagnetic push rod 122 is fixedly communicated with a pressure regulating hose 124. One side of the top of the plastic spacer 2 is fixedly connected with a hollow block 125, and the pressure regulating hose 124 is communicated with the hollow block 125. The bottom of the pressure regulating hose 124 is fixedly inserted with a liquid injection pipe 126, and the liquid injection pipe 126 is communicated with the inside of the pressure cylinder 5. Hydraulic oil 127 is filled on the side of the pressure regulating piston 123 away from the electromagnetic push rod 122 inside the hollow column 121. Elastic sealing sleeves 128 are sleeved on the outer sides of the respective pull ropes 94, and each elastic sealing sleeve 128 is arranged between the pressure regulating piston 123 and the pressure cylinder 5. The electromagnetic push rod 122 is electrically connected to the controller 3. The elastic sealing sleeve 128 can prevent the hydraulic oil 127 from leaking through the connection between the pull rope 94 and the pressure cylinder 5.
[0033] The pressing groove 13 is formed in the bottom of the plastic cushion block 2, and an elastic sealing film 14 is installed inside the pressing groove 13. The nursing box 1 is equipped with a liquid supply unit 15, and the liquid supply unit 15 is communicated with the inside of the pressing groove 13. The liquid supply unit 15 includes a liquid storage cavity 151 and an installation cavity 152 arranged inside the nursing box 1. The controller 3 and the hollow column 121 are both arranged inside the installation cavity 152. The inside of the liquid storage cavity 151 is filled with disinfected alcohol. A peristaltic pump 153 is fixedly installed on the side wall of the nursing box 1, and the suction end of the peristaltic pump 153 is communicated with the inside of the liquid storage cavity 151. The liquid outlet end of the peristaltic pump 153 is fixedly communicated with an infusion tube 154, and the liquid outlet end of the infusion tube 154 is fixedly communicated with a liquid inlet flexible tube 155. The liquid inlet flexible tube 155 is communicated with the inside of the pressing groove 13. A reflux flexible tube 156 is fixedly inserted on the side of the bottom of the pressing groove 13 away from the liquid inlet flexible tube 155. A reflux rigid tube 157 is fixedly inserted on the cavity wall of the liquid storage cavity 151, and the reflux rigid tube 157 is communicated with the reflux flexible tube 156. A pressure regulating valve 158 is installed inside the reflux rigid tube 157. A hydraulic detection probe 159 is inserted into the end face of the plastic cushion block 2, and the detection end of the hydraulic detection probe 159 is arranged inside the pressing groove 13. The controller 3 controls the operation of the pressure regulating valve 158 according to the electrical signal fed back by the hydraulic detection probe 159. A refrigeration component 17 is arranged inside the liquid storage cavity 151. The hydraulic detection probe 159 can detect the liquid pressure and convert the pressure into an electrical signal and feed it back to the controller 3.
[0034] The refrigeration component 17 includes a semiconductor refrigerator 171 fixedly inserted on the side wall of the liquid storage cavity 151, and the refrigeration end of the semiconductor refrigerator 171 is arranged inside the liquid storage cavity 151. A heat dissipation fan 172 is fixedly inserted on the side wall of the installation cavity 152. A plurality of heat dissipation holes 173 are formed in the top of the installation cavity 152. The semiconductor refrigerator 171 and the heat dissipation fan 172 are both electrically connected to the controller 3. When the semiconductor refrigerator 171 works, its refrigeration end can transfer the heat of the disinfected alcohol to its heat end, so as to realize the refrigeration of the disinfected alcohol.
[0035] The disinfection unit 16 is installed on the bottom of the plastic cushion block 2, and the disinfection unit 16 is communicated with the liquid supply unit 15. The disinfection unit 16 includes a plastic frame 161 fixedly inserted on the bottom of the plastic cushion block 2, and a frame-shaped groove 162 is formed in the bottom of the plastic frame 161. A plurality of shunt tubes 163 are fixedly inserted on the groove wall of the frame-shaped groove 162, and an electric control valve 164 is installed inside each shunt tube 163. Each shunt tube 163 is communicated with the inside of the pressing groove 13. The plastic cushion block 2 is equipped with a detection and start component 18, and the controller 3 controls the operation of each electric control valve 164 according to the electrical signal fed back by the detection and start component 18. The plastic frame 161 can deform along with the plastic cushion block 2 to ensure that it can fit on the patient's body surface.
[0036] The detection starting component 18 includes a detection tube 181 fixedly inserted inside the plastic cushion block 2, and the detection tube 181 communicates with the inside of the frame-shaped groove 162. A humidity-sensitive element 182 is arranged inside the detection tube 181. An insulating bracket 183 corresponding to the position of the detection tube 181 is fixedly installed at the top of the plastic cushion block 2, and the humidity-sensitive element 182 is installed at the bottom of the insulating bracket 183. The humidity-sensitive element 182 is electrically connected to the controller 3, and each electric control valve 164 is electrically connected to the controller 3. Within a certain humidity range, the resistance of the humidity-sensitive element 182 decreases as the humidity increases.
[0037] The operating principle of the present invention is described as follows: When performing hemostasis protection on the postoperative incision of a patient, the movable end of the binding strap 10 is passed around the patient's back so that the plastic cushion block 2 is located at the thoracic incision of the patient. Then, the movable end of the binding strap 10 is passed through the adjustment channel 111. Then, the incision of the patient is disinfected and covered with a dressing. Then, the plastic cushion block 2 is placed at the incision so that the gauze pad 4 covers the dressing. Subsequently, the connecting block 8 is abutted against the side wall of the plastic cushion block 2, and the movable end of the binding strap 10 is pulled so that the binding strap 10 exerts an appropriate binding force on the patient, and the plastic cushion block 2 is stably bound to the patient's body. Then, the adjustment bolt 113 is rotated so that the pressing block 112 is stably abutted against the binding strap 10, thereby fixing the binding strap 10 and the connecting block 8. Subsequently, the medical staff sets appropriate pressing force and tension force on the controller 3 according to the patient's body type, incision size, position, etc., and then starts the controller 3;
[0038] After the controller 3 is started, it will immediately control the electromagnetic push rod 122 to work. The electromagnetic push rod 122 will push the pressure regulating piston 123 to move, so as to push the hydraulic oil 127 inside the hollow column 121 through the pressure regulating hose 124, the hollow block 125 and the liquid injection pipe 126 into the pressure cylinder 5. Under the action of the hydraulic oil 127, the moving piston 6 will move in the direction away from the connecting block 8, so as to gradually tighten the pull rope 94, so that the tension detector 92 detects the tension. When the tension value reaches the tightening force preset by the medical staff, the controller 3 controls the electromagnetic push rod 122 to maintain the current energizing current intensity. When the patient breathes, the patient inhales, and his chest will bulge. At this time, due to the body bulge, the tension on the strap 10 increases, so the tension detected by the tension detector 92 will also increase synchronously. After the tension detected by the tension detector 92 increases, the controller 3 will control the current intensity flowing into the electromagnetic push rod 122 to decrease synchronously, so that the regulating piston starts to move back. At this time, under the action of the tension, the moving piston 6 starts to move back, and the excess hydraulic oil 127 will flow back into the hollow column 121. When the moving piston 6 moves back, the pull rope 94 will move outward, so the strap 10 will drive the connecting block 8 to move in the direction away from the plastic cushion block 2, that is, when the patient inhales and the chest bulges, the strap 10 will drive the connecting block 8 to move in the direction away from the plastic cushion block 2. Cooperating with the pull rope 94, the length between the movable end of the strap 10 and the plastic cushion block 2 can be increased. Therefore, the binding force of the strap 10 on the patient is reduced, so as to balance the increase in the pressure between the incision and the plastic cushion block 2 caused by the chest bulge when the patient inhales, ensure that the binding force on the patient's incision remains stable, avoid further increasing the pain of the incision due to excessive binding pressure, and can avoid bleeding from the incision due to excessive pressure. Similarly, when the patient exhales, since the chest bulge disappears, the tension detected by the tension detector 92 decreases, so the controller 3 will control the electromagnetic push rod 122 to perform an extending action again, so that the moving piston 6 moves in the direction away from the connecting block 8 again until the tension detected by the tension detector 92 reaches the set value;
[0039] After the controller 3 is started, the controller 3 also controls the peristaltic pump 153 to work. The peristaltic pump 153 pumps out the disinfected alcohol in the liquid storage chamber 151 and transports the disinfected alcohol to the compression groove 13 through the infusion tube 154 and the liquid inlet flexible hose 155. As the disinfected alcohol in the compression groove 13 increases, the hydraulic pressure in the compression groove 13 becomes higher. At this time, the elastic sealing membrane 14 begins to expand under the action of the hydraulic pressure, so as to cooperate with the gauze pad 4 to apply pressure to the patient's incision (this pressure directly acts on the incision from the vertical direction to ensure the compression hemostasis effect on the incision). After the hydraulic detection probe 159 detects that the hydraulic pressure reaches the hydraulic value preset by the medical staff, the hydraulic detection probe 159 feeds back an electrical signal to the controller 3. At this time, the controller 3 controls the pressure regulating valve 158 to be energized and opened, so that the excess disinfected alcohol entering the compression groove 13 flows back to the liquid storage chamber 151 through the return flexible hose 156 and the return rigid tube 157. Secondly, the controller 3 also controls the semiconductor cooler 171 and the cooling fan 172 to work. When the semiconductor cooler 171 works, it can refrigerate the disinfected alcohol in the liquid storage chamber 151 (the refrigeration temperature is 15°C ± 3°C) and transfer the heat from the refrigeration end to the heating end. Under the action of the cooling fan 172, the air flow in the installation cavity 152 is discharged through the heat dissipation holes 173. When the air flow passes through the semiconductor cooler 171, it can transfer the heat at its hot end to ensure the continuous refrigeration effect of the semiconductor cooler 171. By reducing the temperature of the disinfected alcohol, the temperature at the incision can be reduced. Through the way of cold compress and compression, the healing of the incision can be promoted, the bleeding at the incision can be reduced, and the bacteria growth at the incision can be reduced to a certain extent, improving the protection effect on the incision. The controller 3 controls the semiconductor cooler 171 to work once every 1 hour, and the single working time is 15 minutes to avoid the long-term low temperature affecting blood circulation;
[0040] After the controller 3 is started, the controller 3 will connect the connection circuit with the humidity-sensitive element 182. Since there is no disinfection alcohol on the gauze pad 4 initially, the humidity at the humidity-sensitive element 182 is relatively low. At this time, the resistance of the humidity-sensitive element 182 is relatively large. Therefore, the measurement circuit of the controller 3 measures that the electrical signal intensity of the connection circuit with the humidity-sensitive element 182 is relatively low. At this time, the controller 3 will control each electromagnetic control valve 164 to be energized and opened. At this time, part of the disinfection alcohol in the pressing groove 13 will flow into the frame groove 162 of the plastic frame 161 through the shunt pipe 163, and then the disinfection alcohol is adsorbed by the gauze pad 4, so that the gauze pad 4 can adsorb the disinfection alcohol. After the gauze pad 4 adsorbs the disinfection alcohol, it can perform antibacterial disinfection around the incision. As the disinfection alcohol is discharged through the shunt pipe 163, part of the disinfection alcohol begins to volatilize under the action of its own volatile characteristics, and carries moisture away through the detection pipe 181. The humidity-sensitive element 182 in the detection pipe 181 will detect an increase in the humidity in the air (the ethanol in the disinfection alcohol is generally 75%, and the water solution is 25%. When ethanol volatilizes, it will carry moisture and escape). At this time, the resistance of the humidity-sensitive element 182 decreases due to the increase in humidity. When the humidity is higher than 65%, the measurement circuit of the controller 3 detects that the electrical signal of the connection circuit with the humidity-sensitive element 182 is higher than 10 mA. Therefore, at this time, the controller 3 will control each electromagnetic control valve 164 to be de-energized and closed. Since the gauze pad 4 adsorbs the disinfection alcohol, the humidity at the humidity-sensitive element 182 will be temporarily higher than 65% under the action of the disinfection alcohol volatilizing in the gauze pad 4. As the disinfection alcohol in the gauze pad 4 becomes less and less, the humidity at the humidity-sensitive element 182 will decrease again. When the humidity is lower than 65%, the controller 3 will control the electromagnetic control valve 164 to open again to replenish the disinfection alcohol for the gauze pad 4 to ensure that the gauze pad 4 maintains a continuous antibacterial disinfection effect around the incision.
[0041] The above are only the preferred embodiments of the present invention and are not intended to limit the present invention. Any modifications, equivalent replacements, improvements, etc. made within the spirit and principle of the present invention shall be included in the protection scope of the present invention.
Claims
1. A postoperative hemostasis nursing device for thoracic surgery rehabilitation, comprising a nursing box (1) and a plastic cushion block (2) arranged on one side of the nursing box (1), a controller (3) is installed on the side wall of the nursing box (1), and a detachable gauze pad (4) is installed at the bottom of the plastic cushion block (2), characterized in that, It further includes: A pressure cylinder (5) fixedly inserted into the side wall of one side of the plastic cushion block (2). A moving piston (6) is slidably arranged inside the pressure cylinder (5), and a support spring (7) is fixedly arranged between the moving piston (6) and the inner wall of the pressure cylinder (5); A connecting block (8) is arranged on one side of the pressure cylinder (5), and a tensile force detection mechanism (9) is jointly installed on the connecting block (8) and the moving piston (6). A strap (10) is fixedly connected to the side wall of the plastic cushion block (2) away from the connecting block (8). The connecting block (8) is equipped with a locking assembly (11), and the strap (10) is connected to the connecting block (8) through the locking assembly (11); A pressure regulating unit (12) is installed inside the nursing box (1) and is communicated with the inside of the pressure cylinder (5). The controller (3) controls the operation of the pressure regulating unit (12) according to the electrical signal fed back by the tensile force detection mechanism (9); A pressing groove (13) is opened at the bottom of the plastic cushion block (2), and an elastic sealing film (14) is installed inside the pressing groove (13). The nursing box (1) is equipped with a liquid supply unit (15), and the liquid supply unit (15) is communicated with the inside of the pressing groove (13); A disinfection unit (16) is installed at the bottom of the plastic cushion block (2), and the disinfection unit (16) is communicated with the liquid supply unit (15).
2. The postoperative hemostasis nursing device for thoracic surgery rehabilitation according to claim 1, wherein, The tensile force detection mechanism (9) includes an installation groove (91) opened on the side wall of the connecting block (8), and a tensile force detector (92) is fixedly installed inside the installation groove (91). A fixed block (93) is installed at the detection end of the tensile force detector (92). A group of pull ropes (94) are fixedly arranged between the side wall of the fixed block (93) and the moving piston (6), and each pull rope (94) is slidably connected to the end of the pressure cylinder (5). The tensile force detector (92) is electrically connected to the controller (3).
3. The postoperative hemostasis nursing device for thoracic surgery rehabilitation according to claim 1, wherein The locking assembly (11) includes an adjustment channel (111) opened inside the connecting block (8). One end of the strap (10) close to the connecting block (8) passes through the adjustment channel (111). A pressing block (112) is slidably connected to the side wall of the adjustment channel (111), and an adjustment bolt (113) is rotatably connected to the side wall of the pressing block (112). The adjustment bolt (113) is threadedly connected to the side wall of the connecting block (8).
4. The postoperative hemostasis nursing device for thoracic surgery rehabilitation according to claim 2, wherein, The pressure regulating unit (12) includes a hollow column (121) fixedly installed inside the nursing box (1), and an electromagnetic push rod (122) is fixedly installed inside the hollow column (121). The telescopic end of the electromagnetic push rod (122) is fixedly connected to a pressure regulating piston (123), and the pressure regulating piston (123) is slidably arranged inside the hollow column (121). One end of the hollow column (121) far from the electromagnetic push rod (122) is fixedly communicated with a pressure regulating hose (124). One side of the top of the plastic cushion block (2) is fixedly connected to a hollow block (125), and the pressure regulating hose (124) is communicated with the hollow block (125). The bottom of the pressure regulating hose (124) is fixedly inserted with a liquid injection pipe (126), and the liquid injection pipe (126) is communicated with the inside of the pressure cylinder (5). Hydraulic oil (127) is filled on the side of the pressure regulating piston (123) far from the electromagnetic push rod (122) inside the hollow column (121). Elastic sealing sleeves (128) are sleeved on the outer sides of the respective draw ropes (94), and the respective elastic sealing sleeves (128) are arranged between the pressure regulating piston (123) and the pressure cylinder (5). The electromagnetic push rod (122) is electrically connected to the controller (3).
5. The postoperative hemostasis nursing device for thoracic surgery rehabilitation according to claim 4, characterized in that, The liquid supply unit (15) includes a liquid storage cavity (151) and an installation cavity (152) arranged inside the nursing box (1). The controller (3) and the hollow column (121) are both arranged inside the installation cavity (152). The liquid storage cavity (151) is filled with disinfected alcohol. A peristaltic pump (153) is fixedly installed on the side wall of the nursing box (1), and the suction end of the peristaltic pump (153) is communicated with the inside of the liquid storage cavity (151). The liquid outlet end of the peristaltic pump (153) is fixedly communicated with an infusion tube (154), and the liquid outlet end of the infusion tube (154) is fixedly communicated with a liquid inlet hose (155). The liquid inlet hose (155) is communicated with the inside of the pressing groove (13). A return hose (156) is fixedly inserted on the side of the bottom of the pressing groove (13) far from the liquid inlet hose (155). A return hard tube (157) is fixedly inserted on the cavity wall of the liquid storage cavity (151), and the return hard tube (157) is communicated with the return hose (156). A pressure regulating valve (158) is installed inside the return hard tube (157). A hydraulic detection probe (159) is inserted into the end face of the plastic cushion block (2), and the detection end of the hydraulic detection probe (159) is arranged inside the pressing groove (13). The controller (3) controls the operation of the pressure regulating valve (158) according to the electrical signal fed back by the hydraulic detection probe (159). A refrigeration component (17) is arranged inside the liquid storage cavity (151).
6. The postoperative hemostasis nursing device for thoracic surgery rehabilitation according to claim 1, wherein, The disinfection unit (16) includes a plastic frame (161) fixedly inserted at the bottom of the plastic cushion block (2), and a frame-shaped groove (162) is formed in the bottom of the plastic frame (161). A plurality of shunt pipes (163) are fixedly inserted in the groove wall of the frame-shaped groove (162), and an electric control valve (164) is installed inside each shunt pipe (163). Each of the shunt pipes (163) is communicated with the inside of the pressing groove (13). The plastic cushion block (2) is provided with a detection and start-up component (18), and the controller (3) controls the operation of each electric control valve (164) according to the electrical signal fed back by the detection and start-up component (18).
7. The postoperative hemostasis nursing device for thoracic surgery rehabilitation according to claim 5, characterized in that, The refrigeration component (17) includes a semiconductor refrigeration device (171) fixedly inserted in the side wall of the liquid storage cavity (151), and the refrigeration end of the semiconductor refrigeration device (171) is arranged inside the liquid storage cavity (151). A heat dissipation fan (172) is fixedly inserted in the side wall of the installation cavity (152). A plurality of heat dissipation holes (173) are formed in the top of the installation cavity (152). The semiconductor refrigeration device (171) and the heat dissipation fan (172) are both electrically connected to the controller (3).
8. The postoperative hemostasis nursing device for thoracic surgery rehabilitation according to claim 6, wherein, The detection and start-up component (18) includes a detection pipe (181) fixedly inserted inside the plastic cushion block (2), and the detection pipe (181) is communicated with the inside of the frame-shaped groove (162). A humidity-sensitive element (182) is arranged inside the detection pipe (181). An insulating bracket (183) corresponding to the position of the detection pipe (181) is fixedly installed on the top of the plastic cushion block (2), and the humidity-sensitive element (182) is installed at the bottom of the insulating bracket (183). The humidity-sensitive element (182) is electrically connected to the controller (3), and each of the electric control valves (164) is electrically connected to the controller (3).
Citation Information
Patent Citations
Postoperative hemostatic nursing device for thoracic surgery rehabilitation
CN211460369U
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