1. Field of the Invention
The present invention relates generally to surgical devices and methods, and more particularly to an endoscopic applicator particularly suitable for delivering surgical fluids, hemostatic agents or the like.
2. Background Discussion
Minimally invasive surgical procedures, such as endoscopic procedures, have become very common. These procedures typically involve one or more small incisions that provide access to the relevant internal surgical site. A trocar, cannula or the like is placed into each incision, and all surgical steps are subsequently performed through the trocar(s) using appropriately sized and designed instruments and devices.
Often times during such surgical procedures it is necessary to deliver medicinal materials, such as liquids, gels or the like, to the surgical site. Delivery to a specific location, and delivery of a specific amount of the material is often desired, such as is the case with anti-adhesion or hemostatic materials. For such materials, general washing or irrigation type delivery methods are unsuitable. Further, many such materials are costly, rendering precise application even more important.
In efforts to address these concerns, many endoscopic applicators have been developed, and those known to the inventors typically involve a long catheter-like outer tube (long enough to pass through the endoscopic trocar or port) having a channel extending therethrough between its proximal and distal ends. The surgical material, typically a fluid or gel-like material, is expressed into the channel (by any suitable means such as a syringe) for delivery to the surgical site. The proximal end includes some type of handle device to enable the user to adequately grip and manipulate the device. A second plunger-like element is sized to fit into the outer tube channel, and when slid therein expresses the material within the outer tube out through its distal end. A representative example of such a prior art applicator 100 is illustrated in
Some known prior art devices of the type shown in
One other known applicator is somewhat similar to that described above, but further includes toward its proximal end (towards the handle portion) an airtight membrane or seal between the outer deliver tube and the inner plunger element to prevent gases within the surgical site from escaping. This device is known as the EndoAvitine® Endscopic Delivery System, which is sold by C.R. Bard, Inc. of New Jersey, and is designed specifically to delivery a collagen hemostat, which is a solid-like material that is pre-loaded into the applicator by the manufacturer. With this device, sliding movement between the outer delivery tube and inner plunger element is possible, but only by overcoming a much larger frictional force caused by the presence of the seal. This frictional force is typically not an issue for the specified application, since, due to it's pre-loaded nature, the plunger is only used to express the solid-like material and therefore only has to travel a small distance under compressive force by the user. This type of design, however, would be unsuitable for endoscopic fluid applicators, where the plunger-like element is first entirely removed from the outer delivery tube so that the surgical fluid can be inserted therein, and subsequently re-inserted and moved substantially entirely through the outer delivery tube to express the fluid. The frictional forces generated by having such a seal at a proximal end would render the device too difficult to manipulate.
Accordingly, it would be desirable to provide a new and improved endoscopic applicator that overcomes the problems described above.
An endoscopic fluid applicator is provided including an outer delivery device having a handle at a proximal end and an elongate tubular element extending outwardly from the handle to a distal end, where the outer delivery device has a channel extending therethrough between the proximal and distal ends, the channel being defined along its length by an inner diameter. Also included is an inner plunger device including a handle at a proximal end and an elongate plunger element extending outwardly from the handle to a distal end, where the elongate plunger element is defined along its length by an outer diameter and is sized and shaped relative to the outer delivery device channel so as to be receivable therein. The elongate plunger element further has a length such that, when received within the outer delivery device channel, it extends at least substantially to the distal end of the outer delivery device. Only proximal end portions of the outer delivery device and inner plunger device are sized and shaped so as to form an interference fit with one another substantially only when the elongate plunger element is fully received within the outer delivery device channel.
According to one embodiment, the elongate plunger element has a proximal end region, a middle region, and a distal end region, and the outer diameter is greater in the proximal end region than in the middle region. The outer delivery device channel may be substantially uniform along its length. In yet another embodiment, the outer diameter of the elongate plunger element at the middle region is approximately 3.2 mm, and the outer diameter at the proximal end region reaches approximately 4.3 mm. The outer diameter of the distal end region of the elongate plunger element may further be approximately 3.7 mm.
In yet another embodiment, the applicator further includes at least one interference element forming the interference fit as between the outer delivery device and the inner plunger device when the elongate plunger element is substantially fully received within the outer delivery device channel. In an alternate embodiment the outer diameter of the elongate tubular element may be less than approximately 5 mm.
Also provided is an endoscopic fluid applicator including an outer delivery device having a handle at a proximal end and an elongate tubular element extending outwardly from the handle to a distal end, where the outer delivery device has a channel extending therethrough between the proximal and distal ends. The applicator further includes an inner plunger device including a handle element at a proximal end and an elongate plunger element extending outwardly from the handle to a distal end, where the elongate plunger element is sized and shaped so as to be slidably receivable within the outer delivery device channel, and means at a proximal end region of the applicator for forming an interference fit between the outer delivery device and inner plunger device substantially only when elongate plunger element is fully inserted within the outer delivery device channel. The interference fit is sufficient to substantially prevent further movement of the inner plunger device relative to the outer delivery device absent exertion of a predetermined amount of force by a user.
According to alternate embodiments, the means for forming an interference fit may be an outwardly tapered proximal end region of the elongate plunger element, which may be a luer taper, may further include at least one interference element positioned between the proximal end regions of the outer delivery device channel and the elongate plunger element, or may be a recess within the handle of the inner plunger device for receiving a corresponding extension portion of the handle of the outer delivery device.
According to various other embodiments, the outer diameter of the elongate tubular element may be less than approximately 5 mm and/or the inner diameter of the outer delivery device channel may be approximately 3.8 mm.
An endoscopic applicator is also provided having an outer delivery device including a handle at a proximal end and an elongate tubular element extending outwardly from the handle to a distal end, where the outer delivery device has a channel extending therethrough between the proximal and distal ends, and an inner plunger device including a handle element at a proximal end and an elongate plunger element extending outwardly from the handle to a distal end, where the elongate plunger element is sized and shaped so as to be slidably receivable within the outer delivery device channel. Also included is a means at a proximal end region of the applicator for forming an threaded fit between the outer delivery device and inner plunger device when the elongate plunger element is substantially fully inserted within the outer delivery device channel. The threaded fit is sufficient to substantially prevent further movement of the inner plunger device relative to the outer delivery device absent further manipulation by a user.
The means for forming an threaded fit further comprises male and female thread forms at the proximal end region of the inner plunger device and outer delivery device channel.
According to one embodiment, the male and female thread forms are Luer taper threads. In another embodiment, the outer diameter of the elongate tubular element is less than 5 mm, and in yet another embodiment, the inner diameter of the outer delivery device channel is approximately 3.8 mm.
a-1c are side-views illustrating an exemplary prior art design and various components thereof;
a and 2b are side-views illustrating components of one embodiment of an applicator according to the present invention;
a-5e illustrate alternate means by which to form an interference fit as between the outer delivery device and inner plunger device.
Referring now to
The outer delivery device includes a channel 222 extending therethrough between the proximal 208 and distal 212 ends, with the size of the channel being defined by an inner diameter d1 of the outer delivery device. Further, the device and channel therethrough include a proximal end region 250, a middle region 251 and a distal end region 252. Although the term “diameter” is used, it is to be understood that the term is not meant to be limited to circular cross-sections, although circular is the preferred embodiment. Further, the term “diameter” is not intended to require a constant diameter along the length of the device, as will be described further below.
The outer diameter d2 and length l1 of the elongate tubular member 210 must be suitable for insertion through an endoscopic port such as a cannula or trocar. According to a preferred embodiment, the inner diameter d1 is approximately 3.8 mm, the outer diameter d2 is approximately 4.8 mm, and the length l1 is approximately 34 cm. With regard to handle element 206, any suitable configuration may be used that adequately allows the user to grasp and manipulate the outer delivery device. In the illustrated embodiment, the handle has a substantially disc-like portion 224 having a length l2 of approximately 10 mm, and a diameter d3 of approximately 2.5 cm, and an extension portion 226 at its proximal end.
The elongate plunger element 218 of the inner plunger device 204 is dimensioned relative to the outer delivery device channel so as to be receivable therein, and slidable therein along a substantial portion of its length. In the illustrated embodiment, the length l3 is further sized such that, when the elongate plunger element is inserted into the outer delivery channel, the distal end 220 of the elongate plunger element is at least substantially aligned with the distal end 212 of the outer delivery device, and preferably extends slightly beyond, as illustrated in greater detail in
Referring now to the proximal end portion 230 of the elongate plunger element, in the illustrated embodiment shown in greater detail in
Although the illustrated embodiment shows an outwardly tapered or flared proximal end portion of the elongate plunger element, it is to be understood that any suitable means for forming an interference or locking fit as between the proximal end portions of the outer delivery device and inner plunger device can be used. For example, the respective handle portions could be appropriately configured so as to form an interference fit therebetween as shown in
It will be apparent from the foregoing that, while particular forms of the invention have been illustrated and described, various modifications can be made without departing from the spirit and scope of the invention. Accordingly, it is not intended that the invention be limited, except as by the appended claims.