Automated Urinary Output Measuring System

Abstract

Disclosed herein is an automated urinary output monitoring system including an automated urinary output monitoring device. The automated urinary output monitoring device includes a load cell assembly, a mounting system having a buffering region configured to reduce vibrations through the automated urinary output monitoring device and allow axial rotation of the automated urinary output monitoring device around a lateral axis, a mounting region configured to couple the automated urinary output monitoring device to a surface, a fluid collection bag attachment, and a console in communication with the load cell assembly.

Description

BACKGROUND

Some current urine monitoring systems use weight based methodologies to determine urine volume and urine flow rate over time. A fluid collection container may be suspended from a weighing device and as urine is captured by the fluid collection container, the weight of the fluid collection container increases. The weighing device may be configured to detect the increase in the weight of the fluid collection container. However, most urine monitoring systems do not travel with a patient as the patient is moved through a hospital setting, requiring clinicians to suspend urine monitoring until a patient is stationed in one location. If a patient has to move frequently within the hospital (e.g., multiple surgeries), critical patient data may not be captured. It would be beneficial to the patient and the clinician to be able to monitor urine output during the patient's entire stay. Disclosed herein is an automated urinary output monitoring system and method of use that address the foregoing.

SUMMARY

Disclosed herein is an automated urinary output monitoring system including an automated urinary output monitoring device. The device includes a device body having a mounting system coupled thereto. The mounting system includes a mounting surface rotatably coupled with the device body, where the mounting surface is configured to secure the automated urinary output monitoring device to an external stabilizing surface. The mounting system further includes a buffering region disposed between the mounting surface and the device body, where the buffering region is configured to isolate the device body from vibrations of the external stabilizing surface. The device further includes a load cell assembly operatively coupled with the device body having a fluid collection bag attachment coupled therewith, where the fluid collection bag attachment is configured to suspend a fluid collection bag therefrom.

The system further includes a console communicatively coupled with the load cell assembly, where the console including one or more processors, and non-transitory computer readable medium having logic stored thereon that, when executed by the one or more processors, performs operations of the system. The operations include (i) receiving a load value applied to the fluid collection bag attachment by the fluid collection bag, (ii) calculating a volume of urine collected within the fluid collection bag based on the load value, and (iii) depicting the volume of urine on a display of the system.

In some embodiments, the mounting system extends laterally away from a back panel of the device body. In some embodiments, the mounting surface includes a number of suction cups, clamps, magnets, or an adhesive configured for securing the mounting surface to the stabilizing surface. In some embodiments, the automated urinary output monitoring device is configured to rotate with respect to the mounting surface due to gravity to maintain a vertical orientation of the device body during use.

In some embodiments, the buffering region is configured to transition between a non-compressed configuration and a compressed configuration in response to a lateral movement of the stabilizing surface. In some embodiments, the mounting surface rotates about an axis of rotation extending through the buffering region.

In some embodiments, the automated urinary output monitoring device includes a front panel including the display and an input interface, where each are in communication with the console. In some embodiments, the input interface includes a plurality of buttons.

In some embodiments, the automated urinary output monitoring device includes one or more module inputs configured to define communication between one or more modules and the console.

In some embodiments, the system receives electrical power from an external power source.

In some embodiments, the operations further include correlating the volume of urine with a time of day and depicting the time of day along with the volume of urine on the display of the system.

In some embodiments, the automated urinary output monitoring device includes a tube holder coupled with the device body, where the tube holder is configured to secure a portion of a drainage tube of the fluid collection bag to the device body.

In some embodiments, the one or more modules includes a temperature sensor coupled with the tube holder, where the temperature sensor is configured to determine a temperature of urine disposed with in the drainage tube, and the operations further include obtaining a temperature measurement of the urine disposed with in the drainage tube and depicting the temperature measurement on the display.

In some embodiments, the automated urinary output monitoring device includes the securing attachment extending upward away from a top side of the device body, where the securing attachment is configured to suspend the automated urinary output monitoring device from a bed rail.

In some embodiments, the console is configured to wirelessly communicate with an external computing device, where the external computing device includes one or more of a tablet, a cell phone, or an electronic medical record (EMR) system, and the operations further include at least one of (i) receiving patient information from the external computing device or (ii) transmitting urine output monitoring data to the external computing device.

In some embodiments, the operations further include receiving a plurality of patient profiles from the EMR system and storing the plurality of the patient profiles on the non-transitory computer readable medium.

In some embodiments, the operations further include depicting patient profile information on the display.

Also disclosed herein is a method of monitoring urine output from a patient performed by a urine output monitoring system. According to some embodiments, the method includes (i) rotating a device body of the urine output monitoring system about an axis of rotation with respect to a mounting surface of the urine output monitoring system so that the device body is vertically oriented; (ii) obtaining a load value from a load cell assembly of the urine output monitoring system, where the load value is defined by a urine collection bag coupled with load cell assembly and the urine collection bag includes a volume of urine collected therein; (iii) calculating the volume of urine based on the load value; (iv) correlating the volume of urine with a time of day; (v) receiving patient identification for the patient from an EMR system; and (vi) depicting the volume of urine, the time of day, and the patient identification on a display of the urine output monitoring system.

In some embodiments, the method further includes transmitting the volume of urine, the time of day, and the patient identification to the EMR system.

In some embodiments, the method further includes obtaining a temperature measurement of the urine disposed within a drainage tube of the urine output monitoring system and depicting the temperature measurement on the display.

These and other features of the concepts provided herein will become more apparent to those of skill in the art in view of the accompanying drawings and following description, which describe particular embodiments of such concepts in greater detail.

DRAWINGS

A more particular description of the present disclosure will be rendered by reference to specific embodiments thereof that are illustrated in the appended drawings. It is appreciated that these drawings depict only typical embodiments of the invention and are therefore not to be considered limiting of its scope. Example embodiments of the invention will be described and explained with additional specificity and detail through the use of the accompanying drawings in which:

FIG. 1 illustrates a plan view of an automated urinary output measuring system, in accordance with some embodiments;

FIG. 2 illustrates a perspective view of the system of FIG. 1, in accordance with some embodiments;

FIG. 3A illustrates perspective view of a back panel of another embodiment of an automated urinary output measuring system, in accordance with some embodiments;

FIGS. 3B-3C illustrate a side view of the automated urinary output measuring device of FIG. 3A including a mounting system, in accordance with some embodiments;

FIG. 4 illustrates a block diagram of some components of the system of FIG. 1 including a console, in accordance with some embodiments; and

FIGS. 5A-5B illustrates a perspective view of the system of FIG. 3A depicting an exemplary method of the mounting system maintaining the automated urinary output measuring system in a vertical orientation, in accordance with some embodiments.

DESCRIPTION

Before some particular embodiments are disclosed in greater detail, it should be understood that the particular embodiments disclosed herein do not limit the scope of the concepts provided herein. It should also be understood that a particular embodiment disclosed herein can have features that can be readily separated from the particular embodiment and optionally combined with or substituted for features of any of a number of other embodiments disclosed herein.

Regarding terms used herein, it should also be understood the terms are for the purpose of describing some particular embodiments, and the terms do not limit the scope of the concepts provided herein. Ordinal numbers (e.g., first, second, third, etc.) are generally used to distinguish or identify different features or steps in a group of features or steps, and do not supply a serial or numerical limitation. For example, “first,” “second,” and “third” features or steps need not necessarily appear in that order, and the particular embodiments including such features or steps need not necessarily be limited to the three features or steps. Labels such as “left,” “right,” “top,” “bottom,” “front,” “back,” and the like are used for convenience and are not intended to imply, for example, any particular fixed location, orientation, or direction. Instead, such labels are used to reflect, for example, relative location, orientation, or directions. Singular forms of “a,” “an,” and “the” include plural references unless the context clearly dictates otherwise.

The term “logic” may be representative of hardware, firmware or software that is configured to perform one or more functions. As hardware, the term logic may refer to or include circuitry having data processing and/or storage functionality. Examples of such circuitry may include, but are not limited or restricted to a hardware processor (e.g., microprocessor, one or more processor cores, a digital signal processor, a programmable gate array, a microcontroller, an application specific integrated circuit “ASIC”, etc.), a semiconductor memory, or combinatorial elements.

Additionally, or in the alternative, the term logic may refer to or include software such as one or more processes, one or more instances, Application Programming Interface(s) (API), subroutine(s), function(s), applet(s), servlet(s), routine(s), source code, object code, shared library/dynamic link library (dll), or even one or more instructions. This software may be stored in any type of a suitable non-transitory storage medium, or transitory storage medium (e.g., electrical, optical, acoustical or other form of propagated signals such as carrier waves, infrared signals, or digital signals). Examples of a non-transitory storage medium may include, but are not limited or restricted to a programmable circuit; non-persistent storage such as volatile memory (e.g., any type of random access memory “RAM”); or persistent storage such as non-volatile memory (e.g., read-only memory “ROM”, power-backed RAM, flash memory, phase-change memory, etc.), a solid-state drive, hard disk drive, an optical disc drive, or a portable memory device. As firmware, the logic may be stored in persistent storage.

The term “computing device” should be construed as electronics with the data processing capability and/or a capability of connecting to any type of network, such as a public network (e.g., Internet), a private network (e.g., a wireless data telecommunication network, a local area network “LAN”, etc.), or a combination of networks. Examples of a computing device may include, but are not limited or restricted to, the following: a server, an endpoint device (e.g., a laptop, a smartphone, a tablet, a “wearable” device such as a smart watch, augmented or virtual reality viewer, or the like, a desktop computer, a netbook, a medical device, or any general-purpose or special-purpose, user-controlled electronic device), a mainframe, internet server, a router; or the like.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by those of ordinary skill in the art.

FIG. 1 illustrates a perspective view of an automated urinary output measuring system 100, in accordance with some embodiments. The automated urinary output monitoring system (system) 100 includes the automated urinary output monitoring device (device) 110 having a device body 112 including a top side 114, a bottom side 116, a front panel 118, and a back panel 120. The device 110 includes a fluid collection bag attachment 122 extending downward from the device body 112, i.e., downward away from the bottom side 116. In some embodiments, the system 100 also includes a fluid collection bag 132 configured for coupling to the fluid collection bag attachment 122 during use. During use, the fluid collection bag 132 may be in fluid communication with a urinary catheter via a drainage tube 133 and collect a volume of fluid (urine) therein by gravity flow, negative pressure flow, or the like. The fluid collection bag 132 may be directly coupled to the fluid collection bag attachment 122 or may be coupled to the fluid collection bag attachment 122 via an intermediate device, such as a hook, a ring, or the like. The fluid collection bag 132 is coupled to the fluid collection bag attachment 122 so that any volume of fluid (urine) within the fluid collection bag 132 or any increase in volume of fluid within the fluid collection bag 132 defines a load (e.g., a hanging load) on the fluid collection bag attachment 122. The device 110 further includes a load cell assembly 140 configured to measure the load on the fluid collection bag attachment 122.

The load cell assembly 140 may be integrated into the bottom side 116 of the device 110 or may be located within the device body 112. The load cell assembly 140 is communicatively coupled with a console 150 of the system 100 wherein the load cell assembly 140 is configured to communicate load cell values (measurements) to the console 150. The load cell assembly 140 may be wired to the console 150 or may be wirelessly coupled with the console 150. The console 150 may reside within the device body 112. In some embodiments, the console 150 may be in wireless communication with an external computing device (e.g., a stand-a-alone computer, a tablet, or cell phone) or electronic medical record (EMR) system so that the console 150 may transmit load cell values to the computing device or the EMR system. Exemplary wireless communication modalities can include WiFi, Bluetooth, Near Field Communications (NFC), cellular Global System for Mobile Communication (“GSM”), electromagnetic (EM), radio frequency (RF), combinations thereof, or the like.

The front panel 118 of the device 110 may include a display 170 integrated into or coupled to the device body 112. The display 170 may be in communication with the console 150 and may be configured to display determined load cell values or other information pertaining the monitoring of urine output. In some embodiments, the front panel 118 of the device 110 may include an input interface 126 in communication with the console 150. In some embodiments, the input interface 126 may include a plurality of buttons 126A configured to allow a user to input information into the system 100 and/or select information to be projected on the display 170. In some embodiments, the plurality of buttons 126A may be organized into a keypad array, positioned around the display 170, or a combination thereof.

The device 110 includes a securing attachment 124 configured to detachably couple the device 110 to a stabilizing surface 190. In some embodiments, the stabilizing surface 190 may include a rail of a hospital bed, an IV pole or the like. In some embodiments, the securing attachment 124 may include a hook, a clamp, or the like. The securing attachment 124 may be configured to allow the device 110 to be suspended from (i.e., hung from) the stabilizing surface 190 so that the device 110 is disposed in a vertical orientation, where the vertical orientation enables the load cell assembly 140 to precisely determine load values applied to the fluid collection bag attachment 122.

FIG. 2 illustrates a perspective view of the automated urinary output measuring device 110, in accordance with some embodiments. In some embodiments, the device body 112 may include one or more module inputs 128 located on one or more sides of the device body 112. In some embodiments, the module inputs 128 may be configured to receive therein or otherwise couple with one or more modules, where the one or more modules may be configured to provide additional functionality to the system 100.

The device 110 may include a tube holder 130 configured for securing a portion of drainage tube 133 to the body 112. The tube holder 130 may be configured to optimally position and hold a drainage tube 133 so that movement of the patient does not affect the load applied to the fluid collection bag attachment 122. If the drainage tube is not adequately positioned and secured, the shape or strain of the drainage tube 1330 may alter the load obtained by the load cell assembly 140, confounding the determination of load cell values.

In some embodiments, the one or more modules may include a temperature sensor 127 coupled with the tube holder 130. The temperature sensor 127 may be configured to determine the temperature of the volume of fluid as the volume of fluid moves through the drainage tube 133 to the fluid collection bag 132.

In some embodiments, the fluid collection bag attachment 122 being fixed to the bottom side 116 of the device body 112 or the fluid collection bag attachment 122 be integrated into or formed into the device body 112. In some embodiments, the fluid collection bag attachment 122 is fixed directly underneath the device body 112, equidistant between the front panel 118 and the back panel 120. The fluid collection bag attachment 122 and the device body 112 may be formed as a single piece. In some embodiments, the device body 112 and the fluid collection bag attachment 122 may be formed of a thermoplastic material (e.g., polyvinyl chloride, polyethylene, polypropylene, polystyrene, polyurethane, nylon, or any other suitable thermoplastic material) formed by 3D printing, injection molding or the like. Advantageously, the device body 112 and the fluid collection bag attachment 122 being formed as a singular piece removes attachment/reattachment of the fluid collection bag attachment 122 and rotation of the fluid collection bag 132 around the fluid collection bag attachment 122, leading to longevity of the device 110 and consistency of the load cell assembly 140 detecting the load of the fluid collection bag attachment 122. In an embodiment, the load cell assembly 140 may be integrated into the fluid collection bag attachment 122. Advantageously, fixing the fluid collection bag attachment 122 to the device body 112 ensures both consistent placement of the fluid collection bag 132 on the fluid collection bag attachment 122 and that the load cell assembly 140 is protected and consistently able to transmit load values to the console 150 during multiple deployments of the system 100 or multiple changes of the fluid collection bag 132.

FIGS. 3A-3C illustrate another embodiment of automated urinary output measuring system 300 that can, in certain respects, resemble components of the automated urinary output measuring system 100 described in connection with FIGS. 1-2. It will be appreciated that all the illustrated embodiments may have analogous features. Accordingly, like features are designated with like reference numerals, having leading digits of “3.” For instance, the device is designated as “110” in FIGS. 1-2, and an analogous device is designated as “310” in FIGS. 3A-3C. Relevant disclosure set forth above regarding similarly identified features thus may not be repeated hereafter. Moreover, specific features of the automated urinary output measuring system 100 and related components shown in FIGS. 1-2 may not be shown or identified by a reference numeral in the drawings or specifically discussed in the written description that follows. However, such features may clearly be the same, or substantially the same, as features depicted in other embodiments and/or described with respect to such embodiments. Accordingly, the relevant descriptions of such features apply equally to the features of the automated urinary output measuring system of FIGS. 3A-3C. Any suitable combination of the features, and variations of the same, described with respect to the coronary automated urinary output measuring system 100 and components illustrated in FIGS. 1-2 can be employed with the automated urinary output measuring system and components of FIGS. 3A-3C, and vice versa.

FIG. 3A illustrates a perspective view of the back panel 320 of the automated urinary output measuring device 310, in accordance with some embodiments. The back panel 320 of the device 310 includes a mounting system 380 configured to allow the device 310 to hang vertically when an orientation of the stabilizing surface 190 is oriented away from a horizontal orientation. For example, the mounting system 380 may facilitate accurate measurement of urine output when the position of the patient is adjusted, such as between a lying position and a sitting position, for example. The mounting system 380 configured facilitate rotation of a mounting surface 382 with respect to the body 312 of the device 310 about an axis 381 so that the device 310 maintains a vertical orientation when the orientation of the stabilizing surface 190 is rotated away from a horizontal orientation. Similar to the securing attachment 324, mounting surface 382 is configured to couple the device 310 to the stabilizing surface 190 (see FIG. 1). In some instances, some stabilizing surfaces 190 (e.g., hospital beds or the like) may have portions of the stabilizing surfaces 190 that change orientation, forcing a device hung by the securing attachment 324 to be removed from the stabilizing surface 190 and to be repositioned to ensure the device 310 remains vertically oriented.

The mounting system 380 couples the device 310 to the stabilizing surface 190 along the axis 381. In some embodiments, the mounting system 380 extends laterally from a back panel 320 of the device 310. During use, the device 310 may be coupled to the stabilizing surface 190 via the securing attachment 324, the mounting system 380, or a combination thereof. In some embodiments, the stabilizing surface 190 be flat or may include portions of a hospital bed, a wall, an IV stand, a bed pole mount, or the like. In some embodiments, the mounting surface 382 may include a mounting mechanism 383 that may include a number (e.g., 1, 2, 3, 4 or more) of suction cups, clamps or magnets. In some embodiments, portions of the mounting surface 382 may include an adhesive configured to secure the mounting system 380 to the stabilizing surface 190. The mounting system 380 may be configured to prevent any sag or rotation of the device 310 except about the axis 381.

The mounting system 380 may also be configured to isolate the load cell system 340 from vibrations of the stabilizing surface 190. The mounting system 380 may include a buffering region 384 disposed between the back panel 320 and the mounting surface 382. The mounting surface 382 may be configured to couple the device 310 to a surface, including the stabilizing surface 190. Advantageously, the mounting surface 382 positions the device 310 to maintain the device in the vertical orientation so the fluid collection bag attachment 322 is suspended in line with the load cell assembly 340 and so that the stability of the device 310 in enhanced, e.g., isolated from vibrational movement of the stabilizing surface 190.

In some embodiments, the buffering region 384 buffers lateral movement of the device 310. In some embodiments, the buffering region 384 may include a spring. In some embodiments, the buffering region 384 may include a damping material such as a rubber or foam material. In some embodiments, the buffering region 384 may also be configured to allows the device 310 to move or rotate axially around the axis 381, allowing the device 310 to be maintained in a vertical orientation regardless of the orientation of the stabilizing surface 190. In some embodiments, the buffering region 384 may be configured (e.g., include stops) to limit rotation of the device 310 around the axis 381. In some embodiments, the user or the weight of the fluid collection bag 132 (see FIGS. 1-2) coupled to the fluid collection bag attachment 322 may rotate the device body 312 axially around the axis 381 to the vertical orientation, as will be described in more detail herein.

FIGS. 3B-3C illustrate a side view of the device 310 including the mounting system 380. In some embodiments, the mounting system 380 may be configured to transition between a non-compressed configuration and a compressed configuration to buffer lateral movement of the device 310. As illustrated in FIG. 3B, in the non-compressed configuration, the buffering region 384 may be fully extended away from the device 310 along the lateral axis. As illustrated in FIG. 3C, in the compressed configuration, the buffering region 384 may be partially or fully compressed toward the device 310 along the axis 381. In some embodiments, the buffering region 384 may collapse upon itself or may laterally slide into the mounting surface 382. The mounting system 380 may transition between the non-compressed configuration and the compressed configuration due to vibrations or sudden lateral movement of the stabilizing surface 190 with respect to the mounting surface 382. While the mounting system 380 is in the non-compressed configuration or the compressed configuration, the device may be rotated about the axis 381. Advantageously, the mounting system 380 stabilizes the device 310 during lateral movement, positions the device 310 in the vertical orientation, and buffers the device 310 from lateral movement impacting the ability of the load cell assembly 340 to determine load values.

In some embodiments, the device 310 may include an accelerometer (not shown) located within the device 310 that may be configured to determine the orientation of the device 310. The accelerometer may be in communication with the console 350 so as to receive accelerometer values from the accelerometer, where the console 350 may use the accelerometer values adjust load values obtained by the load cell assembly 340 to enhance the measurement accuracy of the load applied to the load cell assembly 340 and calculate the volume of fluid within the fluid collection bag 132 taking into account the orientation of the device 310. In some embodiments, the device 310 may include a gyroscope (not shown) that may be configured to stabilize the load cell assembly 340, such as maintain the device 310 in the vertical orientation and/or inhibit vibrations of the device 310 from affecting the ability of the load cell assembly 340 to detect load cell values. In some embodiments, the FIG. 4 illustrates a block diagram of some components of the system 100 including the console 150, in accordance with some embodiments. In some embodiments, the console 150 may include one or more processors 452, an energy source 454, non-transitory computer readable medium (“memory”) 456 and a plurality of logic modules. In some embodiments, the energy source 454 may be configured to provide power to the display 170 and the load cell assembly 140. In some embodiments, the energy source 154 may include an external power source. In some embodiments, wherein the external power source 154 is not connected to the console, the console 150, the display 170 and the load cell assembly 140 may not be operable.

For illustrative purposes, logic of the console 150 may be divided into a number of logic modules that may include load cell receiving logic 458, load cell correlation logic 460, module receiving logic 462, input interface receiving logic 464, display logic 466, and a data store 468.

The load cell receiving logic 458 may generally be configured to receive electrical signals (i.e., load cell values) from the load cell assembly 140. In some embodiments, the load cell receiving logic 458 may be configured to constantly (e.g., at a high sampling rate) receive the load cell values. In some embodiments, the sampling rate may be defined by the user, such as a sampling rate of every 5 minutes for example. In some embodiments, the load cell receiving logic 458 may be configured to receive the load cell values upon a defined change or difference from a previous load cell values.

The load cell correlation logic 460 may be configured to correlate the received load cell value with a volume of urine collected within the fluid collection bag 132. In some embodiments, the load cell correlation logic 460 may be configured correlate the volume of urine with a time of day value. In other words, the load cell correlation logic 460 may attach time stamp to each the volume of urine. By way of summary, a volume of urine may be calculated for each load cell value, and each volume of urine may include an attached time stamp.

The module receiving logic 462 may be configured to receive data from any of the one or more modules coupled with module inputs 128. The module receiving logic 462 may also be configured to receive data wirelessly from an external source, such as the external computing device or the EMR system. For example, the module receiving logic 462 may receive patient identification information from the EMR system and the volume of urine values to a specific patient. In some embodiments, the module receiving logic 462 may receive patient identification information for a plurality of patients and the patient information may be stored in the data store 468. The module receiving logic 462 may also be configured to receive/obtain temperature data from the temperature sensor 127 and correlate the temperature data with the volume of urine values.

In some embodiments, the input interface receiving logic 464 may be configured to receive input from the user via the input interface 126 including the plurality of buttons 126A. The input interface receiving logic 464 may, in response to the input, change a mode of operation, such as change the load cell sampling rate, for example. The user may also input various settings, such as a volume capacity for the fluid collection bag 132. The user may also define a number of alert limits for the system, such as a leak alert associated in a decrease in load cell values, or a low urine output rate, for example.

In some embodiments, the display logic 466 may be configured to project urine output information on the display 170, such as the determined load cell values, the correlated volume values, the time of day values, the patient identification information, the urine temperature data, and/or module data from the one or more modules. The display logic 466 may also be configured to transmit the urine output information to the external computing device or the EMR system.

In some embodiments, the data store 468 may be configured to store the detected load cell values, the correlated volume values, the time of day values, and the module data values. The data store 468 may be configured to store multiple patient profiles as may be input by the user or received from the EMR system. In some embodiments, the data store 468 may be configured to record and store all data received, generated, obtained, or otherwise utilized by the system 100.

FIGS. 5A-5B illustrate a perspective view of the system 300 depicting an exemplary method of the mounting system 380 maintaining the system 300 in the perpendicular position, in accordance with some embodiments. As illustrated in FIG. 5A, the device 310 may be coupled to the stabilizing surface 190 by the mounting system 380 with the fluid collection bag 132 coupled to the fluid collection bag attachment 322. The stabilizing surface 190 may include a portion of a hospital bed being in a parallel configuration, wherein the parallel configuration includes the portion of the stabilizing surface 190 being parallel to a floor surface. The stabilizing surface 190 may transition from the parallel configuration towards a perpendicular configuration, wherein the perpendicular configuration includes the portion of the stabilizing surface 190 being perpendicular to the flood surface. The mounting system 380 (e.g., the buffering region 384) may allow the device 310 to be rotated around the lateral axis to maintain the device 310 in the perpendicular position, as illustrated in FIG. 5B. The device 310 is continuously coupled to the stabilizing surface 190 while maintaining the perpendicular position. Advantageously, maintaining the device 310 and more specifically the load cell assembly 340 perpendicular to the ground allows the load cell assembly 340 to accurately detect the load of the fluid collection bag 132.

While some particular embodiments have been disclosed herein, and while the particular embodiments have been disclosed in some detail, it is not the intention for the particular embodiments to limit the scope of the concepts provided herein. Additional adaptations and/or modifications can appear to those of ordinary skill in the art, and, in broader aspects, these adaptations and/or modifications are encompassed as well. Accordingly, departures may be made from the particular embodiments disclosed herein without departing from the scope of the concepts provided herein.

Claims

1. An automated urinary output monitoring system, comprising: an automated urinary output monitoring device, comprising: a device body;a mounting system operatively coupled with the device body, the mounting system including: a mounting surface rotatably coupled with the device body, the mounting surface configured to secure the automated urinary output monitoring device to an external stabilizing surface; anda buffering region disposed between the mounting surface and the device body, the buffering region configured to isolate the device body from vibrations of the external stabilizing surface;a load cell assembly operatively coupled with the device body;a fluid collection bag attachment coupled with the load cell assembly, the fluid collection bag attachment configured to suspend a fluid collection bag therefrom; anda console communicatively coupled with the load cell assembly, the console including one or more processors, and non-transitory computer readable medium having logic stored thereon that, when executed by the one or more processors, performs operations, including: receiving a load value applied to the fluid collection bag attachment by the fluid collection bag;calculating a volume of urine collected within the fluid collection bag based on the load value;depicting the volume of urine on a display of the system.

2. The system according to claim 1, wherein the automated urinary output monitoring device includes a tube holder coupled with the device body, the tube holder configured to secure a portion of a drainage tube of the fluid collection bag to the device body.

3. The system according to claim 1, wherein the mounting system extends laterally away from a back panel of the device body.

4. The system according to claim 1, wherein the mounting surface includes a mounting mechanism including a number of suction cups, clamps, magnets, or an adhesive configured for securing the mounting surface to the stabilizing surface.

5. The system according to claim 1, wherein the mounting surface is configured to rotate with respect to the device body to maintain a vertical orientation of the device body during use.

6. The system according to claim 1, wherein the automated urinary output monitoring device is configured to rotate with respect to the mounting surface due to gravity when the mounting surface is secured to the stabilizing surface.

7. The system according to claim 1, wherein the buffering region is configured to transition between a non-compressed configuration and a compressed configuration in response to a lateral movement of the stabilizing surface.

8. The system according to claim 1, wherein the mounting surface rotates about an axis of rotation extending through the buffering region.

9. The system according to claim 1, wherein the automated urinary output monitoring device includes the securing attachment extending upward away from a top side of the device body, the securing attachment configured to suspend the automated urinary output monitoring device from a bed rail.

10. The system according to claim 1, wherein the automated urinary output monitoring device includes a front panel including the display and an input interface, each in communication with the console.

11. The system according to claim 10, wherein the input interface includes a plurality of buttons.

12. The system according to claim 1, wherein the system receives electrical power from an external power source.

13. The system according to either claim 1, wherein the operations further include: correlating the volume of urine with a time of day; anddepicting the time of day along with the volume of urine on the display.

14. The system according to claim 2, wherein the automated urinary output monitoring device includes one or more module inputs configured to define communication between one or more modules and the console.

15. The system according to claim 14, wherein: the one or more modules includes a temperature sensor coupled with the tube holder, the temperature sensor configured to measure a temperature of urine disposed within the drainage tube; andthe operations further include: obtaining a temperature measurement of the urine disposed with in the drainage tube; anddepicting the temperature measurement on the display.

16. The system according to claim 1, wherein: the console is configured to wirelessly communicate with an external computing device, the external computing device including one or more of a tablet, a cell phone, or an electronic medical record (EMR) system; andthe operations further include at least one of: receiving patient information from the external computing device; ortransmitting urine output monitoring data to the external computing device.

17. The system according to claim 16, wherein the operations further include: receiving a plurality of patient profiles from the EMR system; andstoring the plurality of the patient profiles on the non-transitory computer readable medium.

18. A method of monitoring urine output from a patient performed by a urine output monitoring system, the method comprising: rotating a device body of the urine output monitoring system about an axis of rotation with respect to a mounting surface of the urine output monitoring system so that the device body is vertically oriented;obtaining a load value from a load cell assembly of the urine output monitoring system, the load value defined by a urine collection bag coupled with load cell assembly, the urine collection bag having a volume of urine collected therein;calculating the volume of urine based on the load value;correlating the volume of urine with a time of day;receiving a patient identification for the patient from an EMR system; anddepicting the volume of urine, the time of day, and the patient identification on a display of the urine output monitoring system.

19. The method according to claim 18, further comprising: transmitting the volume of urine, the time of day, and the patient identification to the EMR system.

20. The method according to claim 18, further comprising: obtaining a temperature measurement of the urine disposed within a drainage tube of the urine output monitoring system; anddepicting the temperature measurement on the display.