Abstract: An implantable device and method for adjustably restricting a selected body lumen such as the urethra of a patient to treat urinary incontinence. The device includes an expandable element or membrane such as a balloon attached pressure-tightly to a flexible conduit at its forward end and includes a rear port portion containing an elastic septum and flow connected to the expandable element by a first passageway. The conduit contains a second passageway which allows it to be slid along an elongated guide probe initially inserted surgically into a patient's body adjacent the body lumen which is to be adjustably restricted. A suitable flowable material is injected from a syringe source into the device rear port sufficient to expand the membrane element and restrict the body lumen to the desired degree. The syringe and guide probe are removed and the skin incision is closed over the rear port end of the implanted device.

Abstract: A portable apparatus and corresponding method is provided for treating or preventing at least one of brain, brain-stem and associated nervous tissue injuries in a mammal suffering from decreased blood flow to the brain. The apparatus includes a flexible enveloping member for enveloping a head, neck and upper back of a mammal. The enveloping member includes outer and inner shells with at least one cavity intermediate the outer and inner shells for holding a coolant fluid within the at least one cavity. A coolant source is provided in communication with the enveloping member.

Abstract: Provided is a device to control fecal incontinence and methods for its use. The device comprises a longitudinal tubular member having attached thereto bilaterally-extending wings for securing the device while in use. The device also comprises an expandable portion for prevention of unwanted defecation during use of the device.

Abstract: A self-contained isolation and environmental protection life support system for shielding a patient contained therein or, alternatively, isolating a contaminated patient from a clean environment while allowing treatment of traumatic injuries to the patient. The system comprises the combination of an environmental control system (ECS) and a containment enclosure that are designed to function in concert with conventional life support stretcher. The ECS component possesses an air management system that is designed and configured to extract contaminated particles and gas from the external air and deliver the same to the patient contained within the containment enclosure. To facilitate such delivery, the containment enclosure is preferably provided with a plurality of tubular passages which are designed to be filled with air provided by the ventilator system to thus cause the containment enclosure to expand to form a semi-rigid structure.

Abstract: Flexible probes are arranged to achieve a desired light distribution pattern for administering light therapy at a treatment site in a patient's body. The flexible probes (20, 20', 92) each include a flexible substrate on which are mounted light emitting devices (30) in spaced-apart array. An optically transparent, biocompatible envelope (36) encloses the flexible substrate and components mounted thereon. In one embodiment, a link (44) couples a pair of the flexible probes together in parallel alignment for insertion at the treatment site. Thereafter, the probes are moved relative to each other within the link to achieve the desired light distribution pattern. In another embodiment, the flexible probes include flexible leaders (70, 72) attached to their distal ends, which terminate in suture tabs (74) that can be affixed to tissue adjacent the treatment site.