Hospital bed warning light management
By designing a control system of multiple device components, sensors and programming protocols on the patient support equipment, the problem that the location of the device components does not comply with the treatment operation protocol is solved, and automatic adjustment is achieved to comply with the treatment operation protocol, improving the quality of care and patient safety.
Patent Information
- Application Number
- CN202380061192.4
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Priority Date
- 2022-09-01
- Filing Date
- 2023-08-31
- Publication Date
- 2025-04-29
AI Technical Summary
The existing patient support equipment cannot effectively determine whether the location of the equipment components complies with the agreement before implementing the treatment operation protocol, resulting in potential harm to the patient.
A patient-supported device control system is designed including multiple device components, sensors, programming baseline operation protocols and user interfaces. The system communicates with multiple device component sensors through the controller to determine whether the treatment operation protocol complies with the baseline operation protocol and automatically adjusts to comply with the treatment operation protocol if it does not comply.
Through this system, it is possible to effectively ensure that the position of the patient's support equipment components complies with the treatment operation protocol, reduce potential harm to the patient, and improve the quality of care.
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Figure CN119907654A_ABST
Abstract
Description
[0001] CROSS-REFERENCE TO RELATED APPLICATIONS
[0002] This application claims priority under 35 U.S.C. §119(e) to U.S. Provisional Application No. 63 / 403,116, filed on September 1, 2022, which is expressly incorporated herein by reference. Background Art
[0003] The present invention relates to determining the hierarchy of patient care protocols to be implemented, for example using sensors of a patient support device such as a hospital bed. More specifically, the present invention relates to a system or method for communicating a treatment protocol and determining whether a patient support device should issue an alert.
[0004] Patient support devices (including mattresses, stretchers, operating room tables, etc.) are commonly used in various care environments to facilitate patient care and transportation. Patient support devices are programmed with protocols to enable users to perform various automated functions related to patient support. Examples of such automated functions include raising or lowering one or more sections of a patient support, adjusting the configuration of a bed frame or support surface or a portion thereof, and activating or deactivating selected treatments, alarms, communications, and other automated features of a patient support.
[0005] Many such patient supports include a frame, a platform supported by the frame, a mattress, a bed rail configured to prevent the patient from getting out of the mattress, and a controller configured to control one or more features of the bed. The patient, caregiver, or visitor may intermittently change the position of one or more components of the patient support device during the day. In some cases, it is important to determine the position of one or more components relative to the patient support device before implementing a treatment operation protocol. In addition, sensors can be used to determine the position of one or more components.
[0006] Monitoring various components of a patient support device may include monitoring position, angle, movement, or other attributes. A caregiver may not be able to determine whether different components are in compliance with a therapeutic operating protocol. The ability of a patient support device to automatically determine compliance may prevent potential harm to the patient. Thus, characterizing components of a patient support device in accordance with any therapeutic operating protocol communicated to a caregiver may provide improved care for the patient. Summary of the invention
[0007] The invention comprises one or more of the features recited in the appended claims and / or the following features, which alone or in any combination may constitute patentable subject matter.
[0008] According to a first aspect of the invention, a patient support device comprises a plurality of device components; a plurality of device component sensors located on the plurality of device components; a baseline operating protocol programmed on the patient support device; a user interface operable to be programmed with a therapeutic operating protocol; and a control system comprising a controller in communication with the plurality of device component sensors, the controller operable to determine whether the therapeutic operating protocol complies with the baseline operating protocol.
[0009] In some embodiments of the patient support device, the controller may function as a protocol conflict manager.
[0010] In one embodiment of the patient support device, if the control system determines that the therapeutic operating protocol does not comply with the baseline operating protocol, the therapeutic operating protocol replaces the baseline operating protocol, and the control system is further operable to communicate with the plurality of device component sensors to ensure compliance with the therapeutic operating protocol.
[0011] In one embodiment of the patient support device, the compliance status of the patient support device to the treatment protocol is projected on the floor. In some embodiments of the patient support device, the plurality of device components are a plurality of bed rails, and the controller is operable to receive a separate signal from each of the plurality of device component sensors to determine whether each of the plurality of bed rails is up or down, and the controller is further operable to process the signal to determine whether the treatment protocol is being complied with.
[0012] In one embodiment of the patient support device, the treatment operating protocol is a CLR (continuous lateral rotation) protocol and the baseline operating protocol includes a baseline bedrail protocol. In some embodiments, the CLR protocol includes having four bedrails in an upward position and the baseline bedrail protocol includes having two bedrails in an upward position. In some embodiments, the CLR protocol replaces the baseline bedrail protocol and the controller projects a warning sign on the floor if the patient support device does not comply with the CLR protocol. In some embodiments, the warning sign is an indication that the patient support device does not comply with the CLR protocol.
[0013] In one embodiment of the patient support device, the CLR protocol replaces the baseline bedrail protocol, and wherein if the controller determines that the patient support device does not have four bedrails in an upward position, the user interface displays a warning sign. In some embodiments, the CLR protocol includes determining the status of other components of the patient support device.
[0014] In one embodiment of the patient support device, the user interface is operable for manual or remote programming.
[0015] According to a second aspect of the invention, a system includes a patient support device, the patient support device including a head end and a foot end; a plurality of patient support members; an indicator light at the foot end; and a controller operable to communicate with the plurality of patient support members and the indicator light. The controller is operable to receive a separate signal from each of the plurality of patient support members to process the signal to determine the position of each patient support member; and a user interface operable to be programmed with a baseline operating protocol and a treatment operating protocol.
[0016] In some embodiments of the system, the controller may function as a protocol conflict manager.
[0017] In one embodiment of the system, the controller is operable to process the signal to determine whether the therapeutic operating protocol complies with the baseline operating protocol. In some embodiments of the system, if the control system determines that the patient support device does not comply with the therapeutic operating protocol, the control system is further operable to communicate with the plurality of device component sensors to ensure compliance with the therapeutic operating protocol.
[0018] In one embodiment of the system, the indicator light projects a compliance status of the patient support device on the floor, and wherein the compliance status is based on the treatment protocol.
[0019] In one embodiment of the system, the therapeutic operating protocol is a CLR protocol, and the user interface is operable to program using the CLR protocol. In some embodiments, the CLR protocol replaces a baseline operating protocol, and wherein the CLR protocol includes having four bedrails in an upward position. In some embodiments, the baseline operating protocol includes a bedrail protocol, and the bedrail protocol includes having two bedrails in an upward position.
[0020] In one embodiment of the system, if the controller determines that the patient support device does not have four bedrails in the upward position, the user interface is operable to display a warning sign. In some embodiments, if the controller determines that the patient support device does not have four bedrails in the upward position, an indication is projected on the floor that the patient support device does not comply with the programmed bedrail protocol. In some embodiments, the CLR protocol also includes determining the status of other components of the patient support device.
[0021] In one embodiment of the system, the user interface is operable for manual or remote programming.
[0022] According to a second aspect of the present invention, a method includes monitoring compliance of a support device with a treatment operation protocol. The method includes the following steps: inputting a baseline operation protocol into a user interface; monitoring signals from a plurality of device component sensors; processing the signals from the plurality of device component sensors using a controller.
[0023] signals, the equipment component sensors being located on a plurality of equipment components; determining positions of a plurality of bedrails based on the signals from the plurality of equipment component sensors; and determining whether the positions of the plurality of bedrails comply with a patient protocol.
[0024] In one embodiment of the method, if the support device is not in compliance with the patient protocol, the method includes the controller communicating with the plurality of device component sensors to ensure compliance with a programmed patient protocol. In another embodiment of the method, the method includes automatically moving a portion of the support device based on the signal from the device component sensor to ensure compliance with the patient protocol. In one embodiment of the method, the method includes projecting the compliance status of the support device on a floor.
[0025] In some embodiments of the method, the controller may function as a protocol conflict manager.
[0026] In one embodiment of the method, the user interface is operable to be programmed using a CLR (Continuous Lateral Rotation) protocol. In some embodiments, the method includes the CLR protocol replacing a conventional bedrail protocol, and the CLR protocol includes having four bedrails in an upward position. In some embodiments, if the controller determines that the patient support device does not have four bedrails in an upward position, the method includes the user interface displaying a warning sign.
[0027] In one embodiment of the method, if the controller determines that the patient support device does not have four bedrails in the upward position, the method includes projecting an indication on the floor that the patient support device does not comply with the programmed bedrail protocol. In one embodiment of the method, the user interface is operable for manual or remote programming.
[0028] Additional features, which alone or in combination with any other feature(s) (such as those listed above and / or in the claims) may constitute patentable subject matter and will become apparent to those skilled in the art upon consideration of the following detailed description of the various embodiments, which illustrate the best mode of implementing the presently perceived embodiments. BRIEF DESCRIPTION OF THE DRAWINGS
[0029] The detailed description makes particular reference to the accompanying drawings, in which:
[0030] Figure 1 is a perspective view of a patient support device according to the present invention, the patient support device including a control system operable to measure signals from a plurality of sensors and process the signals;
[0031] Figure 2 is a schematic diagram of warning signs that are inconsistent with the patient bedrail protocol;
[0032] {HRBTL-23012-CNPT / 02161386v1}-4-
[0033] Figure 3 yes Figure 1 a block diagram of a portion of a control system of a patient support device;
[0034] Figure 4 is a decision tree executed by the control system to determine whether the user interface has been programmed with a therapeutic operation protocol;
[0035] Figure 5 is an illustration of one embodiment of a display screen including a home icon, a still icon, a sleep data icon, a motion icon, and a help icon;
[0036] Figure 6 is an illustration of one embodiment of a display screen including a bed rail protocol icon;
[0037] Figure 7 is an illustration of one embodiment of a current bedrail protocol screen displayed upon activating the bedrail protocol icon;
[0038] Figure 8 is an illustration of one embodiment of an information screen when a CLR protocol information icon is activated;
[0039] Fig. 9 is an illustration of one embodiment of a current bedrail protocol screen showing a CLR protocol icon selected;
[0040] Fig.10 It is a schematic diagram of the bed rail status consistent with the treatment operation protocol. DETAILED DESCRIPTION
[0041] exist Figure 1 An illustrative patient support apparatus 10 embodied as a hospital bed is shown in FIG. Figure 1The bed 10 has a frame 20 including a base frame 22 supported on casters 24. The fixed base frame 22 further supports a gravity frame 30, and an adjustably positionable mattress support upper frame 34 further supports a mattress 18. The bed 10 also includes a headboard 12 located at a head end 46 of the bed 10, a footboard 16 located at a foot end 48 of the bed 10, and movable bedrails 14A-D coupled to the upper frame 34 of the bed 10. The bed 10 also includes a user interface 54 located on one of the bedrails 14A-D. Figure 1 The bed 10 of the embodiment of FIG. 1 is generally configured to adjustably position the upper frame 34 relative to the base 22 to adjust the position of a patient supported on the mattress 18 .
[0042] Conventional structures and devices may be provided to adjustably position the upper frame 34, and such conventional structures and devices may include, for example, linkages, actuators, and other moving components and devices coupled between the base 22 and the gravity frame 30 and / or between the gravity frame 30 and the upper frame 34. The position of the upper frame 34 and the mattress 18 relative to the base 22 or the gravity frame 30 is controlled, for example, by the patient control pendant 56 or the user interface 54. For example, the upper frame 34 may be adjustably positioned to be generally tilted from the head end 46 to the foot end 48, or vice versa. In addition, the upper frame 34 may be adjustably positioned so that the head section 44 of the mattress 18 is positioned between a minimum and maximum tilt angle (e.g., 0-65 degrees) relative to the horizontal or the bed board, and the upper frame 34 may also be adjustably positioned so that the seat portion (not shown) of the mattress 18 is positioned at a maximum {HRBTL-23012-CNPT / 02161386v1}-5-
[0043] Those skilled in the art will recognize that the upper frame 34 or portions thereof may be adjustably positioned in other orientations, and the present invention also contemplates such other orientations.
[0044] One or more components of the patient support device may be communicated by an icon 32 projected on the floor and / or an icon 33 illuminated on a frame member of the bed 10. Examples of structures for projecting icons 32 on the floor or illuminating icons 33 on the frame are disclosed in WO2016196403A1 and US20180184984A1 (each of which is incorporated herein by reference to disclose structures for projecting icons on the floor). The projected icon 32 may be used to indicate whether a component of the patient support device 10 complies with a baseline operating protocol used by the patient. In some embodiments, the bed rail status of the patient support device 10 may be communicated by an icon 32 projected on the floor. The projected icon 32 may be used to indicate whether the bed rails 14A-D of the patient support device 10 comply with a baseline operating protocol. The therapeutic operating protocol may be programmed into the user interface 54 by a caregiver or user.
[0045] For example, the treatment operation protocol may be a CLR (Continuous Lateral Rotation) protocol that requires all four bed rails 14A-D to be raised before the CLR begins. Currently, caregivers face significant challenges in caring for patients with pulmonary therapy on a patient platform. Many of these treatments include patient rotation. Rotational therapy typically includes lateral rotation of the patient support device 10 for patients requiring pulmonary therapy or bedsore prevention or treatment. The rotatable support surface typically includes a mattress 18 on the bed 10 that is rotated laterally by an air support system when all bed rails 14A-D are in the upward position. As shown in FIG. Figure 2 As shown, the projected icon 32 may not indicate a warning even though the patient support device 10 is not in compliance with the treatment operating protocol but is in compliance with the baseline operating protocol. Although the bed rail 14A is lowered, the projected icon 32 is a green flag indicating compliance. This effect may exist due to the different requirements of the two protocols used simultaneously (the baseline protocol that defines the nominal bed condition and the treatment protocol that is selectively applied only when treatment is being performed). The present invention solves the management of inconsistent requirements of the protocols that are active simultaneously.
[0046] exist Figure 3 In one illustrative embodiment, shown diagrammatically in FIG. 1 , the bed 10 has a control system 26 that includes a controller 28, a scale module 50, component modules (e.g., a bedrail module 52), and a user interface 54. The bed 10 can communicate with the hospital information system 36 via a communication infrastructure 110. The scale module 50 of the bed 10 is used to measure the motion of a patient occupying the bed 10 by measuring signals from load sensors 66, 68, 70, 72. The bedrail module 52 of the bed 10 is used to determine the operation of the bedrails 14A-D by measuring signals from sensors 82, 84, 86, 88.
[0047] In the illustrated embodiment, the controller 28, the scale module 50, the component module (eg, the bed rail module 52) {HRBTL-23012-CNPT / 02161386v1}-6-
[0048] Each of the controller 28, the scale module 50, the bedrail module 52, and the user interface 54 includes a processor 62 and a storage device 64. The processor 62 and the storage device 64 are used in the controller 28, the scale module 50, the bedrail module 52, and the user interface 54. The storage device 64 includes instructions that, when executed by the processor 62, cause the processor 62 to perform functions associated with a particular one of the controller 28, the scale module 50, the bedrail module 52, and the user interface 54.
[0049] In some embodiments, the treatment protocol may require changing the position of more than one component of the bed 10 (e.g., bed rails 14A-D, head end 48, etc.). For example, the treatment protocol may require all bed rails 14A-D to be in a specific position, or require the head end 46 to be at a specific angle. Figure 4 As shown, in step 112, the controller 28 is operable to act as a protocol conflict manager to execute a decision tree to determine whether the user interface 54 has been programmed with a therapeutic operating protocol. If the user interface 54 has been programmed with a therapeutic operating protocol, then in step 116, the therapeutic operating protocol will replace the baseline operating protocol. Then, in step 118, the controller 28 is operable to identify components of the bed 10 (e.g., bedrails 14A-D, head end 48, etc.) that require a different orientation in the therapeutic operating protocol than in the baseline operating protocol. Then, in step 120, the controller 28 is operable to communicate with sensors (e.g., sensors 82, 84, 86, 88) in the identified component modules of the bed 10 (e.g., bedrail module 52) to determine whether they comply with the therapeutic operating protocol.
[0050] If it is determined in step 122 that the components of the bed 10 (e.g., bedrails 14A-D, head end 48, etc.) comply with the therapeutic operating protocol, then no warning or alert is issued in step 124. If it is determined in step 122 that the components of the bed 10 (e.g., bedrails 14A-D, head end 48, etc.) do not comply with the therapeutic operating protocol, then a warning or alert is issued in step 126. If the controller 28 determines in step 112 that the user interface 54 has not been programmed with the therapeutic operating protocol, then in step 114 the controller 28 is operable to determine whether the components of the bed 10 (e.g., bedrails 14A-D, head end 48, etc.) comply with the baseline operating protocol. If it is determined in step 114 that the components of the bed 10 (e.g., bedrails 14A-D, head end 48, etc.) comply with the baseline operating protocol, then no warning or alert is issued in step 124. If it is determined in step 114 that the components of the bed 10 (e.g., bedrails 14A-D, head end 48, etc.) do not comply with the baseline operating protocol, then a warning or alert is issued in step 126.
[0051] The components of the control system 26 communicate with each other to share information and distribute the functions of the bed 10. The processor 62 of each of the controller 28, the scale module 50, the component modules (e.g., the bed rail module 52), and the user interface 54 can also operate based on instructions from the storage device 64 to communicate with the controller 28, the scale module 50, the component modules (e.g., the bed rail module 52), and other modules in the user interface 54 using the communication protocol. It should be understood that the term processor herein includes any microprocessor, microcontroller, processor circuit, control circuit, pre-programmed device or capable of accessing a storage device and executing non-transient instructions to perform any of the inventions herein {HRBTL-23012-CNPT / 02161386v1}-7-
[0052] In the illustrated embodiment, the control system 26 uses a conventional controller area network (CAN) for communication between subsystems, but it should be understood that any of a variety of networking and communication solution protocols may be used in the control system 26.
[0053] Return to reference Figure 3 , bedrail module 52 is a functional controller of bedrails 14A-D and includes a processor 62 and a storage device 64. Processor 62 communicates with bedrails 14A-D. Sensor assembly 60 includes separate sensors for determining the position of each of bedrails 14A-D. Signals from sensors 82, 84, 86, and 88 are used to determine the position of bedrails 14A-D and make inferences regarding compliance with any patient bedrail protocols that a user may have entered on patient interface 54. Such determinations will improve patient safety and provide a more adequate and accurate analysis of the patient's condition related to the patient support device. In addition, bed 10 can record the existence of a therapeutic operating protocol and send the data to an electronic medical record. As Figure 2 As shown, the treatment protocol may be indicated on the user interface 54. The display screen 94 may include a status panel 98 that indicates whether treatment has been stopped due to non-compliance with the treatment protocol. The status panel 98 may include additional information.
[0054] The display screen 94 of the user interface 54 may include more than one input icon. Figure 5As shown, the home screen 132 on the display screen 94 includes a home icon 134, a move up icon 136, a balance icon 138, a physiological icon 140, and a settings icon 142. When any of the icons are activated, the controller 28 receives user input commands from the graphic display screen 94. Based on the user input commands on the display 94 and the data processed by the processor 62, the controller 28 controls various functions of the bed 10, such as the pneumatic system and / or raising or lowering different portions of the bed 10. In some embodiments, based on the user input commands on the display 94 and the data processed by the processor 62, the controller 28 controls the functions of one or more actuators in the bed 10. In some embodiments, based on the user input commands on the display 94 and the data processed by the processor 62, the controller 28 controls the functions of the bedrails 14A-D.
[0055] like Figure 6 As shown, when the caregiver activates the settings icon 142, the controller 28 prompts the caregiver to select bed features on the features screen 146. Figure 7 As shown, the caregiver can activate the bed rail protocol icon 144 (in Figure 6 14A-D) to cause the controller 28 to call up the current bedrail protocols screen 148. The current bedrail protocols screen 148 of the user interface 54 may list different treatment operation protocols that require certain bedrail 14A-D positions, including the CLR protocol. The current bedrail protocols screen 148 includes a CLR protocol information icon 152 that the caregiver may activate to cause the controller 28 to display a Figure 8 Information about the CLR protocol is shown on the information screen 156 in FIG. Selecting the "Yes" icon 158 on the information screen 156 activates the CLR protocol. Fig. 9 , when the caregiver activates the "Yes" icon 158 on the information screen 156, the CLR {HRBTL-23012-CNPT / 02161386v1}-8-
[0056] The protocol icon 150 is selected. The controller 28 is operable to identify the CLR protocol as the therapeutic operating protocol to replace any baseline operating protocol. The caregiver may activate the "Accept" icon on the current bedrail protocol screen 148 to confirm the selection of the CLR protocol.
[0057] Fig.10 The figure shows that if the controller 28 is operable to determine a therapeutic operating protocol in lieu of a baseline operating protocol, the projected icon 32 may indicate a bedrail status indicating that the bed 10 does not comply with the therapeutic operating protocol. Fig.10 In FIG. 1 , since 14A is lowered, the projected icon 32 does not indicate compliance.
[0058] While the present invention relates to particular embodiments, it will be understood by those skilled in the art that various changes in form and details may be made without departing from the subject matter set forth in the following claims.
Claims
1. A patient support device comprising: Multiple equipment components, a plurality of equipment component sensors, the plurality of equipment component sensors being located on the plurality of equipment components, a baseline operating protocol programmed on the patient support device, a user interface operable to be programmed with a therapeutic operation protocol, and a control system including a controller in communication with the plurality of device component sensors, the controller operable to determine whether the therapeutic operating protocol complies with the baseline operating protocol, wherein the treatment operating protocol is a continuous lateral rotation (CLR) protocol and the baseline operating protocol comprises a baseline bedrail protocol, and Wherein the CLR protocol includes having four bedrails in the up position and the baseline bedrail protocol includes having less than four bedrails in the up position.
2. A patient support device according to claim 1, wherein: If the control system determines that the therapeutic operating protocol does not comply with the baseline operating protocol, the therapeutic operating protocol replaces the baseline operating protocol, and the control system is further operable to communicate with the plurality of device component sensors to ensure compliance with the therapeutic operating protocol.
3. The patient support device of claim 1, wherein: The compliance status of the patient support device to the treatment protocol is projected onto the floor.
4. The patient support device of claim 1 , wherein the plurality of device components are a plurality of bed rails, and wherein the controller is operable to receive a separate signal from each of the plurality of device component sensors to determine whether each of the plurality of bed rails is up or down, and the controller is further operable to process the signal to determine whether the therapy protocol is being complied with.
5. The patient support device of claim 1, the CLR protocol replacing the baseline bedrail protocol, and wherein the controller projects a warning sign on the floor if the patient support device does not comply with the CLR protocol.
6. The patient support device of claim 5, wherein the warning indicia is an indication that the patient support device is not compliant with the CLR protocol.
7. The patient support device of claim 1, the CLR protocol replacing the baseline bedrail protocol, and wherein the user interface displays a warning sign if the controller determines that the patient support device does not have four bedrails in an up position.
8. The patient support device of claim 1, wherein the CLR protocol includes determining status of other components of the patient support device.
9. A patient support device according to claim 1, wherein the user interface is operable for manual or remote programming.
10. A system comprising: a patient support device, the patient support device comprising a head end and a foot end, Multiple patient support components, an indicator light, the indicator light being located at the foot end, and a controller operable to communicate with the plurality of patient supports and the indicator light, the controller operable to receive a separate signal from each of the plurality of patient supports to process the signal to determine a position of each patient support, and A user interface is operable to be programmed with a baseline operating protocol and a therapeutic operating protocol.
11. The system of claim 10, wherein the controller is operable to process the signal to determine whether the therapeutic operating protocol complies with the baseline operating protocol.
12. The system according to claim 10, wherein: If the control system determines that the patient support device is not in compliance with the therapeutic operating protocol, the control system is further operable to communicate with the plurality of device component sensors to ensure compliance with the therapeutic operating protocol.
13. The system of claim 10, wherein the indicator light projects a compliance status of the patient support device onto the floor, and wherein the compliance status is based on the treatment procedure protocol.
14. The system of claim 10, wherein the therapeutic procedure protocol is a continuous lateral rotation (CLR) protocol, and wherein the user interface is operable to program using the CLR protocol.
15. The system of claim 14, wherein the CLR protocol replaces a baseline operating protocol, and wherein the CLR protocol includes having four bed rails in an upward position.
16. The system of claim 15, wherein the baseline operating protocol comprises a bedrail protocol, {HRBTL-23012-CNPT / 02161386v1} -2- The bedrail protocol includes having less than four bedrails in the up position.
17. The system of claim 16, wherein: The user interface is operable to display a warning sign if the controller determines that the patient support device does not have four bedrails in the upward position.
18. The system of claim 16, wherein: If the controller determines that the patient support device does not have four bedrails in the up position, an indication is projected on the floor that the patient support device does not comply with the programmed bedrail protocol.
19. The patient support device of claim 15, wherein the CLR protocol further comprises determining a status of other components of the patient support device.
20. The system of claim 10, wherein the user interface is operable for manual or remote programming.
21. A method of monitoring compliance of a support device with a therapeutic operation protocol, the method comprising the steps of: Enter the baseline operating protocol into the user interface, Monitor signals from multiple equipment component sensors, processing the signals from the plurality of equipment component sensors using a controller, wherein the equipment component sensors are located on a plurality of equipment components, determining positions of a plurality of bedrails based on the signals from the plurality of equipment component sensors, and A determination is made as to whether the positions of the plurality of bedrails comply with patient protocol.
22. The method according to claim 21, wherein: If the support device is not in compliance with the patient protocol, the method includes the controller communicating with the plurality of device component sensors to ensure compliance with a programmed patient protocol.
23. The method of claim 22, wherein the method includes automatically moving a portion of the support device based on the signal from the device component sensor to ensure compliance with the patient protocol.
24. The method of claim 21, wherein the method includes projecting a compliance status of the support device onto the floor.
25. The method according to claim 21, wherein: The user interface is operable to be programmed using a continuous lateral rotation (CLR) protocol.
26. The method according to claim 25, wherein: The method includes CLR protocol instead of conventional {HRBTL-23012-CNPT / 02161386v1} -3- A bedrail protocol, and wherein the CLR protocol includes having four bedrails in an upward position.
27. The method according to claim 26, wherein: If the controller determines that the patient support device does not have four bedrails in the upward position, the method includes the user interface displaying a warning sign.
28. The method according to claim 26, wherein: If the controller determines that the patient support device does not have four bedrails in the up position, the method includes projecting an indication on the floor that the patient support device does not comply with a programmed bedrail protocol.
29. The method of claim 21, wherein the user interface is operable for manual or remote programming.
Citation Information
Patent Citations
Patient support apparatus having vital signs monitoring and alerting
US20180184984A1
Patient support apparatus
WO2016196403A1