The present invention pertains generally to catheters that are advanced into the vasculature of a patient to perform a medical/surgical procedure. More particularly, the present invention pertains to systems and methods for guiding a catheter through the vasculature of a patient over a guide wire. The present invention is particularly, but not exclusively, useful as an over-the-wire catheter that is modified to provide an open access for manipulation of its guide wire at a location proximate the distal end of the catheter.
Interventional surgical procedures typically require that a catheter be somehow advanced through the vasculature of a patient to a predetermined site. Catheters, however, are typically designed for a particular purpose that is to be accomplished after the catheter has been positioned in the vasculature. Therefore, as a practical matter, a particular catheter may not necessarily have the structural wherewithal to effectively navigate the vasculature on its own. Consequently, the advancement of a catheter into the vasculature is often accomplished with assistance from other means, such as a pre-positioned guide wire. As can be easily appreciated, the pre-positioning of the guide wire, and the subsequent advancement of the catheter along the guide wire, must be done with the utmost care and precision.
Presently there are two well-known methods for advancing a catheter along a guide wire. These methods are generally known as: 1) the over-the-wire method; and 2) the monorail method. For the first, i.e. the over-the-wire method, the catheter is formed with a guide wire lumen that extends the entire length of the catheter. Thus, the entire catheter follows the wire during its advancement into the vasculature. A significant advantage for this method is that the “pushability” of the catheter is substantially enhanced. On the other hand, for the monorail method, only a portion of the catheter is formed with a guide wire lumen. Accordingly, part of the catheter can remain free of the catheter to enhance the individual manipulability of the catheter.
Depending on the particular medical/surgical procedure that is being performed, both methods of guide wire use have their advantages. It can happen for some specific procedures, however, that the ability to select between an over-the-wire method and a monorail method may be advantageous. For instance, procedures such as a device exchange or the crossing of a bifurcation lesion could easily give rise to the need for such a selection. Moreover, for some procedures it may be desirable to actually change from one method of guide wire use to the other during the procedure.
In light of the above it is an object of the present invention to provide a catheter system that can be selectively used either as an over-the-wire type catheter or as a monorail type catheter. Another object of the present invention is to provide a catheter system that allows the operator (i.e. physician) direct access both to the catheter and to the guide wire at selected locations along the length of the catheter. Still another object of the present invention is to provide a catheter system that is relatively simple to manufacture, is easy to use and is cost effective.
A catheter system in accordance with the present invention includes a catheter that is specifically designed to facilitate the advancement of the catheter over a guide wire and into the vasculature of a patient. To do this, the present invention provides a catheter that permits changes in the structural interaction of the catheter with the guide wire. Specifically, the catheter of the present invention allows the operator to selectively change between an over-the-wire and a monorail method of guide wire usage. More generally, the catheter system of the present invention permits an over-the-wire type operation, a monorail type operation, or a hybrid combination of the two. It also allows the operator access to the guide wire, at selected locations along the length of the catheter.
Structurally, the catheter of the present invention has a proximal end and a distal end with a main lumen that extends along the length of the catheter between the two ends. Also, the catheter has a distal bracket and a proximal bracket. Specifically, the distal bracket is formed on the catheter to extend from the distal end of the catheter in a proximal direction. It surrounds and defines a distal guide wire lumen. Similarly, the proximal bracket is formed on the catheter to extend from the proximal end of the catheter in a distal direction. It surrounds and defines a proximal guide wire lumen. A consequence of this is that a lateral access is established between the distal bracket and the proximal bracket. In order to help stabilize a guide wire in the lateral access, the surface of the catheter between the distal bracket and the proximal bracket can be formed with a groove that is dimensioned to receive the guide wire therein.
As envisioned for the present invention, an inflatable angioplasty balloon can be mounted on the distal end of the catheter in fluid communication with the main lumen. Also, a Y-site can be attached to the proximal end of the catheter. If used, one branch of the Y-site is placed in fluid communication with the main lumen. Thus, the Y-site establishes a main port that can be used for an inflation/deflation of the balloon. The other branch of the Y-site can then be used for the guide wire. Specifically, this other branch of the Y-site establishes a proximal end port that connects with the proximal guide wire lumen of the proximal bracket. At the distal end of the catheter, the distal bracket provides a distal end port that allows the guide wire to be introduced into the guide wire lumen of the distal bracket. As indicated above, the proximal and distal guide wire lumens can act in concert with each other to establish a comprehensive guide wire lumen for the catheter.
In an alternate embodiment of the present invention, the catheter can be formed with a central bracket that is located between the distal bracket and the proximal bracket. For this embodiment, the central bracket will effectively divide the lateral access into a proximal lateral access and a distal lateral access. Structurally and functionally, the central bracket is essentially the same as either the proximal bracket or the distal bracket.
In its operation, the present invention envisions that a guide wire will be pre-positioned in the vasculature of a patient. The extracorporeal end of the guide wire can then be inserted into the distal end port of the catheter and received into the distal guide wire lumen. Additional advancement of the catheter over the guide wire will then bring the exposed extracorporeal end of the guide wire past the lateral access and into the vicinity of the proximal bracket. At this point, the guide wire can be selectively inserted into the proximal guide wire lumen of the proximal bracket. If so, the guide wire will exit the proximal bracket through the proximal end port and the catheter can thereafter be used as an over-the-wire catheter. Otherwise, when the guide wire is not passed through the proximal bracket, the guide wire is restrained by only the distal bracket and can stay free from the catheter at the lateral access. In this case, the catheter can be used in a monorail methodology. It will be appreciated that the catheter's method of guide wire usage can be changed at any time during a procedure, either by selectively inserting the guide wire through the proximal bracket (over-the-wire), or not inserting the guide wire through the proximal bracket (monorail).
The novel features of this invention, as well as the invention itself, both as to its structure and its operation, will be best understood from the accompanying drawings, taken in conjunction with the accompanying description, in which similar reference characters refer to similar parts, and in which:
Referring initially to
In
In detail, for the over-the-wire configuration of catheter 10 (see
In the monorail configuration for catheter 10 (see
An alternate embodiment for the present invention is shown as the catheter 10′ in
For purposes of this disclosure, the catheter 10 is shown to be a so-called “balloon catheter.” Specifically, in
As envisioned for the present invention, the interaction of the catheter 10 with a guide wire 16 will most often happen after the guide wire 16 has been pre-positioned in the vasculature of the patient 14. To begin, the extracorporeal end of guide wire 16 will first be inserted through the distal end port 34 of the distal bracket 28. As the guide wire 16 then exits from the distal bracket 28, the operator has a choice. One choice is to do no more, and use the catheter 10 in a monorail configuration. The other choice is to insert the guide wire 16 into the guide wire lumen 38 of the proximal bracket 30 until it extends from the proximal end port 26 at the Y-site 22. The operator can then use the catheter 10 in its over-the-wire configuration. As will be appreciated by the skilled artisan, the configurations are selectively interchangeable at any time.
While the particular Over-The-Wire Catheter With Lateral Access as herein shown and disclosed in detail is fully capable of obtaining the objects and providing the advantages herein before stated, it is to be understood that it is merely illustrative of the presently preferred embodiments of the invention and that no limitations are intended to the details of construction or design herein shown other than as described in the appended claims.