Other Coding
Item
inouye risk score >3 calculated on coventry claims
boolean
C3846158 (UMLS CUI [1])
Medicare Advantage Beneficiary Age
Item
medicare advantage beneficiaries age > 65 years
boolean
C2713369 (UMLS CUI [1,1])
C3853043 (UMLS CUI [1,2])
C0001779 (UMLS CUI [1,3])
Eligibility Duration
Item
continuous eligibility > 12 months prior to study
boolean
C1548635 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Ability Telephone Contact
Item
ability to be contacted via telephone
boolean
C0085732 (UMLS CUI [1,1])
C0039457 (UMLS CUI [1,2])
C0332158 (UMLS CUI [1,3])
Informed Consent
Item
subject is willing and able to provide informed consent
boolean
C0021430 (UMLS CUI [1])
Protocol Compliance
Item
willing to comply with all study procedures and be available for the duration of the study
boolean
C0525058 (UMLS CUI [1])
Cancer treatment | Chemotherapy | Therapeutic radiology procedure
Item
active cancer treatment (i.e. chemotherapy or radiation) in the past 6 months
boolean
C0920425 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
Skilled nursing facility
Item
living anywhere other than a community setting [i.e. skilled nursing facility (snf)]
boolean
C0037265 (UMLS CUI [1])
Just-in-time member
Item
just-in-time (jit) members
boolean
C1517626 (UMLS CUI [1,1])
C0680022 (UMLS CUI [1,2])
Members Geographic Location
Item
members with a geographic location > 60 from either st. louis or kansas city, mo.
boolean
C0680022 (UMLS CUI [1,1])
C0017446 (UMLS CUI [1,2])
Solid organ transplant Recipient
Item
solid organ transplant recipients
boolean
C0730400 (UMLS CUI [1,1])
C1709854 (UMLS CUI [1,2])
Study Subject Participation Status
Item
active enrollment in another clinical research study
boolean
C2348568 (UMLS CUI [1])