Method and System for Tracking Inventory and Usage of Pharmaceuticals in Medical Facilities
20220301694 · 2022-09-22
Inventors
Cpc classification
G06F16/2379
PHYSICS
G16H40/20
PHYSICS
G16H20/10
PHYSICS
International classification
G16H40/20
PHYSICS
G16H20/10
PHYSICS
Abstract
Method and system for tracking the inventory and reimbursement status of an inventory of drug doses held at medical facilities and administered to patients are disclosed. In one embodiment, the methods comprise facilitating the addition of drug doses into an inventory database, facilitating the assignment of specific doses to specific patients, and facilitating the transfer of drug doses from one location to another, all accomplished without the necessity of creating and/or scanning machine readable data carriers.
Claims
1. A method comprising: modifying, in a computerized inventory tracking system, a database comprising inventory counts and identification information of drug doses received by a medical facility from a drug distributor or manufacturer; modifying, in a computerized inventory tracking system, a database through creation of an association of a specific drug dose with a specific patient; and, modifying, in a computerized inventory tracking system, a database through revision of inventory counts of drug doses whose inventory location has changed;
2. The method of claim 1, wherein the identification information of drug doses includes a drug dose manufacturing lot number and an expiration date.
3. The method of claim 1, wherein the inventory counts of drug doses are updated by extracting the lot number of an incoming batch of drug doses from a machine readable data carrier associated with the drug dose through the use of a machine readable data carrier reading device and subsequently specifying the quantity received of that lot, or by manually entering the lot number and expiration date of an incoming batch of drug doses and subsequently specifying the quantity received of that lot.
4. The method of claim 1, wherein an association between a drug dose and the patient who receives said drug dose is established by specifying a patient who will be receiving the drug dose and subsequently clicking the unique identifying number of the drug dose from a listing of available drug doses and subsequently moving the cursor of the mouse over a specified area of a computer screen therein establishing the association.
5. The method of claim 1, wherein an association between a drug dose and the patient who receives said drug dose is established by specifying a patient who will be receiving the drug dose and subsequently scanning a machine readable data carrier associated with the drug dose using a machine readable data carrier reading device.
6. The method of claim 1, wherein inventory counts and inventory locations of drug doses may be revised by specifying a quantity of drug doses from available drug doses with a specific lot number to be transferred to a different location.
7. The method of claim 1, wherein inventory counts and inventory locations of drug doses may be revised by scanning a machine readable data carrier encoded with a uniquely identifying serial number.
8. A non-transitory computer readable storage medium comprising instructions which, when executed by a processor, cause the processor to perform steps comprising: modifying, in a computerized inventory tracking system, a database comprising inventory counts and identification information of drug doses received by a medical facility from a drug distributor or manufacturer; modifying, in a computerized inventory tracking system, a database through creation of an association of a specific drug dose with a specific patient; and, modifying, in a computerized inventory tracking system, a database through revision of inventory counts of drug doses whose inventory location has changed;
9. The computer readable storage medium of claim 8, wherein the identification information of drug doses includes a drug dose manufacturing lot number and an expiration date.
10. The computer readable storage medium of claim 8, wherein the inventory counts of drug doses are updated by extracting the lot number of an incoming batch of drug doses from a machine readable data carrier associated with the drug dose through the use of a machine readable data carrier reading device and subsequently specifying the quantity received of that lot, or by manually entering the lot number and expiration date of an incoming batch of drug doses and subsequently specifying the quantity received of that lot.
11. The computer readable storage medium of claim 8, wherein an association between a drug dose and the patient who receives said drug dose is established by specifying a patient who will be receiving the drug dose and subsequently clicking the unique identifying number of the drug dose from a listing of available drug doses and subsequently moving the cursor of the mouse over a specified area of a computer screen therein establishing the association.
12. The computer readable storage medium of claim 8, wherein an association between a drug dose and the patient who receives said drug dose is established by specifying a patient who will be receiving the drug dose and subsequently scanning a machine readable data carrier associated with the drug dose using a machine readable data carrier reading device.
13. The computer readable storage medium of claim 8, wherein inventory counts and inventory locations of drug doses may be revised by specifying a quantity of drug doses from available drug doses with a specific lot number to be transferred to a different location.
14. The computer readable storage medium of claim 8, wherein inventory counts and inventory locations of drug doses may be revised by scanning a machine readable data carrier encoded with a uniquely identifying serial number.
15. A computer system comprising: a non-transitory computer-readable storage medium storing executable computer program instructions, the computer program instructions comprising instructions that when executed cause a computer processor to perform steps comprising: modifying a database having inventory counts and identification information of drug doses received by a medical facility from a drug distributor or manufacturer; modifying a database through creation of an association of a specific drug dose with a specific patient; and, modifying a database through revision of inventory counts of drug doses whose inventory location has changed;
16. The computer system of claim 15, wherein the identification information of drug doses includes a drug dose manufacturing lot number and an expiration date.
17. The computer system of claim 15, wherein the inventory counts of drug doses are updated by extracting the lot number of an incoming batch of drug doses from a machine readable data carrier associated with the drug dose through the use of a machine readable data carrier reading device and subsequently specifying the quantity received of that lot, or by manually entering the lot number and expiration date of an incoming batch of drug doses and subsequently specifying the quantity received of that lot.
18. The computer system of claim 15, wherein an association between a drug dose and the patient who receives said drug dose is established by specifying a patient who will be receiving the drug dose and subsequently clicking the unique identifying number of the drug dose from a listing of available drug doses and subsequently moving the cursor of the mouse over a specified area of a computer screen therein establishing the association.
19. The computer system of claim 15, wherein an association between a drug dose and the patient who receives said drug dose is established by specifying a patient who will be receiving the drug dose and subsequently scanning a machine readable data carrier associated with the drug dose using a machine readable data carrier reading device.
20. The computer system of claim 15, wherein inventory counts and inventory locations of drug doses may be revised by specifying a quantity of drug doses from available drug doses with a specific lot number to be transferred to a different location.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0008] To enable the PI to be easily understood and readily practiced, the PI will now be described for purposes of illustration and not limitation, in connection with the following figures wherein:
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DETAILED DESCRIPTION OF THE INVENTION
[0017] The PI will now be described in greater detail by reference to the accompanying drawings in which illustrated embodiments of the invention are provided. The PI may also be embodied in alternate forms not herein described, and should not be construed as limited to the embodiments set forth here; these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art. Like numbers will refer to like elements throughout this document, and to provide clarification on various terms used throughout the text, a glossary follows which is intended to set forth the intended meaning of these terms:
[0018] drug assignment—the identification of drug doses that have been or will be administered to particular patients and the recording of such within the TS databases.
[0019] virtual—related to activity that occurs within the context of computer software operation, such as manipulating databases or representing places or actions that exist within that context.
[0020] machine readable data carrier—any tag or label containing an encoded message that is affixed to a drug dose and subsequently scanned or decoded by a compatible device and decoded for further processing, including but not limited to RFID tags and barcodes of multiple different symbologies.
[0021] manufacturer—a drug dose processing concern, performing industrial-scale synthesis of pharmaceutical drugs; or, a drug compounder, a drug dose processing concern that prepares medications according to a unique recipe that combines, mixes, or alters ingredients in order to treat specific illnesses or conditions.
[0022] Those skilled in the art will recognize that, while the description of the PI contained herein is focused on pharmaceutical products, the methods and processes described will apply equally to other distributed material. It should also be recognized that as federal guidelines evolve, the methods, systems and processes which are addressed herein will be redefined as necessary to accommodate those new guidelines.
[0023] Drug doses received by an end user intended for patient treatment are always identified with a human readable production lot number and an expiration date. In some cases, end users may make use of the TS, through the use of a suitable machine readable data carrier reading device, to enter into the inventory database of the TS each drug dose that has been furnished by a manufacturer or a distributor with a machine readable data carrier containing an identifying product number that usually but not necessarily contains the drug NDC, the production lot number assigned to the drug dose, the drug dose expiration date, and in some cases an encoded serial number. To enter into the inventory database of the TS those drug doses that are received from a manufacturer and do not contain a pre-printed or installed machine readable data carrier, a serialized machine readable data carrier for each drug dose may be created by drug distributor personnel or the end user and be affixed to or maintained in close proximity to each drug dose so that each drug dose received by the end user may be cross checked, through the use of a suitable machine readable data carrier reading device, against the list of doses claimed to have been shipped by the drug dose source. To enter into the inventory database of the TS those drug doses that are received from a manufacturer or distributor and contain a pre-printed or installed machine readable data carrier that does not contain a serialized machine readable data carrier, an end user may choose to create and affix a serialized machine readable data carrier for each drug dose, or alternatively may choose to identify each dose by lot number, such that doses from a specific lot number are not differentiated from one another when entered into the inventory database of the TS.
[0024] Because an end user may receive several hundred or more drug doses in a day, the PI facilitates the entry of drug doses into the inventory database by introducing the processes detailed in
[0027] As drug doses are entered into the inventory database by following the process described in
[0028] Those skilled in the art will recognize that the process flow and the configuration of the user input screen (the Add Inventory screen) accessed for the entry of drug doses into the inventory database are not limited to the embodiment of the PI described in
[0029] Following receipt of drug doses from a drug dose source and subsequent entry of drug doses into the inventory database, drug doses are administered to patients according to the treatment plan developed by a health care provider. Because a given drug dose selected to be administered to a patient, having previously been entered into the inventory database, may or may not be associated with a machine readable data carrier, the PI describes a general process in
[0030] Those skilled in the art will recognize that the process flow and the configuration of the user input screen (the Assign Dose screen) accessed for the assignment of drug doses to patients are not limited to the embodiment of the PI described in
[0031] Because most group medical practices receive and maintain the great majority of pharmaceutical inventory for the entire group at the main or central location, drug doses are generally entered into inventory as having been received and stocked at the main or central location. When patients are to be subsequently examined and treated at one or more RL, drug doses are removed from physical inventory from the main or central office, packed in suitable containers, and shipped or transported to one or more RL for patient treatment. Doses may also be physically relocated among all offices whenever the supply of drug doses warrants such a physical relocation of drug doses.
[0032] In addition to the physical movement of doses from one location to another, doses must be virtually relocated from the initial inventory location to the RL so that drug dose inventory counts as reported by the TS database remain correct relative to the number of doses of a given drug at a given location. Because drug doses selected to be transferred to an alternate location, having previously been entered into the inventory database, may or may not be associated with a machine readable data carrier, the PI describes a general process in
[0033] Those skilled in the art will recognize that the process flow and the configuration of the user input screen (the Inventory Adjustment screen) accessed for the virtual relocation of drug doses are not limited to the embodiment of the PI described in
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