Showing 21-25 of 38 faqs:
Why is there not a higher volume of patients with EASI?

While assessments like EASI and the SCORAD index are commonly used in clinical trials, they are not practical for clinical practice because they are time-consuming and were not developed and validated for routine care. The dataset is a reflection of assessments conducted in routine care.

How does OM1 identify Non-Radiographic Axial Spondyloarthritis (nr-axSpA)?

OM1 flags a cohort of nr-AxSpA patients within the OM1 AxSpA dataset via clinical abstraction and machine learning (ML).Patients can also be identified using ICD-10 diagnosis code M45.A, Non-radiographic axial spondyloarthritis, effective October 2020.  The nr-AxSpA observation identifies patients who have been flagged with a non-radiographic status (True/False) and the qualifying date on which they[…]

Can phenotypes be identified in the SLE patient population?

Yes. The PremiOM SLE dataset includes deep clinical data, including laboratory assessments, observed and estimated disease activity measures, and treatments in patients with systemic disease. These data can be used in a range of methods to determine either a priori defined or machine-learning identified phenotypes. Please find our Lupus ebook for additional information.

Is the methodology behind the estimated SLEDAI scores validated?

Yes. The machine-learning based methodology for estimating SLEDAI scores for patients is fully validated and published (Alves P, Bandaria J, Leavy MB, et al. Validation of a machine learning approach to estimate Systemic Lupus Erythematosus Disease Activity Index score categories and application in a real-world dataset. RMD Open. 2021 May;7(2):e001586. (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141448/)