Ultrasonic authentication for dialysis

11504458 ยท 2022-11-22

Assignee

Inventors

Cpc classification

International classification

Abstract

A system for blood treatment can include a dialysis machine and an ultrasonic authentication device connected to the blood treatment machine, the ultrasonic authentication device configured to scan a label and send signals containing label information to the dialysis machine.

Claims

1. A system for blood treatment, the system comprising a dialysis machine; and an ultrasonic authentication device connected to the dialysis machine, the ultrasonic authentication device configured to scan a label using ultrasonic signals and to send identified label information to the dialysis machine.

2. The system of claim 1, further comprising a controller configured to generate a user notification of required label authentication before a treatment begins.

3. The system of claim 1, wherein the label information comprises a lot number, a material description, a sku, an expiration date, a size, and/or a concentration.

4. The system of claim 1, wherein the label information is positioned on a clear label.

5. The system of claim 1, further comprising a consumable having a label configured to be scanned by the ultrasonic authentication device.

6. The system of claim 5, wherein the consumable is a saline bag, a dialyzer, a tubing set, and/or a drug.

7. A method of operating a dialysis system, the method comprising: scanning a label with an ultrasonic authentication device connected to a dialysis machine, the ultrasonic authentication device being configured to scan the label using ultrasonic signals and to send identified label information to the dialysis machine; comparing the label information against stored information to determine whether the label corresponds to a required consumable for the dialysis machine; and instructing the user to proceed or halt setup based on the compared information.

8. The method of claim 7, wherein the label is positioned on a consumable being installed on the dialysis machine.

9. The method of claim 7, wherein the label is a clear label.

10. The method of claim 7, wherein the label information comprises a lot number, a material description, a sku, an expiration date, a size, and/or a concentration.

11. The method of claim 7, wherein the consumable is a saline bag, a dialyzer, a tubing set, and/or a drug.

Description

DESCRIPTION OF DRAWINGS

(1) FIG. 1 shows a blood treatment system including a blood treatment machine and an ultrasonic authentication device where the blood treatment machine is configured to identify label information.

(2) FIG. 2 shows the ultrasonic authentication device of FIG. 1.

(3) FIG. 3 shows a method of using an ultrasonic identification device in preparation for a dialysis treatment.

DETAILED DESCRIPTION

(4) In certain aspects, an ultrasonic authentication device can be used to identify information from labels on items used in a dialysis treatment. These items can removeable or connectable to a blood treatment device (e.g., disposables, accessories, fluids, and/or drugs.)

(5) FIG. 1 shows a blood treatment system 100 that includes a blood treatment machine (e.g., hemodialysis machine 102) and an ultrasonic authentication device 104, connected to hemodialysis machine 102. The ultrasonic authentication device 104 includes an ultrasonic signal transmitter 106 configured to send ultrasonic signals. An ultrasonic signal receiver 108 is configured to receive reflected ultrasonic signals.

(6) In FIG. 1, the hemodialysis machine 102 and ultrasonic authentication device 104 are connected electronically. A user interface 132 is mounted on or integrated in the hemodialysis machine 102 and is operably controlled by a controller (e.g., a controller 202 shown in FIG. 2) of the hemodialysis machine 102. The user interface 132 can be configured to display information related to the labeling information received by the ultrasonic signal receiver 108. This labeling information can include information related to the function or source of the item (e.g., lot number, description, sku, expiration date, size, and/or concentration.)

(7) In operation, a blood pump 122 of the hemodialysis machine 102 pumps blood through an extracorporeal circuit 117 connected to the hemodialysis machine 102. More specifically, the blood pump 122 draws blood out of a patient 101 via an arterial patient line 118 and forces the blood through a blood chamber of a dialyzer 112. As the blood passes through the blood chamber of dialyzer 112, dialysate passes through a dialysate chamber of the dialyzer 112, so that the blood is cleared of toxins. The cleansed blood then flows through a venous air trap 120 where any air in the blood is collected and is returned to the patient via a venous patient line 110. A saline bag 107 is connected to the venous air trap 120 for introducing saline into the cleansed blood.

(8) In some cases, before identifying the label information, the controller 202 of hemodialysis machine 102 will generate a notification to notify the operator that label information is required. The notification may be visual, auditory, and/or vibrational.

(9) After the ultrasonic authentication is completed, label information is transmitted from the ultrasonic authentication device 104 to hemodialysis machine 102 via the ultrasonic signal transmitter 106 and the ultrasonic signal receiver 108. The ultrasonic signal receiver 108 receives the label information and user interface 132 then optionally displays the label information, an error, and/or further instructions to the user.

(10) FIG. 2 is a schematic illustration of the ultrasonic authentication device 104 including the ultrasonic signal transmitter 106 and the ultrasonic signal receiver 108. The saline bag 107 is an exemplary disposable and includes a label 109. The label 109 can be formed from different labeling applications (e.g., clear labels, paper labels, and/or solid foil/metal labels.) In this example, a user places the bag before the ultrasonic authentication device 104 before use. The ultrasonic authentication device 104 transmits high-frequency sound waves 204 directed at the label 109 and receives reflected waves 206. Based on the reflected waves 206 the controller 202 identifies labeling information from the label 109. In some cases, the received labeling information is displayed to the user on the user interface 132. In other cases, the received labeling information is first compared against expected information. If the information matches expected or acceptable parameters, the treatment or set up is allowed to progress. If the information does not match, the user can be shown an error (e.g., a request to rescan, the reason for rejection, and/or a request to scan a new saline bag.)

(11) FIG. 3 is a flow chart illustrating a method 300 using an ultrasonic identification device in preparation for a dialysis treatment. To prepare for treatment, the hemodialysis machine 102 notifies 304 the user (e.g., via the user interface 132) that authentication is required before connecting a saline bag. Then, the label of the saline bag is scanned 306 by the ultrasonic authentication device when the user places the label near the ultrasonic authentication device. A controller of the HD machine then compares 308 the received label information with expected information. If the label information matches the expected information, the user is instructed to proceed 310 with machine set up. If the information does not match, the user is shown an error (e.g., a request to rescan, the reason for rejection, and/or a request to scan a new saline bag). While FIG. 3 illustrates a method for verifying label information of a saline bag, other connectable components of a dialysis system could be similarly verified.

(12) Alternative Implementations

(13) The examples described herein can be implemented in a variety of ways without departing from the scope of the specification.

(14) While the authentication device 104 is generally shown as part of the hemodialysis machine 102, in some cases, the authentication device could be detachable or connectable to a medical device.

(15) While the saline bag 107 and the label 109 are generally described, labels for other removable components could also be used. For example, a label on the extracorporeal circuit or the dialyzer could be authenticated using the authentication device 104.

(16) Elements of different implementations described herein may be combined to form other implementations not specifically set forth above. Elements may be left out of the structures described herein without adversely affecting their operation. Furthermore, various separate elements may be combined into one or more individual elements to perform the functions described herein.

(17) Various embodiments discussed herein may be combined with each other in appropriate combinations in connection with the system described herein. Additionally, in some instances, the order of steps in a method may be modified, where appropriate. Further, various aspects of the systems described herein may be implemented using software, hardware, a combination of software and hardware and/or other computer-implemented modules or devices having the described features and performing the described functions.

(18) Software implementations of aspects of the system described herein may include executable code that is stored in a computer-readable medium and executed by one or more processors. The computer-readable medium may include volatile memory and/or non-volatile memory, and may include, for example, a computer hard drive, ROM, RAM, flash memory, portable computer storage media such as a CD-ROM, a DVD-ROM, a flash drive and/or other drive with, for example, a universal serial bus (USB) interface, and/or any other appropriate tangible or non-transitory computer-readable medium or computer memory on which executable code may be stored and executed by a processor. The system described herein may be used in connection with any appropriate operating system.

(19) Several implementations have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the description. Accordingly, other implementations are within the scope of the following claims.