HK1188551B - Medical device for use with a stoma - Google Patents

Description

FIELD OF INVENTION

This invention relates to a device for use in percutaneous applications by patients who have undergone surgery as a result of which an opening or stoma has been left in the wail of a hollow body cavity, such as an intestine, and/or in the abdominal wall.

BACKGROUND OF THE INVENTION

For patients having intestinal surgery or other operations to repair or remove a section of intestine, it is frequently necessary to perform a colostomy operation or an ileostomy operation. With a colostomy, the large intestine is brought through the abdominal wall, and with an ileostomy, the small intestine is brought through the abdominal wall, in each case, an opening called a stoma is created to provide a conduit for allowing elimination of waste material from the patient's body. Drainage or discharge from the digestive system of the patient takes place through the opening or stoma in the abdominal wall. The body duct protruding from the abdominal wall is typically sutured or otherwise adhered to the skin surrounding the opening. A flexible bag or other receiving means is typically attached to the stoma to collect and retain liquid, solid, and gaseous waste material eliminated through the stoma.

An exemplary such procedure is illustrated in Figures 1A and 1B, showing a loop ileostomy 10. The stoma 14 is created by cutting the loop of the intestine protruding from the abdomen. Upstream section 13 of the intestine empties the intestinal contents through the stoma. A mucous fistula 11 is formed on the downstream end 12 of the intestine, typically blocking that section from receiving intestinal contents while the stoma is in place. A shunt 5 is sometimes used between the skin and the loop of intestine.

Externalizing the intestine to form a stoma has disadvantages. It is sometimes difficult to control the flow of intestinal contents and there arises a consequential risk of infection and skin irritation. Attachment of ostomy appliances for collection of the intestinal matter can also be difficult Stenosis and prolapse of the intestine are additional risks with this type of procedure.

A similar procedure might be undertaken to connect two hollow body cavities or organs within the body, thereby allowing one organ to drain into another. For instance, a stoma, may be created in a hoilow body cavity within the body in order to allow the cavity to drain into the GI tract.

US4119100 discloses a surgical device for discharge of faecal matter from the colon. The device comprises a bent drainage duct whose inner end lies within the lumen of the colon and is surrounded by an inflatable bag for filling the lumen, the outer end of the duct projects through the side of the inflatable bag and through the wall of the colon. The outer end of the duct is held in position by a flange which lies against the surface of the patient's skin and is coupled to the duct.

US5261898 discloses a temporary colostomy apparatus for diverting the fecal stream and comprising an open ended excrement tube including a fecal receiving end having a liquid inflatable balloon on the outside thereof. A dissolvable and absorbable band is snugly wrapped around the outside of the colon at a preselected location. The tube is inserted inside the colon through a slit opening, so that the balloon is further inward but adjacent the band. The balloon is inflated so that the outer circular periphery thereof contacts the inside surface of the arrested colon and has a circumference slightly larger than the band. The inflated balloon and the band are in an abutting relationship with a common area of the colon sandwiched therebetween, to prevent outward movement of the tube. A retainer ring is positioned on the disposal end of the tube and pressed against the outside of the body to prevent inward movement of the tube. A disposable bag is secured to the disposal end of the tube on the outside of the body for collecting the fecal stream fully diverted into the receiving end of the tube. The colon is sutured to the abdominal wall adjacent the surgical openings in the colon and abdomen, to further stabilize the position of the tube inside the colon. When normal colon and rectal bowel functions could be resumed and prior to any substantial dissolving of the band, the balloon is deflated and the excrement tube is removed from the colon. The band remains encircled around the colon and in time the band is dissolved, absorbed and excreted from the body.

US2010114128 describes methods and devices for treating obesity, and more particularly, methods and devices for performing gastric bypass. In one exemplary embodiment a gastric bypass procedure is provided that includes forming a gastro-entero anastomosis between a stomach and an intestine and forming an entero-entero anastomosis between a portion of the intestine distal to the gastro-entero anastomosis and a portion of the intestine proximal to the gastro-entero anastomosis. A surrogate path is formed between the esophagus and the gastro-entero anastomosis to at least partially direct fluid from the esophagus to the intestine by way of the gastro-entero anastomosis, thereby bypassing the stomach. A variety of devices that are particularly useful in gastric bypass procedures are also disclosed. The devices include anastomotic devices that can be coupled to or integrally formed with a shunt. The devices can include a plurality of tubular bodies that are configured to have an adjustable length. Still further, methods for repairing an abdominal aortic aneurysm and leaking heart valve are also disclosed.

US3818511 describes a medical prosthesis for ducts or conduits and method of manufacture. An exemplary embodiment is an arteriovenous shunt having a cannula terminated in a funnel in which the interior included angle ranges from 15 DEG - 30 DEG . The funnel is of an implantable, resilient silicone rubber into which a woven, flexible Dacron skirt is molded to enable suturing and tissue ingrowth at the anastomotic juncture. The silicone is of a medical type which is body tissue-compatible, and has sufficient elasticity and resilience to permit compliance during pulsatile fluid flow, storage and return of fluid kinetic energy, and accommodation to various sizes of vessels, ducts, or conduits. Actual experimental use shows improved results compared to prior types of tip-type cannulae.

SUMMARY OF THE INVENTION

The invention is related to a device described according to the appended claims.

Applicant has addressed the many disadvantages associated with conventional stomas by providing a device that can be utilized with a stoma and, for example, eliminates the need to externalize an intestine through the abdominal wall. In an exemplary embodiment, the invention provides a device including a proximal portion adapted for placement intermediately within an intestine, or other hollow body cavity or organ, to capture and divert contents; the proximal portion being expandable, optionally by using a self-expandable nitinol stent, from an initial state with an initial diameter smaller than a diameter of the intestine for insertion of the proximal portion into the intestine, for example, into an expanded state with a diameter greater than the initial diameter for engaging the proximal portion with an inner wall of the intestine; and a distal portion, connected to the proximal portion, adapted to extend through the abdominal wall, or alternatively into another hollow body cavity or organ, to conduct the contents out of the proximal portion. The device also includes a valve connected to the distal portion to provide continence, allowing contents to be selectively discharged from the distal portion. The device includes a transitional portion connecting the proximal portion to the distal portion.

The proximal portion is optionally compressible from the expanded state for removal of the proximal portion from the intestine or other hollow body cavity or organ.

The distal portion has an adjustable length, either through compression, or by removing portions of the device in a controlled manner. The distal portion is also optionally corrugated. The device may be flexible, crush resistant, and kink resistant.

A method of draining hollow body cavity contents is provided comprising the steps of (a) making an incision in the GI tract; (b) making an incision into the hollow body cavity wall; (c) inserting through said incisions a device according to the present invention; (d) positioning said proximal portion within the hollow body cavity; (e) deploying said proximal portion to capture and divert hollow body cavity contents; and (f) positioning said distal portion within the GI tract to drain the hollow body cavity contents out of the proximal portion and into the GI tract.

Also described is a method of diverting intestinal contents from an intestine without bringing the intestine through an abdomen comprising the steps of (a) making an incision through the abdominal wall; (b) making an incision into the intestine without severing an entire diameter of the intestine; (c) percutaneously inserting through the incisions a device of the present invention; (d) positioning the proximal portion Within the intestine; (e) deploying the proximal portion to capture and divert intestinal contents; and (f) positioning the distal portion to extend through the abdominal wall to conduct the intestinal contents out of the proximal portion. Optionally, the method includes the step of attaching a valve to the device to provide continence allowing intestinal contents to be selectively discharged from the device. Further optional steps include attaching the intestine to an inner wall of the abdomen to seal the intestine, and adjusting the length of the distal portion to account for the thickness of the abdominal wall. The method also alternatively includes the step of removing said device from the intestine.

DESCRIPTION OF THE DRAWINGS

• FIG. 1A is a side view of a loop ileostomy according to the prior art.
• FIG. 1B is a schematic side view of a loop ileosotmy according to the prior art.
• FIG. 2 is a side view of an exemplary embodiment of the present invention.
• FIG. 3 is a side view of another exemplary embodiment of the present invention.
• FIG. 4 is a side view of another exemplary embodiment of the present invention.
• FIG. 5 is a side view of another exemplary embodiment of the present invention.
• FIG. 6 is a side view of another aspect of the present invention.
• FIG. 7 is a side view of another aspect of the present invention.
• FIG. 8 is a side view of another exemplary embodiment of the present invention.
• FIG. 9 is a side view of another aspect of the present invention.
• FIG. 10 is a side view of another embodiment of the present invention.
• FIG. 11 is a side view of the embodiment of FIG. 10 commencing inversion.
• FIG. 12 is a perspective view of the embodiment of FIG. 10 partially inverted.
• FIG. 13 is a side view of one embodiment of the device of the present invention preferentially bent into a C-shape orientation.
• FIG. 14 is a perspective view of the device of FIG. 13 in use.
• FIG. 15 is a perspective view of another embodiment of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

Figure 2 illustrates an exemplary embodiment of a device according to the present invention. A proximal portion 10 of the device is disposed intermediately within an intestine 11. "Intermediately" as used herein means within the length of the intestine, as opposed to at a surgically severed end thereof. Proximal portion 10 is adapted to capture and divert intestinal contents from within intestine 11. The material of construction for proximal portion 10 may be durable biocompatible barrier material that prevents leaks and allows intestinal contents to pass along the internal length of proximal portion 10 without sticking to it. These attributes may be achieved by the material itself, or by combining the material with a suitable coating. Preferably, proximal portion 10 is made of a multilayer construction of fluoropolymer, such as expanded polytetrafluoroethylene (ePTFE). Alternative materials for proximal portion 10 include other fluoropolymers (such as FEP), polyethylene, polypropylene, polyolefins, polyimides, polyesters, silicone, fluorosilicone, and bioabsorbable materials, such as polymers and copolymers of PGA, TMC, PLA and any combination of any of these materials. In certain embodiments, the barrier material of the proximal portion may comprise at least one aperture therein.

Proximal portion 10 includes support structure 19. Support structure 19 is preferably a self-expanding material, such as nitinol. Alternatively, support structure 19 is stainless steel or other biocompatible metal or polymer which is expandable by the application of an external force, such as balloon-expandable materials. Also alternatively, support structure 19 may be formed of a polymeric material. Support structure 19 may be bioabsorbable or nonbioabsorbable.

Support structure 19 may be disposed on the inside or the outside of the perimeter of distal portion 10; that is, support structure 19 may be around the outside of the ePTFE (for example) used for the proximal portion 10, or it may be disposed inside the ePTFE used for proximal portion 10. It could alternatively be sandwiched between layers or coatings of the material used for proximal portion 10. In any case, it is attached to the ePTFE (for example) and is used to exert an outward force that engages the inner wall of intestine 11 and secures proximal portion 10 in place therein, allowing intestinal contents to be substantially fully diverted from intestine 11.

Support structure 19 enables proximal portion 10 to be expandable, from an initial state with an initial diameter smaller than the diameter of intestine 11 for insertion of the proximal portion into intestine 11, into an expanded state with a diameter greater than said initial diameter, for engaging the proximal portion 10 with an inner wall 12 of intestine 11. Proximal portion 10 is also compressible from its expanded state for removal of proximal portion from intestinal 11.

In Figure 3, support structure 19 extends the length of proximal portion 10 and beyond, extending into intestine 11 below proximal portion 10. This structure provides for added reinforcement, and therefore patency, of intestine 11 at the stoma site. It limits twisting or kinking of intestine 11 near the stoma site, providing the benefit of preventing narrowing (such as by occlusion or obstruction) of intestine 11 leading to an undesirable slowdown of intestinal flow.

Figure 4 illustrates an example in which support structure 19 is included in distal portion 13. The support structure can be of the same alternative constructions as described above in connection with proximal portion 10.

Figure 15 depicts yet another alternative support structure 19 in which portions along the length of the device are unsupported while regions of both the distal portion 13 and the proximal portion 10 are supported.

As shown in Figures 2 -4, the device also includes a distal portion 13, connected to proximal portion 10. Distal portion 13 may be adapted to extend through abdominal wall 14 to conduct the intestinal contents out of proximal portion 10. At least distal portion 13 may be kink resistant to prevent twisting or kinking thereof. This may be done by constructing distal portion 13 of any biocompatible material that can be made into a tube. Preferably, distal portion 13 is made of ePTFE, reinforced by a support structure similar to that described above in connection with support structure 19. Figure 4 illustrates the support structure for distal portion 13 as a series of nitinol rings. Alternatively, the reinforcement can be FEP. In certain embodiments, the material of the distal portion may comprise at least one aperture therein.

Distal portion 13 has an adjustable length to accommodate different width of abdominal wall 14. The adjustable length may be provided by selection of material that is cut to size, or by use of corrugated or telescoping construction to facilitate compressibility or extension.

Exemplary devices may further comprise a funnel structure (not shown) at the distal end of the device which could assist in preventing migration or movement of the device and potentially avoid pull through of the device through the stoma.

The device of the present invention includes a transitional portion 15 connecting proximal portion 10 to distal portion 13 for attaching intestine 11 to an inner wall 16 of the abdominal wall 14. A flange or other securing means 18 is optionally also included at the opening to connect and seal distal portion 13 to the patient's skin.

In alternative embodiments, the device of the present invention includes a valve incorporated at any point along the device, preferably the valve could be connected to either said proximal portion 11 or said distal portion 13 for providing continence to the patient, thereby allowing intestinal contents to be selectively discharged from distal portion 13. A valve located in proximal portion 11 may provide an advantage in that the larger diameter of the valve opening could allow for easier passage of material and potentially reduce the risk of blockage. For example, a valve may be located in a proximal portion of the device but controlled from the distal portion.

Figure 5 depicts an embodiment of the present invention including retention means 51, which can be barbs or scales or the like, on proximal portion 52 for retaining device 50 in place within the intestine. Support structure 53 in this embodiment comprises nitinol stent rings that extend the entire length from proximal portion 52 through and including distal portion 54. In this embodiment, device 50 also includes a retention collar 55 and an iris valve 56 pneumatically actuated. Retention collar 55 is designed to be on the inside wall of the abdomen to prevent movement or migration of device 50 out of the patient. Iris valve 56 is intended to allow a patient to have control over the external release of intestinal contents and is designed to be disposed outside the body.

Figure 6 illustrates another aspect of the invention. Figure 6 shows a dual disc fistula collar 60. Collar 60 is preferably made from a bioresorbable material that is designed to last as long as the device is intended to be in place. A more permanent device may be used, and for example, an ePTFE scaffold can be used with the bioresorbable material. The purpose of fistula collar 60 is to anchor the inside of the intestine to the abdominal wall. This provides support for the device that passes through the middle of collar 60 via lumen 63. This facilitates sealing of the intestine so that intestinal contents do not leak in the abdominal cavity. A retention collar (55, Figure 5) on device 50 keeps device 50 from being withdrawn into the abdominal cavity. End 61 of collar 60 is designed to be placed inside the intestine, while end 62 is designed to be placed against the abdominal wall. Compression cords 64 are pulled after placement to allow accordion effect of central lumen 63 to clamp down on device 50 and draw the intestine towards the abdominal wall.

Figure 7 illustrates an intestinal plug 70 which is used to seal the natural fistula channel that remains after removal of the device. Intestinal plug 70, as with dual disc fistula collar 60, can be made from a bioresorbable material, alone or with a scaffold made, for example, of ePTFE to provide strength and longer life. The dual disc fistula collar 60 is left behind in vivo after removal of the device. The design of intestinal plug 70 is similar to dual disc fistula collar 60 but without the central lumen 63. End 71 of intestinal plug 70 is designed to be placed in the intestine, and end 72 is designed to be placed against the abdominal wall. Compression cords 74 pull the two discs 71 and 72 together.

Figure 8 illustrates the in-dwelling device shown post-placement and before removal. Proximal portion 81 diverts intestinal contents. Dual disc fistula collar 82 anchors the device in place. Retention collar 83 prevents the device from retracting into the intestine. Iris valve 84 allows patient to control release of intestinal contents. Compression cords 85 seal and pull intestine toward abdominal wall. Support structure 86 in this embodiment is a nitinol frame which comprises a spine that creates a preferential bend in the device that helps hold it in place within the intestine but is flexible enough to allow removal of the device with a removal sheath. Note that the bottom of the device bend is held in place by the dual disc fistula collar 82.

Figure 9 illustrates removal of the device. A removal sheath 90 is used to compress the device so that it can be removed percutaneously, ideally in an outpatient setting. Removal sheath 90 is a hollow polymeric tube sized to allow the withdrawal of the device 91, in the illustrated example, into the central lumen of the removal sheath 90. Removal sheath 90 is rigid enough to prevent collapse or accordioning when removing device 91. Tensioning members 92 are attached to the end of device 91 (after removal of the valve) to pull the stent graft into the sheath. The sheath is advanced as the tensioning members are pulled to completely capture device 91 then removed from the patient. Figure 9 is an illustration of device 91 in the process of being retracted into sheath 90.

An alternative method of removal is demonstrated in Figures 10-12 wherein the proximal end of the device can be inverted into the main channel of the device for ease of removal. Figure 10 shows an embodiment of the present invention comprising a radial component 101 that reduces the diameter of the proximal portion 10, or at least the proximal end 103 of the device 100. In communication with the radial component 101 is a tensioning member 102, which may be in the form of, for example, a tensioning cord or retrieval line. The tensioning cord or retrieval line may be a separate member from the radial component or may be pan extended end portion of the radial component. Upon force being applied to the tensioning member, as in FIG. 11, tension is applied to the radial component 101 which reduces the diameter of at least the proximal end of the device and anchor fins 111, positioned circumferentially on the proximal portion and/or proximal end of the device are disengaged from the surrounding tissues. Once the proximal end is so reduced, additional force applied to the tensioning member 102 serves to pull the proximal end of the device into a main channel of the device and begin the inversion process as shown in Figure 12. The larger diameter of the proximal portion is thereby reduced.

In yet another example, the device can be pulled apart in a controlled manner in order to ease removal from the intestine or other hollow body cavity or organ. In one embodiment, to facilitate the pull apart method the device may comprise a retrieval line that is attached directly to the proximal end of the support frame, such as a nitinol, one piece, wire frame. Pulling on the retrieval line would pull the proximal end of the support out of the graft material. Continued tension on the retrieval line would continue to pull the nitinol wire free of the graft material in a continuous length. In one example, when enough of the wire has been pulled out that the supported proximal region has a diameter similar to that of the stoma, the device can be removed. Alternatively, where a device comprises a one piece nitinol wire support frame but no retrieval line is present, one could begin pulling on the distal end of the nitinol wire. This method would require the user to unravel most of the device prior to removal as the largest diameter portion of the device would be unraveled last.

As described above, the devices of the present invention further comprise a preferential bending mechanism which imparts a radius of curvature to a region of the device, preferentially in one direction, upon expansion of the device. The region of the device capable of achieving a radius of curvature may be located in the proximal portion of the device, the distal portion of the device or any transitional portion therebetween. The preferential bending mechanism may be in the form of a spine along one side of a region of the device. Where the device comprises a support frame, an asymmetrical support frame on opposing sides could provide a suitable spine to achieve preferential bending of the device upon expansion. As shown in Figure 11, where the device comprises a support frame 53, longer apical distances 112 between apices 113 on adjacent stent rings along at least a region of one side of the device could provide a spine for the device and would be a suitable preferential bending mechanism. Alternatively, the preferential bending mechanism may be in the form of bridging members along a length of device connecting adjacent stent rings on one side of the device thereby creating a spine. Alternatively, a spine could comprise an area of denser barrier material along one side of a region of the device or any other longitudinal stiffening member. Figure 13 shows the device preferentially bent along the spine 150 of the device 100 in order to render the device into a c-shape or j-shape. In Figure 15 the spine 150 of the device comprises a longitudinal support structure along one side of an otherwise unsupported region of the device which provides a suitable preferential bending mechanism.

The preferential bending mechanism may further comprise a locking feature that allows the device to remain in the bent position, until such time as the lock is removed or opened. One advantage to locking the device into a preferentially bent orientation is that the device itself can operate as a clamp, thereby clamping surrounding tissues and eliminating the need for supplemental anchoring means to keep the anchor in place and prevent migration. Generally, the proximal portion of the device would be located within a first hollow body cavity or organ and the distal end of the device could be located in a second hollow body cavity, suitable for receiving drainage from the first, or, alternatively, through the abdominal wall. However, the devices may further be held in place by adherence to the surrounding tissue, for example, by suturing or other means. Figure 14 shows a locked and preferentially bent device 100 in use and connecting two hollow body cavities or organs.

Any number of active agents, such as antimicrobials, may also be included as fillers or coatings in conjunction with any of the embodiments described herein.

While particular embodiments of the present invention have been illustrated and described herein, the present invention should not be limited to such illustrations and descriptions. It should be apparent that changes and modifications may be incorporated and embodied as part of the present invention within the scope of the following claims.

Claims (15)

1. A device comprising;

   a. a proximal portion (10) adapted for placement within a hollow body cavity to capture and divert said hollow body cavity contents; at least said proximal portion (10) being expandable, from an initial state with an initial diameter for insertion of said proximal portion (10) into the hollow body cavity, into an expanded state for engaging hollow body cavity tissues with a diameter greater than said initial diameter; and

   b. a distal portion (13) having an adjustable length, adapted to extend through a stoma in a wall of said hollow body cavity to conduct the hollow body cavity contents out of the proximal portion (10);

   c. a transitional portion (15) connecting the proximal portion (10) and the distal portion (13);

   d. wherein the proximal portion (10) includes a support structure (19) which is used to exert an outward force that engages the inner wall of the hollow body cavity and secures the proximal portion (10) therein; and

   e. a bending mechanism that imparts a radius of curvature to a region of the device in one direction upon expansion of the device.
2. The device of claim 1 wherein said distal portion (13) and said proximal portion (10) comprise at least one layer of a barrier material.
3. The device of claim 2 wherein the support structure (19) comprises an expandable support frame with a length and a channel extending therethrough.
4. The device of claim 1 wherein in the initial state the device is substantially axially oriented and in the expanded state the device comprises at least one region with a radius of curvature.
5. The device of claim 4 wherein the bending mechanism is a longitudinal stiffening member, or wherein the bending mechanism further comprises a locking component.
6. The device of claim 3 wherein the support frame (19) has a substantially round cross section, and optionally wherein the support frame (19) is asymmetrical on opposing sides of said channel.
7. The device of claim 1 wherein said proximal portion (10) further comprises a radial component (101) that reduces the diameter of said proximal portion (10) upon tensioning.
8. The device of claim 7 wherein said device further comprises a tensioning member (102) in communication with the radial component (101), and optionally wherein said tensioning member (102) is oriented within said channel and extends from said proximal portion (10) to said distal portion (13).
9. The device of claim 1 wherein said proximal portion further comprises an anchoring component (111).
10. The device of claim 2 wherein said layer of barrier material comprises at least one aperture.
11. The device of claim 1 wherein the hollow body cavity is selected from an intestine, a stomach, a gall bladder, a bladder, a pseudocyst, a peritoneal cavity, and a thoracic cavity, or wherein the distal portion (13) is positioned within the gastrointestinal tract, or wherein the distal portion (13) is positioned through the abdominal wall, or further comprising a valve connected to said device providing continence allowing intestinal contents to be selectively discharged from said distal portion (13).
12. The device of claim 1 wherein said transitional portion (15) comprises a dual disk fistula collar (60).
13. The device of claim 1 wherein said distal portion (13) is expandable, from an initial state with an initial diameter into an expanded state with a diameter greater than said initial diameter, and optionally wherein said proximal (10) and distal portions (13) are compressible from said expanded state for removal from the hollow body cavity, or wherein said distal portion (13) is corrugated.
14. The device of claim 3 wherein said expandable frame (19) is nitinol, or wherein said expandable frame (19) is stainless steel, or wherein said expandable frame (19) is a polymer, or wherein said expandable frame (19) is bioresorbable.
15. The device of claim 1 comprising a retention means (51) on the proximal portion (10) for retaining the device in place within the hollow body cavity, and optionally further comprising a retention collar (55) and an iris valve (56).