COIL CATHETER, METHOD OF USE, AND METHOD OF MANUFACTURE
20210069470 ยท 2021-03-11
Inventors
Cpc classification
A61M25/0017
HUMAN NECESSITIES
A61M25/005
HUMAN NECESSITIES
A61M25/0074
HUMAN NECESSITIES
A61M25/007
HUMAN NECESSITIES
A61M25/0102
HUMAN NECESSITIES
A61M25/0068
HUMAN NECESSITIES
International classification
Abstract
A catheter device and manufacturing process for manufacturing the catheter device, wherein the catheter device has a halo-shaped coiled portion extending away from a perpendicular stem portion through a swan neck portion. Eyelets on the halo coil portion and swan neck portion facilitate flow out of the bladder through the catheter device vertical to the catheter, rather than perpendicularly as is the case with existing catheters. The catheter device is formed by using a straight catheter tube, heating and cooling it within a formed mold to have the halo coil and swan neck, such that it can be straightened using a pusher and stylet, inserted into the body while straightened, and thereafter return to its coiled shape when the stylet is removed.
Claims
1. A catheter system comprising: a catheter body; a coil having a swan neck element and a right-angle element; and said swan neck configured to allow for dynamic movement and further configured to relax to allow for snap back in proximity with a sphincter.
2. The system of claim 1, further comprising: a long-segmented catheter portion configured to be converted to a short catheter iteration after collecting fluid.
3. The system of claim 1, further comprising: a suture-to-tube portion configured to allow for bridging said sphincter, positioning the catheter body, and removing the catheter body.
4. The system of claim 1, further comprising: at least one eyelet along a horizontal plane of said catheter body along said coil, said at least one eyelet configured to facilitate and enhance flow through the catheter; and whereby said at least one eyelet further are configured to reduce biofilm production about said catheter body.
5. The system of claim 1, further comprising: a stylet, a guide wire channel, and a pusher coupled together for placement with said a tethering suture.
6. The system of claim 5, further comprising: a snap cap configured to keep said suture from migrating and further configured to provide visual validation of placement of said catheter body; and said snap cap comprising a magnet.
7. The system of claim 1, further comprising: said catheter body configured to be transformed from a first, straight orientation into a second, coiled orientation comprising said coil having said swan neck element and said right-angle element.
8. A method of inserting a catheter, the method comprising the steps: inserting a catheter in a first, straightened orientation using a pusher and a stylet; placing said catheter in a selected location; removing said stylet, thereby transforming said catheter from said first, straightened orientation to a second, coiled orientation comprising a catheter body, a coil having a swan neck element and a right-angle element; and allowing for dynamic movement of said catheter with said swan neck; and relaxing said swan neck thereby allowing for snap back of said catheter in proximity with a sphincter.
9. The method of claim 8, further comprising the steps: draining through said catheter via at least one eyelet located along a horizontal plane of said catheter body along said coil; and reducing biofilm production about said catheter body with said at least one eyelet.
10. The method of claim 8, further comprising the steps: draining through said catheter and said pusher to a tube connected to an external reservoir; removing said external reservoir and said tube; and continuing draining through said catheter and said pusher.
11. A method of manufacturing a catheter, the method comprising the steps: placing catheter tube in a straight orientation into a mold base, said mold base comprising a forming block having a swan neck form portion and a halo coil form portion; positioning portions of said straight catheter tube within said forming block about said swan neck form portion and said halo coil form portion; capping said mold with a mold cap and securing said mold cap to said mold base; heating said mold with a heating element; cooling said mold with a chiller after ceasing the heating of said mold by deactivating said heating element; deactivating said chiller; removing said mold cap; and removing said catheter tube, now comprising a coil having a swan neck element and a right-angle element.
12. The method of claim 11, further comprising the step of placing a tubing support protector into said catheter tube prior to placing said catheter tube into said mold base.
13. The method of claim 11, wherein at least one eyelet is located along a horizontal plane of said catheter tube along said coil, said at least one eyelet configured to facilitate and enhance flow through the catheter.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0027] The drawings constitute a part of this specification and include exemplary embodiments of the present invention illustrating various objects and features thereof.
[0028]
[0029]
[0030]
[0031]
[0032]
[0033]
[0034]
[0035]
[0036]
[0037]
[0038]
[0039]
[0040]
[0041]
[0042]
[0043]
[0044]
[0045]
[0046]
[0047]
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
I. Introduction and Environment
[0048] As required, detailed aspects of the present invention are disclosed herein, however, it is to be understood that the disclosed aspects are merely exemplary of the invention, which may be embodied in various forms. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a basis for the claims and as a representative basis for teaching one skilled in the art how to variously employ the present invention in virtually any appropriately detailed structure.
[0049] Certain terminology will be used in the following description for convenience in reference only and will not be limiting. For example, up, down, front, back, right and left refer to the invention as orientated in the view being referred to. The words, inwardly and outwardly refer to directions toward and away from, respectively, the geometric center of the aspect being described and designated parts thereof. Forwardly and rearwardly are generally in reference to the direction of travel, if appropriate. Said terminology will include the words specifically mentioned, derivatives thereof and words of similar meaning.
[0050] The directional terms proximal and distal require a point of reference. In this application, the point of reference in determining direction is from the perspective of the patient. Therefore, the term proximal will always refer to a direction that points into the patient's body, whereas distal will always refer to a direction that points out of the patient's body.
II. Preferred Embodiment Catheter System 2
[0051] As shown in a typical environment in
[0052] The catheter 4 stem 8 passes through the prostate gland 14 and the end of the stem is located in proximity with the external sphincter 18. This system facilitates flow from the bladder 16 through the catheter 4 via eyelets 22, located at least at the swan neck section 7 and at the proximal coil tip 23 of the coil portion 6, and out through the urethra 20.
[0053]
[0054]
[0055]
[0056]
III. System 52 for Manufacture of Catheter System 2
[0057]
[0058]
[0059] The mold cap 46 is removed as shown in
IV. Method 102 of Using Catheter System 2
[0060]
[0061] A check is then made at 124 and a determination made whether flow is optimal with the pusher 36 in place. If not, the pusher will remain. If so, the pusher can be removed at 126 so that flow is entirely facilitated using the catheter 4 in the body. The process then ends at 128 until such a time that the catheter is to be removed.
V. Method 152 of Manufacturing System 52 for Manufacture of Catheter System 2
[0062]
[0063] The catheter and protector are then inserted into the mold at 160, using the swan neck form 44 and the halo form 40 of the mold base 34. The mold is capped at 162 and heated at 164 as described above. A check using the temperature gauge 54 is made at 166 to determine if the proper temperature has been reached. If not, heating continues. If so, temperature is maintained at 168 for 15 minutes, after which the chiller is activated at 170 to cool the mold.
[0064] A check to determine if the mold has reached its cooled temperature below 80 degrees Fahrenheit at 172. If not, chilling continues. If so, then the chiller is deactivated at 174, the mold is opened at 176, and the formed catheter 4 is removed at 178, ending the process at 180.
[0065] It is to be understood that while certain embodiments and/or aspects of the invention have been shown and described, the invention is not limited thereto and encompasses various other embodiments and aspects.