Glomerular Disease
Abstract
A phenotype for identifying patients with glomerular disease based on diagnoses and kidney biopsy procedures.
Downloadable content for this Phenotype includes two R files (cohorts.R and driver.R) and a specs folder, which includes the required concept sets.
Funder(s)
Provenance
Developed as part of the Preserving Kidney Function in Children with Chronic Kidney Disease (PRESERVE) study.
Description
The glomerular disease computable phenotype will identify a cohort of patients meeting criteria for glomerular disease based on criteria developed as part of the GLEAN study.
Inclusion Criteria
Broad pathways into the cohort:
- 2 or more glomerular inclusion diagnoses on different dates OR
- 1 or more glomerular inclusion diagnoses AND 1 or more kidney biopsy which is not post-transplant Inclusion diagnoses with special requirements:
- 1 or more “other_code_req” diagnosis AND 1 or more additional glomerular inclusion diagnosis on a different date OR 1 or more kidney biopsy that is not post-transplant
- 1 or more
neph_reqdiagnosis that is associated with a nephrology visit
Exclusion Criteria
- Inclusion events occur after
age_ub_years(defaults to 30), before the minimum date cutoff or after the maximum date cutoff, or after the patient’s endpoint date - Kidney biopsy occurs after a kidney transplant.
Vocabulary
Clinical Subjects
Related Publications
Creative Commons license
Except where otherwised noted, this item's license is described as a CC-BY Attribution 4.0 license.