Abstract: An in-the-ear (ITE) physiological measurement device (2) includes a structure (4) formed for easy insertion into multiple shaped and sized ear canals. An inflatable balloon (6) surrounds an end portion of the structure (4) to be positioned in the ear. Optionally, a mushroom shaped tip (22) is connected with an end of the structure (4) and carries a plurality of sensors (8). Inflation of the balloon (6) expands the tip (22) radially to position the sensors (8) proximate to vascular tissue within the ear canal. Once suitably positioned, the one or more sensors (8) sense physiological signals from the vascular tissue and bone structure.

Abstract: A physiological parameter measuring device (14) is disposed within or near an ear canal of a subject (16) to non-invasively sense at least one physiological parameter of the subject which one physiological parameter is associated with at least one physiological condition of the subject. An analyzing device (48) is operatively coupled to the physiological parameter measuring device (14) to analyze the sensed physiological parameter and detect the physiological condition of the subject (16). Based on the detection and analysis of the physiological condition of the subject (16), a stimulating device (20) stimulates the subject (16) with the physiological parameter measuring device (14) within or near the ear canal of the subject (16) to mitigate the physiological condition of the subject (16).

Abstract: A highly portable biometric monitor is disclosed. At least one remote sensor member (12, 12?) includes one or more biometric sensors (20, 22, 24, 25) configured for operative coupling with a patient. A neck collar (14, 114, 214, 314, 414) includes electronics (36, 40, 42, 44, 46, 48) for operating the at least one remote sensor member. The at least one remote sensor member is separate from and not disposed on the neck collar. Optionally, the collar also includes one or more biometric sensors (53). A communication link (18) operatively connects the remote sensor member and the electronics of the neck collar. A motion sensor (26) and position sensor (28) may be disposed with the one or more biometric sensors to sense movement and position, and the electronics (36, 40, 42, 44, 46, 48) configured to account for error in a signal produced by the one or more biometric sensors due to movement sensed by the motion sensor or position sensed by the position sensor.

Abstract: Medical vital signs (110) are captured, recorded, processed, and a signal quality assessment (160) is computed based on signal waveform components such as slope, amplitude, time to rise, time at peak, and degree to which signal peaks (420) and valleys (430). The signal assessment (160) may be used as a basis for rating the quality (130) of the underlying vital signal, to increase the quality of the signal by removing noisy segments and physiologically impossible peaks (424) and valleys (434), to detect a parameter value (120), to label a waveform (140), or to prompt an alarm (550) to indicate the signal has reached a critical level and issue a warning to the user of the vital data. The signal and the assessment are stored in an indexed, searchable data storage memory (590) from which the signals may be retrieved and displayed (300).

Abstract: An apparatus (10) for predicting patient respiratory stability includes a patient data memory (24) which stores patient data for a patient (12) and an analyzer (34) in communication with the memory computes a measure of patient respiratory stability. The analyzer applies one or more rules to the patient data that are based on a plurality of parameters which in combination, have been identified as being predictive of patient respiratory instability, such as mean airway pressure (MAWP), plateau pressure (PP), arterial oxygen saturation (SaO2 or SpO2), and heart rate (HR). Based on the application of the rules, the analyzer determines the measure of patient respiratory stability.

Abstract: A physiological parameter measuring device (14) is disposed within or near an ear canal of a subject (16) to non-invasively sense at least one physiological parameter of the subject which one physiological parameter is associated with at least one physiological condition of the subject. An analyzing device (48) is operatively coupled to the physiological parameter measuring device (14) to analyze the sensed physiological parameter and detect the physiological condition of the subject (16). Based on the detection and analysis of the physiological condition of the subject (16), a stimulating device (20) stimulates the subject (16) with the physiological parameter measuring device (14) within or near the ear canal of the subject (16) to mitigate the physiological condition of the subject (16).

Abstract: A highly portable biometric monitor is disclosed. At least one remote sensor member (12, 12?) includes one or more biometric sensors (20, 22, 24, 25) configured for operative coupling with a patient. A neck collar (14, 114, 214, 314, 414) includes electronics (36, 40, 42, 44, 46, 48) for operating the at least one remote sensor member. The at least one remote sensor member is separate from and not disposed on the neck collar. Optionally, the collar also includes one or more biometric sensors (53). A communication link (18) operatively connects the remote sensor member and the electronics of the neck collar. A motion sensor (26) and position sensor (28) may be disposed with the one or more biometric sensors to sense movement and position, and the electronics (36, 40, 42, 44, 46, 48) configured to account for error in a signal produced by the one or more biometric sensors due to movement sensed by the motion sensor or position sensed by the position sensor.

Abstract: A metal pallet includes a first deck subassembly, first and second bumpers, and a plurality of risers. The first deck subassembly includes a plurality of deck boards. The first bumper connects to at least one of the deck boards along a first peripheral edge of the first deck subassembly. The second bumper connects to at least one of the deck boards along a second peripheral edge of the first deck subassembly. The first peripheral edge is oriented approximately normal to the second peripheral edge. The plurality of risers connects to the first deck subassembly for spacing the first deck subassembly above an associated surface upon which the pallet rests. A second deck subassembly can also be employed.

Abstract: A portable physiological monitoring device (12) includes a receiver (22) that wirelessly receives physiological measurements from each of a plurality of in-the-ear probes (14) upon entering a communication range of one of the in-the-ear probes (14). The portable physiological monitoring device (12) farther includes a display (30) for presenting the physiological measurements.

Abstract: An in-the-ear (ITE) physiological measurement device (2) includes a structure (4) formed for easy insertion into multiple shaped and sized ear canals. An inflatable balloon (6) surrounds an end portion of the structure (4) to be positioned in the ear. Optionally, a mushroom shaped tip (22) is connected with an end of the structure (4) and carries a plurality of sensors (8). Inflation of the balloon (6) expands the tip (22) radially to position the sensors (8) proximate to vascular tissue within the ear canal. Once suitably positioned, the one or more sensors (8) sense physiological signals from the vascular tissue and bone structure.

Abstract: In a medical monitoring system (10), one or more biometric monitors (20, 21, 22, 23, 24, 26, 66) collect data of a plurality of monitored biometric parameters. An expression evaluator (72) evaluates a user-defined expression incorporating one or more of the monitored biometric parameters to generate data for a user-defined biometric parameter. A further processing component (32, 50, 52, 54, 55, 56, 57, 58, 60, 62, 88) performs processing and display of data of at least one parameter selected from the monitored bio-metric parameters and the user-defined biometric parameter. The further processing component operates in the same way regardless of whether the at least one parameter is selected from the monitored biometric parameters or the user-defined biometric parameter.

Abstract: In a patient monitoring system (10), shorter interval physiological parameters and longer interval clinical data are collected from a monitored patient (12). A composite acuity score generator (70) generates or updates a composite acuity score indicative of wellbeing of the patient (12) based at least on the sensed physiological parameters and the longer interval data. A monitor (22, 56) displays current values of at least one of selected sensed physiological parameters, longer interval data, and the composite acuity score.

Abstract: Sanding and screening are steps in floor finishing that produce large quantities of fine dust which is difficult to remove and which plugs porous filter elements of dust collection systems. Dust collection is enhanced with a floor screening attachment for a floor machine. A vacuum system with a liquid filtering medium is provided to collect dust produced during screening. A dust collection unit is also disclosed to collect and separate sawdust produced by sanding which can cause foaming of a liquid filter medium.

Abstract: A metal pallet includes a first deck subassembly, first and second bumpers, and a plurality of risers. The first deck subassembly includes a plurality of deck boards. The first bumper connects to at least one of the deck boards along a first peripheral edge of the first deck subassembly. The second bumper connects to at least one of the deck boards along a second peripheral edge of the first deck subassembly. The first peripheral edge is oriented approximately normal to the second peripheral edge. The plurality of risers connects to the first deck subassembly for spacing the first deck subassembly above an associated surface upon which the pallet rests. A second deck subassembly can also be employed.

Abstract: Sanding and screening are steps in floor finishing that produce large quantities of fine dust which is difficult to remove and which plugs porous filter elements of dust collection systems. Dust collection is enhanced with a floor screening attachment for a floor machine. A vacuum system with a liquid filtering medium is provided to collect dust produced during screening. A dust collection unit is also disclosed to collect and separate sawdust produced by sanding which can cause foaming of a liquid filter medium.

Abstract: Sanding and screening are steps in floor finishing that produce large quantities of fine dust which is difficult to remove and which plugs porous filter elements of dust collection systems. Dust collection is enhanced with a floor screening attachment for a floor machine. A vacuum system with a liquid filtering medium is provided to collect dust produced during screening. A dust collection unit is also disclosed to collect and separate sawdust produced by sanding which can cause foaming of a liquid filter medium.

Abstract: Sanding and screening are steps in floor finishing that produce large quantities of fine dust which is difficult to remove and which plugs porous filter elements of dust collection systems. Dust collection is enhanced with a floor screening attachment for a floor machine. A vacuum system with a liquid filtering medium is provided to collect dust produced during screening. A dust collection unit is also disclosed to collect and separate sawdust produced by sanding which can cause foaming of a liquid filter medium.