Abstract: An stretch resistant plantar fascia support system is provided. The stretch resistant plantar fascia support system is adhesively applied to the foot of a patient for providing relief from plantar fasciitis. A portion of the stretch resistant plantar fascia support system is adhesively attached to the bottom surface of the foot for reducing stress on the plantar fascia.

Abstract: A heel supporting and protective boot for bed-ridden patients, comprising unitary exterior and interior body forms which contain fiber filling and an angled foam wedge. Sewn tube holes on both sides allow for insertion of medical tubing. The inner fabric of the boot is antibacterial and moisture absorbent, while the outer fabric is moisture repellant. Left and right “Y-straps” provide secure upper and lower fastening of the boot as it envelops the patient's foot and lower leg. Two “loop” straps and a T-stabilizer stabilize the boot and keep the foot at a 90 degree angle to help eliminate foot drop. An opening at the heel of the boot and a circular cutout in the foam wedge allow the heel to remain exposed to air, provide proper elevation, and enhance blood circulation. The device enhances the healing of existing ulcers and minimizes the occurrence of foot drop and new pressure points.

Abstract: The present invention is directed to hygiene articles comprising nanofibers. The nanofibers are made from a melt film fibrillation process with a polymer composition having a melt flow rate of less than about 400 decigram per minute. The nanofibers, having a diameter of less than 1 micron, must comprise a significant number of the fibers in one layer of the web contained by the hygiene article. The hygiene articles include diapers, training pants, adult incontinence pads, catamenials products such as feminine care pads and pantiliners, tampons, personal cleansing articles, personal care articles, and personal care wipes including baby wipes, facial wipes, and feminine wipes.

Abstract: A composite wound dressing apparatus promotes healing of a wound via the use of a micropump system housed within a wound dressing member. The micropump system includes a miniature pump that applies a subatmospheric pressure to the wound to effectively draw wound fluid or exudate away from the wound bed without the need for an external vacuum source. Hence, the wound dressing and micropump system is portable which allows the patient mobility that is unavailable when an external vacuum source is used. The patient does not need to be constrained for any period of time while exudate is being removed from the wound.

Abstract: A dental appliance may have an incisor reception zone and first and second canine reception zones. The top portions of the canine reception zones may have a greater thickness that the top portion of the incisor reception zone. The top portions of the canine reception zones may also be elastic.

Abstract: A ventilator that delivers air at different pressures to a patient during inspiratory and expiratory cycles of breathing and that cycles from inspiratory to expiratory operation when the patient's respiratory flow passes a threshold level. The threshold generally increases from the beginning of inspiration to the end of inspiration. The increase can be linear over all or only a portion of the inspiratory cycle, and the threshold can be adjusted so that cycling is prevented during the initial portion of an inspiratory cycle. The minimum and maximum levels may both be functions of peak flow and the threshold may increase as a function of elapsed inspiratory time. The rate at which the threshold increases from a minimum level to a maximum level may be adjustable for individual patient needs and may be determined from previous breaths.

Abstract: A surgical drape comprising a base sheet defining a base sheet aperture, an absorbent pad attached to the base sheet and defining a pad aperture positioned in substantial alignment with the base sheet aperture, and a linear tear polymer pane attached to the base sheet and absorbent pad and defining a fenestration in substantial alignment with the base sheet and pad apertures. The base sheet, absorbent pad and linear tear polymer pane are operatively arranged to tear in communication with one another when the drape is torn away from a patient. The linear tear polymer pane further and has an adhesive strip to adhere the drape to the patient's body when the drape is in position during surgery.

Abstract: A traction apparatus which impresses a desired traction force to a body to be pulled is provided.

Abstract: The adhesive bandage consists of a support with one surface having pressure sensitive adhesive and a wound covering pad placed centrally on it, which are covered by two protective detachable tear away tabs. The tear away tab consists of a single layer over the adhesive surface of the support and becomes two layered over the pad region. The two layers are fused at the zone of fusion near the margin of the pad, but are otherwise free from each other. The layer close to the pad, called inner barrier layer, completely covers the pad area. The outer layer, also called grasping layer, partially covers the barrier layer and the pad, and is folded upon itself to give sufficient length. When the outer layer is grasped to pull apart the releasable tear away tabs the inner barrier layer prevents contact of the finger to the pad. As one pulls apart the tear away tabs the barrier layers unfold and prevent contact of the fingers with the wound and wound exudates, preventing cross contamination.

Abstract: A therapeutic pressure strap for applying pressure across a muscle or muscle groups on a mammalian limb is described. The strap is particularly well suited for treating “tennis elbow”. The strap contains an adjustable fastening means for securing and tightening the strap around a limb. The strap also possesses a plurality of pressure members (e.g., elongated rubber tubes) that apply separate and discrete areas or points of pressure in a line across a muscle or muscle group and generally perpendicular to the longitudinal axis of the limb.

Abstract: An ultrathin sole strap with a pair of heel tabs and an ultrathin arch strap formed of flexible, non-resilient non-stretch woven microfiber material having an adhesive layer on an underside surface for adhesive application to a foot individually or in combination. The sole strap is adhered along the ball, the midfoot, and the heel of the foot, and the heel tabs are adhered to the back side of the heel in crossed relation. The sole strap functions as a tensile load bearing member in the region between the ball and the heel of the foot during the heel contact phase, weight bearing midstance phase, and propulsion phases of a walking gait cycle, to bear major tensile loads and stresses which would otherwise be absorbed primarily by the plantar fascia. The arch strap adhered transversely over the sole support strap and arch of the foot provides additional support and stability.

Abstract: Systems and methods for detecting an obstructive sleep apnea event are disclosed herein. The systems and methods may use an electrical output generating ionic polymer metal composite sensor attached to a region in an airway passage in an oral cavity. The electrical output may be wirelessly transmitted as a signal for indication of an obstructive sleep apnea event. The signal may be further analyzed for treatment of the obstructive sleep apnea event.

Abstract: Magnetic devices and implantation methods are provided for use in the treatment of obstructive sleep apnea. The devices include a sheet-like element having ferromagnetic qualities. The device may also include a permanent magnet attached to the sheet-like element by magnetic forces. The devices are implanted in soft tissue surrounding the airway and in tissue space beneath the pharyngeal wall to exert forces on and/or change the shape of the soft tissue. The magnetic devices may also include a bladder containing a magnetorheological fluid that stiffens soft tissue when exposed to a magnetic field.

Abstract: The various embodiments of the present inventions provide stabilization devices and methods for use of the stabilization devices with minimally invasive gynecological procedures such as methods of preventing pregnancy by inserting intrafallopian contraceptive devices into the fallopian tubes.

Abstract: A surgical cover has a second absorbent region which is overlapped by a fluid absorbent and fluid permeable material section having outer edges and adjoining edge regions. The surgical cover as such extends in a longitudinal direction LR between an upper end and a lower end. The absorbent material section is undetachably fixed across the entire circumference on the upper side of the base cover material of the surgical cover and is substantially not connected to the base cover material outside of the edge regions such that a pocket is formed between the absorbent material section and the fluid impermeable base cover material. At least one of the edge regions of the absorbent material section has a fluid barrier formed by a joining element which undetachably fixes the material section to the upper side of the base cover material.

Abstract: A male contraceptive device includes a condom-like sheath that is placed over the male genital member and has a flavor-infusing agent disposed within the distal end. The distal end is operable to release, eject, or secrete the flavor-altered semen during male ejaculation. The condom-like sheath is shaped to elastically conform to the elongated shape of a male genital member. The sheath has an open proximal end for receiving the male genital member and the distal end has a distal tip that is selectively closed. The distal tip defines a reservoir containing the flavor-infusing agent and is operable, upon pressure of seminal fluid entering the reservoir, to cause the flavor profile or characteristic of the seminal fluid to be altered and to permit the release of the seminal fluid that has entered the reservoir.

Abstract: An apparatus for use with a protective cup is disclosed. The apparatus includes a plurality of support members which may position the protective cup in a preferred position relative to a user's body, and secure the protective cup in the preferred position. The plurality of support members may connect to the protective cup or a protective support configured to receive the protective cup. The apparatus may be configured to protect the user's groin region, such as the user's crotch area, pubic bone and genitals. The apparatus may also be configured to protect the user's buttocks or legs, such as the user's hips, thighs, shins or knees.

Abstract: A surgical drape and method of providing a sterile surface therewith is provided. The drape is configured to cover an upper portion of a radiation shield and includes a flexible wall providing a cavity sized to receive the upper portion of the radiation shield. The flexible wall has a rear wall portion configured to cover at least in part a rear portion of the radiation shield and a front wall portion configured to cover a front portion of the radiation shield. The front wall portion extends to an upper front free edge and the rear wall portion extends to an upper rear free edge. At least one fastener is attached to at least one of the front and rear wall portions adjacent respective ones of the upper front free edge and rear free edge. The fastener is configured to releasably fix the front and rear walls to the radiation shield.

Abstract: A mechanically advantaged progressive spinal system and method, wherein a string- and pulley-free strap arrangement facilitates adjustment of tension and enhances patient delivered muscle strength, wherein posterior plate curvature may be quickly and easily adjusted to best accommodate a patient's lordosis and kyphosis, and wherein modular components allow for adaptation of mobility and support to improving patient needs.

Abstract: An adhesive preparation comprising a stretchable support and an adhesive layer laminated on at least one side of the support, wherein the stretchable support comprises a interlock woven fabric subjected to crimping processing, the adhesive layer contains 10% by mass or more of methyl salicylate with respect to the total mass of the layer, the whole adhesive preparation has moisture permeability of 1 to 350 g/m2·24 hr measured at a temperature of 40° C. and a relative humidity of 90%, and the methyl salicylate has a plasma AUC0-24 ranging from 3.0 to 60.0 ng·hr/mL in terms of a mean±standard deviation, and salicylic acid as a metabolite of the methyl salicylate has a plasma AUC0-24 ranging from 5000 to 13000 ng·hr/mL in terms of a mean±standard deviation, when the adhesive preparation is applied to a human skin for 8 hours such that an application amount of the adhesive layer applied is 50 to 300 g/m2 and a contact area is 280 cm2.