ArticleBMC musculoskeletal disorders2018
Cohort identification of axial spondyloarthritis in a large healthcare dataset: current and future methods.
Article in BMC musculoskeletal disorders, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Machine learning models with time-series clinical features to predict radiographic progression in patients with ankylosing spondylitis.Journal of rheumatic diseases · 2024Article
- The Annual Diagnostic Prevalence of Ankylosing Spondylitis and Axial Spondyloarthritis in the United States Using Medicare and MarketScan Databases.ACR open rheumatology · 2021Article
- Utility of the Current Procedural Terminology Codes for Prophylactic Stabilization for Defining Metastatic Femur Disease.Journal of the American Academy of Orthopaedic Surgeons. Global research & reviews · 2020Article
- Early differential diagnosis of ankylosing spondylitis among patients with low back pain in primary care.BMC family practice · 2020Article
- Clinical features in primary care electronic records before diagnosis of ankylosing spondylitis: a nested case-control study.BMC family practice · 2020Article
- Incorporating natural language processing to improve classification of axial spondyloarthritis using electronic health records.Rheumatology (Oxford, England) · 2020Article
- Application of machine learning in the diagnosis of axial spondyloarthritis.Current opinion in rheumatology · 2019Review
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Authors and funding
7 authors.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundBig data research is important for studying uncommon diseases in real-world settings. Most big data studies in axial spondyloarthritis (axSpA) have been limited to populations identified with billing codes for ankylosing spondylitis (AS). axSpA is a more inclusive concept, and reliance on AS codes does not produce a comprehensive axSpA study population. The first objective was to describe our process for establishing an appropriate sample of patients with and without axSpA for developing accurate axSpA identification methods. The second objective was to determine the classification performance of AS billing codes against the chart-reviewed axSpA reference standard.
methodsVeteran Health Affairs clinical and administrative data, between January 2005 and June 2015, were used to randomly select patients with clinical phenotypes that represented high, moderate, and low likelihoods of an axSpA diagnosis. With chart review, the sampled patients were classified as Yes axSpA, No axSpA or Uncertain axSpA, and these classification assignments were used as the reference standard for determining the positive predictive value (PPV) and sensitivity of AS ICD-9 codes for axSpA.
resultsSix hundred patients were classified as Yes axSpA (26.8%), No axSpA (68.3%), or Uncertain axSpA (4.8%). The PPV and sensitivity of an AS ICD-9 code for axSpA were 83.3% and 57.3%, respectively.
conclusionsStandard methods of identifying axSpA patients in a large dataset lacked sensitivity. An appropriate sample of patients with and without axSpA was established and characterized for developing novel axSpA identification methods that are anticipated to enable previously impractical big data research.
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