<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kim JS</submitter><funding>National Institute of Arthritis and Musculoskeletal and Skin Diseases</funding><funding>Sara and Alex Othon Research Fund</funding><funding>Jerome L. Greene Foundation</funding><funding>Chresanthe Staurulakis Memorial Fund</funding><funding>Johns Hopkins inHealth initiative</funding><funding>Manugian Family Scholar</funding><funding>NIH/NIAMS</funding><funding>Scleroderma Research Foundation</funding><funding>Donald B. and Dorothy L. Stabler Foundation</funding><funding>Nancy and Joachim Bechtle Precision Medicine Fund for Scleroderma</funding><pagination>197-207</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12919693</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>78(2)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>In complex diseases, it is challenging to assess a patient's disease state, trajectory, treatment exposures, and risk of multiple outcomes simultaneously, efficiently, and at the point of care.&lt;h4>Methods&lt;/h4>We developed an interactive patient-level data visualization and analysis tool (VAT) that automates illustration of the trajectory of a patient with scleroderma across multiple organs and illustrates this relative to a reference population, including patient subgroups who share risk factors with the index patient, to improve estimation of disease state. We conducted VAT usability testing with patients and clinicians. We then embedded results from internally cross-validated, Bayesian multivariate mixed models that calculate an individual's risk of critical events, usi</pubmed_abstract><journal>Arthritis care &amp; research</journal><pubmed_title>Development of a Personalized Visualization and Analysis Tool to Improve Clinical Care in Complex Multisystem Diseases With Application to Scleroderma.</pubmed_title><pmcid>PMC12919693</pmcid><funding_grant_id>R01AR073208</funding_grant_id><funding_grant_id>K24AR080217</funding_grant_id><funding_grant_id>P30AR070254</funding_grant_id><pubmed_authors>Orbai AM</pubmed_authors><pubmed_authors>Smithwright R</pubmed_authors><pubmed_authors>Shah AB</pubmed_authors><pubmed_authors>Shah AA</pubmed_authors><pubmed_authors>Pitts SI</pubmed_authors><pubmed_authors>Hummers LK</pubmed_authors><pubmed_authors>Stewart W</pubmed_authors><pubmed_authors>Rosen A</pubmed_authors><pubmed_authors>Scott J</pubmed_authors><pubmed_authors>Kim JS</pubmed_authors><pubmed_authors>Koher D</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Woods A</pubmed_authors><pubmed_authors>Aslanbeik P</pubmed_authors><pubmed_authors>Zeger SL</pubmed_authors><pubmed_authors>Fisher L</pubmed_authors><pubmed_authors>Smith LN</pubmed_authors><pubmed_authors>Tibbils B</pubmed_authors><pubmed_authors>Gurses AP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of a Personalized Visualization and Analysis Tool to Improve Clinical Care in Complex Multisystem Diseases With Application to Scleroderma.</name><description>&lt;h4>Objective&lt;/h4>In complex diseases, it is challenging to assess a patient's disease state, trajectory, treatment exposures, and risk of multiple outcomes simultaneously, efficiently, and at the point of care.&lt;h4>Methods&lt;/h4>We developed an interactive patient-level data visualization and analysis tool (VAT) that automates illustration of the trajectory of a patient with scleroderma across multiple organs and illustrates this relative to a reference population, including patient subgroups who share risk factors with the index patient, to improve estimation of disease state. We conducted VAT usability testing with patients and clinicians. We then embedded results from internally cross-validated, Bayesian multivariate mixed models that calculate an individual's risk of critical events, usi</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-16T10:06:14.69Z</modification><creation>2026-07-09T10:48:55.22Z</creation></dates><accession>S-EPMC12919693</accession><cross_references><pubmed>40654109</pubmed><doi>10.1002/acr.25613</doi></cross_references></HashMap>