Abstract:
A medical electrode system (10) includes an electrically non-conductive backing material (12) and a flexible, electrically conductive patch (14) disposed on the backing material (12). An electrically non-conductive facing material (16) is disposed over the patch which includes an aperture (24) therein for exposing a portion of the patch (14), said aperture (24) having a maximum dimension smaller than a minimum dimension of the patch (14). A lead wire (20) electrically connected to the patch (14) and a separate electrically conductive gel pad (30) is provided for releasably coupling the patch to a body part (34), the gel pad (30) having a minimum dimension larger than the aperture's maximum dimension and formed from a material enabling the gel means to be removed, intact, from said body part and patch. The gel pad (30) may further include a drug suitable for iontophoretic delivery. A strap system (76, 78) enables the patches (14) and backing material (12) to be applied in a compressing manner on a body part, and in one embodiment, the entire system is both stretchable and flexible.
Abstract:
A catheter comprising a flexible elongate tubular member (22) having proximal and distal extremities. A deflection tip (31) is carried by the distal extremity of the flexible tubular member and has a curved deflecting surface (29). The flexible elongate member has a plurality of lumens (26) therein extending through the distal extremity of the flexible elongate member and opening onto the curved deflecting surface of the deflecting tip. A plurality of arms (41) are slidably mounted in the lumens. Each of the arms has a plurality of electrodes (57) spaced-apart longitudinally thereon. A control mechanism (101) is secured to the proximal extremity of the flexible elongate member and is coupled to the plurality of arms for moving the distal extremities of the arms into engagement with the deflection tip to cause the arms to deflect proximally and outwardly from the deflection tip.
Abstract:
An EEG monitor utilizes a portable acquisition module (14) and a substantially stationary processing module (12). The EEG signals are acquired and converted to an oversampled stream of digital signals by a sigma-delta modulator (64) located in the data acquisition module. The signals are then filtered by a decimation filter (62) located in the processing module. Additional means are also provided to monitor the electrode leads to detect when the leads become unplugged. The monitor provides all power to the data acquisition module over a single twisted line which transmits data as well.
Abstract:
A biofeedback system (10) provides detection of bioelectric signals in a range of 0-90 Hz. A bioelectric signal (26) is amplified by a preamplifier (22). The composite amplitude of the amplified signal (24) is calculated by performing a fast Fourier transform on the amplified signal to calculate amplitudes of bandwidths in the range of the detected signal. Particular bandwidths of interest can be selected and displayed on a computer (26). The display permits training of the person being monitored with audio or verbal feedback.
Abstract:
An electrode system includes a nonconductive material (12) and straps (36) for positioning and holding the nonconductive material (12) along with lead wires (30) for electrically connecting the fabric patches (14) to a remote monitor or pulse generator. An electrically conductive adhesive gel pad (16) is provided for releasably coupling the flexible conductive fabric patch (14) to the body part. The pad (16) is selectively removable from the fabric patch (14), enabling removal of the patch (14) from the gel pad (16) while the latter remains adhered to a body part. This facilitates release of the conductive fabric patch (14) and separate disposal of the adhesive gel pad (16).
Abstract:
Determining the brain condition of a human between normal and abnormal as determined by dementia, and selectively between dementia of the Alzheimer's-type and multi-infarct dementia is effected. Measures of electrical output, spectral ratio and coherence value of the brain are determined. Selected scores are applied to the electrical output, spectral ratio and coherence values. A relationship between the scores and additionally the scored value of a coherence ratio are effected to obtain a diagnostic evaluation. Measurements are taken by electrodes (13).
Abstract:
Apparatus for mounting electrodes (10) on a human body in order to obtain human biosignals is disclosed. The apparatus includes close fitting clothing apparatus (70), a plurality of electrodes (10) mounted to the close fitting clothing apparatus (70), removable cover sheet apparatus (78) for providing a sterile interface between the skin and at least one of the electrodes (10) and joining apparatus for joining the removable cover sheet apparatus (78) to at least one of the plurality of electrodes (10). A variety of applications of the apparatus are also disclosed, including apparatus (130) for detecting drowsiness in a subject and for alerting the subject as a result and a fetal biosignal probe (200).
Abstract:
Heart performance is evaluated by collecting ultrasound images of at least one chamber of the heart of a patient after peak exercice (204, 206). The images are subsequently displayed and analyzed to determine the presence and degree of heart disease, such as coronary artery disease (CAD). Collecting (212) the images is done continuously at a rate of at least eight images per heart beat synchronized to a predetermined point in each heart beat over a time period (214) which is normally sufficient to capture ischemic events resulting form the peak exercise (204, 206). Each image thus synchronized (212) represents a similar condition of each heart beat, thereby facilitating accurate comparisons. Collecting of images can be interrupted to eliminate blank or obscured images while the ultrasound sensor is repositioned (216, 224). The collected images can be displayed and subsequently analyzed to determine the presence and degree of heart disease by comparing the images from successive heart beats.
Abstract:
A swallowable electrode (10) or an esophageal catheter (201) are formed with a porous (111) or roughened region (113) capable of receiving a cream or jell form of topical anesthetic. The anesthetic can be covered with a dissolvable medium. Located on each side of the anesthetic is a metal conductor (107, 109) coupled to a flexible wire (103) extending from the device. Upon positioning of the metal members in an individual's esophagus, adjacent a posterior heart surface, the protective medium dissolves (102) exposing the topical anesthetic to portions of the esophagus adjacent to the two conducting members (107, 109). A lumen (221) in the catheter can be provided to deliver the anesthetic to the esophagus. The exposed anesthetic can be absorbed by the adjacent region of the esophagus thereby providing for more comfortable esophageal cardiac pacing.
Abstract:
The non-stringy hydrogels of this invention are comprised of a homogeneous uniform mixture of water and at least one water-soluble high molecular weight polymer. Suitable mixtures may be derived from poly(ethylene oxide) and water or poly(vinyl pyrrolidone), a viscosity-enhancing hydrophilic polymer and water, and further, may optionally contain an effective amount of a water-soluble electrolyte to provide conductive non-stringy materials. These polymeric mixtures which are crosslinked by exposure to radiant energy provide gel-like solids which are sufficiently tacky and adhesive to adhere to the subjects' skin and yet are substantially non-stringy and non-aggressive such that contact with such hydrogels imparts less discomfort to the user. In addition, the consumer utilizing the products of this invention would not experience the objectionable sticky, stringy sensation associated with existing conductive adhesive gels.