Patient support systems facilitate care of patients in a health care setting. Exemplary patient support systems include patient support apparatuses such as hospital beds, stretchers, gurneys, cots, trolleys, and wheelchairs, as well as traditional chairs, seats, benches, and tables. Various adjustable or movable patient support apparatuses may include a base and a litter upon which the patient is ultimately supported. Patient support apparatuses often also have a lift system that may be used to raise and lower the litter, and thus the patient, relative to the base. The patient support apparatuses have the potential of being in numerous different positioning orientations as the litters and support components attached thereto typically have several sections, such as a fowler section, a seat section, and a foot section, with the fowler and foot sections being capable of articulation relative to the seat section.
In the day to day operations of medical facilities, patients may need to be transferred from one patient support system or patient support apparatus to another patient support system or patient support apparatus. In many instances, patients are not ambulatory. These patients may need to be moved with the supervision and/or assistance of nursing and medical staff, and the patient immobility may make the transfer process more complex than anticipated. For example, the two patient support apparatuses may not be properly aligned or in preferential positions with respect to one another, or they may be disposed at incompatible heights. Further, supporting features such as rails may not be in appropriate positions, and the patient support apparatuses may not be in ergonomic positions relative to the particular caregiver providing lifting assistance in the transfer process, which may lead to an overexertion by the caregiver. As such, there remains a need for improved patient transfer systems and methods with minimal physical lifting or handling from the caregiver.
The present teachings will become more fully understood from the detailed description and the accompanying drawings, wherein:
It should be noted that the figures set forth herein are intended to exemplify the general characteristics of the systems, methods, and devices among those of the present technology, for the purpose of the description of certain aspects. These figures may not precisely reflect the characteristics of any given aspect, and are not necessarily intended to define or limit specific embodiments within the scope of this technology. Further, certain aspects may incorporate features from a combination of figures, while other aspects may incorporate only portions of features from a single figure.
The present technology generally provides automated systems and methods for coordinating a transfer of a patient between two patient support apparatuses. When transferring a patient from one patient support apparatus to another, various considerations are often thought-out in order to have a preferential configuration of a patient support surface of a transferring support apparatus relative to a patient support surface of a receiving support apparatus. In various aspects, the present technology provides systems and methods for determining advantageous patient transfer positions of an occupied transferring patient support apparatus and an unoccupied receiving patient support apparatus. The technology provides automated methods of driving one or both of the transferring and receiving patient support apparatuses into preferred or optimal positions prior to the transfer the patient, with minimal adjustment of the apparatuses provided by the caregiver.
For a more complete understanding of the present teachings, initial reference is made to
The exemplary gatch-type hospital bed 20 as shown in
The litter 26 of the bed 20 of
The various patient support apparatuses 18 may also include a plurality of side rails, collectively referred to by reference number 46. For example, the bed of
As shown in
In various aspects, the controller 54 may be located out of view, for example, secured in the base 22 or coupled to the litter 26, as appropriate. The controller 54 may alternatively be an external unit that is wired to the bed 20 or communicates via wireless communication. Thus, the bed 20 may also be provided with one or more communication module configured to establish a wireless communication. Various wireless communication protocols may be used, including Bluetooth, near-field communication (NFC), infrared communication, radio wave communication, cellular network communication, and wireless local area network communication (Wi-Fi). In certain aspects, the communication module may be a part of the controller 54. The wireless communication may provide compatibility with information management systems. Not only can the patient support apparatuses 18 be coupled to the controller 54 using wireless communication protocols, one or more patient support apparatuses 18 can establish a communication link directly or indirectly with one another in order to share data, information, and exhibit control.
The physical construction of any of the base 22, the lifts 24, the litter 26, the support deck 28, the headboard 30, the footboard 32, and/or the side rails 46 may alternatively be similar to that as disclosed in commonly assigned, U.S. Pat. No. 7,690,059 issued to Lemire et al., and entitled HOSPITAL BED; or as disclosed in commonly assigned U.S. Pat. No. 8,689,376 issued to Becker et al. and entitled PATIENT HANDLING DEVICE INCLUDING LOCAL STATUS INDICATION, ONE-TOUCH FOWLER ANGLE ADJUSTMENT, AND POWER-ON ALARM CONFIGURATION; or as embodied in the commercially available S3 bed sold by Stryker Corporation of Kalamazoo, Mich., and documented in the Stryker Maintenance Manual for Stryker's MedSurg Bed, Model 3002 S3, (doc. 3006-609-002 Rev D), published in 2010, the complete disclosures of each of which is hereby incorporated herein by reference. It should also be understood that the construction of any of base 22, lifts 24, frame/litter 26, deck, headboard 30, footboard 32 and/or side rails 46 may also take on forms different from what is disclosed in these documents.
In various aspects, the methods may begin by locating the two patient support apparatuses that will be involved in the transfer, and coordinating an initial movement and positioning of at least one patient support apparatus as indicated by method feature 92. The two patient support apparatuses may be manually selected, or they may be selected using an automated process. For example, in the event there is more than one patient support apparatus available for use, considerations may be made with respect to the type or kind of patient support apparatus preferred; the current position of both apparatuses relative to one another; the range of motion of each apparatus; the type of mattresses and/or patient support surfaces provided; and the availability of any accessories that may be of assistance. Depending on the particular patient and case-by-case considerations, it may be preferable to move the patient from a left-to-right direction, or from a right-to-left direction. Thus the types and relative locations of the two patient support apparatuses may need to be considered and/or approved by a caregiver for the patient transfer to take place.
In certain aspects, the systems and methods described herein may include a feature of requesting or activating the transfer process as indicated by method feature 94. In certain aspects, confirmation of a request for transfer may be a prerequisite before the remainder of the transfer process continues. In one non-limiting example, this may include the use of a “transfer” button that may be provided on a user interface, or the like, for verification purposes.
The systems and methods of the present technology include various safety checks and safety considerations during the various stages of the transfer process. As indicated by method feature 96, the methods may include checking that the patient support apparatuses are at all relevant times in sufficient proximity to one another. As indicated by method feature 98, if the patient support apparatuses become separated more than a threshold distance from one another, the method may stop or pause, waiting for the apparatuses to again have the proper proximity. As indicated by method feature 100, the system may be configured to provide a visual or audio indication that the apparatuses are not ready to continue with the transfer process. In certain examples, this may require the involvement and/or override by a caregiver or other user. Similarly, as indicated by method feature 102, the methods may include checking that the brakes of patient support apparatuses are at all relevant times are properly set, engaged, or locked. As indicated by method feature 104, if the brakes become unlocked, they may be reset or reengaged and subsequently verified as indicated in method feature 106. The method may stop or pause, waiting for the apparatuses to again have the proper brake settings as necessary. Similarly, as indicated by method feature 100, the system may be configured to provide a visual or audio indication that the apparatuses are not ready to continue with the transfer process if there is an error with the brakes or if the brake settings are not appropriate for the transfer process. Additional relevant safety checks that may be monitored may include erecting or locking a side rail, receiving an indication that the two apparatuses remain properly coupled (as explained in more detail below), and receiving an indication that any spatial gaps between the two apparatuses is minimized or removed (also as explained in more detail below).
Once the apparatuses are aligned and positioned, and the various safety checks are in order, the methods may include performing a load check in order to verify the presence of the patient, as indicated by method feature 108. As shown in the simplified flowchart, the presence of a load will likely indicate the apparatus is a transferring patient support apparatus, and will permit various changes to movable components of the patient support apparatus as indicated by method feature 110. Alternatively, the absence of a load will likely indicate the apparatus is a receiving patient support apparatus, and will permit various changes to movable components of the patient support apparatus as indicated by method feature 112. Further details of the assignment of the patient apparatuses with a status of a transferring or receiving apparatus will be discussed in more detail below. Various configurations and settings may be monitored throughout the transfer process as indicated by method feature 114. If any of the configurations or settings of the patient support apparatuses are determined to be inappropriate or in error, the system may be configured to provide a visual or audio indication that the apparatuses are not ready to continue with the transfer process as indicated by method feature 100. Once the apparatuses are properly configured and all safety checks are complete, the transfer process can begin as indicated by method feature 116. In various aspects, an indication is provided to a caregiver or user that it is safe to transfer the patient between the two patient support apparatuses. For example, the systems may provide an audio or visual indication to a caregiver indicating that at least one or more safety feature is met.
As briefly mentioned above, at least one patient support apparatus may be equipped with a controller 54 and/or a communication module configured to communicate and/or otherwise exchange general information and specifications. In the event one of the patient support apparatuses is a passive device, for example, without any controller or communication module, the controller 54 of the other patient support apparatus may be configured to ascertain a model number, or equivalent identification of the passive device. In other instances, the passive device may be provided with a beacon, an RFID device, or an equivalent mechanism to broadcast identifying information, current setting or configuration information, and/or specifications to the controller 54. A caregiver may also manually provide certain identifying information as required. In aspects where both patient support apparatuses include a controller or communication module, the methods may include establishing a communication link between the two patient support apparatuses. As described above, the communication may be established using at least one wireless protocol, such as Bluetooth, near-field communication (NFC), infrared communication, radio wave communication, cellular network communication, and wireless local area network communication (Wi-Fi).
In certain aspects, the features of locating and aligning the transferring patient support apparatus 132 adjacent the receiving patient support apparatus 136 may include an autonomous movement of a location of at least one of the transferring patient support apparatus 132 and the receiving patient support apparatus 136 with respect to one another. For example, the controller 54 may be configured to operate at least one powered wheel 58, or similar automated drive mechanism to provide various movements and alignments. In certain aspects, the two patient support apparatuses can be placed in close proximity to one another, and a caregiver or user can initiate an automated process of the patient support apparatuses autonomously aligning with one another. Once located and aligned in the appropriate proximity with one another, the systems and methods may include checking the status of the brakes of one or both of the patient support apparatuses. In various aspects, the controller 54 may be provided with programmable instructions to engage, lock, and disengage a brake or similar safety feature that prevents or minimizes a movement of the patient support apparatuses. In other aspects, one or more brake can be configured to be engaged, locked, and disengaged remotely and/or manually.
Either before or after locating and aligning the transferring patient support apparatus 132 adjacent the receiving patient support apparatus 136, the present technology includes adjusting at least one position of a movable component of one or both of the transferring patient support apparatus 132 and the receiving patient support apparatus 136 in order to have a preferred configuration for transferring the patient 134. In various aspects, the patient support apparatuses are provided with one or more automated means of driving one or more movable components to particular configurations suitable for transferring a patient. Adjusting the position of a movable component may ultimately include repositioning a movable component with the ultimate purpose of adjusting an overall height of the patient support surface 38 or a portion thereof. In various aspects, this may include a movement of the lifts 24, shortening or extending a length of the legs 74, pivoting a movable structure coupled to the deck structure 28, 64 such as a head section 40, a back section 68, a foot section 42, a leg section 72, etc.
In various aspects, adjusting a height position of at least one of the transferring patient support apparatus 132 and the receiving patient support apparatus 136 includes obtaining or measuring a current height of at least one of the transferring patient support apparatus 132 and the receiving patient support apparatus 136. If the heights cannot be obtained by the controller 54, the methods may include measuring the current height using at least one of an optical sensor, a displacement sensor, a magnetic (hall) sensor, or the like, located on the respective patient support apparatus. In other aspects, one or more current height may be manually provided as an input by a caregiver. If an actual height dimension cannot be obtained, relative differences in height between the two apparatuses 132, 136 can be determined and the heights can be adjusted based on the relative difference. For example, if the patient support apparatuses use a column lift, a relative height difference between adjacent apparatuses can be determined using a hall sensor. Alternatively, if the patient support apparatuses use a scissor lift, it is envisioned that an optical sensor can measure an angle of the each of the lift mechanisms and determine a relative height difference based on the difference in angular measurements.
The height of the patient support surfaces may be adjusted in order to arrive at what is referred to herein as an optimal transfer height for the patient transfer process, which can reviewed and determined based on many different variables and patient-specific information. In addition to an optimal transfer height, there may be one or more optimal angular orientations of various movable components of the patient support apparatuses that ultimately have an influence on a position of at least a portion of a patient supporting surface.
In various aspects, algorithms and logic for the determination of an optimal transfer height and/or optimal angular orientations may be programmed in the controller 54 and may depend on the use of any auxiliary transfer aid devices. By way of non-limiting examples, the optimal transfer height may be based on one or more of a patient's: age, weight, height, medical condition, injury, cognitive state, the presence and location of dressings, the use of other medical equipment (IV fluid dispensers, catheters, medical electrodes and electrical contacts, etc.). Such patient-specific information may be manually entered by a care giver, or may be requested or obtained by one of the patient support apparatuses. In certain aspects, the patient support apparatus can use an internal sensor to determine a current weight or height of the patient. With renewed reference to
In addition to being based on patient-specific information, an optimal transfer height can additionally or alternatively be based in whole or in part using caregiver-specific information. In this regard, the optimal transfer height may be based on ergonomic conditions, or be based on a combination of information, such as patient weight along with strength and/or height of a caregiver, etc. Non-limiting examples of caregiver-specific information may include age, weight, waist height, and total height of the caregiver. In addition to physical characteristics, caregiver-specific information may also include information such as gender, occupation (nurse, assistant, orderly), years of experience, maximum desired lifting capacity, lift restrictions, etc. In certain aspects, the caregiver-specific information can be manually entered, programmed into a wearable device that is associated with the caregiver, or otherwise retrieved through the controller 54. It is also envisioned that the patient support apparatus may include one or more camera or optical sensor 138 (
In various aspects, the optimal transfer height of the two patient support apparatuses may be such that the height of the patient support surface of the receiving patient support apparatus 136 be slightly lower than the height of the adjacent patient support surface of the transferring patient support apparatus 132. In this regard, it may be easier to transfer the patient 134 in a downward movement as well as a lateral movement between the two patient support apparatuses.
Once the patient support apparatuses are configured with movable components at appropriate positions and with an appropriate height of the patient support surfaces, the systems and methods of the present technology may include coupling the two patient support apparatuses together to minimize or prevent unintended relative movement between the apparatuses. In various aspects, portions of the respective bases 22, legs 74, side rails 46, 78, wheels 34, 76, or other suitable components of the adjacent patient support apparatuses may be temporarily coupled to one another. In various aspects, the coupling can be accomplished using a mechanical or magnetic coupling mechanism. The coupling (and subsequent uncoupling) may be manually engaged, remotely controlled, or be operated by an algorithm or programmable instructions in the controller 54 or equivalent control mechanism. Non-limiting examples of mechanical couplings may include the use of latches, gripping mechanisms, and the like. Where magnetic coupling mechanisms are used, they may preferably include electromagnets that can be actuated in a controlled manner. Electromagnets having an appropriately selected strength may be attached to various locations on the respective bases 22, legs 74, side rails 46, 78, wheels 34, 76, or other suitable components of the adjacent patient support apparatuses. Once the patient has been transferred, the receiving patient support apparatus can be uncoupled from the transferring patient support apparatus.
In various aspects, the systems and methods of the transferring the patient may include the use of one or more auxiliary transfer aid device configured to assist with a movement of the patient. Non-limiting examples of auxiliary transfer aid devices, also called lateral sliding aids, presently considered useful with the present technology include an adjustable air bladder, a sheet transfer device, an anchor body wedge system, and/or a bridge transport device.
With renewed reference to
The physical construction of the sheet transfer device 144 or anchor body wedges 148 may alternatively be similar to that as disclosed in U.S. Pat. App. Pub. No. 2017/0296415 by Fowler et al., and entitled APPARATUS AND SYSTEM FOR TURNING AND POSTIONING A PATIENT, assigned to Sage Products, LLC, the complete disclosure of which is hereby incorporated herein by reference.
Depending on the design of the patient support apparatuses, certain apparatuses may be provided with mattresses or other patient support features that are not necessarily lined up or flush with one another when the two patient support apparatuses are located and aligned adjacent one another. In this regard, there may be a spatial gap between the mattresses or patient support features. An example of a spatial gap 155 is provided in
In still further aspects, it may be desired to continue use of the mattress or patient support feature that is currently used with the transferring patient support apparatus 132. In this regard, the receiving patient support apparatus 136 may be configured as having a base 22 or other supporting frame component, but without a litter 26 or without a mattress 36. The methods of transferring the patient may include transferring a mattress or litter component with a mattress (and carrying the patient) from the transferring patient support apparatus 132 to the receiving patient support apparatus. In various aspects, this may include the use of a rail system component designed to permit the smooth transfer between patient support apparatuses.
The following examples provide additional guidance and further illustrate various aspects of the systems and methods of the present technology. The following examples illustrate various configurations of two patient support apparatuses prior to the transfer of the patient, and should be read with reference to the representative figure to which each pertains. It should be understood that these examples are provided for illustrative purposes and are not to be construed as limiting the scope of the present technology.
The foregoing description is provided for purposes of illustration and description and is in no way intended to limit the disclosure, its application, or uses. It is not intended to be exhaustive or to limit the disclosure. Individual elements or features of a particular embodiment are generally not limited to that particular embodiment, but, where applicable, are interchangeable and can be used in a selected embodiment, even if not specifically shown or described. The same may also be varied in many ways. Such variations should not be regarded as a departure from the disclosure, and all such modifications are intended to be included within the scope of the disclosure.
As used herein, the phrase at least one of A, B, and C should be construed to mean a logical (A or B or C), using a non-exclusive logical “or.” It should be understood that the various steps within a method may be executed in different order without altering the principles of the present disclosure. Disclosure of ranges includes disclosure of all ranges and subdivided ranges within the entire range, including the endpoints.
As used herein, the terms “comprise” and “include” and their variants are intended to be non-limiting, such that recitation of items in succession or a list is not to the exclusion of other like items that may also be useful in the devices and methods of this technology. Similarly, the terms “can” and “may” and their variants are intended to be non-limiting, such that recitation that an embodiment can or may comprise certain elements or features does not exclude other embodiments of the present technology that do not contain those elements or features.
The broad teachings of the present disclosure can be implemented in a variety of forms. Therefore, while this disclosure includes particular examples, the true scope of the disclosure should not be so limited since other modifications will become apparent to the skilled practitioner upon a study of the specification and the following claims. Reference herein to one aspect, or various aspects means that a particular feature, structure, or characteristic described in connection with an embodiment or particular system is included in at least one embodiment or aspect. The appearances of the phrase “in one aspect” (or variations thereof) are not necessarily referring to the same aspect or embodiment. It should be also understood that the various method steps discussed herein do not have to be carried out in the same order as depicted, and not each method step is required in each aspect or embodiment.
This application claims priority to U.S. Provisional Patent Application Ser. No. 62/722,257, filed on Aug. 24, 2018, and which is incorporated by reference in its entirety.
Number | Date | Country | |
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62722257 | Aug 2018 | US |