Trachea opens intubate
Technical Field
The utility model relates to the technical field of medical appliances, in particular to a tracheotomy cannula.
Background
Tracheotomy is a common operation for relieving dyspnea caused by laryngeal dyspnea, respiratory dysfunction or retention of lower respiratory tract secretion, and 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. The tracheotomy cannula is an artificial airway used after tracheotomy of a patient, is widely used clinically, and has the following defects in the clinical application process:
1. After tracheostomy tubes, it is often necessary to place oxygen and/or humidification conduits within the tracheostomy tube to assist the patient in respiratory and airway humidification. When oxygen or humidifying liquid is input to a patient, the oxygen pipeline or the humidifying pipeline is mostly inserted into the tracheostomy tube from the upper end opening of the tracheostomy tube, and then the oxygen pipeline or the humidifying pipeline is wound and fixed on the outer wall of the upper end opening of the tracheostomy tube or other exposed parts of the tracheostomy tube by using a medical adhesive tape so as to ensure continuous supply of the oxygen and the humidifying liquid and prevent blockage of the respiratory tract caused by dry sputum. If the medical adhesive tape is firmly fixed, the medical adhesive tape is required to be torn off when the oxygen pipeline or the humidifying pipeline is replaced every time, and the tracheotomy intubation is extremely easy to twist to stimulate a patient to cause cough and even take off the tube in the adhesive tape tearing process. The method not only makes the patient feel uncomfortable, but also brings inconvenience to life and medical care, and threatens the life safety of the patient when serious.
2. The current blocking balloon 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 tracheostomy tube.
3. It was found that ischemic injury of the tracheal mucosa occurred when the pressure between the cuff and tracheal wall exceeded the perfusion pressure of the tracheal mucosa capillaries (20-30 mmHg). The long-time over inflation of the cuff can also cause the tracheal mucosa pressed by the cuff to generate edema necrosis, ulcer formation and tracheal cartilage necrosis, fibrous tissue hyperplasia and/or tracheal collapse, thereby forming tracheal stenosis, and the injury caused by 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.
4. The section from the subglottal to 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 this, the present utility model aims to provide a tracheostomy tube, which overcomes one of the technical problems of the existing tracheostomy tube.
In order to achieve the above purpose, the technical scheme adopted by the utility model is as follows:
A tracheotomy cannula comprises a four-cavity pipeline, a conical balloon and a fixing belt, wherein the four-cavity pipeline comprises a main cavity, one end of the main cavity is connected with a subglottic suction cavity, the subglottic suction cavity is connected with an oxygen and/or humidifying cavity, the other end side wall of the main cavity is respectively communicated with a balloon filling port, a subglottic suction port and an oxygen and/or humidifying port, the conical balloon is fixedly sleeved on the peripheral wall of the subglottic suction cavity, the balloon filling port is communicated with the conical balloon, the subglottic suction port is communicated with the subglottic suction cavity, the oxygen and/or humidifying port is communicated with the oxygen and/or humidifying cavity, the fixing belt is sleeved on the peripheral wall of the main cavity, and the fixing belt is used for fixing the balloon filling port, the subglottic suction port, the oxygen and/or humidifying port.
As one implementation mode, the outer wall of the subglottal suction lumen is provided with a subglottal suction tube opening in a penetrating way, and the subglottal suction tube opening is positioned on one side of the conical balloon.
As one embodiment, the end of the tapered balloon having the larger outer diameter is adjacent to the subglottal suction tube opening.
As one embodiment, the subglottal suction port is provided with a subglottal suction duct in communication with the subglottal suction lumen.
As an embodiment, the oxygen and/or humidification port is provided with an oxygen and/or humidification pipe in communication with the oxygen and/or humidification lumen.
As one embodiment, the balloon filling port is provided with a balloon filling pipe in communication with the tapered balloon.
As one implementation mode, the balloon filling pipeline is communicated with and provided with a pressure indicating balloon, and the side wall of the pressure indicating balloon is provided with 3 circular pressure indicating windows at intervals.
As one implementation mode, the fixing belt is of a strip-shaped structure, and fixing holes are formed in the fixing belt.
Compared with the prior art, the tracheostomy tube has the beneficial effects that:
The utility model is characterized in that one end of a main pipe cavity is connected with respiratory auxiliary equipment or is directly opened, the other end with a conical balloon is inserted into a trachea, gas is mainly introduced into and discharged from the respiratory system through the main pipe cavity, then the conical balloon is inflated through an inflation port of the balloon to enable the conical balloon to be inflated, the effect of plugging the trachea is achieved, only the outer side surface with larger diameter of the conical balloon is wedged into the trachea to be contacted with the tracheal mucosa, the rest most part 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 the tracheal intubation is conveniently inserted into the trachea in a contracted state of the conical balloon through the conical design, furthermore, one end of the subglottal suction port is connected with the subglottal suction port, and the subglottal suction port is opened at one side of the conical balloon, so that secretion on the conical balloon can be sucked out through the subglottal suction port on one side of the subglottal suction lumen, in addition, the utility model can accurately estimate the bulge value of 3 pressure indication windows on the balloon through observing the pressure indication window.
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 the tracheostomy tube of the present utility model;
FIG. 2 is a schematic partial end view of a tracheostomy tube of the present utility model;
FIG. 3 is a schematic view of the structure of the pressure indicating balloon of the present utility model;
FIG. 4 is a schematic view in partial cutaway of a tracheostomy tube of the present utility model;
Fig. 5 is a reference diagram comparing the use of the tapered balloon of the present utility model with a conventional balloon.
Reference numerals illustrate:
10. Four-cavity pipeline, 11, main cavity, 12, subglottal suction cavity, 13, oxygen and/or humidification cavity, 14, balloon filling port, 15, subglottal suction port, 16, oxygen and/or humidification port, 17, subglottal suction tube opening, 18, pressure indicating balloon, 19, pressure indicating window, 20, conical balloon, 30, fixing band.
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.
Referring to fig. 1 to 5, the embodiment provides a tracheostomy tube, which comprises a four-cavity tube 10 and a conical balloon 20, wherein the four-cavity tube 10 comprises a main cavity 11, one end of the main cavity 11 is connected with a subglottal suction cavity 12, the subglottal suction cavity 12 is connected with an oxygen and/or humidification cavity 13, the other end side wall of the main cavity 11 is respectively communicated with a balloon filling port 14, a subglottal suction port 15 and an oxygen and/or humidification port 16, the conical balloon 20 is fixedly sleeved on the peripheral wall of the subglottal suction cavity 12, the balloon filling port 14 is communicated with the conical balloon 20, the subglottal suction port 15 is communicated with the subglottal suction cavity 12, and the oxygen and/or humidification port 16 is communicated with the oxygen and/or humidification cavity 13.
Wherein, subglottal suction port 15 intercommunication is provided with subglottal suction pipeline, subglottal suction pipeline with subglottal suction lumen 12 is linked together, oxygen and/or humidification port 16 intercommunication is provided with oxygen and/or humidification pipeline, oxygen and/or humidification pipeline with oxygen and/or humidification lumen 13 are linked together, sacculus filling port 14 intercommunication is provided with sacculus filling pipeline, sacculus filling pipeline with toper sacculus 20 is linked together.
In order to better define the balloon filling port 14, the subglottal suction port 15, the oxygen and/or the humidification port 16, the present embodiment further includes a fixing band 30, wherein the fixing band 30 is sleeved on the outer peripheral wall of the main lumen 11, and the fixing band 30 is used for fixing the balloon filling port 14, the subglottal suction port 15, the oxygen and/or the humidification port 16. Further, the fixing strap 30 has a strip structure, and fixing holes are formed in the fixing strap 30.
Optionally, a subglottal suction tube opening 17 is formed on the outer wall of the subglottal suction lumen 12 in this embodiment, and the subglottal suction tube opening 17 is located at one side of the conical balloon 20. In addition, the end of the tapered balloon 20 having the larger outer diameter is adjacent to the subglottal suction tube opening 17.
As shown in fig. 4, the conical balloon 20 of the present embodiment has an overlapping structure, and the middle of the conical balloon 20 is provided with a through hole along the axial direction, and the middle of both ends of the conical balloon 20 are respectively overlapped inward and adhered to the outer wall of the subglottal suction lumen 12 through the overlapping portion, so that the connection between the conical balloon 20 and the subglottal suction lumen 12 is more convenient and reliable.
As shown in fig. 3, the balloon filling pipe of this embodiment is provided with pressure indicating balloons 18 in a communicating manner, and the side walls of the pressure indicating balloons 18 are provided with 3 circular pressure indicating windows 19 at intervals. Wherein, 3 pressure indication windows 19 all have film structure constitution, and the film thickness of 3 pressure indication windows 19 is all different, makes 3 pressure indication windows 19's swell pressure value all different from this to pressure indication sacculus 18 is under the condition of different pressure, and the swell quantity of pressure indication window 19 is different demonstration.
The utility model is characterized in that one end of a main pipe cavity 11 is connected with breathing auxiliary equipment or is directly opened, the other end with a conical balloon 20 is penetrated into the main pipe, gas is mainly introduced into and discharged from the respiratory system through the main pipe cavity 11, then the conical balloon 20 is inflated through a balloon inflation port 14 to enable the conical balloon 20 to be inflated, the effect of plugging the gas pipe is achieved, only the outer side surface with a larger diameter of the conical balloon 20 is wedged into the gas pipe to be contacted with the gas pipe mucosa, the rest of the conical balloon 20 is not contacted with the gas pipe mucosa, the conical balloon 20 is prevented from being excessively pressed against the gas pipe mucosa, folds are fewer in a contracted state of the conical balloon 20 so as to facilitate the insertion of the tracheotomy intubation into the gas pipe, furthermore, one end of the conical balloon 20 is connected with a subglottal suction port 15, and the other end of the subglottal suction port is opened at the outer wall of the subglottal suction pipe cavity 12, thus, the subglottal suction port 15 can be used for sucking the conical balloon 20 through the subglottal suction pipe opening 17 on one side of the subglottal suction pipe cavity 12, and the pressure of the balloon 20 can be accurately estimated, and the pressure of the utility model can be accurately indicated by the pressure value of the balloon is estimated by the bulge value of the balloon 20.
The above examples merely represent a few embodiments of the present utility model, which are described in more detail and are not to be construed as limiting the scope of the inventive tracheostomy tube. 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.