SLOTTED GUIDEWIRE PROTECTOR AND ADVANCING DEVICE AND METHOD
20190255298 ยท 2019-08-22
Assignee
Inventors
Cpc classification
A61M2025/0293
HUMAN NECESSITIES
A61M2025/09125
HUMAN NECESSITIES
A61M2025/018
HUMAN NECESSITIES
A61M2025/09116
HUMAN NECESSITIES
A61M25/0169
HUMAN NECESSITIES
International classification
Abstract
A guidewire advancing device used in connection with medical devices for providing intravascular access for advancing substantial length of guidewire used to place such medical devices within the anatomical structure. A method of managing substantial length of guidewire for use with medical devices. The guidewire advancing device includes a longitudinally extending wire guide which is removably secured to the medical device and which includes a longitudinally extending channel. The guidewire extends the length of the channel to be advanced along the channel.
Claims
1. A guidewire advancing device for use with a medical device and for advancing a guidewire having a proximal and distal end to achieve intravascular placement of the medical device comprising: a wire guide longitudinally extending between a proximal and distal end; a channel defined by an outer surface of said wire guide and extending a predetermined distance between said proximal and distal ends of said wire guide, said channel being configured for receipt of the guidewire and for movement of said guidewire along the length of said channel; a proximal cap positioned along the proximal end of the wire guide and defining a seat for receipt of the guidewire; a guidewire stay connected to the proximal end of the guidewire; and a brace for connecting said wire guide to the medical device.
2. A guidewire advancing device according to claim 1 wherein said guidewire stay is configured to selectively cooperate with said proximal cap.
3. A guidewire advancing device according to claim 1 wherein said guidewire stay defines an aperture for receipt of the proximal end of said guidewire.
4. A guidewire advancing device according to claim 1 wherein said brace includes a seat for receipt of said guidewire advancing device.
5. A guidewire advancing device according to claim 4 further comprising a coupling wherein said coupling cooperates with said brace for securing said advancing device to the medical device.
6. A guidewire advancing device according to claim 5 further comprising at least one post extending between said brace and said coupling for clamping said guidewire advancing device to said medical device.
7. A guidewire advancing device according to claim 5 wherein said brace is removable from said coupling.
8. A guidewire advancing device according to claim 1 wherein said guidewire stay includes a finger tab and a stop wherein said stop is configured for receipt within said channel and connected to the proximal end of said guidewire.
9. A guidewire advancing device according to claim 1 wherein said channel predetermined length extends substantially the length of said advancing device from said proximal to said distal ends thereof.
10. A guidewire advancing device according to claim 1 wherein said advancing device length defined between said proximal and distal ends is substantially the length of the medical device selectively connected by said coupling.
11. A method of using a guidewire advancing device for advancing a guidewire to achieve intravascular placement of a medical device comprising the steps of: positioning the guidewire advancing device adjacent an outer surface of the medical device; connecting the guidewire advancing device to said medical device with a brace; advancing the guidewire along the length of the guidewire advancing device within a channel defined by said guidewire advancing device so as to advance the guidewire into the medical device and through a needle for obtaining vascular access for medical device placement; and removing the brace and the guidewire advancing device when vascular access is achieved.
12. A method according to claim 11 further comprising the step of providing a guidewire stay on a proximal end of the guidewire and a proximal cap on a proximal end of said guidewire advancing device and wherein said guidewire stay and said proximal cap cooperate to prevent loss of the guidewire proximal end.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION OF THE INVENTION
[0018] The present invention will now be described in detail hereinafter by reference to the accompanying drawings. The invention is not intended to be limited to the embodiments described; rather, this detailed description is provided to enable any person skilled in the art to make and practice the invention.
[0019] As used herein, the terms proximal and distal (excluding horizontal cross-sections) are used to refer to the axial ends of the assembly. The term proximal end refers to the end closely adjacent the user of the assembly and the term distal end refers to the end of the assembly to be intravascularly positioned.
[0020] The guidewire advancing device 10, as shown in
[0021] For the purposes of its use with the rapid insertion venous catheter, the wire 15 is preassembled into the proximal end of the venous access needle 13. Alternatively, the guidewire may be inserted into the access needle after initiation of the procedure, that is, it is not pre-loaded into the needle. The device 10 may also be used in a manner as to be contained within the housing of a peripheral IV (PIV) or midline/extended dwell peripheral IV (EDPIV) device, or as a mechanism to be used in conjunction with any type and configuration of a peripheral or central line. One skilled in the art of vascular access and minimally invasive procedures could also envision a device that could contain this mechanism not only for peripheral or central venous access, but also for arterial access as is seen in arterial lines for invasive vital sign monitoring, hemostatic vascular sheaths for venous/arterial procedures, or access components, such as peel-away sheaths, for example. Additionally, the guidewire device 10 described herein could be used in conjunction or incorporated in a device used for percutaneous access into any cavity as is seen in image-guided drain/catheter placements into an abscess, the renal collecting system, biliary system, or any space or potential space of the human body.
[0022] The catheter 12 is a disposable, single use device that is made of a biocompatible material. The needle and guidewire may be made of known materials, such as steel, nitinol, or a composition including one or both. The guidewire 15, according to one aspect, is formed of a flexible material to accommodate anatomical complications such as complex and tortuous vasculature. Commonly used materials are a polymeric coated or metallic wire.
[0023] The needle 13 has an insertion tip and is hollow and may be formed of a surgical grade stainless steel, such as an 18-22 gauge, as is common in the art.
[0024] As shown, the guidewire 15 extends along the length of the hollow needle 13. The proximal end of the guidewire 15 preferably includes visible marks at regular intervals, for example, 1 cm, to indicate the depth of the wire. This avoids placement too deep within the vasculature, but of sufficient depth for catheter placement. The guidewire 15 may be formed of material known in the art, such as a composite with a nitinol core to provide a blend of stiffness and flexibility, for effective torque control and venous navigation.
[0025] The guidewire advancing device 10, as shown in
[0026] The guidewire advancing device 10 also includes a tapered distal end 38, a proximal cap 28, and a guidewire stay 27 positioned on the proximal end of the guidewire. The proximal cap 28 is also slotted and defines a channel to allow passage of the guidewire 15. The proximal cap 28 and the guidewire stay 27 communicate with each other and are held in place by either static friction or a screwing thread mechanism analogous to a Luer Lock device. The tapered distal end 38 is configured for receipt by the needle hub 16. The distal end 38 may be integrally formed with the wire guide 22 or, as shown, separately formed wherein the wire guide 22 is inserted therein. The needle hub 16, shown in
[0027] The guidewire advancing device 10 further includes a brace 20. Brace 20 shown in
[0028] The wire guide 22 may be of any desired length, such as substantially the length of the catheter 12 as shown. The channel 25 is open on its proximal end wherein the guidewire 15 extends along the length of the channel 25 and the guidewire stay extends proximally from the wire guide 22 as shown in
[0029] As shown, the wire guide 22 is linear. It is within the scope of the present invention, however, to provide the wire guide in a non-linear configuration, such as curvilinear, or a combination of portions which are linear and non-linear.
[0030] In operation, the guidewire 15 is preferably preloaded in the wire guide 22. The wire guide tip 38 articulates with the needle hub 16. The wire guide 22 is then connected to the catheter 12. The brace 20 of guidewire advancing device 10 mates with the catheter coupling 21, such as by a snap fit. The needle 13 is then inserted into the target vessel for treatment.
[0031] For treatment, the guidewire 15 is advanced distally to extend beyond the distal tip of the needle 13 and further into the target vessel for treatment. The length of the guidewire 15 is restrained by but slideable along the wire guide channel 25. Once positioned, the physician, utilizing the guidewire stay 27 as a handle, distally advances the guidewire 15. As it is advanced, the guidewire 15 curves upwardly, out of the channel 25, as shown in
[0032]
[0033] Upon completion of guidewire 15 placement within the target vessel as necessary for the medical procedure, the wire guide 22 may be removed by applying appropriate force to disconnect the connection between the catheter coupling 21 and the brace 20. The catheter 12 may then be advanced along the length of the guidewire 15 until placed within the target vessel. The guidewire 15 and the needle 13 may then be withdrawn, leaving the catheter 12 in-dwelling within the vessel.
[0034] While exemplary embodiments have been shown and described above for the purpose of disclosure, modifications to the disclosed embodiments may occur to those skilled in the art. The disclosure, therefore, is not limited to the above precise embodiments and that changes may be made without departing from its spirit and scope.