Four-in-one trachea cannula
Technical Field
The utility model relates to the technical field of medical instruments, in particular to a four-in-one trachea cannula.
Background
The tracheal intubation is a treatment method for relieving dyspnea caused by laryngeal dyspnea, respiratory dysfunction or retention of secretion of the lower respiratory tract, can keep the respiratory tract of a patient smooth, improve dyspnea caused by various reasons, correct the anoxic state of the patient and the like.
Currently, tracheal intubation is widely used clinically. The following defects exist in the clinical application process, namely 1, the current plugging saccule is cylindrical. After filling, the balloon can press the inner wall of the trachea of the longer section, so that the mucous membrane of the longer section of the inner wall of the trachea is pressed. In addition, the balloon with the shape has more folds in the contracted state, which affects the insertion of the trachea cannula. 2, research shows that when the pressure between the cuff and the tracheal wall exceeds the perfusion pressure (20-30 mmHg) of the tracheal mucosa capillary vessel, ischemic injury occurs to the tracheal mucosa. Prolonged over-inflation of the cuff can also cause oedema necrosis, ulceration and tracheal cartilage necrosis of the tracheal mucosa pressed by the cuff, fibrous tissue proliferation and/or tracheal collapse, which in turn creates a tracheal stenosis. The harm of the airway stenosis is large and the treatment difficulty is high. The detection method of the cuff filling pressure comprises three methods (1) a finger touch method, namely, the finger touch indication air bag is similar to the nose tip in elasticity to indirectly judge the cuff filling pressure, and the method is most commonly adopted in the emergency tracheal intubation. This approach is highly subjective and often results in over inflation of the cuff. (2) The cuff pressure gauge detects the filling pressure of the cuff reliably and accurately. However, manual measurement does not effectively control the cuff pressure and can cause the cuff to leak when connecting and disconnecting the pressure tube. The cuff inflation pressure is thus often set to be somewhat higher than the target value using a cuff pressure gauge. (3) Automatic inflator continuous pressure measurement or continuous cuff pressure monitoring systems have great advantages in continuously monitoring cuff pressure and stabilizing cuff pressure, but are expensive and difficult to popularize in clinical practice. And 3, the section from the subglottal part to the upper part of the tracheal cannula balloon generates more secretion, but is not easy to suck out to form a potential infection source.
Disclosure of utility model
Based on the above, the utility model aims to provide a four-in-one trachea cannula so as to overcome one of the technical problems of the existing tracheotomy cannula.
In order to achieve the above purpose, the technical scheme adopted by the utility model is as follows:
The four-in-one trachea cannula comprises a cannula main pipe, a saccule filling pipe, a glottic suction pipe, a glottic flushing pipe and a conical saccule, wherein the saccule filling pipe, the glottic suction pipe and the glottic flushing pipe are respectively arranged in the cannula main pipe;
The conical balloon is fixedly sleeved on the peripheral wall of one end, close to the inclined socket, of the cannula main pipe, one end, close to the inclined socket, of the smaller diameter of the conical balloon, one end of the balloon filling pipe penetrates through the cannula main pipe and is communicated with the conical balloon, the other end of the balloon filling pipe penetrates through the cannula main pipe and stretches out of the cannula main pipe, and glottis suction openings and glottis flushing openings are formed in the side wall, close to the larger diameter end of the conical balloon, of the cannula main pipe at intervals;
One end of the glottic suction tube penetrates through the cannula main tube and is communicated with the glottic suction opening, the other end of the glottic suction tube penetrates through the cannula main tube and extends out of the cannula main tube, one end of the glottic flushing tube penetrates through the cannula main tube and is communicated with the glottic flushing opening, and the other end of the glottic flushing tube penetrates through the cannula main tube and extends out of the cannula main tube.
As one embodiment, the end of the balloon filling tube extending out of the cannula main tube is located at one side of the auxiliary joint, the end of the glottis suction tube extending out of the cannula main tube is located at one side of the auxiliary joint, and the end of the glottis flushing tube extending out of the cannula main tube is located at one side of the auxiliary joint.
As one implementation mode, one end of the balloon filling pipe extending out of the cannula main pipe is communicated with a pressure indicating balloon, and a plurality of circular pressure indicating windows are arranged on the side wall of the pressure indicating balloon at intervals.
As an implementation mode, 3 circular pressure indication windows are arranged on the side wall of the pressure indication balloon at intervals, each pressure indication window is formed by a film structure, and the film thickness of each pressure indication window is unequal.
As one embodiment, the glottic suction opening is located between the glottic irrigation port and the tapered balloon.
As one embodiment, the spacing between the glottis suction opening and the tapered balloon is 5mm to 15mm.
As an implementation mode, the side wall of the inclined socket is provided with a through hole in a penetrating mode.
As one embodiment, the conical balloon is adhesively fixed on the cannula main tube.
Compared with the prior art, the four-in-one trachea cannula has the beneficial effects that:
The utility model is characterized in that one end of a main intubation tube is connected with respiratory auxiliary equipment or is directly opened, the other end with a conical balloon is inserted into the trachea, gas mainly passes through an internal channel of the main intubation tube and enters and exits a respiratory system, then the conical balloon is inflated through a balloon inflation tube so as to achieve the effect of blocking the trachea, only the outer side surface with larger diameter of the conical balloon is embedded into the trachea to be contacted with the tracheal mucosa, the rest of the conical balloon is not contacted with the tracheal mucosa, the conical balloon is prevented from being excessively pressed against the tracheal mucosa, and moreover, the conical balloon is designed to have fewer folds in the contracted state of the conical balloon so as to facilitate the insertion of the main intubation tube into the trachea.
For a better understanding and implementation, the present utility model is described in detail below with reference to the drawings.
Drawings
FIG. 1 is a schematic view of a four-in-one endotracheal tube according to the present utility model;
FIG. 2 is a second schematic view of a four-in-one endotracheal tube according to the present utility model;
FIG. 3 is an enlarged schematic view of portion A of FIG. 2;
FIG. 4 is a schematic view of the structure of the pressure indicating balloon of the present utility model;
fig. 5 is a schematic partial cross-sectional view of a four-in-one endotracheal tube according to the present utility model.
The reference numerals indicate 10, a cannula main pipe, 11, an auxiliary joint, 12, an inclined socket, 13, a glottic suction opening, 14, a glottic flushing opening, 20, a balloon filling pipe, 21, a pressure indicating balloon, 22, a pressure indicating window, 30, a glottic suction pipe, 40, a glottic flushing pipe and 50, a conical balloon.
Detailed Description
For further illustration of the various embodiments, the utility model is provided with the accompanying drawings. The accompanying drawings, which are incorporated in and constitute a part of this disclosure, illustrate embodiments and together with the description, serve to explain the principles of the embodiments. With reference to these matters, one of ordinary skill in the art will understand other possible implementations and advantages of the present utility model.
In the description of the present utility model, it should be understood that the terms "center", "longitudinal", "lateral", "length", "width", "thickness", "upper", "lower", "left", "right", "top", "bottom", "inner", "outer", "axial", "radial", "circumferential", etc. indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings, are merely for convenience in describing the present utility model and simplifying the description, and do not indicate or imply that the devices or elements referred to must have a specific orientation, be configured and operated in a specific orientation, and thus are not to be construed as limiting the present utility model.
In the related art, the tracheal intubation is widely used clinically. The following defects exist in the clinical application process, namely 1, the current plugging saccule is cylindrical. After filling, the balloon can press the inner wall of the trachea of the longer section, so that the mucous membrane of the longer section of the inner wall of the trachea is pressed. In addition, the balloon with the shape has more folds in the contracted state, which affects the insertion of the trachea cannula. 2, research shows that when the pressure between the cuff and the tracheal wall exceeds the perfusion pressure (20-30 mmHg) of the tracheal mucosa capillary vessel, ischemic injury occurs to the tracheal mucosa. Prolonged over-inflation of the cuff can also cause oedema necrosis, ulceration and tracheal cartilage necrosis of the tracheal mucosa pressed by the cuff, fibrous tissue proliferation and/or tracheal collapse, which in turn creates a tracheal stenosis. The harm of the airway stenosis is large and the treatment difficulty is high. The detection method of the cuff filling pressure comprises three methods (1) a finger touch method, namely, the finger touch indication air bag is similar to the nose tip in elasticity to indirectly judge the cuff filling pressure, and the method is most commonly adopted in the emergency tracheal intubation. This approach is highly subjective and often results in over inflation of the cuff. (2) The cuff pressure gauge detects the filling pressure of the cuff reliably and accurately. However, manual measurement does not effectively control the cuff pressure and can cause the cuff to leak when connecting and disconnecting the pressure tube. The cuff inflation pressure is thus often set to be somewhat higher than the target value using a cuff pressure gauge. (3) Automatic inflator continuous pressure measurement or continuous cuff pressure monitoring systems have great advantages in continuously monitoring cuff pressure and stabilizing cuff pressure, but are expensive and difficult to popularize in clinical practice.
In view of this, the present embodiment provides a four-in-one tracheal cannula, which can effectively avoid the excessive compression of the tracheal mucosa by the tapered balloon 50, can suck out the secretion on the tapered balloon 50 through the glottis suction tube 30, and can accurately estimate the pressure value in the tapered balloon 50.
Referring to fig. 1 to 4, the embodiment provides a four-in-one tracheal cannula, which comprises a cannula main tube 10, a balloon filling tube 20, a glottic suction tube 30, a glottic flushing tube 40 and a conical balloon 50, wherein the balloon filling tube 20, the glottic suction tube 30 and the glottic flushing tube 40 are respectively arranged in the cannula main tube 10, one end of the cannula main tube 10 is connected with an auxiliary connector 11, the other end of the cannula main tube 10 is provided with an inclined socket 12, the conical balloon 50 is fixedly sleeved on the peripheral wall of one end of the cannula main tube 10, which is close to the inclined socket 12, one end of the conical balloon 50, which is smaller in diameter, is close to the inclined socket 12, one end of the balloon filling tube 20 penetrates through the cannula main tube 10 and is communicated with the conical balloon 50, the other end of the balloon filling tube 20 penetrates through the cannula main tube 10 and stretches out of the outside, the cannula main tube 10 is provided with a glottic suction opening 13, which is spaced apart from the side wall of one end, which is close to one end of the conical balloon main tube 50, which is larger in diameter, and the glottic flushing tube 10 penetrates through the other end of the cannula main tube 10, and the end of the conical balloon filling tube 20 penetrates through the glottic flushing tube 10, and the end of the suction tube 10 is communicated with the glottic flushing tube 10, and the end of the suction tube is stretched out of the end of the main tube 10.
Optionally, an end of the balloon filling tube 20 extending out of the cannula main tube 10 is located at one side of the auxiliary joint 11, an end of the glottis suction tube 30 extending out of the cannula main tube 10 is located at one side of the auxiliary joint 11, and an end of the glottis flushing tube 40 extending out of the cannula main tube 10 is located at one side of the auxiliary joint 11.
In other words, the cannula main tube 10 of the present embodiment has one end of the auxiliary joint 11 as an input end, and one ends of the balloon filling tube 20, the glottic suction tube 30 and the glottic flushing tube 40 respectively extend out of the side wall of the cannula main tube 10 and are as close to the auxiliary joint 11 as possible, so that, in use, the auxiliary joint 11, the balloon filling tube 20, the glottic suction tube 30 and the glottic flushing tube 40 can be disposed in an exposed manner by extending the end of the cannula main tube 10 provided with the inclined socket 12 into the air intake tube, so as to facilitate the manipulation of each member.
Optionally, a pressure indicating balloon 21 is provided on the end of the balloon filling tube 20 extending out of the cannula main tube 10, and a plurality of circular pressure indicating windows 22 are provided on the side wall of the pressure indicating balloon 21 at intervals. Wherein, 3 circular pressure indication windows 22 are spaced apart from each other on the side wall of the pressure indication balloon 21, each pressure indication window 22 is formed by a film structure, and the film thickness of each pressure indication window 22 is not equal.
As shown in fig. 4, the tapered balloon 50 of the present embodiment has an overlapping structure, and the middle of the tapered balloon 50 is provided with a through hole along the axial direction, and the middle of two ends of the tapered balloon 50 are respectively overlapped inward and adhered to the outer wall of the cannula main tube 10 through the overlapping part, so that the connection between the tapered balloon 50 and the cannula main tube 10 is more convenient and reliable.
Optionally, the glottic suction opening 13 is located between the glottic irrigation port and the tapered balloon 50. Furthermore, the spacing between the glottis suction opening 13 and the tapered balloon 50 is 5mm to 15mm. In addition, a through hole is formed through the sidewall of the inclined socket 12.
Compared with the prior art, the utility model has the advantages that one end of the intubation main tube 10 is connected with respiratory auxiliary equipment or is directly opened, the other end with the conical balloon 50 is inserted into the trachea, gas is mainly led into and out of the respiratory system through the internal channel of the intubation main tube 10, then the conical balloon 50 is inflated through the balloon inflation tube 20, so that the effect of plugging the trachea is achieved, only the outer side surface with larger diameter of the conical balloon 50 is embedded into the trachea to be contacted with the tracheal mucosa, the rest of the conical balloon 50 is not contacted with the tracheal mucosa, the conical balloon 50 is prevented from being excessively pressed against the tracheal mucosa, and wrinkles are fewer in the contracted state of the conical balloon 50 so as to facilitate the insertion of the intubation main tube 10 into the trachea, in addition, secretion on the conical balloon 50 can be sucked out through the glottic suction tube 30, in addition, the 3 pressure indication windows 22 on the balloon 21 can be accurately expanded out of the conical balloon 50 through observing the inflation degree and quantity of the pressure indication window, and the suction tube 40 can be prevented from being more stimulated by the suction tube 40 of a user, and the suction tube 30 is prevented from being more severely stimulated by the suction tube 40, and the suction tube is prevented from being more severely stimulated by the suction tube 30.
The above examples merely represent several embodiments of the present utility model, which are described in more detail and are not to be construed as limiting the scope of the four-in-one endotracheal tube of the present utility model. It should be noted that it will be apparent to those skilled in the art that several variations and modifications can be made without departing from the spirit of the utility model, which are all within the scope of the utility model.