Age
Item
1. female or male patient aged > 18 years old.
boolean
C0001779 (UMLS CUI [1])
Kidney Failure, Chronic | Dialysis | Patient Appropriate Kidney Transplantation
Item
2. esrd patient (on dialysis or preemptive) who is a potential candidate for kidney transplantation
boolean
C0022661 (UMLS CUI [1])
C0011946 (UMLS CUI [2])
C0030705 (UMLS CUI [3,1])
C1548787 (UMLS CUI [3,2])
C0022671 (UMLS CUI [3,3])
Laparoscopic sleeve gastrectomy
Item
3. undergone laparoscopic sleeve gastrectomy procedure > 3 months prior to enrollment.
boolean
C1960816 (UMLS CUI [1])
Informed Consent
Item
4. subjects have signed and dated the informed consent to participate in the study.
boolean
C0021430 (UMLS CUI [1])
Pharmaceutical Preparations Interaction Astagraf XL | Pharmaceutical Preparations Interaction Prograf | Pharmaceutical Preparations Interaction MMF
Item
1. patients taking a drug known to interact with astagraf xl, prograf®, or mmf.
boolean
C0013227 (UMLS CUI [1,1])
C0687133 (UMLS CUI [1,2])
C3666776 (UMLS CUI [1,3])
C0013227 (UMLS CUI [2,1])
C0687133 (UMLS CUI [2,2])
C0678125 (UMLS CUI [2,3])
C0013227 (UMLS CUI [3,1])
C0687133 (UMLS CUI [3,2])
C0209368 (UMLS CUI [3,3])
Hypersensitivity Astagraf XL | Hypersensitivity Prograf | Hypersensitivity MMF
Item
2. patients that have an allergy to astagraf xl, prograf®, or mmf.
boolean
C0020517 (UMLS CUI [1,1])
C3666776 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0678125 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0209368 (UMLS CUI [3,2])
Astagraf XL | Prograf | MMF
Item
3. patients currently taking astagraf xl, prograf®, or mmf.
boolean
C3666776 (UMLS CUI [1])
C0678125 (UMLS CUI [2])
C0209368 (UMLS CUI [3])
Leak Complication Postoperative
Item
4. post-surgical leak complication
boolean
C0332234 (UMLS CUI [1,1])
C0009566 (UMLS CUI [1,2])
C0032790 (UMLS CUI [1,3])
Adherence failed Laparoscopic sleeve gastrectomy Follow-up | Adherence failed Clinic Visits
Item
5. patients failing to adhere to post laparoscopic sleeve gastrectomy follow-up recommendations and clinic visits
boolean
C1510802 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C1960816 (UMLS CUI [1,3])
C3274571 (UMLS CUI [1,4])
C1510802 (UMLS CUI [2,1])
C0231175 (UMLS CUI [2,2])
C0008952 (UMLS CUI [2,3])
Medical condition Severe Treatment required for | Medical condition Severe | Requirement Treatment chronic | Medical condition Interferes with Study Subject Participation Status
Item
6. patients with any severe medical condition requiring acute or chronic treatment that in the investigator's opinion would interfere with study participation.
boolean
C3843040 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0332121 (UMLS CUI [1,3])
C3843040 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C1514873 (UMLS CUI [3,1])
C0087111 (UMLS CUI [3,2])
C0205191 (UMLS CUI [3,3])
C3843040 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C2348568 (UMLS CUI [4,3])
Pregnancy | Breast Feeding
Item
7. pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive laboratory test
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Pharmaceutical Preparations Interfere with Blood tacrolimus level | Pharmaceutical Preparations Interfere with Mycophenolate level | Drugs, Non-Prescription | Herbal Supplements | Grapefruit | GRAPEFRUIT JUICE
Item
8. currently taking or planning to initiate of any medications that could interfere with tacrolimus and/or mycophenolate blood levels, including over the counter (otc) medications, herbal supplements, grapefruit or grapefruit juice.
boolean
C0013227 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C1271702 (UMLS CUI [1,3])
C0013227 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C3669267 (UMLS CUI [2,3])
C0013231 (UMLS CUI [3])
C1504473 (UMLS CUI [4])
C0995150 (UMLS CUI [5])
C0452456 (UMLS CUI [6])
Exposure to Investigational Therapy
Item
9. subjects who have been exposed to an investigational therapy within 30 days prior to enrollment or 5 half-lives of the investigational product, whichever is greater.
boolean
C0332157 (UMLS CUI [1,1])
C0949266 (UMLS CUI [1,2])