Surgical procedures where medical devices need to be inserted into an incision in order to perform an operation can potentially be very invasive and extensive. Operations such as spinal surgery or similarly dangerous operations require adequate visibility and access to the area being operated on in order for the surgery to be safe and effective. In order to reduce post-operative healing time, scarring, and potentially other complications which may arise from making large incisions, minimally invasive techniques for inserting the instruments are desirable.
Consequently, medical professionals try to minimize complications such as those listed by making smaller incisions. Smaller incisions, however, make it more difficult to insert medical instruments and limit access and visibility within the incision. Because of this, there is a need in the field for a minimally invasive system and method for inserting medical instruments into a small incision without having a detrimental effect on the ability of a medical professional to effectively operate. Minimally invasive techniques can reduce the intra-operative damage and reduce the post-operative recovery time.
According to one embodiment of the present specification, a transitional dilator includes a dilator body having a proximal end and a distal end, in which the dilator body defines a sleeve orifice configured to receive an implant placement tube. A round tip is formed on the distal end of the dilator body, wherein the round tip defines a converging orifice terminating at an exit orifice configured to closely mate with a serial dilator. The round tip including a converging orifice further includes a wall split configured to receive the implant placement tube and expand to accommodate passage of the implant placement tube through the exit orifice.
In another exemplary embodiment, a method of inserting an implant placement tube includes: inserting a serial dilator in a wound; placing a transitional dilator over the serial dilator, wherein a tip of the transitional dilator is closely mated to the diameter of the serial dilator and configured to expand when forced open; inserting an implant placement tube into the transitional dilator; and forcing the placement tube through the tip of the transitional dilator, expanding the tip to displace surrounding soft tissue. The method may further include removing the serial dilator from the transitional dilator to create a pathway for implant placement.
The accompanying drawings illustrate various embodiments of the principles described herein and are a part of the specification. The illustrated embodiments are merely examples and do not limit the scope of the claims.
Throughout the drawings, identical reference numbers designate similar, but not necessarily identical, elements.
The present specification relates to dilators for use during surgical operations. Specifically, a transitional dilator used to transition between an initial serial dilator and an implant placement tube is described herein. According to one exemplary embodiment, the transitional dilator is configured to expand the wound into which the serial dilator was placed so that the implant placement tube may be easily placed without causing unnecessary damage to tissue. Once the transitional dilator is inserted, according to one exemplary embodiment, the serial dilator may be removed to create a pathway to allow for surgical instruments to be used in the area being operated on, and the placement tube may be used to retain the incision open while a medical implant is inserted.
As used in the present specification and in the appended claims, the term “dilator” will be broadly understood to mean an instrument or tool that is used to dilate or widen an opening such as a surgical incision or a wound. The dilator may accomplish this, according to one exemplary embodiment, by displacing the soft tissue surrounding the opening. Also as used in the present specification and in the appended claims, the terms “incision” and “wound” are to be broadly interpreted to include any incision, portal, access point, wound or other opening made in a body where the operation is to take place.
In the following description, for purposes of explanation, numerous specific details are set forth in order to provide a thorough understanding of the present systems and methods. It will be apparent, however, to one skilled in the art that the present systems and methods may be practiced without these specific details. Reference in the specification to “an embodiment,” “an example” or similar language means that a particular feature, structure, or characteristic described in connection with the embodiment or example is included in at least that one embodiment, but not necessarily in other embodiments. The various instances of the phrase “in one embodiment” or similar phrases in various places in the specification are not necessarily all referring to the same embodiment.
As used in the present specification, the serial dilator (100) may be used as an initial dilator for other procedures such as medical implants or the like, or alternatively may serve a plurality of purposes by providing a suction access in addition to the dilation functionality. The embodiment of
The exemplary transitional dilator (200) illustrated in
According to the exemplary embodiment illustrated in
The implant placement tube (300), according to one exemplary embodiment, is a hollow structure with an outer perimeter (305) measuring less than an inner perimeter (240) of the sleeve orifice (220) of the transitional dilator (200) so that the implant placement tube (300) may be inserted into the transitional dilator (200) via the sleeve orifice (220). While a square shaped implant placement tube (300) is illustrated in
As the implant placement tube (300) is inserted into and pushed through the transitional dilator (200), the tube reaches the round tip (225) where the inner perimeter (240) of the dilator body (205) begins to converge to the smaller perimeter of the exit orifice (235). The round tip (225) of the dilator (200) has at least one wall split (245) that allows the inner diameter of the round tip (225) to be expanded, such that as the implant placement tube (300) is pushed through the transitional dilator (200), the act of pushing the tube (300) through the round tip (225) causes the exit orifice (235) to expand to allow further penetration of the tube (300). The exemplary transitional dilator (200) of
Use of the transitional dilator (200) in conjunction with a serial dilator (100) and an implant placement tube (300) is shown in greater detail in
Once the exit orifice (235) of the transitional dilator (200) has been inserted into the incision, the implant placement tube (300) is inserted into the sleeve orifice (220) of the transitional dilator (200), as depicted in
According to one exemplary embodiment illustrated herein, the converging orifice (230) includes four elastic wall flaps (700) and four elastic corner flaps (705), each corner flap (705) being connected to a rounded section (710) of the exit orifice (235). The rounded sections (710) of the exit orifice (235) form a closed circular shape when in a non-expanded state. When the round tip (225) is in an expanded state, the rounded sections (710) are displaced away from each other due to the outward force from the implant placement tube (300). According to one exemplary embodiment, the round tip (225) is made from an elastically deformable material to allow the wall flaps (700) and corner flaps (705) to straighten and extend away from one another and radially outward from the center of the exit orifice. In the expanded state, the inner perimeter of the converging orifice (230) and the exit orifice (235) is increased to greater than the outer perimeter (305) of the implant placement tube (300) so that the implant placement tube (300) can be pushed all the way through the transitional dilator and into the surgical site of the wound. As the exit orifice (235) is moved into an expanded state, the rounded sections (710) push outward against the soft tissue surrounding the exit orifice (235) and expand the opening of the incision. Additionally, the transitional dilator (200) is shaped such that as the exit orifice (235) expands, the rounded sections (710) also push slightly upward, which may help hold the dilator (200) within the wound and prevent the dilator from slipping out during the operation.
When the incision has been expanded sufficiently and the exit orifice (235) is in its expanded state, the implant placement tube (300) may be placed in the incision. Expanding the incision will allow a surgeon to more easily see the operating area and use operating instruments in the area by providing light, irrigation, suction, and various medical instruments. Also, the implant placement tube (300) may have a sufficient inner perimeter to allow a surgeon to place larger items in the operating area without the need to make a longer incision. The serial dilator (100) may be removed from the incision and the transitional dilator (200) once the implant placement tube (300) is in place to clear the way for any instruments or for the implantation of other medical devices.
According to one exemplary embodiment, the round tip (225) may be integrally formed with the rest of the dilator body (205). The dilator body (205) may include a compliant hinged connection (715) with the round tip (225) at a transition area where the inner perimeter (240) of the transitional dilator (200) begins to converge. The compliant hinged connection (715) made be made by creating a wall thickness of the dilator body (205) that is thinner at the transition area than at the rest of the dilator body (205), thus allowing the wall and corner flaps (700, 705) to bend outward by flexing at the thinner wall thickness. An integrally formed dilator body (205), including the round tip (225), may allow for the transitional dilator (200) to be formed from a single mold or using a simple process. Alternatively, the round tip (225) may be coupled to the dilator body (205) by any number of hinge features including, but in no way limited to, a pined hinge, a flap hinge, and the like.
As illustrated, the wall splits (245) may extend past the hinged connection (715) or transition area and up into the main body portion. Extending the splits as such would allow portions of the round tip (225) to extend farther radially outward without putting too much strain on the hinged connection (715) or material from which the dilator (200) is made.
According to another embodiment, the round tip (225) may be attached to the rest of the dilator body by a separate hinged connection. The hinged connection may be such that the portion of the dilator body with a constant outer perimeter is formed separately from that of the round tip, and the round tip is connected after manufacture by a hinge piece that allows the wall flaps and the corner flaps to bend outward when a force is applied from within the dilator body. The hinge piece may be spring loaded such that in a resting state the exit orifice has a tight circular shape and closely mates the serial dilator when first installed.
The placement tube (300) may also be anchored to the transitional dilator (200) to prevent movement with respect to the transitional dilator once the tube has been inserted. The tube may be anchored using a spike or other protrusion at the distal end of the tube that hooks onto or is inserted into a portion of the dilator, preventing longitudinal movement of the tube. The tube may alternatively be configured to allow a modular spike or other attachment to be connected to both the placement tube and the dilator to anchor the tube and dilator to one another.
The transitional dilator (200) may be any shape suitable to receive a like-shaped implant replacement tube (300), or any such tube shaped so that the dilator holds the tube in place laterally and guides the tube into the incision. The dilator may be rectangular at the sleeve orifice (220) and the tube may be rectangular to fit within the dilator. The dilator may alternatively be square at the sleeve orifice, with the tube also being square so that the tube fits within the dilator. The exit orifice (235) is preferably the same shape as the serial dilator so that the exit orifice closely mates with the serial dilator (100) regardless of the orientation of either the transitional dilator or the serial dilator.
Other variations of the present specification may include a transitional dilator (200) that is made from multiple materials so that when the exit orifice (225) expands, the wall flaps (700) and corner flaps (705) are still connected by a second, stretchable material. The converging orifice of the round tip may have fewer or more flaps than shown in the figures, and the wall splits (245) may be located and designed in any fashion suitable for operating under the principles described herein.
When the operation or implantation is finished, the transitional dilator (200) and the implant placement tube (300) may be easily removed and disposed of. The dilators and tube are made from sterilized materials that prevent contamination in the incised area. The materials may also be made of disposable/recyclable materials for single-use to maintain a sterile operating environment. The transitional dilator, serial dilator, and placement tube may be made using inexpensive materials and mass-produced to further reduce costs.
In accordance with the transitional dilator described herein, a method (800) of inserting an implant placement tube includes first inserting (805) a serial dilator in a wound. After the serial dilator has been inserted in the wound to sufficiently expand the opening of the wound, a transitional dilator is placed (810) over the serial dilator, wherein a tip of the transitional dilator is closely mated to the diameter of the serial dilator and is configured to expand when forced open. An implant placement tube is then inserted (815) into the transitional dilator. The placement tube is forced (820) through the tip of the transitional dilator, expanding the tip to displace surrounding soft tissue. The method may also include removing the serial dilator to create a pathway for implant placement, as well as to provide visibility, light, and room for other medical instruments.
In another exemplary embodiment, the method further includes anchoring the implant placement tube to the transitional dilator after inserting the tube into the dilator and into the wound. The implant placement tube may be anchored to the dilator with a spike or protrusion formed on the distal end of the tube. Alternatively, a modular protrusion may be attached separately to both the dilator and the placement tube at any location in order to stabilize the tube and dilator and to prevent the tube from moving within the dilator.
The preceding description has been presented only to illustrate and describe embodiments of the invention. It is not intended to be exhaustive or to limit the invention to any precise form disclosed. Many modifications and variations are possible in light of the above teaching. Modification of the above disclosure may include only pieces of the system as exclusive members or combinations of pieces to form a useful application in which various described elements of the disclosure are not incorporated. As specific embodiments of the system and method have been described, it is important to recognize that each embodiment may be used alone or in conjunction pieces of the other embodiments.
The present application claims priority under 35 U.S.C. § 119(e) from the following previously-filed Provisional Patent Application, U.S. Application No. 61/049,628, filed May 1, 2008, entitled “Distally Expandable Dilation Tube,” and which is incorporated herein by reference in its entirety.
Number | Date | Country | |
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61049628 | May 2008 | US |