A dosimetry device includes at least one sensor in a housing and a dosimetry processing device with a memory. The dosimetry processing device is coupled to the at least one sensor in the housing. The dosimetry processing device is configured to execute programmed instructions stored in the memory co
A dosimetry device includes at least one sensor in a housing and a dosimetry processing device with a memory. The dosimetry processing device is coupled to the at least one sensor in the housing. The dosimetry processing device is configured to execute programmed instructions stored in the memory comprising: obtaining readings from the sensor; storing the readings; conducting an analysis of the stored readings to determine an injury risk assessment; and outputting at least one of the conducted analysis of the determined injury risk assessment or the stored readings.
대표청구항▼
1. A dosimetry device for use in an ambient environment, the device comprising: a housing configured to be secured to at least one location on a person such that the person is wearing or carrying the housing in the ambient environment;at least one sensor at least partially disposed within the housin
1. A dosimetry device for use in an ambient environment, the device comprising: a housing configured to be secured to at least one location on a person such that the person is wearing or carrying the housing in the ambient environment;at least one sensor at least partially disposed within the housing and accessible to the ambient environment, the at least one sensor being configured to derive a plurality of parametric signals from either a) acceleration readings generated from movement of the person, or b) pressure readings generated from perturbations propagating in the ambient environment, resulting from an identified event;at least one memory device disposed within the housing, the at least one memory device including a plurality of memory locations, the plurality of memory locations being configured to store personal medical history data of the person that is wearing or carrying the housing in the ambient environment, aggregate medical history data, and parametric data corresponding to the plurality of parametric signals;a control circuit disposed in the housing and coupled to the at least one sensor and the at least one memory device, the control circuit being configured to tailor and adjust an individualized injury threshold for the person based on the personal medical history data and the aggregate medical history data and store the tailored and adjusted individualized injury threshold prior to the identified event, and the control circuit being further configured to provide in real time an injury risk assessment corresponding to the identified event by determining whether one or more of the plurality of parametric signals exceeds the stored individualized injury threshold for the person; andat least one input/output (I/O) device coupled to the control circuit, the at least one I/O device being configured to provide the injury risk assessment in response to an assessment analysis request, whereby medical treatment of the person is guided according to the injury risk assessment that is provided by the I/O device, when the one or more of the plurality of parametric signals exceeds the stored individualized injury threshold for the person. 2. The device of claim 1, wherein the at least one sensor includes an inertial measurement sensor configured to measure an acceleration of the housing in real time, the plurality of parametric signals including at least one acceleration signal corresponding to the measured acceleration. 3. The device of claim 2, wherein the inertial measurement sensor includes a three-axis accelerometer, the at least one acceleration signal providing three-axis acceleration data in substantially real time. 4. The device of claim 2, wherein the inertial measurement sensor includes a gyroscope device, the at least one acceleration signal providing rotational acceleration data in substantially real time. 5. The device of claim 2, wherein the control circuit is configured to compare the measured acceleration with the individualized injury threshold stored in the at least one memory device to derive the injury risk assessment. 6. The device of claim 1, wherein the at least one sensor includes a pressure sensor configured to measure air pressure based on the sonic perturbations propagating in the ambient environment. 7. The device of claim 6, wherein the control circuit is configured to compare the measured air pressure with the individualized injury threshold stored in the at least one memory device to derive the injury risk assessment. 8. The device of claim 1, wherein the at least one sensor includes: a pressure sensor coupled to the control circuit, the pressure sensor being configured to measure air pressure based on the sonic perturbations propagating in the ambient environment;an inertial measurement sensor coupled to the control circuit, the inertial measurement sensor being configured to measure an acceleration of the housing in real time; andwherein the control circuit is configured to compare the measured air pressure and the measured acceleration with the individualized injury threshold stored in the at least one memory device to derive the injury risk assessment. 9. The device of claim 8, wherein the personal medical history data corresponds to personal medical history or injuries previously sustained by the person prior to the identified event. 10. The device of claim 8, wherein the aggregate medical history data is based on group medical history data or injury assessment data obtained from other dosimetry devices over a period of time. 11. The device of claim 8, wherein the at least one I/O device includes a display, the display being configured to display a probability that the person has sustained a predetermined injury with human readable indicia based on the injury risk assessment. 12. The device of claim 1, wherein the at least one memory includes a look-up table that obtains the injury risk assessment by relating the personal medical history data, the aggregate medical history data and the parametric data. 13. The device of claim 1, wherein the control circuit is configured to update the personal medical history data based on the injury risk assessment. 14. The device of claim 1, wherein the plurality of parametric signals include a date and a time stamp corresponding to an occurrence of the identified event. 15. The device of claim 1, further comprising a power supply configured to provide electrical energy to the device from a non-stationary or portable power source. 16. The device of claim 15, wherein the power source includes a battery device. 17. The device of claim 16, wherein the battery device is rechargeable. 18. The device of claim 15, wherein the power source includes a device configured to harvest energy from a renewable energy source. 19. The device of claim 1, wherein the at least one sensor includes a global positioning device (GPD) configured to provide GPD data corresponding to a location of the housing. 20. The device of claim 19, wherein the control circuit is configured to estimate a location of the identified event based on the GPD data and the parametric signals. 21. The device of claim 20, further comprising a transmitter portion configured to transmit the housing location, the identified event location, and injury risk assessment to an external receiver. 22. The device of claim 1, further comprising a transceiver coupled to the control circuit, the transceiver being configured to provide injury risk assessment to an external receiver. 23. The device of claim 22, wherein the transceiver is configured to receive data or instructions from an external transmitter. 24. The device of claim 1, further comprising a non-rechargeable or disposable battery. 25. The device of claim 1, wherein the device is disposable after the at least one I/O device has provided the injury risk assessment in response to at least one assessment analysis request.
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