Abstract: A temperature determination method includes temporarily contacting a forehead of a subject with a first surface of a removable patch, and exposing a second surface of the patch opposite the first surface to ambient conditions. The method also includes sensing a temperature of the first surface of the patch while the first surface is in contact with the forehead at a first location thereon, sensing a temperature of the second surface of the patch, and calculating a sub-skull temperature of the subject based on the sensed temperatures of the first and second surface.

Abstract: A manual neurological testing device for measuring a subject's reaction time comprising: a releasable holding member operable to be grasped by the subject; a stimulus device coupled with the releasable holding member, the stimulus device outputting a perceivable stimulus; and a measurement device coupled with the releasable holding member, the measurement device measuring the subject's reaction time for grasping the releasable holding member relative to the perceivable stimulus.

Abstract: A disposable biosensor test strip is provided that includes a plurality of penetrating members. Each penetrating member is associated with a capillary chamber that has a depth suitable for capillary flow of blood and holds a volume of less than about 1.0 .?l of the blood sample. A working electrode and a counter or reference electrode are disposed within the capillary chamber. A reagent is proximal to or in contact with at least the working electrode. The reagent includes an enzyme and a mediator. The reagent reacts with glucose to produce an electroactive reaction product. A blood sample, containing glucose, is applied into the capillary chamber. The capillary chamber directs capillary flow of the blood sample into contact with the reagent to cause the blood sample to at least partially solubilize or hydrate the reagent. The blood sample is detected in the capillary chamber. The electroactive reaction product is electro-oxidized or electro-reduced at the working electrode.

Abstract: A system and method for predicting the onset of glaucoma uses a Finite Element Model (FEM) to obtain a response profile of the Optical Nerve Head (ONH) inside an eye. To do this, the FEM is programmed with data from first and second images of the ONH that are respectively taken at the beginning and the end of an imposed pressure differential (e.g. over a range of about 8kPa). The FEM is then subjected to a sequence of pressure increments and the resultant profile is compared with empirical data to predict an onset of glaucoma.

Abstract: A sample collection container adapted to be connected to, and disconnected from, a sample collection adapter and a sample collection container cap. The sample collection adapter has a downward sloping interior surface that provides a free-flowing path for samples provided by a subject to the sample collection container. The sample collection adapter may have a three-dimensional rim that is curved in two different non-parallel planes.

Abstract: A steerable device, such as a steerable catheter, may include a control handle and an insertion shaft extending outwardly therefrom. In use, the insertion shaft is navigated to an area of interest for examination and/or treatment thereof. The steerable device may include a steering system that controls the deflection angle of the distal end of the insertion shaft in two or more non-planar directions for navigating the insertion shaft to the area of interest. The steering system may also include a locking mechanism for arresting or partially arresting the movement of the distal end of the insertion shaft in a first direction independent of arresting or partially arresting the movement of the distal end in a second non-planar direction.

Abstract: Methods for determining structural integrity of a bone within the spine of a patient, the bone having a first aspect and a second aspect, wherein the second aspect separated from the first aspect by a width and located adjacent to a spinal nerve. The methods involve (a) applying an electrical stimulus to the first aspect of the bone; (b) electrically monitoring a muscle myotome associated with the spinal nerve to detect if an onset neuro-muscular response occurs in response to the application of the electrical stimulus to the first aspect of the bone; (c) automatically increasing the magnitude of the electrical stimulus to until the onset neuro-muscular response is detected; and (d) communicating to a user via at least one of visual and audible means information representing the magnitude of the electrical stimulus which caused the onset neuro-muscular response.

Abstract: The invention is directed to tissue cutting members and biopsy devices with such tissue cutting member for separating a tissue specimen from a patient's body at a target site. The tissue cutting member is slidably disposed within an inner lumen of an elongated probe member of the biopsy device to cut a tissue specimen drawn into the interior of an outer cannula of the biopsy device through a tissue receiving aperture in the probe. The tissue cutting member has a tubular distal portion with a distal tip having an outer tissue cutting edge, an inner tissue receiving aperture, and a longitudinally oriented opening with a closed proximal end and open distal end which opens to the inner tissue receiving aperture to facilitate flaring of the distal tubular portion. The cutting member has at least one opening in a wall of the tubular portion to maintain a vacuum during use.

Abstract: A tissue penetration device and method of using same that may include a lancet module or sampling module. The sampling module may optionally be in a cartridge configuration and include sampling and analyzing functions, which may be integrated.

Abstract: An integrated sampling device defines a first opening and a second opening. The first opening is connected to a channel for drawing fluid automatically towards a test media upon incision by an incision portion. The second opening is positioned over the test media allowing manual sampling of fluid if the channel fails to draw a sufficient amount of fluid onto the test media.

Abstract: The present invention relates to methods and devices for formation of microconduits in tissue, particularly using an impedance sensing drill to form microconduits. One embodiment of the invention is an impedance sensing drill comprising a drilling assembly, a control module, mechanically connected to the drilling assembly for controlling the depth of drilling by the drilling assembly; and a sensor, electrically connected to the drilling assembly and control module for detecting a change in an electrical impedance of a material being drilled. Another embodiment is a method of forming a microconduit in a material, which comprises the steps of drilling into the material, monitoring an electrical impedance of the material, and stopping the drilling into the material when a change in the impedance is detected, thereby forming microconduit.

Abstract: A system for delivering information through a computer. The system comprises: data collecting means for collecting personal data including menstrual data regarding a menstrual cycle on a woman from a user; phase identification means for identifying a phase within the menstrual cycle; storage means for storing predetermined information; selection means for selecting information from the storage means, which is personalized based on the phase identified by the phase identification means; and delivery means for delivering the personalized information.

Abstract: A method and system for regulating contact pressure of a sensor is provided. In accordance with an embodiment, a sensor includes a collapsible material capable of regulating the localized component contact pressure exerted on a tissue between a threshold which ensures proper contact between the sensing component and monitoring site but which minimizes incidents of excessive localized pressures which could result in tissue damage over prolonged use. This localized contact pressure range is maintained over a wide range of sensor application pressures. In one embodiment, a window is provided in the sensor and a colorimetric indication of the compression or expansion of the collapsible material may be determined through the window.

Abstract: The present invention provides for a device and a kit for collecting body fluids. The device includes a body fluid collection portion comprising a body fluid absorbing material. The body fluid connecting portion has a free edge and is hingedly connected at the edge opposite to the free edge to a first support panel and a second support panel. A base panel is hingedly connected to the first support panel or the second support panel. In a first folded condition the body fluid collection portion is sandwiched between the first support panel and the second support panel in a substantially face contacting relationship.

Abstract: An intracranial pressure monitoring system and method. The system includes an auditory stimulation and recording unit, which includes a stimulation controller, a memory for storing waveforms, a device for comparing received waveforms with stored waveforms, and an alarm operable based upon that comparison. The system includes at least one cranial electrode attachable to a patient, and an auditory stimulation device, operable by the stimulation controller. The stimulation device is a pair of acoustic ear inserts, each of which is connected to and operated by an auditory stimulator activated by the stimulation controller. In the method, a patient is auditorially stimulated to evoke a received waveform indicative of intracranial pressure, a comparison is generated by comparing the received waveform with one of an established patient baseline waveform and an established normal waveform, and an alarm is generated responsive to that comparison.

Abstract: Monitoring the status of an absorbent article can be desirable to various users in various situations. A monitoring device for use with an absorbent article is provided. The monitoring device includes a sensing device and a signaling device. The sensing device is configured to sense a physiological indication related to the absorbent article wearer. The functionality of the monitoring device may be updateable, for instance, by utilizing firmware updates, hardware or user interface changes, software installations, etc. Thus, the monitoring device of the present invention may be utilized over an entire lifespan from infants to elderly without the need for costly replacement or installation of an entirely new monitoring system.

Abstract: A biopsy device comprises a body, a needle, and a cutter operable to sever tissue protruding through a lateral aperture of the needle. A vacuum pump is in fluid communication with the cutter. A fluid pump is in fluid communication with the needle. A fluid pump actuation assembly is operable to actuate the fluid pump to deliver a bolus of fluid to the needle based on movement of the cutter. A valve assembly responsive to cutter movement is operable to selectively couple the needle with the fluid pump, couple the needle with atmospheric air, or seal the needle relative to the fluid pump and atmospheric air. The fluid from the fluid pump and atmospheric air cooperate with the vacuum to urge severed tissue samples proximally through the cutter. Components operable to actuate the cutter and the fluid pump include coaxial lead screws having different pitch diameters.

Abstract: A biopsy device includes a body portion, a tip, at least one blade, and a cutter. The cannula defines at least one lumen. The cannula has a transverse aperture configured to receive tissue. The tip is located at the distal end of the cannula, and may include at least two concave surfaces. The blade extends longitudinally from the tip. A second blade may also extend longitudinally from the tip. Blades may be axially staggered relative to the cannula. Blades may also have lengths that differ from one another. In addition, a blade may have a pointed distal end, or may have a curved distal edge. The configuration of the blade and tip may provide reduced force to penetrate tissue. The blade and tip may produce a cut length that is greater than or equal to the length of the outer perimeter of the cannula.

Abstract: A selective filtering collection and delivery system for collecting and delivering autogenous bone to and from a surgical site is provided. The selective filtering collection device includes a suction nozzle, suction nozzle assembly and a vacuum source. Disposed in parallel between the suction nozzle assembly and the vacuum source are a removable filter cartridge and a filter bypass tube. A switch on the suction nozzle assembly may be actuated to provide suction to the suction nozzle through either the bypass tube or through the filter cartridge. When suction is applied through the filter cartridge, autogenous bone is collected on a filter medium within the cartridge. Additionally, the cartridge may be removed and directly placed into a delivery device. The delivery device includes a ratchet system that actuates a plunger base to accurately extrude the bone material from the filter cartridge into the desired surgical location.

Abstract: The present invention generally relates to a medical surgical device and specifically a wire guide for percutaneous placement within a body cavity. The flexibility of the wire guide may be varied while it is in place within the body vessel.