A detection device for medical pipe blocking device
By designing a detection device for tracheotomy, the problems of inconvenient sealing of airbag sleeves and difficulty in regulating exhaust volume are solved, real-time monitoring and alarm of gas oxygen content are achieved, and patients' rehabilitation efficiency and medical staff's work efficiency are improved.
Patent Information
- Application Number
- CN202510138986.7
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-02-08
- Publication Date
- 2025-04-04
- Estimated Expiration
- Not applicable · inactive patent
AI Technical Summary
The prior art is inconvenient to seal the airbag cannula during tracheotomy, unable to adjust the discharge volume, and unable to monitor the oxygen content of the gas in real time, affecting the patient's recovery and the work efficiency of medical staff.
A detection device for medical tube plugging device is designed, including a control module, an oxygen saturation monitoring module, a data transmission module, a monitoring module and an alarm module. By connecting components, exhaust components and control components, convenient sealing and exhaust volume adjustment of the airbag sleeve is realized, and real-time monitoring and alarm is carried out through the oxygen saturation monitoring module.
It improves the convenience of sealing the airbag casing and the ability to regulate the exhaust volume during tracheotomy, realizes real-time monitoring and alarm of gas oxygen content, reduces the work intensity and nursing workload of medical staff, and promotes the rehabilitation of patients.
Smart Images

Figure CN119746263A_ABST
Abstract
Description
Technical Field
[0001] The invention relates to the technical field of medical consumables, and in particular to a detection device for a medical pipe blocking device. Background Art
[0002] Tracheotomy is to cut open the cervical trachea and insert a metal tracheal tube and a silicone tube. It is a common surgery to relieve dyspnea caused by laryngeal dyspnea, respiratory dysfunction or retention of lower respiratory tract secretions.
[0003] The balloon cannula should be removed as soon as possible after the patient's condition stabilizes, and the cannula should be blocked before removal. However, the existing technology still has some defects in the process of blocking and testing the balloon cannula:
[0004] 1. In the existing technology, when sealing the airbag sleeve, adhesive tape is mostly used to stick the adhesive tape to the end of the airbag sleeve, which makes the sealing of the airbag sleeve inconvenient;
[0005] 2. At the same time, according to the existing technology, the balloon cannula is blocked, and the discharge volume of the balloon cannula after blocking cannot be adjusted, thus affecting the process of extubation and thus affecting the patient's recovery time;
[0006] 3. The existing technology is not convenient for real-time monitoring of the oxygen content of the gas at the balloon sleeve. Medical staff usually perform irregular testing, which results in the medical staff being unable to know the patient's condition in time, affecting the patient's recovery, and causing the medical staff to have a large workload and high work intensity.
[0007] In view of the above problems, the inventor proposes a detection device for a medical tube blocking device to solve the above problems. Summary of the invention
[0008] In order to solve the above-mentioned problems, the purpose of the present invention is to provide a detection device for a medical pipe blocking device.
[0009] In order to solve the above technical problems, the present invention adopts the following technical solutions: a detection device for a medical tube blocking device, the detection device comprising a control module, an oxygen saturation monitoring module, a data transmission module, a monitoring module and an alarm module;
[0010] The oxygen saturation monitoring module is connected to the data transmission module by signal, the data transmission module is connected to the monitoring module by signal, and the monitoring module is connected to the alarm module by signal;
[0011] The monitoring module is connected to the control module by signal, and the control module is connected to the oxygen saturation monitoring module by signal;
[0012] The terminal device of the control module includes a hollow sleeve, and the terminal device of the oxygen saturation monitoring module includes an oxygen saturation monitoring probe and a signal line, wherein the oxygen saturation monitoring probe is fixedly mounted at the axial position of one end of the hollow sleeve, one end of the signal line is fixedly mounted at the signal interface end of the oxygen saturation monitoring probe, and the other end of the signal line extends to the outside of the hollow sleeve and is fixed on the hollow sleeve;
[0013] A connecting component is provided at one end of the hollow sleeve, an exhaust component is provided on the hollow sleeve, and a control component for controlling the exhaust size is provided between the hollow sleeve and the exhaust component.
[0014] Preferably, the connecting assembly includes an outer jacket, which is fixedly mounted on one end of the hollow sleeve, forming a connecting cavity between the inner wall of the outer jacket and the outer wall of the hollow sleeve, a first sealing ring is fixedly mounted on the inner wall of the outer jacket, and a second sealing ring is fixedly mounted on the outer wall of one end of the hollow sleeve.
[0015] Preferably, the exhaust assembly includes an isolation disk, which is fixedly mounted on the inner wall of a hollow sleeve, one end of the hollow sleeve is provided with a plurality of first exhaust holes distributed in a ring array, a semicircular exhaust channel is provided on the isolation disk, and the other end of the hollow sleeve is provided with a plurality of second exhaust holes distributed in a ring array.
[0016] Preferably, a semicircular disk is rotatably provided on one side of the isolation disk, and the size of the semicircular disk is larger than the size of the semicircular exhaust channel.
[0017] Preferably, the control component includes a rotating shaft, one end of the rotating shaft is fixedly connected to the axial center position of the semi-circular disk, the other end of the rotating shaft is rotatably connected to the axial center position of the other end of the hollow sleeve, the other end of the hollow sleeve is fixedly installed with a device box, a rotating rod is rotatably installed inside the device box, one end of the rotating rod and the other end of the rotating shaft are both fixedly installed with bevel gears, and the two bevel gears are meshingly connected.
[0018] Preferably, a micro motor is fixedly provided inside the device box, and a driving output end of the micro motor is fixedly connected to the other end of the rotating rod.
[0019] Compared with the prior art, the present invention has the following beneficial effects:
[0020] 1. In the present invention, the end of the trachea in the neck is made to enter the connecting cavity through the function of the connecting assembly, and the silicone sleeve entering the connecting cavity is firmly sealed and connected with the outer jacket and the hollow sleeve through the contractility of the first sealing ring and the second sealing ring, thereby conveniently realizing the blocking of the silicone sleeve for tracheotomy, thereby effectively improving the convenience of the blocking of the silicone sleeve for tracheotomy;
[0021] 2. In the present invention, the overlap degree between the semicircular disk and the semicircular exhaust channel is controlled by the cooperation of the exhaust component and the control component, so that the hollow sleeve is in a state of full blockage, half blockage or any exhaust size, thereby conveniently realizing the adjustment of the exhaust volume of the tracheotomy silicone sleeve, thereby effectively improving the patient's recovery time;
[0022] 3. In the present invention, the oxygen content of the gas at the silicone cannula is monitored in real time through the oxygen saturation monitoring module, and the monitored data is transmitted to the monitoring module by the data transmission module. The medical staff reads the oxygen content data received by the monitoring module. If the oxygen content data is low, the alarm module sounds an alarm. When the medical staff operates the monitoring module, the control module receives the instruction from the monitoring module to control the exhaust volume of the silicone cannula on the patient's neck, thereby conveniently realizing the real-time monitoring of the oxygen content of the gas at the silicone cannula on the patient's neck, which makes it convenient for the medical staff to know the patient's respiratory condition in time, which is beneficial to the patient's recovery and reduces the nursing workload and work intensity of the medical staff. BRIEF DESCRIPTION OF THE DRAWINGS
[0023] In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings required for use in the embodiments or the description of the prior art will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the present invention. For ordinary technicians in this field, other drawings can be obtained based on these drawings without paying creative work.
[0024] Figure 1 The present invention is a schematic diagram of the composition of a detection device for a medical pipe blocking device.
[0025] Figure 2 It is a schematic structural diagram of the hollow sleeve of the present invention.
[0026] Figure 3 Another structural schematic diagram of the hollow sleeve of the present invention.
[0027] Figure 4 It is a schematic diagram of the separation structure of the first sealing ring, the second sealing ring and the outer jacket of the present invention.
[0028] Figure 5 It is a schematic diagram of the cutaway structure of the hollow sleeve of the present invention.
[0029] Figure 6 It is a schematic diagram of the cutaway structure of the hollow sleeve and the device box of the present invention.
[0030] Figure 7 It is a schematic diagram of the separation structure of the semi-circular disk and the isolation disk of the present invention.
[0031] In the figure: 100, control module; 200, oxygen saturation monitoring module; 300, data transmission module; 400, monitoring module; 500, alarm module; 600, bed recording module; 700, data recording module; 1, hollow sleeve; 11, U-shaped pull ring; 12, oxygen saturation monitoring probe; 13, signal line; 2, connecting assembly; 21, outer jacket; 22, connecting cavity; 23, first sealing ring; 24, second sealing ring; 3, exhaust assembly; 31, isolation disk; 32, first exhaust hole; 33, semicircular exhaust channel; 34, second exhaust hole; 35, semicircular disk; 36, sealing pad; 37, semicircular slider; 38, circular slide; 4, control assembly; 41, rotating shaft; 42, equipment box; 43, rotating rod; 44, bevel gear; 45, micro motor; 46, fixing bracket. DETAILED DESCRIPTION
[0032] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.
[0033] Example: Figure 1-7 As shown, the present invention provides a detection device for a medical tube blocking device, the detection device includes a control module 100, an oxygen saturation monitoring module 200, a data transmission module 300, a monitoring module 400 and an alarm module 500;
[0034] The oxygen saturation monitoring module 200 is connected to the data transmission module 300 by signal, the data transmission module 300 is connected to the monitoring module 400 by signal, the monitoring module 400 is connected to the alarm module 500 by signal, the monitoring module 400 is connected to the control module 100 by signal, the control module 100 is connected to the oxygen saturation monitoring module 200 by signal, the oxygen saturation monitoring module 200 can monitor the oxygen content of the gas at the silicone cannula (the silicone cannula is a silicone tube placed in the tracheotomy of the patient's neck trachea to relieve the patient's symptoms such as dyspnea and suffocation), the monitored data is transmitted to the monitoring module 400 by the data transmission module 300, and the medical staff reads the oxygen content data received by the monitoring module 400. If the oxygen content data is low, the alarm module 500 sounds an alarm, and when the medical staff operates the monitoring module 400, the control module 100 receives the instruction from the monitoring module 400 to control the exhaust volume of the silicone cannula in the patient's neck;
[0035] The terminal device of the control module 100 includes a hollow sleeve 1, and the terminal device of the oxygen saturation monitoring module 200 includes an oxygen saturation monitoring probe 12 and a signal line 13. The oxygen saturation monitoring probe 12 is provided to read the oxygen content of the gas at the silicone sleeve of the patient's neck. The oxygen saturation monitoring probe 12 is fixedly installed at the axial position of one end of the hollow sleeve 1, and one end of the signal line 13 is fixedly installed at the signal interface end of the oxygen saturation monitoring probe 12, and the other end of the signal line 13 extends to the outside of the hollow sleeve 1 and is fixed on the hollow sleeve 1;
[0036] A U-shaped pull ring 11 is fixedly installed at the other end of the hollow sleeve 1. The U-shaped pull ring 11 is provided to facilitate the operator to pull the hollow sleeve 1 away from the end of the silicone sleeve on the patient's neck;
[0037] A connecting component 2 is provided at one end of the hollow sleeve 1, an exhaust component 3 is provided on the hollow sleeve 1, and a control component 4 for controlling the exhaust size is provided between the hollow sleeve 1 and the exhaust component 3. By arranging the connecting component 2, the exhaust component 3 and the control component 4, the connecting component 2 can facilitate medical staff to fix the hollow sleeve 1 on the end of the patient's silicone sleeve, and at the same time facilitate medical staff to remove the hollow sleeve 1 from the end of the silicone sleeve, thereby improving convenience. The exhaust component 3 has a variety of exhaust volumes, which are controlled by the control component 4, so that the exhaust of the silicone sleeve is divided into full blockage, half blockage and exhaust of any size.
[0038] The detection device also includes a bed recording module 600 and a data recording module 700. The bed recording module 600 and the data recording module 700 are connected to the control module 100 by signal. The bed recording module 600 can record the bed signal of the department ward for medical staff to know, and the data recording module 700 can record the patient's oxygen saturation data.
[0039] The connecting component 2 includes an outer jacket 21, which is fixedly installed at one end of the hollow sleeve 1. A connecting cavity 22 is formed between the inner wall of the outer jacket 21 and the outer wall of the hollow sleeve 1. A first sealing ring 23 is fixedly installed on the inner wall of the outer jacket 21, and a second sealing ring 24 is fixedly installed on the outer wall of one end of the hollow sleeve 1. By arranging the outer jacket 21 at the end of the hollow sleeve 1, and arranging the connecting cavity 22, the first sealing ring 23 and the second sealing ring 24, when the end of the silicone sleeve is inserted into the interior of the connecting cavity 22, the first sealing ring 23 and the second sealing ring 24 are made contractible, so that the silicone sleeve entering the connecting cavity 22 is firmly sealed and connected with the outer jacket 21 and the hollow sleeve 1. By pulling the U-shaped pull ring 11 in the reverse direction, the hollow sleeve 1, the outer jacket 21 and the silicone sleeve can be separated, and the operation is convenient.
[0040] The exhaust assembly 3 includes an isolation disk 31, which is fixedly mounted on the inner wall of the hollow sleeve 1. One end of the hollow sleeve 1 is provided with a plurality of first exhaust holes 32 distributed in a ring array, and the isolation disk 31 is provided with a semicircular exhaust channel 33. The other end of the hollow sleeve 1 is provided with a plurality of second exhaust holes 34 distributed in a ring array. By arranging the first exhaust holes 32 and the second exhaust holes 34 on the hollow sleeve 1, when the patient breathes, the breathed gas can be connected to the outside through the first exhaust holes 32 and the second exhaust holes 34. By arranging the isolation disk 31 in the hollow sleeve 1 and arranging the semicircular exhaust channel 33 on the isolation disk 31, the gas entering the hollow sleeve 1 can realize the connection between the first exhaust hole 32 and the second exhaust hole 34 from the semicircular exhaust channel 33.
[0041] A semicircular disk 35 is rotatably provided on one side of the isolation disk 31. The size of the semicircular disk 35 is larger than that of the semicircular exhaust channel 33. By setting the semicircular disk 35 slightly larger than the semicircular exhaust channel 33, when the semicircular disk 35 revolves around the axis of the isolation disk 31 as the center of the circle, the amount of inhaled and exhaled gas can be controlled. When the semicircular disk 35 completely overlaps with the semicircular exhaust channel 33, it is a full blocking mode, and the cervical trachea cannot inhale or exhale gas, and the patient breathes through the mouth instead.
[0042] A sealing gasket 36 is fixedly provided on one side of the semi-circular disk 35, and one side of the sealing gasket 36 is in movable contact with one side of the isolation disk 31. By providing the sealing gasket 36, the sealing gasket 36 can improve the sealing between the semi-circular disk 35 and the isolation disk 31 to prevent gas from flowing in or overflowing.
[0043] A semicircular slider 37 is fixedly installed on one side of the semicircular disk 35, and a circular groove 38 is opened on one side of the isolation disk 31. The semicircular slider 37 and the inner wall of the circular groove 38 are slidably connected. By setting the semicircular slider 37 and the circular groove 38, the semicircular slider 37 can slide circumferentially in the circular groove 38, thereby ensuring the stability of the semicircular disk 35 during the circular rotation process.
[0044] The control component 4 includes a rotating shaft 41, one end of the rotating shaft 41 is fixedly connected to the axis center position of the semi-circular disk 35, and the other end of the rotating shaft 41 is rotatably connected to the axis center position of the other end of the hollow sleeve 1. By driving the rotating shaft 41 to rotate, the rotating shaft 41 can make the semi-circular disk 35 revolve in a circle, thereby realizing the control of the size of gas intake and discharge. A device box 42 is fixedly installed on the other end of the hollow sleeve 1, and a rotating rod 43 is rotatably installed inside the device box 42. One end of the rotating rod 43 and the other end of the rotating shaft 41 are fixedly installed with a bevel gear 44, and the two bevel gears 44 are meshingly connected. By driving the rotating rod 43 to rotate, the rotating rod 43 can rotate the rotating shaft 41 through the two bevel gears 44.
[0045] A micro motor 45 is fixedly installed inside the device box 42. The driving output end of the micro motor 45 is fixedly connected to the other end of the rotating rod 43. By turning on the micro motor 45, the driving shaft of the micro motor 45 can rotate the rotating rod 43. A fixing frame 46 is fixedly installed on the fixed end of the micro motor 45. The fixing frame 46 is fixedly installed on the top wall of the device box 42. By setting the fixing frame 46, the fixing frame 46 can support and fix the micro motor 45, thereby improving the stability of the micro motor 45.
[0046] Working principle: When the patient's neck trachea needs to be blocked, the medical staff first holds the U-shaped pull ring 11, aligns the outer jacket 21 with the neck trachea, and allows the end of the neck trachea to enter the connecting cavity 22. At this time, with the contractibility of the first sealing ring 23 and the second sealing ring 24, the silicone sleeve entering the connecting cavity 22 is firmly sealed and connected with the outer jacket 21 and the hollow sleeve 1;
[0047] After connection, the oxygen saturation monitoring probe 12 reads the oxygen content of the gas inhaled and exhaled at the silicone sleeve of the patient's neck;
[0048] If the oxygen content is high, the medical staff starts the micro motor 45, the driving shaft of the micro motor 45 can rotate the rotating rod 43, the rotating rod 43 can rotate the rotating shaft 41 through two bevel gears 44, and the rotating shaft 41 can make the semicircular disk 35 revolve in a circle on the isolation disk 31. At this time, the semicircular disk 35 gradually overlaps with the semicircular exhaust channel 33. By controlling the overlap degree of the semicircular disk 35 and the semicircular exhaust channel 33, the size of the gas inhaled or exhaled through the hollow sleeve 1 is controlled;
[0049] If the oxygen content is low, the drive shaft of the micromotor 45 rotates in the opposite direction, so that the semicircular disk 35 gradually staggers with the semicircular exhaust channel 33, and the semicircular exhaust channel 33 is fully opened, thereby conveniently realizing the sealing of the tracheotomy silicone sleeve and the adjustment of the exhaust volume, thereby effectively improving the convenience of the tracheotomy silicone sleeve sealing and effectively improving the patient's recovery time.
[0050] Obviously, those skilled in the art can make various changes and modifications to the present invention without departing from the spirit and scope of the present invention. Thus, if these modifications and variations of the present invention fall within the scope of the claims of the present invention and their equivalents, the present invention is also intended to include these modifications and variations.
Claims
1. A detection device for a medical pipe plugging device, characterized in that: The detection device comprises a control module (100), an oxygen saturation monitoring module (200), a data transmission module (300), a monitoring module (400) and an alarm module (500); The oxygen saturation monitoring module (200) is signal-connected to the data transmission module (300), the data transmission module (300) is signal-connected to the monitoring module (400), and the monitoring module (400) is signal-connected to the alarm module (500); The monitoring module (400) is signal-connected to the control module (100), and the control module (100) is signal-connected to the oxygen saturation monitoring module (200); The terminal device of the control module (100) comprises a hollow sleeve (1), and the terminal device of the oxygen saturation monitoring module (200) comprises an oxygen saturation monitoring probe (12) and a signal line (13), wherein the oxygen saturation monitoring probe (12) is fixedly mounted at an axial position at one end of the hollow sleeve (1), one end of the signal line (13) is fixedly mounted at a signal interface end of the oxygen saturation monitoring probe (12), and the other end of the signal line (13) extends to the outside of the hollow sleeve (1) and is fixed on the hollow sleeve (1); A U-shaped pull ring (11) is fixedly mounted on the other end of the hollow sleeve (1); A connecting component (2) is provided at one end of the hollow sleeve (1), an exhaust component (3) is provided on the hollow sleeve (1), and a control component (4) for controlling the exhaust size is provided between the hollow sleeve (1) and the exhaust component (3).
2. A detection device for a medical pipe blocking device as claimed in claim 1, characterized in that: The detection device further comprises a bed recording module (600) and a data recording module (700), wherein the bed recording module (600) and the data recording module (700) are connected to the control module (100) by signals.
3. A detection device for a medical pipe blocking device as claimed in claim 1, characterized in that: The connecting assembly (2) comprises an outer jacket (21), the outer jacket (21) being fixedly mounted on one end of the hollow sleeve (1), a connecting cavity (22) being formed between the inner wall of the outer jacket (21) and the outer wall of the hollow sleeve (1), a first sealing ring (23) being fixedly mounted on the inner wall of the outer jacket (21), and a second sealing ring (24) being fixedly mounted on the outer wall of one end of the hollow sleeve (1).
4. A detection device for a medical pipe blocking device as claimed in claim 1, characterized in that: The exhaust assembly (3) comprises an isolation disk (31), wherein the isolation disk (31) is fixedly mounted on the inner wall of a hollow sleeve (1), one end of the hollow sleeve (1) is provided with a plurality of first exhaust holes (32) distributed in a ring-shaped array, the isolation disk (31) is provided with a semicircular exhaust channel (33), and the other end of the hollow sleeve (1) is provided with a plurality of second exhaust holes (34) distributed in a ring-shaped array.
5. A detection device for a medical pipe blocking device as claimed in claim 4, characterized in that: A semicircular disk (35) is rotatably provided on one side of the isolation disk (31), and the size of the semicircular disk (35) is larger than the size of the semicircular exhaust passage (33).
6. A detection device for a medical pipe blocking device as claimed in claim 5, characterized in that: A sealing gasket (36) is fixedly provided on one side of the semicircular disk (35), and one side of the sealing gasket (36) is in movable contact with one side of the isolation disk (31).
7. A detection device for a medical pipe blocking device as claimed in claim 5, characterized in that: A semicircular slider (37) is fixedly mounted on one side of the semicircular disk (35), a circular slide groove (38) is provided on one side of the isolation disk (31), and the semicircular slider (37) and the inner wall of the circular slide groove (38) are slidably connected.
8. A detection device for a medical pipe blocking device as claimed in claim 5, characterized in that: The control assembly (4) comprises a rotating shaft (41), one end of the rotating shaft (41) is fixedly connected to the axis center position of the semi-circular disk (35), the other end of the rotating shaft (41) is rotatably connected to the axis center position of the other end of the hollow sleeve (1), the other end of the hollow sleeve (1) is fixedly mounted with a device box (42), a rotating rod (43) is rotatably mounted inside the device box (42), one end of the rotating rod (43) and the other end of the rotating shaft (41) are both fixedly mounted with bevel gears (44), and the two bevel gears (44) are meshingly connected.
9. A detection device for a medical pipe blocking device as claimed in claim 8, characterized in that: A micro motor (45) is fixedly arranged inside the device box (42), and a driving output end of the micro motor (45) is fixedly connected to the other end of the rotating rod (43).
10. A detection device for a medical pipe blocking device according to claim 9, characterized in that: A fixing frame (46) is fixedly mounted on the fixed end of the micro motor (45), and the fixing frame (46) is fixedly mounted on the top wall of the device box (42).