The present invention relates generally to the field of orthopaedics, and, more particularly, to an orthopaedic injection restrictor apparatus and method.
Total joint arthroplasty (“joint replacement”) is the surgical replacement of a joint with a prosthesis. A typical conventional joint replacement procedure often includes anchoring a longitudinal stem, keel, post, or the like of the prosthesis into the medullary canal of a bone of the affected joint with an acrylic polymer or other suitable synthetic cement.
For some such procedures, it has been desirable to restrict the initial injection of the cement to a particular depth within the medullary canal.
The present invention provides an orthopaedic injection restrictor apparatus. The apparatus includes a nozzle. The nozzle includes an elongated portion. The apparatus further includes an orthopaedic plug. The orthopaedic plug includes a first portion releasably engaged with the elongated portion of the nozzle and further includes a plurality of flaps extending radially outwardly from its first portion.
In an alternative embodiment, the present invention provides an apparatus for restricting injection of a substance to a depth in a cavity within a bone. The apparatus includes a means for injecting the substance into the cavity and a means, releasably engaged with the injecting means, for plugging the cavity.
In another alternative embodiment, the present invention provides a method for restricting injection of a substance into a cavity within a bone with a plug. The method includes the steps of injecting the substance into the cavity and ejecting the plug into the cavity simultaneously with the injecting step.
The above-noted features and advantages of the present invention, as well as additional features and advantages, will be readily apparent to those skilled in the art upon reference to the following detailed description and the accompanying drawings.
Like reference numerals refer to like parts throughout the following description.
Exemplary apparatus 100 includes an exemplary injection nozzle 110. Among other things, nozzle 110 is configured to convey bone cement or any other suitable injection substance from a suitable controllable supply (not shown) into the bone cavity. In the exemplary embodiment nozzle 110 is disposable, made from injection molded High Density Polyethylene (“HDPE”), and gamma sterilized prior to use. In alternative embodiments, nozzle 110 may be reusable, made from any other suitable surgical material, and autoclaved or otherwise suitably sterilized prior to use. Nozzle 110 includes a base 120. Base 120 includes a generally cylindrical fitting 130. Among other things, fitting 130 is configured to connect to the injection substance supply. Fitting 130 has a plurality of generally planar external sidewall portions or flats 140 and internal screw threads 150. Base 120 also includes an elongated crown 160 extending axially from fitting 130. Nozzle 110 further includes an elongated tube 170 extending from crown 160. Tube 170 has a smooth inner sidewall 174 (see
Exemplary apparatus 100 further includes an exemplary disk-like or fan-like orthopaedic plug 190. Among other things, plug 190 is configured to resiliently radially collapse or fold down to fit through a relatively smaller diameter opening leading into a relatively larger diameter cavity and to unfold or fan back out inside the cavity (after clearing the opening) to effectively plug or stopper the cavity vis-a-vis the injection substance. In the exemplary embodiment plug 190 is made from HDPE and gamma sterilized prior to use. In alternative embodiments, plug 190 may be made from any other suitable biocompatible material and autoclaved or otherwise suitably sterilized prior to use. In some of the alternative embodiments, plug 190 may also be bio-absorbable. Plug 190 has near side or a nozzle engagement side facing generally toward nozzle 110 as indicated by directional arrows 200. Plug 190 includes a centralized boss 210 (see
In the exemplary embodiment the flexibility of the HDPE resiliently hinges flaps 220 to boss 210. Further, flaps 220 are sized to have a radius 224 (see
Exemplary apparatus 100 further includes a plurality of graduations 230 marked on tube 170. In the exemplary embodiment, graduations 230 are implemented as black bands that are suitably painted or otherwise marked onto tube 170. In alternative embodiments, graduations 230 may be otherwise marked or embossed onto, etched or molded into, or affixed to tube 170 in any other suitable manner.
Directional arrows 240 and directional arrows 250 are discussed further below in connection with operation of exemplary apparatus 100.
In operation of exemplary apparatus 100, a surgeon or other operator decides the depth to which a synthetic cement or other substance is to be injected into an intramedullary canal, a pre-drilled bone site, or any other similar bone cavity such as those typically involved in a total or partial joint arthroplasty. The operator may choose to set the depth to which the substance will be injected by removing plug 190 from tube 170 and then cutting off tube 170 at or about one of graduations 230, thus reducing the overall length of nozzle 110 to a corresponding known value; or, alternatively, the operator may choose to visually gauge the depth by reference to graduations 230 during insertion of tube 170 into the cavity as discussed further below. In any event, via fitting 130 nozzle 110 is connected to a suitable controllable supply of cement or other suitable injection substance.
Next, with boss 210 of plug 190 inserted into channel 180 of tube 170, plug 190 and tube 170 are inserted into the cavity along the general direction of arrow 240 (see
Next, the substance is injected into the cavity. The injection simultaneously ejects boss 210 (and thus, plug 190) from tube 170. Nozzle 110 is withdrawn from the cavity, while plug 190 remains lodged within the cavity (via flaps 220) to block the injected substance from spreading into undesired areas.
Similar operations for alternative plug 260 as opposed to plug 190 and/or for other alternative embodiments of apparatus 100 should be readily appreciated.
The foregoing description of the invention is illustrative only, and is not intended to limit the scope of the invention to the precise terms set forth. Further, although the invention has been described in detail with reference to certain illustrative embodiments, variations and modifications exist within the scope and spirit of the invention as described and defined in the following claims.