Other

Pfizer Hospital Products Group, Inc.

Biagio Ravo

Thomas E Sloane, Jr

Christine L Regan

An artificial anus includes a hollow tubular support member, having a cylindrical body portion and a pair of radially-extending flanges at the two opposed open ends of the body portion, and a releasable plug for sealingly closing the hollow support member. The support member is suitable for implantation within an opening in the abdominal wall of the patient, with one of the radially-extending flanges lying upon the dermis or subcutaneous tissue, the other of the flanges lying on the fascia or peritoneum, and the end of the patient's colon received within the support member. Inner and outer layers of at least a portion of the cylindrical body portion are capable of receiving soft tissue ingrowth. A pressure transducer of electrical contact is provided on the support member and connected to an electrode in contact with the patient's skin, so that when the colon becomes pressurized the patient is signalled that the plug should be released. The device can be modified to serve as an artificial bladder or implantable body access device.

Implantable reservoir adapted to receive and store structural devices

An artificial anus includes a hollow tubular support member, having a cylindrical body portion and a pair of radially-extending flanges at the two opposed open ends of the body portion, and a releasable plug for sealingly closing the hollow support member. The support member is suitable for implantation within an opening in the abdominal wall of the patient, with one of the radially-extending flanges lying upon the dermis or subcutaneous tissue, the other of the flanges lying on the fascia or peritoneum, and the end of the patient's colon received within the support member. Inner and outer layers of at least a portion of the cylindrical body portion are capable of receiving soft tissue ingrowth. A pressure transducer or electrical contact is provided on the support member and connected to an electrode in contact with the patient's skin, so that when the colon becomes pressurized the patient is signalled that the plug should be released. The device can be modified to serve as an artificial bladder or implantable body access device.

Implantable device

A technique whereby leakage from an anastomosis and problems directly resulting from such leakage are eliminated. The technique is an anastomosis procedure for securing intraintestinal bypass graft formed preferably of a soft latex or silastic tube with a radiopaque axial line for x-ray observation after implantation. The ends of the tube are sutured or stapled to the mucosal or submucosal linings, and after a period of about 10 to 15 days during which the anastomosis is healing, the bypass graft separates naturally from the wall of the intestine, and is finally expelled naturally from the anus. This graft prevents leakage at the anastomosis and thus substitutes for and makes unnecessary a colostomy or any other diversionary procedure.

Surgical method for using an intraintestinal bypass graft

The intestinal graft is a graft formed of a thin wall latex or silastic tube of various widths and lengths. The upper circular end of the tube and vertical seam are reinforced by fabric which contains a radiopaque filament. When the graft is joined to the submucosal layer of the bowel proximal to the usual anastomosis, it will prevent salivary esophago-gastrointestinal secretions, food, and fecal flow from coming in contact with the anastomotic closure site. The graft will thus prevent leakage from any intestinal anastomosis and will guarantee a healed anastomosis by the time the graft is naturally expelled from rectum.

Intraintestinal bypass tube

An improved intraintestinal bypass graft for attachment in the lumen of a resectioned intestine or duct upstream of the anastomosis site in order to protect the healing anastomosis comprises an elongated tube formed of a thin, highly flexible, water-impervious wall material terminating at its distal end in a short, reduced diameter nipple. The surgical procedure for implanting the bypass graft can be simplified and shortened in time by readily fitting the distal nipple over one end of an elongated pliable leader, or alternatively over the terminal anvil nut of a circular anastomosis surgical stapler, and then drawing the leader or stapler body through the patient's anus to pull the distal end of the bypass graft out of the anus. The need to tie the distal end of the bypass graft to the leader or surgical stapler is eliminated.

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New York, NY, United States of America

Biagio Ravo