CN212118731U - Breathing mask and ventilation treatment equipment - Google Patents

Abstract

The utility model relates to a respirator and therapeutic equipment of ventilating relates to respiratory device technical field. The utility model relates to a breathing mask, which comprises a frame, a gasket, a bent pipe and a head belt component; the liner is arranged on the frame and forms an air-communicating cavity with the frame; the headband assembly is connected with the frame to fix the cushion and the frame on the head of a patient, the elbow is rotatably arranged on the frame, the interface is arranged on the elbow and comprises an insertion pipe block fixedly connected with the elbow or integrally connected with the elbow, the insertion pipe block is used for being connected with a medical pipeline, the rigidity of the insertion pipe block is smaller than that of the elbow, the interface is arranged on the elbow, the medical pipeline can be inserted through the interface, the patient can be treated by using the breathing mask without taking off the breathing mask, and therefore the breathing mask can meet the use requirement of the medical environment of the patient.

Description

Breathing mask and ventilation treatment equipment

Technical Field

The utility model relates to a treatment technical field of ventilating especially relates to a respirator and treatment of ventilating equipment.

Background

Noninvasive positive pressure ventilation has been widely used for Obstructive Sleep Apnea (OSA), chronic obstructive pulmonary emphysema (COPD), and the like, without the need for surgically inserting a tube into the patient's airway, using a blower to deliver a continuous pressure ventilation (CPAP) or a variable pressure ventilation, such as a bi-level pressure that varies with the patient's respiratory cycle or an autoregulated pressure that varies with the monitored condition of the patient, through tubing and a patient interface. This pressure-supported therapy is also commonly used for treatments such as obstructive sleep hypopnea, Upper Airway Resistance Syndrome (UARS), or congestive heart failure.

Non-invasive ventilation therapy includes interface devices on the face of a patient that are generally classified into four different contact patterns: a nasal mask covering only the nose, an oral mask covering only the mouth, an oral-nasal mask (also called a full face mask) covering the mouth and the nose, and a nasal cushion mask inserted into the nostrils. During treatment, an external blower is a pressure support device, such as a ventilator, and a patient interface couples the pressure of the gas provided by the ventilator to the patient's airway to deliver a flow of breathing gas to the patient's airway.

The full face mask can be divided into a face mask with exhaust and a face mask without exhaust according to different exhaust modes. The exhaust mask is provided with a special exhaust hole at the mask end so as to facilitate the exhaust of the breathing waste gas, and is mainly used in the household environment. The waste respiratory gas without exhaust mask is usually exhausted from the pipeline or the end of the respirator, and is mostly used in medical environment.

When a patient wears the breathing mask for treatment, the exhaust gas exhaled by the patient cannot be completely exhausted, so that the exhaust gas CO is generated₂And (4) retention. CO retention₂Is referred to as the dead space.

In most cases the treatment of the patient is chronic. The patient uses the no mask of arranging to treat under the hospital environment, need purchase the face mask of arranging of family expenses in addition after the discharge, can't continue to use medical no mask of arranging. In one instance, a patient may need to insert a medical tube (e.g., an endoscopic tube, a feeding tube, etc.) through the mouth or nostrils during treatment using the mask. In another use case, the mask is provided with a safety valve hole for preventing suffocation.

Existing full-face masks are generally classified into two types, one type being a face mask with exhaust (as shown in fig. 38) suitable for use in a domestic environment, and the other type being a face mask without exhaust (as shown in fig. 39) suitable for use in a medical environment. The two masks differ in whether the mask has an exhaust. A vented mask suitable for use in a domestic environment is generally composed of a mask body 100 and an elbow 200. The mask body typically includes a vent aperture 110. The exhaust apertures 110 are used to exhaust the exhaust exhaled by the patient when the mask is in use. Of course, the vent apertures 110 may also be provided in the elbow 200. Typically, the mask body 100 and elbow 200 are not removable from each other.

In practice, it has been found that a patient may need to insert medical tubing (e.g., endoscope tubes, feeding tubes, etc.) through the mouth or nostrils during treatment using the mask, and thus a single mask function may not be adequate for multiple use environments.

SUMMERY OF THE UTILITY MODEL

In order to solve the whole or partial problems, the utility model provides a breathing mask and ventilation therapy equipment, which can be inserted into a medical pipeline by replacing a bent pipe so as to satisfy different use environments.

According to a first aspect of the present invention, there is provided a respiratory mask comprising a frame, a cushion, an elbow, and a headgear assembly; the gasket is arranged on the frame and forms an air-through cavity with the frame; the headgear assembly is connected with the frame to secure the cushion and the frame to the head of the patient; the elbow is rotatably arranged on the frame, the elbow is detachably connected with the frame, and the elbow is at least configured into two different structures to be matched with the frame.

In one embodiment, the cannula block is made of a flexible material, preferably a silicone material.

In one embodiment, the cannula block is provided with a cannula hole, the cannula hole is provided with a sealing unit, and the medical tube extends into the elbow tube via the sealing unit.

In one embodiment, the sealing unit includes a thick sealing region disposed on the wall of the cannula hole, a thin sealing region connected to the thick sealing region, and a thin sealing slit disposed on the thin sealing region, through which the medical tubing can extend into the elbow.

In one embodiment, the sealing slit is configured as a "straight", "m", "S" or "square" slit.

In one embodiment, the sealing slit has a slit width of 0.1 to 2.0 mm.

In an embodiment, still be provided with on the return bend and be used for holding the intubate piece interface of intubate piece, the intubate piece includes interior lamella and the outer lamella that sets gradually from inside to outside, interior lamella with be provided with the draw-in groove between the outer lamella, be provided with the card limit along circumference on the inner wall of intubate piece interface, the draw-in groove with card limit looks block is in order to restrict the degree of freedom of intubate piece along the trompil direction.

In one embodiment, the cannula block interface further comprises a rotation stopping protrusion arranged at the circumferential edge of the cannula block interface, the outer sheet layer is provided with a rotation stopping groove, and the rotation stopping protrusion is clamped with the rotation stopping groove to limit the rotation freedom degree of the cannula block.

In one embodiment, the elbow includes an elbow body including a first pipe region and a second pipe region disposed at an included angle, the first pipe region being coupled to the frame, the insertion block being disposed on the second pipe region.

In one embodiment, the first tube area includes at least two deformation areas, and a gap is disposed between adjacent deformation areas, where the gap is used to provide a corresponding space for the deformation areas to elastically deform.

According to a second aspect of the present invention, there is provided a ventilation therapy device comprising a breathing mask as described above.

Compared with the prior art, the utility model has the advantages of: through set up the interface on the return bend, can insert medical pipeline through the interface, make patient use respirator treatment period, need not take off respirator and just can carry out other treatments to make respirator can satisfy the operation requirement of patient's medical environment.

Drawings

The present invention will be described in more detail hereinafter based on embodiments and with reference to the accompanying drawings.

Fig. 1 and 2 are schematic perspective views of a breathing mask in an embodiment of the present invention;

fig. 3a is an exploded view of a respiratory mask in an embodiment of the present invention;

fig. 3b is an exploded view of a respiratory mask in another embodiment of the present invention;

fig. 4 and 5 are schematic structural views of an intermediate member in an embodiment of the present invention;

FIG. 6 is a cross-sectional view at A-A of FIG. 5;

fig. 7 is a schematic perspective view of an elbow pipe according to an embodiment of the present invention;

FIG. 8 is an exploded view of the elbow of FIG. 7;

FIGS. 9 and 10 are schematic perspective views of the elbow body shown in FIG. 7;

FIG. 11 is a front view of the elbow mounted respiratory mask of FIG. 7;

FIG. 12 is a cross-sectional view of FIG. 11 at B-B;

FIG. 13 is a cross-sectional view at C-C of FIG. 11;

FIG. 14 is an enlarged view of FIG. 12 at D;

FIG. 15 is an enlarged view of FIG. 13 at E;

FIGS. 16-19 are half sectional views of the elbow shown in FIG. 7;

fig. 20 is a schematic perspective view of an elbow pipe according to an embodiment of the present invention;

FIG. 21 is an exploded view of the elbow of FIG. 20;

FIGS. 22 and 23 are schematic perspective views of the elbow body shown in FIG. 20;

fig. 24 and 25 are schematic perspective views of an elbow pipe according to an embodiment of the present invention;

figures 26 and 27 are schematic perspective views of an elbow according to an embodiment of the invention;

FIG. 28 is a schematic structural view of the elbow of FIG. 26 (with the cannula block not shown);

FIG. 29 is a front view of the elbow of FIG. 28;

FIG. 30 is a cross-sectional view at F-F of FIG. 29;

FIG. 31 is a perspective view of the cannula block of FIG. 26;

FIG. 32 is a front view of the cannula block of FIG. 31;

FIG. 33 is a cross-sectional view at G-G of FIG. 32;

FIG. 34 is an enlarged view of FIG. 33 at H;

FIG. 35 is an assembled schematic view of the elbow of FIG. 26;

FIG. 36 is a cross-sectional view of FIG. 35 at I-I;

FIG. 37 is a diagram of a directional definition for a respiratory mask in an embodiment of the present invention;

fig. 38 and 39 are schematic views of the structure of a prior art respiratory mask.

Description of the drawings of fig. 1-37:

1-forehead pad; 2-a liner; 3-a frame; 341-tumbling air stream;

4-bending the pipe; 41-elbow body; 42-safety valve plate; 43-elbow fitting; 44-cannula block; 45-exhaust fine seams;

411-first tube zone; 412-a second tube region; 413-a limiting pipe area; 414-buckle; 415-a bump; 416-a vent; 417-relief valve bore; 418-notch; 419-cannula block interface; 419 a-rotation stop projection; 419 b-card edge;

411 a-deformation zone; 411 b-sealing area;

4151-stop protrusion; 4152-clearance protrusions;

441-inner sheet layer; 442-an outer sheet layer; 443-a rotation stopping groove; 444-cannula hole; 445-sealing the card slot; 446-seal thick area; 447-a thin sealing region; 448-sealing the thin seam;

451-front section of slit; 452-rear section of slot;

5-an intermediate piece; 51-a card slot; 52-stop projection.

The drawings of fig. 38 and 39 illustrate:

100-a mask body; 200-bending the pipe; 110-exhaust orifice.

Detailed Description

The present invention will be further explained with reference to the accompanying drawings.

As shown in fig. 1 and 2, the present invention provides a respiratory mask, which comprises a frame 3, a headband assembly, a forehead pad 1 and a cushion 2 respectively arranged on the frame 3, wherein the cushion 2 is arranged on the frame 3 and forms an air cavity with the frame 3, and the headband assembly is connected with the frame 3 to fix the cushion 2 and the frame 3 on the head of a patient. Wherein, the frame 3 is rotatably provided with an elbow 4, and the elbow 4 is detachable with the frame 3. Therefore, when in use, different bent pipes 4 can be selected according to the use environment and assembled on the frame 3, so as to realize diversified purposes.

Generally, polycarbonate materials (PC materials for short) having both transparency and cost are often used for the frame 3 and the bent pipe 4. When two same materials are matched to rotate, the rotation abnormal sound is easily caused due to the consistent hardness and strength of the materials. In order to effectively solve the above-mentioned abnormal rotation sound problem, as shown in fig. 3a, the present invention provides an intermediate member 5 for connecting with the bent pipe 4 on the frame 3, and the intermediate member 5 is configured to be rotatably and detachably connected with at least one of the frame 3 and the bent pipe 4.

In other words, one embodiment is: the intermediate piece 5 can be fixedly mounted on the frame 3, while the elbow 4 can rotate around the intermediate piece 5 and the elbow 4 is detachably connected with the intermediate piece 5; the other implementation mode is as follows: the intermediate piece 5 and the elbow 4 can not rotate relatively, but the two can rotate around the frame 3 integrally and are connected with the frame 3 detachably; yet another embodiment is: the intermediate piece 5 is both rotatably and detachably connected to the frame 3 and to the elbow 4.

Furthermore, the intermediate piece 5 is of a different material than the elbow 4. For example, the intermediate member 5 may be made of a polypropylene material (PP material for short). By the design, the problem of abnormal rotating sound between the bent pipe 4 and the intermediate piece 5 can be effectively solved.

In order to facilitate the regulation of the undesired exhaust flow at the whole assembly gap of the breathing mask, the intermediate piece 5 is preferably fixedly arranged on the frame 3, and the intermediate piece 5 is rotatably connected with the elbow 4.

Further, there are various fixing means between the intermediate member 5 and the frame 3. For example, the intermediate member 5 may be firmly attached to the frame 3 by ultrasonic welding, gluing, or the like, or may be directly assembled to the frame 3 and fixedly attached thereto.

In a preferred embodiment, the intermediate piece 5 can be connected to the frame 3 in an assembled manner in order to reduce costs. Specifically, as shown in fig. 4 to 6, the intermediate member 5 includes a locking groove 51 provided on an outer surface thereof, the locking groove 51 is annularly provided on the outer surface of the intermediate member 5, and after the intermediate member 5 is assembled with the frame 3, the locking groove 51 is engaged with the frame 3 to restrict a degree of freedom of the intermediate member 5 in the inserting and extracting direction so that the intermediate member 5 cannot be pulled out from the frame 3.

Optionally, in order to limit the rotational degree of freedom of the intermediate member 5 relative to the frame 3, a first rotation stop protrusion (not shown) is disposed on the slot 51, and a rotation stop groove is disposed at a corresponding position on the frame 3, and the first rotation stop protrusion and the rotation stop groove cooperate to limit the rotational degree of freedom between the intermediate member 5 and the frame 3.

The utility model discloses all not prescribing a limit to the shape of first spline arch and spline recess, can understand ground, as long as can carry out the first spline arch and the spline recess that splines to frame 3 and middleware 5 with the complex mode and all fall into within the protection scope of the utility model.

Optionally, an interference fit or partial interference fit is formed between the intermediate piece 5 and the frame 3 to limit the rotational freedom between the intermediate piece 5 and the frame 3. The principle of limiting the rotational degree of freedom between the intermediate member 5 and the frame 3 by interference fit or partial interference fit is to limit the rotational degree of freedom of the intermediate member 5 by means of friction.

It should be noted that, the local interference fit of the present invention may be that the intermediate member 5 or the frame 3 is provided with a local protrusion (not shown) at the fitting position, and the local interference fit is formed at the local protrusion position during assembly. The utility model discloses do not prescribe a limit to these local bellied shapes and positions.

Because of the way of arranging the first rotation stopping protrusion and the rotation stopping groove, the intermediate piece 5 is required to be arranged on the frame 3 along a specific direction, so that the first rotation stopping protrusion is just clamped in the rotation stopping groove; the local interference fit easily causes a large local deformation of the intermediate member 5, which is not favorable for controlling the size and the exhaust flow.

Therefore, in the present invention, it is preferable that the intermediate member 5 and the frame 3 are in interference fit with each other to limit the rotational degree of freedom of the intermediate member 5.

The elbow 4 will be described in detail below.

In some embodiments, as shown in fig. 7-19, elbow 4 is suitable for use in a vented mask in a domestic environment.

Specifically, as shown in fig. 7 and 8, elbow 4 includes elbow body 41 and elbow fitting 43, with one end of elbow body 41 connected to frame 3, the other end of elbow body 41 fixedly or integrally connected to elbow fitting 43, and elbow fitting 43 for connection to an intake conduit of a ventilator. The elbow main body 41 and the elbow joint 43 may be fixedly connected by ultrasonic welding, adhesive, or the like.

Additionally, the elbow 4 may also include a safety valve 42 disposed between the elbow body 41 and the elbow fitting 43, the safety valve 42 being configured to cooperate with a safety valve aperture 417 as described below.

Further, as shown in FIGS. 9 and 10, elbow body 41 includes a first tube section 411 for connection to intermediate piece 5 and a second tube section 412 for connection to elbow fitting 43, with an included angle between first tube section 411 and second tube section 412. Elbow main body 41 further includes a stopper tube area 413 connecting first tube area 411 and second tube area 412, respectively, and when first tube area 411 is connected to frame 3, stopper tube area 413 can restrict the degree of freedom of elbow main body 41 in the insertion and removal direction.

The intermediate part 5 comprises a stop projection 52 arranged on its inner surface, and a catch 414 is arranged on the outer wall of the first tube section 411 at a corresponding position, the stop projection 52 cooperating with the catch 414 to limit the freedom of the pipe bend 4 in the plugging direction.

The elbow body 41 also includes a protrusion 415, the protrusion 415 for mating contact with the intermediate piece 5 to form the vent slot 45, when the vent slot 45 is vented, a tumble flow 341 can be formed at the interface of the elbow 4 and the frame 3. The tumbling airflow 341 can entrain a portion of the entrapped CO2, reducing the volume of dead space to some extent, reducing the repetitive breathing of CO 2.

The number of the catches 414 is at least 2, and the number of the projections 415 is at least 3. Preferably, the number of the catches 414 is the same as the number of the projections 415, and the catches 414 and the projections 415 are arranged at equal intervals in the circumferential direction of the elbow 4.

Specifically, as shown in FIGS. 11-14, the exhaust slot 45 includes a forward slot section 451 and a rearward slot section 452. The front sipe section 451 is formed as follows: as shown in fig. 15, the protrusion 415 includes a position-limiting protrusion 4151 on the outer wall of the first tube area 411, after the position-limiting protrusion 4151 is in contact fit with the intermediate member 5, a slit front section 451 is formed between the inner wall of the intermediate member 5 and the outer wall of the first tube area 411 to perform air exhaust, and after the position-limiting protrusion 4151 is in contact fit with the intermediate member 5, the degree of freedom of the elbow 4 in the circumferential direction can be limited.

The rear slotted segment 452 is formed as follows: as shown in fig. 15, the protrusion 415 further includes a gap protrusion 4152 located on the side wall of the position limiting pipe area 413, after the gap protrusion 4152 is in contact fit with the intermediate member 5, a slit rear section 452 is formed between the end surface of the intermediate member 5 and the end surface of the position limiting pipe area 413 to perform air exhaust, and after the gap protrusion 4152 is in contact fit with the intermediate member 5, the degree of freedom of the elbow 4 in the inserting and extracting direction can be limited.

Specifically, the height of the clearance projection 4152 is 0.08 to 0.3mm, preferably 0.1 to 0.2 mm.

Further, the width of the rear sipe section 452 is determined by the gap protrusion 4152 and is smaller than the width of the front sipe section 451. The amount of exhaust flow through the exhaust slit 45 between the intermediate piece 5 and the elbow main body 41 is also determined by the clearance projection 4152.

Further, as shown in fig. 10, the second tube area 412 is provided with an exhaust hole 416 for exhausting the breathing waste gas, and the diameter of the exhaust hole 416 is 0.65-0.9mm, preferably 0.70-0.8 mm.

As shown in fig. 12, the second tube area 412 is further provided with a safety valve hole 417 located below the exhaust hole 416, the flow from the ventilator can apply a pushing force to the safety valve plate 42, and the safety valve hole 417 is blocked when the safety valve plate 42 is pushed; when the respirator has a single fault (fig. 19), the safety valve plate 42 is restored under the action of the self elasticity and is in a natural state, and the safety valve hole 417 is opened by the safety valve plate 42 in the natural state so as to prevent asphyxia.

The elbow 4 described in the above embodiments is applied to a ventilator with a mask, and is divided into two states of inhaling and exhaling during normal operation of the ventilator.

Specifically, as shown in fig. 16, in the inspiratory state, air pressure from the ventilator pushes the safety valve 42 up and blocks the safety valve hole 417. The flow from the ventilator is partially delivered to the patient and partially exhausted through exhaust port 416 and exhaust slot 45. Wherein the air flow exiting through the exhaust slots 45 forms a tumbling air flow 341 in front of the patient's mouth and nose.

As shown in fig. 17-18, during an expiratory condition, air pressure from the ventilator pushes the safety flap 42 up and blocks the safety valve aperture 417. When the patient exhales more than the ventilator, as shown in fig. 17, the airflow from the ventilator is entirely exhausted through the exhaust holes 416, and a portion of the patient's exhaled exhaust gases are exhausted through the exhaust holes 416 and another portion are exhausted through the exhaust slits 45, wherein the airflow exhausted through the exhaust slits 45 forms a tumbling airflow 341 in front of the patient's mouth and nose.

When the patient exhales less than the ventilator, as shown in fig. 18, a portion of the flow from the ventilator exits the exhaust holes 416 and another portion of the flow exits the exhaust slots 45 along with the patient's exhaled exhaust gases, wherein the flow exiting through the exhaust slots 45 creates a relative tumble flow 341 in front of the patient's mouth and nose. In the event of a single failure of the ventilator, as shown in fig. 19, the safety valve 42 recovers under its own elastic force and is in a natural state, blocking the ventilator duct and opening the safety valve hole 417. The patient can now breathe through the vent hole 416, vent slit 45 and safety valve hole 417, thereby preventing asphyxia.

The exhaust mask with the elbow 4 has at least the following advantages: when the air flow is exhausted through the exhaust slot 45, a tumble flow 341 is formed at the interface of the elbow 4 and the frame 3. While tumbling stream 341 can entrain a portion of the retained CO₂Thereby reducing the volume of dead space and reducing CO to a certain extent₂Is repeated.

Note that the arrows in fig. 15 to 19 show the flow direction of the air flow.

In other embodiments, as shown in fig. 20-23, elbow 4 is suitable for use in a zero-exhaust mask in a medical environment.

Specifically, the elbow 4 includes an elbow body 41 and an elbow joint 43, one end of the elbow body 41 is connected to the frame 3, the other end of the elbow body 41 is fixedly or integrally connected to the elbow joint 43, and the elbow joint 43 is configured to be connected to an intake conduit of a ventilator. The elbow main body 41 and the elbow joint 43 may be fixedly connected by ultrasonic welding, adhesive, or the like. Additionally, the elbow 4 may also include a safety valve 42 disposed between the elbow body 41 and the elbow fitting 43.

Further, elbow body 41 includes a first tube section 411 for connection to intermediate piece 5 and a second tube section 412 for connection to elbow fitting 43, with an included angle between first tube section 411 and second tube section 412. Elbow main body 41 further includes a stopper tube area 413 connecting first tube area 411 and second tube area 412, respectively, and when first tube area 411 is connected to frame 3, stopper tube area 413 can restrict the degree of freedom of elbow main body 41 in the insertion and removal direction.

As shown in fig. 22 and 23, the first tube region 411 includes at least two deformation regions 411a, and a notch 418 is disposed between adjacent deformation regions 411a, and the notch 418 is used to provide a corresponding space for the deformation regions 411a to be elastically deformed. The deformation zone 411a is elastically deformable when the bent tube 4 is inserted into the frame 3 (or the intermediate piece 5) so as to make the notch 418 smaller and thus enable the first tube zone 411 to be inserted into the intermediate piece 5; when the bent pipe 4 is inserted into the frame 3 (or the intermediate member 5), the deformation region 411a is restored and the notch 418 is enlarged to engage the first pipe region 411 with the frame 3 (or the intermediate member 5).

The utility model discloses quantity to breach 418 and arrange all not inject. In the embodiment shown in fig. 22, the deformation regions 411a may be provided in four.

Preferably, the notches 418 are equally spaced, in other words, the width of the deformation zone 411a is equal, in order to facilitate the machining.

Further, the deformation zone 411a is provided with a catch 414, and specifically, the catch 414 is provided at a circumferential edge outside the deformation zone 411 a. The intermediate piece 5 comprises a stop projection 52 arranged on its inner surface, the stop projection 52 cooperating with the catch 414 to limit the freedom of the pipe bend 4 in the plugging direction. The snaps 414 may be distributed on the outer wall of the deformation zone 411a along a circumferential circumference or a half circumference or a part of the deformation zone 411 a.

The diameter of the circle where the buckle 414 is located is slightly larger than the inner diameter of the hole for accommodating the buckle 414 in the middle piece 5, so when the elbow 4 is connected with the middle piece 5, the deformation area 411a can be elastically deformed, and due to the arrangement of the notch 418, the deformation area 411a has a space for generating elastic deformation, and the diameter of the circle where the buckle 414 is located can be reduced after the deformation area 411 generates elastic deformation, so that the buckle can be smoothly inserted into the middle piece 5, and once the buckle 414 is clamped with the stopping protrusion 52, the deformation area 411a can be restored to a natural state, so that the degree of freedom of the elbow 4 in the plugging direction can be limited through the combined action of the deformation area 411a and the buckle 414.

Further, the first tube region 411 further includes a sealing region 411b connected to the deformation region 411a, and the thickness of the sealing region 411b is greater than that of the deformation region 411a, so that the sealing region 411b forms a sealing connection with the frame 3. The sealing area 411b is in contact fit with the intermediate piece 5 during assembly to limit the rotational freedom of the elbow 4 in the circumferential direction. At the same time, a seal is formed between the elbow 4 and the intermediate piece 5, thereby minimizing the amount of unintended venting between the elbow 4 and the intermediate piece 5.

The second tube section 412 is connected to the elbow fitting 43 and has a relief valve opening 417 disposed therein. The safety valve hole 417 has the effect that when a single failure of the respirator or the blockage of a breathing pipeline occurs, the safety valve plate 42 is restored under the action of the elastic force of the safety valve plate and is in a natural state, the breathing pipeline is blocked, the safety valve hole 417 is opened, and the asphyxia can be prevented.

The elbow 4 described in the above embodiments is applied to a non-exhaust mask.

In particular, when the ventilator is operating normally. Air pressure from the ventilator pushes the safety valve flap 42 up and blocks the safety valve aperture 417. At this time, the patient breathes through the ventilator end or a separate exhaust. When the respirator is in single failure or the breathing pipeline is blocked, the safety valve plate 42 restores the original extension state under the action of the self elastic force and opens the safety valve hole 417. The patient can now breathe through the safety valve aperture 417, preventing asphyxia.

In other embodiments, the elbow 4 is suitable for use in a zero-exhaust mask in a medical environment.

In this embodiment, the elbow 4 includes an elbow body 41 and an elbow joint 43, one end of the elbow body 41 is connected to the frame 3, the other end of the elbow body 41 is fixedly connected or integrally connected to the elbow joint 43, and the elbow joint 43 is used for connecting to an intake conduit of a ventilator. The elbow main body 41 and the elbow joint 43 may be fixedly connected by ultrasonic welding, adhesive, or the like.

Unlike the previous embodiment, the elbow 4 of the present embodiment does not have the vent hole 416 and the safety valve hole 417, so that the elbow 4 of the present embodiment is applied to a non-exhaust mask, and a patient should breathe through a respirator end or a separate exhaust device.

In other embodiments, as shown in fig. 24 and 25, elbow 4 is suitable for use in a zero-exhaust mask in a medical environment.

In this embodiment, elbow body 41 includes a first tube section 411 for connection to intermediate piece 5 and a second tube section 412 for connection to elbow fitting 43, with an included angle between first tube section 411 and second tube section 412. And the first tube region 411 and the second tube region 412 are integrally formed.

Therefore, unlike the previous embodiments, the limiting tube area 413 is not provided in the present embodiment.

The first tube region 411 includes a deformation region 411a and a sealing region 411 b. The deformation area 411a can deform when the elbow 4 is inserted into or pulled out of the frame 3. In addition, the deformation area 411a may further include a catch 414 and a notch 418. The arrangement of the latch 414 and the notch 418 can refer to the previous embodiments, and will not be described herein.

The second tube section 412 is operatively connected to a ventilator circuit. Since the limiting tube area 413 is not provided in the present embodiment, the degree of freedom of the elbow 4 in the inserting and extracting direction can be limited by the top of the second tube area 412 and the buckle 414.

In other embodiments, as shown in fig. 3b and fig. 26-36, the elbow 4 is suitable for use in a non-exhaust mask in a medical environment.

Unlike the previous embodiments, the elbow 4 of the present embodiment is capable of being inserted into a medical tube (e.g., an endoscopic tube, a feeding tube, etc.).

Specifically, the elbow 4 is provided with a connector for connecting with a medical tube. The medical tube can be extended into the elbow 4 through the interface to treat the patient without removing the breathing mask.

Elbow 4 includes elbow body 41 and the interface includes a cannula block 44. The cannula block 44 may be made of a relatively soft material, such as silicone or rubber. In addition, the cannula block 44 may be integrated with the elbow body 41 by a secondary encapsulation or assembly.

Preferably, the cannula block 44 is made of silicone material and is assembled with the elbow body 41. In use, a medical tube can be inserted through the cannula block 44 without cross-sectional mask treatment.

28-30, elbow body 41 includes first and second tube sections 411, 412 for connection to intermediate member 5, with the first and second tube sections 411, 412 forming an angle therebetween.

The first tube region 411 includes at least two deformation regions 411a, and a gap 418 is disposed between adjacent deformation regions 411a, and the gap 418 is used to provide a corresponding space for the deformation regions 411a to elastically deform. The deformation zone 411a is elastically deformable when the bent tube 4 is inserted into the frame 3 (or the intermediate piece 5) so as to make the notch 418 smaller and thus enable the first tube zone 411 to be inserted into the intermediate piece 5; when the bent pipe 4 is inserted into the frame 3 (or the intermediate member 5), the deformation region 411a is restored and the notch 418 is enlarged to engage the first pipe region 411 with the frame 3 (or the intermediate member 5).

The utility model discloses quantity to breach 418 and arrange all not inject. In the embodiment shown in fig. 28, the deformation regions 411a may be provided in four.

Preferably, the notches 418 are equally spaced, in other words, the width of the deformation zone 411a is equal, in order to facilitate the machining.

Further, the deformation zone 411a is provided with a catch 414, and specifically, the catch 414 is provided at a circumferential edge outside the deformation zone 411 a. The intermediate piece 5 comprises a stop projection 52 arranged on its inner surface, the stop projection 52 cooperating with the catch 414 to limit the freedom of the pipe bend 4 in the plugging direction. The snaps 414 may be distributed on the outer wall of the deformation zone 411a along a circumferential circumference or a half circumference or a part of the deformation zone 411 a.

The diameter of the circle where the buckle 414 is located is slightly larger than the inner diameter of the hole for accommodating the buckle 414 in the middle piece 5, so that when the elbow 4 is connected with the middle piece 5, the deformation area 411a is elastically deformed, and due to the arrangement of the notch 418, the deformation area 411a has a space for generating elastic deformation, and the diameter of the circle where the buckle 414 is located is reduced after the deformation area 411 generates elastic deformation, so that the elbow can be smoothly inserted into the middle piece 5, and once the buckle 414 is clamped with the stopping protrusion 52, the deformation area 411a is restored to a natural state, so that the elbow 4 can be smoothly inserted into or pulled out of the middle piece 5 through the combined action of the deformation area 411a and the buckle 414.

28-30, an intubation block interface 419 is provided in the second tube section 412 for receiving the intubation block 44. Cannula block interface 419 may be a hole in second tube section 412 to facilitate mounting and securing cannula block 44. Cannula block interface 419 may be configured in any shape, such as circular, oval, or square.

Cannula block interface 419 includes a second detent protrusion 419a and a catch 419 b. Here, the second rotation stop protrusion 419a may be provided at any position of the peripheral edge of the cannula block interface 419 and protrudes in the axial direction thereof, which functions to restrict the rotational freedom of the cannula block 44 while indicating the mounting direction of the cannula block 44.

The gripping edge 419b is a ring or partial protrusion around the circumference of the cannula block interface 419, whereby the gripping edge 419b defines the smallest aperture size of the cannula block interface 419. Therefore, the clamping edge 419b functions to limit the degree of freedom of the cannula block 44 in the opening direction, so that the cannula block 44 is not easily pulled off when the medical tube is inserted into the elbow main body 41.

Further, when cannula block 44 is installed in cannula block interface 419, the outside surface of cannula block 44 is flush with the outside surface of elbow 4. To accomplish this, cannula block 44 is shaped to conform to cannula block interface 419. Specifically, as shown in fig. 31-34, the cannula block 44 includes an inner sheet 441 and an outer sheet 442 disposed in an inside-out sequence. The curvature of the inner and outer sheets 441, 442 conforms to the curvature of the mounting surface of the elbow body 41. Understandably, the consistent curvature of the cannula block 44 and the elbow body 41 allows for a perfect fit between the two, thereby providing no cosmetic differences and/or obtrusiveness.

Further, as shown in FIGS. 31-34, a seal slot 445 is provided between the inner sheet 441 and the outer sheet 442, the seal slot 445 configured to mate with the bead 419b of the elbow body 41 during assembly. The outer sheet 442 is also provided with a detent 443, and the detent 443 is configured to engage the second detent protrusion 419a of the elbow body 41 during assembly.

The cannula block 44 is provided with a cannula hole 444 in a central region thereof, the cannula hole 444 sequentially penetrating the inner sheet 441 and the outer sheet 442, and different sizes of the cannula hole 444 may be provided according to the type of medical tubing to be inserted. Typically, the cannula bore 444 has a 6-10mm diameter.

Furthermore, the cannula hole 444 is provided with a sealing unit, and the sealing unit is used for realizing free insertion of the medical tube and playing a role in sealing when the medical tube is inserted, so that the unexpected air leakage is reduced.

Specifically, the sealing unit includes a sealing thin region 447, a sealing thick region 446, and a sealing slit 448 opened on the sealing thin region 447. The seal thick region 446 is a thicker seal region for connecting the seal thin region 447 and the cannula bore 444 and supporting and securing the seal thin region 447.

The thin sealing region 447 has a thickness of between 0.1 and 1.0mm, preferably between 0.2 and 0.6 mm.

The sealing slit 448 may be configured in a "straight" shape, a "meter" shape, an "S" shape, a "mouth" shape, or the like. In view of the process shaping and sealing effect, it is preferable that the sealing slit 448 is configured as an "S" type sealing slit.

The width of the sealing slit 448 may be 0.1-2.0mm, preferably 0.4-0.8 mm.

As shown in FIGS. 35 and 36, during assembly, the retaining edge 419b of the elbow body 41 is inserted into the sealing retaining groove 445 of the cannula block 44, and the second rotation stop protrusion 419a of the elbow body 41 is inserted into the rotation stop groove 443 of the cannula block 44, so that the elbow body 41 and the cannula block 44 are stably assembled, and the medical tube can be inserted along the cannula hole 444.

Further, the plane of the thin sealing region 447 of the cannula block 44 determines the orientation of the cannula bore 444. The included angle beta between the medical tube and the bent tube along the plugging direction determines the smoothness of the medical tube when the medical tube is plugged. Typically, the included angle β is greater than or equal to 45 °.

As shown in fig. 37, the definition of the above direction in the present invention is as follows:

the outer plane of the frame 3 at the matching position with the bent pipe 4 is a reference plane alpha, and the direction vertical to the reference plane alpha is the plugging and unplugging direction of the bent pipe 4; the direction parallel to the reference plane α is a circumferential direction (or may also be referred to as a radial direction).

In addition, the utility model also provides a treatment of ventilating equipment, and it includes foretell respirator, and respirator and equipment such as breathing machine link to each other.

While the invention has been described with reference to a preferred embodiment, various modifications may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In particular, the technical features mentioned in the embodiments can be combined in any way as long as there is no structural conflict. The present invention is not limited to the particular embodiments disclosed herein, but encompasses all technical solutions falling within the scope of the claims.

Claims (11)

1. A respiratory mask comprising a frame (3), a cushion (2), an elbow (4) and a headgear assembly; characterized in that the gasket (2) is arranged on the frame (3) and forms an air-through cavity with the frame (3); the headgear assembly being connected to the frame (3) to secure the cushion (2) and the frame (3) to the head of the patient; the elbow (4) is rotatably arranged on the frame (3), an interface is arranged on the elbow (4), the interface comprises a cannula block (44) fixedly connected or integrally connected with the elbow (4), the cannula block (44) is used for being connected with a medical pipeline,

wherein the stiffness of the cannula block (44) is less than the stiffness of the elbow (4).

2. The respiratory mask of claim 1, wherein the cannula block (44) is made of a flexible material.

3. The respiratory mask of claim 2, wherein the flexible material is a silicone material.

4. A breathing mask according to claim 3, wherein the cannula block (44) is provided with a cannula hole (444), the cannula hole (444) is provided with a sealing unit, and the medical tubing extends into the elbow (4) via the sealing unit.

5. The respiratory mask according to claim 4, wherein the sealing unit comprises a sealing thick region (446) provided on a wall of the cannula hole (444), a sealing thin region (447) connected to the sealing thick region (446), and a sealing slit (448) provided on the sealing thin region (447), the medical tubing being extendable into the elbow (4) via the sealing slit (448).

6. A facial mask according to claim 5, wherein the sealing slit (448) is configured as a line, meter, S or mouth slit.

7. A facial mask according to claim 5 or 6, wherein the sealing slit (448) has a slit width of 0.1-2.0 mm.

8. The respiratory mask according to claim 4, wherein an intubation block interface (419) for accommodating the intubation block (44) is further disposed on the elbow (4), the intubation block (44) includes an inner sheet layer (441) and an outer sheet layer (442) which are sequentially disposed from inside to outside, a clamping groove (445) is disposed between the inner sheet layer (441) and the outer sheet layer (442), a clamping edge (419b) is disposed on an inner wall of the intubation block interface (419) along a circumferential direction, and the clamping groove (445) is clamped with the clamping edge (419b) to limit a degree of freedom of the intubation block (44) along an opening direction.

9. The respiratory mask of claim 8, wherein the cannula block interface (419) further comprises a rotation stop protrusion (419a) disposed at a circumferential edge of the cannula block interface (419), wherein the outer sheet (442) is provided with a rotation stop groove (443), and wherein the rotation stop protrusion (419a) engages with the rotation stop groove (443) to limit a rotational degree of freedom of the cannula block (44).

10. The respiratory mask of claim 2, wherein the elbow (4) comprises an elbow body (41), the elbow body (41) comprising a first tube region (411) and a second tube region (412) disposed at an included angle, the first tube region (411) being connected to the frame (3), the cannula block (44) being disposed on the second tube region (412).

11. A ventilation therapy device comprising a respiratory mask as claimed in any one of claims 1 to 10.

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