Adult | Age
Item
adult patients, >/= 18 years of age
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Chronic Hepatitis C Genotype
Item
chronic hepatitis c genotype 1
boolean
C0524910 (UMLS CUI [1,1])
C1533728 (UMLS CUI [1,2])
Therapy naive | PEGINTERFERON Absent | Interferon Absent | Ribavirin Absent
Item
treatment-naïve, i.e. have not been previously treated with pegylated interferon, standard interferon and ribavirin
boolean
C0919936 (UMLS CUI [1])
C0982327 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C3652465 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0035525 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Serum Hepatitis C RNA positive
Item
confirmed serum positive hcv rna
boolean
C0229671 (UMLS CUI [1,1])
C0855842 (UMLS CUI [1,2])
Liver Fibrosis Histology | Liver Fibrosis Fibroscan
Item
liver fibrosis confirmed histologically or by fibroscan up to 24 months before treatment
boolean
C0239946 (UMLS CUI [1,1])
C0344441 (UMLS CUI [1,2])
C0239946 (UMLS CUI [2,1])
C4522043 (UMLS CUI [2,2])
Medical contraindication Pegasys | Medical contraindication Copegus
Item
any contraindications according to the summary of product characteristics for pegasys or copegus
boolean
C1301624 (UMLS CUI [1,1])
C1176430 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C1170183 (UMLS CUI [2,2])
HBV coinfection | Human immunodeficiency virus (HIV) coinfection
Item
co-infection with hepatitis b or hiv
boolean
C2242656 (UMLS CUI [1])
C4062778 (UMLS CUI [2])
Patients Post Transplantation
Item
post-transplant patients
boolean
C0030705 (UMLS CUI [1,1])
C0687676 (UMLS CUI [1,2])
C0040732 (UMLS CUI [1,3])
Kidney Failure, Chronic | Creatinine clearance measurement
Item
end stage renal disease (creatinine clearance < 15 ml/min)
boolean
C0022661 (UMLS CUI [1])
C0373595 (UMLS CUI [2])
Immunotherapy
Item
patients treated with immunotherapy
boolean
C0021083 (UMLS CUI [1])
Pregnancy | Gender Partner Pregnancy
Item
pregnant women and male partners of women who are pregnant
boolean
C0032961 (UMLS CUI [1])
C0079399 (UMLS CUI [2,1])
C0682323 (UMLS CUI [2,2])
C0032961 (UMLS CUI [2,3])
Childbearing Potential Contraceptive methods Unable | Childbearing Potential Contraceptive methods Unwilling | Gender Partner Childbearing Potential | Gender Contraceptive methods Unable | Gender Contraceptive methods Unwilling
Item
female patients of childbearing potential and male patients with female partners of childbearing potential who are unable or unwilling to use effective and continuous contraception during the treatment and for 4 months (females) and 7 months (males) thereafter
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
C0079399 (UMLS CUI [3,1])
C0682323 (UMLS CUI [3,2])
C3831118 (UMLS CUI [3,3])
C0079399 (UMLS CUI [4,1])
C0700589 (UMLS CUI [4,2])
C1299582 (UMLS CUI [4,3])
C0079399 (UMLS CUI [5,1])
C0700589 (UMLS CUI [5,2])
C0558080 (UMLS CUI [5,3])