Trachea intubation system

By introducing a protective catheter into the tracheal intubation system and setting it outside the lens, the problem of cross-infection of the lens in the prior art is solved, and the effect of reducing cross-infection and simplifying cleaning is achieved.

CN223248598UActive Publication Date: 2025-08-22TIANJIN MEDICAL UNIVERSITY GENERAL HOSPITAL +1
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Patent Information

Application Number
CN202421911458.8
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2024-08-08
Publication Date
2025-08-22
Estimated Expiration
2034-08-08

AI Technical Summary

Technical Problem

In the existing tracheal intubation, the endoscope is directly connected to the tracheal intubation, which causes the lens to extend into the human body to easily cause cross-infection and is complicated to clean.

Method used

A tracheal intubation system is designed, including an endoscope, a protective catheter and a tracheal intubation. The disposable tube of the protective catheter and the connecting sub-tube sleeve are arranged outside the mirror body, the connecting sub-tube can be detachedly connected to the operating part, and the tube body of the tracheal intubation and the handle can be detached. The mirror body is tightly covered by the disposable tube to prevent the mirror body from being exposed away from the operating part.

Benefits of technology

Reduces the risk of cross-infection, simplifies the cleaning process of the endoscopy, and ensures that the intubation process is visualized and does not cause trauma to the human body.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model provides a trachea cannula system, and relates to the technical field of trachea cannula. The trachea cannula system comprises an endoscope, and the endoscope comprises an operation part and an endoscope body connected to one side of the operation part; the protective catheter comprises a disposable tube and a connecting sub-tube connected to one side of the disposable tube; the disposable tube and the connecting sub-tube are arranged outside the mirror body in a sleeving manner, and the connecting sub-tube is detachably connected with the operation part; the trachea cannula comprises a handle and a cannula body connected to one end of the handle; the disposable tube is sleeved with the tube body and the handle, and the handle is detachably connected with the connecting sub-tube. According to the tracheal intubation system, the protective catheter is arranged, the disposable tube of the protective catheter and the connecting sub-tube completely cover the endoscope body, when the tracheal intubation system is inserted into the trachea of the human body, the connecting sub-tube is arranged outside the human body, and the part, extending into the trachea of the human body, of the endoscope body is tightly covered by the disposable tube, so that the end, away from the operation part, of the endoscope body is prevented from being exposed outside; and the possibility of cross infection is reduced.
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Description

Technical Field

[0001] The present application relates to the technical field of endotracheal intubation, and in particular to an endotracheal intubation system. Background Art

[0002] Endotracheal tubes are commonly used in medical settings. Their primary function is to ensure a clear airway and provide the necessary oxygen supply. Existing endotracheal tubes are typically used in conjunction with an endoscope. During use, the endoscope is inserted into the endotracheal tube, which is then inserted into the human trachea. The portion of the endoscope that extends into the tube also enters the human trachea along with the tube, posing a risk of cross-infection. After use, the endoscope is cleaned for the next use. However, when an endoscope is used in conjunction with an endotracheal tube, it needs to be reused repeatedly, which can easily lead to cross-infection. To achieve sterilization, the endoscope needs to be cleaned multiple times, making the process complicated. Utility Model Content

[0003] The purpose of this application is to provide a tracheal intubation system to address the above problems.

[0004] The present application provides a tracheal intubation system, comprising:

[0005] An endoscope, comprising an operating portion and a scope connected to one side of the operating portion;

[0006] a protective catheter, the protective catheter comprising a disposable tube and a connecting sub-tube connected to one side of the disposable tube; the disposable tube and the connecting sub-tube are both sleeved outside the scope, and the connecting sub-tube is detachably connected to the operating portion;

[0007] The endotracheal cannula comprises a handle and a tube body connected to one end of the handle; the tube body and the handle are sleeved outside the disposable tube, and the handle is detachably connected to the connecting sub-tube.

[0008] According to the technical solution provided in certain embodiments of the present application, the operating portion has a connector at one end close to the mirror body, and a protrusion is provided on the outer wall of the connector; a groove is provided on the inner wall of the connecting sub-tube, the connecting sub-tube is sleeved outside the connector, and the protrusion is clamped in the groove.

[0009] According to the technical solutions provided in certain embodiments of the present application, a plurality of first arc-shaped cuts and second arc-shaped cuts are alternately provided on the outer wall of the tube body along the extension direction of the tube body, and the bending direction of the first arc-shaped cuts is opposite to the bending direction of the second arc-shaped cuts.

[0010] According to the technical solutions provided in certain embodiments of the present application, the central angle corresponding to the first arc-shaped incision is greater than 180°, and the central angle corresponding to the second arc-shaped incision is greater than 180°.

[0011] According to the technical solution provided in certain embodiments of the present application, the handle has an insertion channel inside, and the insertion channel includes a first channel and a second channel that are connected to each other. The second channel is a trumpet-shaped structure, and its small-diameter end is connected to the first channel. The end of the first channel away from the second channel is connected to the interior of the tube body.

[0012] According to the technical solution provided in certain embodiments of the present application, the connecting sub-tube has a cannula connecting portion on the side close to the disposable tube, the cannula connecting portion extends into the second channel, the outer wall of the cannula connecting portion abuts against the inner wall of the second channel, the cross-section of the second channel is elliptical, and the outer contour of the cannula connecting portion is elliptical.

[0013] According to the technical solutions provided in certain embodiments of the present application, the inner wall of the tube is spray-coated with a first film.

[0014] According to the technical solutions provided in certain embodiments of the present application, the outer wall of the tube is covered with an elastic membrane.

[0015] According to the technical solutions provided in certain embodiments of the present application, the inner and outer sides of one end of the tube body away from the handle are spray-coated with a second film.

[0016] Compared with the prior art, the present application has the following beneficial effects: The present application provides an endotracheal intubation system, comprising an endoscope, the endoscope comprising an operating portion and a scope body connected to one side of the operating portion; the scope body is provided with a disposable tube and a connecting sub-tube for protecting the catheter, and the connecting sub-tube is detachably connected to the operating portion; the disposable tube is provided with a tube body and a handle for the endotracheal tube, and the handle is detachably connected to the connecting sub-tube. During use, the endotracheal intubation system is connected to an oxygen supply device and then inserted into the human body. The endoscope allows visualization of the insertion process to avoid trauma to the human body. After the endotracheal intubation system is inserted into the trachea, the protective catheter and endoscope can be removed from the endotracheal tube, and other instruments can be inserted into the handle of the endotracheal tube for treatment. In the prior art, the endoscope is directly connected to the endotracheal tube, and the portion of the endoscope extending into the tube body enters the human trachea along with the tube body, resulting in a risk of cross-infection at the end of the end of the endoscope away from the operating part; the present application provides a protective catheter, and the disposable tube of the protective catheter and the connecting sub-tube completely cover the endoscope. When the endotracheal tube system is inserted into the human trachea, the connecting sub-tube is placed outside the human body, and the portion of the endoscope extending into the human trachea is tightly covered by the disposable tube, thereby avoiding exposure of the end of the endoscope away from the operating part to the outside, thereby reducing the possibility of cross-infection.

[0017] It should be understood that the description of technical features, technical solutions, beneficial effects or similar language in this application does not imply that all features and advantages can be realized in any single embodiment. On the contrary, it is understood that the description of a feature or beneficial effect means that a specific technical feature, technical solution or beneficial effect is included in at least one embodiment. Therefore, the description of a technical feature, technical solution or beneficial effect in this specification does not necessarily refer to the same embodiment. Furthermore, the technical features, technical solutions and beneficial effects described in the present embodiment can also be combined in any appropriate manner. Those skilled in the art will understand that the embodiment can be implemented without one or more specific technical features, technical solutions or beneficial effects of a specific embodiment. In other embodiments, additional technical features and beneficial effects can also be identified in specific embodiments that do not embody all embodiments. BRIEF DESCRIPTION OF THE DRAWINGS

[0018] In order to more clearly illustrate the technical solutions in the embodiments of the present application, the following briefly introduces the drawings required for use in the description of the embodiments. Obviously, the drawings described below are only some embodiments of the present application. For ordinary technicians in this field, other drawings can be obtained based on these drawings without any creative work.

[0019] Figure 1 A schematic diagram of the structure of the endotracheal intubation system provided in an embodiment of the present application;

[0020] Figure 2 A schematic structural diagram of an endoscope provided in an embodiment of the present application;

[0021] Figure 3 A schematic structural diagram of a protective conduit provided in an embodiment of the present application;

[0022] Figure 4 A schematic diagram of the structure of the endotracheal tube provided in an embodiment of the present application;

[0023] Figure 5 A schematic structural diagram of the second channel of the endotracheal tube provided in an embodiment of the present application;

[0024] Figure 6 A schematic diagram of the structure of the tube body provided in an embodiment of the present application;

[0025] Figure 7 A schematic diagram of the stepped structure of the tube body provided in an embodiment of the present application;

[0026] Figure 8 This is a connection diagram of the endotracheal intubation system provided in an embodiment of the present application.

[0027] The text annotations in the figure represent:

[0028] 1. Operating part; 2. Scope body; 3. Connecting sub-tube; 4. Disposable tube; 5. Handle; 6. Tube body; 7. Endoscope; 8. Protective catheter; 9. Endotracheal tube; 11. Connector; 12. Protrusion; 21. Camera; 32. Groove; 33. Intubation tube connection; 51. Second channel; 52. Air supply pipe; 61. First arc-shaped incision; 62. Second arc-shaped incision; 63. First film; 64. Elastic membrane. DETAILED DESCRIPTION

[0029] In order to enable those skilled in the art to better understand the technical solutions of the present application, the technical solutions in the embodiments of the present application will be clearly and completely described below in conjunction with the accompanying drawings. The description in this section is only exemplary and explanatory and should not have any limiting effect on the scope of protection of the present application. Specifically, the embodiments described are only part of the embodiments of the present application, not all of the embodiments. Based on the embodiments in the present application, all other embodiments obtained by ordinary technicians in this field without making creative work should fall within the scope of protection of the present application.

[0030] It should be noted that similar reference numerals and letters represent similar items in the following figures. Therefore, once an item is defined in one figure, it does not need to be further defined or explained in subsequent figures. In addition, the terms "including" and "having" and any variations thereof are intended to cover non-exclusive inclusions. For example, a process, method, system, product or apparatus that includes a series of steps or units is not necessarily limited to those steps or units explicitly listed, but may include other steps or units that are not explicitly listed or inherent to these processes, methods, products or apparatuses.

[0031] Please refer to Figures 1 to 4 This embodiment provides a tracheal intubation system, including:

[0032] An endoscope 7 includes an operating portion 1 and a scope 2 connected to one side of the operating portion 1;

[0033] The protective conduit 8 includes a disposable tube 4 and a connecting sub-tube 3 connected to one side of the disposable tube 4; the disposable tube 4 and the connecting sub-tube 3 are both sleeved outside the scope body 2, and the connecting sub-tube 3 is detachably connected to the operating part 1;

[0034] The endotracheal cannula 9 includes a handle 5 and a tube body 6 connected to one end of the handle 5; the tube body 6 and the handle 5 are sleeved outside the disposable tube 4, and the handle 5 is detachably connected to the connecting sub-tube 3.

[0035] The endoscope comprises an operating portion 1 and a mirror body 2 connected to one side of the operating portion 1; the operating portion 1 has a hand-held portion, which is covered with a rubber sleeve for easy grasping of the endoscope; a camera 21 is installed at the end of the mirror body 2 away from the operating portion 1, and the curvature and length of the mirror body 2 meet the structural characteristics of the human trachea, so that the tracheal intubation system can enter the human body under visual conditions, and the mirror body 2 is an arc-shaped hard mirror body, which can provide sufficient support for the tracheal intubation system; the disposable tube 4 is a flexible transparent tube, the inner diameter of the disposable tube 4 matches the outer diameter of the mirror body 2, and the disposable tube 4 is replaced after use to reduce the risk of cross infection; a first through hole is opened inside the connecting sub-tube 3, and one end of the disposable tube 4 is inserted into the first through hole The hole is in the hole to realize the connection between the connecting sub-tube 3 and the disposable tube 4. The disposable tube 4 and the connecting sub-tube 3 are both sleeved on the outside of the mirror body 2 to protect the mirror body 2 from damage during use. The end of the connecting sub-tube 3 away from the disposable tube 4 is detachably connected to the operating part 1; the handle 5 is hollow inside, and the outer contour of the handle 5 conforms to ergonomics, ensuring that it is more comfortable to hold and reducing the burden on the hand when holding for a long time; the outer wall of the tube body 6 is in contact with the inner wall of the handle 5, and an air supply pipe 52 extends from the outer wall of the handle 5. The interior of the air supply pipe 52 is connected to the interior of the tube body 6, which is convenient for connecting to the oxygen supply equipment, so that the endotracheal tube 9 can supply air to the human body when it is inserted, thereby ensuring the patient's blood oxygen concentration during treatment.

[0036] When in use, first connect the air supply pipe 52 to the oxygen supply equipment, and then insert the tracheal intubation system into the human body. The endoscope 7 makes the insertion process visual to avoid trauma to the human body. After the tracheal intubation system is inserted into the trachea, the protective catheter 8 and the endoscope 7 can be removed from the tracheal intubation 9, and other instruments (such as therapeutic instruments) can be inserted into the handle 5 of the tracheal intubation 9. In the prior art, the endoscope 7 is directly connected to the endotracheal tube 9, and the portion of the scope 2 that extends into the tube body 6 enters the human trachea together with the tube body 6, resulting in a risk of cross-infection at the end of the scope 2 away from the operating part 1; however, the present application provides a protective catheter 8, and the disposable tube 4 of the protective catheter 8 and the connecting sub-tube 3 completely cover the scope 2. When the endotracheal tube system is inserted into the human trachea, the connecting sub-tube 3 is placed outside the human body, and the portion of the scope 2 that extends into the human trachea is tightly covered by the disposable tube 4, thereby avoiding exposure of the end of the scope 2 away from the operating part 1 to the outside, thereby reducing the possibility of cross-infection.

[0037] In a preferred embodiment, the operating portion 1 has a connector 11 at one end close to the mirror body 2, and a protrusion 12 is provided on the outer wall of the connector 11; a groove 32 is provided on the inner wall of the connecting sub-tube 3, the connecting sub-tube 3 is sleeved on the outside of the connector 11, and the protrusion 12 is clamped in the groove 32.

[0038] Please refer to Figure 2 and Figure 3The end of the operating part 1 close to the mirror body 2 has a cylindrical connector 11, and a second through hole is provided inside the connector 11, and the mirror body 2 is inserted into the second through hole; a protrusion 12 is provided on the outer wall of the connector 11 at the end away from the mirror body 2; a groove 32 is provided on the inner wall of the connecting sub-tube 3 away from the disposable tube 4, and the groove 32 has an opening at the end away from the disposable tube 4, and the shape and size of the groove 32 match the protrusion 12; when assembling the endoscope 7 and the protective catheter 8, the mirror body 2 end of the endoscope 7 is inserted from the side of the connecting sub-tube 3 away from the disposable tube 4, and the mirror body 2 is located in the disposable tube 4, and the protrusion 12 on the connector 11 slides into the open end of the groove 32 and is engaged in the groove 32 to prevent the endoscope 7 and the protective catheter 8 from rotating relative to each other during use.

[0039] In a preferred embodiment, a plurality of first arcuate cuts 61 and second arcuate cuts 62 are alternately provided on the outer wall of the tube body 6 along the extension direction of the tube body 6 , and the bending direction of the first arcuate cuts 61 is opposite to the bending direction of the second arcuate cuts 62 .

[0040] Please refer to Figure 6 The tube body 6 is made of a hard material, such as 304 stainless steel, to prevent the tube body 6 from being deformed due to the material being too soft when it enters the trachea and is compressed; the provision of multiple first arc-shaped cuts 61 and multiple second arc-shaped cuts 62 reduces the rigidity of the tube body 6 to a certain extent, so that multiple gaps are formed on the wall of the tube body 6. The multiple gaps provide the tube body 6 with space that can be extended or contracted, so that the tube body 6 can bend, so that no stress shielding is generated when the tube body 6 enters the human body cavity, thereby avoiding damage to the human body to a certain extent.

[0041] In a preferred embodiment, the central angle corresponding to the first arc-shaped cutout 61 is greater than 180°, and the central angle corresponding to the second arc-shaped cutout 62 is greater than 180°.

[0042] Please refer to Figure 6 The central angles of the first arc-shaped cutout 61 and the second arc-shaped cutout 62 are both greater than 180°, which allows the tube body 6 to have more space for expansion or contraction and can be bent in any direction with a greater degree of bendability.

[0043] In a preferred embodiment, the handle 5 has an insertion channel inside, and the insertion channel includes a first channel and a second channel 51 that are connected to each other. The second channel 51 is a trumpet-shaped structure, and its small-diameter end is connected to the first channel. The end of the first channel away from the second channel 51 is connected to the inside of the tube body 6.

[0044] Please refer to Figure 5The inner diameter of the first channel is consistent with the outer diameter of the tube body 6, and the tube body 6 extends into the first channel; the large-diameter end of the second channel 51 faces the connecting sub-tube 3, and the small-diameter end is connected to the first channel, which facilitates the disposable tube 4 to extend into the tube body 6 or be pulled out from the tube body 6 along the second channel 51 and the first channel, and also facilitates subsequent other instruments to extend into the tube body 6 along the insertion channel.

[0045] In a preferred embodiment, the connecting sub-tube 3 has a cannula connecting portion 33 on the side close to the disposable tube 4. The cannula connecting portion 33 extends into the second channel 51. The outer wall of the cannula connecting portion 33 abuts against the inner wall of the second channel 51. The cross-section of the second channel 51 is elliptical, and the outer contour of the cannula connecting portion 33 is also elliptical.

[0046] Please refer to Figure 8 The cross section of the second channel 51 is elliptical, and the outer contour of the cannula connecting portion 33 is elliptical, and the two are matched. During use, the cannula connecting portion 33 is prevented from rotating relative to the second channel 51, and the protective catheter 8 is prevented from rotating relative to the handle 5, thereby preventing the protective catheter 8 from driving the endoscope 7 to rotate and causing the lens to shift, thereby accurately monitoring the process and position of the tracheal cannula being inserted into the human body.

[0047] In a preferred embodiment, the inner wall of the tube body 6 is spray-coated with a first film 63 .

[0048] Please refer to Figure 7 The first film 63 makes the inner wall of the tube body 6 smooth, making it easy for the disposable tube 4 and other various instruments to be inserted.

[0049] In a preferred embodiment, the outer wall of the tube body 6 is covered with an elastic membrane 64 .

[0050] Please refer to Figure 7 The elastic membrane 64 is used to prevent the tube body 6 from leaking during use, which may cause a decrease in blood oxygen content, and also makes the instrument smoother when inserted into the human body.

[0051] In a preferred embodiment, the end of the tube body 6 away from the handle 5 is spray-coated with a second film inside and outside.

[0052] The end of the tube body 6 away from the handle 5 is the tube head, and the inside and outside of the tube head are sprayed with a second film. The second film is used to ensure that the tube head is smooth and not sharp, and to prevent the tube head from causing trauma to the human trachea during the process of being inserted into the human trachea.

[0053] This article uses specific examples to illustrate the principles and implementation methods of this application. The description of the above embodiments is only used to help understand the method and core ideas of this application. The above is only the preferred implementation method of this application. It should be pointed out that due to the limitations of textual expression, there are objectively infinite specific structures. For ordinary technicians in this technical field, without departing from the principles of the present invention, they can also make several improvements, modifications or changes, and can also combine the above technical features in an appropriate manner; these improvements, modifications, changes or combinations, or the direct application of the inventive concept and technical solution to other occasions without improvement, should be regarded as the scope of protection of this application.

Claims

1. A tracheal intubation system, characterized in that: include: An endoscope (7), comprising an operating portion (1) and a scope (2) connected to one side of the operating portion (1); A protective conduit (8), the protective conduit (8) comprising a disposable tube (4) and a connecting sub-tube (3) connected to one side of the disposable tube (4); the disposable tube (4) and the connecting sub-tube (3) are both sleeved outside the scope body (2), and the connecting sub-tube (3) is detachably connected to the operating portion (1); A tracheal cannula (9) is provided, comprising a handle (5) and a tube body (6) connected to one end of the handle (5); the tube body (6) and the handle (5) are sleeved outside the disposable tube (4), and the handle (5) is detachably connected to the connecting sub-tube (3).

2. The endotracheal intubation system according to claim 1, characterized in that: The operating portion (1) has a connector (11) at one end close to the mirror body (2), and a protrusion (12) is provided on the outer wall of the connector (11); a groove (32) is provided on the inner wall of the connecting sub-tube (3), the connecting sub-tube (3) is sleeved outside the connector (11), and the protrusion (12) is clamped in the groove (32).

3. The endotracheal intubation system according to claim 1, characterized in that: A plurality of first arc-shaped cutouts (61) and second arc-shaped cutouts (62) are alternately provided on the outer wall of the tube body (6) along the extension direction of the tube body (6), and the bending direction of the first arc-shaped cutouts (61) is opposite to the bending direction of the second arc-shaped cutouts (62).

4. The endotracheal intubation system according to claim 3, characterized in that: The central angle corresponding to the first arc-shaped incision (61) is greater than 180°, and the central angle corresponding to the second arc-shaped incision (62) is greater than 180°.

5. The endotracheal intubation system according to claim 1, characterized in that: The handle (5) has an insertion channel inside, and the insertion channel includes a first channel and a second channel (51) that are connected to each other. The second channel (51) is a trumpet-shaped structure, and its small-diameter end is connected to the first channel. The end of the first channel away from the second channel (51) is connected to the inside of the tube body (6).

6. The endotracheal intubation system according to claim 5, characterized in that: The connecting sub-tube (3) has a cannula connecting portion (33) on a side close to the disposable tube (4), and the cannula connecting portion (33) extends into the second channel. The outer wall of the cannula connecting portion (33) abuts against the inner wall of the second channel (51). The cross section of the second channel is elliptical, and the outer contour of the cannula connecting portion (33) is also elliptical.

7. The endotracheal intubation system according to claim 1, characterized in that: The inner wall of the tube body (6) is spray-coated with a first film (63).

8. The endotracheal intubation system according to claim 1, characterized in that: The outer wall of the tube body (6) is covered with an elastic membrane (64).

9. The endotracheal intubation system according to claim 1, characterized in that: The end of the tube body (6) away from the handle (5) is spray-coated with a second film inside and outside.