The present technology is generally related to non-contact patient monitoring.
Many conventional medical monitors require attachment of a sensor to a patient in order to detect physiologic signals from the patient and to transmit detected signals through a cable to the monitor. These monitors process the received signals and determine vital signs such as the patient's pulse rate, respiration rate, and arterial oxygen saturation. For example, a pulse oximeter is a finger sensor that can include two light emitters and a photodetector. The sensor emits light into the patient's finger and transmits the detected light signal to a monitor. The monitor includes a processor that processes the signal, determines vital signs (e.g., pulse rate, respiration rate, arterial oxygen saturation), and displays the vital signs on a display.
Other monitoring systems include other types of monitors and sensors, such as electroencephalogram (EEG) sensors, blood pressure cuffs, temperature probes, air flow measurement devices (e.g., spirometer), and others. Some wireless, wearable sensors have been developed, such as wireless EEG patches and wireless pulse oximetry sensors.
Video-based monitoring is a field of patient monitoring that uses one or more remote video cameras to detect physical attributes of the patient. This type of monitoring can also be called “non-contact” monitoring in reference to the remote video sensor(s), which does/do not contact the patient. The remainder of this disclosure offers solutions and improvements in this field.
The techniques of this disclosure generally relate to non-contact, video-based patient monitoring, wherein at least one region of interest (ROI) of a patient is defined, and wherein at least one image capture device captures two or more images of the ROI. A processor calculates a change in depth of at least one portion of the ROI within the two or more images and assigns a visual indicator to a display based at least in part on the calculated change in depth.
In another aspect, the disclosure provides for assignment of the visual indicator based on a sign of the change in depth or magnitude of the change in depth, including average or instantaneous average change in depth over time. In other aspects, the visual indicator includes a color, shade, pattern, concentration and/or an intensity. In other aspects, the visual indicator is overlaid onto a portion of the ROI. In other aspects, the visual indicator is overlaid in real time. In other aspects, the tidal volume signal is displayed in real time.
In another aspects, a graphic is provided with a visual indicator when the tidal volume indicates that a patient is inhaling and/or exhaling. In other aspects, the monitoring system provides for threshold target tidal volumes, representing risks of hypoventilation, hyperventilation, obstructive lung disease indication, etc.
The details of one or more aspects of the disclosure are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the techniques described in this disclosure will be apparent from the description and drawings, and from the claims.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
Many aspects of the present disclosure can be better understood with reference to the following drawings. The components in the drawings are not necessarily to scale. Instead, emphasis is placed on illustrating clearly the principles of the present disclosure. The drawings should not be taken to limit the disclosure to the specific embodiments depicted but are for explanation and understanding only.
The following disclosure describes video-based patient monitoring systems and associated methods for detecting and/or monitoring patient breathing and related parameters. As described in greater detail below, systems and/or methods configured in accordance with embodiments of the present technology are configured to recognize and/or identify a patient and to define one or more regions of interest (ROI's) on the patient. Additionally or alternatively, the system and/or methods are configured to capture one or more images (e.g., a video sequence) of the ROI's and/or to measure changes in depth of regions (e.g., one or more pixels or groups of pixels) in the ROI's over time. Based, at least in part, on these measurements, the systems and/or methods can assign one or more visual indicators to regions of one or more of the ROI's. In these and other embodiments, the systems and/or methods generate various breathing parameter signals of all or a subset of the ROI's. The breathing parameter signals can include tidal volume, minute volume, and/or respiratory rate, among others. In these and other embodiments, the systems and/or methods can analyze the generated signals and can trigger alerts and/or alarms when the systems and/or methods detect one or more breathing abnormalities. In these and still other embodiments, the systems and/or methods can display (e.g., in real-time) all or a subset of the assigned visual indicator(s) and/or of the generated signals on a display, e.g., to provide a user (e.g., a caregiver, a clinician, a patient, etc.) a visual indication of the patient's breathing. For example, the systems and/or methods can overlay the assigned visual indicator(s) onto the captured images of the patient to indicate: (i) whether the patient is breathing; and/or, (ii) whether a patient's breathing is abnormal.
Specific details of several embodiments of the present technology are described herein with reference to
The camera 114 can capture a sequence of images over time. The camera 114 can be a depth sensing camera, such as a Kinect camera from Microsoft Corp. (Redmond, Washington). A depth sensing camera can detect a distance between the camera and objects within its field of view. Such information can be used, as disclosed herein, to determine that a patient 112 is within the FOV 116 of the camera 114 and/or to determine one or more ROI's to monitor on the patient 112. Once a ROI is identified, the ROI can be monitored over time, and the changes in depth of regions (e.g., pixels) within the ROI 102 can represent movements of the patient 112 associated with breathing. As described in greater detail in U.S. Provisional Patent Application Ser. No. 62/614,763, those movements, or changes of regions within the ROI 102, can be used to determine various breathing parameters, such as tidal volume, minute volume, respiratory rate, etc. Those movements, or changes of regions within the ROI 102, can also be used to detect various breathing abnormalities, as discussed in greater detail in U.S. Provisional Patent Application Ser. No. 62/716,724. The various breathing abnormalities can include, for example, apnea, rapid breathing (tachypnea), slow breathing, intermittent or irregular breathing, shallow breathing, obstructed and/or impaired breathing, and others. U.S. Provisional Patent Application Ser. Nos. 62/614,763 and 62/716,724 are incorporated herein by reference in their entirety.
In some embodiments, the system 100 determines a skeleton-like outline of the patient 112 to identify a point or points from which to extrapolate a ROI. For example, a skeleton-like outline can be used to find a center point of a chest, shoulder points, waist points, and/or any other points on a body of the patient 112. These points can be used to determine one or more ROI's. For example, a ROI 102 can be defined by filling in area around a center point 103 of the chest, as shown in
In another example, the patient 112 can wear specially configured clothing (not shown) that includes one or more features to indicate points on the body of the patient 112, such as the patient's shoulders and/or the center of the patient's chest. The one or more features can include visually encoded message (e.g., bar code, QR code, etc.), and/or brightly colored shapes that contrast with the rest of the patient's clothing. In these and other embodiments, the one or more features can include one or more sensors that are configured to indicate their positions by transmitting light or other information to the camera 114. In these and still other embodiments, the one or more features can include a grid or another identifiable pattern to aid the system 100 in recognizing the patient 112 and/or the patient's movement. In some embodiments, the one or more features can be stuck on the clothing using a fastening mechanism such as adhesive, a pin, etc. For example, a small sticker can be placed on a patient's shoulders and/or on the center of the patient's chest that can be easily identified within an image captured by the camera 114. The system 100 can recognize the one or more features on the patient's clothing to identify specific points on the body of the patient 112. In turn, the system 100 can use these points to recognize the patient 112 and/or to define a ROI.
In some embodiments, the system 100 can receive user input to identify a starting point for defining a ROI. For example, an image can be reproduced on a display 122 of the system 100, allowing a user of the system 100 to select a patient 112 for monitoring (which can be helpful where multiple objects are within the FOV 116 of the camera 114) and/or allowing the user to select a point on the patient 112 from which a ROI can be determined (such as the point 103 on the chest of the patient 112). In other embodiments, other methods for identifying a patient 112, identifying points on the patient 112, and/or defining one or more ROI's can be used.
The images detected by the camera 114 can be sent to the computing device 115 through a wired or wireless connection 120. The computing device 115 can include a processor 118 (e.g., a microprocessor), the display 122, and/or hardware memory 126 for storing software and computer instructions. Sequential image frames of the patient 112 are recorded by the video camera 114 and sent to the processor 118 for analysis. The display 122 can be remote from the camera 114, such as a video screen positioned separately from the processor 118 and the memory 126. Other embodiments of the computing device 115 can have different, fewer, or additional components than shown in
The computing device 210 can communicate with other devices, such as the server 225 and/or the image capture device(s) 285 via (e.g., wired or wireless) connections 270 and/or 280, respectively. For example, the computing device 210 can send to the server 225 information determined about a patient from images captured by the image capture device(s) 285. The computing device 210 can be the computing device 115 of
In some embodiments, the image capture device(s) 285 are remote sensing device(s), such as depth sensing video camera(s), as described above with respect to
The server 225 includes a processor 235 that is coupled to a memory 230. The processor 235 can store and recall data and applications in the memory 230. The processor 235 is also coupled to a transceiver 240. In some embodiments, the processor 235, and subsequently the server 225, can communicate with other devices, such as the computing device 210 through the connection 270.
The devices shown in the illustrative embodiment can be utilized in various ways. For example, either the connections 270 and 280 can be varied. Either of the connections 270 and 280 can be a hard-wired connection. A hard-wired connection can involve connecting the devices through a USB (universal serial bus) port, serial port, parallel port, or other type of wired connection that can facilitate the transfer of data and information between a processor of a device and a second processor of a second device. In another embodiment, either of the connections 270 and 280 can be a dock where one device can plug into another device. In other embodiments, either of the connections 270 and 280 can be a wireless connection. These connections can take the form of any sort of wireless connection, including, but not limited to, Bluetooth connectivity, Wi-Fi connectivity, infrared, visible light, radio frequency (RF) signals, or other wireless protocols/methods. For example, other possible modes of wireless communication can include near-field communications, such as passive radio-frequency identification (RFID) and active RFID technologies. RFID and similar near-field communications can allow the various devices to communicate in short range when they are placed proximate to one another. In yet another embodiment, the various devices can connect through an internet (or other network) connection. That is, either of the connections 270 and 280 can represent several different computing devices and network components that allow the various devices to communicate through the internet, either through a hard-wired or wireless connection. Either of the connections 270 and 280 can also be a combination of several modes of connection.
The configuration of the devices in
In these and other embodiments, the system 100 can define other regions of interest in addition to or in lieu of the ROI's 102, 351, 352, 353, and/or 354. For example, the system 100 can define a ROI 356 corresponding to the patient's chest (e.g., the ROI 351 plus the ROI 354) and/or a ROI 357 corresponding to the patient's abdomen (e.g., the ROI 352 plus the ROI 353). In these and other embodiments, the system 100 can define a ROI 358 corresponding to the right side of the patient's chest or torso (e.g., the ROI 353 and/or the ROI 354) and/or a ROI 359 corresponding to the left side of the patient's chest or torso (e.g., the ROI 351 and/or the ROI 352). In these and still other embodiments, the system 100 can define one or more other regions of interest than shown in
Using two images of the two or more captured images, the system can calculate change(s) in depth over time between the image capture device and one or more regions (e.g., one or more pixels or groups of pixels) within a ROI. For example, the system can compute a difference between a first depth of a first region 467 in the ROI 102 in image 461 (a first image of the two or more captured images) and a second depth of the first region 467 in the ROI 102 in image 462 (a second image of the two or more captured images). With these differences in depth, the system can determine if a region is moving toward the camera or away from the camera. In some embodiments, the system can assign visual indicators (e.g., colors, patterns, shades, concentrations, intensities, etc.) from a predetermined visual scheme to regions in an ROI based on their movement. The visual indicators can correspond to changes in depth computed by the system (e.g., to the signs and/or magnitudes of computed changes in depth). As shown in
In these and other embodiments, the shade of the assigned colors can be positively correlated with the magnitude of a computed change in depth. As shown in
Although the visual indicators displayed in the images 461 and 462 illustrated in
In these and other embodiments, the concentration (e.g., the density) of an assigned pattern can be relative to an amount of excursion of a region in an ROI over time. For example, as shown in image 463 illustrated in
As a result, a user (e.g., a clinician, nurse, etc.) of the system is able to quickly and easily determine a number of patient breathing characteristics of a patient based on displayed visual indicators. For example, a user is able to quickly and easily determine that a patient is breathing (based on the presence of visual indicators displayed) and whether the patient is currently inhaling or exhaling (based on the particular visual indicators displayed). In addition, a user and/or the system is able to quickly and easily detect one or more breathing abnormalities. For example, the user and/or the system can determine that a patient is currently experiencing paradoxical breathing (e.g., when the chest and abdomen are moving in opposite directions) based on the difference in visual indicators displayed over the patient's chest and abdomen. As another example, the user and/or the system can determine whether a patient is straining to breathe based on the presence of visual indicators on a patient's neck or based on characteristics of visual indicators (e.g., low intensity, low concentration, no visual indicators displayed, etc.) displayed over specific regions (e.g., the abdomen) of the patient.
The images 581 and 582 differ from the images 461 and/or 462, however, in that the aggregate ROI 102 is displayed with spatially uniform visual indicators across the ROI 102. As shown in
In other embodiments, the system can assign and/or display visual indicators based on displacement of a majority of the regions in the ROI 102. For example, the system can assign and/or display the same intensity of the first color 471 to all regions in the aggregate ROI 102 when the system determines that a majority of the regions in the ROI 102 have moved toward the image capture device over time (e.g., that a majority of the regions in the ROI 102 have exhibited negative changes in depth across two capture images). In these and other embodiments, the system can assign and/or display the same intensity of the second color 472 to all regions in the aggregate ROI 102 when the system determines that a majority of the regions in the ROI 102 have moved away from the image capture device over time (e.g., that a majority of the regions in the ROI 102 have exhibited positive changes in depth across two capture images).
Regardless of the visual scheme employed, the system can display (e.g., in real-time) the assigned visual indicators over corresponding regions of the ROI in a captured image to visually portray the computed changes in depths. For example, the assigned visual indicators can be displayed within the ROI 102 and overlaid onto a depth image (e.g., a 3-D representation of a surface, including point clouds, iso-surfaces (contours), wire frames, etc.), an RGB image, and infrared image, an MM image, and/or CT image of the patient 112, among other image types of the patient 112. Thus, the assigned visual indicators can exaggerate or emphasize changes in depths detected by the system. In turn, a user (e.g., a caregiver, a clinician, a patient, etc.) can quickly and easily determine whether or not a patient 112 is breathing based on whether or not the colors get brighter, or the patterns get darker/denser, during a breath (that is, based on whether or not the visual indicators displayed on the ROI 102 correspond to one or more breathing cycles of the patient 112).
Additionally or alternatively, a user can quickly and easily determine a phase (e.g., inhalation and/or exhalation) of a patient's breathing. For example, a large majority of the ROI 102 in the generated image 461 illustrated in
As shown in
In some embodiments, the visual indicators overlaid onto the patient 112 can vary along the inhalation portion and/or the exhalation portion of the patient's breathing. For example,
The intensities of the visual indicators displayed across all regions in the ROI 102 in the images 711-716, 821-826, 931-936, and 1041-1046 correspond to a position along the patient's breathing cycle. In some embodiments, the system can display the first color 471 across all regions in the ROI 102 while the patient 112 is inhaling, and the intensity of the first color 471 displayed within the ROI 102 can increase as the tidal volume signal 691 (
In these and other embodiments, the system can display the second color 472 across all regions in the ROI 102 while the patient 112 is exhaling, and the intensity of the second color 472 displayed within the ROI 102 can increase as the tidal volume signal 691 decreases. For example, the system can display the image 714 (
In
Although the generated images 711-716, 821-826, 931-936, and 1041-1046 (
Another approach for visually representing a patient's breathing cycle, based on images captured with a depth sensing camera, is shown in
The images 1261-1263 and 1371-1373 differ from the images 461, 462, 463, 581, 582, 711-716, 821-826, 931-936, 1041-1046, and/or 1141-1146, however, in that amount (e.g., area) of the ROI 102 filled with one or more visual indicators corresponds to a position along the patient's breathing cycle and/or to an amount (e.g., volume) of air within the patient's lungs. Referring to
Referring to
Although the generated images 1261-1263 and 1371-1373 are illustrated and displayed with an aggregate ROI 102 in
In some embodiments, a user and/or the system can define one or more inhalation target tidal volumes for a patient 112. As shown in
In these and other embodiments, a user and/or the system can define one or more other threshold target tidal volumes in addition to or in lieu of the threshold target tidal volume 1495. For example, a user and/or the system can define a second inhalation threshold tidal volume 1496 (
As shown in
The line plot 1480 illustrated in
In some embodiments, the system can display a visualization of the patient's breathing in real-time such that the current display corresponds to a current position of the patient's breathing within the patient's breathing cycle relative to one or more of the threshold target tidal volumes 1495-1498. For example, the system can display the generated image 1521 (
Although the third color 1533 is illustrated in the image 1523 as spatially uniform across all regions in the ROI 102, the third color 1533 in other embodiments can spatially vary across the regions in the ROI 102. For example, various shades of the third color 1533 can be used to provide an indication of the amount of excursion a particular region of the ROI 102 experienced across two or more images in a video sequence. In these and other embodiments, the intensity and/or shade of the third color 1533 can vary (e.g., increase and/or decrease) across two or more generated images as the tidal volume increases and/or decreases to, for example, provide an indication of the current position of the patient's breathing within the patient's breathing cycle. In these and still other embodiments, the system can trigger other audio and/or visual alerts in addition to or in lieu of the third color 1533. For example, the system (i) can display a check mark or other graphic and/or (ii) can trigger a first audio alert/alarm to indicate that the patient's breathing has met and/or exceeded the threshold target tidal volume 1495.
As discussed above, in some embodiments a user and/or the system can set and/or define a second threshold target tidal volume 1496 (
In some embodiments, as the tidal volume signal 1481 (
As discussed above, in some embodiments a user and/or the system can set and/or define a threshold target tidal volume 1497. For example, a user and/or the system can define and/or set the threshold target tidal volume 1497 such that it represents a volume of air exhaled that, if not met, can indicate the patient 112 is experiencing one or more medical conditions, such as obstructive lung disease. In these and other embodiments, as the tidal volume signal 1481 (
Although the fifth color 1535 is illustrated in the image 1644 as spatially uniform across all regions in the ROI 102, the fifth color 1535 in other embodiments can spatially vary across the regions in the ROI 102. For example, various shades of the fifth color 1535 can be used to provide an indication of the amount of excursion a particular region of the ROI 102 experienced across two or more images in a video sequence. In these and other embodiments, the intensity and/or shade of the fifth color 1535 can vary (e.g., increase and/or decrease) across two or more generated images as the tidal volume increases and/or decreases to, for example, provide an indication of the current position of the patient's breathing within the patient's breathing cycle. In these and still other embodiments, the system can trigger other audio and/or visual alerts/alarms in addition to or in lieu of the fifth color 1535. For example, the system (i) can display a check mark or other graphic and/or (ii) can trigger a third audio alert/alarm to indicate that the patient's breathing has met and/or dropped below the threshold target tidal volume 1497.
As discussed above, the threshold target tidal volume 1497 can represent a target volume of air exhaled from a patient's lungs. For example, a user and/or the system can define and/or set the threshold target tidal volume 1497 to represent a target volume of air that, if not met, can indicate the patient 112 is experiencing various medical conditions, such as obstructive lung disease. Thus, if a patient 112 is unable to or has difficulty exhaling enough air out of his/her lungs such that the tidal volume signal 1481 does not meet and/or drop below the threshold target tidal volume 1497 in one or more cycles of the patient's breathing (e.g., a scenario not illustrated by the tidal volume signal 1481 in
As discussed above, in some embodiments a user and/or the system can set and/or define a threshold target tidal volume 1498 (
As shown in
In contrast with the previous cycle of the patient's breathing, during the subsequent cycle of the patient's breathing, the patient 112 begins exhaling before the tidal volume signal 1481 meets and/or exceeds the threshold target tidal volume 1495. As discussed above, the threshold target tidal volume 1495 in some embodiments can represent a volume of air below which the patient 112 is at risk of hypoventilation. The system can notify the user that the patient's breathing did not meet and/or exceed the threshold target tidal volume 1495 (e.g., that the patient 112 did not inhale enough air and/or is at risk of hypoventilation) by changing (e.g., the color of) the visual indicators within the ROI 102 of the visualization of the patient's breathing cycle, displaying one or more other graphics, and/or triggering one or more other audio and/or visual alerts/alarms. For example, the system (i) can display a seventh color (not shown) within the ROI 102, (ii) can display an “X” or other graphic, (iii) can flash the display, and/or (iv) can trigger a sixth audio alert and/or alarm.
In some embodiments, the amount of the ROI 102 filled with one or more visual indicators in the images 1761-1764 can correspond to a position along the patient's breathing cycle and/or to an amount (e.g., a volume) of air within the patient's lungs. For example, the system can display the image 1761 (
In some embodiments, as the tidal volume signal 1481 (
In these and other embodiments, as the tidal volume signal 1481 (
In some embodiments, as the tidal volume signal 1481 (
In some embodiments, as the tidal volume signal 1481 (
In these and other embodiments, as the tidal volume signal 1481 (
In some embodiments, as the tidal volume signal 1481 (
As discussed above, in contrast with the previous cycle of the patient's breathing, the tidal volume signal 1481 plateaus and begins to decrease in the subsequent cycle (as shown by the tidal volume signal 1481 at points 1408-1410 illustrated in
The routine 2090 can begin at block 2091 by recognizing a patient within a field of view (FOV) of the image capture device, defining one or more regions of interest (ROI's) on the patient, and/or setting one or more threshold target tidal volumes. In some embodiments, the routine 2090 can recognize the patient by identifying the patient using facial recognition hardware and/or software of the image capture device. In these embodiments, the routine 2090 can display the name of the patient on a display screen once the routine 2090 has identified the patient. In these and other embodiments, the routine 2090 can recognize a patient within the FOV of the image capture device by determining a skeleton outline of the patient and/or by recognizing one or more characteristic features (e.g., a torso of a patient). In these and still other embodiments, the routine 2090 can define one or more ROI's on the patient in accordance with the discussion above with respect to
In some embodiments, the routine 2090 can define the one or more threshold target tidal volumes based, at least in part, on one or more patient factors. For example, the routine 2090 can define the one or more threshold target tidal volumes based on demographics and/or disease state(s) of the patient. In these and other embodiments, the routine 2090 can define one or more threshold target tidal volumes based on one or more previous breathing cycles of the patient. For example, the routine 2090 can monitor one or more previous breathing cycles of the patient to define one or more ranges of tidal volumes indicative of normal patient ventilation. In some embodiments, the routine 2090 can define (i) one or more inhalation target tidal volumes and/or (ii) one or more exhalation target tidal volumes. For example, the routine 2090 (a) can define an inhalation threshold target tidal volume representative of a volume of inhaled air below which the patient is at risk of hypoventilation and/or (b) can define an inhalation threshold target tidal volume representative of a volume of inhaled air above which the patient is at risk of hyperventilation. Additionally or alternatively, the routine 2090 (a) can define an exhalation threshold target tidal volume representative of a volume of exhaled air that, if not met, can indicate that the patient is suffering one or more medical conditions, such as obstructive lung disease and/or (b) can define an exhalation threshold target tidal volume representative of a volume of air that, if exceeded, can indicate that the patient is not breathing and/or that the patient's breathing is strained, inhibited, restricted, and/or obstructed.
At block 2092, the routine 2090 can capture two or more images of one or more ROI's. In some embodiments, the routine 2090 can capture the two or more images of the one or more ROI's by capturing a video sequence of the one or more ROI's. In these and other embodiments, the routine 2090 can capture the two or more images of the one or more ROI's by capturing separate still images of the one or more ROI's. The routine 2090 can capture the two or more still images at a rate faster than a period of the patient's respiration cycle to ensure that the two or more still images occur within one period of the patient's respiration cycle.
At block 2093, the routine 2090 can measure changes in depth of one or more regions in one or more ROI's over time. In some embodiments, the routine 2090 can measure changes in depth of regions in the one or more ROI's by computing a difference between a depth of a region of a ROI in a first captured image of the ROI and a depth of the same region in a second captured image of the ROI.
At block 2094, the routine 2090 can generate one or more breathing parameter signals. In some embodiments, the routine 2090 generates a volume gain signal and/or a volume loss signal for one or more ROI's. In these and other embodiments, the routine 2090 generates a tidal volume signal for one or more ROI's. In these and still other embodiments, the routine 2090 generates one or more other breathing parameter signals for one or more ROI's. For example, the routine 2090 can generate an inhalation-to-exhalation ratio for one or more ROI's, a degree of consistency value indicating consistency in the volume of each breath for one or more ROI's, a trending and/or an absolute minute volume signal for one or more ROI's, a respiratory rate signal for one or more ROI's, a SpO2 signal for one or more ROI's, and/or an absolute tidal volume signal for one or more ROI's, among others.
At block 2095, the routine 2090 can analyze one or more of the breathing parameter signals generated at block 2094 to determine one or more positions of the patient's breathing within the patient's breathing cycle. For example, the routine 2090 can determine whether the patient is currently breathing and/or whether the patient is currently inhaling and/or exhaling. In these and other embodiments, the routine 2090 can determine the one or more positions of the patient's breathing relative to one or more defined threshold target tidal volumes. For example, if the routine 2090 determines that the patient is currently inhaling, the routine 2090 can determine whether the tidal volume signal is at or above an inhalation threshold target tidal volume previously defined by the routine 2090. If the routine 2090 determines that the patient is currently exhaling, the routine 2090 can determine whether the tidal volume signal is at or below one or more exhalation threshold target tidal volumes defined by the routine 2090. In these and other embodiments, the routine 2090 can determine whether the tidal volume signal is within and/or outside one or more ranges of normal patient ventilation defined by the routine 2090.
At block 2096, the routine 2090 can assign one or more visual indicators to one or more regions in the one or more ROI's. In some embodiments, the one or more visual indicators can be colors, patterns, shades, concentrations, intensities, etc. In these and other embodiments, the routine 2090 can assign the one or more visual indicators in accordance with a predetermined visual scheme. In these and still other embodiments, the routine 2090 can assign one or more visual indicators to one or more regions in accordance with the discussion above with respect to
At block 2097, the routine 2090 can display one or more visual indicators assigned at block 2096 over corresponding regions of one or more ROI's and/or can display one or more of the breathing parameter signals generated at block 2094. In some embodiments, the routine 2090 can display the one or more visual indicators in accordance with the discussion above with respect to
At block 2098, the routine 2090 can trigger one or more alerts and/or alarms. In some embodiments, the routine 2090 can trigger the one or more alerts and/or alarms by changing the visual indicators displayed in the ROI 102, by flashing the display, by displaying one or more other graphics, and/or by triggering one or more other visual and/or audio alerts/alarms. For example, the routine 2090 can trigger the one or more alerts/alarms in accordance with the discussion above with respect to
Although the steps of the routine 2090 are discussed and illustrated in a particular order, the routine 2090 in
As shown in
In some embodiments, a user can select which image type to view the patient 112 and/or the user can toggle the display of the visualization of the ROI 102 on and/or off. In these and other embodiments, the user can define the ROI 102 within a selected image type. For example, a user can define a ROI 102 to align with a patient's torso within an RGB image of the patient 112. This can be helpful, for example, when a portion of the patient 112 is hidden from an image capture device's FOV (e.g., when a patient 112 is underneath a blanket). Although the visualizations of the patient's breathing are confined to regions within the ROI 102 in the images of the patients 112 in
The above detailed descriptions of embodiments of the technology are not intended to be exhaustive or to limit the technology to the precise form disclosed above. Although specific embodiments of, and examples for, the technology are described above for illustrative purposes, various equivalent modifications are possible within the scope of the technology, as those skilled in the relevant art will recognize. For example, while steps are presented in a given order, alternative embodiments can perform steps in a different order. Furthermore, the various embodiments described herein can also be combined to provide further embodiments. Moreover, any one of the visual indicators (e.g., colors) described herein can be the same visual indicator (e.g., color) as and/or a different visual indicator (e.g., color) than any one of the other visual indicators (e.g., colors) described herein. Any one of the audio and/or visual alerts/alarms described herein can be the same as and/or a different than any one of the other audio and/or visual alerts/alarms described herein. In addition, one or more other colors, sequences of colors, patterns, shades, densities, intensities, concentrations, and/or visual indicators than shown in the embodiments illustrated herein are within the scope of the present technology. Furthermore, any one of the visual indicators described herein can be spatially uniform across an ROI in a generated image, can spatially vary across an ROI in a generated image, can remain constant throughout all or a portion of a patient's breathing cycle, and/or can vary throughout all or a portion of the patient's breathing cycle. Any of the displayed visual indicators can be displayed apart (e.g., independent) from the one or more regions of an ROI on which they are based. As an example, the visual indicators can be displayed within a box having a different (e.g., smaller or larger) area than the ROI or a region within the ROI. The box can be displayed over the ROI, at another location (e.g., apart from), or separate from the ROI on the display. The visual indicators can be based on one or more regions of the ROI. The visual indicators can be displayed within, fill in, or empty from the box to provide a user information about a patient's breathing cycles.
The systems and methods described herein can be provided in the form of tangible and non-transitory machine-readable medium or media (such as a hard disk drive, hardware memory, etc.) having instructions recorded thereon for execution by a processor or computer. The set of instructions can include various commands that instruct the computer or processor to perform specific operations such as the methods and processes of the various embodiments described here. The set of instructions can be in the form of a software program or application. The computer storage media can include volatile and non-volatile media, and removable and non-removable media, for storage of information such as computer-readable instructions, data structures, program modules or other data. The computer storage media can include, but are not limited to, RAM, ROM, EPROM, EEPROM, flash memory or other solid-state memory technology, CD-ROM, DVD, or other optical storage, magnetic disk storage, or any other hardware medium which can be used to store desired information and that can be accessed by components of the system. Components of the system can communicate with each other via wired or wireless communication. The components can be separate from each other, or various combinations of components can be integrated together into a monitor or processor or contained within a workstation with standard computer hardware (for example, processors, circuitry, logic circuits, memory, and the like). The system can include processing devices such as microprocessors, microcontrollers, integrated circuits, control units, storage media, and other hardware.
From the foregoing, it will be appreciated that specific embodiments of the technology have been described herein for purposes of illustration, but well-known structures and functions have not been shown or described in detail to avoid unnecessarily obscuring the description of the embodiments of the technology. To the extent any materials incorporated herein by reference conflict with the present disclosure, the present disclosure controls. Where the context permits, singular or plural terms can also include the plural or singular term, respectively. Moreover, unless the word “or” is expressly limited to mean only a single item exclusive from the other items in reference to a list of two or more items, then the use of “or” in such a list is to be interpreted as including (a) any single item in the list, (b) all of the items in the list, or (c) any combination of the items in the list. Where the context permits, singular or plural terms can also include the plural or singular term, respectively. Additionally, the terms “comprising,” “including,” “having” and “with” are used throughout to mean including at least the recited feature(s) such that any greater number of the same feature and/or additional types of other features are not precluded. Furthermore, as used herein, the term “substantially” refers to the complete or nearly complete extent or degree of an action, characteristic, property, state, structure, item, or result. For example, an object that is “substantially” enclosed would mean that the object is either completely enclosed or nearly completely enclosed. The exact allowable degree of deviation from absolute completeness may in some cases depend on the specific context. However, generally speaking the nearness of completion will be so as to have the same overall result as if absolute and total completion were obtained. The use of “substantially” is equally applicable when used in a negative connotation to refer to the complete or near complete lack of an action, characteristic, property, state, structure, item, or result.
From the foregoing, it will also be appreciated that various modifications can be made without deviating from the technology. For example, various components of the technology can be further divided into subcomponents, or various components and functions of the technology can be combined and/or integrated. Furthermore, although advantages associated with certain embodiments of the technology have been described in the context of those embodiments, other embodiments can also exhibit such advantages, and not all embodiments need necessarily exhibit such advantages to fall within the scope of the technology. Accordingly, the disclosure and associated technology can encompass other embodiments not expressly shown or described herein.
The present application is a continuation application of U.S. application Ser. No. 16/713,265 filed Dec. 13, 2019, entitled “Depth Sensing Visualization Modes for Non-Contact Monitoring” which claims the benefit of priority to U.S. Provisional Patent Application Ser. No. 62/779,964, filed Dec. 14, 2018, the entire contents of which are incorporated herein by reference.
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Number | Date | Country | |
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20230200679 A1 | Jun 2023 | US |
Number | Date | Country | |
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62779964 | Dec 2018 | US |
Number | Date | Country | |
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Parent | 16713265 | Dec 2019 | US |
Child | 18173008 | US |