This invention relates generally to medication compliance management and, more particularly, to methods and systems for cueing patients when to take their medications, controlling medication dispensing based on compliance to the prescribed dosage, and determining that the dosage has been take by the patient.
There are many devices designed to control medication dispensing. The field may be segmented into (a) devices that are stand alone and must be pre-programmed for reminders, etc. and are also examined by bring the device back to it point of origin to determine medication compliance, and (b) devices that have a network capability so that programming and compliance can be remotely monitored. Aten et al. U.S. Pat. No. 4,674,652 is an example of the first case and Rose et al. U.S. Pat. No. 4,695,954 is an example of the second case. Many newer disclosures (1998 and later) appear to incorporate some option for remote control or integration into some type of record keeping system.
Physically, such devices can be separated into (a) those that support preparation of medication in a pharmacy for distribution to the patient (pharmacy automation systems)—one such is described in Williams et al. U.S. Pat. No. 5,646,912 and Liff et al. U.S. Pat. No. 5,713,485; (b) those that are designed to support presentment of medications to patients in a hospital or medical care setting (and therefore support multiple medication to multiple patients, typically focusing on prevention of medication error making by the medical staff)—one such is described in Halvorson U.S. Pat. No. 4,847,764; (c) medication dispenser design for patient use in the home (or sometimes assisted living)—these device are for single patient users (many including U.S. Pat. Nos. 4,939,705, 5,752,620, 5,710,551, 5,751,661, etc.); and (d) devices that are design to provide medication mixes versus those design to provide and monitor compliance to a single medication (many including U.S. Pat. Nos. 4,674,652, 4,748,600, 4,911,327, 5,159,581. 5,246,136, 5,752,621, etc.).
The basic purpose of these devices is to (a) remind the patient to take medicine in compliance to prescription (first described in Carlson U.S. Pat. No. 4,223,801 and later in Aten et al. U.S. Pat. No. 4,674,652), (b) to assure that medicine can only be taken in a compliant manner (also described in Aten et al. U.S. Pat. No. 4,674,652), and (c) to determine that compliance has occurred (described in many cited patents, but in Aten et al. U.S. Pat. No. 4,674,652 as when the patient removes a medication vial). Some devices expect the patient to enter or notify his/her compliance (Hemmann, et al. U.S. Pat. No. 5,805,051), some measure compliance by (a) measuring a medication preparation cycle as a compliant action (Aten et al. U.S. Pat. No. 4,674,652), (b) measuring a medication removal as a compliance action (taking off a vial lid Walters U.S. Pat. No. 5,751,661; raising the lid of the dispenser Ridgeway U.S. Pat. No. 5,710,551), or (c) indirectly measuring compliance (for instance by counting medication cap removals as a compliance action—Pearson U.S. Pat. No. 5,752,620).
Finally, some devices (a) exploit existing standard medical packaging (for instance pill vials Abdulhay et al. U.S. Pat. No. 7,213,721 or Walters U.S. Pat. No. 5,751,661), (b) some require use specialized packaging (for instance blister packs that fit the dispenser Parkhurst, Canadian Patent CA 2145193, 1993, Parkhurst et al. U.S. Pat. No. 5,412,372, Benouali U.S. Pat. No. 6,973,371, and Fabricius et al. U.S. Pat. No. 7,170,823), and (c) some require re-packaging or feeding of the medications (for instance dumping from a standard vial into the dispensing device in some device specific manner Aten et al. U.S. Pat. No. 4,674,652, Hasey U.S. Pat. No. 6,766,219).
Most of the personal medication dispensers disclosed fall into one only a few alternative mechanical architectures: (a) caps that fasten onto standard medical vials (Jean-Pierre 2004, Hamilton et al. U.S. Pat. No. 4,939,705, Walters U.S. Pat. No. 5,751,661); (b) controlled drawer or filing cabinet forms (Halvorson U.S. Pat. No. 4,847,764, Williams U.S. Pat. No. 5,263,596, Blechl, et al. U.S. Pat. No. 5,377,864, Fedor, et al. U.S. Pat. No. 5,790,409, Higham, et al. U.S. Pat. No. 5,745,366); (c) two dimensional matrices (usually with pop-up pill areas covers—Schwartz 2004, Agans U.S. Pat. No. 5,159,581, Parkhurst et al. U.S. Pat. No. 5,412,372, Ridgeway U.S. Pat. No. 5,710,551, Gilmore U.S. Pat. No. 6,138,865, Lucas U.S. Pat. No. 6,221,010); (d) rotating carrousels (Urquhart U.S. Pat. No. 4,748,600, Urquhart et al. U.S. Pat. No. 4,971,221, Loidl U.S. Pat. No. 5,246,136, Kurtenbach U.S. Pat. No. 5,582,323, Chorosinsici et al. U.S. Pat. No. 5,945,651, Shusterman U.S. Pat. No. 6,304,797, Sahai et al. U.S. Pat. No. 5,971,594, Papp et al. U.S. Pat. No. 6,439,422, Papp U.S. Pat. No. 6,848,593, Conley U.S. Pat. No. 7,044,302); (e) moving conveyors (with pill reservoirs separated by some means like a vials or paddle wheels, for instance Aten et al. U.S. Pat. No. 4,674,652 or Hasey U.S. Pat. No. 6,766,219); and (f) drop down vials/tubes or compartment systems where the pills are release to gravity feed into the discharge cup (Aten et al. U.S. Pat. No. 4,674,652, Abdulhay et al. U.S. Pat. No. 7,213,721).
As is apparent from the above, however, that there is no device that is (a) highly portable, (b) uses standard medical pill vials, (c) can accommodate multiple pill types, (d) counts pill dispenses pill-by-pill (as opposed to cap openings), (e) only allow dispenses that are consistent with medical prescription to the patient, (f) incorporated into a (wireless) network interface that can update vial programming and can relay pill dispensing at near real time rates to a centrally located secure network (web-based) medical record, which also accepts and integrates medical data taken by other remote devices describing the patient's condition coordinated with medical compliance data for that patient.
Combining these features into the size and low cost necessary for a cap-type dispenser has been beyond the state-of-the-art for prior systems. Therefore prior units were either built to be full featured at the expense of device size or had important features removed to keep cost and size small enough to be a medication cap form factor.
This invention resides in a medication compliance management system and method of using the same. The system includes a base station including a first communications interface, and a pill dispensing cap adapted to replace the cap of a standard pill vial. The pill dispensing cap includes a pill transfer mechanism operative to load a single pill from the vial and dispense that pill to a user, and an interface configured to communicate with the base station and inform the base station that the single pill has been dispensed. In the preferred embodiment, the base station further includes a second communications interface operative to provide compliance information to a remote location.
To conserve battery power, the pill transfer mechanism relies on gravity to load a single pill from the vial and dispense that pill to a user. The transfer mechanism further includes an interchangeable chamber to accommodate pills of different sizes.
The first communications interface is preferably a short-range wireless communications interface, enabling compliance information to be automatically transferred to the base station when the pill dispenser in proximate to the base station. The second communications interface preferably uses a plain old telephone service (POTS) interface, allowing the most number of users to communicate with healthcare personnel at one or more remote locations.
In the preferred embodiment, the base station includes a code reader to determine the type of pill or other medication contained in the vial, and an interface allowing at least a portion of this information to be loaded into the pill dispensing cap. The pill dispensing cap preferably includes an audible or visual alert to remind a user to take the medication contained in the vial. The compliance information typically includes a time stamp indicating the time that a pill was taken, and/or the number of pills taken over a given period of time.
There are several applications that need methods to monitor and manage medication compliance. These include assembling medications for supply or resale in the pharmacy setting, delivering and monitoring the delivery of medication to patients in a hospital or group care setting (i.e. supporting accurate delivery to multiple patient from a shared delivery source or card), and assuring medication compliance to the individual patient in a home of assisted living setting. This invention resides in a medication compliance management device (MCMD) and system focused primarily on the third application: assuring medication compliance to the individual patient in a home of assisted living setting and secondarily supporting accurate home-based clinical trials of new medications.
To support these applications, the disclosed MCMD has the following features:
An important aspect of the system architecture is the modularity and portability that is achieved by the secure wireless communications between the base module and multiple Dispenser Caps. This is in contrast to several existing systems that form a large package for multiple medications and similar functionalities.
The main components of the system are:
The disclosed medication cap/dispensing system is diagramed in
Either to assure medication compliance, or to automated the prescription refilling process, the invention incorporates a small and inexpensive automated medication vial cap that (a) fits the present standard vials, (b) supports multiple pill sizes and quantities, (c) can be programmed at home or at the pharmacy with the patient's prescription dosages and dose times, (d) provide patient reminders to take the medicine, (e) allows the patient to only take the prescribed dosages (within the prescribed dosage time window), (f) monitors that the dose are taken through direct pill counting at the time dispensing, (g) reports this data back to a central monitoring database (and clinical users that have access to this data) through a wireless network. The wireless network can also be used to insert medical dispenser cap programming and can assure that the proper physical vial is attached to the properly programmed cap.
Item (2) in
Items (3)-(5) in
Item (6) in
The clinician or pharmacist can pull data records patient-by-patient and dispenser-by-dispenser (9) through a secure Internet connection (browser). This data can be (10) used for many useful medical applications, including (a) verifying that the patient is compliant with his/her medically prescribed treatment, (b) assuring that the patient receives timely refills, (c) providing an audit trail that a medical practitioner can correlate with other patient tests or physiological signs, and (d) providing statistical patient compliance data to minimize drug dosing errors.
In this system shown in
The Web and Database Servers and Web Server Software is based on industry standards, which are FDA approved, HIPAA compliant, and are being used by many telehealth patients and clinical users.
The data collection server collects data from a plurality of base modules. The data collection server has an open interface to enable connectivity to legacy systems. It includes software for a Medical Database to include website specific interfaces for patients, Pharmacists, Practitioners/Nurses, and System Management (for inventory, billing, insurance, and user management). All user types (Providers, Patients, Managers) have secure password/login ID entrance portals.
Medical Staff Login Pages have Prescription Pages (for the medicine compliance and cap programming function), Procedure Pages, Patient Information Pages, Data Report Pages, Medication Compliance Report pages, Device Traclcing Pages, Report Generation, Compliance Reports, Manual Data Entry Pages and PDA/WAP support for Provider's pagers. Patient Login Pages include Patient Information Pages and Data Report Pages. Management & Provider staff has the ability to add/archive physicians, pharmacists, etc., enter prescription data (times, types, dosages, etc.), add new device types into the device management capabilities, perform minor cosmetic changes (screen and report layouts), and can perform Provider, Patient, and Medical Staff tasks with Manual Data Entry Pages, Compliance and Patient data reports, Global Inventory Management and Insurance Provider Management. The Database will include all fields requested, plus will include Transaction Log and History Tables.
The Pill Dispenser is the device shown in
The Pill Dispenser twists onto a pill vial (13) that has been prescribed with the full prescription quantity before any pills have been administered by the patient. The patient removes the standard pill vial cap after receiving a prescription and replacing it with the Pill Dispenser or this operation being done by the pharmacist prior to deliver of the combination to the patient.
In this disclosure, “standard pill vial” is intended to mean existing as well as yet-to be-developed pill containers in which prescription and over-the-counter medications are provided. With appropriate dimensional modification that would be apparent to a person of sldll in the art, the Pill Dispenser is adaptable to non-child resistant, screw-on and child-resistant container varieties. By way of example,
The Pill Dispenser components are as follows: 2 Body halves (1) and (10), an Orientating Funnel (12), an Interchangeable Slider (5) with a Spring Return (6), a Slider Safety Lock (7) with Spring Return (6), a Dispensed Pill Access Panel (11), a Batteries (8) and a Cover (9), a PC-Board (3) and Cover (2) and screws to hold the assembly together. (4) shows a typical pill that fits the slider (5). (14) and (15) show the device assembled in perspective and as a side section, respectively.
When the Safety is un-Locked, the LED and audible indications change until a pill is properly dispensed. This allows the cavity of the Pill Slide to be exposed in order for the patient to lightly shake the device (4), causing a single Pill to Funnel downward into the cavity. The dimensions of the cavity are designed to the particular Pill prescribed to the patient. The boundary conditions of the Pill Slide cavity dimensions allow a single pill to be captured, separating it from the Pill Vial. When the PC-Board electronics detect that a Pill has been properly accepted into the cavity (5), a signal to the patient will be lighted (6). This will notify to the patient to proceed with dispensing the pill.
Pushing the external button of the Pill Slide linearly inward until the pill reaches the Pill Access area dispenses the Pill (7). The smooth top feature of the Pill Slide keeps the remaining Pills left in the vial. The separated Pill will move and be exposed behind the transparent plastic Pill Access Panel. The PC-Board electronics will also signal with an indication that the Pill is accessible and the patient will be able to open the Pill Access Panel to retrieve the prescribed Pill for ingestion (8). The PC-Board electronics will then tale account of the Pill being dispensed, as it is removed form the access compartment (9).
The Safety Lock then automatically reengages the locking feature and locks the Pill Slide in the closed position until the process needs to be repeated by the patient at the prescribed intervals (10). As part of return to its original operational state, the dispenser interrogates it internal medicine dispensing event table, and if any data has been stored (i.e. a dispensing event had occurred), the PC board microcomputer imitates a query cycle to see if it is sufficiently near to a base module to upload the accumulated medicine dispensing event table (11). If so, this is done, otherwise the device returns to its quiescent sleep state to conserve battery power.
Referring to
Referring to
The base module uplinks (coordinates) with the web servers through the data collection servers for messages, alerts and changes in medication regimen. The base module uses its LCD screen to display messages (1.) To guide the user and (2.) to provide any tailored messaging or counseling. The base module has an audible for interaction. In the optional form the base unit may also include additional (serial) ports or wireless protocols for acquiring and relaying data from other medical devices to the central servers used in a telehealth applications. The barcode scanning sensor can be removed if human operator (patient or pharmacist) checking/validation is substituted. Or the code can be in another form using alternative means of sensing, such as RFID (Radio Frequency Identification Devices).
This application claims priority from U.S. Provisional Patent Application Ser. No. 60/888,156, filed Feb. 5, 2007, the entire content of which is incorporated herein by reference.
Number | Date | Country | |
---|---|---|---|
60888156 | Feb 2007 | US |