1. A computer-implemented system for administering a drug registry database, comprising:
an electronic database containing at least a plurality of healthcare claims of a plurality of patients and a plurality of new drugcomparator drug pairings;
an electronic user interface configured to
display the plurality of new drugcomparator drug pairings, wherein each new drug is added to the database when a threshold number of healthcare claims for the new drug have been received and wherein each comparator drug paired with a new drug that has substantially similar medical indications as the new drug; and
receive a selection of the new drugcomparator drug pairing, and filter parameters input by a user; and
a computer-implemented analysis engine configured to
search the healthcare claims stored in the database to identify a first and second group of patients satisfying the filter parameters input by the user, wherein the first group includes patients with claim data indicating use of the new drug and the second group includes patients with claim data indicating use of the comparator drug;
identify a comparative occurrence of one or more existing medical conditions or new medical conditions in the first and second groups of patients; and
calculate a probability value indicating a relative likelihood that a patient taking the new drug will have each of the one or more new or existing medical conditions in comparison to a likelihood that a patient taking the comparator drug will have each of the one or more new or existing medical conditions;
wherein the electronic user interface displays each new or existing medical condition and the probability value for the new drug and the comparator drug in accordance with one or more report parameters entered by the user.
2. The system according to claim 1, wherein the display generated by the electronic user interface includes demographic characteristics, prevalence of diagnosis, prevalence of procedures, prevalence of drug class, or healthcare utilization.
3. The system according to claim 1, wherein the filter parameters include one or more diagnosis codes, procedure codes, drug categories, or demographic characteristics.
4. A computer-implemented method for administering a drug registry database, comprising:
storing a plurality of healthcare claims for a plurality of patients on a computing device and a plurality of new drugcomparator drug pairings;
displaying on an electronic user interface a plurality of new drugcomparator drug pairings, wherein each new drug is added to the database when a threshold number of healthcare claims for the new drug have been received and wherein each comparator drug paired with a new drug that has substantially similar medical indications as the new drug;
receiving a selection of the new drugcomparator drug pairing, and filter parameters input by a user;
searching by a computer-implemented analysis engine the healthcare claims stored in the database to identify a first and second group of patients satisfying the filter parameters input by the user; wherein the first group includes patients with claim data indicating use of the new drug and the second group includes patients with claim data indicating use of the comparator drug;
identifying a comparative occurrence of one or more existing medical conditions or new medical conditions in the first and second groups of patients;
calculating a probability value indicating a relative likelihood that a patient taking the new drug will have each of the one or more new or existing medical conditions in comparison to a likelihood that a patient taking the comparator drug will have each of the one or more new or existing medical conditions; and
displaying each new or existing medical condition and the probability value for the new drug and the comparator drug in accordance with one or more report parameters entered by the user.
5. The method according to claim 4, wherein the display
generated by the electronic user interface includes demographic characteristics, prevalence of diagnosis, prevalence of procedures, prevalence of drug class, or healthcare utilization.
6. The method according to claim 4, wherein the filter parameters include one or more diagnosis codes, procedure codes, drug categories, or demographic characteristics.
The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.
1. A method of recording information on a user recordable multi-layer record carrier having a plurality of information layers including at least a first information layer and a second information layer for storing information, the method comprising acts of:
receiving data content to be recorded on the user recordable multi-layer record carrier;
recording the data content on the user recordable multi-layer record carrier such that the data content is substantially evenly distributed between each of the plurality of information layers and recorded in compliance with a ROM (read only memory) record carrier standard, wherein portions of the data content are recorded in data areas of the first and second information layers such that the data areas are superjacent; and
shifting middle zone areas of at least the first and second information layers towards an inner radius of the disc such that inner radius data areas of the first and second information layers are filled with a portion of the recorded data content if the user recordable multi-layer record carrier is recorded with less than a full capacity of the user recordable multi-layer record carrier.
2. The method of claim 1, wherein the recordable multi-layer record carrier is an optical disk.
3. The method of claim 1, wherein recording comprises acts of dividing the received data content into portions of substantially equal size, and recording the portions of the data content to the data areas of the plurality of information layers.
4. The method of claim 3, wherein dividing the data content into portions of substantially equal size comprises an act of dividing the data content based on recording time.
5. The method of claim 3, wherein dividing the data content into portions of substantially equal size comprises an act of dividing the data content based on a size of the data content to be recorded.
6. The method of claim 1, wherein the data content is video data.
7. The method of claim 1, wherein the data content is audio data.
8. The method of claim 1, wherein the data content is audiovisual data.
9. A user recordable multi-layer record carrier, said record carrier comprising:
a plurality of information layers including at least a first information layer and a second information layer for storing data content recorded on the user recordable multi-layer record carrier such that the data content is substantially evenly distributed between each of the plurality of information layers and recorded in compliance with a ROM (read only memory) record carrier standard,
wherein portions of the data content are recorded in data areas of the first and second information layers such that the data areas are of substantially equal size and are superjacent and wherein middle zone areas of at least the first and second information layers are shifted towards an inner radius of the disc such that inner radius data areas of the first and second information layers are filled with a portion of the recorded data content if the user recordable multi-layer record carrier is recorded with less than a full capacity of the user recordable multi-layer record carrier.
10. A method of recording information on a user recordable multi-layer optical disc having a plurality of information layers, the method comprising acts of:
receiving data content to be recorded on the user recordable multi-layer optical disk; and
recording the data content in data areas of the plurality of information layers such that the data content is substantially evenly distributed between each of the plurality of information layers and recorded in compliance with a ROM (read only memory) record carrier standard,
wherein recording includes an act of shifting middle zone areas of the plurality of information layers towards an inner radius of the disc if the user recordable multi-layer optical disk is recorded with less than a full capacity of the user recordable multi-layer optical disk such that the data area of the plurality of information layers are (i) substantially equal size, (ii) substantially filled with a portion of the recorded data content and are (iii) spatially aligned.
11. The method of claim 10, wherein recording the data content comprises an act of dividing the data content into portions of substantially equal size, and recording the portions of the data content to the data areas of the plurality of information layers.
12. The method of claim 11, wherein dividing the data content into portions of substantially equal size comprises an act of dividing the data content based on recording time.
13. The method of claim 11, wherein dividing the data content into portions of substantially equal size comprises an act of dividing the data content based on a size of the data content to be recorded.
14. The method of claim 10, wherein the data content is video data.
15. The method of claim 10, wherein the data content is audio data.
16. The method of claim 10, wherein the data content is audiovisual data.