The present invention is concerned with alternative catheter arrangements for use in a variety of medical applications. Specifically, but not exclusively, the catheters described herein may be used in urethral catheterisation, surgical drainage and in stomach decompression tubes and enteral (gastric and small intestine) feeding tubes.
An example of the use of catheters is where patients' micturition (urination) can be problematic. We consider briefly the use of urethral catheters as one example of the importance of catheters in general. Their use may be for various reasons including patient age, patients being infirm or because of patients suffering post-operative complications. In such situations the patient may have lost, or have limited ability to control micturition (passage of urine). Some male patients may have simple obstruction to the bladder, caused by enlargement of the prostate and may be too ill or frail to undergo surgery.
In general, the majority of patients requiring urethral catheterisation will have some failure of the function of the bladder or of its control mechanisms and the procedure is of increasing relevance as the population in the western world ages. The bladder is a muscular organ and, as the muscle of this organ weakens with age, the ability of the bladder to contract and thus empty satisfactorily, is lost. A small number of patients are incontinent due to the muscular valves that control micturition ceasing to function and bladder catheterisation is the treatment of last resort. Elderly demented patients may also present with incontinence and this may be due to lack of cognitive function rather than dysfunction of the lower urinary tract but all require urethral catheterisation.
Current solutions to these situations may include the insertion along the urinary passage into the bladder of either a temporary intermittent catheter or an in-dwelling catheter that will remain in place for a number of weeks. The bladder can then be drained through the catheter and out of the body. These solutions are simple to use and are reliable by virtue of the simplicity of design.
However, although simple to use and reliable in operation, existing urethral catheters present their own drawbacks and complications. These include blockages and bladder inflammation with the latter usually associated with Catheter Associated Urinary Tract Infection. (CAUTI).
Blockages occur for a number of reasons. For example, the lining of the bladder can occlude the drainage port in the catheter dependent on its position relative to the wall within the bladder. Another complication occurs when the bladder wall becomes irritated by the presence of the catheter and the response of the glands in the bladder wall is to become inflamed and produce mucus which then blocks the drainage port of the urethral catheter. This is particularly the case for in-dwelling catheters i.e. catheters that are in-situ for longer periods of time. Separately, blockages within the bladder can be caused by post-operative blood clots resulting from prostate surgery or tumour surgery in the bladder that has resulted in a raw area that bleeds.
In summary, although existing urethral catheters are simple to use, they do present complications that frequently require the catheter to be removed and replaced. Disadvantageously this thereby consumes important clinician time, causes distress to the patient further increases the risk of CAUTI, and importantly increases overall costs.
The Applicant has devised an alternative approach to catheterisation and specifically a catheter design that advantageously addresses a number of the drawbacks of existing catheter technology. Furthermore, the Applicant has devised a design that can advantageously be used not just to address complications with urethral catheters but also to address complications with surgical drainage, gastric decompression and naso-gastric and naso-intestinal enteral feeding. The novel and inventive approach to catheter design is not limited to catheters for human use; the approach may equally be applied in these areas for veterinary procedures.
Aspects of the invention are set out in the accompanying claims.
Viewed from a first aspect of an invention described herein there is provided, a catheter comprising an elongate generally cylindrical body and a catheter tip for insertion into a human or animal, the elongate generally cylindrical body comprising a first fluid ingress lumen and a second fluid egress lumen for communicating fluid along the elongate generally cylindrical body to and from the catheter tip, wherein the catheter tip comprises a first portion integral with the elongate generally cylindrical body, a second portion distal to the first portion and defining the distal end of the catheter and an intermediate fluid ingress/egress region located between the first and second portions, wherein the intermediate fluid ingress/egress region is in the form of an open section of the elongate cylindrical body exposing the first and second lumens to allow for fluid communication; the catheter tip further comprising a base portion extending between the first and second catheter tip portions; and wherein the fluid ingress lumen extends through a predetermined length of the base portion and is arranged in use to discharge fluid from an outlet port to direct fluid away from the base portion and into the intermediate fluid ingress/egress region.
Thus, an alternative catheter geometry is provided that causes fluid to flow into and out of the bladder in such a way that blockages or occlusion of outlet passages can be avoided. Further advantages are described herein.
Specifically the open nature of the intermediate ingress/egress region (also called the aspiration port) provides a volume or zone in which irrigation fluid can mix with surrounding urine and pass to the egress port. Advantageously, the way in which the outlet port is geometrically configured prevents a mucosa or similar from coming into close contact with the catheter proximate to an outlet and blocking the catheter in use.
The intermediate fluid ingress/egress region may be in the form of a generally concave recess in the cylindrical body extending towards the base, the recess defining an upper opening relative to the base which intersects with the lumens to allow fluid flow to and from the lumens. Such a recess may be conveniently moulded for example in a material suitable for use in a body.
In such an arrangement the recess may advantageously intersect with the base and first and second catheter tip portions to define a smooth and continuous surface profile. This facilitates smooth fluid flow and prevents trauma caused by the catheter contracting the muscosa or vein wall, for example. It also prevents fluid turbulence.
At least a portion of the intermediate fluid ingress/egress region may extend more than 180 degrees around the circumference of the cylindrical body. Such an angle advantageously provides sufficient structural material strength to the distal end of the catheter whilst providing the recess described above and herein. For example, at least a portion of the intermediate fluid ingress/egress region may extend between 180 degrees and 190 degrees around the circumference of the cylindrical body.
The fluid egress lumen may be coaxial with the elongate generally cylindrical body and intersect with the intermediate fluid ingress/egress region to allow fluid flow therefrom. Such a configuration facilitates fluid flow, allows the geometry to be conveniently manufactured and allows a minimal overall diameter of catheter to be achieved. Alternatively it allows a large cross-section of lumen for a given cross-sectional area.
The fluid ingress lumen may extend along the elongate generally cylindrical body and intersect with the intermediate fluid ingress/egress region from the base portion to allow fluid flow substantially perpendicularly therefrom. Thus, fluid entering the intermediate region or zone has a component of movement away from the catheter in a direction that advantageously intersects with tissue, such as mucosa or vein walls that may be proximate thereto. Thus, a hydraulic pressure and thus force can be applied to maintain the space between the mucosa and the ingress and egress ports. Fluid may advantageously be arranged to flow from an outlet of the fluid ingress lumen so as to flow away from the inlet to the egress lumen.
Viewed in cross-section, the intermediate fluid ingress/egress region may advantageously have a smooth generally U shaped, ‘bowl’ shape or ‘concave’ profile. Thus a space or void can be created by the fluid flow, allowing urine or other fluid to be drained to pass towards the egress port.
The second portion of the catheter tip defining the distal end of the catheter may also have a smooth generally curved outer surface. In effect, a ‘bullet’ or ‘convex’ geometry may be provided. Such a surface profile advantageously allows the catheter to be inserted along the urethra or vein with minimal discomfort or trauma to the patient and furthermore advantageously allows for smooth fluid flow around the catheter tip once in situ in the body.
The second portion of the catheter tip defining the distal end of the catheter may be inclined with respect to the elongate axis of the catheter. This may, for example, be inclined at an angle of between 15 degrees and 30 degrees. Such an inclination allows the catheter to be navigated or inserted through the urethra with minimal trauma and pain to the patient. For example, the second portion may be inclined at an angle of approximately 15 degrees.
The catheter may also advantageously comprise an expandable member located circumferentially with respect to the elongate generally cylindrical body and movable radially outwards from the body surface. Such an expandable member allows the catheter (a) to be inserted with the member in an un-expanded state, thereby minimising the diameter of the catheter and (b) provides a mechanism to selectively secure the catheter in place by expansion of the member at an appropriate position and to an appropriate diameter.
In one example, the expandable member may be in the form of a circumferentially located balloon expandable between a first position in alignment with the outer surface of the elongate body and a second position radially spaced from the body. A balloon conveniently allows a light and simple expandable member to be provided that may be expanded with a fluid such as water or saline solution.
The catheter may also comprise a lumen extending along the elongate body and in fluid communication with the expandable member to cause selective expansion or retraction of the expandable member. Thus the member can be accurately controlled.
The elongate, generally cylindrical body, may comprise a first lumen for fluid egress and two radially opposing lumens, a first being a fluid ingress lumen and a second being in fluid communication with an expandable member. The expandable member may be in the form of a balloon which may be selectively expanded by means of a fluid.
Furthermore, the expandable member may be positioned at least 4 cm from the tip of the catheter to the midpoint of the expandable member inflation channel i.e. a midpoint at which the balloon is inflated.
For a surgical drain, the expandable member (for example balloon) may be positioned 10, 20 or 30 cm from the tip of the catheter to the midpoint of the expandable (for example balloon) inflation channel i.e a midpoint at which the balloon is inflated from the channel.
The catheter may be formed from any suitable material. However the catheter may advantageously be formed from a material selected from an aromatic polyurethane teflon, polyvinylchloride (PVC) and silicone. Such materials are soft enough to prevent trauma in a patient, convenient to manufacture and provide sufficient structure strength for the application.
They are also tolerated by the human body. Polyurethane is particularly advantageous since or any given outer diameter of catheter the greatest internal diameter of lumen can be achieved whilst maintaining sufficient structural strength of the catheter. Furthermore, it is also more biocompatible with the human body than other materials.
For example, the catheter may be formed from a polyurethane material having a Shore Hardness of between 85 and 90 Shore A.
The maximum length of the intermediate fluid ingress/egress region extending between the first portion of the catheter tip and the second portion of the catheter tip when measured along the axis of the catheter may be less than 15 mm.
Viewed from a further aspect there is provided a catheter as described herein wherein the catheter is a urethral catheter or surgical drainage catheter.
Viewed from yet another aspect there is provided a urethral catheter comprising an elongate generally cylindrical body and a catheter tip for insertion into and along a urethra,
Viewed from a still further aspect there if provided a method of urethral or surgical drainage or gastric decompression or enteral feeding tube for use in the stomach and small intestine by means of a catheter as claimed in any preceding claim, the method comprising the steps of inserting a catheter into a body, causing fluid to ingress into a body and removing fluid from the body through the fluid egress lumen
Aspects of catheters described herein may also be used in peripheral venous catheters and central venous catheters for delivery of intravenous fluids, blood drugs and parenteral nutrition and in addition to irrigation and drainage of fluids.
The outside diameter of the catheters may vary depending on application but in general will be between 5.3 mm and 6.6 mm (16-20 Fr) for urethral catheters with a maximum internal diameter between 3.9 mm and 5.2 mm. Venous catheters will have a smaller outer diameter, typically less than 16 Fr.
Aspects of the invention will now be described, by way of example only, with reference to the accompanying figures in which:
While an invention described herein is susceptible to various modifications and alternative forms, specific embodiments are shown by way of example in the drawings and are herein described in detail. It should be understood however that drawings and detailed description attached hereto are not intended to limit the invention to the particular form disclosed but rather the invention is to cover all modifications, equivalents and alternatives falling within the spirit and scope of the claimed invention.
It will be recognised that the features of the aspects of the invention(s) described herein can conveniently and interchangeably be used in any suitable combination. As stated earlier, it will be recognised that the invention covers not only individual embodiments but also combinations of the embodiments that have been discussed herein.
Any reference to prior art documents in this specification is not to be considered an admission that such prior art is widely known or forms part of the common general knowledge in the field.
As used in this specification, the words “comprises”, “comprising”, and similar words, are not to be interpreted in an exclusive or exhaustive sense. In other words, they are intended to mean “including, but not limited to”.
The invention is further described with reference to the following examples. It will be appreciated that the invention as claimed is not intended to be limited in any way by these examples.
A catheter apparatus comprises the catheter 2 itself, which is the component which is inserted along the urethra of the patient. The distal end of the catheter 2 comprises a small aperture 3 through which urine may pass from the patient's bladder. The urethral catheter includes balloon 4 which may be inflated with inflation line 5 to maintain the position of the catheter inside the bladder. Once inserted, the catheter 2 is then coupled to the drainage tube 6 which is in turn connected to a collection bag 7 (with optional outlet port 8).
In use, the catheter is inserted and connected to the bag and urine can be drained from the patient's bladder.
Referring back to
The applicant has established that the majority of medical tubes/catheters have, as their outflow/aspiration port(s), punched outside ports that present a narrow flat surface typically approximating to less than 50-75° of the circumference of the outer diameter (OD) of the tube/catheter (as illustrated in
As illustrated by
Conversely,
Furthermore, the design of the outflow port is such that the outflow fluid characteristics are novel by virtue of being diffuse rather than concentrated from the tip of existing venous catheters, the “fire-hose effect” (a term in the art) which when aimed at the inside of the lining of the vein causing trauma and inflammation that leads to the development of thrombophlebitis and venous thrombosis, complications that limit the use of peripheral and central vein catheters. Thus, further arrangements described herein provided an improved venous catheter arrangement.
Importantly, as shown in
In the example shown in
Cross-sectional views 7A, 7B and 7C illustrate cross-sectional views through the uretheral catheter at the identified points (A-A′; B-B′ and C-C′ respectively). This catheter comprises 3 lumens passing along the elongate body of the catheter. The purpose of each lumen will be described below.
The uretheral catheter comprises a proximal end 17 which is in the form of a generally cylindrical elongate body. At the opposing end is the catheter tip 18.
The arrangement in
Lumen 20 extends along the elongate body and fluidly connects with a balloon 22 arrangement forming a radially expandable element of the embodiment. Introducing a fluid along the lumen 20 causes the balloon to expand as illustrated in
In each of
The catheter cross-section may be conveniently manufactured using an extrusion process. This allows for a range of cross-sections to be created. The cross-sections shown in
In the examples shown in
As shown the generally concave profile of this region intersects with the cylindrical body, the end portion of the catheter and the base to define an ‘open’ or ‘bowl’ region through which fluid may easily flow. Fluid flows in multiple directions as will be described with reference to
The cross-section shown in
The relative areas in mm2 are shown for each of 16, 18 and 20 Fr catheters. It will be recognised that these areas are only examples and that slight deviations from these parameters may also function.
The fluid flows associated with the catheter will now be described with reference to
The tip 18 is formed of 3 distinct portions or regions. Specifically, the tip 18 comprises:
Referring back to
As discussed above with reference to
In effect, the recess defines an upper opening intersecting with the lumens 19 and 21 and thus allowing fluid communication into and out of the region.
Returning to
As shown in
Returning to
The outlet 29 may also comprise a recess as illustrated by the dashed line at outlet 29 in
Furthermore, the upper extend i.e. the most distal end of the upper part of the outlet may be curved and may generally follow the profile of the catheter in an upwards direction and terminate at the intersection of the outlet 29 and recess 26 (illustrated by the sharp and curved profile proximal to the arrow F1 in
The irrigation fluid serves a number of purposes as described in further detail with reference to
The primary function of the ingress fluid through the catheter and to the catheter outlet port 29 is to provide a flow which applies an outward pressure against a mucosa or blood clots dietary contents or bladder lining or stomach lining that might otherwise obscure the fluid ingress/egress region. As shown in
As shown in
The new catheter geometries provide a number of advantages including reduction in the incidence of uretheral catheter blockage, improved bladder drainage, reduced incidence of urinary infection and to reduced incidence of clot retention following urogenital tract surgery.
There may occasionally, despite the novel design of the drainage port, be a tendency of the mucosa to abut with the catheter and prolapse down within the cavity of the drainage port 26 blocking the flow of urine 19. However, the continuous irrigation flow F2 will force the mucosa (M) out of the orifice of the drainage port 26 thereby maintaining an open and continuous flow path to the outlet lumen 19 as illustrated by flow F3.
In effect the geometry of the tip of the catheter described herein functions in 2 complementary ways:
These two supporting surfaces or portion cooperate with the fluid flow and the angle of opening of the intermediate opening to allow for continuous flow through the catheter; something that is not possible with existing catheter designs.
Two additional features of the new geometry have been established by the applicant and are illustrated in
Furthermore, the bullet tip and aspiration port may advantageously be angled upwards of the main body of the catheter (as shown in
This angle A may be between 16 degrees and 30 degrees, but is advantageously 30 degrees.
This is in order to facilitate passage of the catheter through the ‘bed’ of the prostate and neck of the bladder. From the manufacturing standpoint, the component constituting the bullet tip and aspiration port is likely to be required to be moulded onto the main body of the tubing—the site of the moulding is where the acute angle (allowing upwards project of the tip of the catheter) will be formed.
The inventions described herein are also applicable to other medical devices such as surgical drains as well as gastric decompression tubes and nasogastric and naso enteral feeding tubes.
Also, the improved design of the aspiration port will enhance the efficiency of drainage thereby reducing bladder sump volume and reducing the incidence of catheter-related urinary infection. As with the nasogastric feeding tube, blockage by bladder mucosal adherence and mucous produced from the wall of an inflamed bladder will be prevented. The ability to be able to apply internal coating to the polyurethane tubing will enable us to apply a bacteriostatic polymer) that will further reduce the incidence of catheter-related urinary infections. Not only will the invention benefit patients undergoing short-term urethral catheterisation but also those with long-term urinary catheterisation. The application of the port design will improve the functioning of venous catheters by virtue of improved flued patterns that in turn will reduce trauma during fluid infusion and thereby the incidence of thrombophlebitis and venous thrombosis that lead to the need for venous catheter withdrawal and replacement.
The reference numerals for
Number | Date | Country | Kind |
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2204656.9 | Mar 2022 | GB | national |
Filing Document | Filing Date | Country | Kind |
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PCT/GB2023/050861 | 3/31/2023 | WO |