Patent Application
20210177564
This invention patent application relates to a particular type of urethral probe, which is now part of the field of hospital/medical use devices and items. This permanent, removable and self-sustainable urethral probe is to be used on living human male and female patients suffering from urethral dysfunction, incontinence and chronic urinary retention, among other secondary causes that affect bladder function in order to provide a natural method for bladder emptying, emulating voiding physiology.
Permanent or intermittent bladder catheterization, along with the use of diapers, have been featured as viable alternatives for patients with bladder emptying dysfunctions, either caused by permanent loss of urination or poor, or lack of, bladder emptying.
Reduction or lack of urethral resistance at any stage of life, in particular on children suffering from neurological diseases, causes the bladder to lose the capacity of storing urine and, therefore, become dysfunctional, leading to atrophy of detrusor muscles and reduction, loss or increase in stimulation from the autonomic nervous system.
Patients suffering reduction or loss of urethral resistance require reinforcing mechanisms in order to stimulate the bladder's neuromuscular system and enable proper urine storage, since the patents that are unable to empty their bladders require mechanisms to make this process viable.
Intermittent catheterization is the most commonly used method for this purpose, with its main inconvenience in that it must be carried out several times during the day, as well as the amount of material required for such (Mazouni et al., 2004).
Urinary incontinence and retention in patients from all age brackets pose a challenging issue for the urological community, particularly in cases where the use of surgically implantable devices cannot be applied, either due to the presence of co-morbidities such as diabetes, severe neurological lesion, low age or elderly patients suffering from said anomalies.
The difficulty of self-catheterization for children and elderly people, particularly female patients, leads to improper bladder emptying which, in turn, leads to damages to the urinary tract and a subsequent renal failure condition, eventually leading to irreversible situations, which may require transplantation or hemodialysis (Ricciotti et al., 1995).
The simplest form of permanent bladder emptying is the Foley probe, which includes an inflatable balloon connected to a collector bag, which is periodically emptied.
Despite properly emptying the bladder, other features of the inflatable balloon such as size, commonly used manufacturing material, as well as the inconvenience itself of an installed inflatable balloon, render it unable to be used in a permanent condition in the aforementioned situations.
Some intra-urethral devices were previously described but failed to prove useful in solving the issue (Yachia, 1997).
In general, it has been determined by the present disclosure that probes belonging to the state of the art are not perfectly adjustable and are not designed for optimal fitting to the genitourinary anatomy.
In face of the aforementioned drawbacks, the permanent, removable and self-sustainable urethral probe was developed, in order to address compactness requisites, featuring a reduced size compared to similar devices belonging to the state of the art; it is also adjustable and designed for perfect fitting to the genitourinary anatomy.
In face of the particularities of the aforementioned state of the art, the probe herein proposed was developed, manufactured in medical grade silicone and including two discs with a central protuberance, one being a proximal fixed disc coupled to the bladder neck and providing occlusion, and the other being a distal sliding disc which, upon adjustment to the external female meatus, or male perineal urethrostomy, provides full urethral occlusion and subsequent continence.
The probe at hand is defined as a tubular body featuring four holes on its proximal end which has 2.5 cm in length
The tubular body is manufactured in flexible and transparent medical grade silicone with a smooth surface and having rounded end (proximal end) and featuring a small 1 mm diameter hole to allow passage of a guide wire, which may prove necessary in some situations to provide easier introduction.
The distal end includes a connector with a cover and an open-close mechanism, which enables bladder emptying whenever required. (
The probe includes a disposable chuck made of polypropylene (
This chuck includes a channel with a 1 mm diameter opening through its entire length, in order to enable potential use of the guide wire, as previously mentioned.
The innovations of this invention are its reduced and adjustable size, and its perfect fitting to the genitourinary anatomy.
There is a special sized probe with an extension of 15 cm between disks to be used in patients who use wheelchairs and are unable to reach and adequately manipulate the device. This chuck is part of the pack that comes with the specific probe and is also made of polypropylene.
The exit ports of the existing probe in the prior art are insufficient in specific cases where the elimination of crystals produced by the patient's kidneys is required.
Another drawback noted is the difficulty of positioning the tube through the patient's bladder and, in addition, the lack of ergonomics of the tube in cases where the patients are wheelchair-bound, as these individuals usually have disability properly reach and handle the device.
The purpose of this patent application is to meet the aforementioned needs and provide patients with a urethral probe that provides greater comfort by having a compact and adjustable dimension perfectly to the genitourinary anatomy as well as providing a disposable mandrel or chuck, which greatly assists in positioning the said rig and finally, to serve the wheelchair patients appropriately, offering a model with dimensions that facilitate the correct manipulation by the wheelchair.
This invention patent application will be described in detail with reference to the drawings listed below, in which:
The probe that is object of this invention patent application is generally indicated by reference number 1 and is manufactured in medical grade silicone including two discs, each with a central protuberance, one being a fixed proximal disc 2 which, when coupled to the bladder neck CV, provides occlusion, and also including a protuberance as indicated by reference 2A; the other being a distal disc 3, with its respective protuberance indicated by reference 3A, with said distal disc 3 being slidable and adjustable to the external female meatus or male perineal urethrostomy in order to provide full occlusion of the patient's urethra, therefore providing continence.
Protuberances 2A and 3A of discs 2 and 3 may feature a substantially conical shape, required for perfect fixation of the probe to the bladder neck CV and the external meatus of the urethra ME in the female and perineal region.
The proximal end 4 of the tubular body 5 of the probe 1 includes 4 holes 2 indicated by reference number 6, through which the urine volume contained inside the bladder B of the patient may be drained through a longitudinal channel 7, traversing the tubular body 5 from the region of the holes 6 up to the lumen 8 located on the distal end 9.
Probe 1 is defined by a tubular body 5 with four holes 6 and 6A, two of them 6A, positioned next to the proximal disc 2 and which are 2.5 cm long.
The existence of four holes is essential to avoid accumulation of crystals provenients from the urine which holds potential to obstruct the probe specially if the device extrapolates the time for replacement. Moreover, the position of the four holes can also be essential to avoid accumulation of crystals provenients from the urine.
The end portion of the proximal end 4 features a rounded tip 4A, which includes a 1 mm diameter hole (indicated as 4A′) in order to allow passage of the aforementioned guide wire (not shown), which does not integrate the claimed subject of this invention.
The distal end 9 of the probe 1 includes a connector 10 with a cover 11 and an open close mechanism that enables emptying of the bladder B when required, as may be assumed upon visualization of
The probe 1 includes a chuck M (as shown on
The chuck M features a shaft-shaped portion M1, which is dimensioned to be inserted through the tubular body 5 of the probe 1; an enlarged distal portion M2 which coincides, when touching the edge of the connector 10, with its end M3 reaching the terminal part of the proximal end 4 of the probe 1, such proximal end 4 including a 1 mm diameter hole indicated as 4A′, as previously mentioned; and a gripping portion M4, through which the chuck M is handled.
The chuck M features a channel M′ for its entire length, through which a guide wire (not shown) is eventually used in the positioning procedure of the probe 1.
It should be noted that hole 4A′, incorporated to the proximal end 4 of the probe 1 is included in full alignment with the channel M′ provided throughout the chuck M.
The state of the art to be considered useful to the understanding of this invention is to be provided by the introduction of the probe 1 through the urethra U up to the bladder neck CV, for female patients.
For male patients required to use the probe, it should be introduced via a minor perineal urethrostomy. As shown in
The guide wire mentioned herein is an accessory, and is not part of this invention, since it is used eventually, in other words, in more complex situations that require easier insertion conditions for the probe.
The probe mentioned herein is indicated, in general, by reference number 1, while both discs included in the probe (discs 2 and 3) are malleable and pose no difficulties for this procedure.
One disc (proximal disc 2) remains in the internal portion of the bladder neck CV (proximal), therefore, inside the bladder B, and the other disc (distal disc 3) is placed on the external meatus of the urethra ME or in the perineal region in the male (
The sliding of the disc 3 through the probe 1 allows adjustment in relation to the length of the urethra U, such adjustment being shown regarding the movement shown by arrow “A”-“B”, as shown by
This mechanism works upon traction exerted by the urologist on the moment of the introduction of the probe 1. After it is fixed to the bladder neck CV (disc 2) and the external urethral meatus ME (disc 3) through the respective protuberances 2A and 3A included on discs 2 and 3 or in the male perineal region.
The probe 1 described herein may be removed or replaced at any time, functioning for six to eight months due to the material used in manufacturing and its reduced size.
Said probe is manufactured with 2 gauges (12 and 14 FR) for children, and 4 (16, 18, 20 and 22 FR) for adults.
The total length of this probe 1 is 7 cm for child models and 8 cm for adult models. A 15 cm is also available to be used in patients with special needs such wheelchairs.
In both cases, both the gauge and the size of the probe 1 may vary according to particular anatomical features of the patient.
