Trachea intubation device

By designing the structure of two airbags and liquid storage chambers in the tracheal intubation device, the problem of fluid substance leakage caused by the incompatibility of the cross-sectional shape of the airbag and the tracheal tube wall is solved, and a more efficient fluid substance interception and regular cleaning effect is achieved.

CN222854389UActive Publication Date: 2025-05-13FIRST HOSPITAL AFFILIATED TO GENERAL HOSPITAL OF PLA
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Patent Information

Application Number
CN202421223747.9
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2024-05-31
Publication Date
2025-05-13
Estimated Expiration
2034-05-31

AI Technical Summary

Technical Problem

In the existing tracheal intubation device, the cross-sectional shape of the airbag and the tracheal tube wall is not perfectly adapted, resulting in the possibility of fluid substance leakage.

Method used

A tracheal intubation device was designed, using two airbags and constructing a reservoir between the two airbags to improve the interception effect of fluid substances.

Benefits of technology

By configuring the two airbags and the reservoir chamber, better fluid material interception effect is achieved, reducing the possibility of leakage, and the fluid material leaking from the airbag and the tracheal wall can be periodically removed.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model discloses a tracheal intubation device which comprises a catheter, the near end of the catheter is located outside the oral cavity of a patient and connected to oxygen supply equipment, and the far end of the catheter is used for being pushed to the far end of the trachea of the patient; the expandable part comprises a first air bag and a second air bag which are connected in series, and a connecting sleeve connected between the first air bag and the second air bag; the radial outer side of the far end of the catheter is sleeved with the first air bag, the connecting sleeve and the second air bag, and the second air bag is located on one side of the far end of the first air bag; the near end of the inflation tube is located on one side of the near end of the catheter, the far end of the inflation tube extends to the far end of the catheter along the catheter and is connected to the expandable component so as to be used for inflating the first air bag and the second air bag, and the near end of the inflation tube is connected to inflation equipment; after the first air bag and the second air bag are inflated and expanded, a liquid storage cavity is defined between the first air bag and the second air bag.
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Description

Technical Field

[0001] The utility model relates to the technical field of medical equipment, in particular to an endotracheal intubation device. Background Art

[0002] Tracheal intubation is a typical means of assisted breathing in an interventional manner. In the prior art, the device for performing tracheal intubation generally includes a catheter and an inflatable balloon attached to the outside of the distal end of the catheter. During the process of performing tracheal intubation, the distal end of the catheter is pushed through the patient's mouth and the proximal end of the trachea to a predetermined position at the distal end of the trachea. Subsequently, the balloon is inflated outside the patient's body using an inflation device so that the balloon is inflated and rests against the wall of the patient's trachea, thereby achieving positioning of the distal end of the catheter and avoiding axial and radial movement of the distal end of the catheter. Another function of the balloon is that the balloon contacts the wall of the trachea to implement a seal, thereby intercepting fluid substances upstream of the balloon (such as secretions such as sputum) from flowing downward along the trachea to the lungs.

[0003] However, there is still a possibility that fluid substances may leak from between the airbag and the wall of the trachea. The reason is that the cross-sectional shape of the airbag after being inflated cannot perfectly match the trachea. The reasons for the inability to perfectly match include: the cross-sectional shapes of the tracheas of different patients are different, while the airbags used are universal airbags with the same cross-sectional shape; the deformation stiffness of the patient's trachea in the front and rear directions is different, while the deformation stiffness of the airbag in all directions is basically the same. Utility Model Content

[0004] In view of the above technical problems existing in the prior art, an embodiment of the utility model provides an endotracheal intubation device.

[0005] In order to solve the above technical problems, the technical solution adopted in the embodiment of the utility model is:

[0006] A tracheal intubation device, comprising:

[0007] a catheter having a proximal end located outside the patient's oral cavity and connected to an oxygen supply device, and a distal end of the catheter for advancement to the distal end of the patient's trachea;

[0008] An expandable component, comprising a first airbag, a second airbag connected in series, and a connecting sleeve connected between the first airbag and the second airbag; the first airbag, the connecting sleeve, and the second airbag are all sleeved on the radial outside of the distal end of the catheter, and the second airbag is located on one side of the distal end of the first airbag;

[0009] An inflation tube, whose proximal end is located on one side of the proximal end of the catheter, and whose distal end extends along the catheter to the distal end of the catheter and is connected to the expandable component, so as to inflate the first airbag and the second airbag, and the proximal end of the inflation tube is connected to an inflation device; wherein:

[0010] After the first airbag and the second airbag are inflated, a liquid storage chamber is defined between the first airbag and the second airbag.

[0011] Preferably, the endotracheal intubation device further comprises a first suction tube;

[0012] The proximal end of the first suction tube is located on one side of the proximal end of the catheter, the proximal end of the first suction tube is connected to a suction device, and the distal end of the first suction tube extends along the catheter to the distal end of the catheter and is connected to the liquid storage chamber for suctioning fluid substances in the liquid storage chamber.

[0013] Preferably, a fluid channel is arranged in the first airbag, and the distal end of the fluid channel passes through the liquid storage cavity; the proximal end of the fluid channel is covered by the proximal end wall of the first airbag;

[0014] An openable sealing gap is formed in the area of ​​the proximal wall of the first airbag opposite to the fluid channel.

[0015] Preferably, the endotracheal intubation device further comprises a second suction tube;

[0016] The proximal end of the second suction tube is located on one side of the proximal end of the catheter, the proximal end of the second suction tube is connected to a suction device, and the distal end of the second suction tube extends along the catheter to the proximal wall of the first balloon for suctioning fluid material upstream of the first balloon.

[0017] Preferably, the middle portion of the proximal wall of the first airbag and the middle portion of the proximal wall of the second airbag are both axially retracted so that the edge of the proximal wall of the first airbag is higher than the middle portion, and the edge of the proximal wall of the second airbag is higher than the middle portion.

[0018] Preferably, the middle section of the inflation tube runs in the inner hole of the catheter, and the distal end and the distal end of the inflation tube both radially pass through the catheter; the middle sections of the first suction tube and the second suction tube are both located in the inner hole of the catheter, and the proximal end and the distal end of the first suction tube and the second suction tube both radially pass through the catheter.

[0019] Preferably, the inflation tube includes a first inflation tube and a second inflation tube; the distal end of the first inflation tube is connected to the first airbag, and the distal end of the second inflation tube is connected to the second airbag.

[0020] Preferably, the distal ends of the first inflation tube and the second inflation tube are both provided with exhaust ports.

[0021] Preferably, a switch valve is installed at the distal end of the first suction pipe and the distal end of the second suction pipe.

[0022] Preferably, the distal ends of the first inflation tube and the second inflation tube are both connected to switch valves.

[0023] Compared with the prior art, the beneficial effects of the endotracheal intubation device disclosed in the utility model are:

[0024] 1. The endotracheal intubation device provided by the utility model is configured with two air bags and a liquid storage chamber is constructed between the two air bags, so that a better interception effect of fluid substances can be achieved, thereby improving the inhibition effect of fluid substance leakage to a certain extent.

[0025] 2. The tracheal intubation device provided by the utility model can regularly remove fluid substances leaked from between the first airbag and the inner tube wall of the trachea.

[0026] The overview of various implementations or examples of the technology described in this utility model is not a comprehensive disclosure of the entire scope or all features of the disclosed technology. BRIEF DESCRIPTION OF THE DRAWINGS

[0027] In the drawings that are not necessarily drawn to scale, the same reference numerals may describe similar parts in different views. The same reference numerals with letter suffixes or different letter suffixes may represent different instances of similar parts. The accompanying drawings generally illustrate various embodiments by way of example and not limitation, and together with the specification and claims, are used to illustrate the embodiments of the utility model. When appropriate, the same reference numerals are used in all drawings to refer to the same or similar parts. Such embodiments are illustrative and are not intended to be exhaustive or exclusive embodiments of the present device or method.

[0028] Figure 1 This is a main cross-sectional view of the endotracheal intubation device provided in an embodiment of the utility model.

[0029] Figure 2 for Figure 1 AA section view.

[0030] Figure 3 This is a view of the endotracheal intubation device provided in an embodiment of the utility model in use.

[0031] Figure 4 for Figure 3 An enlarged view of part B (using the first suction tube to suck the fluid substance in the liquid storage chamber).

[0032] Figure 5 for Figure 3 An enlarged view of part B (using the second suction tube to suck the fluid substance on one side of the proximal end of the first airbag).

[0033] Reference numerals:

[0034] 10-expandable component; 11-first airbag; 111-proximal wall; 111-sealed gap; 112-fluid channel; 1121-hard lining tube; 12-second airbag; 121-proximal wall; 13-connecting sleeve; 14-liquid storage chamber; 20-catheter; 31-first inflation tube; 311-first exhaust port; 32-second inflation tube; 321-second exhaust port; 41-first suction tube; 42-second suction tube; 51-inflation device; 52-suction device; 61-first switch valve; 62-second switch valve; 63-third switch valve; 64-fourth switch valve; 100-trachea. DETAILED DESCRIPTION

[0035] Unless otherwise defined, the technical terms or scientific terms used in the present invention shall have the usual meanings understood by persons with ordinary skills in the field to which the present invention belongs. The words "first", "second" and similar words used in the present invention do not indicate any order, quantity or importance, but are only used to distinguish different components. Words such as "include" or "comprise" and the like mean that the elements or objects appearing before the word include the elements or objects listed after the word and their equivalents, without excluding other elements or objects. Words such as "connect" or "connected" and the like are not limited to physical or mechanical connections, but may include electrical connections, whether direct or indirect. "Up", "down", "left", "right" and the like are only used to indicate relative positional relationships. When the absolute position of the described object changes, the relative positional relationship may also change accordingly.

[0036] In order to keep the following description of the embodiments of the present invention clear and concise, the present invention omits detailed descriptions of known functions and known components.

[0037] like Figures 1 to 5 As shown, an embodiment of the utility model discloses an endotracheal intubation device, which includes: a catheter 20, an expandable component 10, an inflation tube, an inflation device 51, a suction tube and a suction device 52.

[0038] During the intubation process, the distal end of the catheter 20 passes through the patient's oral cavity and the proximal end of the trachea 100 in sequence and is pushed to the distal end of the trachea 100, while the proximal end of the catheter 20 is located outside the oral cavity. The proximal end of the catheter 20 is connected to an oxygen supply device, which is used to provide oxygen to the catheter 20, so that the provided oxygen is directly supplied to the patient's lungs through the catheter 20.

[0039] like Figure 3 and Figure 4 As shown, the expandable component 10 is attached to the distal end of the catheter 20. The expandable component 10 is pushed to the distal end of the trachea 100 along with the distal end of the catheter 20. After being pushed to the distal end of the trachea 100, the expandable component 10 is expanded to contact the inner tube wall of the trachea 100, thereby supporting and positioning the distal end of the catheter 20 to limit the axial and radial movement of the distal end of the catheter 20. In the present utility model, the expandable component 10 includes two airbags, that is, a first airbag 11 and a second airbag 12. The first airbag 11 and the second airbag 12 are connected in series. The first airbag 11 and the second airbag 12 are connected by a connecting sleeve 13. The first airbag 11, the connecting sleeve 13 and the second airbag 12 are all sleeved on the radial outer side of the distal end of the catheter 20 and fixed relative to the catheter 20. The first airbag 11 is located on one side of the proximal end of the second airbag 12.

[0040] The inflation tube includes a first inflation tube 31 and a second inflation tube 32; the middle tube section of the first inflation tube 31 runs in the inner hole of the catheter 20, the proximal end of the first inflation tube 31 passes through the proximal end of the catheter 20 and is located on the outside of the oral cavity, the distal end of the first inflation tube 31 passes through the outside of the catheter 20 and extends into the first airbag 11, the middle tube section of the second inflation tube 32 runs in the inner hole of the catheter 20, the proximal end of the second inflation tube 32 passes through the proximal end of the catheter 20 and is located on the outside of the oral cavity, and the distal end of the second inflation tube 32 passes through the outside of the catheter 20 and extends into the second airbag 12. The proximal ends of the first inflation tube 31 and the second inflation tube 32 are both connected to the inflation device 51, and the proximal end of the first inflation tube 31 is installed with a first switch valve 61, and the upstream of the first switch valve 61 is provided with a first exhaust port 311, and the proximal end of the second inflation tube 32 is installed with a second switch valve 62, and the upstream of the second switch valve 62 is provided with a second exhaust port 321. In this way, after the expandable component 10 is pushed to the distal end of the trachea 100, the first switch valve 61 and the second switch valve 62 are opened, and the inflation device 51 is used to synchronously inflate the first airbag 11 and the second airbag 12 through the first inflation tube 31 and the second inflation tube 32, so that the first airbag 11 and the second airbag 12 are expanded and contact the tube wall.

[0041] After the two airbags are inflated, since the two airbags are arranged in series at intervals, a chamber is formed between the two airbags and the inner tube wall of the trachea 100. In this way, if the sealing effect between the first airbag 11 and the inner tube wall of the trachea 100 is poor, resulting in an undesirable leakage of the fluid material upstream of the expandable component 10 (i.e., upstream of the first airbag 11), the chamber can collect the leaked fluid material. At the same time, the second airbag 12 performs a second sealing and interception on the fluid material, thereby improving the interception effect of the fluid material to a certain extent. In addition, the two airbags in series have better compliance with the direction of the patient's trachea 100, which is conducive to positioning the distal end of the catheter 20 and facilitating the airbag to intercept the fluid material. Since the chamber is used to collect fluid materials, it may be called a liquid storage chamber 14.

[0042] The suction tube includes a first suction tube 41 and a second suction tube 42; the main tube section of the first suction tube 41 is located in the inner hole of the catheter 20, the proximal end of the first suction tube 41 extends out of the proximal end of the catheter 20 and is located outside the oral cavity, the distal end of the first suction tube 41 extends to the position of the liquid storage chamber 14, and radially extends into the liquid storage chamber 14 to be used for sucking the fluid material in the liquid storage chamber 14, the main tube section of the second suction tube 42 is located in the inner hole of the catheter 20, the proximal end of the second suction tube 42 extends out of the proximal end of the catheter 20 and is located outside the oral cavity, the distal end of the second suction tube 42 extends to one side of the proximal end of the first airbag 11, and the end passes through the catheter 20 and faces the proximal wall 111 of the first airbag 11 for sucking the fluid material on the proximal side of the first airbag 11 (i.e., upstream of the expandable component 10). The proximal end of the first suction pipe 41 and the proximal end of the second suction pipe 42 are both connected to the suction device 52. The proximal end of the first suction pipe 41 is installed with a third switch valve 63, and the proximal end of the second suction pipe 42 is installed with a fourth switch valve 64. If the first switch valve 61 is opened, Figure 5 As shown, the suction device 52 can suck the fluid material into the liquid storage chamber 14 through the first suction pipe 41. If the second switch is turned on, as shown in FIG. Figure 4 As shown, the suction device 52 can suck the intercepted fluid material toward the proximal end of the first airbag 11 through the second suction tube 42 .

[0043] The first airbag 11 is provided with a plurality of fluid channels 112, which are arranged circumferentially, the distal end of each fluid channel 112 passes through the liquid storage chamber 14, the proximal end of the fluid channel 112 is covered by the proximal wall 111 of the first airbag 11, and a hard lining tube 1121 is provided in each fluid channel 112 to support the fluid channel 112. The proximal wall 111 of the first airbag 11 and the region corresponding to each fluid channel 112 are provided with a sealing gap 1111, preferably, the sealing gap 1111 is opened at an angle, so that the sealing gap 1111 has a wider sealing surface, and the sealing gap 1111 is opened by elastic deformation based on the pressure difference on both sides.

[0044] The following describes the method for using the above-mentioned endotracheal intubation device.

[0045] The catheter 20 is inserted into the patient's trachea 100, and the distal end of the catheter 20 is pushed to the distal end of the trachea 100, the first switch valve 61 and the second switch valve 62 are opened, and the first airbag 11 and the second airbag 12 are inflated synchronously using an inflating device 51 such as an inflatable kettle, such as Figure 3 As shown, the first airbag 11 and the second airbag 12 are expanded to contact the inner tube wall of the trachea 100 .

[0046] The proximal end of the catheter 20 is connected to an oxygen supply device, and the oxygen supply device is used to actively supply oxygen to maintain the patient's breathing.

[0047] During the period of maintaining the patient's breathing by using the oxygen supply device, fluid substances can be pumped out periodically. The fluid substances can be pumped out in the following two ways.

[0048] First way:

[0049] like Figure 5 As shown, the third switch valve 63 is opened, and the suction device 52 sucks fluid material into the liquid storage chamber 14 between the two airbags through the first suction tube 41. If there is fluid material in the area, the fluid material is removed by the first suction tube 41. At this time, the sealing gap 1111 at the proximal end of the fluid channel 112 is opened to balance the pressure in the liquid storage chamber 14. If there is no fluid material on the proximal side of the first airbag 11, the gas enters the liquid storage chamber 14 through the fluid channel 112 to balance the pressure in the liquid storage chamber 14. If there is fluid material on the proximal side of the first airbag 11, the fluid material enters the liquid storage chamber 14 through the fluid channel 112 and is then removed by the first suction tube 41, thereby also removing the fluid material on the proximal side of the first airbag 11. This method is a necessary suction method during the entire use of the tracheal intubation device.

[0050] Second way:

[0051] like Figure 4As shown, the fourth switch valve 64 is opened, and the suction device 52 sucks the fluid material on one side of the proximal end of the first airbag 11 through the second suction tube 42. This method can only suck the fluid material on one side of the proximal end, but cannot suck the fluid material in the liquid storage chamber 14. This method is an unnecessary suction method during the entire use of the endotracheal intubation.

[0052] Before removing the endotracheal tube device from the patient's trachea 100, first, open the first exhaust port 311 so that the first airbag 11 is first deflated and contracted, and the fluid material (if any) intercepted by the first airbag 11 will flow down into the liquid storage chamber 14, and then, use the first suction tube 41 to suck the fluid material into the liquid storage chamber 14, so as to completely remove the fluid material, and then, open the second exhaust port 321 to allow the second airbag 12 to be deflated and contracted. Since the fluid material in the liquid storage chamber 14 is completely removed, no fluid material will flow back into the lungs. Finally, remove the endotracheal tube device from the trachea 100.

[0053] In some preferred embodiments, the middle portion of the proximal wall 111 of the first airbag and the middle portion of the proximal wall 121 of the second airbag 12 are both axially retracted, so that the edge of the proximal wall 111 of the first airbag is higher than the middle portion, and the edge of the proximal wall 121 of the second airbag 12 is higher than the middle portion. This structure is conducive to the airbag intercepting fluid substances.

[0054] In addition, although exemplary embodiments have been described in the present invention, the scope includes any and all embodiments based on the present invention with equivalent elements, modifications, omissions, combinations (e.g., various embodiments intersecting schemes), adaptations or changes. The elements in the claims will be interpreted broadly based on the language adopted in the claims, and are not limited to the examples described in this specification or during the implementation of this application, and the examples will be interpreted as non-exclusive. Therefore, this specification and examples are intended to be considered as examples only, and the true scope and spirit are indicated by the following claims and the full scope of their equivalents.

[0055] The above description is intended to be illustrative rather than restrictive. For example, the above examples (or one or more of them) can be used in combination with each other. For example, a person of ordinary skill in the art can use other embodiments when reading the above description. In addition, in the above-mentioned specific embodiments, various features can be grouped together to simplify the utility model. This should not be interpreted as an intention that a disclosed feature that is not required to be protected is necessary for any claim. On the contrary, the subject matter of the utility model may be less than all the features of a specific disclosed embodiment. Thus, the following claims are incorporated into the specific embodiments as examples or embodiments, wherein each claim is independently used as a separate embodiment, and it is considered that these embodiments can be combined with each other in various combinations or arrangements. The scope of the utility model should be determined with reference to the attached claims and the full scope of equivalent forms granted by these claims.

[0056] The above embodiments are only exemplary embodiments of the present invention and are not intended to limit the present invention. The protection scope of the present invention is defined by the claims. Those skilled in the art may make various modifications or equivalent substitutions to the present invention within the essence and protection scope of the present invention, and such modifications or equivalent substitutions shall also be deemed to fall within the protection scope of the present invention.

Claims

1. A tracheal intubation device, characterized in that: include: a catheter having a proximal end located outside the patient's oral cavity and connected to an oxygen supply device, and a distal end of the catheter for advancement to the distal end of the patient's trachea; An expandable component, comprising a first airbag, a second airbag connected in series, and a connecting sleeve connected between the first airbag and the second airbag; the first airbag, the connecting sleeve, and the second airbag are all sleeved on the radial outside of the distal end of the catheter, and the second airbag is located on one side of the distal end of the first airbag; An inflation tube, whose proximal end is located on one side of the proximal end of the catheter, and whose distal end extends along the catheter to the distal end of the catheter and is connected to the expandable component, so as to inflate the first airbag and the second airbag, and the proximal end of the inflation tube is connected to an inflation device; wherein: After the first airbag and the second airbag are inflated, a liquid storage chamber is defined between the first airbag and the second airbag.

2. The endotracheal intubation device according to claim 1, characterized in that: The endotracheal intubation device also includes a first suction tube; The proximal end of the first suction tube is located on one side of the proximal end of the catheter, the proximal end of the first suction tube is connected to a suction device, and the distal end of the first suction tube extends along the catheter to the distal end of the catheter and is connected to the liquid storage chamber for suctioning fluid substances in the liquid storage chamber.

3. The endotracheal intubation device according to claim 2, characterized in that: A fluid channel is arranged in the first airbag, and the distal end of the fluid channel passes through the liquid storage cavity; the proximal end of the fluid channel is covered by the proximal end wall of the first airbag; An openable sealing gap is formed in the area of ​​the proximal wall of the first airbag opposite to the fluid channel.

4. The endotracheal intubation device according to claim 3, characterized in that: The endotracheal intubation device also includes a second suction tube; The proximal end of the second suction tube is located on one side of the proximal end of the catheter, the proximal end of the second suction tube is connected to a suction device, and the distal end of the second suction tube extends along the catheter to the proximal wall of the first balloon for suctioning fluid material upstream of the first balloon.

5. The endotracheal intubation device according to claim 1, characterized in that: The middle parts of the proximal wall of the first airbag and the proximal wall of the second airbag are both axially retracted so that the edge of the proximal wall of the first airbag is higher than the middle part, and the edge of the proximal wall of the second airbag is higher than the middle part.

6. The endotracheal intubation device according to claim 4, characterized in that: The middle section of the inflation tube runs in the inner hole of the catheter, and the distal end and the distal end of the inflation tube both radially pass through the catheter; the middle sections of the first suction tube and the second suction tube are both located in the inner hole of the catheter, and the proximal end and the distal end of the first suction tube and the second suction tube both radially pass through the catheter.

7. The endotracheal intubation device according to claim 3, characterized in that: The inflation tube includes a first inflation tube and a second inflation tube; the distal end of the first inflation tube is connected to the first airbag, and the distal end of the second inflation tube is connected to the second airbag.

8. The endotracheal intubation device according to claim 7, characterized in that: The distal ends of the first inflation tube and the second inflation tube are both provided with exhaust ports.

9. The endotracheal intubation device according to claim 4, characterized in that: A switch valve is installed at the distal end of the first suction pipe and the distal end of the second suction pipe.

10. The endotracheal intubation device according to claim 7, characterized in that: The distal ends of the first inflation tube and the second inflation tube are both connected with switch valves.