Vladimir Rigodon

Data Analyst

Vladimir Rigodon

Vlad is a Clinical Data Analyst at the Renal Research Institute, collaborating with multidisciplinary teams to foster data stewardship and advance research initiatives. 

As clinical data analyst at RRI, he specializes in renal research and clinical trial support. He has over a decade of progressive experience in clinical data management and analysis, leveraging tools like R, SAS, Oracle, and SQL to extract and customize complex reporting requirements and provide actionable insights to stakeholders.

Before joining RRI, Vlad was a SAS programmer with Fresenius’s Custom Reporting and Data Analytics (CRDA) group, supporting the Global Medical Office and its partners. He began his career at Frenova Renal Research as a Clinical Research Associate (CCRA), where he monitored clinical trials to ensure protocol adherence and compliance with regulatory standards. His growing interest in bioinformatics and data analytics led him to transition into an analyst role, managing study-specific data extracts, contracts, and data licenses, while serving as a key liaison for project teams and programmers.

Vlad holds an MD and has a background in nutrition. He is currently pursuing a PhD at the Pontifical Catholic University of Paraná (PUCPR) in Brazil.

Recent Articles by Vladimir Rigodon

  • Peritoneal dialysis international
    January 20, 2026
    Anemia-independent prognostic value of iron deficiency in incident peritoneal dialysis patients
    Vladimir Rigodon, Murilo Guedes, Peter G Pecoits, Brianna Hartley, Yue Jiao, Len A Usvyat, Dinesh K Chatoth, Jeffrey L Hymes, Franklin W Maddux, Jeroen Kooman, Thyago P Moraes, Jochen G Raimann, Peter Kotanko, John W Larkin, Roberto Pecoits-Filho
    Background and objectivesIron plays a critical role beyond erythropoiesis, yet the prognostic significance of iron deficiency (ID) independent of anemia remains poorly defined in the peritoneal dialysis (PD) population. This study aimed to evaluate the association between iron status, specifically transferrin saturation (TSAT), and mortality in PD patients, independent of hemoglobin levels.Design, setting, participants, and measurementsWe conducted a retrospective cohort study of 11,013 adults who initiated PD at a large US dialysis network between December 2004 and January 2011. Patients had at least 180 days on PD and baseline data on TSAT, ferritin, hemoglobin, albumin, and white blood cell count. The primary outcome was all-cause mortality. Broadly adjusted associations between iron parameters and mortality were assessed using Cox proportional hazards models and restricted cubic splines, with adjustments for demographic, clinical, treatment-related, and laboratory variables including hemoglobin and ESA use.ResultsIron deficiency, defined as TSAT ≤20%, was present in 10% of patients at PD initiation. The cohort was 54% male and 70% Caucasian, with a mean age of 55 years; 39% had diabetes. While 91% received erythropoiesis-stimulating agents, only 34% received IV iron. After comprehensive adjustment, TSAT ≤20% remained independently associated with increased mortality (adjusted HR: 1.26; 95% CI: 1.12-1.42). Spline analyses showed a sharp rise in mortality risk at TSAT levels below 25%. Ferritin was inconsistently associated with mortality risk. During follow-up, 2704 deaths occurred (24.6% of the cohort) over a median 440-day follow-up.ConclusionsIron deficiency is common in incident PD patients and is associated with increased mortality risk, independent of anemia. These findings challenge current anemia-centric treatment paradigms and suggest that iron status, particularly TSAT, should be routinely assessed in PD patients regardless of hemoglobin levels. A prospective, randomized trial is warranted to evaluate whether proactive iron management improves outcomes in this population.

At RRI, data isn’t just numbers; it’s a powerful tool that drives innovation, improves patient outcomes, and transforms the way we care for individuals with kidney disease.

Vladimir Rigodon
Data Analyst