The present invention relates to a nasal flushing catheter, and more particularly to an innovative nasal flushing catheter for cleaning the mucus and crust deeply within the nasal cavity and nasopharynx to improve the symptoms of chronic sinusitis.
Despite not life-threatening, the chronic sinusitis by the diagnostic criteria of symptoms lasting more than 12 weeks is a troubling disease. Currently, there is no cure for the disease. The main symptoms of nasal obstruction, foreign body sensation in the throat and cough would bother the patient relentlessly and may even lasting life-long. Antibiotics are only used for control of acute infection, and surgical operation is a method to remove the obstruction or to restore the patency of sinus orifice to prevent acute episode of sinusitis. No matter what the treatment is taken, the disease remains unchanged, and the symptoms persist. Hence, the otolaryngologists recommend long-term home-remedy of nasal flushing treatment at least twice a day.
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The nasal secretions can be understood through a cold process. Running nose occurs in the early stage. The nasal discharge at this stage is a kind of clear liquid without mucus and can be completely evaporated. Afterwards, the discharge becomes tenacious and difficult to expel which is called mucus. Then, the secretion becomes jelly-like scab, and finally solid booger (crust). The mucus, scab and crust are the three states of mucus. The symptoms of chronic sinusitis are due to accumulation of these three patterns of mucus within the nasal cavity body. The symptoms of common cold rarely last more than 4 weeks, while the symptoms of chronic sinusitis persist much longer. Only chronic sinusitis has symptoms persisting more than 12 weeks, therefore, can be used as a diagnostic criteria. If no other obstructive causes such as polyps or tumors present, the diagnosis can be confirmed. The allergic rhinitis or hay fever so on may also present with severe nasal obstruction persisting from a long time, but is always accompanied by a lot of watery nasal discharge and absence of foreign body sensation in the throat. As long as the allergen disappears, the symptoms disappear. In addition, allergic rhinitis is a periodic and seasonal disease, while chronic sinusitis is a life-long persisting disease.
The so called nasal obstruction is a sense of exertion effect on respiration due to blockage of nasal passage. Because the nasal passage is composed of front to back slit like spaces, significant area reduction of these spaces at any coronal plane of nasal cavity may cause nasal obstruction. In the early period of chronic sinusitis, the mucus secreted into nasal cavity from sinuses, does not cause significant area reduction of nasal passage. Due to its stickiness, the slow migration of mucus by gravity precludes the appreciation of its presence. Hence, the patient would not consciously expel it out. The mucus migrates by gravity to form a thin layer onto the turbinate. Because the respiratory air is not block in this area, the mucus in thin layer is quickly dried by the respiratory air to become even much thinner crust coating on the turbinate. Repeated coating of the crust results in gradual enlargement of turbinates until the severe narrowing of nasal passage. Meanwhile due to the aerodynamics, the configuration of the turbinate is retained and may be difficult to distinguish from as that caused by mucosal swelling in allergic rhinitis. The situation progresses until significant nasal obstruction forces the patient to seek medical treatment. At this time, the nasal passages become narrow, even the viscosity of mucus remains unchanged, it is more difficult to expel due to increased relative viscosity, and finally it causes complete obstruction beginning from the upper part of nasal cavity. This is so called insidious onset of symptoms. The mucus continuously discharges from the opening of the upper nasal meatus and the middle nasal meatus, and spreads from the top to down. This causes a suspended conglomerated mass on the upper part of nasal cavity while the lower part of nasal cavity remains more patent. The downstream of mucus still contacts with the respiratory air, and becomes the hardest crust state (shown in
The interchange of mucus, jelly-like scab and solid booger (crust) can be observed in in-vitro experiments. The mucus exposed in the air will become jelly-like scab, and the jelly-like scab will become solid booger. The volume may shrink more than 10 times from liquid mucus to solid booger. The duration depends on the degree of humidity and the air circulation. Conversely, if the solid booger is soaked in the water for one hour, it will become half-solid scab, and then it gradually becomes mucus. This is the rational of nasal flushing treatment for chronic sinusitis and all medical experts recommend conventional nasal flushing device for this treatment. However, some of our family members and our friends with chronic sinusitis followed the instruction of medical expert using conventional nasal flushing device, the symptom improvement was very limit initially and gave up quickly due to unsatisfactory therapeutic effect.
All conventional nasal flushing devices are similar in basic structures. Please refer
The fundamental problem of conventional nasal flushing devices is its direction of spouts. These devices can only produce frontal back single directional spouts by a big nozzle placed in nasal vestibule. Although this single directional spouts can rinse the whole nasal cavity in normal person, this spouts can only pass through the wide and non-obstructed inferior meatus to nasopharynx but cannot reach the narrow and obstructed middle and superior meatus in severe cases of chronic sinusitis. These narrow and obstructed areas can only be rinse effectively by multi-directional spouts perpendicular to the nasal passage by a catheter placed in middle and superior nasal meatus. Therefore we filed a patent application as following.
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We first collected a lot of mucus to paste on many plastic plates and left the mucus dried to become solid crust. These plastic plates were kept in upright position to avoid fluid stasis for simulating the nasal meatus in flushing condition. The crust areas of the plastic plates were flushed by 3 different strength spouts and variable angles related to the up-right plastic plate. The strength of the spouts was classified as following: 1. Low pressure spouts under 45 cm vertical height; 2. Medium pressure spouts between 45 to 90 cm vertical height and 3. High pressure spouts over 90 cm vertical height. The relationship between strength as well as angle of spouts and the fluidity of crust after flushing were observed as following: 1. the stronger the spout, the better fluidity of crust after flushing, 2. vertical angle spout has the best flushing effect. The results of this experiment can explain the unsatisfactory effect of the prior nasal flushing catheter as following. Since the nasal cavity is a slit like air passage, when the catheter is too large and can only be placed at the inferior wide portion of middle nasal meatus or the para-septal space, only the spouts parallel and aligned to the slit can pass through the slit, but they are parallel spouts related to the slit, therefore the crust has to be penetrated is the depth of the slit measured in centimeter range which may require strong spouts to achieve the purpose; but if the catheter is small enough to be placed at the deep narrow recess of middle and superior nasal meatus, the crust at this target area can be rinsed directly by vertical spouts and the crust has to be penetrated is the thickness of crust measured in millimeter range, this only require weak spouts. Centimeter and millimeter is a huge difference around 10 times. The 30 cm spouts by the prior nasal flushing catheter placed at inferior wide portion of nasal meatus or middle para-septal space D2 is obviously inadequate to effectively rinse the deep narrow recesses of nasal meatus illuminated by the above experiment. Further, when the parallel spout entering the narrow slit space, the crust within this space can absorb the water to expand its volume causing more severe nasal obstruction; this explains why 30 cm spouts are not completely satisfactory in nasal flushing treatment.
These are the fundamental problems of our prior nasal flushing catheter. The resolutions are 1. To increase the strength of spouts without increasing the outer diameter of catheter, and 2. To make better controllability of small catheter.
On the priority date of the present patent application (Oct. 14, 2015), the prior nasal flushing catheter has not been patented and not commercialized. All medical experts in the world by then still recommended conventional nasal flushing device for nasal flushing treatment (chronic sinusitis-Medscape reference; chronic sinusitis-Mayo Clinic) and the Sinus Rinse of NeilMed pharmaceutical INC. was a favorite conventional nasal flushing device in the United States of America. Because the prior nasal flushing catheter was only a document among the vast if not indefinite data of patent applications in the whole world, no-body paid attention to this document and the advantage of the prior nasal flushing catheter could not be appreciated. Since the catheter was not commercialized and its advantage was not appreciated, it was impossible to try this catheter to find its disadvantage. Therefore, the fundamental problems of the prior nasal flushing catheter was impossible to be discovered by any other person, not mention to conceive these solutions, we therefore file this patent application.
Therefore, the purpose of the present invention is to provide a better flushing catheter having stronger spouts and/or better controllability for entering the narrow crooked nasal passages.
The flushing catheter includes a catheter body and a connector formed outside of the catheter body. The said catheter body is made of silicone, latex, thermoplastic elastomer or other soft and elastic materials, therefore can be operated by patient to place into the nasal cavity and nasopharynx. The catheter body has a closed end, an open end on the opposite side. Multiple side-holes are made near the closed end of the catheter body.
Another technique of an embodiment of the present invention is that the catheter body is not larger than 1.0 mm in outer diameter.
Another technique of an embodiment of the present invention is that the catheter body is not larger than 1.0 mm in outer diameter. The side-holes are linear in shape and parallel to the catheter body.
Another technique of an embodiment of the present invention is that the flushing catheter further includes a tapered end metallic stylet undergone anticorrosive treatment providing within the lumen of the nasal flushing catheter.
Another technique of an embodiment of the present invention is that the flushing catheter further includes multiple different length and uniform diameter metallic stylets undergone anticorrosive treatment providing within the lumen of the nasal flushing catheter.
Another technique of an embodiment of the present invention is that the stylets are made of tungsten alloy undergone anticorrosive treatment with diameter not larger than 0.1 mm.
Another technique of an embodiment of the present invention is that the total area of multiple side-holes on the catheter body is between 3.367 mm2˜4.123 mm2 in range.
Another technique of an embodiment of the present invention is that the total area of multiple side-holes on the catheter body is between 2.381 mm2˜3.367 mm2 in range.
Another technique of an embodiment of the present invention is that the total area of multiple side-holes on the catheter body is smaller than 2.381 mm2.
Another technique of an embodiment of the present invention is that the plurality of side-holes is more densely distributed when closer to the closed end.
The advantages of this invention are to improve the efficiency and efficacy of nasal flushing treatment by optimal strength of spouts and to improve the controllability of the small and soft catheter by the stylet inside the catheter, and by the design of the connector and total area of side-holes, the stronger thin spouts can be produced.
For the examiners to clearly understand the technical features and the content of the present invention, the present invention is hereinafter described in details with the accompanying drawings and the expression in the form of two preferred embodiments. In addition, prior to the detailed description, it should be noted that same or similar reference numerals are used to designate the same or similar elements.
The relevant features and the technical fields of the present invention will be illuminated by the description of the preferred embodiments as well as the accompanying drawings.
Please refer to
In the first preferred embodiment, the nasal flushing catheter 6 includes a catheter body 61, and a connector 62 formed outside of the catheter body 61. The said catheter body 61 is made of silicone, latex, thermoplastic elastomers or other soft and elastic material which can be operated by patient to put into the nasal cavity and nasopharynx. The catheter body 61 has a closed end 611 and an open end 612 on the opposite side of the closed end 611. A plurality of side-holes 613 is circumferentially distributed in a segment near the closed called flushing section 610. The plurality of the said plurality of side-holes 613 may be evenly distributed or denser distribution closer to the closed end 611 (as shown in
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The following is the detailed description about the manufacture of catheter, the relationship between the side-holes and the height of the vertical spout, the manufacture of side-holes as well as their arrangement, the relationship between the catheter and the side-holes, the design of stylet, the connector, the selection of the syringe, the actual operation, and the improvement of the therapeutic effect for nasal flushing catheter 6 of the present invention.
The Manufacture of Catheter
The said catheter body 61 is made of silicone, latex, thermoplastic elastomer or other soft and elastic materials. The said catheter body 61 has a closed end 611, an open end 612 on the opposite side of the closed end 611, and a flushing section 610 near the closed end having a plurality of side-holes 613 disposed circumferentially. The widest inferior nasal meatus H1 and the inferior para-septal space 13 of the nasal cavity, are not wider than 4 mm in normal person, and may be 2.5 mm or even narrower than 1.5 mm in patients with chronic sinusitis. The narrowest superior nasal meatus, is usually not wider than 1.5 mm in normal person, and even narrower than 1 mm in patients with chronic sinusitis. Therefore, the outer diameter of the catheter of the present invention is not larger than 4 mm, and preferably, between 0.5˜2.5 mm. A catheter with outer diameter less than 1.0 mm is called a micro-catheter. A micro-catheter may have 0.6 mm or even 0.3 mm inner diameter. Because micro-catheter may be easy to burst during flushing action, an additional small end-hole may reduce the possibility of such risk. The wall thickness of catheter is less than 1 mm, and preferably between 0.1˜0.6 mm.
The Relationship Between the Side-Holes and the Height of the Vertical Spout
The average initial velocity (V0) of side-holes 613 spout can determine the average vertical height h. The equations can be deducted as followings: V0=gt or t=V0/g, wherein, g is the gravitational constant 9.8 m/sec2, t is the time reaching the vertical apex. The maximum vertical apex h, can be determined by the equation h=1/2(gt2), plugging t=V0/g, and h=1/2(g)(V0/g)2=V02/2g or V02=2gh; furthermore, the average initial velocity (V0) of side-holes 613 spout can be determined by the injection rate (IR) and the total area of side-holes (TA), the equation is as following: V0=IR/TA, when applies to the function V02=2gh, and then will get (IR/TA)2=2gh, or TA2=IR2/2gh, or TA=√{square root over (IR2/2gh)}. Even the 10 cc, 20 cc, 50 cc, 60 cc, and 100 cc syringes 7 are all available easily, for considering the operability and avoiding choking phenomenon by large flow of water, the 10 cc syringe 7 may be the best choice. Hence, the 10 cc syringe 7 was chosen as a standard syringe of the present invention. Manual injection of a 10 cc syringe may reach a injection rate (IR) from 5 cc/sec to 15 cc/sec, hence, the medium value of 10 cc/sec is chosen as the standard injection rate. Under this standard injection rate, spout of 30 cm can be expected by side-holes 613 with total area TA=√{square root over (100/(2×9.8 m×0.3 m))}=4.123 mm2; similarly, spout of 45 cm can be expected by side-holes 613 with total area TA=√{square root over (100/(2×9.8 m×0.45 m))}=3.367 mm2 and spout of 90 cm can be expected by side-holes 613 with total area TA=√{square root over (100/(2×9.8 m×0.9 m))}=2.381 mm2. In conclusion, a catheter with a total area of side-holes 613 between 3.367 mm2˜4.123 mm2 to produce 30˜45 cm low pressure spouts is called a low pressure catheter; a catheter with a total area of side-holes 613 between 2.381 mm2˜3.367 mm2 to produce 45˜90 cm medium pressure spouts is called a medium pressure catheter; a catheter with less than 2.381 mm2 total area side-holes 613 to produce over 90 cm high pressure spouts is called a high pressure catheter. Due to the prior invention can already eject 30 cm spouts, the low pressure spout is defined as 30˜45 cm.
The Manufacture and Arrangement of Side-Holes
The said side-holes 613 can be produced by traditional method of removing a part of the catheter wall, and can also be produced by puncturing method using a solid metallic needle with a conical tip. The size of side-holes is between 0.1 mm and 1 mm, and preferably between 0.2 mm and 0.5 mm. The number of 0.5 mm diameter side-holes can be made from 4.123 mm2 total area is 4.123 mm2÷0.5 mm÷0.5 mm÷0.785=21 the number of 0.3 mm side-holes is 58 and the number of 0.2 mm side-holes is 131. The number of 0.5 mm diameter side-holes can be made from 3.367 mm2 total area is 3.367 mm2÷0.5 mm÷0.5 mm÷0.785=17 the number of 0.3 mm side-holes is 47 and the number of 0.2 mm side-holes is 107. The number of 0.5 mm diameter side-holes can be made from 2.381 mm2 total area is 12, the number of 0.3 mm side-holes is 33 and the number of 0.2 mm side-holes is 75.
During forceful injection, the closer to the closed end it is, the higher the intraluminal pressure is. Therefore, the side-holes 613 are designed to be more densely disposed near the closed end 611 (as shown in
The Relationship Between the Catheter and the Side-Holes
The height of spout can be determined by the injection rate (IR) and the total area of side-holes (TA), but only when the catheter can endure high pressure. Because of nasal cavity size, the catheter cannot expand unlimitedly, and the height of spout cannot either. Therefore, the height of high pressure spouts is defined as above 90 cm. Under a given outer diameter of the catheter body 61, the thinner the wall of the catheter is, the larger the inner diameter is and the lower the resistance on forceful injection, but easier to cause elastic fatigue. The said elastic fatigue will cause dilatation of the side-holes, increasing the total area of side-holes 613 and reducing the strength of spouts. However, the thicker wall and the smaller inner diameter of the catheter may cause smaller flow rate and greater resistance, which is not good for forceful injection to eject strong spouts. Therefore, the wall thickness and the inner diameter must be balanced. Although the stronger spouts may be more effective, however, stronger spouts may cause tingling sensation, and is also accompanied with smaller total area resulting in smaller number of side-holes that only smaller area can be cover during the flushing action, in other words, it is less efficient. Therefore if the symptoms are not so bad, the mucus is not so sticky and the solid crust is not so much, then the medium pressure or low pressure spouts may be enough to improve the symptoms. Besides, the area of side-holes for medium pressure or low pressure catheter is larger, the resulting larger number of side-holes can be disposed longer on the catheter to cover a larger area during flushing action, in other word, medium pressure or low pressure catheter is less effective but more efficient. Therefore, the three kinds of catheters have their definite indication, and no one shall be given up.
The Design of Stylet
A catheter with larger outer diameter and thicker wall has better controllability. However, a catheter should be smaller than the narrowest part of the insertion route to the target area of nasal cavity, a catheter smaller than 2 mm or even 1.0 mm in outer diameter may be difficult to operation and advancement. In addition to the hardness of the catheter, a gradual transition from hard to soft toward the distal close-end is necessary for excellent controllability. An easy solution to this problem is to put metallic stylet within the lumen of catheter. The metallic stylet should be undergone anticorrosive treatment. The metallic stylet 8 may be single in number having a tapered end or multiple in number with uniform diameter and different in length (as shown in
The Connector
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The Selection of the Syringe
Even the 20 cc, 30 cc, and 60 cc syringes 7 are all available, they are not easy to operate due to their large size; therefore, a 10 cc syringe is the choice. However, the syringes 7 must be adjusted according the diameter of the catheter body 61. A catheter body 61 over 2 mm in outer diameter may use 10 cc syringe 7; a catheter body 61 with 1.5˜2 mm outer diameter may use 5˜10 cc syringe 7; a catheter body 61 having 1˜1.5 mm outer diameter may use 1˜5 cc syringe 7; A micro-catheter with less than 1 mm in outer diameter may use 1˜2 cc syringe 7 in order to avoid bursting of the catheter.
The Actual Operation
The handmade catheter of the prior nasal flushing catheter had been tried by our family members and close friends before filing the present invention for more than 2 years, meanwhile, the catheter of the present invention has also been tried for more than one year, hence, we have a lot of experiences and are familiar with all details of flushing treatment. Although the computed tomography can objectively assess the efficacy, the subjective assessment by the patient is more important. There are two issues for assessing the therapeutic effect: one is the amount of mucus wash out during or after flushing, the more the amount of mucus the better it is; the other is subjective feeling of symptom improvement, such as the severity of nasal obstruction, foreign body sensation in the throat and cough, of course these symptoms related to quality of sleep and daytime activity. Both of them have to be considered. If a patient using the catheter of the prior invention (
If the result of computed tomography is like
If the result of computed tomography is like
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From the above description, a patient can choose a catheter as needed. Due to the presence of the stylet 8, the nasal flushing catheter has better controllability and is easy to enter the superior nasal meatus F1, middle nasal meatus G1, lower nasal meatus H1 and the nasopharynx J to clean mucus and solid crust.
From the above detailed description of the embodiments, it can be known that the nasal flushing catheter of the present invention has the following effects:
1. It is possible to flush the narrow nasal passages directly by a micro-catheter which is easy to be operated.
2. Due to the improvement of the connector 62, a catheter can eject stronger spouts to improving cleansing effect without increasing the diameter.
3. The strength of the spouts can be predicted by the total area of side-holes 613, so that the stronger the spout, the better the effect.
4. Through the controllability of the catheter, the position of the catheter body 61 can be adjusted in the nasopharynx J, thus strong spouts can be ejected to clean the mucus and solid crust within the nasopharynx J.
The nasal flushing catheter of the present invention can overcome the disadvantages of the prior nasal flushing device by better controllability to achieved deep insertion to small deep recess of the nasal cavity and by stronger spouts to penetrate solid crust. This is very important in improving the symptoms of patients with chronic sinusitis. Meanwhile, it is also convenient for the patient in travelling.
The above descriptions are only explanations according to the five preferred embodiments, and should not limit the scope the present invention. It is to be understood that many other possible modifications and variations can be made without departing from the spirit and scope of the invention as hereinafter claimed.
Filing Document | Filing Date | Country | Kind |
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PCT/CN2015/091911 | 10/14/2015 | WO | 00 |