Prosthetic penile implants with tethered rear tip extenders and related methods
09801723 · 2017-10-31
Assignee
Inventors
Cpc classification
B29C45/00
PERFORMING OPERATIONS; TRANSPORTING
B29C2045/0093
PERFORMING OPERATIONS; TRANSPORTING
B29L2031/7532
PERFORMING OPERATIONS; TRANSPORTING
B29K2083/00
PERFORMING OPERATIONS; TRANSPORTING
Y10T29/49826
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
International classification
Abstract
Rear tip extenders having a tether attached to a collar for penile implants that can be mounted onto a respective cylinder forward of a fluid line (that communicates with a scrotal pump) to prevent full separation or detachment from the cylinder during a revision procedure can be fabricated by molding. The fabrication methods include: providing a mold with a mold cavity configured to define three attached members of defined shapes, including a rear tip extender, a collar and a tether attaching the rear tip extender and collar; and flowably introducing moldable material into the mold cavity to form the collar, rear tip extender and attached tether as a molded assembly.
Claims
1. A method of fabricating a penile implant, comprising: providing a mold with a mold cavity configured to define three attached members of defined shapes, including a rear tip extender, a collar and a tether attaching the rear tip extender and collar; and flowably introducing moldable material into the mold cavity to form the collar, rear tip extender and attached tether as a molded assembly.
2. The method of claim 1, further comprising sterilizing the molded assembly for medical use.
3. The method of claim 1, wherein the rear tip extender is sized and configured to attach to an end portion of an elongate cylinder of a penile prosthesis implant, wherein the collar is sized and configured to reside against an outer surface of the cylinder, and wherein the collar is sized to be loosely held on the cylinder with an inner diameter that is between 10-50% greater than an outer diameter of the cylinder and/or is configured to expand when the cylinder expands due to inflation.
4. The method of claim 1, wherein the rear tip extender comprises a rear tip cap with a closed end.
5. The method of claim 1, wherein the moldable material comprises silicone rubber.
6. The method of claim 1, wherein the collar comprises at least one arcuate recess.
7. The method of claim 1, wherein the collar comprises a plurality of circumferentially spaced apart arcuate recesses.
8. The Method of claim 1, wherein the providing the mold is a first mold to form a first molded assembly with the collar, rear tip extender and attached tether, and wherein the method further comprises: providing a second mold with a mold cavity configured to define three attached members of defined shapes, including a rear tip extender, a collar and a tether attaching the rear tip extender and collar; and flowably introducing moldable material into the mold cavity of the second mold to form the collar, rear tip extender and attached tether as a seconded molded assembly, wherein the rear tip extender of the second molded assembly has a shorter or longer length than the rear tip extender of the first molded assembly.
9. The method of claim 8, wherein the collar, tether and/or rear tip extender of the second molded assembly has a different color than the collar, tether and/or rear tip extender of the first molded assembly.
10. The method of claim 1, wherein the tether is a single tether.
11. The method of claim 1, wherein the tether has a width that is between about 0.001 inches to about 0.1 inches.
12. The method of claim 1, wherein the collar is between about 0.1 inches to about 0.5 inches in axial length.
13. The method of claim 1, wherein the tether has a length between about 0.5 inches to about 10 inches.
14. The method of claim 1, wherein the tether has a length between about 0.5 inches to about 5 inches and a width between about 0.001 inches to about 0.1 inches.
15. The method of claim 1, further comprising providing at least one core rod to cooperate with the mold cavity, the at least one core rod shaped to form the collar to have at least one arcuate recess.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DESCRIPTION OF EMBODIMENTS OF THE INVENTION
(20) The present invention will now be described more fully hereinafter with reference to the accompanying figures, in which embodiments of the invention are shown. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. Like numbers refer to like elements throughout. In the figures, certain layers, components or features may be exaggerated for clarity, and broken lines illustrate optional features or operations unless specified otherwise. In addition, the sequence of operations (or steps) is not limited to the order presented in the figures and/or claims unless specifically indicated otherwise. In the drawings, the thickness of lines, layers, features, components and/or regions may be exaggerated for clarity and broken lines illustrate optional features or operations, unless specified otherwise.
(21) The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used herein, the singular forms, “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises,” “comprising,” “includes,” and/or “including” when used in this specification, specify the presence of stated features, regions, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, regions, steps, operations, elements, components, and/or groups thereof.
(22) It will be understood that when a feature, such as a layer, region or substrate, is referred to as being “on” another feature or element, it can be directly on the other feature or element or intervening features and/or elements may also be present. In contrast, when an element is referred to as being “directly on” another feature or element, there are no intervening elements present. It will also be understood that, when a feature or element is referred to as being “connected”, “attached” or “coupled” to another feature or element, it can be directly connected, attached or coupled to the other element or intervening elements may be present. In contrast, when a feature or element is referred to as being “directly connected”, “directly attached” or “directly coupled” to another element, there are no intervening elements present. Although described or shown with respect to one embodiment, the features so described or shown can apply to other embodiments. The term “distal” refers to a direction or location that is closer to or toward a patient while the term “proximal” refers to the opposing direction or a location that is further away from the patient.
(23) Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the present application and relevant art and should not be interpreted in an idealized or overly formal sense unless expressly so defined herein.
(24) The term “tether” refers to a flexible or semi-rigid member that extends between and attaches two separate components.
(25) The term “about” means that the recited number or value can vary by +/−20%.
(26) The term “sterile” means that the noted device or material meets or exceeds defined medical guidelines of cleanliness and is substantially (if not totally) without contaminants so as to be suitable for medical uses.
(27) The term “semi-rigid” means that the implant is flexible but has sufficient rigidity to substantially maintain its three-dimensional shape under normal loading in the body.
(28) The term “instructional media” refers to electronic and/or paper manuals, videos, user guides, or the like illustrating and/or describing pre-surgical assembly steps and/or a surgical procedure using the tethered penile implant.
(29) Referring now to the figures,
(30) The tether 70 is typically attached to or integrally formed onto a wall or the outer surfaces of both the collar 60 and the RTE 25. Although shown in most embodiments as a single tether, more than one tether may be used.
(31) The tether 70 can comprise a thread, strap, suture, wire or other elongate member. The tether 70 can be flexible. The tether 70 can be semi-rigid. The tether 70 can be an integrally molded component of the collar 60.
(32) The collar 60 can be a unitary monolithic component of suitable medical grade material. The collar 60 can comprise silicone rubber or other medical grade suitable elastomeric or polymeric material. The collar 60 can also comprise a biocompatible, non-cytotoxic metal or ceramic. The collar 60 can comprise a combination of materials.
(33) The collar 60 can include at least one arcuate recess 61 (
(34) The collar 60 can be provided in different sizes for different sizes of cylinders 20. The collar 60 can optionally abut the outer surface of the cylinder 20 at the rear end portion 20r or may reside loosely against the outer surface of the cylinder 20 (e.g., so as to not contact at least a portion of the outer wall of the cylinder thereat). The collar 60 can have any suitable axial length and any suitable cross-sectional width and is not required to matably correspond to the cylinder outer diameter. The collar 60 can be between about 0.1 inches to about 0.5 inches in axial length but other lengths may also be suitable.
(35) In some embodiments, the collar 60 can have an axially extending centerline 60c that is concentric with an axially extending centerline 20c of the cylinder 20 as shown in
(36) In some embodiments, as shown in
(37) The collar 60 can be configured to be able to expand in response to inflation/expansion of the cylinders 20 so as not to provide undue compression on the cylinder when in an expanded configuration. The collar 60 can have an accordion, undulated or pleated segment or segments to facilitate expansion and/or may be formed of a resilient, flexible and/or otherwise expandable material.
(38) In some embodiments, the collar 60 can reside loosely against the outer wall of the cylinder and is not required to expand with the expansion of the cylinder 20. The collar 60 can have an inner wall with a cross-sectional width that is 10-50% larger than an outer diameter of the cylinder 20.
(39) The collar 60 can be in the shape of a disk (e.g., with a substantially circular opening). The collar 60 can be in other shapes not requiring a circular opening or circular external outer Wall shape. The collar 60 can have any closed geometric shape, e.g., oval, polygonal, triangular and the like.
(40) The tether 70 can have the same material as the collar 60 or the RTE 25 or may comprise a different material. The tether 70 has a length sufficient to extend from at least a front end portion of the RTE 25 to the collar 60; typically, the tether 70 has a length between about 0.5 inches to about 10 inches, typically between about 0.5 inches to about 5 inches. The tether 70 can be longer as it can reside in local tissue and when pulled, it pulls the RTE along with the collar upon a revision or other surgery to provide a positive retention of the two components.
(41) As shown in
(42) The RTE 25 can be a rear tip end cap (with a closed end tip) as shown in
(43) In some embodiments, the collar 60, tether 70 and RTE 25 can be provided pre-assembled as an assembly 25a and provided in a kit 100 of different sizes of RTEs 25 (
(44) In some embodiments, the tether 70 is moldably attached to the collar 60 and RTE 25. In some embodiments, the tether 70 is adhesively attached to the respective collar 60 and/or RTE 70. In some embodiments, the collar 60 is mechanically fastened to the tether 70 and/or RTE 70 using, for example, hooks, VELCRO (e.g., loop and hook), or mechanical slide and channel, tongue and groove, rivets, pins or clamp attachment configurations.
(45) In some embodiments, the assembly 25a includes a single RTE 25 and tether 70 attached to a respective collar 60 as shown, for example, in
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(50) As the RTEs 25 can be provided in different lengths, the collars 60 or tethers 70 (or both) can be color-coded to represent a length of the RTE for facilitating physician size selection.
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(53) The method may optionally include providing a plurality of collars, each attached to a different length rear tip extender (block 227). The collars can be color-coded to designate a particular length rear tip extender (block 228).
(54) The placing steps can be carried out at a surgical site prior to implanting the cylinder in a patient (block 247).
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(56) The mold shape for the collar can include arcuate regions that form longitudinally extending arcuate recesses in the collar (block 272). The moldable material can include (or be made totally of) silicone rubber (block 277).
(57) The method can include sterilizing the assembly for medical use (block 282).
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(59) The foregoing is illustrative of the present invention and is not to be construed as limiting thereof. Although a few exemplary embodiments of this invention have been described, those skilled in the art will readily appreciate that many modifications are possible in the exemplary embodiments without materially departing from the novel teachings and advantages of this invention. Accordingly, all such modifications are intended to be included within the scope of this invention as defined in the claims. In the claims, means-plus-function clauses, if used, are intended to cover the structures described herein as performing the recited function and not only structural equivalents but also equivalent structures. Therefore, it is to be understood that the foregoing is illustrative of the present invention and is not to be construed as limited to the specific embodiments disclosed, and that modifications to the disclosed embodiments, as well as other embodiments, are intended to be included within the scope of the appended claims. The invention is defined by the following claims, with equivalents of the claims to be included therein.